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形狀
powder
包裝
pkg of 1 × 10 mg (870710P-10mg)
pkg of 1 × 5 mg (870710P-5mg)
製造商／商標名
Avanti Research™ - A Croda Brand 870710P
應用
lipidomics
脂質類型
coenzymes
運輸包裝
dry ice
儲存溫度
−20°C
SMILES 字串
O[C@@](C(NCCC(NCCSC(CCCCCCCCC)=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/C31H54N7O17P3S.3H3N/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);3*1H3/t20-,24?,25+,26+,30-;;;/m1.../s1
InChI 密鑰
IWPPTKRPCYMCQM-HGTZWQFESA-N
一般說明
10:0 Coenzyme A, also known as decanoyl Coenzyme A, is a coenzyme A derivative of decanoic acid. It is a medium-chain acyl CoA and is an intermediate of fatty acid metabolism. Decanoyl-CoA acts as a CqsA (acyl-CoA transferase) substrate for the synthesis of 3-aminotridecan-4-one (amino-CAI-1).
應用
Decanoyl Coenzyme A has been used as an internal standard to measure the decanoyl-CoA in the standard mixture analyzed with reversed phase ultrahigh performance liquid chromatography (UHPLC).
包裝
5 mL Amber Glass Screw Cap Vial (870710P-10mg)
5 mL Amber Glass Screw Cap Vial (870710P-5mg)
法律資訊
Avanti Research is a trademark of Avanti Polar Lipids, LLC
儲存類別代碼
11 - Combustible Solids
Robert C Kelly et al.
Nature chemical biology, 5(12), 891-895 (2009-10-20)
Vibrio cholerae, the bacterium that causes the disease cholera, controls virulence factor production and biofilm development in response to two extracellular quorum-sensing molecules, called autoinducers. The strongest autoinducer, called CAI-1 (for cholera autoinducer-1), was previously identified as (S)-3-hydroxytridecan-4-one. Biosynthesis of
László Abrankó et al.
Journal of chromatography. A, 1534, 111-122 (2018-01-02)
Fatty acyl-Coenzyme A species (acyl-CoAs) are key biomarkers in studies focusing on cellular energy metabolism. Existing analytical approaches are unable to simultaneously detect the full range of short-, medium-, and long-chain acyl-CoAs, while chromatographic limitations encountered in the analysis of
Jake M Stout et al.
The Plant journal : for cell and molecular biology, 71(3), 353-365 (2012-02-23)
The psychoactive and analgesic cannabinoids (e.g. Δ(9) -tetrahydrocannabinol (THC)) in Cannabis sativa are formed from the short-chain fatty acyl-coenzyme A (CoA) precursor hexanoyl-CoA. Cannabinoids are synthesized in glandular trichomes present mainly on female flowers. We quantified hexanoyl-CoA using LC-MS/MS and
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