SMB00010
环素
≥95% (LC/MS-ELSD)
别名:
Albocyclin, Cineromycin-β-methylaether, Ingramycin
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关于此项目
经验公式（希尔记法）:
C18H28O4
化学文摘社编号:
分子量:
308.41
MDL编号:
UNSPSC代码:
12352205
PubChem化学物质编号:
NACRES:
NA.25
方案
≥95% (LC/MS-ELSD)
表单
solid
应用
metabolomics
vitamins, nutraceuticals, and natural products
储存温度
−20°C
SMILES字符串
O1[C@@H]([C@H](CC\C=C(\[C@H](\C=C\[C@](\C=C\C1=O)(O)C)OC)/C)C)C
InChI
1S/C18H28O4/c1-13-7-6-8-14(2)16(21-5)9-11-18(4,20)12-10-17(19)22-15(13)3/h8-13,15-16,20H,6-7H2,1-5H3/b11-9+,12-10+,14-8+/t13-,15+,16-,18+/m0/s1
InChI key
BYWWNDLILWPPJP-REXWONOSSA-N
一般描述
Natural product derived from fungal source.
警示用语：
Danger
危险声明
危险分类
Acute Tox. 3 Oral
储存分类代码
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
法规信息
新产品
此项目有
历史批次信息供参考:
Albocycline- and carbomycin-type macrolides, inhibitors of human prolyl endopeptidases.
C Christner et al.
The Journal of antibiotics, 51(3), 368-371 (1998-05-20)
R C Thomas et al.
The Journal of antibiotics, 35(12), 1658-1664 (1982-12-01)
The structure and absolute configuration of the macrolide antibiotic albocycline (1a) has been determined by X-ray crystallographic analysis on the derived p-bromobenzoate (1b). The absolute configuration of albocycline is 4R, 7S, 12S, 13R.
A new inhibitor of melanogenesis, albocycline K3, produced by Streptomyces sp. OH-3984.
S Takamatsu et al.
The Journal of antibiotics, 49(5), 485-486 (1996-05-01)
Biosynthesis of albocycline: origin of the carbon skeleton.
A Taddei et al.
The Journal of antibiotics, 50(6), 526-528 (1997-06-01)
Robert V O'Brien et al.
The Journal of antibiotics, 67(1), 89-97 (2013-12-05)
The increasing availability of DNA sequence data offers an opportunity for identifying new assembly-line polyketide synthases (PKSs) that produce biologically active natural products. We developed an automated method to extract and consolidate all multimodular PKS sequences (including hybrid PKS/non-ribosomal peptide
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