- 1. (2S,5R,6R)-6-((R)-2-Amino-2-phenylacetamido)-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo(3.2.0)heptane-2-carboxylic Acid
- [semi-synthetic derivative of penicillin that functions as an orally active broad-spectrum antibiotic. ( CSP )] (UMLS (NCI) C0002680) =Organic Chemical; Antibiotic ;
| - 3. [S-(R*,R*)]-3-Acetyl-1,5-dihydro-4-hydroxy-5-(1-methylpropyl)-2H-pyrrol-2-one
- [3-Acetyl-5-sec-butyl-4-hydroxy-3-pyrrolin-2-one. A metabolite found in a strain of the fungus Alternaria tenuis Auct. which functions as an antibiotic with antiviral and antineoplastic properties, and may also act as a mycotoxin. ( MSH )] (UMLS (NCI) C0039531) =Organic Chemical; Pharmacologic Substance; Hazardous or Poisonous Substance
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- 2. (S-(R*,R*))-1,2,3,4-butanetetrol,1,4-dimethanesulfonate
- [A substance that is being studied as a treatment for cancer. It belongs to the family of drugs called alkylating agents. ( NCI )] (UMLS (NCI) C0076959) =Organic Chemical; Pharmacologic Substance ;
| - 4. [S-(R*,R*)]-9-[4,5-dimethoxy-2-[(1,2,3,4-tetrahydro-6,7-dimethoxy-2-methyl-1-isoquinolinyl)-methyl]phenoxy]-5,6,6a,7-tetrahydro-1,2,10-trimethoxy-6-methyl-4H-dibenzo[de,g]quinoline
- [A natural aporphine benzylisoquinoline vinca alkaloid with antineoplastic activity. Thalicarpine binds to and inhibits p-glycoprotein, the multidrug resistance efflux pump. Thalicarpine also induces single-strand breaks in DNA and arrests cancer cells at the G2/M and G1 phase of the cell cycle. (NCI04) ( NCI )] (UMLS (NCI) C0039735) =Organic Chemical; Pharmacologic Substance ;
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