Discovery of 4-(phenyl)thio-1H-pyrazole derivatives as agonists of GPR109A, a high affinity niacin receptor
暂无分享,去创建一个
[1] Sunkyung Lee,et al. Discovery of 4-(phenyl)thio-1H-pyrazole derivatives as agonists of GPR109A, a high affinity niacin receptor , 2015, Archives of Pharmacal Research.
[2] I. Gaidarov,et al. Differential tissue and ligand-dependent signaling of GPR109A receptor: implications for anti-atherosclerotic therapeutic potential. , 2013, Cellular signalling.
[3] D. Connolly,et al. (1aR,5aR)1a,3,5,5a-Tetrahydro-1H-2,3-diaza-cyclopropa[a]pentalene-4-carboxylic acid (MK-1903): a potent GPR109a agonist that lowers free fatty acids in humans. , 2012, Journal of medicinal chemistry.
[4] W. Greenlee,et al. Discovery of SCH 900271, a Potent Nicotinic Acid Receptor Agonist for the Treatment of Dyslipidemia. , 2012, ACS medicinal chemistry letters.
[5] S. Tunaru,et al. Nicotinic acid- and monomethyl fumarate-induced flushing involves GPR109A expressed by keratinocytes and COX-2-dependent prostanoid formation in mice. , 2010, The Journal of clinical investigation.
[6] J. Benovic,et al. Internalization of the Human Nicotinic Acid Receptor GPR109A Is Regulated by Gi, GRK2, and Arrestin3* , 2010, The Journal of Biological Chemistry.
[7] M. Forrest,et al. Discovery of a biaryl cyclohexene carboxylic acid (MK-6892): a potent and selective high affinity niacin receptor full agonist with reduced flushing profiles in animals as a preclinical candidate. , 2010, Journal of medicinal chemistry.
[8] J. Violin,et al. beta-Arrestin1 mediates nicotinic acid-induced flushing, but not its antilipolytic effect, in mice. , 2009, The Journal of clinical investigation.
[9] P. D. Boatman,et al. Nicotinic acid receptor agonists. , 2008, Journal of medicinal chemistry.
[10] D. Connolly,et al. Effects of a niacin receptor partial agonist, MK-0354, on plasma free fatty acids, lipids, and cutaneous flushing in humans. , 2008, Journal of clinical lipidology.
[11] Ning Ren,et al. Molecular modeling aided design of nicotinic acid receptor GPR109A agonists. , 2008, Bioorganic & medicinal chemistry letters.
[12] D. Connolly,et al. Nicotinic Acid Receptor Agonists Differentially Activate Downstream Effectors* , 2007, Journal of Biological Chemistry.
[13] A. IJzerman,et al. Nicotinic acid receptor subtypes and their ligands , 2007, Medicinal research reviews.
[14] D. Connolly,et al. Analogues of acifran: agonists of the high and low affinity niacin receptors, GPR109a and GPR109b. , 2007, Journal of medicinal chemistry.
[15] S. Offermanns. The nicotinic acid receptor GPR109A (HM74A or PUMA-G) as a new therapeutic target. , 2006, Trends in pharmacological sciences.
[16] Z. Benyó,et al. GPR109A (PUMA-G/HM74A) mediates nicotinic acid-induced flushing. , 2005, The Journal of clinical investigation.
[17] L. Carlson,et al. Nicotinic acid: the broad‐spectrum lipid drug. A 50th anniversary review , 2005, Journal of internal medicine.
[18] H. Matsushime,et al. Molecular identification of nicotinic acid receptor. , 2003, Biochemical and biophysical research communications.
[19] S. Dowell,et al. Molecular Identification of High and Low Affinity Receptors for Nicotinic Acid* , 2003, The Journal of Biological Chemistry.
[20] James Inglese,et al. Development of an intact cell reporter gene beta-lactamase assay for G protein-coupled receptors for high-throughput screening. , 2003, Analytical biochemistry.
[21] S. Tunaru,et al. PUMA-G and HM74 are receptors for nicotinic acid and mediate its anti-lipolytic effect , 2003, Nature Medicine.
[22] R. P. Eaton,et al. Kinetic studies of plasma free fatty acid and triglyceride metabolism in man. , 1969, The Journal of clinical investigation.
[23] J. Flinn,et al. Reduction of serum cholesterol levels and beta-lipoprotein cholesterol levels by nicotinic acid. , 1959, A.M.A. archives of internal medicine.
[24] A. Hoffer,et al. Influence of nicotinic acid on serum cholesterol in man. , 1955, Archives of biochemistry and biophysics.
[25] L. Carlson. NICOTINIC ACID ─ THE BROAD SPECTRUM LIPID DRUG , 2006 .
[26] M. Guerin,et al. Pharmacological modulation of cholesteryl ester transfer protein, a new therapeutic target in atherogenic dyslipidemia. , 2004, Pharmacology & therapeutics.