Compound ID | 3596

Update compound information

YM-13115

Synonym(s): YM13115  |  YM 13115

Class: Beta-lactam (cephalosporin)

Spectrum of activity: Gram-positive  &  Gram-negative
Details of activity: Active against Enterobacteriaceae, Streptococcus pyogenes, and Streptococcus pneumoniae; cell wall synthesis inhibitor
Description: Semisynthetic compound derived from cephalosporin; resistant to hydrolysis by penicillinase (i.e. TEM-1, OXA-1, OXA-2, PSE-3), staphylococcal penicillinase, and chromosomal cephalosporinase
Institute where first reported: Yamanouchi Pharmaceutical Co., Ltd., Tokyo 174, Japan
Year first mentioned: 1985
Development status: Experimental
Chemical structure(s):
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Molecular weight: 644.68
Iso. SMILES: CC(C)(C(=O)O)O/N=C(/C1=CSC(=N1)N)\C(=O)N[C@H]2[C@@H]3N(C2=O)C(=C(CS3)CSC4=C(C(=O)NS4)C(=O)O)C(=O)O
InChI Key: VAWGRRAOBMTZDZ-ABNFUVILSA-N
Can. SMILES: CC(C)(C(=O)O)O/N=C(/C1=CSC(=N1)N)\C(=O)N[C@@H]2C(=O)N3C(=C(CS[C@H]23)CSC4=C(C(=O)NS4)C(=O)O)C(=O)O
InChI: InChI=1S/C21H20N6O10S4/c1-21(2,19(35)36)37-25-9(7-5-40-20(22)23-7)13(29)24-10-14(30)27-11(17(33)34)6(3-38-15(10)27)4-39-18-8(16(31)32)12(28)26-41-18/h5,10,15H,3-4H2,1-2H3,(H2,22,23)(H,24,29)(H,26,28)(H,31,32)(H,33,34)(H,35,36)/b25-9-/t10-,15-/m1/s1
External links:
PubChem link: https://pubchem.ncbi.nlm.nih.gov/compound/13338940
Citation: https://journals.asm.org/doi/10.1128/aac.27.4.565

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