Setembro 2013 vol. 1 num. 1 - Brazilian Meeting on Organic Synthesis 2011

Abstract - Open Access.

Idioma principal

SYNTHESIS AND EVALUATION OF POSSIBLE SUBTYPESELECTIVE ANTAGONISTS OF NICOTINIC ACETYLCHOLINE RECEPTORS

López, Jhon J. ; Pérez, Edwin G. ;

Abstract:

Development of selective agonists or antagonists for the Nicotinic acetylcholine receptors (nAChR) may result in new and potentially useful therapeutic agents. It has been reported in the literature that potent and selective nAChR antagonists could be used for the treatment of nicotine dependence and may be an efficacious adjuvant therapy in many different oncologic protocols. nAChr antagonists studied previously by us having an indole ring core, N1-alkyl groups and a quaternized moiety showed potency but little selectivity.

Abstract:

Palavras-chave: Quinucludine, reductions, biological activity,

Palavras-chave: ,

DOI: 10.5151/chempro-14bmos-R0375-1

Referências bibliográficas
  • [1] 1 Dasgupta, p.; Kinkade, R.; Joshi, B.; DeCook, C.; Haura, E.; Chellappan, S. Proc. Natl. Acad. Sci. U.S.A.., 2006, 103, 6332.
  • [2] 2 Grozio, A.; Peleari, L.; Catassi, A.; Servent, D.; Cilli, M.; Piccardi, F.; Paganuzzi, M.; Cesario, A.; Granote, P.; Mourier, G.; Russo, P. Int. J. Cancer, 2008, 122, 1911.
  • [3] 3 Pérez, E. P.; Eibl, C.; Gundisch, D.; Cassels B. K. Bioorg. Med. Chem. 2011. Acepted.
Como citar:

López, Jhon J.; Pérez, Edwin G.; "SYNTHESIS AND EVALUATION OF POSSIBLE SUBTYPESELECTIVE ANTAGONISTS OF NICOTINIC ACETYLCHOLINE RECEPTORS", p. 375 . In: In Blucher Chemistry Proceedings, São Paulo, v. 1, n. 1, Setembro.2013. São Paulo: Blucher, 2013.
ISSN 2318-4043, DOI 10.5151/chempro-14bmos-R0375-1

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