نتایج جستجو برای: propoxy

تعداد نتایج: 252  

2008
Guo-Zhi Zhang Mei Zhao Xiao-Ling Zhang Jian-Ping Ma Dian-Shun Guo

Mol-ecules of the title compound, C(40)H(44)O(8), adopt a partial cone conformation. The dihedral angles between the planes of the aromatic rings and the mean plane through the methyl-ene C atoms bridging the aromatic rings are 35.74 (7), 85.86 (5), 87.77 (4) and 89.95 (5)°. Two opposite aryl rings are approximately parallel to each other; the others are at an inter-planar angle of 52.41 (6)°. ...

Journal: :The Journal of pharmacology and experimental therapeutics 2007
Huiling Liu Jerry M Farley

Airway submucosal gland cell (SMGC) secretions are under the control of various neurotransmitters and hormones. Interactions between different pathways, such as those mediated by cAMP and Ca(2+), in controlling mucus or electrolyte secretions are not well understood. Prostaglandin E(2) (PGE(2)) or forskolin has been shown to enhance acetylcholine (ACh)-induced short circuit current (I(SC)) in S...

Journal: :Acta Crystallographica Section E Structure Reports Online 2009

Journal: :Drug metabolism and disposition: the biological fate of chemicals 2007
Felix Waldmeier Ulrike Glaenzel Bernard Wirz Lukas Oberer Dietmar Schmid Michael Seiberling Jessica Valencia Gilles-Jacques Riviere Peter End Sujata Vaidyanathan

Aliskiren (2(S),4(S),5(S),7(S)-N-(2-carbamoyl-2-methylpropyl)-5-amino-4-hydroxy-2,7-diisopropyl-8-[4-methoxy-3-(3-methoxypropoxy)phenyl]-octanamid hemifumarate) is the first in a new class of orally active, nonpeptide direct renin inhibitors developed for the treatment of hypertension. The absorption, distribution, metabolism, and excretion of [(14)C]aliskiren were investigated in four healthy ...

Journal: :The Journal of pharmacology and experimental therapeutics 2005
Gerard B Fox Timothy A Esbenshade Jia Bao Pan Richard J Radek Kathleen M Krueger Betty B Yao Kaitlin E Browman Michael J Buckley Michael E Ballard Victoria A Komater Holly Miner Min Zhang Ramin Faghih Lynne E Rueter R Scott Bitner Karla U Drescher Jill Wetter Kennan Marsh Martine Lemaire Roger D Porsolt Youssef L Bennani James P Sullivan Marlon D Cowart Michael W Decker Arthur A Hancock

Acute pharmacological blockade of central histamine H3 receptors (H3Rs) enhances arousal/attention in rodents. However, there is little information available for other behavioral domains or for repeated administration using selective compounds. ABT-239 [4-(2-{2-[(2R)-2-methylpyrrolidinyl]ethyl}-benzofuran-5-yl)benzonitrile] exemplifies such a selective, nonimidazole H3R antagonist with high aff...

Journal: :The Journal of pharmacology and experimental therapeutics 2016
Kazumi Koga Mitsukane Yoshinaga Yoshikatsu Uematsu Yuji Nagai Naoki Miyakoshi Yoko Shimoda Masayuki Fujinaga Takafumi Minamimoto Ming-Rong Zhang Makoto Higuchi Norikazu Ohtake Tetsuya Suhara Shigeyuki Chaki

A novel pyridopyrimidin-4-one derivative, N-tert-butyl-2-[2-(3-methoxyphenyl)-6-[3-(morpholin-4-yl)propoxy]-4-oxopyrido[2,3-d]pyrimidin-3(4H)-yl]acetamide (TASP0434299), was characterized as a radioligand candidate for arginine vasopressin 1B (V1B) receptor. TASP0434299 exhibited high binding affinities for human and rat V1B receptors with IC50 values of 0.526 and 0.641 nM, respectively, and po...

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