Synthesis and pharmacological activity of 5 substituted 2 (N,N dialkylaminoethyl)amino and 2 N methylpiperazinyl 1,3,4 thiadiazoles

DOI: 10.1002/jps.2600640732

Source and publish data:

Journal of Pharmaceutical Sciences p. 1250 - 1252 (1975)

Update date:2022-09-26

Topics:

Authors:

Lalezari

Shafiee Shafiee

Badaly Badaly

Salimi Salimi

Khoyi Khoyi

Abtahi Abtahi

Zarrindast

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

Article abstract of DOI:10.1002/jps.2600640732

Full text of DOI:10.1002/jps.2600640732

Products guided by the article

Product name:1-methyl-4-[5-(4-nitro-phenyl)-[1,3,4]thiadiazol-2-yl]-piperazine

Cas No:57709-48-5

R&D Labs maybe for 57709-48-5

Shanghai Profirst Co., Ltd.

Contact:+86-21-38122007

Address:2, Lane 1123, Kangqiao Road, Pudong New Area, Shanghai
MENGNA

Contact:18698110882

Address:1303 No2 building,LuoMa Garden,YongAn Road,Hexi District,Tianjin city
henan victory industry co.ltd

Contact:86-371-63655023

Address:No.85,jinshui road,zhengzhou,China
N&R INDUSTRIES,INC

Contact:Tel:+86-29-88764861 Fax:+86-29-88764861

Address:Rm#2107, Block A, Epin Meidao Building, Gaoxin Rd, Hi-Tech Zone, Xi’an, China
Hangzhou Yingshanhua Pigment Chemicals Co.,Ltd.

Contact:+86-0150-58101658

Address:Nanyang Economic DevelopmentZong,Xiaoshan,Hangzhou,China

Relevant to this article

Doi:10.1021/jo00871a001
(1976)
Natural product inspired library synthesis - Identification of 2,3-diarylbenzofuran and 2,3-dihydrobenzofuran based inhibitors of Chlamydia trachomatis

Doi:10.1016/j.ejmech.2017.11.099
(2018)
Doi:10.1016/S0008-6215(00)84179-8
(1975)
Light controlled protein release from a supramolecular hydrogel

Doi:10.1039/c002565h
(2010)
A new synthesis of 4-alkyl/aryl-5,6-dihydro-2H-pyrano[3,2-c]quinoline-2,5-diones and molecular rearrangement of their 3-bromo derivatives to 2-alkyl/aryl-4-oxo-4,5-dihydrofuro[3,2-c]quinoline-3-carboxylic acids

Doi:10.3987/COM-02-9681
(2003)
Copper promoted desulfurization towards the synthesis of isothiocyanates

Doi:10.1016/j.tetlet.2016.11.086
(2017)

Article Doi