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Izumi Kamo

Takeda Pharmaceutical Company

25

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351

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Increasing effects of selective 5-HT2C receptor stimulation on evoked momentary urethral closure in female rats and humans.

2021 Journal of Pharmacology and Experimental Therapeutics
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Discovery of 5-Chloro-1-(5-chloro-2-(methylsulfonyl)benzyl)-2-imino-1,2-dihydropyridine-3-carboxamide (TAK-259) as a Novel, Selective, and Orally Active α1D Adrenoceptor Antagonist with Antiurinary Frequency Effects: Reducing Human Ether-a-go-go-Related Gene (hERG) Liabilities

2016 Journal of Medicinal Chemistry
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Corrigendum to “Design, structure–activity relationship, and highly efficient asymmetric synthesis of 3-phenyl-4-benzylaminopiperidine derivatives as novel neurokinin-1 receptor antagonists” [Bioorg. Med. Chem. 19 (2011) 6430–6446]

2014 Bioorganic & Medicinal Chemistry
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Novel 3-phenylpiperidine-4-carboxamides as highly potent and orally long-acting neurokinin-1 receptor antagonists with reduced CYP3A induction.

2012 Bioorganic & Medicinal Chemistry
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Design, structure–activity relationship, and highly efficient asymmetric synthesis of 3-phenyl-4-benzylaminopiperidine derivatives as novel neurokinin-1 receptor antagonists

2011 Bioorganic & Medicinal Chemistry
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Increased urethral resistance by periurethral injection of low serum cultured adipose-derived mesenchymal stromal cells in rats

2011 International Journal of Urology
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Kondensiertes Pyridinderivat und seine Verwendung

2008
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Composé hétérocyclique condensé et son utilisation

2007
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Méthode de dépistage in-vivo

2007
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Effect of TAK-637, a Tachykinin NK1-Receptor Antagonist, on Lower Urinary Tract Function in Cats

2001 Japanese Journal of Pharmacology
- Izumi Kamo
- Takayuki Doi
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Citations (8)