Pyrrolidinohydroquinazolines––a novel class of CCR3 modulators
摘要:
A novel class of CCR3 modulators is described. Starting with lead compound 4a (K-i: 110 nM), which turned out to be all antagonist of eotaxin at the CCR3 receptor, further optimization led to compound 8b (K-i: 28 nM), which surprisingly proved to be an agonist. (C) 2004 Elsevier Ltd. All rights reserved.
Novel N-(3-cyano-4-alkylthien-2-yl) ureas are selective pre- and/or post-emergent herbicides.
新型N-(3-氰基-4-烷基噻吩-2-基)脲类化合物是选择性的前期和/或后期除草剂。
Synthesis and nitration of some 4-cyclopropyl- and 4-(p-cyclopropylphenyl)-2-aminothiophenes
作者:T. P. Surikova、V. D. Zakharova、S. S. Mochalov、Yu. S. Shabarov
DOI:10.1007/bf00479336
日期:1988.8
SURIKOVA, T. P.;ZAXAROVA, V. D.;MOCHALOV, S. S.;SHABAROV, YU. S., XIMIYA GETEROTSIKL. SOED.,(1988) N 8, S. 1045-1049
作者:SURIKOVA, T. P.、ZAXAROVA, V. D.、MOCHALOV, S. S.、SHABAROV, YU. S.
DOI:——
日期:——
US3956315A
申请人:——
公开号:US3956315A
公开(公告)日:1976-05-11
Pyrrolidinohydroquinazolines––a novel class of CCR3 modulators
作者:Ralf Anderskewitz、Rolf Bauer、Gisela Bodenbach、Dirk Gester、Bernd Gramlich、Gerd Morschhäuser、Franz W. Birke
DOI:10.1016/j.bmcl.2004.11.039
日期:2005.2
A novel class of CCR3 modulators is described. Starting with lead compound 4a (K-i: 110 nM), which turned out to be all antagonist of eotaxin at the CCR3 receptor, further optimization led to compound 8b (K-i: 28 nM), which surprisingly proved to be an agonist. (C) 2004 Elsevier Ltd. All rights reserved.