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质量水平
方案
≥90%
表单
solid
储存温度
−20°C
SMILES字符串
[Li].CC(C)(COP(O)(=O)OP(O)(=O)OCC1OC(C(O)C1OP(O)(O)=O)n2cnc3c(N)ncnc23)C(O)C(=O)NCCC(=O)NCCSC(=O)c4ccccc4
InChI
1S/C28H40N7O17P3S.Li.H/c1-28(2,22(38)25(39)31-9-8-18(36)30-10-11-56-27(40)16-6-4-3-5-7-16)13-49-55(46,47)52-54(44,45)48-12-17-21(51-53(41,42)43)20(37)26(50-17)35-15-34-19-23(29)32-14-33-24(19)35;;/h3-7,14-15,17,20-22,26,37-38H,8-13H2,1-2H3,(H,30,36)(H,31,39)(H,44,45)(H,46,47)(H2,29,32,33)(H2,41,42,43);;
InChI key
HBWPXONQNHVILU-UHFFFAOYSA-N
一般描述
苯甲酰基辅酶A(苯甲酰基CoA)是CoA依赖性环氧化物途径中的一个中间体,在苯甲酸酯-CoA连接酶存在下由苯甲酸酯合成。它可进一步转化为2,3-环氧苯甲酰辅酶A,该步骤由苯甲酰辅酶A还原酶(BoxA)和苯甲酰辅酶A加氧酶(BoxB)进行催化。
生化/生理作用
苯甲酰辅酶A(苯甲酰CoA)可用于苯甲酸酯的代谢研究。 苯甲酰CoA是苯甲酰辅酶A(CoA)氧化环氧酶系统BoxAB的组成部分。 苯甲酰辅酶A也可作为底物,用于表征特定的醇酰基转移酶。苯甲酰辅酶A可用作合成联苯和二苯并呋喃植物抗毒素(聚酮化合物衍生物)的起始底物。
苯甲酰辅酶A(苯甲酰CoA)是苯甲酰CoA还原酶的底物(图框A) 和用于III型聚酮化合物合酶的一种起始底物。它还可充当植物酶联苯合酶(BIS)和二苯甲酮合酶(BPS)的底物。苯甲酰辅酶A是细菌睾丸酮丛毛单胞菌中龙胆酸盐途径的一个效应子。它也可以作为底物用于表征特定醇酰基转移酶和N-酰基转移酶测定。
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
Eyeshields, Gloves, type N95 (US)
从最新的版本中选择一种:
Phytochemistry, 72(8), 700-710 (2011-04-01)
Volatile esters are key compounds of kiwifruit flavour and are formed by alcohol acyltransferases that belong to the BAHD acyltransferase superfamily. Quantitative RT-PCR was used to screen kiwifruit-derived expressed sequence tags with proposed acyltransferase function in order to select ripening-specific
The Journal of biological chemistry, 286(33), 29241-29248 (2011-06-03)
The coenzyme A (CoA)-dependent aerobic benzoate metabolic pathway uses an unprecedented chemical strategy to overcome the high aromatic resonance energy by forming the non-aromatic 2,3-epoxybenzoyl-CoA. The crucial dearomatizing reaction is catalyzed by three enzymes, BoxABC, where BoxA is an NADPH-dependent
Biochimica et biophysica acta, 1814(12), 1609-1615 (2011-06-16)
BoxA is the reductase component of the benzoyl-coenzyme A (CoA) oxidizing epoxidase enzyme system BoxAB. The enzyme catalyzes the key step of an hitherto unknown aerobic, CoA-dependent pathway of benzoate metabolism, which is the epoxidation of benzoyl-CoA to the non-aromatic
Journal of plant physiology, 168(9), 944-951 (2011-02-19)
Sorbus aucuparia cell cultures accumulate biphenyl and dibenzofuran phytoalexins in response to elicitor treatment. These polyketide derivatives arise from the starter substrate benzoyl-CoA, the biosynthesis of which is largely unresolved. Two CoA ligases involved are cinnamate:CoA ligase and benzoate:CoA ligase
A versatile biosynthetic approach to amide bond formation
Green Chemistry, 20(15), 3426-3431 (2018)
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