The effect of lipophilic substituents on the H2-histaminergic activity of some close analogues of impromidine

DOI: 10.1002/ardp.19923250805

Source and publish data:

Archiv der Pharmazie p. 471 - 476 (1992)

Update date:2022-08-02

Topics:

Authors:

Sellier Sellier

Elz Elz

Buschauer

Schunack

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

Article abstract of DOI:10.1002/ardp.19923250805

The cimetidine-like moiety of the potent H₂-agonist impromidine (9a) and three closely related guanidines (10a, 11a, and 12a) which are modified in the imidazolylpropyl portion, has been replaced by 2-[(2-pyridyl)methylthio]ethyl, 2-(benzylthio

Full text of DOI:10.1002/ardp.19923250805

Products guided by the article

Product name:Carbamimidic acid, N-benzoyl-N'-[2-[(phenylmethyl)thio]ethyl]-, phenyl ester

Cas No:112758-77-7

R&D Labs maybe for 112758-77-7

Shenzhen Hongyuan Import & Export Co., Ltd.

Contact:0755-26407171

Address:Shenzhen Hongyuan Chemical New Materials Technology Co., Ltd.
Changzhou Foreign Trade Corp

Contact:+86-519-86623222

Address:29F/D, 99 Yanling West Road, Changzhou, Jiangsu, China
Zhengzhou Minzhong Pharmaceutical Co.,ltd

Contact:0086-371-65797115

Address:15/F,Jiangshan Bldg, NO.126 Huanghe Road,Zhengzhou, China
MENGNA

Contact:18698110882

Address:1303 No2 building,LuoMa Garden,YongAn Road,Hexi District,Tianjin city
QINGDAO NEW FLOURISH INTERNATIOANAL TRADE CO., LTD.

Contact:+86 532 80861829

Address:No. 1, Yinchuan East Road, 266061, Qingdao, China

Relevant to this article

A highly selective and synthetically facile aqueous-phase cyanide probe

Doi:10.1016/j.tetlet.2008.08.115
(2008)
Alkylfluorenyl substituted N-heterocyclic carbenes in copper(i) catalysed hydrosilylation of aldehydes and ketones

Doi:10.1039/c5dt01888a
(2015)
Synthesis of saframycins. I. Total synthesis (+/-)-saframycin B and its congeners.

Doi:10.1248/cpb.35.2158
(1987)
ACYLATION OF AROMATIC AMINODICARBOXYLIC ACIDS

Doi:10.1007/BF00960132
(1987)
Oxidative addition of nitroalkanes to dinuclear gold(I) ylide complexes. The characterization by X-ray crystallography of Au₂(ylide)₂(NO₂)₂, a nitro complex of gold(II)

Doi:10.1021/om00094a032
(1988)
Doi:10.1016/S0020-1693(00)82117-9
(1987)

Article Doi