Clindamycin hydrochloride 21462-39-5,chemical research,C18H34Cl2N2O5S
Product Name: | Clindamycin hydrochloride |
Synonyms: | (2S-TRANS)-METHYL 7-CHLORO-6,7,8-TRIDEOXY-6[[(1-METHYL-4-PROPYL-2-PYRROLIDINYL)CARBONYL]AMINO]-1-THIO-L-THREO-ALPHA-D-GALACTO-OCTOPYRANOSIDE;(7S)-7-CHLORO-7-DEOXYLINCOMYCIN HYDROCHLORIDE;7(S)-CHLORO-7-DEOXYLINCOMYCIN;7(S)-CHLORO-7-DEOXYLINCOMYCIN HCL;7[S]-CHLORO-7-DEOXYLINCOMYCIN HYDROCHLORIDE;CLEOCIN;CLEOCIN HYDROCHLORIDE;CLINDAMYCIN HCL |
CAS: | 21462-39-5 |
MF: | C18H34Cl2N2O5S |
MW: | 461.44 |
EINECS: | 244-398-6 |
Product Categories: | Antibiotic Explorer;Peptide Synthesis/Antibiotics;Carbohydrates & Derivatives;Heterocycles;Intermediates & Fine Chemicals;Pharmaceuticals;Sulfur & Selenium Compounds;CLINSOL;antibiotic;Antimicrobial;API;Inhibitors |
Clindamycin hydrochloride Usage And Synthesis |
Chemical Properties | White Solid |
Usage | antibacterial, inhibits protein synthesis |
Usage | Clindamycin hydrochloride is a salt of clindamycin, a semi-synthetic lincosamide. The hydrochloride salt forms at the basic N-ethylproline moiety and is the preferred pharmaceutical formulation. Like other members of the lincosamide family, clindamycin is a broad spectrum antibiotic with activity against anaerobic bacteria and protozoans. Clindamycin hydrochloride acts by binding to the 23S ribosomal subunit, blocking protein synthesis. Clindamycin hydrochloride has been extensively studied with over 8,000 literature citations. |
Usage | Labelled Clindamycin. Semi-synthetic antibiotic prepared from Lincomycin;Labeled Clindamycin, intended for use as an internal standard for the quantification of Clindamycin by GC- or LC-mass spectrometry. |
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