Licensed by Pfizer Catalog No.S2457
Molecular Weight(MW): 461.44
Clindamycin HCl inhibits protein synthesis by acting on the 50S ribosomal, used for the treatment of bacterial infections.
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Choose Selective Anti-infection Inhibitors
|Description||Clindamycin HCl inhibits protein synthesis by acting on the 50S ribosomal, used for the treatment of bacterial infections.|
Clindamycin is a classical inhibitor of bacterial protein synthesis, by binding to the 23S ribosomal RNA of the 50S ribosomal subunit. 
|In vivo||Clindamycin hydrochloride results in fast absorption after oral administration in dogs, with a mean absorption time (MAT) of 0.87 hour, and bioavailability is 72.55%. Clindamycin hydrochloride results in total clearance (CL) of Clindamycin after both IV and oral administration (0.503 vs. 0.458 L/h/kg) in dogs. Clindamycin hydrochloride results in volume of distribution at steady-state (IV) at 2.48 L/kg, indicating a wide distribution of clindamycin in body fluids and tissues. Clindamycin serum concentrations after IV and oral administration remain above 0.5 μg/mL approximately for 10 hours.  Clindamycin hydrochloride significantly reduces oral malodor from the dogs' baseline levels through 42 days. Clindamycin hydrochloride also results in significant reductions in dental plaque, dental calculus, and gingival bleeding in dogs.  Clindamycin hydrochloride (2.5 mg/lb), after ultrasonic scaling, root planing, and polishing (USRP) , has a significant effect on plaque and pocket depth measures of periodontal disease but not on gingivitis in canine.  Clindamycin hydrochloride results in complete remission ratio of 71.4% (15/21) in dogs with canine superficial bacterial pyoderma after treat within 14 to 28 days. |
|In vitro||DMSO||92 mg/mL (199.37 mM)|
|Water||92 mg/mL (199.37 mM)|
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Clinical Trial Information
|NCT Number||Recruitment||interventions||Conditions||Sponsor/Collaborators||Start Date||Phases|
|NCT03845790||Recruiting||Other: Blood and microdialysis samples||Surgical Site Infection||Poitiers University Hospital||May 26 2019||Phase 1|
|NCT02782078||Active not recruiting||Biological: Clindamycin and rifampicin dosages||Staphylococcal Infections||Assistance Publique - Hôpitaux de Paris||March 6 2017||Not Applicable|
|NCT03267225||Unknown status||--||VA Drug Interaction||Dr Valerie ZELLER|Fondation Ophtalmologique Adolphe de Rothschild|Groupe Hospitalier Diaconesses Croix Saint-Simon||January 2016||--|
|NCT02629770||Recruiting||Drug: usual antibiotic treatment||Arthritis Infectious|Bone Diseases Infectious||Groupe Hospitalier Diaconesses Croix Saint-Simon|Fondation Ophtalmologique Adolphe de Rothschild||December 2015||--|
|NCT02475876||Active not recruiting||Drug: Clindamycin|Drug: trimethoprim-sulfamethoxazole||Bacterial Infections||Michael Cohen-Wolkowiez|Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)|Duke University||November 2015||Phase 1|
Answers to questions you may have can be found in the inhibitor handling instructions. Topics include how to prepare stock solutions, how to store inhibitors, and issues that need special attention for cell-based assays and animal experiments.
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