Clindamycin Size:Contact [email protected] for quotation Smiles: CN1C2=CC=CC=C2C(=O)N(C)C2=CN=C(NC3=CN(N=C3)C3CCNCC3)N=C12

Smiles: CN1C2=CC=CC=C2C(=O)N(C)C2=CN=C(NC3=CN(N=C3)C3CCNCC3)N=C12

2R)-2-[2-(3

(2011) Bioorg Med Chem

18(12):3396-406

InChiKey: DXOUQSZKEPSXBC-UHFFFAOYSA-N

Clindamycin Size:Contact [email protected] for quotation Smiles: CN1C2=CC=CC=C2C(=O)N(C)C2=CN=C(NC3=CN(N=C3)C3CCNCC3)N=C12Clindamycin is an oral protein synthesis inhibitory agent that has the ability to suppress the expression of virulence factors in Staphylococcus aureus at sub inhibitory concentrations (sub MICs). Clindamycin resistance results from enzymatic methylation of the antibiotic binding site in the 50S ribosomal subunit (23S rRNA). Clindamycin decreases the production of Panton Valentine leucocidin (PVL), toxic shock staphylococcal toxin (TSST 1) or alpha