berninamycin A

berninamycin A 구조식 이미지
카스 번호:
58798-97-3
상품명:
berninamycin A
동의어(영문):
Berninamycin;berninamycin A;BerninaMycin, U27810;Alaninamide, L-threonyl-2-[(1Z)-1-amino-1-propen-1-yl]-5-methyl-4-oxazolecarbonyl-2,3-didehydroalanyl-3-methyl-L-threonyl-2-(1-aminoethenyl)-5-methyl-4-oxazolecarbonyl-2,3-didehydroalanyl-6-[2-(1-aminoethenyl)-4-oxazolyl]-5-(4-carboxy-2-thiazolyl)-2-pyridinecarbonyl-2,3-didehydroalanyl-2,3-didehydro...
CBNumber:
CB01361481
분자식:
C51H51N15O15S
포뮬러 무게:
1146.11
MOL 파일:
58798-97-3.mol

berninamycin A 속성

녹는점
>290°
저장 조건
Store at -20°C
용해도
DMSO에 용해됨
물리적 상태
고체
물리적 상태
단단한 모양
색상
하얀색

안전

berninamycin A C화학적 특성, 용도, 생산

용도

Berninamycin A is an antibiotic discovered in 1976 from a strain of Streptomyces. Berninamycin A is a macrocyclic "peptide" comprising atypical amino acids linked to thiazole and oxazoles. Chemically very complex, berninamycin A is an inducer of tipA, a gene that controls the bacterial transcription regulators, TipAL and TipAS, that are central to multidrug resistance. Berninamycin A is closely related to siomycin, a recently discovered inhibitor of oncogenic transcription factor, FoxM1.

효소 저해제

This fungal antibiotic (FW = 1146.12 g/mol; CAS 58798-97-3; Soluble in DMSO), also known as Antibiotic U27810, from Streptomyces bernensis inhibits protein biosynthesis by binding to a complex formed by ribosomal 23S and the L11 protein, thereby disrupting the function of the ribosome’s A site and inhibiting protein synthesis in Gram-positive bacteria. In this respect, it has the same mode of action as thiostrepton. Streptomyces bernensis and Streptomyces azureus, which produce berninamycin and thiostrepton, respectively, possess similar ribosomal RNA methylases that mediate specific pentose-directed methylation of 23S ribosomal RNA, rendering the modified ribosomes resistant to these antibiotics.

berninamycin A 준비 용품 및 원자재

원자재

준비 용품


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