8-Aminoquinolines as anticoccidials - I

DOI: 10.1016/S0960-894X(97)10024-5

Source and publish data:

Bioorganic and Medicinal Chemistry Letters p. 2585 - 2588 (1997)

Update date:2022-08-03

Topics:

Authors:

Armer, Richard E.

Barlow, Jacqueline S.

Dutton, Christopher J.

Greenway, David H.J.

Greenwood, Sean D.W.

Lad, Nita

Tommasini, Ivan

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

Article abstract of DOI:10.1016/S0960-894X(97)10024-5

The proposed ring metabolites of the 8-aminoquinoline antimalarial, pentaquine, 1, have been synthesised and their biological activity as anticoccidial agents investigated in vivo. Several analogues in which this metabolic pathway had been blocked were also synthesised and their anticoccidial activity measured.

Full text of DOI:10.1016/S0960-894X(97)10024-5

Products guided by the article

Product name:N-(5-Bromo-6-methoxy-quinolin-8-yl)-N'-isopropyl-pentane-1,5-diamine

Cas No:199383-92-1

R&D Labs maybe for 199383-92-1

Feis International Trade Co,. Ltd

Contact:13961823444-18235944442

Address:Wuxi jiangsu
Beijing Zhongshuo Pharmaceutical T & D Co.,Ltd

Contact:0086-10-64430626

Address:ea No 16, HEPINGLI,DONGCHENG DISTRICT,BEIJING,P.R.CHINA.
SINO Industries Company Limited(expird)

Contact:86-29-85369724

Address:No.111, Jiefang Road, Xi’an, China
NEWSTAR CHEM ENTERPRISE LTD.

Contact:0572-2722882

Address:1201,F3,xinghuibandao,
Santow Laboratory Limited

Contact:+86-371-55981030

Address:Room 1571, Macalline Soho, No.1, Shangdu Road, Zhengzhou, Henan

Relevant to this article

Preparation of cyclic α-hydroxy ketones from δ- and ε-keto acids induced by the generation of a novel acyl anion equivalent from the carboxyl group

Doi:10.1248/cpb.45.1729
(1997)
Biohydroxylations of Cbz-protected alkyl substituted piperidines by Beauveria bassiana ATCC 7159

Doi:10.1039/a805800h
(1998)
A 1,6-ring closure mechanism for (+)-δ-cadinene synthase?

Doi:10.1021/ja211820p
(2012)
Spontaneous dimerization of 2-(4-methylphenylamino)thiophene

Doi:10.1007/BF02253121
(1997)
Nucleophilic phosphanylation of fluoroaromatic compounds with carboxyl, carboxymethyl, and aminomethyl functionalities - An efficient synthetic route to amphiphilic arylphosphanes

Doi:10.1002/(SICI)1099-0682(199801)1998:1<73::AID-EJIC73>3.0.CO;2-M
(1998)
Optically active cantharidin analogues possessing selective inhibitory activity on Ser/Thr protein phosphatase 2B (calcineurin): Implications for the binding mode

Doi:10.1016/j.bmc.2005.05.013
(2005)

Article Doi