Compound ID | 3480

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Bay v 3522

Class: Beta-lactam

Agent Type: Synthetic; Small molecule; Direct acting;
Spectrum of activity: Gram-positive & Gram-negative
Mechanism of action: Cell wall synthesis inhibitor
Target Pathogen: Active against Enterobacteriaceae but to a lesser extent compared to Gram-positives including methicillin-resistant Staphylococcus aureus
Description: Synthetic compound (cephalosporin); oral cephem; activity against Gram-negatives is inferior to cefuroxime but activity against Gram-positive is superior to cefuroxime, cefixime, and cephalexin
Year first mentioned: 1990
Development status: Experimental
Chemical structure(s):
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Molecular weight: 445.52
Iso. SMILES: C/C=C\C1=C(N2[C@@H]([C@@H](C2=O)NC(=O)[C@@H](C3=CC4=C(C=C3)N=C(S4)N)N)SC1)C(=O)O
InChI Key: GSPMBQQDLRBMID-AGGBKSKLSA-N
Can. SMILES: C/C=C\C1=C(C(=O)O)N2C(=O)[C@H]([C@H]2SC1)NC(=O)[C@@H](C3=CC4=C(C=C3)N=C(N)S4)N
InChI: InChI=1S/C19H19N5O4S2/c1-2-3-9-7-29-17-13(16(26)24(17)14(9)18(27)28)23-15(25)12(20)8-4-5-10-11(6-8)30-19(21)22-10/h2-6,12-13,17H,7,20H2,1H3,(H2,21,22)(H,23,25)(H,27,28)/b3-2-/t12-,13-,17-/m1/s1
External links:
PubChem link: https://pubchem.ncbi.nlm.nih.gov/compound/6440069
Citation: https://journals.asm.org/doi/10.1128/aac.34.5.813

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