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Chemical design of peripherally acting compounds.
Jackson, W R; Copp, F C; Cullen, J D; Guyett, F J; Rae, I D; Robinson, A J; Pothoulackis, H; Serelis, A K; Wong, M.
Afiliación
  • Jackson WR; Department of Chemistry, Monash University, Melbourne, Victoria, Australia.
Clin Exp Pharmacol Physiol ; 19(1): 17-23, 1992 Jan.
Article en En | MEDLINE | ID: mdl-1623633
1. Some guanidines, related in structure to mianserin and to 2-methyl-1,2,9,13b-tetrahydro-3H-dibenz[c,f]imadazo[1,5a] azepin-3-imine hydrobromide (WAL 801), have been synthesized and shown to be peripherally acting 5-HT2 antagonists. Structurally related compounds but not bearing a charged ionic group have been shown to have central activity. 2. Computer-aided molecular modelling has been used to establish a 5-HT2 pharmacophore. 3. The principle of exclusion from the CNS by incorporating a highly polar group to a biologically active molecule has been extended to the design and synthesis of a peripherally acting analgesic.
Asunto(s)
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Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Antagonistas de la Serotonina / Simulación por Computador / Diseño de Fármacos / Dibenzazepinas / Imidazoles / Mianserina Idioma: En Revista: Clin Exp Pharmacol Physiol Año: 1992 Tipo del documento: Article País de afiliación: Australia Pais de publicación: Australia
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Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Antagonistas de la Serotonina / Simulación por Computador / Diseño de Fármacos / Dibenzazepinas / Imidazoles / Mianserina Idioma: En Revista: Clin Exp Pharmacol Physiol Año: 1992 Tipo del documento: Article País de afiliación: Australia Pais de publicación: Australia