New arylhexahydropyrimidinediones: Synthesis, benzodiazepine receptor affinity and anticonvulsant activity

DOI: 10.1016/0223-5234(96)80371-0

Source and publish data:

European Journal of Medicinal Chemistry p. 335 - 339 (1996)

Update date:2022-08-05

Topics:

Authors:

Guillon Guillon

Daoust Daoust

Radulovic

Boulouard

Dallemagne

Legrand Legrand

Rault Rault

Quermonne

Robba Robba

Read Full Text PDF DownLoad Join now for total 90,000,000 free articles

Article abstract of DOI:10.1016/0223-5234(96)80371-0

Synthesis of new 3-alkyl-6-arylhexahydropyrimidine-2,4-dione derivatives was achieved starting from various benzaldehydes. Their affinity towards the benzodiazepine receptor and their anticonvulsant effect were evaluated.

Full text of DOI:10.1016/0223-5234(96)80371-0

Products guided by the article

Product name:3-[3N'-(2-chloroethyl)ureido]-3-phenylpropionic acid

Cas No:176901-40-9

R&D Labs maybe for 176901-40-9

Shanghai HengXun Pharmaceutical Tech. Co., Ltd.

Contact:86-86-52730756

Address:Room 603, No. 240, Tianmuzhong Road, Zhabei, Shanghai, China
XI'AN CHUKANG BIOTECHNOLOGY CO.,LTD

Contact:29-63685658 63685359

Address:Room 3-1202,Building 1,Oriental oasis,East of Xianning Road,Xi'an,Shaanxi 710043 P.R.China
Suzhou BEC Fine Chemicals Co., Ltd.

website:http://www.bek.com.cn

Contact:0512-68095917　 18913193865

Address:6, Jin Shan Road, Suzhou New District, 215011 China Suzhou Nations Pharmaceutical Innovation Center Inside
Changzhou Yongxu Chemical Co.,Ltd

Contact:86-0519-85286591

Address:Room 1812,Wanda Plaza B,Xinbei District,Changzhou,Jiangsu,China
Jinan Yijialian Economic and Trade Development Co., Ltd.

Contact:+86 0531-66729596

Address:jinan

Relevant to this article

A combined experimental and TD-DFT investigation of three disperse azo dyes having the nitroterephthalate skeleton

Doi:10.1016/j.dyepig.2013.10.035
(2014)
Bismuth (III) chlorides; an efficient and selective catalyst for deprotection of 1,1-diacetates

Doi:10.1080/00397919908086439
(1999)
A convenient asymmetric synthesis of α-1-arylalkylamines through the enantioselective hydrogenation of enamides

Doi:10.1021/ja953872n
(1996)
Streptonigrin and related compounds. 6. Synthesis and activity of some quinoxaline analogues

Doi:10.1002/jhet.5570330238
(1996)
Carboranes. II. The preparation of 1- and 1,2-substituted carboranes

Doi:10.1021/ic50010a008
(1963)
Exceptionally persistent nitrogen-centered free radicals. Syntheses, ESR spectra, isolation, and X-ray crystallographic structures of N-(arylthio)-2-tert-butyl-4,6-diarylphenylaminyl and N-(arylthio)-4-tert-butyl-2,6-diarylphenylaminyl radicals

Doi:10.1021/jo960347d
(1996)

Article Doi