+++6 журналов: ACS(3) SciencDir(3)

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1. J. Med. Chem., 1993, 36 (23), pp 3693–3699
Development of high-affinity 5-HT3 receptor antagonists. Structure-affinity relationships of novel 1,7-annulated indole derivatives. 1
Ineke van Wijngaarden, Derk Hamminga

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http://dx.doi.org/10.1021/jm00075a026

2. J. Med. Chem., 1995, 38 (4), pp 669–685
Synthesis, Structure-Activity Relationships, and Pharmacological Evaluation of Pyrrolo[3,2,1-ij]quinoline Derivatives: Potent Histamine and Platelet Activating Factor Antagonism and 5-Lipoxygenase Inhibitory Properties. Potential Therapeutic Application in Asthma
Dominique Paris, Michel Cottin, Patrice Demonchaux,

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http://dx.doi.org/10.1021/jm00004a013

3. Bioorganic & Medicinal Chemistry Letters, 11, 6, 2001, pp 845-848
N-Aminoindoline derivatives as inhibitors of 5-lipoxygenase
Corinne Audouina, Nathalie Mestdagh, Marie-Agnès Lassoie

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http://dx.doi.org/10.1016/S0960-894X(01)00077-4

4. Bioorganic & Medicinal Chemistry Letters, 10, 9, 2000, pp 919-921
Pyrrolo[3,2,1-ij]quinoline derivatives, a 5-HT2c receptor agonist with selectivity over the 5-HT2a receptor: potential therapeutic applications for epilepsy and obesity
Methvin Isaac, , Abdelmalik Slassi, Anne O'Brien, Louise Edwards

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http://dx.doi.org/10.1016/S0960-894X(00)00141-4

5. J. Am. Chem. Soc., 1958, 80 (12), pp 3009–3012
Novel Reductions of N-Nitrosodibenzylamines—A New Reaction
C. G. Overberger, Joseph G. Lombardino, Richard G. Hiskey

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http://dx.doi.org/10.1021/ja01545a028

6. European Journal of Medicinal Chemistry, 42, 7, 2007, pp 1004-1013
Design, synthesis and melatoninergic activity of new unsubstituted and β,β′-difunctionalised 2,3-dihydro-1H-pyrrolo[3,2,1-ij]quinolin-6-alkanamides
Andrew Tsotinisa, Maria Panoussopoulou

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http://dx.doi.org/10.1016/j.ejmech.2007.01.005

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