Compound ID | 428

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KST-150290

Class: Beta-lactam (cephalosporin)

Spectrum of activity: Gram-positive
Details of activity: Was tested against 473 clinical isolates and it was found there was a preference for Gram positive bacteria. The MICs were lower than both cefdinir and cefpirome against Streptococcus pyogens 308A, S. aureus 285 and Enterococcus faecium MD 8b.
Description: Frosco, MaryBeth, Laura E. Lawrence, and John F. Barrett. "Interscience Conference on Antimicrobial Agents and Chemotherapy (ICAAC)." Expert opinion on investigational drugs 6, no. 12 (1997): 1951-1968.
Institute where first reported: Korea Research Institute of Chemical Technology, Korea
Year first mentioned: 1997
Highest developmental phase: Preclinical
Development status: Inactive
Chemical structure(s):
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Molecular weight: 514.47
Iso. SMILES: COC1=NOC(=C1)/C=C/C2=C(N3C(C(C3=O)NC(=O)/C(=N\O)/C4=CSC(=N4)N)SC2)C(=O)[O-].[Na+]
InChI Key: MDBPARROFWIGCU-WVBDDRPWSA-M
Can. SMILES: COC1=NOC(=C1)/C=C/C2=C(C(=O)[O-])N3C(=O)C(C3SC2)NC(=O)/C(=N\O)/C4=CSC(=N4)N.[Na+]
InChI: InChI=1S/C18H16N6O7S2.Na/c1-30-10-4-8(31-23-10)3-2-7-5-32-16-12(15(26)24(16)13(7)17(27)28)21-14(25)11(22-29)9-6-33-18(19)20-9;/h2-4,6,12,16,29H,5H2,1H3,(H2,19,20)(H,21,25)(H,27,28);/q;+1/p-1/b3-2+,22-11-;
External links:
PubChem link: https://pubchem.ncbi.nlm.nih.gov/compound/23693946
Citation:

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