Synthesis, cytostatic and trichomonacide activities of 3,5-bis-(halomethyl)pyrazoles

DOI: 10.1016/0223-5234(87)90034-1

Source and publish data:

European Journal of Medicinal Chemistry p. 445 - 451 (1987)

Update date:2022-08-02

Topics:

Authors:

Iturrino

Navarro Navarro

Rodriguez-Franco

Contreras

Escario Escario

Martinez

Del Rosario Pardo

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

Article abstract of DOI:10.1016/0223-5234(87)90034-1

Full text of DOI:10.1016/0223-5234(87)90034-1

Products guided by the article

Product name:diethyl 4-bromo-1H-pyrazole-3,5-dicarboxylate

Cas No:115414-01-2

R&D Labs maybe for 115414-01-2

Chengdu NoVi Biotechnology Co., Ltd.(expird)

Contact:13551243286/028-81458053

Address:NO.168-1-224 JULONG ROAD WUHOU DISTRICT, CHENGDU CITY,SICHUAN PROVINCE
CHEM PLUS

Contact:0027-717-456976

Address:2ND FLOOR, 325 VAUSE ROAD, OVERPORT, 4001, SOUTH AFRICA
Cerametek Materials（ShenZhen）Co., Ltd.

Contact:+86-755-2324.2554

Address:A3-#9, YongChuan Street, Suite 501
shanghai hekang chemical co.ltd

Contact:021-54173790

Address:328 WuHe Road, Building #A, 2nd Floor, Minhang, Shanghai 201109, China
Alway Chem, China

website:http://www.alwaychem.com

Contact:+86-532-8586-4000, 8586-5000

Address:NO.51, TAIPING ROAD, QINGDAO, CHINA. 266001

Relevant to this article

Structural and Synthetic Studies of the Spore Germination Autoinhibitor Gloeosporone

Doi:10.1021/ja00226a041
(1988)
Doi:10.1002/ardp.19773100204
(1977)
The effect of linker length on binding affinity of a photoswitchable molecular glue for DNA

Doi:10.1016/j.bmc.2009.01.053
(2009)
Oxidation of Biginelli reaction products: Synthesis of 2-unsubstituted 1,4-dihydropyrimidines, pyrimidines, and 2-hydroxypyrimidines

Doi:10.1055/s-0028-1087920
(2009)
Application of 7-endo-trig Pictet-Spengler cyclization to the formation of the benzazepine ring: Synthesis of benzazepinoindoles

Doi:10.1002/ejoc.200801201
(2009)
Discovery of indolin-2-one derivatives as potent PAK4 inhibitors: Structure-activity relationship analysis, biological evaluation and molecular docking study

Doi:10.1016/j.bmc.2017.04.047
(2017)

Article Doi