A Novel Potent and Selective Histamine H3 Receptor Antagonist Enerisant: In Vitro Profiles, In Vivo Receptor Occupancy, and Wake-Promoting and Procognitive Effects in Rodents von Hino, Noriko, Marumo, Toshiyuki, Kotani, Makiko, Shimazaki, Toshiharu, Kaku-Fukumoto, Ayaka, Hikichi, Hirohiko, Karasawa, Jun-ichi, Tomishima, Yasumitsu, Komiyama, Hiroko, Tatsuda, Emi, Nozawa, Dai, Nakamura, Toshio, Chaki, Shigeyuki

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Antipsychotic profiles of TASP0443294, a novel and orally active positive allosteric modulator of metabotropic glutamate 2 receptor von Hikichi, Hirohiko, Hiyoshi, Tetsuaki, Marumo, Toshiyuki, Tomishima, Yasumitsu, Kaku, Ayaka, Iida, Izumi, Urabe, Hiroki, Tamita, Tomoko, Yasuhara, Akito, Karasawa, Jun-ichi, Chaki, Shigeyuki

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HET0016, a potent and selective inhibitor of 20‐HETE synthesizing enzyme von Miyata, Noriyuki, Taniguchi, Kazuo, Seki, Takayuki, Ishimoto, Tsuyoshi, Sato‐Watanabe, Mariko, Yasuda, Yoshiko, Doi, Mariko, Kametani, Shunichi, Tomishima, Yasumitsu, Ueki, Tomokazu, Sato, Masakazu, Kameo, Kazuya

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A Novel Potent and Selective Histamine H 3 Receptor Antagonist Enerisant: In Vitro Profiles, In Vivo Receptor Occupancy, and Wake-Promoting and Procognitive Effects in Rodents von Hino, Noriko, Marumo, Toshiyuki, Kotani, Makiko, Shimazaki, Toshiharu, Kaku-Fukumoto, Ayaka, Hikichi, Hirohiko, Karasawa, Jun-Ichi, Tomishima, Yasumitsu, Komiyama, Hiroko, Tatsuda, Emi, Nozawa, Dai, Nakamura, Toshio, Chaki, Shigeyuki

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Xantholipin, a novel inhibitor of HSP47 gene expression produced by Streptomyces sp von Terui, Yuichi, Yiwen, Chu, Jun-ying, Li, Ando, Tsutomu, Yamamoto, Haruaki, Kawamura, Yoji, Tomishima, Yasumitsu, Uchida, Saeko, Okazaki, Tadayasu, Munetomo, Eiji, Seki, Takayuki, Yamamoto, Koji, Murakami, Shigeru, Kawashima, Akira

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Neurophysiologic and Antipsychotic Profiles of TASP0433864, a Novel Positive Allosteric Modulator of Metabotropic Glutamate 2 Receptor von Hiyoshi, Tetsuaki, Marumo, Toshiyuki, Hikichi, Hirohiko, Tomishima, Yasumitsu, Urabe, Hiroki, Tamita, Tomoko, Iida, Izumi, Yasuhara, Akito, Karasawa, Jun-ichi, Chaki, Shigeyuki

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N -Alkylidenearylcarboxamides as new potent and selective CB2 cannabinoid receptor agonists with good oral bioavailability von OHTA, Hiroshi, ISHIZAKA, Tomoko, TATSUZUKI, Makoto, YOSHINAGA, Mitsukane, IIDA, Izumi, TOMISHIMA, Yasumitsu, TODA, Yoshihisa, SAITO, Shuji

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Imine derivatives as new potent and selective CB2 cannabinoid receptor agonists with an analgesic action von OHTA, Hiroshi, ISHIZAKA, Tomoko, TATSUZUKI, Makoto, YOSHINAGA, Mitsukane, IIDA, Izumi, YAMAGUCHI, Tomomi, TOMISHIMA, Yasumitsu, FUTAKI, Nobuko, TODA, Yoshihisa, SAITO, Shuji

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Sulfonamide derivatives as new potent and selective CB2 cannabinoid receptor agonists von OHTA, Hiroshi, ISHIZAKA, Tomoko, YOSHINAGA, Mitsukane, MORITA, Aki, TOMISHIMA, Yasumitsu, TODA, Yoshihisa, SAITO, Shuji

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N-Alkylidenearylcarboxamides as new potent and selective CB sub(2) cannabinoid receptor agonists with good oral bioavailability von Ohta, Hiroshi, Ishizaka, Tomoko, Tatsuzuki, Makoto, Yoshinaga, Mitsukane, Izumi IIda, Tomishima, Yasumitsu, Toda, Yoshihisa, Saito, Shuji

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N-Alkylidenearylcarboxamides as new potent and selective CB(2) cannabinoid receptor agonists with good oral bioavailability von Ohta, Hiroshi, Ishizaka, Tomoko, Tatsuzuki, Makoto, Yoshinaga, Mitsukane, Iida, Izumi, Tomishima, Yasumitsu, Toda, Yoshihisa, Saito, Shuji

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Imine derivatives as new potent and selective CB 2 cannabinoid receptor agonists with an analgesic action von Ohta, Hiroshi, Ishizaka, Tomoko, Tatsuzuki, Makoto, Yoshinaga, Mitsukane, Iida, Izumi, Yamaguchi, Tomomi, Tomishima, Yasumitsu, Futaki, Nobuko, Toda, Yoshihisa, Saito, Shuji

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Sulfonamide derivatives as new potent and selective CB 2 cannabinoid receptor agonists von Ohta, Hiroshi, Ishizaka, Tomoko, Yoshinaga, Mitsukane, Morita, Aki, Tomishima, Yasumitsu, Toda, Yoshihisa, Saito, Shuji

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N-Alkylidenearylcarboxamides as new potent and selective CB 2 cannabinoid receptor agonists with good oral bioavailability von Ohta, Hiroshi, Ishizaka, Tomoko, Tatsuzuki, Makoto, Yoshinaga, Mitsukane, Iida, Izumi, Tomishima, Yasumitsu, Toda, Yoshihisa, Saito, Shuji

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Biological evaluation of sphingomyelin analogues as inhibitors of sphingomyelinase von TAGUCHI, Minoru, GODA, Ken-Ichi, KOBORI, Takeo, SUGIMOTO, Kikuo, AKAMA, Tomoko, YAMAMOTO, Kyoko, SUZUKI, Taizo, TOMISHIMA, Yasumitsu, NISHIGUCHI, Mariko, ARAI, Koshi, TAKAHASHI, Kenzo

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Design and synthesis of 1-(4-benzoylphenyl)imidazole derivatives as new potent 20-HETE synthase inhibitors von NAKAMURA, Toshio, ISHII, Takaaki, MIYATA, Noriyuki, TANIGUCHI, Kazuo, TOMISHIMA, Yasumitsu, UEKI, Tomokazu, SATO, Masakazu

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Sphingomyelin analogues as inhibitors of sphingomyelinase von Taguchi, Minoru, Sugimoto, Kikuo, Goda, Ken-ichi, Akama, Tomoko, Yamamoto, Kyoko, Suzuki, Taizo, Tomishima, Yasumitsu, Nishiguchi, Mariko, Arai, Koshi, Takahashi, Kenzo, Kobori, Takeo

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ChemInform Abstract: N‐Alkylidenearylcarboxamides as New Potent and Selective CB 2 Cannabinoid Receptor Agonists with Good Oral Bioavailability von Ohta, Hiroshi, Ishizaka, Tomoko, Tatsuzuki, Makoto, Yoshinaga, Mitsukane, Iida, Izumi, Tomishima, Yasumitsu, Toda, Yoshihisa, Saito, Shuji

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ChemInform Abstract: N-Alkylidenearylcarboxamides as New Potent and Selective CB2 Cannabinoid Receptor Agonists with Good Oral Bioavailability von Ohta, Hiroshi, Ishizaka, Tomoko, Tatsuzuki, Makoto, Yoshinaga, Mitsukane, Iida, Izumi, Tomishima, Yasumitsu, Toda, Yoshihisa, Saito, Shuji

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Design and Synthesis of 1-(4-Benzoylphenyl)imidazole Derivatives as New Potent 20-HETE Synthase Inhibitors von Nakamura, Toshio, Ishii, Takaaki, Miyata, Noriyuki, Taniguchi, Kazuo, Tomishima, Yasumitsu, Ueki, Tomokazu, Sato, Masakazu

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