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

Wuhan Pengo Technology.,Ltd.

Contact:+86-27-67841589

Address:Add: 999 Gaoxin Road, Donghu New Technology Development Zone, Wuhan City, Hubei, China
puyang hongda shengdao new material co.,ltd.

Contact:+86-393- 4896278

Address:No.29 East Zhongyuan Road
CGeneTech (Suzhou, China) Co., Ltd.

Contact:+86-512-62956962

Address:Room 101，Bld C11,218 Xinghu Rd.,Suzhou industrial Park
Hangzhou Zyter Biological & Chemical Technology Co., Ltd.

website:http://www.zyterpharm.com

Contact:+86-18858184290

Address:West Wenyi Road, Cangqian, Yuhang
Shandong Ailitong New Material Co.,Ltd

Contact:+86-536-3226266

Address:zhongjia village, putong town , qingzhou city,Shandong Province,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