Compound ID | 432

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CP6679

Synonym(s): CP-6679  |  CP 6679  |  ME1209

Class: Beta-lactam

Agent Type: Semisynthetic; Small molecule; Direct acting;
Spectrum of activity: Gram-positive & Gram-negative
Mechanism of action: Cell wall synthesis inhibitor
Propensity to select resistant mutants: Lower propensity to select for resistant strains than ceftazidime
Description: Injectable cephalosporin; Yoshida T, Ida I, Kurazono M, et al. ME1209 (CP6679), a new parenteral Cephalosporin II. In vitro and in vivo activity against Pseudomonas aeruginosa. 38th Intersci Conf Antimicrob Agents Chemother. 1998.
Institute where first reported: Meiji Seika Kaisha, Japan
Year first mentioned: 1995
Development status: Experimental
Chemical structure(s):
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Molecular weight:
Iso. SMILES: C[C@H](C1=[N+](C=C2N1C=CS2)CC3=C(N4[C@@H]([C@@H](C4=O)NC(=O)/C(=N\OCF)/C5=NSC(=N5)N)SC3)C(=O)[O-])NC=O
InChI Key: KCRGWNKTMMXMIR-USTRZADQSA-N
Can. SMILES: C[C@H](C1=[N+](CC2=C(C(=O)[O-])N3C(=O)[C@H]([C@H]3SC2)NC(=O)/C(=N\OCF)/C4=NSC(=N4)N)C=C5N1C=CS5)NC=O
InChI: InChI=1S/C21H20FN9O6S3/c1-9(24-8-32)17-29(5-11-30(17)2-3-38-11)4-10-6-39-19-13(18(34)31(19)14(10)20(35)36)25-16(33)12(27-37-7-22)15-26-21(23)40-28-15/h2-3,5,8-9,13,19H,4,6-7H2,1H3,(H4-,23,24,25,26,28,32,33,35,36)/b27-12-/t9-,13-,19-/m1/s1
External links:
PubChem link: https://pubchem.ncbi.nlm.nih.gov/substance/273351054
Citation: https://doi.org/10.1007/s101560200024

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