| Identification | Back Directory | [Name]
hexanoyl CoenzyMe A (aMMoniuM salt) | [CAS]
799812-81-0 | [Synonyms]
06:0 Coenzyme A
hexanoyl CoenzyMe A (aMMoniuM salt)
HEXANOYL COENZYME A (AMMONIUM SALT);06:0 COENZYME A | [Molecular Formula]
C27H55N10O17P3S | [MDL Number]
MFCD22416618 | [MOL File]
799812-81-0.mol | [Molecular Weight]
916.769 |
| Chemical Properties | Back Directory | [storage temp. ]
-20°C | [form ]
powder | [Major Application]
lipidomics | [InChIKey]
MXEFXWIYODKXEJ-WSHYHEJESA-N | [SMILES]
O[C@@](C(NCCC(NCCSC(CCCCC)=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+] |
| Hazard Information | Back Directory | [Uses]
06:0 Coenzyme A has been used as an internal standard in ultra-high performance liquid chromatography–tandem mass spectrometry for quantitative analysis of fatty-acyl-Coenzyme A species in biological samples. | [Biological Activity]
06:0 Coenzyme Aalso known as hexanoyl coenzyme Ais a derivate of short-chain fatty acid hexanoate. It might be an intermediate of fatty acid metabolism. It acts as a source of N-acyl chain in the synthesis of N-hexanoyl-L-homoserine lactone (HHL) by LuxI homologue RhlI(VsmI). Hexanoyl coenzyme A also acts as a precursor for the synthesis of olivetolic acid (OLA)a polyketide metabolite. N-hexanoyl-CoA is preferred over N-octanoyl-CoA as an acyl donor substrate by GO at (ghrelin O-acyltransferase). |
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| Company Name: |
cjbscvictory
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| Telephone: |
13348960310 13348960310 |
| Website: |
www.weikeqi-biotech.com/ |
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