Description

Arachidonoyl CoA triammonium is used as a substrate in the synthesis of Arachidonoyl amino acids. Arachidonoyl CoA triammonium directly interacts with FadR to inhibit binding at its DNA targets[1][2].–Applications–Formula-C41H75N10O17P3S-Citation–References-[1]Jeffrey M McCue, et al. In vitro synthesis of arachidonoyl amino acids by cytochrome c. Prostaglandins Other Lipid Mediat. 2009 Nov;90(1-2):42-8.|[2]Melissa Ellermann, et al. The Canonical Long-Chain Fatty Acid Sensing Machinery Processes Arachidonic Acid To Inhibit Virulence in Enterohemorrhagic Escherichia coli. mBio. 2021 Jan 19;12(1):e03247-20.-CASNumber–MolecularWeight-1105.08-Compound Purity–SMILES-O[C@H]1[C@@H](O[C@@H]([C@H]1OP(O)(O)=O)COP(OP(OCC(C)(C)[C@@H](O)C(NCCC(NCCSC(CCC/C=CC/C=CC/C=CC/C=CCCCCC)=O)=O)=O)(O)=O)(O)=O)N2C3=NC=NC(N)=C3N=C2.N.N.N-Research_Area-Others-Solubility-10 mM in DMSO-Target-Biochemical Assay Reagents-Isoform–Pathway-Others-MCE Product type-Enzyme