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化驗
~90% (HPLC)
形狀
solid
雜質
≤10% water
溶解度
H2O: 50 mg/mL, clear, colorless
儲存溫度
−20°C
SMILES 字串
[Li+].[Li+].[Li+].C\C=C\C(=O)SCCNC(=O)CCNC(=O)[C@H](O)C(C)(C)COP([O-])(=O)OP([O-])(=O)OC[C@H]1O[C@H]([C@H](O)[C@@H]1OP(O)([O-])=O)n2cnc3c(N)ncnc23
InChI
1S/C25H40N7O17P3S.3Li/c1-4-5-16(34)53-9-8-27-15(33)6-7-28-23(37)20(36)25(2,3)11-46-52(43,44)49-51(41,42)45-10-14-19(48-50(38,39)40)18(35)24(47-14)32-13-31-17-21(26)29-12-30-22(17)32;;;/h4-5,12-14,18-20,24,35-36H,6-11H2,1-3H3,(H,27,33)(H,28,37)(H,41,42)(H,43,44)(H2,26,29,30)(H2,38,39,40);;;/q;3*+1/p-3/b5-4+;;;/t14-,18-,19-,20+,24-;;;/m1.../s1
InChI 密鑰
LUYQFKSDLNQLEG-OUWZIDFPSA-K
應用
巴豆酰辅酶A(巴豆酰-CoA)可用作抗结核和抗疟疾药物研究的底物,帮助鉴定和表征恶性疟原虫烯酰-ACP还原酶(PfENR)等酶以及其他可能成为有效药物靶标的烯酰辅酶A还原酶。 巴豆酰-CoA可用作β-羟基酰基-酰基载体蛋白(ACP)脱水酶(FabZ)动力学研究的底物类似物。
其他說明
通过丁酰-CoA/巴豆酰-CoA组合对一般酰基-CoA脱氢酶进行氧化还原;大鼠肝微粒体反式-2-烯酰-CoA还原酶的纯化
儲存類別代碼
11 - Combustible Solids
水污染物質分類(WGK)
WGK 3
閃點(°F)
Not applicable
閃點(°C)
Not applicable
個人防護裝備
Eyeshields, Gloves, type N95 (US)
其他客户在看
Biochemical and biophysical research communications, 524(3), 730-735 (2020-02-10)
Post-translational modifications (PTMs) play pivotal roles in controlling the stability and activity of the tumor suppressor p53 in response to distinct stressors. Here we report an unexpected finding of a short chain fatty acid modification of p53 in human cells.
A new β-hydroxyacyl-acyl carrier protein dehydratase (FabZ) from Helicobacter pylori: Molecular cloning, enzymatic characterization, and structural modeling.
Biochemical and Biophysical Research Communications, 12, 1078-1086 (2005)
Purification of rat liver microsomal trans-2-enoyl-CoA reductase.
Preparative biochemistry, 17(4), 315-325 (1987-01-01)
FEBS letters, 581(8), 1561-1566 (2007-03-27)
An NADH-dependent trans-2-enoyl-CoA reductase (EC1.1.1.36) from the Gram negative spirochete Treponema denticola was identified, expressed and biochemically characterized. The recombinant protein is a monomeric enzyme with a molecular mass of 44 kDa with a specific activity of 43+/-4.8 U/mg (micromol
IUBMB life, 61(11), 1083-1091 (2009-10-28)
A structure-based approach has been adopted to develop 2'-substituted analogs of triclosan. The Cl at position 2' in ring B of triclosan was chemically substituted with other functional groups like NH(2), NO(2) and their inhibitory potencies against PfENR were determined.
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