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Clindamycin

克林黴素

Mechanism of action:

Clindamycin 是一種林克醯胺類抗生素(lincosamide antibiotic)。Clindamycin 能可逆性結合在細菌核糖體 50S 亞基上,特別是與 23S rRNA 的 peptidyl transferase 中心結合。這能阻止肽鏈延長並干擾轉位(translocation),阻斷蛋白質合成,抑制細菌生長。

​Reference(s):

1. Daum RS et al. (2007). Clinical practice: Skin and soft-tissue infections caused by methicillin-resistant Staphylococcus aureus. N Engl J Med. 


2. Klempner MS et al. (1981). Clindamycin uptake by human neutrophils. J Infect Dis. 


3. Lamont RF et al. (2005). Can antibiotics prevent preterm birth—the pro and con debate. BJOG.

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