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Amino Acids|July 8, 2010
Towards non-peptide ANG II AT1 receptor antagonists based on urocanic acid: rational design, synthesis and biological evaluationGeorge Agelis, Amalia Resvani, Minos-Timotheos Matsoukas, et al.Journal of Computer-Aided Molecular Design|July 13, 2010
An efficient synthesis of a rationally designed 1,5 disubstituted imidazole AT(1) angiotensin II receptor antagonist: reorientation of imidazole pharmacophore groups in losartan reserves high receptor affinity and confirms docking studiesGeorge Agelis, Panagiota Roumelioti, Amalia Resvani, et al.Current Molecular Pharmacology|April 21, 2018
Transdermal Delivery of AT1 Receptor Antagonists Reduce Blood Pressure and Reveal a Vasodilatory Effect on Kidney Blood VesselsMichaila Michalatou, Maria Eleni Androutsou, Markos Antonopoulos, et al.European Journal of Medicinal Chemistry|August 15, 2012
The discovery of new potent non-peptide Angiotensin II AT1 receptor blockers: a concise synthesis, molecular docking studies and biological evaluation of N-substituted 5-butylimidazole derivativesGeorge Agelis, Amalia Resvani, Serdar Durdagi, et al.Molecules (Basel, Switzerland)|June 29, 2013
Facile and efficient syntheses of a series of N-benzyl and N-biphenylmethyl substituted imidazole derivatives based on (E)-urocanic acid, as angiotensin II AT1 receptor blockersGeorge Agelis, Konstantinos Kelaidonis, Amalia Resvani, et al.Journal of Medicinal Chemistry|January 6, 2006
Design, synthesis, and molecular modeling of a novel amide-linked cyclic GnRH analogue cyclo(4-9)[Lys4,D-Trp6,Glu9]GnRH: stimulation of gonadotropin gene expressionMaria K Keramida, Theodore Tselios, Efthimia Mantzourani, et al.Combinatorial Chemistry & High Throughput Screening|May 31, 2014
An efficient synthetic method and theoretical calculations of olmesartan methyl ether: study of biological function of AT1 antagonismDimitrios Ntountaniotis, George Agelis, Amalia Resvani, et al.European Journal of Medicinal Chemistry|February 5, 2013
Rational design, efficient syntheses and biological evaluation of N,N'-symmetrically bis-substituted butylimidazole analogs as a new class of potent Angiotensin II receptor blockersGeorge Agelis, Amalia Resvani, Catherine Koukoulitsa, et al.Pageof 2