Name: Clindamycin Sulfoxide
Rating: 5 (10 reviews)

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HIT ID:HIT214320748
Cas No:22431-46-5
常用名:Clindamycin Sulfoxide
IUPAC:(2S,4R)-N-[(1S,2S)-2-chloro-1-[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-methanesulfinyloxan-2-yl]propyl]-1-methyl-4-propylpyrrolidine-2-carboxamide
IUPAC:(2S,4R)-N-[(1S,2S)-2-chloro-1-[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-methanesulfinyloxan-2-yl]propyl]-1-methyl-4-propylpyrrolidine-2-carboxamide
InChI key:XSLGFIQRVCXUEU-NXMZTFJRSA-N

分子式:C18H33ClN2O6S
分子量:440.98
氢键供体数 (HBD):
氢键受体数 (HBA):
LogP:
SMILES:[H][C@@]1(O[C@@H]([C@H](O)[C@@H](O)[C@H]1O)S(C)=O)[C@H](NC(=O)[C@@H]1C[C@@H](CCC)CN1C)[C@H](C)Cl
SMILES:[H][C@@]1(O[C@@H]([C@H](O)[C@@H](O)[C@H]1O)S(C)=O)[C@H](NC(=O)[C@@H]1C[C@@H](CCC)CN1C)[C@H](C)Cl

Clindamycin sulfoxide is an active metabolite of the antibiotic clindamycin . It is formed via S-oxidation of clindamycin primarily by the cytochrome P450 (CYP) isoform CYP3A4. Clindamycin sulfoxide inhibits the growth of P. prevotti, B. fragilis, and C. sordelli in vitro with MIC values of 2, 2, and 1 mg/L, respectively.

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