Clindamycin- 13 C,d 3 is the 13 C- and deuterium labeled Clindamycin. Clindamycin is an orally active and broad-spectrum bacteriostatic lincosamide antibiotic. Clindamycin can inhibit bacterial protein synthesis, possessing 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-haemolysin (Hla). Clindamycin also can be used for researching malaria. In Vitro Stable heavy isotopes of hydrogen, carbon, and other elements have been incorporated into drug molecules, largely as tracers for quantitation during the drug development process. Deuteration has gained attention because of its potential to affect the pharmacokinetic and metabolic profiles of drugs. MCE has not independently confirmed the accuracy of these methods. They are for reference only. Form:Solid
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Clindamycin-13C,d3
CAS number：2140264-63-5 molecular formula：C1713CH30D3ClN2O5S
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| Chinese alias | 克林霉素-13C,d3 | ||
| English alias | - | ||
| CAS number | 2140264-63-5 | molecular formula | C1713CH30D3ClN2O5S |
| molecular weight | 428.99 g/mol | Exact mass | - |
| PSA | - | logp | - |
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