Informação sobre produto
- (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
- Ver mais sinónimos
- 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)
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.
Propriedades químicas
Consulta técnica sobre: 3D-AC178993 Clindamycin hydrochloride - 94%
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