- 1. (+)-(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;
| - 6. 153Sm-EDTMP
- (UMLS (NCI) C0772051) Samarium Sm 153 Lexidronam;
Samarium Sm-153 EDTMP;
Samarium-153 EDTMP;
Samarium-153 Ethylenediaminetetramethylenephosphonate;
Samarium-153 Ethylenediaminetetramethylenephosphonic Acid;
Sm-153 EDTMP =Organic Chemical; Pharmacologic Substance; Indicator, Reagent, or Diagnostic Aid |
- 2. (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 ;
| - 7. 9S-6'-Methoxy-cinchonan-9-ol, Mono-D-gluconate(salt)
- [The gluconate salt form of quinidine, an alkaloid with antimalarial and antiarrhythmic (Class la) properties. Quinidine gluconate exerts its anti-malarial activity by acting primarily as an intra-erythrocytic schizonticide through association with the hemepolymer (hemozoin) in the acidic food vacuole of the parasite thereby preventing further polymerization by heme polymerase enzyme. This results in accumulation of toxic heme and death of the parasite. Quinidine gluconate exerts its antiarrhythmic effects by depressing the flow of sodium ions into cells during phase 0 of the cardiac action potential, thereby slowing the impulse conduction through the atrioventricular (AV) node, reducing the maximal rate of phase 0 depolarization and prolonging the refractory period. Quinidine gluconate also reduces the slope of phase 4 depolarization in Purkinje-fibres resulting in slowed conduction and reduced automaticity in the heart. ( NCI )] (UMLS (NCI) C0072869) =Organic Chemical; Pharmacologic Substance =QUINIDINE;
=(9S)-6'-Methoxycinchonan-9-ol Sulfate (2:1) (salt);
QUINIDINE GLUCONATE 80 MG/ML;
QUINIDINE GLUCONATE 324 MG |
- 3. (2S)-2-Methylbutanoic Acid, (1S,3R,7S,8S,8aR)-1,2,3,7,8,8a-Hexahydro-3,7-dimethyl-8-[2-[(2R,4R)-tetrahydro-4-hydroxy-6-oxo-2H-pyran-2-yl]ethyl]-1-naphthalenyl Ester
- [HMG coA reductase inhibitor which inhibits cholesterol biosynthesis and thus lowers blood cholesterol levels; also blocks isoprenylation of protein CAAX motifs. ( CSP )] (UMLS (NCI) C0024027) =Organic Chemical; Pharmacologic Substance ;
=antihypercholesterolemic agent;
[CV350] ANTILIPEMIC AGENTS;
naphthalene;
=[1S-[1alpha,3alpha,7beta,8beta(2S*,4S*),8abeta]]-1,2,3,7,8,8a-Hexahydro-3,7-dimethyl-8-[2-(tetrahydro-4-hydroxy-6-oxo-2H-pyran-2-yl)ethyl]-1-naphthalenyl 2,2-dimethylbutanoate;
LOVASTATIN 10 MG;
LOVASTATIN 20 MG;
LOVASTATIN 40 MG;
| - 8. Smear, Tzanck
- (UMLS (HL7) C1547938) =Intellectual Product =Specimen Source Codes;
|
- 4. (9S)-6'-Methoxycinchonan-9-ol Sulfate (2:1) (salt)
- [The sulfate salt form of quinidine, an alkaloid with antimalarial and antiarrhythmic (Class la) properties. Quinidine sulfate exerts its anti-malarial activity by acting primarily as an intra-erythrocytic schizonticide through association with the hemepolymer (hemozoin) in the acidic food vacuole of the parasite thereby preventing further polymerization by heme polymerase enzyme. This results in accumulation of toxic heme and death of the parasite. Quinidine sulfate exerts its antiarrhythmic effects by depressing the flow of sodium ions into cells during phase 0 of the cardiac action potential, thereby slowing the impulse conduction through the atrioventricular (AV) node, reducing the rate of phase 0 depolarization and prolonging the refractory period. Quinidine sulfate also reduces the slope of phase 4 depolarization in Purkinje-fibres resulting in slowed conduction and reduced automaticity in the heart. ( NCI )] (UMLS (NCI) C0034415) =Organic Chemical; Pharmacologic Substance ;
=QUINIDINE;
9S-6'-Methoxy-cinchonan-9-ol, Mono-D-gluconate(salt);
quinidine polygalacturonate;
=QUINIDINE SULFATE 200 MG;
QUINIDINE SULFATE 100 MG;
QUINIDINE SULFATE 300 MG | - 9. smegma
- [A white secretion of the sebaceous glands of the foreskin. ( NCI )] (UMLS (CSP) C0037359) =Body Substance
|
- 5. (S)-1-(3-Mercapto-2-methyl-1-oxopropyl)-L-proline
- [potent and specific inhibitor of peptidyl dipeptidase A; it acts to suppress the renin-angiotensin system and inhibits blood pressure responses to exogenous angiotensin. ( CSP )] (UMLS (NCI) C0006938) =Amino Acid, Peptide, or Protein; Pharmacologic Substance =Amino Acids, Cyclic;
[CV800] ACE INHIBITORS;
PROLINE;
=CAPTOPRIL 100 MG;
CAPTOPRIL 12.5 MG;
CAPTOPRIL 25 MG;
CAPTOPRIL 50 MG;
| - 10. Smell
- (UMLS (HL7) C1547044) =Quantitative Concept =Kind of quantity;
|
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