Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C20H28N2O7S |
Molecular Weight | 440.511 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 5 / 5 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
[H][C@]12[C@@H](C)C(S[C@H]3CNC(=O)C3)=C(N1C(=O)[C@]2([H])[C@@H](C)O)C(=O)OCOC(=O)C(C)(C)C
InChI
InChIKey=ZNOVVAJWYUBFMI-JIFFNSBPSA-N
InChI=1S/C20H28N2O7S/c1-9-14-13(10(2)23)17(25)22(14)15(16(9)30-11-6-12(24)21-7-11)18(26)28-8-29-19(27)20(3,4)5/h9-11,13-14,23H,6-8H2,1-5H3,(H,21,24)/t9-,10-,11-,13-,14-/m1/s1
CS-834 is a beta-lactam antibiotic of a carbapenem class, developed by the Japanese company Sankyo Co. Ltd. CS-834 is an ester-type prodrug of the active metabolite R-95867. The drug showed potent and well balanced antibacterial activity as well as stability against dehydropeptidase-I. The in vivo efficacy of CS-834 was evaluated in murine systemic infections caused by 16 strains of gram-positive and -negative pathogens. The efficacy of CS-834 was in many cases superior to those of cefteram pivoxil, cefpodoxime proxetil, cefdinir, and cefditoren pivoxil, especially against infections caused by S. aureus, penicillin-resistant S. pneumoniae, E. coli, Citrobacter freundii, and Proteus vulgaris. Pharmacokinetics of CS-834 was evaluated in healthy male volunteers, but no further clinical development of the drug was reported.
Approval Year
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100000144853
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SUB121726
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H26S03B779
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DTXSID30935699
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157542-49-9
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admin on Fri Dec 15 15:29:38 GMT 2023 , Edited by admin on Fri Dec 15 15:29:38 GMT 2023
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177994
Created by
admin on Fri Dec 15 15:29:38 GMT 2023 , Edited by admin on Fri Dec 15 15:29:38 GMT 2023
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ACTIVE MOIETY
SUBSTANCE RECORD