Compound ID | 1220
Synonym(s): Primaxin
Class: Beta-lactam (thienamycin)
Spectrum of activity: | Gram-positive & Gram-negative |
Combined with other compounds: | |
Description: | Cilastatin inhibits the human renal dehydropeptidase preventing systemic degradation of imipenem |
Institute where first reported: | Merck |
Highest developmental phase: | Approved by FDA in 1985 |
Development status: | Approved |
Reason Dropped: | Other formulations were discontinued |
Chemical structure(s): | |
Canonical SMILES: | C[C@H]([C@@H]1[C@H]2CC(=C(C(=O)O)N2C1=O)SCCN=CN)O |
Isomeric SMILES: | C[C@H]([C@@H]1[C@H]2CC(=C(N2C1=O)C(=O)O)SCCN=CN)O |
InChI: | InChI=1S/C12H17N3O4S/c1-6(16)9-7-4-8(20-3-2-14-5-13)10(12(18)19)15(7)11(9)17/h5-7,9,16H,2-4H2,1H3,(H2,13,14)(H,18,19)/t6-,7-,9-/m1/s1 |
InChI Key: | ZSKVGTPCRGIANV-ZXFLCMHBSA-N |
Structure link: | https://pubchem.ncbi.nlm.nih.gov/compound/104838 |
External links: | |
Guide to Pharmacology: | cilastatin |
Patent: | US7507814B2 |