Chemistry and Hypoglycemic Activity of Benzimidoylpyrazoles

DOI: 10.1021/jm00144a031

Source and publish data:

Journal of Medicinal Chemistry p. 1521 - 1525 (1981)

Update date:2022-09-26

Topics:

Authors:

Shroff, James R.

Bandurco, Victor

Desai, Rohit

Kobrin, Sidney

Cervoni, Peter

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

Article abstract of DOI:10.1021/jm00144a031

A series of benzimidoylpyrazoles was synthesized and evaluated as hypoglycemic agents.Methyl 1-(N-cyclohexylbenzimidoyl)-5-methyl-3-pyrazolecarboxylate (13) and methyl 1--5-methyl-3-pyrazolecarboxylate (33) are two of the m

Full text of DOI:10.1021/jm00144a031

Products guided by the article

Product name:1-{[(Z)-2-Methoxy-phenylimino]-phenyl-methyl}-5-methyl-1H-pyrazole-3-carboxylic acid methyl ester

Cas No:79508-06-8

R&D Labs maybe for 79508-06-8

Du-Hope International Group

website:http://www.np-chem.com

Contact:0086-25-52346877

Address:199, Jian Ye Road, Nanjing, China
Guangxi Bonger Pharmaceutical Co., Ltd

website:http://napo.lookchem.com/

Contact:+86-18817331185

Address:Donghai Industrial Zone, Tiandong Country,Guangxi,China
Beijing Century Richap Chemistry Co.,Ltd

Contact:+86- 010-64455497

Address:Guannan County, Lianyungang City, Jiangsu Province, China
taizhou creating bio-pharm co.,ltd.

Contact:+86- 576- 88827176

Address:715 room ,unit A.junyue Building,Jiaojiang,Taizhou,Zhejiang,China
xujianqiang

Contact:86-21-57725962

Address:shanghai

Relevant to this article

REDUCTIVE AMINATION OF l-MENTHOL BY ALIPHATIC NITRILES

Doi:10.1007/BF00568510
(1981)
Synthesis of the azaspiracid-1 trioxadispiroketal

Doi:10.1021/ol048581a
(2004)
Doi:10.1021/ja01175a004
(1949)
Stereochemical studies on medicinal agents. 25. Absolute configuration and analgetic potency of beta-1,2-dimethyl-4-phenyl-4-(propionyloxy)piperidine enantiomers

Doi:10.1021/jm00343a002
(1982)
Palladium-Catalyzed Desulfurative Amide Formation from Thioureas and Arylboronic Acids

Doi:10.1002/cctc.202001099
(2020)
Synthesis of novel fused β-lactams by intramolecular 1,3-dipolar cycloadditions. 3. 6-phenoxacetamido-7-oxo-1,3-diazabicyclo[3.2.0] heptane-2-carboxylic acids

Doi:10.1016/S0040-4039(00)87517-6
(1982)

Article Doi