Title : Exploration of a fundamental substituent effect of alpha-ketoheterocycle enzyme inhibitors: Potent and selective inhibitors of fatty acid amide hydrolase - DeMartino_2008_Bioorg.Med.Chem.Lett_18_5842 |
Author(s) : DeMartino JK , Garfunkle J , Hochstatter DG , Cravatt BF , Boger DL |
Ref : Bioorganic & Medicinal Chemistry Lett , 18 :5842 , 2008 |
Abstract :
A series of C4 substituted alpha-ketooxazoles were examined as inhibitors of the serine hydrolase fatty acid amide hydrolase in efforts that further define and generalize a fundamental substituent effect on enzyme inhibitory potency. Thus, a plot of the Hammett sigma(m) versus -logK(i) provided a linear correlation (R(2)=0.90) with a slope of 3.37 (rho=3.37), that is of a magnitude that indicates that of the electron-withdrawing character of the substituent dominates its effects (a one unit change in sigma(m) provides a >1000-fold change in K(i)). |
PubMedSearch : DeMartino_2008_Bioorg.Med.Chem.Lett_18_5842 |
PubMedID: 18639454 |
Inhibitor | LEI104 |
DeMartino JK, Garfunkle J, Hochstatter DG, Cravatt BF, Boger DL (2008)
Exploration of a fundamental substituent effect of alpha-ketoheterocycle enzyme inhibitors: Potent and selective inhibitors of fatty acid amide hydrolase
Bioorganic & Medicinal Chemistry Lett
18 :5842
DeMartino JK, Garfunkle J, Hochstatter DG, Cravatt BF, Boger DL (2008)
Bioorganic & Medicinal Chemistry Lett
18 :5842