UMLS. CSP-HL7-ICD9CM-NCI-NDFRT-RXNORM
%
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
H H+ H1 HA HB HC HD HE HF HG HH HI HK HL HM HN HO HP HQ HR HS HT HU HV HX HY HZ
HIA HIB HIC HID HIE HIF HIG HII HIL HIM HIN HIP HIR HIS HIT HIV
selected terms: 21 page 1 of 1

1. (1H-Indol-3-ylmethyl)carbamodithioic Acid, Methyl Ester
(UMLS (NCI) C0258434) =Organic Chemical; Pharmacologic Substance
12. H. INFLUENAE SEPTICEMIA
(UMLS (ICD9CM) C0276029) =Disease or Syndrome
2. 1-(1H-Indol-4-yloxy)-3-((1-methylethyl)amino)-2-propanol
[An aryloxypropanolamine derivative with antihypertensive property. Pindolol competitively binds to beta-adrenergic receptors, resulting in a decrease in beta-adrenergic activities, i.e., vasodilation, and negative chronotropic and inotropic effects. In addition, this agent blocks serotonin (5-HT) 1A receptors, thereby increasing the available serotonin in the brain. Increased serotonin levels augment the antidepressant action of selective serotonin reuptake inhibitors and monoamine oxidase inhibitors. ( NCI )] (UMLS (NCI) C0031937) =Organic Chemical; Pharmacologic Substance =Propanolamines;
[CV100] BETA-BLOCKERS/RELATED =PINDOLOL 10 MG;
PINDOLOL 5 MG;
13. H. INFLUENZAE INFECT NOS
(UMLS (ICD9CM) C0019073) =Disease or Syndrome ;
3. 1H-Indene-3-acetic Acid, 5-Fluoro-2-methyl-1-((4-(methylsulfonyl)phenyl)methylene), (Z)
(UMLS (NCI) C0953857) =Organic Chemical; Pharmacologic Substance
14. H.INFLUENZAE PNEUMONIA
(UMLS (ICD9CM) C0276026) =Disease or Syndrome
4. 1H-Indole-2-carboxylic Acid, 1-(2-((1-(ethoxycarbonyl)butyl)amino)-1-oxopropyl)octahydro-,(2S-(1(R*(R*))2alpha,3abeta,7abeta))-, compound with 2-Methyl-2-propanamine(1:1)
[The tert-butylamine salt of perindopril, the ethyl ester of a non-sulfhydryl angiotensin converting enzyme (ACE) inhibitor with antihypertensive property. Upon hydrolysis, perindopril erbumine is converted to its active form perindoprilat, which inhibits ACE, thereby blocks the conversion of angiotensin I to angiotensin II. This prevents angiotensin II-mediated vasoconstriction, decreases angiotensin II-stimulated aldosterone secretion from the adrenal cortex, and consequently promotes diuresis and natriuresis. ( NCI )] (UMLS (NCI) C0244718) =Organic Chemical; Pharmacologic Substance ;
=Perindopril;
=PERINDOPRIL ERBUMINE 2 MG;
PERINDOPRIL ERBUMINE 4 MG;
PERINDOPRIL ERBUMINE 8 MG
15. hind brain
[part of the brain developed from the posterior of the three primary brain vesicles of the embryonic neural tube; it comprises the metencephalon (cerebellum and pons) and myelencephalon (medulla oblongata). ( CSP )] (UMLS (CSP) C0035507) =Body Part, Organ, or Organ Component ;
=brain stem;
=Cerebellar;
medulla oblongata;
pons;
reticular formation
5. 1H-Indole-3-butanoic Acid
(UMLS (NCI) C0063503) =Organic Chemical
16. Hindgut
(UMLS (NCI) C0231053) =Body Part, Organ, or Organ Component
6. 1H-Indole-3-ethanamine, N,N-dimethyl-5-(1H-1,2,4-triazol-1-ylmethyl)-, Monobenzoate
[The benzoate salt form of rizatriptan, a member of the triptan class agents with anti-migraine property. Rizatriptan benzoate selectively binds to and activates serotonin (5-HT) 1B receptors expressed in intracranial arteries, and to 5-HT 1D receptors located on peripheral trigeminal sensory nerve terminals in the meninges and central terminals in brain stem sensory nuclei. Receptor binding results in constriction of cranial vessels and inhibition of nociceptive transmission, thereby providing relief of migraine headaches. Rizatriptan benzoate may also relief migraine headaches by inhibition of pro-inflammatory neuropeptide release. ( NCI )] (UMLS (NCI) C0772420) Rizatriptan Benzoate;
RIZATRIPTAN BENZOATE PREPARATION =Organic Chemical; Pharmacologic Substance ;
=RIZATRIPTAN;
=RIZATRIPTAN BENZOATE 10 MG;
RIZATRIPTAN BENZOATE 5 MG
17. Hindgut Carcinoid Neoplasm
(UMLS (NCI) C1334029) Hindgut Carcinoid Tumor =Neoplastic Process ;
7. 1H-indole-3-methanol
[A substance that is being studied as a cancer prevention drug. It is found in cruciferous vegetables. ( NCI )] (UMLS (NCI) C0063491) =Organic Chemical; Pharmacologic Substance ;
18. Hindu
[A complex body of social, cultural, and religious beliefs and practices evolved in and largely confined to the Indian subcontinent and marked by a caste system, an outlook tending to view all forms and theories as aspects of one eternal being and truth, and the practice of the way of works, the way of knowledge, or the way of devotion as a means of release from the round of rebirths. (From Webster, 3d ed) ( MSH )] (UMLS (HL7) C0019550) =Idea or Concept ;
=religion;
Religious Affiliation
8. 2(H)-Indol-2-one, 4-(2-(dipropylamino)ethyl)-1,3-dihydro-, Monohydrochloride
[The hydrochloride salt form of ropinirole, a non-ergot dopamine agonist with antiparkinsonian property. Acting as a substitute for dopamine, ropinirole hydrochloride binds to and activates dopamine D2 and D3 receptors within the caudate putamen in the brain, thereby improving motor function. ( NCI )] (UMLS (NCI) C0771840) 4-(2-(Dipropylamino)ethyl)-2-indolinone Monohydrochloride;
Ropinirole Hydrochloride;
ROPINIROLE HYDROCHLORIDE PREPARATION;
SK&F 101468-A =Organic Chemical; Pharmacologic Substance ;
=ROPINIROLE;
=ROPINIROLE HYDROCHLORIDE 4 MG;
ROPINIROLE HYDROCHLORIDE 0.25 MG;
ROPINIROLE HYDROCHLORIDE 0.5 MG;
ROPINIROLE HYDROCHLORIDE 2 MG;
ROPINIROLE HYDROCHLORIDE 1 MG;
ROPINIROLE HYDROCHLORIDE 5 MG;
ROPINIROLE HYDROCHLORIDE 3 MG
19. Hindu: Other
(UMLS (HL7) C1546361) =Idea or Concept ;
=religion;
9. 2H-Indol-2-one, 5-(2-(4-(1,2-benzisothiazol-3-yl)-1-piperazinyl)ethyl)-6-chloro-1,3-dihydro-
[A benzothiazolylpiperazine derivative and an atypical antipsychotic agent with an antischizophrenic property. Ziprasidone functions as an antagonist at the dopamine D2 and serotonin 5-HT2A and 5-HT1D receptors, and as an agonist at the 5-HT1A receptor. Ziprasidone also inhibits the synaptic reuptake of serotonin and norepinephrine. The mechanism of action by which ziprasidone exerts its antischizophrenic effect is unknown but is potentially mediated through a combination of dopamine D2 and serotonin 5-HT2 antagonism. This agent also has antagonistic activity against histamine H1 and alpha-1-adrenergic receptors. ( NCI )] (UMLS (NCI) C0380393) =Organic Chemical; Pharmacologic Substance ;
=Piperazines;
thiazole;
[CN709] ANTIPSYCHOTICS, OTHER;
=ZIPRASIDONE 20 MG;
ZIPRASIDONE 40 MG;
ZIPRASIDONE 60 MG;
ZIPRASIDONE 80 MG
20. Hindu: Shaivites
(UMLS (HL7) C1546362) =Idea or Concept =religion;
10. 4H-Indol-4-one, 3-ethyl-1,5,6,7-tetrahydro-2-methyl-5-(4-morpholinylmethyl)-, Monohydrochloride
[The hydrochloride salt form of molindone, a dihydroindolone compound with antipsychotic and anti-schizophrenic properties not structurally related to other major tranquilizers. Molindone hydrochloride exerts its effect by blocking dopamine receptors, probably D2 and D3, in the reticular activating and limbic systems, thereby decreasing dopamine excess in the brain. This leads to a reduction of spontaneous locomotion and aggressiveness, suppression of conditioned response, antagonism of stereotyped behaviour and hyperactivity induced by amphetamines. ( NCI )] (UMLS (NCI) C0282249) =Organic Chemical; Pharmacologic Substance ;
=MOLINDONE;
=MOLINDONE HYDROCHLORIDE 100 MG;
MOLINDONE HYDROCHLORIDE 20 MG/ML;
MOLINDONE HYDROCHLORIDE 50 MG;
MOLINDONE HYDROCHLORIDE 10 MG;
MOLINDONE HYDROCHLORIDE 25 MG;
MOLINDONE HYDROCHLORIDE 5 MG;
21. Hindu: Vaishnavites
(UMLS (HL7) C1546363) =Idea or Concept =religion;
11. 5H-indolo(2,3-a)pyrrolo(3,4-c)carbazole-5,7(6H)-dione,1,11-dichloro-12,13-dihydro-12-(4-O-methyl-beta-D-glucopyranosyl)
[An anticancer drug that belongs to the family of drugs called antineoplastic antibiotics. ( NCI )] (UMLS (NCI) C0073012) =Organic Chemical; Antibiotic ;

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