Preparation and antidiabetic activity of new 3-methyl-5-phenylpyrazolesulfonylurea derivatives

DOI: 10.1002/jps.2600700607

Source and publish data:

Journal of Pharmaceutical Sciences p. 602 - 605 (1981)

Update date:2022-07-30

Topics:

Authors:

Soliman Soliman

Feid-Allah

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

Article abstract of DOI:10.1002/jps.2600700607

Full text of DOI:10.1002/jps.2600700607

Products guided by the article

Product name:C₂₃H₂₆N₄O₂S₂

Cas No:78794-38-4

R&D Labs maybe for 78794-38-4

HANGZHOU TOYOND BIOTECH CO., LTD

Contact:+86-571-86965177

Address:No. 189, Fengqi East Road, Hangzhou, China
Jiangsu Willing Bio-Tech Co ltd

website:http://www.willingbio.com/

Contact:+86 18796908173

Address:No 18 Guoqiao Road
Nanjing lanbai chemical Co.,Ltd.

Contact:+86-25-85499326

Address:Room 908, 9F Taiyue Building,No.285 Heyan Road
Wuhan Hanye Chemical New Material Co.,Ltd

Contact:+86-27-85308141

Address:LiuDian, Panlongcheng Economic Development Zone, HuangPi district, Wuhan, Hubei 430311 P.R.China
Anhui Xinyuan Technology Co.,Ltd

Contact:0086-559-3515800

Address:No.16 Zijin Rd, Circular Economic Zone, Huizhou District, Huangshan Anhui China

Relevant to this article

Stereoselective oxidation of aryl-substituted vicinal diols into chiral α-hydroxy aldehydes by re-engineered propanediol oxidoreductase

Doi:10.1021/cs400824h
(2013)
Stereoselective reductive rearrangement of α-hydroxy epoxides: A new method for synthesis of 1,3-diols

Doi:10.1021/jo981097z
(1999)
A recyclable Ru-based metathesis catalyst

Doi:10.1021/ja983222u
(1999)
Artificial aldolases from peptide dendrimer combinatorial libraries

Doi:10.1039/b607342e
(2006)
The high-anti conformation of 7-halogenated 8-aza-7-deaza-2'- deoxyguanosines: A study of the influence of modified bases on the sugar structure of nucleosides

Doi:10.1002/(SICI)1522-2675(19990113)82:1<105::AID-HLCA105>3.0.CO;2-3
(1999)
Dehydrogenative Diboration of Alkynes Catalyzed by Ir/CO/^tBuNC System

Doi:10.1016/j.jorganchem.2020.121614
(2021)

Article Doi