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Merck

63410

Sigma-Aldrich

丙二酰胺辅酶A 四锂盐

≥90% (HPLC)

别名:

丙二酰胺辅酶a四锂盐

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About This Item

经验公式(希尔记法):
C24H34Li4N7O19P3S
分子量:
877.31
分類程式碼代碼:
41106305
PubChem物質ID:
NACRES:
NA.51

品質等級

化驗

≥90% (HPLC)

形狀

solid

雜質

≤12% water

溶解度

H2O: 50 mg/mL, clear, colorless

儲存溫度

−20°C

SMILES 字串

[Li+].[Li+].[Li+].[Li+].CC(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)[C@@H](O)C(=O)NCCC(=O)NCCSC(=O)CC(O)=O

InChI

1S/C24H38N7O19P3S.4Li/c1-24(2,19(37)22(38)27-4-3-13(32)26-5-6-54-15(35)7-14(33)34)9-47-53(44,45)50-52(42,43)46-8-12-18(49-51(39,40)41)17(36)23(48-12)31-11-30-16-20(25)28-10-29-21(16)31;;;;/h10-12,17-19,23,36-37H,3-9H2,1-2H3,(H,26,32)(H,27,38)(H,33,34)(H,42,43)(H,44,45)(H2,25,28,29)(H2,39,40,41);;;;/q;4*+1/p-4/t12-,17-,18-,19+,23-;;;;/m1..../s1

InChI 密鑰

DQLXXYMNINXQSV-QTRRCMKVSA-J

生化/生理作用

丙二酰辅酶A是一种辅酶A衍生物,可用于脂肪酸和聚酮合成,以及胯线粒体膜转移酮戊二酸。丙二酰辅酶A是由乙酰辅酶A羧化酶介导的乙酰辅酶A的羧化反应形成的。

其他說明

丙二酰胺辅酶a在克隆胰岛β细胞葡萄糖刺激的胰岛素分泌中的作用

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)


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Lars Robbel et al.
Biochemistry, 50(27), 6073-6080 (2011-06-10)
Biosynthesis of the hydroxamate-type siderophore erythrochelin requires the generation of δ-N-acetyl-δ-N-hydroxy-L-ornithine (L-haOrn), which is incorporated into the tetrapeptide at positions 1 and 4. Bioinformatic analysis revealed the FAD-dependent monooxygenase EtcB and the bifunctional malonyl-CoA decarboxylase/acetyltransferase Mcd to be putatively involved
Dea Hwan Kim et al.
Plant physiology and biochemistry : PPB, 47(11-12), 991-997 (2009-09-08)
In this study, a flavonoid malonyltransferase (OsMaT-2) was cloned from Oryza sativa, and the recombinant protein OsMaT-2 was purified via affinity chromatography. OsMaT-2 utilized a variety of flavonoid glucosides, including flavanone glucosides, flavone glucosides, flavonol glucosides, and isoflavone glucosides as
Koichiro Kogawa et al.
Journal of plant physiology, 164(7), 886-894 (2006-08-05)
The crude malonyltransferase from the petals of Clitoria ternatea was characterized enzymatically to investigate its role on the biosynthetic pathways of anthocyanins and flavonol glycosides. In C. ternatea, a blue flower cultivars (DB) and mauve flower variety (WM) accumulate polyacylated
Heather Seidle et al.
Journal of bacteriology, 186(8), 2499-2503 (2004-04-03)
Cfa1 was overproduced in Escherichia coli and Pseudomonas syringae, and the degree of 4'-phosphopantetheinylation was determined. The malonyl-coenzyme A:acyl carrier protein transacylase (FabD) of P. syringae was overproduced and shown to catalyze malonylation of Cfa1, suggesting that FabD plays a
Christopher J Arthur et al.
ACS chemical biology, 4(8), 625-636 (2009-06-27)
Malonylation of an acyl carrier protein (ACP) by malonyl Coenzyme A-ACP transacylase (MCAT) is fundamental to bacterial fatty acid biosynthesis. Here, we report the structure of the Steptomyces coelicolor (Sc) fatty acid synthase (FAS) ACP and studies of its binding

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