B1638
苯甲酰辅酶 A 锂盐
≥90%
别名:
苯甲酰 CoA 锂盐
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关于此项目
经验公式（希尔记法）:
C28H40N7O17P3S
化学文摘社编号:
分子量:
871.64
NACRES:
NA.51
PubChem Substance ID:
UNSPSC Code:
41106305
MDL number:
Form:
solid
Assay:
≥90%
InChI key
HBWPXONQNHVILU-UHFFFAOYSA-N
SMILES string
[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);;
assay
≥90%
form
solid
storage temp.
−20°C
Quality Level
General description
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。
Biochem/physiol Actions
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。
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Catrin S Günther et al.
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
Liv J Rather et al.
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
Mariam M Gaid et al.
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
Cornelia Chizzali et al.
Beilstein journal of organic chemistry, 8, 613-620 (2012-05-09)
Biphenyls and dibenzofurans are the phytoalexins of the Pyrinae, a subtribe of the plant family Rosaceae. The Pyrinae correspond to the long-recognized Maloideae. Economically valuable species of the Pyrinae are apples and pears. Biphenyls and dibenzofurans are formed de novo
Duo Wang et al.
Nature communications, 13(1), 1369-1369 (2022-03-18)
Lysine benzoylation (Kbz) is a recently discovered post-translational modification associated with active transcription. However, the proteins for maintaining and interpreting Kbz and the physiological roles of Kbz remain elusive. Here, we systematically characterize writer, eraser, and reader proteins of histone
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