Clindamycin
An antibiotic that stops bacterial growth by blocking protein synthesis, effective against a wide range of skin, respiratory, and soft tissue infections. It is particularly valued for treating infections caused by anaerobic bacteria and certain drug-resistant organisms.
Peso molecular
424,9830 g/mol
LogP
2,20
TPSA
128,00 Ų
Regla de cinco de Lipinski
Cumple
Áreas terapéuticas
Clases de fármacos
Mecanismo de acción
Binds 50S ribosomal subunit inhibiting protein synthesis.
Pharmacokinetics (PK)
Pharmacodynamics (PD)
Binds 50S ribosomal subunit inhibiting protein synthesis.
Estructura 2D
Cite this structure
Embed this structure
SMILES
CCC[C@@H]1C[C@@H](C(=O)N[C@@H]([C@H]2O[C@H](SC)[C@H](O)[C@@H](O)[C@H]2O)[C@H](C)Cl)N(C)C1
InChI
InChI=1S/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+/m0/s1
Molecular Formula
C18H33ClN2O5S
HBD / HBA
4 / 7
Enlaces Rotables
7
Átomos Pesados
27
Clindamycin may reduce renal tubular secretion of methotrexate, raising methotrexate levels and increasing the risk of haematological and GI toxicity.
Clindamycin may enhance the anticoagulant effect of warfarin by disrupting vitamin K-producing gut flora, leading to unpredictable INR elevations and increased bleeding risk during and shortly after the antibiotic course.
No side effects recorded
Side effect data is not yet available for this drug.
Preguntas frecuentes
An antibiotic that stops bacterial growth by blocking protein synthesis, effective against a wide range of skin, respiratory, and soft tissue infections. It is particularly valued for treating infections caused by anaerobic bacteria and certain drug-resistant organisms.
Binds 50S ribosomal subunit inhibiting protein synthesis.
Key pharmacokinetic parameters for Clindamycin: Half-life: 2-3 hours.
Yes, Clindamycin is an approved drug. It has reached clinical phase 4. It is classified as a Small molecule.
Related Drugs
Same Drug Class
References & Data Sources
- ChEMBL — European Bioinformatics Institute (EBI). CHEMBL1753. Open-access bioactivity database.
- PubChem — National Center for Biotechnology Information (NCBI). CID 446598. Chemical information database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-03-04.
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