LKT Labs

Biochemicals for Life Science Research

Clindamycin Palmitate Hydrochloride

Clindamycin Palmitate Hydrochloride

Product ID C4534
Cas No. 25507-04-4
Purity ≥98%
Product Unit SizeCostQuantityStock
10 mg $107.80 In stock
50 mg $257.70 In stock
100 mg $357.70 In stock
Bulk Quote

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Description

Clindamycin is a lincosamide antibiotic that exhibits antibacterial, anti-protozoan, anti-parasitic, and antimalarial activities. Clindamycin displays efficacy against anaerobic gram negative bacteria, Streptococcus, and Staphylococcus (particularly MRSA). Clindamycin binds 23S rRNA of the ribosomal 50S subunit, preventing translocation and protein synthesis. When co-administered with other anti-parasitic compounds, clindamycin is also occasionally used to treat Plasmodium infection.

Product Info

Cas No.

25507-04-4
Purity

≥98%
Formula

C34H63ClN2O6S • HCl
Formula Wt.

699.85
Chemical Name

(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 palmitate hydrochloride
IUPAC Name

[6-[2-chloro-1-[(1-methyl-4-propylpyrrolidine-2-carbonyl)amino]propyl]- 4,5-dihydroxy-2-methylsulfanyloxan-3-yl] hexadecanoate;hydrochloride
Melting Point

141-143°C
Solubility

Soluble in water, ethanol (330 mg/mL).

Appearance

Almost White Crystal Powder

Shipping and Storage

Store Temp

Ambient
Ship Temp

Ambient

Downloads

MSDS

C4534 MSDS PDF
Info Sheet

C4534 Info Sheet PDF

References

Takem EN, D'Alessandro U. Malaria in pregnancy. Mediterr J Hematol Infect Dis. 2013;5(1):e2013010. PMID: 23350023.

Sireesha P, Setty CR. Detection of various types of resistance patterns and their correlation with minimal inhibitory concentrations against clindamycin among methicillin-resistant Staphylococcus aureus isolates. Indian J Med Microbiol. 2012 Apr-Jun;30(2):165-9. PMID: 22664431.

Wilson DN. On the specificity of antibiotics targeting the large ribosomal subunit. Ann N Y Acad Sci. 2011 Dec;1241:1-16. PMID: 22191523.

Schlünzen F, Zarivach R, Harms J, et al. Structural basis for the interaction of antibiotics with the peptidyl transferase centre in eubacteria. Nature. 2001 Oct 25;413(6858):814-21. PMID: 11677599.

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