Clindamycin

CHEMBL1753 Phase 4 Disetujui Small molecule
Half-Life
2-3 hours
Bioavailability
Protein Binding
Molecular Weight
425.0 g/mol
LogP
2.2
Phase
4

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.

Berat Molekul

424,9830 g/mol

LogP

2,20

TPSA

128,00 Ų

Lipinski RO5

Lulus

Area Terapeutik

Kelas Obat

Mekanisme Kerja

Binds 50S ribosomal subunit inhibiting protein synthesis.

Pharmacokinetics (PK)

Half-Life 2-3 hours

Pharmacodynamics (PD)

Mekanisme

Binds 50S ribosomal subunit inhibiting protein synthesis.

Struktur 2D

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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

Ikatan yang Dapat Dirotasi

7

Atom Berat

27

Primary Target

No side effects recorded

Side effect data is not yet available for this drug.

Pertanyaan yang Sering Diajukan

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

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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.

Penyangkalan Medis

This content is for educational and informational purposes only. It is not a substitute for professional medical advice, diagnosis, or treatment. Always consult a qualified healthcare provider before making medication decisions.

Data sources: ChEMBL, PubChem, DailyMed.