Synthesis and Evaluation of N, N-Di-n-propyltetrahydrobenz [f] indol-7-amine and Related Congeners as Dopaminergic Agonists

DE Nichols, JM Cassady, PE Persons…

Index: Nichols, David E.; Cassady, John M.; Persons, Paul E.; Yeung, Ming C.; Clemens, James A.; Smalstig, E. Barry Journal of Medicinal Chemistry, 1989 , vol. 32, # 9 p. 2128 - 2134

Full Text: HTML

Citation Number: 23

Abstract

An evaluation of 6-[2-(di-n-propylamino) ethyl] indole (4), its rigid analogue N, N-di-n-propyl- 5, 6, 7, 8-tetrahydro-benz [flindol-7-amine (5), and some related congeners, for ability to suppress serum prolactin in reserpinized rats, revealed modest biological activity in this in vivo model of dopaminergic activity. Although the indole NH in these compounds can be considered to be oriented" meta" with respect to the ethylamine side chain, compounds ...

Related Articles:

Transition state imbalance in the deprotonation of substituted 2-tetralones by hydroxide ion

[Journal of the American Chemical Society, , vol. 119, # 52 p. 12722 - 12726]

Synthesis and Evaluation of N, N-Di-n-propyltetrahydrobenz [f] indol-7-amine and Related Congeners as Dopaminergic Agonists

[Journal of Medicinal Chemistry, , vol. 32, # 9 p. 2128 - 2134]

Synthesis and Evaluation of N, N-Di-n-propyltetrahydrobenz [f] indol-7-amine and Related Congeners as Dopaminergic Agonists

[Journal of Medicinal Chemistry, , vol. 32, # 9 p. 2128 - 2134]

Synthesis and Evaluation of N, N-Di-n-propyltetrahydrobenz [f] indol-7-amine and Related Congeners as Dopaminergic Agonists

[Journal of Medicinal Chemistry, , vol. 32, # 9 p. 2128 - 2134]

Synthesis and Evaluation of N, N-Di-n-propyltetrahydrobenz [f] indol-7-amine and Related Congeners as Dopaminergic Agonists

[Journal of Medicinal Chemistry, , vol. 32, # 9 p. 2128 - 2134]

More Articles...