3-Phenylpyrrolidines: synthesis and evaluation of the in vitro binding affinity at D1 and D2 receptors

DOI: 10.1016/0223-5234(92)90155-T

Source and publish data:

European Journal of Medicinal Chemistry p. 407 - 411 (1992)

Update date:2022-08-04

Topics:

Authors:

Crider, A M

Andersen, P H

Cruse, S F

Ghosh, D

Harpalani, A

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

Article abstract of DOI:10.1016/0223-5234(92)90155-T

A variety of 3-phenylpyrrolidines were synthesized and evaluated for their dopamine binding affinity in rat striatal tissue in vitro using <3H> SCH 23390 and <3H> spiperone as the D1 and D2 selective radioligands, respectively.Maximal D1 and D2 receptor b

Full text of DOI:10.1016/0223-5234(92)90155-T

Products guided by the article

Product name:2,5-Pyrrolidinedione, 1-butyl-3-(3,4-dimethoxyphenyl)-

Cas No:143883-79-8

R&D Labs maybe for 143883-79-8

Ji'nan Orgachem Pharmaceutical Co.,Ltd

Contact:+86-531-82687810

Address:Jinan
shanghai Tauto Biotech Co., Ltd

website:http://www.tautobiotech.com/en/index.htm

Contact:+86-21-51320588 ext. 8025

Address:No. 326, Aidisheng Rd , Zhangjiang Hi-tech Park, Shanghai , P.R.CHINA
Jining tiansheng chemical co.,ltd.

Contact:+86-537-5158722

Address:ROOM 1011, BLOCK B, CUIDU INTERNATIOAL BUSINESS CENTER, JINING CITY, CHINA
Guangxi Nanning Guangtai Agriculture Chemical Co.,Ltd

Contact:+86-771-2311266

Address:Room703,Building12, Software Park Phase II,NO.68,Keyuan Road,Nanning City,Guangxi,China
Jiaxing Carry Bio-Chem Technology Co.,Ltd

website:http://www.carrybiotech.com

Contact:0573-82788958

Address:Add.Fl 3th, Pharm Vally,Kaichuang Rd, Xiuzhou District, Jiaxing, Zhejiang,314031,China

Relevant to this article

Magnetic interaction between two triplet nitrene units through diphenylsilane and 1,2-diphenyldisilane couplers

Doi:10.1021/ja00073a006
(1993)
Use of Strain-Release for the Diastereoselective Construction of Quaternary Carbon Centers

Doi:10.1021/jacs.1c03492
(2021)
A New Synthesis of α-Fluoro-α,β-unsaturated Ketones and Esters based on Organoselenium Methodology

Doi:10.1039/c39920001148
(1992)
The structure-activity relationships of L3MBTL3 inhibitors: Flexibility of the dimer interface

Doi:10.1039/c3md00197k
(2013)
Enantioselective catalytic borane reductions of achiral ketones: Synthesis and application of new catalysts prepared from (S)-tert-leucine and (S)-azetidinecarboxylic acid

Doi:10.1080/00397919208019066
(1992)
Pd-catalyzed C-H olefination of (hetero)arenes by using saturated ketones as an olefin source

Doi:10.1002/anie.201208627
(2013)

Article Doi