Compound ID | 325

Update compound information

BMS-247243

Class: Beta-lactam (cephalosporin)

Spectrum of activity: Gram-negative
Details of activity: Cell wall inhibitors; active against resistant Gram positive bacteria such as MRSA
Institute where first reported: Bristol-Myers Squibb, UK
Year first mentioned: 2000
Highest developmental phase: Preclinical
Development status: Inactive
Chemical structure(s):
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Molecular weight: 838.84
Iso. SMILES: CC1=CC(=CC(=[N+]1CCC[N+]2(CCOCC2)C)C)SCC3=C(N4[C@@H]([C@@H](C4=O)NC(=O)CSC5=C(C=C(C(=C5)Cl)/C=C/C(=O)NCC(=O)[O-])Cl)SC3)C(=O)[O-]
InChI Key: MOYDKLWHWUTKTI-LDCQLTLFSA-N
Can. SMILES: CC1=[N+](CCC[N+]2(C)CCOCC2)C(=CC(=C1)SCC3=C(C(=O)[O-])N4C(=O)[C@H]([C@H]4SC3)NC(=O)CSC5=CC(=C(/C=C/C(=O)NCC(=O)[O-])C=C5Cl)Cl)C
InChI: InChI=1S/C36H41Cl2N5O8S3/c1-21-13-25(14-22(2)41(21)7-4-8-43(3)9-11-51-12-10-43)52-18-24-19-54-35-32(34(48)42(35)33(24)36(49)50)40-30(45)20-53-28-16-26(37)23(15-27(28)38)5-6-29(44)39-17-31(46)47/h5-6,13-16,32,35H,4,7-12,17-20H2,1-3H3,(H2-2,39,40,44,45,46,47,49,50)/b6-5+/t32-,35-/m1/s1
External links:
PubChem link: https://pubchem.ncbi.nlm.nih.gov/compound/9811231
Citation:

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