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Farmaco (Societa Chimica Italiana : 1989)|January 1, 1996
(E)-(methyloxyimino)acetamides as analogues of neuroleptic benzamides: synthesis and D2-dopaminergic binding affinityA Lapucci, M Macchia, E Orlandini, et al.
Chemistry & Biology|July 8, 1998
A high-affinity subtype-selective agonist ligand for the thyroid hormone receptorG Chiellini, J W Apriletti, H A Yoshihara, et al.
Molecular and Cellular Endocrinology|June 14, 2011
Effects of the thyroid hormone derivatives 3-iodothyronamine and thyronamine on rat liver oxidative capacityP Venditti, G Napolitano, L Di Stefano, et al.
Neurochemistry International|March 1, 1996
The serotonin transporter from human brain: purification and partial characterizationA Rotondo, G Giannaccini, L Betti, et al.
The Journal of Experimental Biology|March 14, 2009
T3 and the thyroid hormone beta-receptor agonist GC-1 differentially affect metabolic capacity and oxidative damage in rat tissuesP Venditti, G Chiellini, A Bari, et al.
The Journal of Endocrinology|April 3, 2010
The TRbeta-selective agonist, GC-1, stimulates mitochondrial oxidative processes to a lesser extent than triiodothyronineP Venditti, G Chiellini, L Di Stefano, et al.
The Journal of Clinical Investigation|July 4, 2001
Thyroid hormone--sympathetic interaction and adaptive thermogenesis are thyroid hormone receptor isoform--specificM O Ribeiro, S D Carvalho, J J Schultz, et al.
Bioorganic & Medicinal Chemistry|January 9, 1999
Synthesis and beta-adrenergic properties of (Z)-N-[3-(alkylamino)-2-hydroxypropylidene](aryl-methyloxy)amines: effects of the configuration around the methyloxyiminomethyl (MOIM) double bond on the biopharmacological properties of MOIM-type beta-blocking agentsA Balsamo, M C Breschi, G Chiellini, et al.
Journal of Medicinal Chemistry|May 13, 1994
The [(methyloxy)imino]methyl moiety as a bioisoster of aryl. A novel class of completely aliphatic beta-adrenergic receptor antagonistsB Macchia, A Balsamo, M C Breschi, et al.
Journal of Medicinal Chemistry|October 15, 1993
Conformationally restrained analogs of sympathomimetic catecholamines. Synthesis, conformational analysis, and adrenergic activity of isochroman derivativesB Macchia, A Balsamo, M C Breschi, et al.
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