A NEW CLASS OF POTENT, SLOWLY REVERSIBLE DEHYDROPEPTIDASE INHIBITORS

被引：0
|
作者：
PARSONS, WH
HAJDU, R
SCHOEN, WR
COMBS, PL
SUNDELOF, J
PATCHETT, AA
机构：
来源：
BIOCHEMISTRY INTERNATIONAL | 1991年 / 23卷 / 06期
关键词：
D O I：
暂无
中图分类号：
Q5 [生物化学]; Q7 [分子生物学];
学科分类号：
071010 ; 081704 ;
摘要：
引用
收藏
页码：1107 / 1115
页数：9
相关论文
共 50 条
  • [41] STUDIES ON NEW DEHYDROPEPTIDASE INHIBITORS .1. TAXONOMY, FERMENTATION, ISOLATION AND PHYSICOCHEMICAL PROPERTIES
    HASHIMOTO, S
    MURAI, H
    EZAKI, M
    MORIKAWA, N
    HATANAKA, H
    OKUHARA, M
    KOHSAKA, M
    IMANAKA, H
    JOURNAL OF ANTIBIOTICS, 1990, 43 (01): : 29 - 37
  • [42] α,β-dehydrophenylalanine choline esters, a new class of reversible inhibitors of human acetylcholinesterase and butyrylcholinesterase
    Grigoryan, Hasmik A.
    Hambardzumyan, Artur A.
    Mkrtchyan, Marina V.
    Topuzyan, Vigen O.
    Halebyan, Ghukas P.
    Asatryan, Ruben S.
    CHEMICO-BIOLOGICAL INTERACTIONS, 2008, 171 (01) : 108 - 116
  • [43] ANTIDIABETIC AGENTS - A NEW CLASS OF REVERSIBLE CARNITINE PALMITOYLTRANSFERASE-I INHIBITORS
    ANDERSON, RC
    BALESTRA, M
    BELL, PA
    DEEMS, RO
    FILLERS, WS
    FOLEY, JE
    FRASER, JD
    MANN, WR
    RUDIN, M
    VILLHAUER, EB
    JOURNAL OF MEDICINAL CHEMISTRY, 1995, 38 (18) : 3448 - 3450
  • [44] Pyrido-imidazodiazepinones as a new class of reversible inhibitors of human kallikrein 7
    Arama, Dominique P.
    Soualmia, Feryel
    Lisowski, Vincent
    Longevial, Jean-Francois
    Bosc, Elodie
    Maillard, Ludovic T.
    Martinez, Jean
    Masurier, Nicolas
    El Amri, Chahrazade
    EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2015, 93 : 202 - 213
  • [45] ENOL CARBAMATES AS A NEW CLASS OF REVERSIBLE INHIBITORS OF FATTY ACID AMIDE HYDROLASE
    Gattinoni, Sonia
    De Simone, Chiara
    Dallavalle, Sabrina
    Fezza, Filomena
    Minetti, Patrizia
    Caprioli, Antonio
    Borsini, Franco
    Cabri, Walter
    Penco, Sergio
    Merlini, Lucio
    Maccarrone, Mauro
    DRUGS OF THE FUTURE, 2009, 34 : 90 - 90
  • [46] Identification of Indole-Based Chalcones: Discovery of a Potent, Selective, and Reversible Class of MAO-B Inhibitors
    Sasidharan, Rani
    Manju, Sreedharannair Leelabaiamma
    Ucar, Gulberk
    Baysal, Ipek
    Mathew, Bijo
    ARCHIV DER PHARMAZIE, 2016, 349 (08) : 627 - 637
  • [47] Discovery of a potent, selective, and efficacious class of reversible α-ketoheterocycle inhibitors of fatty acid amide hydrolase effective as analgesics
    Boger, DL
    Miyauchi, H
    Du, W
    Hardouin, C
    Fecik, RA
    Cheng, H
    Hwang, I
    Hedrick, MP
    Leung, D
    Acevedo, O
    Guimaraes, CRW
    Jorgensen, WL
    Cravatt, BF
    JOURNAL OF MEDICINAL CHEMISTRY, 2005, 48 (06) : 1849 - 1856
  • [48] A class of potent tyrosinase inhibitors: Alkylidenethiosemicarbazide compounds
    Liu, Jinbing
    Cao, Rihui
    Yi, Wei
    Ma, Chunming
    Wan, Yiqian
    Zhou, Binhua
    Ma, Lin
    Song, Huacan
    EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2009, 44 (04) : 1773 - 1778
  • [49] NEW CLASS OF POTENT ANALGESICS
    VIDA, JA
    SAMOUR, CM
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 1973, : 21 - &
  • [50] The first synthesis of substituted azepanes mimicking monosaccharides:: a new class of potent glycosidase inhibitors
    Li, HQ
    Blériot, Y
    Chantereau, C
    Mallet, JM
    Sollogoub, M
    Zhang, YM
    Rodríguez-García, E
    Vogel, P
    Jiménez-Barbero, J
    Sinaÿ, P
    ORGANIC & BIOMOLECULAR CHEMISTRY, 2004, 2 (10) : 1492 - 1499
12345