Effect of structural modification of the hydrantoin ring on anticonvulsant activity

DOI: 10.1021/jm50001a012

Source and publish data:

Journal of Medicinal Chemistry p. 601 - 606 (1985)

Update date:2022-07-30

Topics:

Authors:

Cortes Cortes

Liao Liao

Watson Watson

Kohn Kohn

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

Article abstract of DOI:10.1021/jm50001a012

Selectively substituted hydantoins (15 examples), 4-hydroxy-2-imidazolidinones (13 examples), 2-imidazolones (10 examples), 2-imidazolidinones (four examples), vicinal diamines (two examples), and simple amino acid derivatives (four examples) have been pr

Full text of DOI:10.1021/jm50001a012

Products guided by the article

Product name:2H-Imidazol-2-one, 1,3-dihydro-1,4-diphenyl-

Cas No:2032-07-7

R&D Labs maybe for 2032-07-7

Zhejiang Hoshine Silicon Industry Co., Ltd.

Contact:86-573-89179966

Address:Zhapu Town, Pinghu City, Zhejiang, China
LinHai Cina Chemical Co., LTD.

Contact:0576-85580989

Address:Pharma-chem zone,Duqiao,Linhai,Zhejiang,China
DU-HOPE INTERNATIONAL GROUP

Contact:+86-25-52346955

Address:199,JIANYE ROAD,NANJING,CHINA
Nantong Chem-land Co., Ltd.

Contact:86 513 85512619

Address:Rm.1306, Building A, Wenfeng Mansion,168 Gongnong Road, Nantong Jiangsu China
Changzhou Qidi Chemical Co., Ltd

website:http://www.czqdhg.com/

Contact:86-519-83382137

Address:128-1-16# HuaYuan Street,Hutang Town,Wujin District,Changzhou City,P.R.China.

Relevant to this article

Anionic ring expansion reactions of oxabicyclo[4.2.1]heptenones. An efficient entry into the carbon framework of oxygenated cembranoids

Doi:10.1016/S0040-4020(01)00778-5
(2001)
Facile synthesis of imidazo[1,5-a]pyrazin-8(7H)-ones from mesoionic 1,3-oxazolium-5-olates via a multistep one-pot transformation

Doi:10.3987/COM-16-13551
(2016)
Synthesis and structure of acyclic bis(ketenimine) complexes of zirconium

Doi:10.1021/om970862h
(1998)
Doi:10.1021/ja01011a023
(1968)
Sequential catalytic isomerization and allylic substitution. Conversion of racemic branched allylic carbonates to enantioenriched allylic substitution products

Doi:10.1021/ja0644273
(2006)
Doi:10.1016/0020-1650(67)80105-3
(1967)

Article Doi