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Clindamycin hydrochloride_Molecular_structure_CAS_21462-39-5)
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Clindamycin hydrochloride

Catalog No. 27543 Name Sigma Aldrich
CAS Number 21462-39-5 Website http://www.sigmaaldrich.com
M. F. C18H34Cl2N2O5S Telephone 1-800-521-8956
M. W. 461.44396 Fax
Purity ≥96.0% (TLC) Email
Storage Chembase ID: 133356

SYNONYMS

IUPAC name
(2S,4R)-N-[(1S,2S)-2-chloro-1-[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(methylsulfanyl)oxan-2-yl]propyl]-1-methyl-4-propylpyrrolidine-2-carboxamide hydrochloride
IUPAC Traditional name
cleocin T gel hydrochloride
Synonyms
Cleocin
(7S)-7-Chloro-7-deoxylincomycin hydrochloride

DATABASE IDS

CAS Number 21462-39-5
Beilstein Number 4070786
MDL Number MFCD07793327
EC Number 244-398-6

PROPERTIES

Empirical Formula (Hill Notation) C18H33ClN2O5S · HCl
Purity ≥96.0% (TLC)
Solubility H2O: soluble50 mg/mL, clear, colorless
MSDS Link Download
Personal Protective Equipment Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
RTECS GF2275000
Storage Temperature 2-8°C
German water hazard class 2

DETAILS

Description (English)
Other Notes
Antibacterial and antiprotozoal antibiotic of the licosamide class.
Review1
Biochem/physiol Actions
Spectrum of Activity: Gram positive cocci and taxoplasma. Especially active against anaerobic bacteria.Mode of Action: Inhibits protein synthesis in bacteria by binding the 50s ribosomal subunit.Clindamycin is a semi-synthetic, lincosamide antibiotic that is prepared from lincomycin. It inhibits bacterial protein synthesis by hydrogen bond interactions with the 23S rRNA component of the 50S ribosomal subunit thus inducing dissociation of the peptidyl-t-RNA complex. Antibacterial and antiprotozoal antibiotic.
Description (简体中文)
Other Notes
Antibacterial and antiprotozoal antibiotic of the licosamide class.
Review1
Biochem/physiol Actions
Spectrum of Activity: Gram positive cocci and taxoplasma. Especially active against anaerobic bacteria.Mode of Action: Inhibits protein synthesis in bacteria by binding the 50s ribosomal subunit.Clindamycin is a semi-synthetic, lincosamide antibiotic that is prepared from lincomycin. It inhibits bacterial protein synthesis by hydrogen bond interactions with the 23S rRNA component of the 50S ribosomal subunit thus inducing dissociation of the peptidyl-t-RNA complex. Antibacterial and antiprotozoal antibiotic.

REFERENCES