91271-79-3Relevant academic research and scientific papers
Mimicking the intramolecular hydrogen bond: Synthesis, biological evaluation, andmolecular modeling of benzoxazines and quinazolines as potential antimalarial agents
Gemma, Sandra,Camodeca, Caterina,Brindisi, Margherita,Brogi, Simone,Kukreja, Gagan,Kunjir, Sanil,Gabellieri, Emanuele,Lucantoni, Leonardo,Habluetzel, Annette,Taramelli, Donatella,Basilico, Nicoletta,Gualdani, Roberta,Tadini-Buoninsegni, Francesco,Bartolommei, Gianluca,Moncelli, Maria Rosa,Martin, Rowena E.,Summers, Robert L.,Lamponi, Stefania,Savini, Luisa,Fiorini, Isabella,Valoti, Massimo,Novellino, Ettore,Campiani, Giuseppe,Butini, Stefania
, p. 10387 - 10404 (2013/02/23)
The intramolecular hydrogen bond formed between a protonated amine and a neighboring H-bond acceptor group in the side chain of amodiaquine and isoquine is thought to play an important role in their antimalarial activities. Here we describe isoquine-based
6-ARYLALKYLAMINO- 2,3,4,5-TETRAHYDRO-1H-BENZO[D]AZEPINES AS 5-HT2C RECEPTOR AGONISTS
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Page/Page column 92-93, (2010/11/26)
The present invention provides 6-substituted 2,3,4,5-tetrahydro-lH- benzo[d]azepines of Formula (I) as selective 5-HT2c receptor agonists for the treatment of 5-HT2c associated disorders including obesity, obsessive/compulsive disorder, depression, and anxiety, where, R6 is -NR10R11, where R10 is substituted phenylalkyl or substituted pyridylalkyl and other substituents are as defined in the specification.
New carboxamide compounds having melanin concentrating hormone antagonistic activity, pharmaceutical preparations comprising these compounds and process for their manufacture
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Page/Page column 45, (2010/02/09)
The present invention relates to carboxamide compounds of general formula I wherein the groups and residues A, B, W, X, Y, Z, R1, R2, R3 and k have the meanings given in claim 1. Moreover the invention relates to process for preparing the above mentioned carboxamides as well as pharmaceutical compositions containing at least one carboxamide according to the invention. In view of their MCH-receptor antagonistic activity the pharmaceutical compositions according to the invention are suitable for the treatment of metabolic disorders and/or eating disorders, particularly obesity, bulimia, anorexia, hyperphagia and diabetes.
