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

InChI: InChI=1/C23H25NO9/c1-24-8-13(24)22(30)6-9-4-11(25)16-17(23(9,31)14(27)7-22)20(32-2)10-5-12(26)21(33-3)19(29)15(10)18(16)28/h5,9,13,26,28-31H,4,6-8H2,1-3H3

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
• Benz(a)anthracene-1,6(2H,5H)-dione, 3,4,4a,12b-tetrahydro-9,12-dimethoxy-3-(1-methyl-2-aziridinyl)-3,7,8,10,12b-pentahydroxy-
• 3,7,8,10,12b-pentahydroxy-9,12-dimethoxy-3-(1-methylaziridin-2-yl)-3,4,4a,12b-tetrahydrotetraphene-1,6(2H,5H)-dione

Azicemicin A

CAS: 154163-93-6

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.

Formula: C₂₃H₂₅NO₉

Color and Shape: Solid

Molecular weight: 459.446

Ref: TM-TN10694