(±)13-HODE cholesteryl ester

(±)13-HODE cholesteryl ester was originally extracted from atherosclerotic lesions and shown to be produced by Cu2+-catalyzed oxidation of LDL. Later studies determined that 15-LO from rabbit reticulocytes and human monocytes were able to metabolize cholesteryl linoleate, a major component of LDL, to 13-HODE cholesteryl ester.Formal Name: (±)-13-hydroxy-9Z,11E-octadecadienoic acid, cholesteryl ester. CAS Number: 167354-91-8. Molecular Formula: C45H76O3. Formula Weight: 665.1. Purity: >98%. Formulation: (Request formulation change), A solution in ethanol. Solubility: DMF: >50 mg/ml, DMSO: >50 mg/ml, Ethanol: >50 mg/ml, Ethanol:PBS (1:10): <10 µg/ml. lambdamax: 234 nm. SMILES: CCCCCC(O)\C=C\C=C/CCCCCCCC(=O)O[C@H]1CC[C@@]2(C)C(=CC[C@H]3[C@@H]4CC[C@H]([C@H](C)CCCC(C)C)[C@@]4(C)CC[C@H]23)C1. InChi Code: InChI=1S/C45H76O3/c1-7-8-16-22-37(46)23-17-14-12-10-9-11-13-15-18-24-43(47)48-38-29-31-44(5)36(33-38)25-26-39-41-28-27-40(35(4)21-19-20-34(2)3)45(41,6)32-30-42(39)44/h12,14,17,23,25,34-35,37-42,46H,7-11,13,15-16,18-22,24,26-33H2,1-6H3/b14-12-,23-17+/t35-,37?,38+,39+,40-,41+,42+,44+,45-/m1/s1. InChi Key: RZXYPSUQZUUHPD-ZCNQQENXSA-N. Side Chain Carbon Sum: 18:2.