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Merck

D5269

Sigma-Aldrich

癸酰辅酶 A 一水合物

≥90%

别名:

Capryl CoA monohydrate, Decanoyl CoA monohydrate

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About This Item

线性分子式:
C31H54N7O17P3S
CAS号:
分子量:
939.80
MDL號碼:
分類程式碼代碼:
41106305
PubChem物質ID:
NACRES:
NA.51

品質等級

化驗

≥90%

形狀

powder

儲存溫度

−20°C

SMILES 字串

O.CCCCCCCCCC(=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/C31H54N7O17P3S.H2O/c1-4-5-6-7-8-9-10-11-22(40)59-15-14-33-21(39)12-13-34-29(43)26(42)31(2,3)17-52-58(49,50)55-57(47,48)51-16-20-25(54-56(44,45)46)24(41)30(53-20)38-19-37-23-27(32)35-18-36-28(23)38;/h18-20,24-26,30,41-42H,4-17H2,1-3H3,(H,33,39)(H,34,43)(H,47,48)(H,49,50)(H2,32,35,36)(H2,44,45,46);1H2/t20-,24-,25-,26+,30-;/m1./s1

InChI 密鑰

IRILGPHKFKSRQN-ASEPKIFHSA-N

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一般說明

癸酰辅酶A是酰基转移酶的底物。 它是人肝脏甘氨酸-N-酰基转移酶的底物。

應用

癸酰辅酶A一水合物已被用于磷脂酰肌醇-4,5-二磷酸盐的抑制研究(LC-CoA) 和人二酰基甘油酰基转移酶1和2测定中。
癸酰辅酶A(癸酰CoA)可通过霍乱弧菌CqsA酶与S-腺苷甲硫氨酸(SAM)偶联,产生有效的群体感应分子3-氨基三嗪-2-烯-4-酮(Ea-CAI-1。

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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Purification and characterization of acyl coenzyme A: alcohol acyltransferase of Neurospora sp.
Yamauchi H, et al.
Agricultural and Biological Chemistry, 53(6), 1551-1556 (1989)
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Rapedius M, et al.
The Journal of biological chemistry, 280(35), 30760-30767 (2005)
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ACS chemical biology, 6(4), 356-365 (2011-01-05)
Vibrio cholerae, the causative agent of the disease cholera, uses a cell to cell communication process called quorum sensing to control biofilm formation and virulence factor production. The major V. cholerae quorum-sensing signal CAI-1 has been identified as (S)-3-hydroxytridecan-4-one, and
H Singh et al.
Journal of lipid research, 37(12), 2616-2626 (1996-12-01)
Peroxisomal matrix proteins were extracted from the highly purified peroxisomes with sodium pyrophosphate, and the membranes were sedimented by high speed centrifugation. Biochemical marker enzyme analyses revealed a quantitative release of a number of well-known peroxisomal matrix proteins from the
Jocelyn E Manning Fox et al.
Metabolism: clinical and experimental, 52(10), 1313-1319 (2003-10-18)
Recent evidence demonstrates that long-chain acyl coenzyme A esters (CoAs) activate cardiac and beta-cell plasma-membrane (pmK(ATP)) adenosine triphosphate (ATP)-sensitive potassium channels. In this study, we have investigated the differential effects of acyl CoAs of short and medium side-chain length on

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