Compound ID | 952
Synonym(s): GV 104326
Class: Beta-lactam (tribactam)
Spectrum of activity: | Gram-positive & Gram-negative |
Details of activity: | Not very active against MRSA though is active in MSSA. Additionally demonstrates strong antimicrobial activity against S. pneumoniae, E. coli and H. influenzae |
Institute where first reported: | GSK, USA |
Year first mentioned: | 1992 |
Highest developmental phase: | Phase 2 (NCT05388448) |
Development status: | Unknown (as of 2025) |
Chemical structure(s): | |
Canonical SMILES: | C[C@H]([C@@H]1[C@H]2[C@H]3CCC[C@@H](C3=C(C(=O)O)N2C1=O)OC)O |
Isomeric SMILES: | C[C@H]([C@@H]1[C@H]2[C@H]3CCC[C@@H](C3=C(N2C1=O)C(=O)O)OC)O |
InChI: | InChI=1S/C14H19NO5/c1-6(16)9-11-7-4-3-5-8(20-2)10(7)12(14(18)19)15(11)13(9)17/h6-9,11,16H,3-5H2,1-2H3,(H,18,19)/t6-,7+,8+,9-,11-/m1/s1 |
InChI Key: | ICFDDEJRXZSWTA-KJFVXYAMSA-N |
Structure link: | https://pubchem.ncbi.nlm.nih.gov/compound/71452 |
External links: | |
Guide to Pharmacology: | sanfetrinem |
Citations: |
|