Search Results - "Ohmi, Takashi"

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    Contribution of Active and Inactive States of the Human 5-HT4d Receptor to the Functional Activities of 5-HT4–Receptor Agonists by Mikami, Tadayoshi, Sugimoto, Hiromi, Naganeo, Rie, Ohmi, Takashi, Saito, Toshiyuki, Eda, Hiroyuki

    “…In the present study, binding affinities of 5-hydroxytryptamine-4 (5-HT4) ligands for the human 5-HT4d receptor were determined using the agonist [3H]5-HT and…”
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    Journal Article
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    Synthesis of benzamide derivatives as TRPV1 antagonists by Shishido, Yuji, Jinno, Madoka, Ikeda, Takafumi, Ito, Fumitaka, Sudo, Masaki, Makita, Naoya, Ohta, Atsuko, Iki-Taki, Ayako, Ohmi, Takashi, Kanai, Yoshihito, Tamura, Tetsuya, Shimojo, Masato

    Published in Bioorganic & medicinal chemistry (01-02-2008)
    “…From hit compounds identified by high throughput screening (HTS), we have found compound 1 as a lead TRPV1 antagonist and confirmed its potential as a…”
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    Journal Article
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    In vitro and in vivo pharmacological characterization of PF-01354082, a novel partial agonist selective for the 5-HT 4 receptor by Mikami, Tadayoshi, Komada, Tohru, Sugimoto, Hiromi, Suzuki, Keiko, Ohmi, Takashi, Kimura, Naoji, Naganeo, Rie, Nakata, Eriko, Nakatani, Keigo, Toga, Tetsuo, Eda, Hiroyuki, Sakakibara, Minoru

    Published in European journal of pharmacology (2009)
    “…The pharmacological profile of PF-01354082, a selective 5-HT 4 receptor partial agonist, was investigated. PF-01354082 displayed high affinity for human 5-HT…”
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    Journal Article
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    In vitro and in vivo pharmacological characterization of PF-01354082, a novel partial agonist selective for the 5-HT(4) receptor by Mikami, Tadayoshi, Komada, Tohru, Sugimoto, Hiromi, Suzuki, Keiko, Ohmi, Takashi, Kimura, Naoji, Naganeo, Rie, Nakata, Eriko, Nakatani, Keigo, Toga, Tetsuo, Eda, Hiroyuki, Sakakibara, Minoru

    Published in European journal of pharmacology (01-05-2009)
    “…The pharmacological profile of PF-01354082, a selective 5-HT(4) receptor partial agonist, was investigated. PF-01354082 displayed high affinity for human…”
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    Journal Article
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