Properties White Solid.
Usage antibacterial, inhibits protein synthesis.
Usage Semi-synthetic antibiotic prepared from Lincomycin.
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.
|Characteristics||A white or almost white, crystalline powder||A white crystalline powder|
|Identification||Infrared Absorption||Infrared Absorption|
|Crystallinity||meets the requirements||meets the requirements|
|Acidity||100mg/ml solution PH 3.0-5.5||4.1|
|Related compounds||clindamycin B ≤ 2.0%||1.05%|
|7-epiclindamycin ≤ 4.0%||0.31%|
|other ind ividual related compound ≤ 1.0%||0.20%|
|total of all related compounds ≤ 6.0%||2%|
|Residual solvents||meets the requirements|
|Assay||not less than 800 µg per mg||871µg /mg|
Clindamycin Hydrochloride on anaerobic bacteria and Gram-positive bacteria was inhibited. Lincomycin antimicrobial spectrum and the same, but the strong antibacterial activity, mainly for clinical osteomyelitis caused by anaerobic bacteria infection, respiratory infection, biliary tract infection, endocarditis, otitis media, skin and soft tissue infections and sepsis.