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Merck
CN

M1762

Sigma-Aldrich

甲基丙二酰辅酶A 四锂盐 水合物

≥90% (HPLC)

别名:

α-甲基丙二酰辅酶 A 四锂盐, 甲基丙二酰辅酶A

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About This Item

经验公式(希尔记法):
C25H36Li4N7O19P3S · xH2O
分子量:
891.34 (anhydrous basis)
MDL编号:
UNSPSC代码:
41106305
PubChem化学物质编号:
NACRES:
NA.51

质量水平

检测方案

≥90% (HPLC)

储存温度

−20°C

SMILES字符串

[Li+].[Li+].[Li+].[Li+].O.CC(C([O-])=O)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/C25H40N7O19P3S.4Li.H2O/c1-12(23(37)38)24(39)55-7-6-27-14(33)4-5-28-21(36)18(35)25(2,3)9-48-54(45,46)51-53(43,44)47-8-13-17(50-52(40,41)42)16(34)22(49-13)32-11-31-15-19(26)29-10-30-20(15)32;;;;;/h10-13,16-18,22,34-35H,4-9H2,1-3H3,(H,27,33)(H,28,36)(H,37,38)(H,43,44)(H,45,46)(H2,26,29,30)(H2,40,41,42);;;;;1H2/q;4*+1;/p-4/t12?,13-,16-,17-,18+,22-;;;;;/m1...../s1

InChI key

ANDKBBZIPFWODN-WLVKLPLXSA-J

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应用

甲基丙二酰辅酶 A (CoA) 已用于超高效液相色谱-质谱法 (UPLC-MS/MS) 中校准曲线的制备。 也用于测定甲基丙二酰辅酶 a 变位酶和甲基丙二酰辅酶 a 差向异构酶活性。
辅酶 A 作为酰基载体,即乙酰辅酶 A 发挥作用。甲基丙二酰辅酶 A (MM-CoA) 是用于研究甲基丙二酰辅酶 A 变位酶(琥珀酰-Ca 形成)、甲基丙二酰辅酶 A 脱羧酶 (EC 4.1.1.41) 和甲基丙二酰辅酶 A 水解酶 (EC 3.1.2.17) 等酶的特异性和动力学的底物。

生化/生理作用

甲基丙二酰辅酶 A (CoA) 是单链脂肪酸、胆固醇和少量氨基酸(如缬氨酸、异亮氨酸、蛋氨酸、苏氨酸)的降解产物。 由丙酰辅酶 a 羧化酶 (PCC) 的活性产生。甲基丙二酰辅酶 A (CoA) 通过甲基丙二酰辅酶 A 变位酶 (MCM) 和维生素 B12 作为辅助因子转化为琥珀酰辅酶 A。低 MCM 活性或维生素 B12 代谢改变导致遗传代谢病甲基丙二酸血症 (MMA)。

象形图

Exclamation mark

警示用语:

Warning

危险声明

危险分类

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

靶器官

Respiratory system

WGK

WGK 3

个人防护装备

dust mask type N95 (US), Eyeshields, Gloves


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Han Y, et al.
Applied and Environmental Microbiology, 78(17), 6194-6202 (2012)
Csaba Paizs et al.
Bioorganic chemistry, 36(6), 261-264 (2008-08-01)
The reported presence of a coenzyme B12-dependent methylmalonyl-CoA mutase in potatoes has been reexamined. The enzyme converting methylmalonyl-CoA was purified to electrophoretic homogeneity. Examination of the reaction product by 1H, 31P NMR and mass spectrometry revealed that it was methylmalonyl-3'-dephospho-CoA.
Valentin Cracan et al.
The Journal of biological chemistry, 285(1), 655-666 (2009-10-30)
Coenzyme B(12) is used by two highly similar radical enzymes, which catalyze carbon skeleton rearrangements, methylmalonyl-CoA mutase and isobutyryl-CoA mutase (ICM). ICM catalyzes the reversible interconversion of isobutyryl-CoA and n-butyryl-CoA and exists as a heterotetramer. In this study, we have
Assay for methylmalonyl coenzyme A mutase activity based on determination of succinyl coenzyme A by ultrahigh-performance liquid chromatography tandem mass spectrometry
Gotoh K, et al.
Analytical and Bioanalytical Chemistry, 407(18), 5281-5286 (2015)
Hannah K D'Ambrosio et al.
iScience, 25(6), 104443-104443 (2022-07-26)
Type I polyketide synthases (PKSs) are multidomain, multimodule enzymes capable of producing complex polyketide metabolites. These modules contain an acyltransferase (AT) domain, which selects acyl-CoA substrates to be incorporated into the metabolite scaffold. Herein, we reveal the sequences of three

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