Search Results - "Ima, Masaki"
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Discovery of Gemilukast (ONO-6950), a Dual CysLT1 and CysLT2 Antagonist As a Therapeutic Agent for Asthma
Published in Journal of medicinal chemistry (13-08-2015)“…An orally active dual CysLT1 and CysLT2 antagonist possessing a distinctive structure which consists of triple bond and dicarboxylic acid moieties is…”
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Discovery of Highly Potent Dual CysLT1 and CysLT2 Antagonist
Published in ACS medicinal chemistry letters (13-11-2014)“…The benzoxazine derivative, (2S)-4-(3-carboxypropyl)-8-{[4-(4-phenylbutoxy)benzoyl]amino}-3,4-dihydro-2H-1,4-benzoxazine-2-carboxylic acid (19, ONO-2050297),…”
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Discovery of a potent, orally available dual CysLT1 and CysLT2 antagonist with dicarboxylic acid
Published in Bioorganic & medicinal chemistry (01-05-2015)“…[Display omitted] A potent, orally available dual CysLT1 and CysLT2 receptor antagonist with a dicarboxylic acid is described…”
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Discovery of Gemilukast (ONO-6950), a Dual CysLT 1 and CysLT 2 Antagonist As a Therapeutic Agent for Asthma
Published in Journal of medicinal chemistry (13-08-2015)Get full text
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5
Discovery of Highly Potent Dual CysLT 1 and CysLT 2 Antagonist
Published in ACS medicinal chemistry letters (13-11-2014)Get full text
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Further optimization of sulfonamide analogs as EP1 receptor antagonists: Synthesis and evaluation of bioisosteres for the carboxylic acid group
Published in Bioorganic & medicinal chemistry (01-11-2006)“…Further optimization of 1 as EP1 antagonist afforded 2b, 8, and 16. 4-{[2-[(2-Furylsulfonyl)(isobutyl)amino]-5-(trifluoromethyl)phenoxy]methyl}benzoic acid…”
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Optimization of sulfonamide derivatives as highly selective EP1 receptor antagonists
Published in Bioorganic & medicinal chemistry (01-12-2006)“…Sulfonamide derivatives 13 and 15–17 were found to be highly potent and selective EP1 receptor antagonists. In vivo EP1 antagonist activity was also…”
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Discovery of heteroaryl sulfonamides as new EP1 receptor selective antagonists
Published in Bioorganic & medicinal chemistry (01-10-2006)“…Heteroaryl sulfonamide derivatives 2–4 were identified as more potent and less lipophilic EP1 receptor antagonists than 1…”
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Enantioselective Synthesis of Lythraceae Alkaloid Lasubine II via Optically Active 2-Isoxazoline
Published in Heterocycles (01-02-2000)Get full text
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