T-type calcium channels inhibitors: a patent review
暂无分享,去创建一个
[1] P. Leeson,et al. The influence of drug-like concepts on decision-making in medicinal chemistry , 2007, Nature Reviews Drug Discovery.
[2] H. Rhim,et al. Synthesis and evaluation of alpha,alpha'-disubstituted phenylacetate derivatives for T-type calcium channel blockers. , 2008, Bioorganic & medicinal chemistry letters.
[3] Kyoichi Ono,et al. Cardiac T-type Ca(2+) channels in the heart. , 2010, Journal of molecular and cellular cardiology.
[4] Steven V. Fox,et al. Short-acting T-type calcium channel antagonists significantly modify sleep architecture in rodents. , 2010, ACS medicinal chemistry letters.
[5] M. Doddareddy,et al. Design, synthesis, and biological evaluation of 1,3-dioxoisoindoline-5-carboxamide derivatives as T-type calcium channel blockers. , 2007, Bioorganic & Medicinal Chemistry Letters.
[6] R. Tsien,et al. Nomenclature of Voltage-Gated Calcium Channels , 2000, Neuron.
[7] Minsoo Han,et al. Exploration of novel 2-alkylimino-1,3-thiazolines: T-type calcium channel inhibitory activity. , 2010, Journal of combinatorial chemistry.
[8] Steven V. Fox,et al. In Vitro Characterization of T-Type Calcium Channel Antagonist TTA-A2 and In Vivo Effects on Arousal in Mice , 2010, Journal of Pharmacology and Experimental Therapeutics.
[9] V. Jevtovic-Todorovic,et al. The role of T-type calcium channels in peripheral and central pain processing. , 2006, CNS & neurological disorders drug targets.
[10] S. Nattel,et al. Differential efficacy of L- and T-type calcium channel blockers in preventing tachycardia-induced atrial remodeling in dogs. , 2001, Cardiovascular research.
[11] D. Abernethy,et al. Pharmacologic and pharmacokinetic profile of mibefradil, a T- and L-type calcium channel antagonist. , 1997, The American journal of cardiology.
[12] E. E. van der Wall,et al. T-channel-selective calcium channel blockade: a promising therapeutic possibility, only preliminarily tested so far: a review of published data. T-Channel Calcium Channel Blocker Study Group. , 1999, American Journal of Therapeutics.
[13] Ji-Hyung Seo,et al. Antitumor activity of 3,4-dihydroquinazoline dihydrochloride in A549 xenograft nude mice. , 2010, Bioorganic & medicinal chemistry letters.
[14] Ming Li,et al. Calcium signaling and T-type calcium channels in cancer cell cycling. , 2008, World journal of gastroenterology.
[15] H. Rhim,et al. Synthesis and SAR studies of a novel series of T-type calcium channel blockers. , 2006, Bioorganic & medicinal chemistry.
[16] T. Snutch,et al. Determinants of voltage-dependent inactivation affect Mibefradil block of calcium channels , 2000, Neuropharmacology.
[17] Jungahn Kim,et al. 3D QSAR studies on 3,4-dihydroquinazolines as T-type calcium channel blocker by comparative molecular similarity indices analysis (CoMSIA). , 2010, Bioorganic & medicinal chemistry letters.
[18] M. Barton,et al. The antihyperalgesic effects of the T-type calcium channel blockers ethosuximide, trimethadione, and mibefradil. , 2005, European journal of pharmacology.
[19] Daniel L Cheney,et al. Design and SAR of selective T-type calcium channel antagonists containing a biaryl sulfonamide core. , 2008, Bioorganic & medicinal chemistry letters.
[20] Steven V. Fox,et al. Discovery of 4,4-Disubstituted Quinazolin-2-ones as T-Type Calcium Channel Antagonists. , 2010, ACS medicinal chemistry letters.
[21] Edmund M. Talley,et al. Differential Distribution of Three Members of a Gene Family Encoding Low Voltage-Activated (T-Type) Calcium Channels , 1999, The Journal of Neuroscience.
[22] J. Gomora,et al. Mibefradil potently blocks ATP-activated K(+) channels in adrenal cells. , 1999, Molecular pharmacology.
[23] P. Lory,et al. T-Type Calcium Channels Are Inhibited by Fluoxetine and Its Metabolite Norfluoxetine , 2006, Molecular Pharmacology.
[24] W. Greenlee,et al. T-type calcium channel blockers: spiro-piperidine azetidines and azetidinones-optimization, design and synthesis. , 2010, Bioorganic & medicinal chemistry letters.
[25] M. Brini,et al. Calcium signalling: a historical account, recent developments and future perspectives , 2000, Cellular and Molecular Life Sciences CMLS.
[26] Hee-Sup Shin,et al. T-type calcium channels and thalamocortical rhythms in sleep: a perspective from studies of T-type calcium channel knockout mice. , 2007, CNS & neurological disorders drug targets.
[27] M. G. Rimoli,et al. T-type channel blocking properties and antiabsence activity of two imidazo[1,2-b]pyridazine derivatives structurally related to indomethacin , 2009, Neuropharmacology.
[28] Steven V. Fox,et al. Discovery of 1,4-substituted piperidines as potent and selective inhibitors of T-type calcium channels. , 2008, Journal of medicinal chemistry.
[29] M. Doddareddy,et al. Synthesis and biological evaluation of novel T-type Ca2+ channel blockers. , 2004, Bioorganic & medicinal chemistry.
[30] H. Satoh. Role of T-type Ca2+ channel inhibitors in the pacemaker depolarization in rabbit sino-atrial nodal cells. , 1995, General pharmacology.
[31] Steven V. Fox,et al. Discovery and expanded SAR of 4,4-disubstituted quinazolin-2-ones as potent T-type calcium channel antagonists. , 2010, Bioorganic & medicinal chemistry letters.
[32] Olivier Poirot,et al. Silencing of the Cav3.2 T‐type calcium channel gene in sensory neurons demonstrates its major role in nociception , 2005, The EMBO journal.
[33] Daesoo Kim,et al. Lack of the Burst Firing of Thalamocortical Relay Neurons and Resistance to Absence Seizures in Mice Lacking α1G T-Type Ca2+ Channels , 2001, Neuron.
[34] N. Akaike,et al. Actions of Ca2+ antagonists on two types of Ca2+ channels in rat aorta smooth muscle cells in primary culture. , 1990, Circulation research.
[35] S. Doran,et al. Antagonism of T-type calcium channels inhibits high-fat diet-induced weight gain in mice. , 2009, The Journal of clinical investigation.
[36] H. Rhim,et al. Synthesis and T-type calcium channel blocking activity of novel diphenylpiperazine compounds, and evaluation of in vivo analgesic activity. , 2010, Bioorganic & medicinal chemistry.
[37] J. Uslaner,et al. T-Type Calcium Channel Antagonism Decreases Motivation for Nicotine and Blocks Nicotine- and Cue-Induced Reinstatement for a Response Previously Reinforced with Nicotine , 2010, Biological Psychiatry.
[38] K. Dyason,et al. Scorpion toxins that block T-type Ca2+ channels in spermatogenic cells inhibit the sperm acrosome reaction. , 2003, Biochemical and biophysical research communications.
[39] Gerald W. Zamponi,et al. Role of voltage-gated calcium channels in ascending pain pathways , 2009, Brain Research Reviews.
[40] Steven V. Fox,et al. Design, synthesis, and evaluation of a novel 4-aminomethyl-4-fluoropiperidine as a T-type Ca2+ channel antagonist. , 2008, Journal of medicinal chemistry.
[41] T. Smith,et al. T-type Ca2+ channels are abnormal in genetically determined cardiomyopathic hamster hearts. , 1994, Circulation research.
[42] Bong Young Chung,et al. Morpholin-2-one derivatives as novel selective T-type Ca2+ channel blockers. , 2006, Bioorganic & medicinal chemistry letters.
[43] Luping Z. Huang,et al. Selective blockade of T-type Ca2+ channels suppresses human breast cancer cell proliferation. , 2008, Cancer letters.
[44] S. D. Kimball,et al. High affinity interaction of mibefradil with voltage‐gated calcium and sodium channels , 2000, British journal of pharmacology.
[45] K. Campbell,et al. Attenuated pain responses in mice lacking CaV3.2 T‐type channels , 2007, Genes, brain, and behavior.
[46] H. Rhim,et al. 3,4-Dihydroquinazoline derivatives as novel selective T-type Ca2+ channel blockers. , 2004, Bioorganic & medicinal chemistry letters.
[47] H. Rhim,et al. Growth inhibition of human cancer cells in vitro by T-type calcium channel blockers. , 2006, Bioorganic & medicinal chemistry letters.
[48] H. Zhuang,et al. NNC 55-0396 [(1S,2S)-2-(2-(N-[(3-Benzimidazol-2-yl)propyl]-N-methylamino)ethyl)-6-fluoro-1,2,3,4-tetrahydro-1-isopropyl-2-naphtyl cyclopropanecarboxylate dihydrochloride]: A New Selective Inhibitor of T-Type Calcium Channels , 2004, Journal of Pharmacology and Experimental Therapeutics.
[49] F. Hofmann,et al. Antihypertensive Effects of the Putative T-Type Calcium Channel Antagonist Mibefradil Are Mediated by the L-Type Calcium Channel Cav1.2 , 2005, Circulation research.
[50] H. Zhuang,et al. A role of functional T-type Ca2+ channel in hepatocellular carcinoma cell proliferation. , 2009, Oncology reports.
[51] B. Nilius,et al. Inhibition by mibefradil, a novel calcium channel antagonist, of Ca2+‐ and volume‐activated Cl− channels in macrovascular endothelial cells , 1997, British journal of pharmacology.
[52] M. de Curtis,et al. Selective increase in T-type calcium conductance of reticular thalamic neurons in a rat model of absence epilepsy , 1995, The Journal of neuroscience : the official journal of the Society for Neuroscience.
[53] H. Rhim,et al. T-type Ca2+ channel blockers suppress the growth of human cancer cells. , 2008, Bioorganic & medicinal chemistry letters.
[54] Gail Mandel,et al. Nomenclature of Voltage-Gated Sodium Channels , 2000, Neuron.
[55] H. Rhim,et al. Synthesis and biological activity of 3,4-dihydroquinazolines for selective T-type Ca2+ channel blockers. , 2005, Bioorganic & medicinal chemistry letters.
[56] Steven V. Fox,et al. Positive Allosteric Interaction of Structurally Diverse T-Type Calcium Channel Antagonists , 2009, Cell Biochemistry and Biophysics.
[57] P. Dayer,et al. Drug–drug interactions of new active substances: mibefradil example , 1999, European Journal of Clinical Pharmacology.