
Archiv der Pharmazie p. 3 - 10 (1996)
Update date:2022-07-29
Topics:
Shigenaga
Manabe
Matsuda
Fujii
Matsuo
As an extension of our study aiming to discover a novel compound with dual activities against histamine and slow-reacting substance (SRS), we synthesized two types of indolylpiperidine derivatives, 3 and 4-20. Testing for in vivo antianaphylactic activity and for in vitro anti-SRS activity revealed that (2E,4E)-5-(3,5-dimethoxy-4-hydroxyphenyl)-N-(2-(4-(1H-indol-3-yl)piper idin-1-yl)ethyl)-2,4-pentadienamide (11) exhibited potent dual activities with ED50 = 0.89 mg/kg and IC50 = 1.43 μM, respectively. However, the plasma concentration of unchanged 11 was very low when administered orally in guinea pigs. This result can be explained by fast formation of a glucuronic acid conjugate.
View Morewebsite:http://www.ringchemicals.com/
Contact:+1-416-493-6870
Address:Toronto, Canada
Contact:86+21-56421993
Address:3F,BUILDING 10,NO.2889 JINKE ROAD, SHANGHAI.
website:https://www.synose.com/
Contact:86-579-82275537
Address:No.1958 Liyu Road , jinhua,zhejiang,China
Taizhou Huading Chemical Co.,Ltd(expird)
Contact:+86-576-88583898
Address:Economic&Technology development zone,Taizhou City,Zhejiang Province,China
Contact:+44 7958 511245
Address:PO Box 469, Manchester, UK
Doi:10.1021/acs.joc.6b01884
(2016)Doi:10.1016/j.ejmech.2011.07.036
(2011)Doi:10.1021/jm00166a010
(1990)Doi:10.1016/j.tetlet.2005.11.022
(2006)Doi:10.1021/jo01264a082
(1969)Doi:10.1021/om980722n
(1998)