C-Attached aminoalkylindoles: potent cannabinoid mimetics

Autor:	Dean A. Haycock, Michael Eissenstat, Joan E. Kuster, Daniel Luttinger, Frances M. Casiano, Kurt A. Josef, Alexandros Makriyannis, Virendra Kumar, James H. Ackerman, Atmaram D. Khanolkar, Jeffrey Abt, Bacon Edward R, Thomas E. D'Ambra, Renee Arnold, John D. Weaver, Malcolm R. Bell, Susan M. Chippari, Joan I. Stevenson, W. Adam G. Hill, Susan Jean Ward, Philip M. Carabateas
Rok vydání:	1996
Předmět:	Agonist Indole test Carbon atom Chemistry Stereochemistry medicine.drug_class medicine.medical_treatment Organic Chemistry Clinical Biochemistry Pharmaceutical Science Ring (chemistry) Biochemistry Combinatorial chemistry Drug Discovery medicine Molecular Medicine Amine gas treating Cannabinoid Molecular Biology
Zdroj:	Bioorganic & Medicinal Chemistry Letters. 6:17-22
ISSN:	0960-894X
DOI:	10.1016/0960-894x(95)00560-g
Popis:	Aminoalkylindoles (AAIs) with potent cannabinoid agonist activity have been synthesized where the aminoalkyl chain is attached to the indole ring via a carbon atom of the cyclic amine.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::8be4d4fe848aed4d5576b63484012c02 https://doi.org/10.1016/0960-894x(95)00560-g Zobrazit plný text záznamu Full Text from ScienceDirect