Compound ID | 1061

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Cefsulodin

Synonym(s): CGP 7174/E

Class: Beta-lactam

Agent Type: Semisynthetic; Small molecule; Direct acting;
Spectrum of activity: Gram-negative
Mechanism of action: Cell wall synthesis inhibitor
Target Pathogen: Active against Pseudomonas
Description: Tosch, W., et al. "In vitro characterization of CGP 7174/E, a Cephalosporin active against Pseudomonas." Current chemotherapy 2 (1978): 843-844. 10th ICAAC p. 843
Institute where first reported: Takeda Pharmaceuticals
Year first mentioned: 1977
Highest development stage: Phase 4
Development status: Inactive
Reason dropped: Poor stability
Chemical structure(s):
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Molecular weight: 532.55
Iso. SMILES: C1C(=C(N2[C@H](S1)[C@@H](C2=O)NC(=O)[C@@H](C3=CC=CC=C3)S(=O)(=O)O)C(=O)[O-])C[N+]4=CC=C(C=C4)C(=O)N
InChI Key: SYLKGLMBLAAGSC-QLVMHMETSA-N
Can. SMILES: C1=CC=C(C=C1)[C@H](C(=O)N[C@@H]2C(=O)N3C(=C(C[N+]4=CC=C(C=C4)C(=O)N)CS[C@H]23)C(=O)[O-])S(=O)(=O)O
InChI: InChI=1S/C22H20N4O8S2/c23-18(27)13-6-8-25(9-7-13)10-14-11-35-21-15(20(29)26(21)16(14)22(30)31)24-19(28)17(36(32,33)34)12-4-2-1-3-5-12/h1-9,15,17,21H,10-11H2,(H4-,23,24,27,28,30,31,32,33,34)/t15-,17-,21-/m1/s1
External links:
PubChem link: https://pubchem.ncbi.nlm.nih.gov/compound/656575
Guide to Pharmacology: cefsulodin
Citation: https://pubmed.ncbi.nlm.nih.gov/6798336/

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