UMLS. CSP-HL7-ICD9CM-NCI-NDFRT-RXNORM
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A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
selected terms: 70,266 page 1 of 703

1.
[ ] (UMLS (ICD9CM) C0730521) Less than 24 completed weeks of gestation =Finding
51. (-)-Cholesterol
[C27H46O, the major fatty steroid alcohol of vertebrate animals, distributed in body tissues, especially the brain and spinal cord, and in animal fats and oils. ( CSP )] (UMLS (NCI) C0008377) =Steroid; Biologically Active Substance ;
=cholestane compound;
Cholestenes;
sterol;
Unclassified Ingredient Preparations =hydroxycholesterol;
cholesterol oxide;
SALICYLIC ACID 40% OINTMENT(GM);
BASLE CREAM,TOP;
ALUMINUM ACETATE/ZINC OXIDE PASTE,TOP;
CHOLESTEROL 3 %;
2. "" w/o Surgery Capability
(UMLS (HL7) C1548830) =Health Care Activity =Consent Type;
52. (-)-Cyclophosphamide
[precursor of an alkylating nitrogen mustard antineoplastic and immunosuppressive agent; used in the treatment of lymphomas, leukemias and other cancers, and as an immunosupressive agent to prevent transplant rejection; its side effect, alopecia, has been used for defleecing sheep; may also cause sterility, birth defects, mutations, and cancer. ( CSP )] (UMLS (NCI) C0010583) =Organophosphorus Compound; Pharmacologic Substance =[AN000] ANTINEOPLASTICS;
phosphamide;
[IM600] IMMUNE SUPPRESSANTS;
Phosphoramide Mustards;
Antineoplastic Alkylating Agent;
=2-oxo-N,3-bis-(2-chloroethyl) tetrahydro-2H-1,3,2-oxazaphosphorin- 2-amine;
CYCLOPHOSPHAMIDE 100 MG;
CYCLOPHOSPHAMIDE 200 MG;
CYCLOPHOSPHAMIDE 500 MG;
CYCLOPHOSPHAMIDE 25 MG;
CYCLOPHOSPHAMIDE 50 MG;
CYCLOPHOSPHAMIDE 2 GM;
CYCLOPHOSPHAMIDE 1 GM;
CYCLOPHOSPHAMIDE 1 GM/VIL;
CYCLOPHOSPHAMIDE 2 GM/VIL
3. ((o-Carboxyphenyl)thio)ethylmercury, Sodium Salt
[An organomercurial compound and derivative of thiosalicyclic acid with antibacterial and antifungal properties. Although the mechanism of action has not been fully elucidated, thimerosal inhibits sulfhydryl-containing active site of various enzymes and binds to sulfhydryl compounds, such as glutathione, cysteine, and SH groups of proteins. In addition, thimerosal activates the InsP3 calcium channel on endoplasmic reticular membrane, thereby triggering the release of calcium from intracellular stores resulting in a calcium-induced calcium-influx of extracellular calcium. Consequently, thimerosal may induce or inhibit cellular functions dependent on calcium signaling. ( NCI )] (UMLS (NCI) C0039867) =Organic Chemical; Pharmacologic Substance ;
=Ethylmercury Compounds;
[DE101] ANTIBACTERIAL, TOPICAL;
Inactive Ingredient Preparations;
=xylometazoline 1 MG/ML Nasal Solution;
BORIC ACID/NA BORATE SOLN IRRG,OPH;
DESOXYRIBONUCLEASE 15000 UNT / FIBRINOLYSIN 25 UNT IRRIGATION SOLUTION;
HEMOPHILUS B CONJUGATE VACCINE INJ;
HEPATITIS B IMMUNE GLOBULIN (IM) INJ;
INFLUENZA VIRUS VACCINE (SPLIT VIRUS),SYRINGE,0.5ML;
INFLUENZA VIRUS VACCINE (SPLIT VIRUS),VIL,5ML;
Polyvinyl Alcohol 0.3 ML/ML Ophthalmic Solution;
Rabies Immune Globulin (Human) Inj 150 IU/ML;
TETANUS IMMUNE GLOBULIN,HUMAN 250UNT/ML INJ,SYRINGE,1ML;
THIMEROSAL SWAB, MEDICATED;
INFLUENZA SUBVIRON VACCINE,VIL,5ML;
INFLUENZA SUBVIRON VACCINE,SYRINGE,0.5ML;
THIMEROSAL 0.001 %;
THIMEROSAL 0.002 %;
THIMEROSAL 0.005 %;
THIMEROSAL 0.01 %;
THIMEROSAL 0.07 %;
THIMEROSAL 1:1000;
THIMEROSAL 0.1 %;
THIMEROSAL 0.004 %
53. (-)-Ephedrine
[alpha- and beta-adrenergic agonist that may also enhance release of norepinephrine; has been used in the treatment of several disorders including asthma, heart failure, rhinitis, and urinary incontinence, and for its central nervous system stimulatory effects in the treatment of narcolepsy and depression. ( CSP )] (UMLS (NCI) C0014479) =Organic Chemical; Pharmacologic Substance ;
=adrenergic agent;
bronchodilator;
Phenethylamines;
Propanolamines;
[AU100] SYMPATHOMIMETICS (ADRENERGICS);
[RE103] BRONCHODILATORS, SYMPATHOMIMETIC,ORAL =PSEUDOEPHEDRINE;
cinnamedrine;
EPHEDRINE HYDROCHLORIDE;
EPHEDRINE SULFATE;
EPHEDRINE TANNATE;
EPHEDRINE HYDROCHLORIDE;
EPHEDRINE SULFATE;
EPHEDRINE TANNATE;
4. (+ -)-Carbovir
[An anti-HIV agent that exerts its effects by inhibiting reverse transcriptase. ( NCI )] (UMLS (NCI) C0054727) =Nucleic Acid, Nucleoside, or Nucleotide; Pharmacologic Substance ;
54. (-)-Epigallocatechin 3-gallate
[A phenolic antioxidant found in a number of plants such as green and black tea. It inhibits cellular oxidation and prevents free radical damage to cells. It is under study as a potential cancer chemopreventive agent. (NCI) ( NCI )] (UMLS (NCI) C0059438) =Organic Chemical; Pharmacologic Substance ;
5. (+)-(4S)-4,11-diethyl-4-hydroxy-9-[(4-piperidino-piperidino)carbonyloxy]-1H-pyrano[3',4':6,7]indolizino[1,2-b]quinol-3,14,(4H,12H)-dione
[DNA topoisomerase I inhibitor. ( CSP )] (UMLS (NCI) C0123931) =Organic Chemical; Pharmacologic Substance ;
=[AN000] ANTINEOPLASTICS;
(+)-Camptothecin;
enzyme inhibitor;
=Irinotecan Hydrochloride
55. (-)-Epothilone B
[A substance that is being studied as a treatment for cancer. It belongs to the family of drugs called epothilones. Also called EPO906. ( NCI )] (UMLS (NCI) C0297960) =Organic Chemical; Pharmacologic Substance
6. (+)-(S)-4,4'-(1-Methyl-1,2-ethanediyl)di(2,6-piperazinedione)
[A drug used to protect the heart from the toxic effects of anthracycline drugs such as doxorubicin. It belongs to the family of drugs called chemoprotective agents. ( NCI )] (UMLS (NCI) C0086444) =Organic Chemical; Pharmacologic Substance ;
=Razoxane;
[CV900] CARDIOVASCULAR AGENTS, OTHER =Dexrazoxane Hydrochloride;
56. (-)-Hydromorphone
[The hydrogenated ketone of morphine, a semi-synthetic opioid with analgesic effects. Hydromorphone selectively binds the mu-opioid receptor which is linked through G-proteins. Binding stimulates the exchange of guanosine triphosphate (GTP) for guanosine diphosphate (GDP) on the G-protein complex and interacts with and inhibits adenylate cyclase located at the inner surface of the plasma membrane. This leads to a reduction in intracellular cyclic 3',5'-adenosine monophosphate (cAMP). Further, voltage-gated potassium channels are activated, thereby causing hyperpolarization and reducing neuronal excitability. In addition, the opening of voltage-gated calcium channels is inhibited, thereby leading to an inhibition of calcium entry and a reduction in the release of various neurotransmitters, including GABA, vasopressin, somatostatin, insulin and glucagons. ( NCI )] (UMLS (NCI) C0012306) =Organic Chemical; Pharmacologic Substance =[CN101] OPIOID ANALGESICS;
Morphine Derivatives =OXYMORPHONE;
HYDROMORPHONE HYDROCHLORIDE;
HYDROMORPHONE 2 MG
7. (+)-1-Beta-D-arabinofuranosyl-5-[(E)-2-bromovi- ny1] uracil
[A synthetic thymidine analogue with potent antiviral activity against herpes simplex and varicella zoster viruses. Sorivudine is phosphorylated into triphosphate form within the cells and this metabolite interferes with viral DNA replication by inhibiting DNA polymerase activity without been incorporated into elongating viral DNA. Due to the dangerous effects of drug-drug interactions via its metabolite, sorivudine has been removed from the market. ( NCI )] (UMLS (NCI) C0207628) =Organic Chemical; Pharmacologic Substance ;
57. (-)-L-alpha-Hydrazino-3,4-dihydroxy-alpha-methylhydrocinnamic Acid
[A hydrazine derivative of dopa. Carbidopa is a peripheral dopa decarboxylase inhibitor that is used as an adjunct to levodopa administration to prevent peripheral biosynthesis of levodopa to dopamine, thereby reducing peripheral side effects. Carbidopa does not penetrate the blood brain barrier so that levodopa, after it reaches the brain, can be metabolized to dopamine by dopa decarboxylase where it exerts its effect on dopamine receptors. ( NCI )] (UMLS (NCI) C0006982) =Organic Chemical; Pharmacologic Substance =[CN500] ANTIPARKINSON AGENTS;
hydrazine;
3-Hydroxy-alpha-methyl-L-tyrosine;
=CARBIDOPA 25 MG;
CARBIDOPA 50 MG;
CARBIDOPA 10 MG;
Carbidopa 12.5 MG / entacapone 200 MG / Levodopa 50 MG Oral Tablet;
CARBIDOPA 37.5 MG;
8. (+)-2-(2-((p-Chloro-alpha-methyl-alpha-phenylbenzyl)oxy)ethyl)-1-methyl Pyrrolidine Fumarate
[A synthetic ethanolamine with anticholinergic, sedative, and histamine H1 antagonistic properties. Clemastine fumarate blocks the H1 histamine receptor and prevents the symptoms that are caused by histamine activity on capillaries, bronchial and gastrointestinal smooth muscles, including vasodilation, increased capillary permeability, bronchoconstriction, and spasmodic contraction of gastrointestinal smooth muscles. This drug also prevents histamine-induced pain and itching of mucous membranes. ( NCI )] (UMLS (NCI) C0546858) =Organic Chemical; Pharmacologic Substance =CLEMASTINE;
=CLEMASTINE FUMARATE 0.67 MG/5ML;
CLEMASTINE FUMARATE 1.34 MG;
CLEMASTINE FUMARATE 2.68 MG;
58. (-)-N -Methyl-3-phenyl-3-(o-tolyloxy)-propylamine Hydrochloride
[The hydrochloride salt of atomoxetine, a phenoxy-3-propylamine derivative and selective non-stimulant, norepinephrine reuptake inhibitor with cognitive-enhancing activity. Although its precise mechanism of action is unknown, atomoxetine appears to selectively inhibit the pre-synaptic norepinephrine transporter, resulting in inhibition of the presynaptic reabsorption of norepinephrine and prolongation of norepinephrine activity in the synaptic cleft. The effect on cognitive brain function may result in improved attention and decreased impulsivity and activity levels. ( NCI )] (UMLS (NCI) C1170741) (-)-N-methyl-gamma(2-methylphenoxy)benzenepropamine Hydrochloride;
ATOMOXETINE HCL;
ATOMOXETINE HCL UNIDENTIFIED;
ATOMOXETINE HCL PREPARATION;
ATOMOXETINE HCL UNIDENTIFIED;
ATOMOXETINE HYDROCHLORIDE =Organic Chemical; Pharmacologic Substance =ATOMOXETINE;
Unclassified Ingredients =atomoxetine 10 MG;
atomoxetine 18 MG;
atomoxetine 25 MG;
atomoxetine 40 MG;
atomoxetine 60 MG;
9. (+)-2-(p-Chloro-alpha-(2-(dimethylamino)ethyl)benzyl)pyridine Maleate(1:1)
[The maleate salt form of dexchlorpheniramine, an alkylamine, and first-generation histamine antagonist with anti-allergic activity. Dexchlorpheniramine maleate competitively blocks H1 receptors, thereby preventing the actions of histamine on bronchial smooth muscle, capillaries and gastrointestinal (GI) smooth muscle. This prevents histamine-induced bronchoconstriction, vasodilation, increased capillary permeability, and GI smooth muscle spasms. ( NCI )] (UMLS (NCI) C0137440) =Organic Chemical; Pharmacologic Substance ;
=DEXCHLORPHENIRAMINE;
=DEXCHLORPHENIRAMINE MALEATE 2 MG/5ML;
DEXCHLORPHENIRAMINE MALEATE 2 MG;
DEXCHLORPHENIRAMINE MALEATE 4 MG;
DEXCHLORPHENIRAMINE MALEATE 6 MG;
59. (-)-Naloxone
[specific opiate antagonist with no agonist activity, a competitive antagonist at mu, delta, and kappa opioid receptors. ( CSP )] (UMLS (NCI) C0027358) =Organic Chemical; Pharmacologic Substance ;
=morphinan;
MORPHINE;
Narcotic Antagonist;
[CN102] OPIOID ANTAGONIST ANALGESICS =NALTREXONE;
NALOXONE HYDROCHLORIDE;
10. (+)-2-Ethoxy-alpha-(((S)-alpha-isobutyl-o-piperidinobenzyl)carbamoyl)-p-toluic Acid
[A benzoic acid derivative belonging to the meglitinide class of antidiabetic agents. Repaglinide blocks ATP-dependent potassium channels in pancreatic beta cells, thereby causing depolarization of the cell membrane and subsequent opening of calcium channels. The increased calcium influx into the pancreatic beta cells induces insulin secretion, thereby lowering blood glucose levels. ( NCI )] (UMLS (NCI) C0246689) =Organic Chemical; Pharmacologic Substance ;
=carbamate;
Piperidines;
[HS502] HYPOGLYCEMIC AGENTS, ORAL;
=REPAGLINIDE 1 MG;
REPAGLINIDE 2 MG;
REPAGLINIDE 0.5 MG
60. (-)-Nicotine
[very poisonous alkaloid; the prototypical agonist at nicotinic cholinergic receptors where it dramatically stimulates neurons and ultimately blocks synaptic transmission; nicotine is important medically because of its presence in tobacco smoke, and is also used as an insecticide. ( CSP )] (UMLS (NCI) C0028040) =Organic Chemical; Pharmacologic Substance; Hazardous or Poisonous Substance =alkaloid;
pyridine;
Solanaceous Alkaloids;
cholinergic agent;
[AD900] ANTIDOTES/DETERRENTS, OTHER;
=nicotine replacement;
Nicotine Polacrilex;
NICOTINE 10 MG/ML;
NICOTINE 10 MG;
NICOTINE 15 MG;
NICOTINE 21 MG;
NICOTINE 14 MG;
NICOTINE 22 MG;
NICOTINE 7 MG;
NICOTINE 11 MG
11. (+)-4-((S)-alpha,2,3-Trimethylbenzyl)imidazole
[An imidazole derivate and active d-isomer of medetomidine with analgesic, anxiolytic and sedative properties. Dexmedetomidine selectively binds to presynaptic alpha-2 adrenoceptors located in the brain, thereby inhibiting the release of norepinephrine from synaptic vesicles. This leads to an inhibition of postsynaptic activation of adrenoceptors, which inhibit sympathetic activity, thereby leading to sedation and anxiolysis. The analgesic effect of this agent is mediated by binding to alpha2-adrenoceptors in the spinal cord. ( NCI )] (UMLS (NCI) C0113293) =Organic Chemical; Pharmacologic Substance =imidazole;
[CN309] SEDATIVES/HYPNOTICS, OTHER =DEXMEDETOMIDINE HCL
61. (-)-Phenylisopropylmethylpropynylamine
[The hydrochloride salt form of selegiline, a levorotatory acetylenic derivative of phenethylamine with antiparkinsonian effect. As a selective monoamine oxidase (MAO) inhibitor, selegiline has the greatest affinity for type B MAO, found mainly in the brain. Selegiline is converted by MAO B to an active moiety, which binds irreversibly at the active site of the enzyme's cofactor FAD (flavin adenine dinucleotide) molecule. This prevents the oxidative deamination of catecholamines and serotonin by MAO B, and leads to an increase in these neurotransmitters' activities resulting in improved motor function. In addition, this agent may inhibit re-uptake of dopamine by the neuron and prolong dopamine activity. ( NCI )] (UMLS (NCI) C0700467) =Organic Chemical; Pharmacologic Substance =l-Deprenyl;
=SELEGILINE HYDROCHLORIDE 5 MG;
12. (+)-4-Amino-3-isoxazolidinone
[An analogue of the amino acid D-alanine with broad-spectrum antibiotic and glycinergic activities. D-cycloserine interferes with bacterial cell wall synthesis by competitively inhibiting two enzymes, L-alanine racemase and D-alanine:D-alanine ligase, thereby impairing peptidoglycan formation necessary for bacterial cell wall synthesis. This agent may be bactericidal or bacteriostatic, depending on its concentration at the infection site and the susceptibility of the organism. In addition, D-cycloserine is an excitatory amino acid and partial agonist at the glycine binding site of the NMDA receptor in the central nervous system (CNS); binding to the central NMDA receptor may result in amelioration of neuropathic pain. ( NCI )] (UMLS (NCI) C0010590) =Amino Acid, Peptide, or Protein; Antibiotic =2-Amino-3-hydroxypropionic Acid;
[AM500] ANTITUBERCULARS =CYCLOSERINE 250 MG;
62. (-)-Quinine
[quinine ascorbate is listed by USP as a smoking deterrent. ( CSP )] (UMLS (NCI) C0034417) =Organic Chemical; Pharmacologic Substance ;
=alkaloid;
Antimalarials;
Cinchona Alkaloids;
1 benzazine;
quinuclidine;
=QUININE SULFATE
13. (+)-6-((4-Chlorophenyl)-1H-1,2,4-triazol-1-ylmethyl)-1-methyl-1H-benzotriazole
[A hormone therapy drug used to decrease the production of estrogen. ( NCI )] (UMLS (NCI) C0286224) =Organic Chemical; Pharmacologic Substance
63. (-)-Salbutamol Hydrochloride
[The hydrochloride salt form of levalbuterol, a relatively selective sympathomimetic beta2 receptor agonist with bronchodilator activity. Levalbuterol hydrochloride binds to beta2-adrenergic receptors in bronchial smooth muscle and activates intracellular adenyl cyclase, thereby increasing the production of cyclic-3', 5'-adenosine monophosphate (cAMP). Increased cAMP levels lead to the activation of protein kinase A, which inhibits the phosphorylation of myosin and lowers intracellular ionic calcium concentrations, resulting in relaxation of bronchial smooth muscles. The increased cyclic AMP concentrations also inhibit the release of inflammatory mediators from mast cells. ( NCI )] (UMLS (NCI) C0772502) 1,3-Benzenedimethanol, alpha1-(((1,1-dimethylethyl)amino)methyl)-4-hydroxy-, Hydrochloride,(alpha1R)-;
LEVALBUTEROL HYDROCHLORIDE;
=Organic Chemical; Pharmacologic Substance
14. (+)-6-[Amino(4-chlorophenyl)(1-methyl-1H-imidazol-5-yl)methyl]-4-(3-chlorophenyl)-1-methyl-2(1H)-quinolinone
[An anticancer drug that inhibits the transformation of normal cells to cancer cells. It belongs to the family of drugs called enzyme inhibitors. ( NCI )] (UMLS (NCI) C1176289) Tipifarnib;
=Organic Chemical; Pharmacologic Substance
64. (-)-Thalidomide
[piperidinyl isoindole originally introduced as a non-barbiturate hypnotic, but withdrawn due to teratogenic effects; it has been reintroduced and used for a number of immunological and inflammatory disorders. ( CSP )] (UMLS (NCI) C0039736) =Organic Chemical; Pharmacologic Substance; Hazardous or Poisonous Substance =[CN100] ANALGESICS;
[CN300] SEDATIVES/HYPNOTICS;
phthalimide;
Piperidones;
Teratogen;
[IM900] IMMUNOLOGICAL AGENTS, OTHER =THALIDOMIDE 50 MG;
THALIDOMIDE 100 MG;
THALIDOMIDE 200 MG
15. (+)-A 127722
(UMLS (NCI) C0663262) =Organic Chemical; Pharmacologic Substance ;
65. (--)-2Amino-3-)3,4-dihydroxyphenyl)propanoic Acid
[naturally occuring form of DOPA and precursor of dopamine; used as an antiparkinsonian agent; unlike dopamine it can be administered orally. ( CSP )] (UMLS (NCI) C0023570) =Amino Acid, Peptide, or Protein; Pharmacologic Substance; Neuroreactive Substance or Biogenic Amine ;
=[CN500] ANTIPARKINSON AGENTS;
dihydroxyphenylalanine =LEVODOPA 100 MG;
LEVODOPA 200 MG;
LEVODOPA 250 MG;
Carbidopa 12.5 MG / entacapone 200 MG / Levodopa 50 MG Oral Tablet;
LEVODOPA 150 MG
16. (+)-Aldosterone
[hormone secreted by the adrenal cortex that regulates electrolyte and water balance by increasing the renal retention of sodium and the excretion of potassium. ( CSP )] (UMLS (NCI) C0002006) =Steroid; Pharmacologic Substance; Hormone
66. (.+ -.)-p-Isobutylhydratropic acid
[nonsteroidal analgesic, antipyretic and anti-inflammatory agent that is a propionic acid derivative. ( CSP )] (UMLS (NCI) C0020740) =Organic Chemical; Pharmacologic Substance ;
=[CN100] ANALGESICS;
NSAIDs;
[CN850] ANTIPYRETICS;
benzoate;
Phenylpropionates;
[MS102] NONSALICYLATE NSAIS, ANTIRHEUMATIC;
[CN104] NONSTEROIDAL ANTI-INFLAMMATORY ANALGESICS;
=IBUPROFEN 100 MG;
IBUPROFEN 100 MG/5ML;
IBUPROFEN 200 MG;
IBUPROFEN 300 MG;
IBUPROFEN 600 MG;
IBUPROFEN 800 MG;
IBUPROFEN 400 MG;
17. (+)-alpha-Tocopherol
[A naturally-occurring form of vitamin E, a fat-soluble vitamin with potent antioxidant properties. Considered essential for the stabilization of biological membranes (especially those with high amounts of polyunsaturated fatty acids), d-alpha-Tocopherol is a potent peroxyl radical scavenger and inhibits noncompetitively cyclooxygenase activity in many tissues, resulting in a decrease in prostaglandin production. Vitamin E also inhibits angiogenesis and tumor dormancy through suppressing vascular endothelial growth factor (VEGF) gene transcription. (NCI04) ( NCI )] (UMLS (NCI) C0969677) .alpha. Tocopherol;
3,4-Dihydro-2,5,7,8-tetramethyl-2-(4,8,12-trimethyltridecyl)-2H-1-benzopyran-6-ol;
alpha Tocopherol;
ALPHA-TOCOPHEROL;
d-Alpha-Tocopherol;
Tocopherol-Alpha;
Tocopherol-D-Alpha;
=Lipid; Pharmacologic Substance; Vitamin
67. (.+-.)-Hexestrol
[A synthetic hydrogenated derivative of diethylstilbestrol (DES). Hexestrol exhibits strong affinity for estrogen receptors that are overexpressed in some types of cancers. When conjugated with a neoplastic drug, hexestrol may selectively concentrate the cytotoxic agent in estrogen receptor-rich tumors. This agent may also be mutagenic. (NCI04) ( NCI )] (UMLS (NCI) C0019467) =Organic Chemical; Pharmacologic Substance; Hormone
18. (+)-alpha-Tocopherol Acetate
[The acetate ester of a fat-soluble vitamin with potent antioxidant properties. Considered essential for the stabilization of biological membranes (especially those with high amounts of polyunsaturated fatty acid), vitamin E is a generic name for a group of compounds known as tocopherols and tocotrienols (tocols). This agent is a potent peroxyl radical scavenger and inhibits noncompetitively cyclooxygenase activity in many tissues, resulting in a decrease in prostaglandin production. Vitamin E also inhibits angiogenesis and tumor dormancy through suppressing vascular endothelial growth factor (VEGF) gene transcription. (NCI04) ( NCI )] (UMLS (NCI) C0078373) =Organic Chemical; Pharmacologic Substance; Vitamin =(+/-)-alpha-Tocopherol;
(+)-alpha-Tocopherol Acetate;
Unclassified Ingredient Preparations;
=(+)-alpha-Tocopherol Acetate;
THICKENUP POWDER;
TOCOPHERYL ACETATE,ALPHA 15 MG;
TOCOPHERYL ACETATE,ALPHA 30 UNT;
OMEGA-3 (N-3) POLYUNSATURATED FATTY ACIDS 1GM CAP;
TOCOPHERYL ACETATE,D-ALPHA 30 MG;
VITAMIN E ACETATE 30 IU;
VITAMIN E ACETATE 30 UNT;
68. (.+-.)-Noradrenaline
[precursor of epinephrine; widespread central and autonomic neurotransmitter, principal transmitter of most postganglionic sympathetic fibers; secreted by the adrenal medulla; used pharmacologically as a sympathomimetic. ( CSP )] (UMLS (NCI) C0028351) =Organic Chemical; Pharmacologic Substance; Neuroreactive Substance or Biogenic Amine =adrenergic agent;
catecholamine;
Adrenal;
Neurotransmitter;
adrenal medulla hormone;
[AU100] SYMPATHOMIMETICS (ADRENERGICS) =Nordefrin;
(2R,3R)-(R)-4-(2-Amino-1-hydroxyethyl)-1,2-benzenediol, 2,3-Dihydoxybutanedioate Monohydrate (1:1) (Salt);
ethylnorepinephrine;
(2R,3R)-(R)-4-(2-Amino-1-hydroxyethyl)-1,2-benzenediol, 2,3-Dihydoxybutanedioate Monohydrate (1:1) (Salt)
19. (+)-Biotin
[water-soluble, enzyme cofactor present in minute amounts in every living cell; occurs mainly bound to proteins or polypeptides and is abundant in liver, kidney, pancreas, yeast, and milk. ( CSP )] (UMLS (NCI) C0005575) =Organic Chemical; Pharmacologic Substance; Vitamin
69. (1 Alpha,11 alpha)-11-(acetyloxy)-1-(methoxymethyl)-2-oxaandrosta-5,8-dieno(6,5,4-bc)furan- 3,7,17-trione
[A potent fungal metabolite isolated from Penicillium wortmannin that selectively inhibits phosphatidylinositol 3-kinase and affects the signal transduction pathway. (NCI) ( NCI )] (UMLS (NCI) C0078517) =Steroid; Pharmacologic Substance; Biologically Active Substance
20. (+)-Camptothecin
[alkaloid isolated from the stem wood of the Chinese tree, Camptotheca acuminata; this compound selectively inhibits the nuclear enzyme DNA topoisomerase type I; several semisynthetic analogs of camptothecin have demonstrated antitumor activity. ( CSP )] (UMLS (NCI) C0006812) =Organic Chemical; Pharmacologic Substance =alkaloid;
[AN000] ANTINEOPLASTICS;
indolizine;
=(s)-10-[(dimethylamino)methyl]-4-ethyl-4,9-dihydroxy-1H-pyrano[3',4':6,7]indolizino[1,2-b]-quinoline-3,14(4H,12H)-dione;
(+)-(4S)-4,11-diethyl-4-hydroxy-9-[(4-piperidino-piperidino)carbonyloxy]-1H-pyrano[3',4':6,7]indolizino[1,2-b]quinol-3,14,(4H,12H)-dione;
(s)-10-[(dimethylamino)methyl]-4-ethyl-4,9-dihydroxy-1H-pyrano[3',4':6,7]indolizino[1,2-b]-quinoline-3,14(4H,12H)-dione
70. (1)-4-(1-Hydroxy-2-(methylamino)ethyl)-1,2-phenylene Dipivalate Hydrochloride
[An ester with sympathomimetic activities. Dipivefrin hydrochloride is a prodrug of epinephrine that, due to its greater lipophilicity, allows for better penetration into the anterior chamber. Once inside the eye, dipivefrin hydrochloride is converted by hydrolysis to epinephrine. Epinephrine enhances the outflow of aqueous humor and decreases the production of aqueous humor by vasoconstriction. This leads to a reduction in intraocular pressure. ( NCI )] (UMLS (NCI) C0700488) =Organic Chemical; Pharmacologic Substance =DIPIVEFRIN;
=DIPIVEFRIN HYDROCHLORIDE 0.1 %;
21. (+)-Catechin
[An antioxidant flavonoid, occurring especially in woody plants as both (+)-catechin and (-)-epicatechin (cis) forms. ( MSH )] (UMLS (NCI) C0007404) =Organic Chemical; Pharmacologic Substance
71. (1,1'-Biphenyl)-2-carboxylic Acid, 4'-((1,4'-dimethyl-2'-propyl(2,6'-bi-1H-benzimidazol)-1'-yl)methyl)-
[A benzimidazole derivative and a non-peptide angiotensin II receptor antagonist with antihypertensive property. Telmisartan selectively antagonizes angiotensin II binding to the AT1 subtype receptor, located in vascular smooth muscle and adrenal gland. The antagonism results in vasodilation and inhibits the angiotensin II-mediated aldosterone production, which in turn leading to a decrease in sodium and water as well as an increase in potassium excretion leading to a subsequent reduction in blood pressure. ( NCI )] (UMLS (NCI) C0248719) =Organic Chemical; Pharmacologic Substance ;
=benzimidazole;
benzoate;
[CV805] ANGIOTENSIN II INHIBITORS;
=TELMISARTAN 40 MG;
TELMISARTAN 80 MG;
TELMISARTAN 20 MG
22. (+)-DX 52-1
[An anticancer drug that belongs to the family of drugs called antitumor antibiotics. It is an anthracycline. ( NCI )] (UMLS (NCI) C0294165) =Organic Chemical; Pharmacologic Substance ;
72. (1,1'-Biphenyl)-3-carboxylic Acid, 2',4'-difluoro-4-hydroxy-
[A difluorophenyl derivate of salicylic acid and a nonsteroidal anti-inflammatory drug (NSAID) with antipyretic, analgesic and anti-inflammatory properties. Diflunisal competitively inhibits both cyclooxygenase (COX) -1 and -2, with higher affinity for COX-1, and subsequently blocks the conversion of arachidonic acid to prostaglandin precursors. This leads to an inhibition of the formation of prostaglandins that are involved in pain, inflammation and fever. Diflunisal differs from other salicylates, in that it is not metabolized to salicylic acid, hence it has a longer half-life. ( NCI )] (UMLS (NCI) C0012228) =Organic Chemical; Pharmacologic Substance ;
=Salicylic Acids;
[MS102] NONSALICYLATE NSAIS, ANTIRHEUMATIC =DIFLUNISAL 500 MG;
DIFLUNISAL 250 MG;
23. (+)-Simalikalactone D
[A quassinoid phytochemical isolated from Simaba multiflora, Quassia africana and other plant species with potential antineoplastic activity. This agent also has antimalarial and antiviral properties. (NCI04) ( NCI )] (UMLS (NCI) C0074548) =Organic Chemical
73. (1,1-Dimethylethyl)-4-methoxyphenol
[A white, waxy solid mixture of 2- and 3-Tert-butyl-4-hydroxyanisole with a faint aromatic odor. Butylated Hydroxyanisole is a widely used synthetic antioxidant in foods, cosmetics and pharmaceuticals mainly to preserve fats and oils. Butylated Hydroxyanisole is reasonably anticipated to be a human carcinogen. (NCI05) ( NCI )] (UMLS (NCI) C0006506) =Organic Chemical; Pharmacologic Substance
24. (+)-UCN-01
[An anticancer drug that belongs to the family of drugs called staurosporine analogues. ( NCI )] (UMLS (NCI) C0950721) UCN-01 =Organic Chemical; Pharmacologic Substance
74. (1-Hydroxyethylidene)bisphosphonic Acid
[As a member of the family of drugs known as bisphosphonates, etidronate differs from endogenous pyrophosphate in its resistance to enzymatic hydrolysis. This agent adsorbs to hydroxyapatite cells and reduces the number of osteoclasts, thereby inhibiting abnormal bone resorption. Etidronate may also directly stimulate bone formation by osteoblasts. (NCI) ( NCI )] (UMLS (NCI) C0015121) =Organophosphorus Compound; Pharmacologic Substance ;
=biphosphonate;
=EHDP;
Risedronic Acid;
25. (+-)-1-(2,4-Dichloro-beta-((4-chlorobenzyl)thio)phenethyl)imidazole Nitrate
[The nitrate salt form of sulconazole, a synthetic imidazole derivative with antifungal property. Sulconazole nitrate inhibits fungal cytochrome P-450 sterol C-14 alpha-demethylation, resulting in the accumulation of fungal 14 alpha-methyl sterols and inhibition of the synthesis of ergosterol, an important component of the fungal cell membrane. Inhibition of ergosterol synthesis leads to a disruption of cell membrane permeability, and ultimately inhibition of cell wall synthesis. In addition, sulconazole nitrate seems to interfere with the autolytic degradation of fungal DNA and RNA. ( NCI )] (UMLS (NCI) C0144004) =Organic Chemical; Pharmacologic Substance ;
=SULCONAZOLE;
=SULCONAZOLE NITRATE 1 %
75. (1-Methyl-DL-piperidine-2-carboxylic acid)-2,6-dimethylanilide hydrochloride
[The hydrochloride salt form of mepivacaine, an amide derivative with local anesthetic properties. At the injection site, mepivacaine hydrochloride acts by binding to specific membrane sodium ion channels in the neuronal cell membranes, thereby inhibiting sodium influx. This leads to a blockage of nerve impulse conduction and results in a loss of sensation. ( NCI )] (UMLS (NCI) C0700542) =Organic Chemical; Pharmacologic Substance =MEPIVACAINE;
=MEPIVACAINE HYDROCHLORIDE 3 %;
MEPIVACAINE HYDROCHLORIDE 1 %;
MEPIVACAINE HYDROCHLORIDE 1.5 %;
MEPIVACAINE HYDROCHLORIDE 2 %;
26. (+-)-1-(3-Chlorophenyl)-2-[(1,1-dimethylethyl)amino]-1-propanone Hydrochloride
[The hydrochloride salt of an aminoketone antidepressant. The molecular mechanism of the antidepressant effect of bupropion is unknown. This agent does not inhibit monoamine oxidase and, compared to classical tricyclic antidepressants, is a weak blocker of the neuronal uptake of serotonin and norepinephrine. Buproprion also weakly inhibits the neuronal re-uptake of dopamine. ( NCI )] (UMLS (NCI) C0700563) =Organic Chemical; Pharmacologic Substance =1-Propanone, 1-(3-Chlorophenyl)-2-((1,1-dimethylethyl)amino)-;
=BUPROPION HYDROCHLORIDE 100 MG;
BUPROPION HYDROCHLORIDE 75 MG;
BUPROPION HYDROCHLORIDE 150 MG
76. (10^3m)3
[LITERAL ( NCI )] (UMLS (NCI) C0439243) =Quantitative Concept
27. (+-)-1-(4-(4-Chlorophenyl)-2-((2,6-dichlorophenyl)thio)butyl)-1H-imidazole Mononitrate
[The nitrate salt form of butaconazole, a synthetic imidazole derivative with fungistatic properties. Butoconazole nitrate interferes with steroid biosynthesis by inhibiting the conversion of lanosterol to ergosterol, thereby changing the fungal cell membrane lipid composition. This alters cell permeability and leads to growth inhibition. Butaconazole nitrate is active against many dermatophytes and yeasts. It also contains antibacterial effects against some gram-positive organisms. ( NCI )] (UMLS (NCI) C0107509) =Organic Chemical; Pharmacologic Substance =butoconazole;
=BUTOCONAZOLE NITRATE 2 %
77. (11alpha,13E)-(+-)-11,16-Dihydroxy-16-methyl-9-oxo-prost-13-en-1-oic Acid Methyl Ester
[A radioprotective agent that belongs to the family of drugs called prostaglandins. ( NCI )] (UMLS (NCI) C0085174) =Eicosanoid; Pharmacologic Substance =Prostaglandins E, Synthetic;
[GA309] ANTIULCER AGENTS, OTHER =Misoprostol 0.2 MG;
Misoprostol 0.1 MG;
28. (+-)-1-Ethyl-6,8-difluoro-1,4-dihydro-7-(3-methyl-1-piperazinyl)-4-oxo-3-quinolinecarboxylic acid, monohydrochloride
[The hydrochloride salt form of lomefloxacin, a synthetic broad-spectrum fluoroquinolone with antibacterial activity. Lomefloxacin hydrochloride inhibits DNA gyrase, a type II topoisomerase involved in the induction or relaxation of supercoiling during DNA replication. This inhibition leads to a decrease in DNA synthesis during bacterial replication, resulting in cell growth inhibition and eventually cell lysis. ( NCI )] (UMLS (NCI) C0770927) Lomefloxacin Hydrochloride;
LOMEFLOXACIN HYDROCHLORIDE PREPARATION =Organic Chemical; Pharmacologic Substance ;
=Lomefloxacin;
=LOMEFLOXACIN HYDROCHLORIDE 400 MG;
78. (11alpha,13E,15S)-11,15-Dihydroxy-9-oxoprost-13-en-1-oic Acid
[The naturally occuring prostaglandin E1 (PGE1) which displays a variety of pharmacologic actions. Alprostadil is a potent vasodilator agent that increases peripheral blood flow, inhibits platelet aggregation, and induces bronchodilation. Used in the treatment of erectile dysfunction, this agent produces corporal smooth muscle relaxation by binding to PGE receptors, resulting in the activation of adenylate cyclase and the subsequent accumulation of 3'5'-cAMP. ( NCI )] (UMLS (NCI) C0002335) =Eicosanoid; Pharmacologic Substance ;
29. (+-)-15-Deoxyspergualin
[A derivative of the antitumor antibiotic spergualin with immunosuppressant activity. Gusperimus inhibits the interleukin-2-stimulated maturation of T cells to the S and G2/M phases and the polarization of the T cells into IFN-gamma-secreting Th1 effector T cells, resulting in the inhibition of growth of activated naive CD4 T cells; this agent may suppress growth of certain T-cell leukemia cell lines. (NCI04) ( NCI )] (UMLS (NCI) C0284559) =Organic Chemical; Pharmacologic Substance ;
79. (11beta)-11,17,21-Trihydroxypregn-4-ene-3,20-dione
[main glucocorticoid secreted by the adrenal cortex; its synthetic counterpart is used, either as an injection or topically, in the treatment of inflammation, allergy, collagen diseases, asthma, adrenocortical deficiency, shock, and some neoplastic conditions. ( CSP )] (UMLS (NCI) C0020268) =Steroid; Pharmacologic Substance; Hormone =[HS051] GLUCOCORTICOIDS;
Pregnenediones;
[DE200] ANTI-INFLAMMATORY, TOPICAL;
[RS100] ANTI-INFLAMMATORIES, RECTAL;
[RS202] HEMORRHOIDAL PREPARATIONS WITH STEROID;
=hydrocortisone 17-butyrate 21-propionate;
HYDROCORTISONE ACETATE;
11beta,17,21-Trihydroxypregn-4-ene-3,20-dione 17-Valerate;
11-beta,17-alpha,21-Trihydroxy-4-pregnene-3,20-dione 17-alpha-butyrate;
Hydrocortisone Cypionate;
Hydrocortisone Sodium Phosphate;
(11beta)-21-(3-Carboxy-1-oxopropyl)-11,17-dihydroxypregn-4-ene-3,20-dione, Monosodium Salt;
HYDROCORTISONE ACETONIDE;
hydrocortisone 17-butyrate 21-propionate;
HYDROCORTISONE ACETATE;
11beta,17,21-Trihydroxypregn-4-ene-3,20-dione 17-Valerate;
11-beta,17-alpha,21-Trihydroxy-4-pregnene-3,20-dione 17-alpha-butyrate;
Hydrocortisone Cypionate;
Hydrocortisone Sodium Phosphate;
(11beta)-21-(3-Carboxy-1-oxopropyl)-11,17-dihydroxypregn-4-ene-3,20-dione, Monosodium Salt;
HYDROCORTISONE POWDER (GM);
HYDROCORTISONE,NONSTERILE PWDR;
HYDROCORTISONE 10 MG;
HYDROCORTISONE 20 MG;
HYDROCORTISONE 25 MG;
HYDROCORTISONE ACETONIDE;
HYDROCORTISONE 5 MG;
Hydrocortisone 1.67 MG/ML;
HYDROCORTISONE 2.5 %;
HYDROCORTISONE 2 %;
HYDROCORTISONE 0.1 %;
HYDROCORTISONE 1 %;
HYDROCORTISONE 1 %WW;
HYDROCORTISONE 0.25 %;
HYDROCORTISONE 100 %;
HYDROCORTISONE 0.5 %
30. (+-)-2-Amino-N-(beta-hydroxy-2,5-dimethoxyphenethyl)acetamide Monohydrochloride
[The hydrochloride salt form of midodrine, a direct-acting prodrug and sympathomimetic agent with antihypotensive properties. Midodrine is converted to its active metabolite, desglymidodrine by deglycination reaction. Desglymidodrine selectively binds to and activates alpha-1-adrenergic receptors of the arteriolar and venous vasculature. This causes smooth muscle contraction and leads to an elevation of blood pressure. Desglymidodrine diffuses poorly across the blood-brain barrier, and is therefore not associated with effects on the central nervous system. ( NCI )] (UMLS (NCI) C0733394) 1-(2',5'-Dimethoxyphenyl)-2-glycinamidoethanol Hydrochloride;
MIDODRINE HYDROCHLORIDE;
MIDODRINE HYDROCHLORIDE PREPARATION;
Midodrine Monohydrochloride =Organic Chemical; Pharmacologic Substance =MIDODRINE;
=MIDODRINE HYDROCHLORIDE 2.5 MG;
MIDODRINE HYDROCHLORIDE 5 MG;
MIDODRINE HYDROCHLORIDE 10 MG
80. (11beta)-11,17,21-Trihydroxypregna-1,4-diene-3,20-dione
[synthetic glucocorticoid with the general properties of the corticosteroids. ( CSP )] (UMLS (NCI) C0032950) =Steroid; Pharmacologic Substance ;
=[HS051] GLUCOCORTICOIDS;
Pregnadienetriols;
corticosteroid analog;
=(6alpha,11beta)-11,17,21-Trihydroxy-6-methylpregna-1,4-diene-3,20-dione;
Prednicarbate;
PREDNISOLONE ACETATE;
Prednisolone Tebutate;
PREDNISOLONE SODIUM PHOSPHATE;
PREDNISOLONE ACETATE;
Prednisolone Tebutate;
PREDNISOLONE SODIUM PHOSPHATE;
PREDNISOLONE POWDER (GM);
PREDNISOLONE 5 MG;
PREDNISOLONE 15 MG/5ML
31. (+-)-4'-(4-(Ethylheptylamino)-1-hydroxybutyl)methanesulfonanilide Fumarate(2:1)(salt)
[The fumarate salt form of ibutilide, a class III antiarrhythmic agent. Ibutilide exerts its effect by activating a slow, inward, predominately sodium current rather than by blocking outward potassium currents. This results in prolongation of atrial and ventricular action potential duration and refractory periods. Ibutilide slightly decreases the sinus rate and atrioventricular (AV) conduction and produces a dose-related prolongation of the QT interval. (NCI05) ( NCI )] (UMLS (NCI) C0123053) =Organic Chemical; Pharmacologic Substance =ibutilide;
=IBUTILIDE FUMARATE 0.1 MG/ML;
81. (11beta)-11,21-Dihydroxypregn-4-ene-3,20-dione
[adrenocortical steroid that has modest but significant activities as a mineralocorticoid and a glucocorticoid. ( CSP )] (UMLS (NCI) C0010124) =Steroid; Pharmacologic Substance; Hormone =[HS051] GLUCOCORTICOIDS;
32. (+-)-alpha-((tert-Butylamino)methyl)-3,5-dihydroxybenzyl Alcohol Sulfate(2:1)(salt)
[The sulfate salt form of terbutaline, an ethanolamine derivative with bronchodilating and tocolytic properties. Terbutaline sulfate selectively binds to and activates beta-2 adrenergic receptors, leading to intracellular adenyl cyclase activation via a trimeric G protein and subsequent increase in cyclic cAMP production. Increased cAMP levels result in relaxation of bronchial and vascular smooth muscle mediated through the activation of protein kinase A (PKA), which phosphorylates proteins in control of muscle tone. cAMP also inhibits calcium ion release from intracellular stores, reduces calcium entry into cells and induces the sequestration of intracellular calcium all of which aids the relaxation of airway muscles. Terbutaline sulfate also increases mucociliary clearance and reduces release of inflammatory cell mediators. ( NCI )] (UMLS (NCI) C0039543) =Organic Chemical; Pharmacologic Substance ;
=TERBUTALINE;
=TERBUTALINE SULFATE 1 MG/ML;
TERBUTALINE SULFATE 2.5 MG;
TERBUTALINE SULFATE 5 MG
82. (11beta)-21-(3-Carboxy-1-oxopropyl)-11,17-dihydroxypregn-4-ene-3,20-dione, Monosodium Salt
[The sodium salt of hydrocortisone succinate with glucocorticoid property. Hydrocortisone sodium succinate is chemically similar to the endogenous hormone that stimulates anti-inflammatory and immunosuppressive activities, in addition to exhibit minor mineralocorticoid effects. This agent binds to intracellular glucocorticoid receptors and is translocated into the nucleus, where it initiates the transcription of glucocorticoid-responsive genes such as various cytokines and lipocortins. Lipocortins inhibit phospholipase A2, thereby blocking the release of arachidonic acid from membrane phospholipids and preventing the synthesis of prostaglandins and leukotrienes, both potent mediators of inflammation. ( NCI )] (UMLS (NCI) C0770560) Cortisol Sodium Succinate;
Hydrocortisone 21-Sodium Succinate;
Hydrocortisone Na Succinate;
Hydrocortisone Sodium Succinate;
HYDROCORTISONE SODIUM SUCCINATE PREPARATION;
Sodium hydrocortisone succinate =Steroid; Pharmacologic Substance ;
=(11beta)-11,17,21-Trihydroxypregn-4-ene-3,20-dione;
=HYDROCORTISONE SODIUM SUCCINATE 125 MG/ML;
HYDROCORTISONE SODIUM SUCCINATE 250 MG;
HYDROCORTISONE SODIUM SUCCINATE 50 MG/ML;
HYDROCORTISONE SODIUM SUCCINATE 500 MG;
HYDROCORTISONE SODIUM SUCCINATE 100 MG;
HYDROCORTISONE SODIUM SUCCINATE 1000 MG
33. (+-)-m-((Ethylamino)-1-hydroxyethyl)phenyl Pivalate
[A prodrug of etilefrine, an adrenergic agonist with vasoconstrictive activity. Etilefrine pivalate is hydrolyzed to etilefrine, which binds to and activates alpha-1-adrenergic receptors of the arteriolar and venous vasculature. This causes smooth muscle contraction and leads to a decrease in venous pooling and increase in blood pressure. This agent may also stimulate beta-1 adrenergic receptors leading to positive chronotropic and inotropic effects. ( NCI )] (UMLS (NCI) C0059855) =Organic Chemical
83. (11beta,16alpha)-21-(3,3-Dimethyl-1-oxobutoxy)-9-fluoro-11-hydroxy-16,17-((1-methylethylidene)bis(oxy))pregna-1,4-diene-3,20-dione
[The hexacetonide salt form of triamcinolone, a synthetic glucocorticosteroid with immunosuppressive and anti-inflammatory activity. Triamcinolone hexacetonide binds to specific cytosolic glucocorticoid receptors and subsequently interacts with glucocorticoid receptor response element on DNA and alters gene expression. This results in an induction of the synthesis of certain anti-inflammatory proteins while inhibiting the synthesis of certain inflammatory mediators. Consequently, an overall reduction in chronic inflammation and autoimmune reactions are accomplished. ( NCI )] (UMLS (NCI) C0077004) =Steroid; Pharmacologic Substance ;
=(11beta,16alpha)-9-Fluoro-11,16,17,21-tetrahydroxypregna-1,4-diene-3,20-dione;
9-alpha-Fluoro-11-beta,21-dihydroxy-16-alpha-isopropylidenedioxy-1,4-pregnadiene,3,20-dione =TRIAMCINOLONE HEXACETONIDE 5 MG/ML;
TRIAMCINOLONE HEXACETONIDE 20 MG/ML;
34. (+-)-Methyl p-(2-hydroxy-3-(isopropylamino)propoxy)hydrocinnamate Hydrochloride
[The hydrochloride salt form of esmolol, a short and rapid-acting beta adrenergic antagonist belonging to the class II anti-arrhythmic drugs and devoid of intrinsic sympathomimetic activity. Esmolol hydrochloride competitively blocks beta1-adrenergic receptors in cardiac muscle and reduces the contractility and cardiac rate of heart muscle, thereby decreasing cardiac output and myocardial oxygen demands. This agent also decreases sympathetic output centrally and blocks renin secretion. At higher doses, esmolol hydrochloride also blocks beta-2 receptors located in bronchial and vascular smooth muscle, thereby leading to smooth muscle relaxation. ( NCI )] (UMLS (NCI) C0700606) =Organic Chemical; Pharmacologic Substance ;
=esmolol;
=ESMOLOL HYDROCHLORIDE 10 MG/ML;
ESMOLOL HYDROCHLORIDE 250 MG/ML;
84. (11beta,16alpha)-9,21-Dichloro-17-[(2-furanylcarbonyl)oxy]-11-hydroxy-16-methylpregna-1,4-diene-3,20-dione
[The furoate salt form of mometasone, a synthetic topical glucocorticosteroid receptor agonist with anti-inflammatory, anti-pruritic and vasoconstrictive properties. Mometasone furoate exerts its effect by binding to cytoplasmic glucocorticoid receptors and subsequently activates glucocorticoid receptor mediated gene expression. This results in synthesis of certain anti-inflammatory proteins, while inhibiting the synthesis of certain inflammatory mediators.. Specifically, mometasone furoate appears to induce phospholipase A2 inhibitory proteins, thereby controlling the release of the inflammatory precursor arachidonic acid from phospholipid membrane by phospholipase A2. ( NCI )] (UMLS (NCI) C0066700) =Steroid; Pharmacologic Substance =Pregnadienediols;
MOMETASONE =MOMETASONE FUROATE 0.1 %
35. (+-)-N,alpha-Dimethylcyclohexaneethylamine
[A propylamine derivative with sympathomimetic property. Propylhexedrine binds to and activates alpha-adrenergic receptors in the mucosa of the respiratory tract, thereby mimicking the actions of norepinephrine and epinephrine. This results in vasoconstriction and reduces swelling and inflammation of the mucous membrane lining, therefore relieving nasal and sinus congestion. ( NCI )] (UMLS (NCI) C0033508) =Organic Chemical; Pharmacologic Substance ;
85. (11beta,16alpha)-9-Fluoro-11,16,17,21-tetrahydroxypregna-1,4-diene-3,20-dione
[synthetic glucocorticoid used in replacement therapy for adrenal insufficiency and as an anti-inflammatory and immunosuppressant in a variety of disorders. ( CSP )] (UMLS (NCI) C0040864) =Steroid; Pharmacologic Substance ;
=[HS051] GLUCOCORTICOIDS;
Pregnadienes;
Steroids, Fluorinated;
corticosteroid analog =9-alpha-Fluoro-11-beta,21-dihydroxy-16-alpha-isopropylidenedioxy-1,4-pregnadiene,3,20-dione;
TRIAMCINOLONE DIACETATE;
1,4-Pregnadiene-2,20-dione-16,17-cyclopentylidenedioxy-9-fluoro-11,21-dihydroxy-21-acetate;
9-alpha-Fluoro-11-beta,21-dihydroxy-16-alpha-isopropylidenedioxy-1,4-pregnadiene,3,20-dione;
TRIAMCINOLONE DIACETATE;
(11beta,16alpha)-21-(3,3-Dimethyl-1-oxobutoxy)-9-fluoro-11-hydroxy-16,17-((1-methylethylidene)bis(oxy))pregna-1,4-diene-3,20-dione;
TRIAMCINOLONE 2 MG;
TRIAMCINOLONE 8 MG;
TRIAMCINOLONE 40 MG/ML;
TRIAMCINOLONE 4 MG;
TRIAMCINOLONE 1 MG
36. (+-)-N-Hydroxy-N-(1-benzo[b]thien-2-ylethyl)-urea
[A synthetic derivative of hydroxyurea with antiasthmatic properties. The leukotriene inhibitor zileuton blocks 5-lipoxygenase, which catalyzes the formation of leukotrienes from arachidonic acid; causes bronchodilation; decreases bronchial mucous secretion and edema; and may prevent or decrease the symptoms of asthma. (NCI04) ( NCI )] (UMLS (NCI) C0081408) =Organic Chemical; Pharmacologic Substance =Hydroxycarbamide;
[RE108] ANTIASTHMA, ANTILEUKOTRIENES =ZILEUTON 600 MG;
86. (11Beta,16alpha)-9-fluoro-11,17,21-trihydroxy-16-methylpregna-1,4-diene-3,20-dione
[anti-inflammatory 9-fluoro-glucocorticoid. ( CSP )] (UMLS (NCI) C0011777) =Steroid; Pharmacologic Substance ;
=[HS051] GLUCOCORTICOIDS;
Pregnadienetriols;
Steroids, Fluorinated;
corticosteroid analog;
[DE200] ANTI-INFLAMMATORY, TOPICAL;
[OP300] ANTI-INFLAMMATORIES, TOPICAL OPHTHALMIC =9-Fluoro-11-beta,21-dihydroxy-16-alpha-methylpregna-1,4-diene-3,20-dione;
Dexamethasone acetate;
DEXAMETHASONE SODIUM PHOSPHATE;
Dexamethasone acetate;
DEXAMETHASONE SODIUM PHOSPHATE;
Dexamethasone 0.1 MG/ML;
DEXAMETHASONE 0.25 MG;
DEXAMETHASONE 0.5 MG;
DEXAMETHASONE 1 MG;
DEXAMETHASONE 1.5 MG;
DEXAMETHASONE 4 MG;
DEXAMETHASONE 6 MG;
DEXAMETHASONE 2 MG;
DEXAMETHASONE 0.5 MG/0.5ML;
DEXAMETHASONE 0.75 MG;
DEXAMETHASONE SODIUMPHOSPHATE;
DEXAMETHASONE 0.1 %;
DEXAMETHASONE 0.04 %;
DEXAMETHASONE 0.012 %
37. (+-)-Verapamil hydrochloride
[The hydrochloride form of Verapamil, which is a phenylalkylamine calcium channel blocking agent. Verapamil inhibits the transmembrane influx of extracellular calcium ions into myocardial and vascular smooth muscle cells, causing dilatation of the main coronary and systemic arteries and decreasing myocardial contractility. This agent also inhibits the drug efflux pump P-glycoprotein which is overexpressed in some multi-drug resistant tumors and may improve the efficacy of some antineoplastic agents. (NCI04) ( NCI )] (UMLS (NCI) C0700468) =Organic Chemical; Pharmacologic Substance =alpha-[3-[[2-(3,4-Dimethoxyphenyl)ethyl]methylamino]propyl]-3,4-dimethoxy-alpha-(1-methylethyl)benzeneacetonitrile;
=VERAPAMIL HYDROCHLORIDE 120 MG;
VERAPAMIL HYDROCHLORIDE 180 MG;
VERAPAMIL HYDROCHLORIDE 240 MG;
VERAPAMIL HYDROCHLORIDE 40 MG;
VERAPAMIL HYDROCHLORIDE 80 MG;
VERAPAMIL HYDROCHLORIDE 2.5 MG/ML;
VERAPAMIL HYDROCHLORIDE 360 MG;
VERAPAMIL HYDROCHLORIDE 200 MG;
VERAPAMIL HYDROCHLORIDE 100 MG;
87. (11beta,16alpha,17beta)-11-Hydroxy-16,17-dimethyl-17-(1-oxopropyl)androsta-1,4-dien-3-one
[A derivative of prednisolone, a synthetic glucocorticoid with anti-inflammatory and immunosuppressive property. Upon binding to the cytosolic glucocorticoid receptor and cell entry, rimexolone activates specific glucocorticoid response elements, resulting in altered gene expression. These include induction of synthesis of anti-inflammatory protein IkappaB-alpha and inhibition of synthesis of nuclear factor kappaB (NFkappa B). As a result, pro-inflammatory cytokine production such as interleukin-1 (IL-1), IL-2 and IL-6 is down-regulated and cytotoxic T-lymphocyte activation inhibited. Therefore, an overall reduction in chronic inflammation and autoimmune reactions may be achieved. ( NCI )] (UMLS (NCI) C0140594) =Steroid; Pharmacologic Substance ;
=Pregnadienes;
[OP300] ANTI-INFLAMMATORIES, TOPICAL OPHTHALMIC;
Unclassified Ingredient Preparations;
=RIMEXOLONE 1 %
38. (+/-)-13-Ethyl-17alpha-hydroxy-18,19-dinorpregn-4-en-20-yne-3-one
[A synthetic progestin commonly used alone or in combination with an estrogen for contraception. Norgestrel suppresses the secretion of luteinizing and follicle-stimulating hormones (LH and FSH), thickens cervical mucus, and slows the transit of ova through the fallopian tubes. This agent also exhibits antiproliferative activity in endometrial tissue and may exhibit chemopreventive and antineoplastic activities in endometrial carcinoma. (NCI04) ( NCI )] (UMLS (NCI) C0028368) =Steroid; Pharmacologic Substance; Hormone =Norpregnenes;
[HS200] CONTRACEPTIVES, SYSTEMIC =(17Alpha)-13-ethyl-17-hydroxy-18,19-dinorpregn-4-en-20-yn-3-one;
Norgestimate;
NORGESTREL 0.5 MG;
NORGESTREL 0.3 MG;
NORGESTREL 75 MCG;
88. (11beta,16beta)-9-Chloro-11-hydroxy-16-methyl-17,21-bis(1-oxopropoxy)pregna-1,4-diene-3,20-dione
[A drug being studied in the treatment of graft-versus-host disease. It belongs to a family of drugs called corticosteroids. ( NCI )] (UMLS (NCI) C0004905) =Steroid; Pharmacologic Substance; Hormone
39. (+/-)-2-(1-Methylethyl)-4-(1-methylethylidene)-2-cyclohexen-1-ol
(UMLS (NCI) C0218671) =Organic Chemical; Pharmacologic Substance ;
89. (11beta,16beta)-9-Chloro-11-hydroxy-16-methyl-17,21-bis(1-oxopropoxy)pregna-1,4-diene-3,20-dione Dipropionate
[The dipropionate salt of a synthetic glucocorticoid with anti-inflammatory and immunomodulating properties. After cell surface receptor attachment and cell entry, beclomethasone enters the nucleus where it binds to and activates specific nuclear receptors, resulting in an altered gene expression and inhibition of proinflammatory cytokine production. ( NCI )] (UMLS (NCI) C0004906) =Steroid; Pharmacologic Substance ;
40. (+/-)-5-[[4-[2-(Methyl-2-pyridinylamino)ethoxy]phenyl]methyl]-2,4-thiazolidinedione, ( Z )-2-Butenedioate (1:1)
[The maleate salt form of rosiglitazone, an orally-active thiazolidinedione with antidiabetic properties and potential antineoplastic activity. Rosiglitazone activates peroxisome proliferator-activated receptor gamma (PPAR-gamma), a ligand-activated transcription factor, thereby inducing cell differentiation and inhibiting cell growth and angiogenesis. This agent also modulates the transcription of insulin-responsive genes, inhibits macrophage and monocyte activation, and stimulates adipocyte differentiation. (NCI04) ( NCI )] (UMLS (NCI) C0795660) Rosiglitazone Maleate;
ROSIGLITAZONE MALEATE PREPARATION =Organic Chemical; Pharmacologic Substance ;
=Rosiglitazone;
=ROSIGLITAZONE MALEATE 4 MG;
ROSIGLITAZONE MALEATE 8 MG;
ROSIGLITAZONE MALEATE 2 MG;
ROSIGLITAZONE MALEATE 1 MG;
90. (11Beta,17beta)-9-fluoro-11,17-dihydroxy-17-methylandrost-4-en-3-one
[A halogenated derivative of 17-alpha-methyltestosterone. Similar to testosterone, fluoxymesterone binds to and activates specific nuclear receptors, resulting in an increase in protein anabolism, a decrease in amino acid catabolism, and retention of nitrogen, potassium, and phosphorus. This agent also may competitively inhibit prolactin receptors and estrogen receptors, thereby inhibiting the growth of hormone-dependent tumor lines. Fluoxymesterone is approximately five times more potent than methyltestosterone. (NCI04) ( NCI )] (UMLS (NCI) C0016366) =Steroid; Pharmacologic Substance; Hormone =Androstenediols;
Steroids, Fluorinated;
[HS100] ANDROGENS/ANABOLICS;
=FLUOXYMESTERONE 10 MG;
FLUOXYMESTERONE 2 MG;
FLUOXYMESTERONE 5 MG;
41. (+/-)-alpha-Tocopherol
[A substance used in cancer prevention. It belongs to the family of drugs called tocopherols. ( NCI )] (UMLS (NCI) C0042874) =Lipid; Pharmacologic Substance; Vitamin =benzopyran;
[DE350] EMOLLIENTS;
(+/-)-alpha-Tocopherol;
[VT000] VITAMINS =(+)-alpha-Tocopherol Acetate;
VITAMIN E OIL;
TOCOPHERYL ACID SUCCINATE,D-ALPHA;
TOCOPHEROL,DL-ALPHA;
(+)-alpha-Tocopherol Acetate;
AMINOBENZOIC ACID LOTION (ML);
PEPTAMEN LIQUID UNFLAVORED,250ML;
PEPTAMEN LIQUID VANILLA,250ML;
ALOE VERA/VITAMIN E OIL,TOP;
CARA-KLENZ,SKIN & WOUND CLEANSER;
CARRINGTON INCONTINENCE SKIN KIT;
ISOCAL HN (VANILLA) LIQUID,240ML;
ISOCAL LIQUID,CAN,240ML;
ISOCAL LIQUID,CAN,360ML; More…
91. (11beta-21-[4-[4-[bis(2-chloroethyl)amino]phenyl]-1-oxobutoxy]-11,17-dihydroxypregna-1,4-diene-3,20-dione
[Ester of CHLORAMBUCIL and PREDNISOLONE used as a combination alkylating agent and synthetic steroid to treat various leukemias and other neoplasms. It causes gastrointestinal and bone marrow toxicity. ( MSH )] (UMLS (NCI) C0032949) =Steroid; Pharmacologic Substance ;
42. (+/-)-N-[4-Cyano-3-(trifluoromethyl)phenyl]-3-[(4-fluorophenyl)sulfonyl]-2-hydroxy-2-methylpropanamide
[An anticancer drug that belongs to the family of drugs called antiandrogens. ( NCI )] (UMLS (NCI) C0285590) =Organic Chemical; Pharmacologic Substance ;
=Anilides;
[AN000] ANTINEOPLASTICS =BICALUTAMIDE 50 MG
92. (123-I)Sodium Iodide
[A radiopharmaceutical containing the radioisotope I-123 with diagnostic property. After absorption, the iodide is distributed through the extracellular fluid of the body and accumulates in the thyroid gland, thereby allowing measurement of thyroid function. ( NCI )] (UMLS (NCI) C0304977) =Indicator, Reagent, or Diagnostic Aid; Inorganic Chemical ;
=IODIDE (AS SODIUM IODIDE);
[DX202] NON-IMAGING AGENTS RADIOPHARMACEUTICALS =Sodium iodide I123 1 MIL;
Sodium iodide I123 0.2 MIL;
SODIUM IODIDE,I-123 100 MIC;
43. (+/-)-Sulforaphane
[A naturally-occurring phytochemical belonging to the class of isothiocyanates. As the aglycone metabolite of glucosinolate glucoraphanin (sulforaphane glucosinolate), sulforaphane acts as an antioxidant and potent stimulator of endogenous detoxifying enzymes. This agent displays anticarcinogenic properties due to its ability to induce phase II detoxification enzymes, such as glutathione S-transferase and quinone reductase, thereby providing protection against certain carcinogens and toxic, reactive oxygen species. Broccoli sprouts contain large amounts of sulforaphane, which is also found in other cruciferous vegetables including cabbage and kale. (NCI04) ( NCI )] (UMLS (NCI) C0163159) =Organic Chemical; Pharmacologic Substance ;
93. (131-I)Sodium Iodide
[A radiopharmaceutical containing the beta- and gamma-emitting radioisotope I-131. After absorption, the iodide is distributed through the extracellular fluid of the body and accumulates in the thyroid gland, thereby allowing the imaging of the thyroid. ( NCI )] (UMLS (NCI) C0304982) =Indicator, Reagent, or Diagnostic Aid; Inorganic Chemical ;
=IODIDE (AS SODIUM IODIDE);
[DX201] IMAGING AGENTS (IN VIVO) RADIOPHARMACEUTICALS =Sodium iodide I131 0.067 MIL/ML;
Sodium iodide I131 100 MIC;
Sodium iodide I131 15 MIL;
Sodium iodide I131 1 MIL;
Sodium iodide I131 2 MIL/ML;
Sodium iodide I131 50 MIL;
Sodium iodide I131 7.05 MIL;
SODIUM IODIDE,I-131 8-100 MIC
44. (-) Strand ssRNA Virus
[A single stranded RNA virus where the RNA strand is the complement of a mRNA. ( NCI )] (UMLS (NCI) C1093214) Negative Sense ssRNA Virus;
Negative Strand ssRNA Virus;
ssRNA Virus, (-) Strand =Virus ;
94. (15S)-15-Methylprostaglandin F(sub 2alpha) Tromethamine
[A synthetic 15-methyl analogue of the naturally occurring prostaglandin F2alpha. Carboprost tromethamine induces myometrium smooth muscle contraction by binding to the prostaglandin F2alpha receptors. This drug can be used to induce contractions to end pregnancy or to induce labour and to control severe postpartum bleeding. Due to its contractile effects on gastrointestinal smooth muscle, carboprost tromethamine can cause vomiting and diarrhea. ( NCI )] (UMLS (NCI) C0054721) =Organic Chemical; Pharmacologic Substance ;
45. (-)-(R)-1-(4,4-Bis(3-methyl-2-thienyl)-3-butenyl)nipecotic Acid, Hydrochloride
[The hydrochloride salt form of tiagabine, a nipecotic acid derivative with anticonvulsant property. Tiagabine hydrochloride inhibits the gamma-aminobutyric acid (GABA) transporter type 1 (GAT1), which is predominantly localized in presynaptic terminals of neurons thereby preventing the reuptake of GABA by the presynaptic endings. Consequently, this increases the level of available GABA within the synaptic cleft, thereby resulting in prolongation of its inhibitory actions. Tiagabine is effective against maximum electroshock seizures and both limbic and generalized tonic-clonic seizures. ( NCI )] (UMLS (NCI) C0772200) 3-Piperidinecarboxylic Acid, 1-(4,4-bis(3-methyl-2-thienyl)-3-buten-yl)-, Hydrochloride,(R)-;
Tiagabine Hydrochloride;
TIAGABINE HYDROCHLORIDE PREPARATION =Organic Chemical; Pharmacologic Substance =TIAGABINE;
=TIAGABINE HYDROCHLORIDE 12 MG;
TIAGABINE HYDROCHLORIDE 16 MG;
TIAGABINE HYDROCHLORIDE 4 MG;
TIAGABINE HYDROCHLORIDE 2 MG
95. (17-alpha)-13-Ethyl-17-hydroxy-11-methylene-18,19-dinorpregn-4-en-20-yn-3-one
[A synthetic form of the naturally occurring female sex hormone progesterone. Etonogestrel binds to the cytoplasmic progesterone receptors in the reproductive system and subsequently activates progesterone receptor mediated gene expression. As a result of the negative feedback mechanism, luteinizing hormone (LH) release is inhibited, which leads to an inhibition of ovulation and an alteration in the cervical mucus and endometrium. ( NCI )] (UMLS (NCI) C0047683) =Steroid; Pharmacologic Substance ;
=[HS200] CONTRACEPTIVES, SYSTEMIC;
Unclassified Ingredients =ETONOGESTREL 0.12 MG
46. (-)-.DELTA.9-Tetrahydrocannabinol
[A synthetic pill form of delta-9-tetrahydrocannabinol (THC), an active ingredient in marijuana that is used to treat nausea and vomiting associated with cancer chemotherapy. ( NCI )] (UMLS (NCI) C0039663) =Organic Chemical; Pharmacologic Substance ;
=[GA700] ANTIEMETICS;
cannabinoid =NABILONE;
DRONABINOL 10 MG;
DRONABINOL 2.5 MG;
DRONABINOL 5 MG;
96. (17Alpha)-13-ethyl-17-hydroxy-18,19-dinorpregn-4-en-20-yn-3-one
[The levorotatory form of norgestrel and synthetic progestogen with progestational and androgenic activity. Levonorgestrel binds to the progesterone receptor in the nucleus of target cells, thereby stimulating the resulting hormone-receptor complex, initiating transcription, and increasing the synthesis of certain proteins. This results in a suppression of luteinizing hormone (LH) activity and an inhibition of ovulation, as well as an alteration in the cervical mucus and endometrium. ( NCI )] (UMLS (NCI) C0023566) =Steroid; Pharmacologic Substance; Hormone ;
=female antifertility drug;
(+/-)-13-Ethyl-17alpha-hydroxy-18,19-dinorpregn-4-en-20-yne-3-one;
[HS800] PROGESTINS;
[HS200] CONTRACEPTIVES, SYSTEMIC =LEVONORGESTREL 0.05 MG;
LEVONORGESTREL 0.15 MG;
LEVONORGESTREL 0.25 MG;
LEVONORGESTREL 0.1 MG;
LEVONORGESTREL 0.75 MG;
LEVONORGESTREL 36 MG;
LEVONORGESTREL 0.05-0.125 MG;
LEVONORGESTREL 52 MG;
47. (-)-2'-Deoxy-5-fluoro-3'-thiacytidine
(UMLS (NCI) C0877876) =Nucleic Acid, Nucleoside, or Nucleotide
97. (17alpha)-19-Norpregna-1,3,5(10)-trien-20-yne-3,17-diol
[semisynthetic alkylated estradiol with a 17-alpha-ethinyl substitution; has high estrogenic potency when administered orally, and is often used as the estrogenic component in oral contraceptives. ( CSP )] (UMLS (NCI) C0015011) =Steroid; Pharmacologic Substance; Hormone =[HS300] ESTROGENS;
estrogen analog;
Norpregnatrienes;
=(17alpha)-3-Methoxy-19-norpregna-1,3,5(10)-trien-20-yn-17-ol;
QUINESTROL;
ETHINYL ESTRADIOL 0.03 MG;
ETHINYL ESTRADIOL 0.5 MG;
ETHINYL ESTRADIOL 0.02 MG;
ETHINYL ESTRADIOL 0.05 MG;
ETHINYL ESTRADIOL 0.035 MG;
ETHINYL ESTRADIOL 0.01 MG;
ETHINYL ESTRADIOL 0.025 MG;
ETHINYL ESTRADIOL 0-35 MCG;
ETHINYL ESTRADIOL 0.015 MG;
ETHINYL ESTRADIOL 0.03-0.04 MG;
ETHINYL ESTRADIOL 0.25 MG;
{7 (Ethinyl Estradiol 0.035 MG / Norethindrone 0.5 MG Oral Tablet) / 7 (Ethinyl Estradiol 0.035 MG / Norethindrone 0.75 MG Oral Tablet) / 7 (Ethinyl Estradiol 0.035 MG / Norethindrone 1 MG Oral Tablet) / 7 (Inert Ingredients 1 MG Oral Tablet) } Pack [Necon 7/7/7 28 Day];
{21 (Ethinyl Estradiol 0.03 MG / Norgestrel 0.3 MG Oral Tablet) / 7 (Inert Ingredients 1 MG Oral Tablet) } Pack [Lo/Ovral 28 Day]
48. (-)-2-(2-Chlorophenyl)-5,7-dihydroxy-8-[(3R,4S)-3-hydroxy-1-methyl-4-piperidinyl]-4H-1-benzopyran-4-one Hydrochloride
[antineoplastic cyclin dependent kinase inhibitor. ( CSP )] (UMLS (NCI) C0281603) =Organic Chemical; Pharmacologic Substance =[AN000] ANTINEOPLASTICS;
enzyme inhibitor;
flavone;
98. (17alpha)-3-Methoxy-19-norpregna-1,3,5(10)-trien-20-yn-17-ol
[A semisynthetic estrogen. Metabolized by the liver to ethynyl estradiol, mestranol serves as the estrogen component in several combination oral contraceptives. (NCI04) ( NCI )] (UMLS (NCI) C0025506) =Steroid; Pharmacologic Substance =[HS300] ESTROGENS;
(17alpha)-19-Norpregna-1,3,5(10)-trien-20-yne-3,17-diol =MESTRANOL 0.1 MG;
MESTRANOL 0.15 MG;
MESTRANOL 0.05 MG;
MESTRANOL 50 MCG
49. (-)-alpha-(1-Aminoethyl)-3,4-dihydroxybenzyl Alcohol
[The levoisomer of nordefrin, a synthetic catecholamine and norepinephrine derivative with sympathomimetic and antihypertensive effects. Levonordefrin's antihypertensive effect is exerted through activation of alpha 2-adrenergic receptors in the cardiovascular control center of the CNS thereby suppressing the sympathetic output from the brain and subsequently lowering blood pressure. Levonordefrin binds to and activates peripheral alpha 2- adrenergic receptors, thereby causing vasoconstriction. ( NCI )] (UMLS (NCI) C0520472) =Organic Chemical; Pharmacologic Substance ;
=Nordefrin;
[DE700] LOCAL ANESTHETICS, TOPICAL =LEVONORDEFRIN 1:20000
99. (17alpha)-Pregna-2,4-dien-20-yno[2,3-d]isoxazol-17-ol
[A synthetic hormone that belongs to the family of drugs called androgens and is used to treat endometriosis. It is being evaluated in the treatment of endometrial cancer. ( NCI )] (UMLS (NCI) C0010961) =Steroid; Pharmacologic Substance =Pregnadienes;
[HS100] ANDROGENS/ANABOLICS =DANAZOL 100 MG;
DANAZOL 50 MG;
DANAZOL 200 MG;
50. (-)-Bactobolin
[A 3-dichloromethylactinobolin antineoplastic antibiotic isolated from various Pseudomonas bacterial species. BN-183 induces apoptosis via a caspase-dependent pathway. This agent also has immunomodulatory properties. (NCI04) ( NCI )] (UMLS (NCI) C0052913) =Organic Chemical; Antibiotic
100. (17beta)-17-(1-Oxopropoxy)androst-4-en-3-one
[A short acting oil-based injectable formulation of testosterone. Testosterone inhibits gonadotropin secretion from the pituitary gland and ablates estrogen production in the ovaries, thereby decreasing endogenous estrogen levels. In addition, this agent promotes the maintenance of male sex characteristics and is indicated for testosterone replacement in hypogonadal males. (NCI04) ( NCI )] (UMLS (NCI) C0039607) =Steroid; Pharmacologic Substance; Hormone =(17Beta)-17-hydroxyandrost-4-en-3-one;
=TESTOSTERONE PROPIONATE POWDER (GM);
TESTOSTERONE PROPIONATE 100 MG/ML;
TESTOSTERONE PROPIONATE 50 MG/ML;
TESTOSTERONE PROPIONATE 25 MG;
TESTOSTERONE PROPIONATE 25 MG/ML

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