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安全信息

870723P

Avanti

23:0 Coenzyme A

Avanti Research™ - A Croda Brand 870723P, powder

别名:

tricosanoyl Coenzyme A (ammonium salt)

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About This Item

经验公式（希尔记法）:
C44H89N10O17P3S
CAS号:
799812-97-8
分子量:
1155.22
MDL编号:
MFCD22416633
UNSPSC代码:
12352211
NACRES:
NA.25

表单

powder

包装

pkg of 1 × 5 mg (870723P-5mg)

制造商/商品名称

Avanti Research™ - A Croda Brand 870723P

应用

lipidomics

脂质类型

coenzymes

运输

dry ice

储存温度

−20°C

SMILES字符串

O[C@@](C(NCCC(NCCSC(CCCCCCCCCCCCCCCCCCCCCC)=O)=O)=O)(C(C)(COP([O-])(OP([O-])(OC[C@H]([C@H]1OP([O-])(O)=O)O[C@H]([C@@H]1O)N2C3=C(C(N)=NC=N3)N=C2)=O)=O)C)[H].[NH4+].[NH4+].[NH4+]

InChI

1S/C44H80N7O17P3S.3H3N/c1-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22-23-24-35(53)72-28-27-46-34(52)25-26-47-42(56)39(55)44(2,3)30-65-71(62,63)68-70(60,61)64-29-33-38(67-69(57,58)59)37(54)43(66-33)51-32-50-36-40(45)48-31-49-41(36)51;;;/h31-33,37-39,43,54-55H,4-30H2,1-3H3,(H,46,52)(H,47,56)(H,60,61)(H,62,63)(H2,45,48,49)(H2,57,58,59);3*1H3/t33-,37?,38+,39+,43-;;;/m1.../s1

InChI key

VWUVJQXOYHTDCP-BHMMHRQOSA-N

相关类别

一般描述

23:0 Coenzyme A, also known as tricosanoyl coenzyme A, is a coenzyme A derivative of tricosylic acid.

应用

23:0 Coenzyme A has been used as a substrate in acylglycerol-3-phosphate-O-acyltransferases (AGPAT 11) assay and ceramide synthase assay.

包装

5 mL Amber Glass Screw Cap Vial (870723P-5mg)

法律信息

Avanti Research is a trademark of Avanti Polar Lipids, LLC

储存分类代码

11 - Combustible Solids

WGK

WGK 3

法规信息

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Anil K Agarwal et al.
Journal of lipid research, 51(8), 2143-2152 (2010-04-07)
The conversion of lysophosphatidic acid (LPA) to phosphatidic acid is carried out by the microsomal enzymes 1-acylglycerol-3-phosphate-O-acyltransferases (AGPATs). These enzymes are specific for acylating LPA at the sn-2 (carbon 2) position on the glycerol backbone and are important, because they
Evgeny V Berdyshev et al.
The Journal of biological chemistry, 284(9), 5467-5477 (2009-01-03)
Novel immunomodulatory molecule FTY720 is a synthetic analog of myriocin, but unlike myriocin FTY720 does not inhibit serine palmitoyltransferase. Although many of the effects of FTY720 are ascribed to its phosphorylation and subsequent sphingosine 1-phosphate (S1P)-like action through S1P(1,3-5) receptors

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