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3,4-dihydroxy Hydrocinnamic acid (L-Aspartic acid dibenzyl ester) amide
For research use only. Not for therapeutic Use.
Acyl-<wbr></wbr>coenzyme A: cholesterol acyltransferase-<wbr></wbr>1 and -<wbr></wbr>2 (ACAT-<wbr></wbr>1 and ACAT-<wbr></wbr>2) catalyze the formation of cholesterol esters from cholesterol and long chain fatty acyl-<wbr></wbr>coenzyme A, and may play a role in the development of atherosclerosis. CAY10485 inhibits human ACAT-<wbr></wbr>1 and ACAT-<wbr></wbr>2 with an IC<sub>50</sub> values of 95 and 81 µM, respectively. It also inhibits copper-<wbr></wbr>mediated oxidation of low density lipoproteins by 91% at a concentration of 2 µM.
Catalog Number | R010664 |
CAS Number | 615264-62-5 |
Synonyms | 3,4-dihydroxy Hydrocinnamic acid (L-Aspartic acid dibenzyl ester) amide |
Molecular Formula | C27H27NO7 |
Purity | ≥95% |
Target | Acyltransferase |
Storage | -20°C |
IUPAC Name | dibenzyl (2S)-2-[3-(3,4-dihydroxyphenyl)propanoylamino]butanedioate |
InChI | InChI=1S/C27H27NO7/c29-23-13-11-19(15-24(23)30)12-14-25(31)28-22(27(33)35-18-21-9-5-2-6-10-21)16-26(32)34-17-20-7-3-1-4-8-20/h1-11,13,15,22,29-30H,12,14,16-18H2,(H,28,31)/t22-/m0/s1 |
InChIKey | SNEUAEKNRYBOTP-QFIPXVFZSA-N |
SMILES | C1=CC=C(C=C1)COC(=O)CC(C(=O)OCC2=CC=CC=C2)NC(=O)CCC3=CC(=C(C=C3)O)O |
Reference | 1.Rudel, L.L.,Lee, R.G., and Cockman, T.L. Acyl coenzyme A: Cholesterol acyltransferase types 1 and 2: structure and function in atherosclerosis. Current Opinion in Lipidology 12, 121-127 (2001). |