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Journal of Medicinal Chemistry|December 8, 2011
Synthesis, biological evaluation, and docking studies of tetrahydrofuran- cyclopentanone- and cyclopentanol-based ligands acting at adrenergic α₁- and serotonine 5-HT1A receptorsAdolfo Prandi, Silvia Franchini, Leda Ivanova Manasieva, et al.European Journal of Medicinal Chemistry|July 4, 2014
High affinity ligands and potent antagonists for the α1D-adrenergic receptor. Novel 3,8-disubstituted [1]benzothieno[3,2-d]pyrimidine derivativesGiuseppe Romeo, Loredana Salerno, Valeria Pittalà, et al.Chemmedchem|December 23, 2008
(2,2-Diphenyl-[1,3]oxathiolan-5-ylmethyl)-(3-phenyl-propyl)-amine: a potent and selective 5-HT(1A) receptor agonistSilvia Franchini, Annalisa Tait, Adolfo Prandi, et al.Molecules (Basel, Switzerland)|June 28, 2023
Dual Anta-Inhibitors Targeting Protein Kinase CK1δ and A2A Adenosine Receptor Useful in Neurodegenerative DisordersBeatrice Francucci, Simone Angeloni, Diego Dal Ben, et al.Bioorganic & Medicinal Chemistry Letters|October 10, 2006
New pyrimido[5,4-b]indoles and [1]benzothieno[3,2-d]pyrimidines: high affinity ligands for the alpha(1)-adrenoceptor subtypesGiuseppe Romeo, Luisa Materia, Gabriella Marucci, et al.Journal of Medicinal Chemistry|March 7, 2003
Structure-activity relationships of acetylcholinesterase noncovalent inhibitors based on a polyamine backbone. 2. Role of the substituents on the phenyl ring and nitrogen atoms of caproctamineVincenzo Tumiatti, Michela Rosini, Manuela Bartolini, et al.Bioorganic & Medicinal Chemistry Letters|April 4, 2020
New 8-amino-1,2,4-triazolo[4,3-a]pyrazin-3-one derivatives. Evaluation of different moieties on the 6-aryl ring to obtain potent and selective human A2A adenosine receptor antagonistsMatteo Falsini, Costanza Ceni, Daniela Catarzi, et al.ACS Medicinal Chemistry Letters|April 19, 2019
Investigation on 2',3'-O-Substituted ATP Derivatives and Analogs as Novel P2X3 Receptor AntagonistsDiego Dal Ben, Michela Buccioni, Catia Lambertucci, et al.Chemmedchem|April 3, 2016
The Length and Flexibility of the 2-Substituent of 9-Ethyladenine Derivatives Modulate Affinity and Selectivity for the Human A2A Adenosine ReceptorAjiroghene Thomas, Michela Buccioni, Diego Dal Ben, et al.Journal of Medicinal Chemistry|April 19, 2002
Structure-activity relationships of methoctramine-related polyamines as muscular nicotinic receptor noncompetitive antagonists. 2. Role of polymethylene chain lengths separating amine functions and of substituents on the terminal nitrogen atomsMichela Rosini, M Gabriele Bixel, Gabriella Marucci, et al.Pageof 11