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Merck
CN

M1762

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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关于此项目

经验公式（希尔记法）:
C25H36Li4N7O19P3S · xH2O
化学文摘社编号:
104809-02-1
分子量:
891.34 (anhydrous basis)
NACRES:
NA.51
PubChem Substance ID:
24896685
UNSPSC Code:
41106305
MDL number:
MFCD10567443

主要文件

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产品名称

甲基丙二酰辅酶A 四锂盐 水合物, ≥90% (HPLC)

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

SMILES string

[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 key

ANDKBBZIPFWODN-WLVKLPLXSA-J

assay

≥90% (HPLC)

form

powder

solubility

H2O: soluble-50 mg/mL, clear, colorless

storage temp.

−20°C

Quality Level

200

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相关类别

Application

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。

Biochem/physiol Actions

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)。

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

存储类别

11 - Combustible Solids

wgk

WGK 3

ppe

dust mask type N95 (US), Eyeshields, Gloves

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
0000508610
0000508612
0000508612
0000508610
0000433520

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Dominique Padovani et al.
Nature chemical biology, 4(3), 194-196 (2008-02-12)
The reactivity and relative rarity of most cofactors pose challenges for their delivery to target enzymes. Using kinetic analyses, we demonstrate that adenosyltransferase, which catalyzes the final step in the assimilation of coenzyme B12, directly transfers the cofactor to methylmalonyl
Filippo Carlucci et al.
Electrophoresis, 28(12), 1921-1925 (2007-05-23)
Methylmalonyl-coenzyme A mutase (MCM) is a 5'-deoxyadenosylcobalamin-linked mitochondrial enzyme that catalyzes the isomerization of L-methylmalonyl-coenzyme A to succinyl-coenzyme A. We described a method for methylmalonyl-CoA and succinyl-CoA separation by CE, suitable for the evaluation of MCM activity. The working conditions
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
Determination of methylmalonyl coenzyme A by ultra high-performance liquid chromatography tandem mass spectrometry for measuring propionyl coenzyme A carboxylase activity in patients with propionic acidemia
Gotoh K, et al.
Journal of Chromatography. B, Biomedical Sciences and Applications, 1046, 195-199 (2017)
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.
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