Clindamycin Palmitate

CHEMBL1201289 Phase 4 Одобрено Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
663.4 g/mol
LogP
10.1
Phase
4

An inactive form of the antibiotic clindamycin that is converted to its active parent compound after absorption. It is used to treat bacterial infections caused by certain anaerobic bacteria and gram-positive organisms, including skin and respiratory tract infections. This salt form is most commonly used in oral liquid preparations for easier dosing.

Молекулярная масса

663,4000 g/mol

LogP

10,10

TPSA

134,00 Ų

Правило пяти Липинского

Не соответствует

Терапевтические области

Pharmacokinetics (PK)

Pharmacodynamics (PD)

2D Структура

SVG PNG

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SMILES

CCCCCCCCCCCCCCCC(=O)O[C@@H]1[C@@H](O)[C@@H](O)[C@@H]([C@H](NC(=O)[C@@H]2C[C@@H](CCC)CN2C)[C@H](C)Cl)O[C@@H]1SC

InChI

InChI=1S/C34H63ClN2O6S/c1-6-8-9-10-11-12-13-14-15-16-17-18-19-21-27(38)42-32-30(40)29(39)31(43-34(32)44-5)28(24(3)35)36-33(41)26-22-25(20-7-2)23-37(26)4/h24-26,28-32,34,39-40H,6-23H2,1-5H3,(H,36,41)/t24-,25+,26-,28+,29+,30-,31+,32+,34+/m0/s1

Molecular Formula

C34H63ClN2O6S

HBD / HBA

3 / 8

Вращаемые Связи

23

Тяжёлые Атомы

44

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.

Часто задаваемые вопросы

An inactive form of the antibiotic clindamycin that is converted to its active parent compound after absorption. It is used to treat bacterial infections caused by certain anaerobic bacteria and gram-positive organisms, including skin and respiratory tract infections. This salt form is most commonly used in oral liquid preparations for easier dosing.

Yes, Clindamycin Palmitate is an approved drug. It has reached clinical phase 4. It is classified as a Small molecule.

{# References & Data Sources section for drug detail pages. Renders standard pharmacological database links plus the drug's data_sources field. #}

References & Data Sources

  • ChEMBL — European Bioinformatics Institute (EBI). CHEMBL1201289. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 16052039. Chemical information database.

Data aggregated from publicly available pharmacological databases. Last updated 2026-03-04.

Медицинский отказ от ответственности

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.