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Mechanism of Action
Clindamycin¿¡ ´ëÇÑ Mechanism_Of_Action Á¤º¸ Systemic/Vaginal-Clindamycin inhibits protein synthesis of bacteria by binding to the 50 S ribosomal subunits of the bacteria. Topical-Clindamycin reduces free fatty acid concentrations on the skin and to suppress the growth of Propionibacterium acnes (Corynebacterium acnes) , an anaerobe found in sebaceous glands and follicles.
Pharmacology
Clindamycin¿¡ ´ëÇÑ Pharmacology Á¤º¸ Clindamycin is an antibiotic, similar to and a derivative of lincomycin. Clindamycin can be used in topical or systemic treatment. It is effective as an anti-anaerobic antibiotic and antiprotozoal.
Absorption
Clindamycin¿¡ ´ëÇÑ Absorption Á¤º¸ Rapidly absorbed after oral administration. Absorption of an oral dose is virtually complete (90%), and the concomitant administration of food does not appreciably modify the serum concentrations; serum levels have been uniform and predictable from person to person and dose to dose.
Pharmacokinetics
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Toxicity
Clindamycin¿¡ ´ëÇÑ Toxicity Á¤º¸ Orally and parenterally administered clindamycin has been associated with severe colitis (pseudomembranous colitis) which may result in patient death. Use of the topical formulation of clindamycin results in absorption of the antibiotic from the skin surface. Diarrhea, bloody diarrhea, and colitis (including pseudomembranous colitis) have been reported with the use of topical and systemic clindamycin.
Drug Interactions
Clindamycin¿¡ ´ëÇÑ Drug_Interactions Á¤º¸ Aluminium The aluminium salt decreases the absorption of lincosamidesAtracurium The agent increases the effect of muscle relaxantDihydroxyaluminium The aluminium salt decreases the absorption of lincosamidesCyclosporine Decreases the effect of cyclosporineDoxacurium The agent increases the effect of muscle relaxantGallamine Triethiodide The agent increases the effect of muscle relaxantMetocurine The agent increases the effect of muscle relaxantMivacurium The agent increases the effect of muscle relaxantPancuronium The agent increases the effect of muscle relaxantPipecuronium The agent increases the effect of muscle relaxantRocuronium The agent increases the effect of muscle relaxantSuccinylcholine The agent increases the effect of muscle relaxantTubocurarine The agent increases the effect of muscle relaxantVecuronium The agent increases the effect of muscle relaxantAttapulgite The aluminium salt decreases the absorption of lincosamidesKaolin The aluminium salt decreases the absorption of lincosamides
CYP450 Drug Interaction
[CYP450 TableÁ÷Á¢Á¶È¸]
Drug Target
[Drug Target]
Description
Clindamycin¿¡ ´ëÇÑ Description Á¤º¸ An antibacterial agent that is a semisynthetic analog of lincomycin. [PubChem]
Dosage Form
Clindamycin¿¡ ´ëÇÑ Dosage_Form Á¤º¸ Capsule OralCream IntravaginalCream TopicalLiquid IntramuscularLiquid IntravenousPowder, for solution OralSolution IntravenousSolution Topical
Drug Category
Clindamycin¿¡ ´ëÇÑ Drug_Category Á¤º¸ Anti-Bacterial AgentsLincomycinsProtein Synthesis Inhibitors
Smiles String Canonical
Clindamycin¿¡ ´ëÇÑ Smiles_String_canonical Á¤º¸ CCCC1CC(N(C)C1)C(=O)NC(C(C)Cl)C1OC(SC)C(O)C(O)C1O
Smiles String Isomeric
Clindamycin¿¡ ´ëÇÑ Smiles_String_isomeric Á¤º¸ CCC[C@@H]1C[C@H](N(C)C1)C(=O)N[C@H]([C@H](C)Cl)[C@H]1O[C@H](SC)[C@H](O)[C@@H](O)[C@H]1O
InChI Identifier
Clindamycin¿¡ ´ëÇÑ InChI_Identifier Á¤º¸ InChI=1/C18H33ClN2O5S/c1-5-6-10-7-11(21(3)8-10)17(25)20-12(9(2)19)16-14(23)13(22)15(24)18(26-16)27-4/h9-16,18,22-24H,5-8H2,1-4H3,(H,20,25)/t9?,10-,11+,12?,13+,14-,15-,16-,18-/m1/s1/f/h20H
Chemical IUPAC Name
Clindamycin¿¡ ´ëÇÑ Chemical_IUPAC_Name Á¤º¸ (2S,4R)-N-[2-chloro-1-[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-methylsulfanyloxan-2-yl]propyl]-1-methyl-4-propylpyrrolidine-2-carboxamide
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