Analysis of the discriminative inhibition of mammalian digestive lipases by 3-phenyl substituted 1, 3, 4-oxadiazol-2 (3H)-ones

…, F Fotiadu, S Canaan, J Leclaire, JF Cavalier

Index: Point, Vanessa; Pavan Kumar; Marc, Sylvain; Delorme, Vincent; Parsiegla, Goetz; Amara, Sawsan; Carriere, Frederic; Buono, Gerard; Fotiadu, Frederic; Canaan, Stephane; Leclaire, Julien; Cavalier, Jean-Francois European Journal of Medicinal Chemistry, 2012 , vol. 58, p. 452 - 463

Full Text: HTML

Citation Number: 19

Abstract

We report here the reactivity and selectivity of three 5-Methoxy-N-3-Phenyl substituted-1, 3, 4-Oxadiazol-2 (3H)-ones (MPOX, as well as meta and para-PhenoxyPhenyl derivatives, ie MmPPOX and MpPPOX) with respect to the inhibition of mammalian digestive lipases: dog gastric lipase (DGL), human (HPL) and porcine (PPL) pancreatic lipases, human (HPLRP2) and guinea pig (GPLRP2) pancreatic lipase-related proteins 2, human pancreatic ...

Related Articles:

N-amination using N-methoxycarbonyl-3-phenyloxaziridine. Direct access to chiral N β-protected α-hydrazinoacids and carbazates

[Vidal, Joelle; Drouin, Jacques; Collet, Andre Journal of the Chemical Society, Chemical Communications, 1991 , # 6 p. 435 - 437]

Curtius and Lossen rearrangements. III. Photolysis of certain carbamoyl azides

[Lwowski,W. et al. Journal of Organic Chemistry, 1975 , vol. 40, p. 2608 - 2612]

More Articles...