Clindamycin Hydrochloride
The hydrochloride salt form of clindamycin used in oral capsules for treating bacterial infections of the skin, lungs, and soft tissues. It works by inhibiting bacterial ribosomal protein synthesis.
Peso molecular
461,4000 g/mol
TPSA
128,00 Ų
Áreas terapéuticas
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.Cl
InChI
InChI=1S/C18H33ClN2O5S.ClH/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);1H/t9-,10+,11-,12+,13-,14+,15+,16+,18+;/m0./s1
Molecular Formula
C18H34Cl2N2O5S
HBD / HBA
5 / 7
Enlaces Rotables
7
Átomos Pesados
28
No targets recorded
Target interaction data is not yet available for this drug.
No interactions recorded
Drug interaction data is not yet available for this compound.
No side effects recorded
Side effect data is not yet available for this drug.
Preguntas frecuentes
The hydrochloride salt form of clindamycin used in oral capsules for treating bacterial infections of the skin, lungs, and soft tissues. It works by inhibiting bacterial ribosomal protein synthesis.
Binds 50S ribosomal subunit inhibiting protein synthesis.
Yes, Clindamycin Hydrochloride is an approved drug. It has reached clinical phase 4. It is classified as a Small molecule.
References & Data Sources
- ChEMBL — European Bioinformatics Institute (EBI). CHEMBL1200588. Open-access bioactivity database.
- PubChem — National Center for Biotechnology Information (NCBI). CID 16051951. Chemical information database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-03-04.
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