
CAS 154163-93-6
:azicemicin A
Description:
Azicemicin A is a natural product belonging to the class of macrolide antibiotics, characterized by its complex structure that includes a large lactone ring. It is derived from the fermentation of specific bacterial strains, particularly those in the genus Micromonospora. Azicemicin A exhibits potent antibacterial activity, particularly against Gram-positive bacteria, making it a subject of interest in pharmaceutical research. Its mechanism of action typically involves inhibition of protein synthesis, which is a common feature among macrolide antibiotics. The compound is known for its unique stereochemistry and functional groups, which contribute to its biological activity and stability. Additionally, azicemicin A has been studied for its potential applications in treating various infections, although its clinical use may be limited by factors such as resistance and toxicity. Overall, azicemicin A represents a significant example of the diverse chemical structures found in natural antibiotics and highlights the ongoing exploration of microbial metabolites in drug discovery.
Formula:C23H25NO9
Synonyms:- Benz[a]anthracene-1,6(2H,5H)-dione, 3,4,4a,12b-tetrahydro-3,7,8,10,12b-pentahydroxy-9,12-dimethoxy-3-(1-methyl-2-aziridinyl)-
- azicemicin A
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Azicemicin A
CAS:<p>Azicemicin A exhibits mild antibacterial activity and shows no acute toxicity when administered via intraperitoneal injection to mice at a dosage of 150 mg/kg.</p>Formula:C23H25NO9Color and Shape:SolidMolecular weight:459.446
