Nalfurafine hydrochloride, a selective κ opioid receptor agonist, has no reinforcing effect on intravenous self-administration in rhesus monkeys von Nakao, Kaoru, Hirakata, Mikito, Miyamoto, Yohei, Kainoh, Mie, Wakasa, Yoshio, Yanagita, Tomoji

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A Double Decarboxylation Reaction of an Oxazolidinone and Carboxylic Acid: Its Application to the Synthesis of a New Opioid Lead Compound von Fujii, Hideaki, Imaide, Satomi, Watanabe, Akio, Yoza, Kenji, Nakajima, Mayumi, Nakao, Kaoru, Mochizuki, Hidenori, Sato, Noriko, Nemoto, Toru, Nagase, Hiroshi

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Effects of TRK-820, a selective kappa opioid receptor agonist, on rat schizophrenia models von Yoshikawa, Satoru, Hareyama, Nana, Ikeda, Ken, Kurokawa, Takahiro, Nakajima, Mayumi, Nakao, Kaoru, Mochizuki, Hidenori, Ichinose, Hiroshi

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Scratching Behavior of ICR-Derived Glomerulonephritis (ICGN) Mice von MIYAMOTO, Yohei, UMEUCHI, Hideo, KUROKAWA, Takahiro, NAKAO, Kaoru, OKANO, Kiyoshi

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Come, You Spirits: An Alternative Afterlife to Shakespeare’s Macbeth and Othello, as Mediated through Japanese Classical Nō and Kyōgen Theatre von Ingham, Michael, Nakao, Kaoru

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Design and synthesis of KNT-127, a δ-opioid receptor agonist effective by systemic administration von Nagase, Hiroshi, Nemoto, Toru, Matsubara, Ayaka, Saito, Manabu, Yamamoto, Naoshi, Osa, Yumiko, Hirayama, Shigeto, Nakajima, Mayumi, Nakao, Kaoru, Mochizuki, Hidenori, Fujii, Hideaki

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Pharmacological Effect of TRK-380, a Novel Selective Human β3 -Adrenoceptor Agonist, on Mammalian Detrusor Strips von Kanie, Sayoko, Otsuka, Atsushi, Yoshikawa, Satoru, Morimoto, Takashi, Hareyama, Nana, Okazaki, Seiji, Kobayashi, Ryosuke, Hasebe, Ko, Nakao, Kaoru, Hayashi, Ryoji, Mochizuki, Hidenori, Matsumoto, Rikiya, Ozono, Seiichiro

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TRK-820, a selective kappa opioid receptor agonist, could effectively ameliorate L-DOPA-induced dyskinesia symptoms in a rat model of Parkinson's disease von Ikeda, Ken, Yoshikawa, Satoru, Kurokawa, Takahiro, Yuzawa, Natsumi, Nakao, Kaoru, Mochizuki, Hidenori

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Involvement of central μ-opioid system in the scratching behavior in mice, and the suppression of it by the activation of κ-opioid system von Umeuchi, Hideo, Togashi, Yuko, Honda, Toshiyuki, Nakao, Kaoru, Okano, Kiyoshi, Tanaka, Toshiaki, Nagase, Hiroshi

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In vitro and in vivo pharmacological characterization of the main metabolites of nalfurafine hydrochloride von Nakao, Kaoru, Togashi, Yuko, Honda, Toshiyuki, Momen, Shinobu, Umeuchi, Hideo, Sakakibara, Shinji, Tanaka, Toshiaki, Okano, Kiyoshi, Mochizuki, Hidenori

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Drug design and synthesis of a novel κ opioid receptor agonist with an oxabicyclo[2.2.2]octane skeleton and its pharmacology von Nagase, Hiroshi, Watanabe, Akio, Nemoto, Toru, Yamaotsu, Noriyuki, Hayashida, Kohei, Nakajima, Mayumi, Hasebe, Ko, Nakao, Kaoru, Mochizuki, Hidenori, Hirono, Shuichi, Fujii, Hideaki

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Synthesis of novel triplet drugs with 1,3,5-trioxazatriquinane skeletons and their pharmacologies. Part 2: Synthesis of novel triplet drugs with the epoxymethano structure (capped... von Nagase, Hiroshi, Koyano, Koji, Wada, Naohisa, Hirayama, Shigeto, Watanabe, Akio, Nemoto, Toru, Nakajima, Mayumi, Nakao, Kaoru, Mochizuki, Hidenori, Fujii, Hideaki

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Investigation of Beckett–Casy model 2: Synthesis of novel 15–16 nornaltrexone derivatives and their pharmacology von Nagase, Hiroshi, Imaide, Satomi, Tomatsu, Miyuki, Nemoto, Toru, Nakajima, Mayumi, Nakao, Kaoru, Mochizuki, Hidenori, Fujii, Hideaki

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Investigation of Beckett–Casy model 1: Synthesis of novel 16,17- seco-naltrexone derivatives and their pharmacology von Imaide, Satomi, Fujii, Hideaki, Watanabe, Akio, Nemoto, Toru, Nakajima, Mayumi, Nakao, Kaoru, Mochizuki, Hidenori, Nagase, Hiroshi

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Synthesis of pyrrolomorphinan derivatives as κ opioid agonists von Fujii, Hideaki, Ida, Yoshihiro, Hanamura, Shinichi, Osa, Yumiko, Nemoto, Toru, Nakajima, Mayumi, Hasebe, Ko, Nakao, Kaoru, Mochizuki, Hidenori, Nagase, Hiroshi

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Investigation of Beckett–Casy model 3: Synthesis of novel naltrexone derivatives with contracted and expanded D-rings and their pharmacology von Nagase, Hiroshi, Imaide, Satomi, Tomatsu, Miyuki, Hirayama, Shigeto, Nemoto, Toru, Sato, Noriko, Nakajima, Mayumi, Nakao, Kaoru, Mochizuki, Hidenori, Gouda, Hiroaki, Hirono, Shuichi, Fujii, Hideaki

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Design and synthesis of a metabolically stable and potent antitussive agent, a novel δ opioid receptor antagonist, TRK-851 von Sakami, Satoshi, Kawai, Koji, Maeda, Masayuki, Aoki, Takumi, Fujii, Hideaki, Ohno, Hiroshi, Ito, Tsuyoshi, Saitoh, Akiyoshi, Nakao, Kaoru, Izumimoto, Naoki, Matsuura, Hirotoshi, Endo, Takashi, Ueno, Shinya, Natsume, Kazuto, Nagase, Hiroshi

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Behavioural Pharmacology: Effects of TRK-820, a selective kappa opioid receptor agonist, on rat schizophrenia models von Yoshikawa, Satoru, Hareyama, Nana, Ikeda, Ken, Kurokawa, Takahiro, Nakajima, Mayumi, Nakao, Kaoru, Mochizuki, Hidenori, Ichinose, Hiroshi

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Antiamnesic action of cromakalim, a potassium channel opener, in mice treated with hypoxia- and cerebral ischemia-type stress stimuli von Nakao, K, Tokuyama, S, Takahashi, M, Kaneto, H, Ueda, H

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Synthesis of pyrrolomorphinan derivatives as K opioid agonists von FUJII, Hideaki, IDA, Yoshihiro, HANAMURA, Shinichi, OSA, Yumiko, NEMOTO, Toru, NAKAJIMA, Mayumi, HASEBE, Ko, NAKAO, Kaoru, MOCHIZUKI, Hidenori, NAGASE, Hiroshi

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