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经验公式（希尔记法）:
C25H39N7Na3O17P3S
化学文摘社编号:
分子量:
903.57
MDL number:
UNSPSC Code:
12352211
NACRES:
NA.25
产品名称
辅酶 A，04:0, Avanti Research™ - A Croda Brand
SMILES string
O[C@@](C(NCCC(NCCSC(CCC)=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].[Na+].[Na+].[Na+]
InChI
1S/C25H42N7O17P3S.3Na/c1-4-5-16(34)53-9-8-27-15(33)6-7-28-23(37)20(36)25(2,3)11-46-52(43,44)49-51(41,42)45-10-14-19(48-50(38,39)40)18(35)24(47-14)32-13-31-17-21(26)29-12-30-22(17)32;;;/h12-14,18-20,24,35-36H,4-11H2,1-3H3,(H,27,33)(H,28,37)(H,41,42)(H,43,44)(H2,26,29,30)(H2,38,39,40);;;/q;3*+1/p-3/t14-,18?,19+,20+,24-;;;/m1.../s1
InChI key
PRMIKLPNYYDDCC-XRHOYZRHSA-K
assay
>99% (TLC)
form
powder
packaging
pkg of 1 × 5 mg (870704P-5mg)
manufacturer/tradename
Avanti Research™ - A Croda Brand
application(s)
lipidomics
lipid type
coenzymes
shipped in
dry ice
storage temp.
−20°C
Biochem/physiol Actions
04:0 Coenzyme A acts as a source of N-acyl chain in the synthesis of N-butanoyl-L-homoserine lactone (BHL) by LuxI homologue RhlI (VsmI). Butanoyl coenzyme A serves as an intermediate in the synthesis of butyrate, which is involved in maintaining colonic homeostasis and gut health. It also has an ability to inhibit citrate synthase (CS).
General description
04:0 Coenzyme A, also known as butanoyl coenzyme A, is a coenzyme A derivative of butanoic acid. 04:0 Coenzyme A is a short-chain acyl CoA and is an intermediate of fatty acid degradation.
Packaging
5 mL Amber Glass Screw Cap Vial (870704P-5mg)
Legal Information
Avanti Research is a trademark of Avanti Polar Lipids, LLC
存储类别
11 - Combustible Solids
wgk
WGK 3
Julian Trachsel et al.
Applied and environmental microbiology, 82(22), 6788-6798 (2016-10-30)
Studying the host-associated butyrate-producing bacterial community is important, because butyrate is essential for colonic homeostasis and gut health. Previous research has identified the butyryl coenzyme A (CoA):acetate-CoA transferase (EC 2.3.8.3) as a gene of primary importance for butyrate production in
J C Lai et al.
Research communications in chemical pathology and pharmacology, 82(3), 331-338 (1993-12-01)
We investigated the hypothesis that one mechanism underlying fatty acid toxicity is the selective inhibition of rate-limiting and/or regulated tricarboxylic acid cycle and related enzymes by fatty acyl coenzyme A (CoA) derivatives by examining the effects of several fatty acyl
Y Jiang et al.
Molecular microbiology, 28(1), 193-203 (1998-05-21)
In Pseudomonas aeruginosa, synthesis of the quorum-sensing signal molecules N-butanoyl-L-homoserine lactone (BHL) and N-hexanoyl-L-homoserine lactone (HHL) requires the Luxl homologue Rhll(Vsml). By using thin-layer chromatography in conjunction with high-performance liquid chromatography (HPLC) and mass spectrometry, we show that purified Rhll
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