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Home > Encyclopedia > Clindamycin hydrochloride monohydrate

Clindamycin hydrochloride monohydrate

pharmaceutical raw materials
Clindamycin hydrochloride monohydrate structure

Clindamycin hydrochloride monohydrate 

structure
  • CAS No:

    58207-19-5

  • Formula:

    C18H34Cl2N2O5S

  • Chemical Name:

    Clindamycin hydrochloride monohydrate

  • Synonyms:

    U-21251F;(7S)-7-CHLORO-7-DEOXYLINCOMYCIN HYDROCHLORIDE;7(S)-CHLORO-7-DEOXYLINCOMYCIN;7(S)-CHLORO-7-DEOXYLINCOMYCIN HCL;7[S]-CHLORO-7-DEOXYLINCOMYCIN HYDROCHLORIDE;(2S-TRANS)-METHYL 7-CHLORO-6,7,8-TRIDEOXY-6[[(1-METHYL-4-PROPYL-2-PYRROLIDINYL)CARBONYL]AMINO]-1-THIO-L-THREO-ALPHA-D-GALACTO-OCTOPYRANOSIDE;(2S-trans)-Methyl 7-Chloro-6,7,8-trideoxy-6[[(1-methyl-4-propyl-2-pyrrolidinyl)carbonyl]amino]-1-thio-L-threo-α-D-galacto-octopyranoside;Clindamycin Hydrochloride Monohydrate

  • Categories:

    Active Pharmaceutical Ingredients  >  Antibiotics

Description

Clindamycin hydrochloride monohydrate is an oral protein synthesis inhibitory agent that has the ability to suppress the expression of virulence factors in Staphylococcus aureus at sub-inhibitory concentrations (sub-MICs). Clindamycin hydrochloride monohydrate resistance results from enzymatic methylation of the antibiotic binding site in the 50S ribosomal subunit (23S rRNA). Clindamycin hydrochloride monohydrate decreases the production of Panton-Valentine leucocidin (PVL), toxic-shock-


White Crystalline Solid

Clindamycin hydrochloride monohydrate Basic Attributes

461.44

478.167114

244-398-6

White to Almost white

29419090

Characteristics

136.79000

1.45600

White Crystalline Solid

143 °C

647ºC at 760 mmHg

345.1ºC

143 ° (C=2, H2O)

Soluble in water

2-8°C

Safety Information

3

NONH for all modes of transport

3

Xi

26-37/39-24/25

GF2275000

Xi

36/37/38

Clindamycin hydrochloride monohydrate Use and Manufacturing

An antibiotic


Clindamycin hydrochloride monohydrate is an antibacterial agent that is a semisynthetic analog of lincomycin.

Drug Function and Efficacy

Clindamycin inhibits bacterial protein synthesis by binding to the 23S RNA of the 50S subunit of the ribosome. It is bacteriostatic and active against various Gram-positive bacteria and anaerobic bacteria.

This ingredient has been used in drugs with the following functions (note: it does not mean that the ingredient itself has the following health functions)

Related Drugs

Registered Holders

  • Zhejiang Hisoar Chuannan Pharmaceutical Co.,Ltd.

    Japan Japan
    Active
  • SUZHOU NUMBER 4 PHARMACEUTICAL FACTORY

    United States United States
    Inactive

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