Clindamycin hydrochloride - 94%

CAS: 21462-39-5

Ref. 3D-AC178993

Información del producto

• Nombre: Clindamycin hydrochloride - 94%
• Sinónimos: (2R,4S)-N-[2-chloro-1-[(2S,3S,4R,5S,6S)-3,4,5-trihydroxy-6-methylsulfanyl-tetrahydropyran-2-yl]propyl]-1-methyl-4-propyl-pyrrolidine-2-carboxamide hydrochloride, 7(S)-Chloro-7-deoxylincomycin hydrochloride, 7-Chloro-7-deoxylincomycin hydrochloride, <span class="text-smallcaps">L</smallcap>-threo-α-<smallcap>D</smallcap>-galacto-Octopyranoside, methyl 7-chloro-6,7,8-trideoxy-6-(1-methyl-4-propyl-<smallcap>L</span>-2-pyrrolidinecarboxamido)-1-thio-, monohydrochloride, trans- α-, <span class="text-smallcaps">L</smallcap>-threo-α-<smallcap>D</span>-galacto-Octopyranoside, methyl 7-chloro-6,7,8-trideoxy-6-[[(1-methyl-4-propyl-2-pyrrolidinyl)carbonyl]amino]-1-thio-, monohydrochloride, (2S-trans)-, <span class="text-smallcaps">L</smallcap>-threo-α-<smallcap>D</span>-galacto-Octopyranoside, methyl 7-chloro-6,7,8-trideoxy-6-[[[(2S,4R)-1-methyl-4-propyl-2-pyrrolidinyl]carbonyl]amino]-1-thio-, hydrochloride (1:1), <span class="text-smallcaps">L</smallcap>-threo-α-<smallcap>D</span>-galacto-Octopyranoside, methyl 7-chloro-6,7,8-trideoxy-6-[[[(2S,4R)-1-methyl-4-propyl-2-pyrrolidinyl]carbonyl]amino]-1-thio-, monohydrochloride, Antirobe vet., Cleocin hydrochloride, ClidamycinHydrochloride, Clinacin, Clindamycin HCl, Clindavet, Clindimycin hydrochloride, Clindomycin hydrochloride, Dalacina, methyl 7-chloro-6,7,8-trideoxy-6-({[(2R)-1-methyl-4-propylpyrrolidinium-2-yl]carbonyl}amino)-1-thio-beta-L-erythro-octopyranoside chloride, methyl 7-chloro-6,7,8-trideoxy-6-{[(4R)-1-methyl-4-propyl-L-prolyl]amino}-1-thio-L-threo-alpha-D-galacto-octopyranoside hydrochloride (1:1)

Descripción

Clindamycin is a lincosamide antibiotic that inhibits the bacterial enzyme, protein synthesis, by binding to the ribosome. It is used in the treatment of a wide range of infections caused by susceptible bacteria. Clindamycin has been shown to have affinity for human plasma proteins and can be detected in blood plasma at concentrations as low as 5 micrograms per millilitre following an intravenous dose. The primary target for clindamycin is the prokaryotic 50S subunit of the ribosome, which binds to the 30S subunit. Clindamycin has been shown to inhibit ionizable antibiotics such as erythromycin and chloramphenicol. Clindamycin also inhibits drug transport into bacteria and can bind to environmental contaminants such as metoprolol and caffeine.

• Marca: Biosynth

Propiedades químicas

• Peso molecular: 461.44 g/mol
• Fórmula: C₁₈H₃₃ClN₂O₅S·HCl
• Color/Forma: Powder