南雲 康行
Nagumo, Yasuyuki
国立研究開発法人国立がん研究センター , がん患者病態生理研究ユニット National Cancer Center , Cancer Pathophysiology Unit
関連記事はまだありません。
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1.
Peripheral-central network analysis of cancer cachexia status accompanied by the polarization of hypothalamic microglia with low expression of inhibitory immune checkpoint receptors.
Yukari Suda; Keiko Nakamura; Fukiko Matsuyama; Yusuke Hamada (+5 著者) Minoru Narita
Molecular brain 17: 20 (2024) Semantic Scholar
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2.
Unexpected Rearrangement Reactions of the 14-Aminonaltrexone Skeleton.
Kenta Maeda; Sayaka Ohrui; Akihisa Tokuda; Yasuyuki Nagumo (+4 著者) Hiroshi Nagase
Organic letters 25: 3407 (2023) Semantic Scholar
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3.
Design and Synthesis of Orexin 1 Receptor-Selective Agonists.
Keita Iio; Kao Hashimoto; Yasuyuki Nagumo; Mao Amezawa (+13 著者) Tsuyoshi Saitoh
Journal of medicinal chemistry 66: 5453 (2023) Semantic Scholar
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4.
Elucidation of the mechanisms of exercise-induced hypoalgesia and pain prolongation due to physical stress and the restriction of movement.
Kenichi Tanaka; Naoko Kuzumaki; Yusuke Hamada; Yukari Suda (+2 著者) Minoru Narita
Neurobiology of pain (Cambridge, Mass.) 14: 100133 (2023) Semantic Scholar
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5.
Discovery of novel orexin receptor antagonists using a 1,3,5-trioxazatriquinane bearing multiple effective residues (TriMER) library.
Tsuyoshi Saitoh; Mao Amezawa; Jumpei Horiuchi; Yasuyuki Nagumo (+14 著者) Hiroshi Nagase
European journal of medicinal chemistry 240: 114505 (2022)
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6.
Discovery of orexin 2 receptor selective and dual orexin receptor agonists based on the tetralin structure: Switching of receptor selectivity by chirality on the tetralin ring.
Keita Iio; Tsuyoshi Saitoh; Ryuichiro Ohshita; Tsubasa Hino (+9 著者) Hiroshi Nagase
Bioorganic & medicinal chemistry letters 60: 128555 (2022) Semantic Scholar
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7.
Essential structure of orexin 1 receptor antagonist YNT-707: Conversion of the 16-cyclopropylmethyl group to the 16-sulfonamide group in d-nor-nalfurafine derivatives.
Koki Katoh; Noriki Kutsumura; Naoshi Yamamoto; Yasuyuki Nagumo (+5 著者) Hiroshi Nagase
Bioorganic & medicinal chemistry letters 59: 128550 (2022) Semantic Scholar
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8.
Discovery of orexin 2 receptor selective and dual orexin receptor agonists based on the tetralin structure: Switching of receptor selectivity by chirality on the tetralin ring
Keita Iio; Tsuyoshi Saitoh; Ryuichiro Ohshita; Tsubasa Hino (+9 著者) Hiroshi NagaseBIOORGANIC & MEDICINAL CHEMISTRY LETTERS 60: (2022) Semantic Scholar -
9.
Effect of removal of the 14-hydroxy group on the affinity of the 4,5-epoxymorphinan derivatives for orexin and opioid receptors.
Koki Katoh; Naoshi Yamamoto; Yukiko Ishikawa; Yoko Irukayama-Tomobe (+5 著者) Hiroshi Nagase
Bioorganic & medicinal chemistry letters 59: 128527 (2022) Semantic Scholar
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10.
Design and synthesis of novel orexin 2 receptor agonists based on naphthalene skeleton.
Tsubasa Hino; Tsuyoshi Saitoh; Yasuyuki Nagumo; Naoshi Yamamoto (+5 著者) Hiroshi Nagase
Bioorganic & medicinal chemistry letters 59: 128530 (2022)
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11.
Synthesis of unnatural morphinan compounds to induce itch-like behaviors in mice: Towards the development of MRGPRX2 selective ligands.
Keita Iio; Noriki Kutsumura; Yasuyuki Nagumo; Tsuyoshi Saitoh (+6 著者) Hiroshi Nagase
Bioorganic & medicinal chemistry letters 56: 128485 (2022) Semantic Scholar
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12.
OX2R-selective orexin agonism is sufficient to ameliorate cataplexy and sleep/wake fragmentation without inducing drug-seeking behavior in mouse model of narcolepsy.
Hikari Yamamoto; Yasuyuki Nagumo; Yukiko Ishikawa; Yoko Irukayama-Tomobe (+8 著者) Masashi Yanagisawa
PloS one 17: e0271901 (2022) Semantic Scholar
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13.
Novel Baeyer-Villiger-type oxidation of 4,5-epoxymorphinan derivatives
Tsubasa Hino; Noriki Kutsumura; Tsuyoshi Saitoh; Naoshi Yamamoto (+3 著者) Hiroshi Nagase
TETRAHEDRON LETTERS 63: (2021) Semantic Scholar
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14.
Discovery of attenuation effect of orexin 1 receptor to aversion of nalfurafine: Synthesis and evaluation of D-nor-nalfurafine derivatives and analyses of the three active conformations of nalfurafine.
Yasuyuki Nagumo; Koki Katoh; Keita Iio; Tsuyoshi Saitoh (+8 著者) Hiroshi Nagase
Bioorganic & medicinal chemistry letters 30: 127360 (2020) Semantic Scholar
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15.
Discovery of attenuation effect of orexin 1 receptor to aversion of nalfurafine: Synthesis and evaluation of D-nor-nalfurafine derivatives and analyses of the three active conformations of nalfurafine (in press)
Yasuyuki Nagumo; Koki Katoh; Keita Iio; Tsuyoshi Saitoh (+8 著者) Hiroshi Nagase
(2020)
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16.
Tonic GABAergic Inhibition Is Essential for Nerve Injury-Induced Afferent Remodeling in the Somatosensory Thalamus and Ectopic Sensations
Yasuyuki Nagumo; Yoshifumi Ueta; Hisako Nakayama; Hironobu Osaki (+3 著者) Mariko Miyata
Cell Reports 31: 107797 (2020) Semantic Scholar
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17.
Structure-Activity Relationship between Thiol Group-Trapping Ability of Morphinan Compounds with a Michael Acceptor and Anti-Plasmodium falciparum Activities
Noriki Kutsumura; Yasuaki Koyama; Tsuyoshi Saitoh; Naoshi Yamamoto (+7 著者) Hiroshi Nagase
Molecules (2020) Semantic Scholar
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18.
Essential structure of orexin 1 receptor antagonist YNT-707, part V: Structure-activity relationship study of the substituents on the 17-amino group.
Tsuyoshi Saitoh; Kazunori Seki; Ryo Nakajima; Naoshi Yamamoto (+6 著者) Hiroshi Nagase
Bioorganic & medicinal chemistry letters 30: 126893 (2020) Semantic Scholar
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19.
Essential structure of orexin 1 receptor antagonist YNT-707, Part IV: The role of D-ring in 4,5-epoxymorphinan on the orexin 1 receptor antagonistic activity.
Saitoh T; Seki K; Nakajima R; Yamamoto N (+7 著者) Nagase H
Bioorganic & medicinal chemistry letters 29: 2655 (2019) Semantic Scholar
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20.
Essential structure of orexin 1 receptor antagonist YNT-707, Part IV: The role of D-ring in 4,5-epoxymorphinan on the orexin 1 receptor antagonistic activity
Saitoh, Tsuyoshi; Seki, Kazunori; Nakajima, Ryo; Yamamoto, Naoshi (+7 著者) Nagase, Hiroshi
Bioorganic & medicinal chemistry letters 29: 2655 (2019) Semantic Scholar
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1.
トワイクロス先生のがん緩和ケア処方薬 : 薬効・薬理と薬の使い方
監訳; 武田文和; 鈴木 勉; 共著パート翻訳; 南雲康行
(担当:分担執筆, 範囲:抗てんかん薬)
医学書院 2013年 (ISBN: 9784260015219)
講演・口頭発表情報はまだありません。
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1. 特願2016-155477: <産業財産権・特許>特願 2016-155477,モルヒナン誘導体及びその医薬用途
長瀬博; 山本直司; 入鹿山容子; 斎藤毅; 柳沢正史; 南雲康行
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