自己紹介
自己紹介
准教授 上井幸司 Koji Uwai
1971年5月生
博士(薬学) 東北大学
TEL : 0143-46-5775
FAX:0143-46-5701
e-mail : uwai(at)mmm.muroran-it.ac.jp
居室:教育研究4号館(H棟)H212-2室
生き方: 納得したうえでやる.やるなら楽しみながら最後までやる.終わったら飲む.
趣味:軽登山、筋トレ
好物:粉物、魚、ポテチ、酒(アルコール)
学歴
1997年3月 東北大学薬学部製薬化学科卒業
1997年3月 東北大学大学院薬学研究科博士課程前期修了
2000年3月 東北大学大学院薬学研究科博士課程後期修了(博士(薬学)取得)
学位論文題目:ドクゼリ (Cicuta virosa) の中枢毒性 C17-多価不飽和アルコールの薬学的研究
職歴
2000年4月 金沢大学薬学部教務職員
2000年9月 ドイツMax-Planck研究所 分子生理学部門博士研究員
(2001年5月より Alexander von Humboldt Fellow)
2002年4月 東北薬科大学助手
2006年4月 東北薬科大学講師
2011年4月 室蘭工業大学くらし環境系領域准教授
2019年4月 室蘭工業大学しくみ解明系領域准教授
受賞歴
1)第15回生体触媒化学シンポジウム ポスター賞(2011年)
2)平成25年度日本医療薬学会 論文賞(学術論文33)
3)Outstanding Poster Award in The 5th Forum on Studies of the Environmental and Public Health Issues in the Asian Mega-cities (EPAM 2014)
4)超異分野学会北海道フォーラム2021 北海道フォーラム賞
著書
1)製剤化のサイエンス 改訂5版,第1部 製剤材料の性質,第2章 分散系,寺田勝英,高山幸三 編集,ネオメディカル,神奈川,2011,pp. 54-96
2)標準薬剤学 改訂第3版,VI 医療と薬剤学,6.医薬品の管理と供給,C 薬局製剤と病院製剤,渡辺善照,芳賀信 編集,南江堂,東京,2012,pp. 570-576
解説等
1)国立大学法人室蘭工業大学編, (分担)中野博人、上井幸司、関千草、 "新しい薬の合成 鏡像異性体を作り分ける", 室蘭工大未来をひらく技術と研究, pp.96-103, 北海道新聞社, Sapporo, Japan (2014).
2)徳樂清孝、上井幸司 “量子ドットを用いたAβ凝集阻害物質の微量ハイスループットスクリーニング法” BIO Clinica 31, 76-81 (2016). (Invited review)
3)田口 莉帆,上井 幸司,東 陽介,箕輪 貴司 ”シソ科植物由来阻害物質によるアミロイドβタンパク質凝集阻害機構の円二色性スペクトルを用いた解析” ,ナノテクノロジーPick Up企画 第9回,NanotechJapan Bulletin
(http://nanonet.mext.go.jp/magazine/?plugin=pgid&id=1367)
4)上井幸司、徳樂清孝, 北海道天然資源を利用して地域・世界を救う ~アオジソの抗認知症機能性食品としての可能性~, グリーンテクノ情報,15巻, 9-13 (2019)
5)倉賀野正弘、上井幸司、徳樂清孝,蛍光イメージング技術を用いたアミロイドβ凝集阻害物質の微量ハイスループットスクリーニングシステム, 分光研究,2020年
6)上井幸司,アルツハイマー病予防を目指した,天然由来のアミロイドβ凝集阻害物質,ファルマシア,57(2),129-133,2021年
7) 山中真也、上井幸司、徳樂清孝 , 家畜衛生用消石灰に関する研究開発~研究背景と粒状化技術~LIME,603,11 ~ 15,2021年
8)中西陽菜,上井幸司,飯森俊文,農場における植物の葉の蛍光分光測定装置,分光研究,2025年
特許
1)特願2023-054595;提出日:2023年3月30日;発明者:西下 直希,徳樂 清孝,上井 幸司,渡邉 真也,倉賀野 正弘;出願人:株式会社カネカ,国立大学法人室蘭工業大学;発明の名称:オルガノイドを用いた凝集性タンパク質に対する凝集抑制活性又は凝集促進活性を評価する方法
2)特許第7446573号,登録日:2024年3月1日
特願2021-15510,提出日:2021年9月24日;発明者:大内 一敏,松村 一雄,山中 真也,徳樂 清孝,上井 幸司,中野 誠一,中野 浩幸;出願人:東洋濾紙株式会社,株式会社コア,国立大学法人室蘭工業大学;発明の名称:呈色組成物
3)特許第6820575号、登録日:2021年1月7日
特願2020-044879、提出日:2020年3月16日
発明者:中野浩幸、中野誠一、徳楽清孝、山中真也、上井幸司
出願人:株式会社コア、国立大学法人室蘭工業大学
発明の名称:可視化剤、これを用いた消毒剤の有効性判定方法及び炭酸化の検出方法
4)PCT/JP2019/51077、提出日:2019年12月26日
発明者:徳楽清孝、上井幸司
出願人:国立大学法人室蘭工業大学
発明の名称:アミロイド形成を評価する方法、装置及びプログラム
5)特許第7166612号,登録日:2020年8月31日
特願2018-242280、提出日:2018年12月26日,発明者:徳楽清孝、上井幸司,出願人:国立大学法人室蘭工業大学,発明の名称:アミロイド形成を評価する方法、装置及びプログラム
6)特許6815003号,登録日:2020年12月24日
特願2016-176927; 提出日:2016年9月9日;発明者:阿部萬千雄、徳樂清孝、山中真也、上井幸司、中野博人;出願人:株式会社コア、国立大学法人室蘭工業大学;発明の名称:消毒剤
7)PCT/JPN2016/57141; 提出日:2016年3月8日;発明者:阿部萬千雄、徳樂清孝、山中真也、上井幸司、中野博人;出願人:株式会社阿部産業、国立大学法人室蘭工業大学;発明の名称:消毒剤
8)特許第6707251号、登録日:2020年6月10日
特願2015-249378; 提出日:2015年12月22日;発明者:徳樂清孝、上井幸司;出願人:国立大学法人室蘭工業大学;発明の名称:アミロイドβタンパク質の凝集阻害組成物
9)特許第6633831号、登録日:2019年12月20日
特願2015-047017; 提出日:2015年3月10日;発明者:阿部萬千雄、徳樂清孝、山中真也、上井幸司、中野博人;出願人:株式会社阿部産業、国立大学法人室蘭工業大学;発明の名称:消毒剤
学術論文
75) On-Site Evaluation of Constituent Content and Functionality of Perilla frutescens var. crispa Using Fluorescence Spectra
Hidemichi Sano, Satoru Kawaguchi, Toshifumi Iimori , Masahiro Kuragano , Kiyotaka Tokuraku and Koji Uwai
Molecules 2023, 28, 7199. https://doi.org/10.3390/
74) New boro amino amide organocatalysts for asymmetric cross aldol reaction of ketones with carbonyl compounds
Zubeda Begum, Chigusa Seki, Yuko Okuyama, Eunsang Kwon, Koji Uwai, Michio Tokiwa, Suguru Tokiwa, Mitsuhiro Takeshita and Hiroto Nakano,
RSC Advances, 2023, 13(2), 888-894.
73) Thiourea fused g-amino alcohol organocatalysts for asymmetric Mannich reaction of b-keto active methylene compounds with imines
Miku Nomura, Zubeda Begum, Chigusa Seki, Yuko Okuyama, Eunsang Kwon, Koji Uwai, Michio Tokiwa, Suguru Tokiwa, Mitsuhiro Takeshita and Hiroto Nakano
RSC Advances, 2023, 13(6), 3715-3722.
72)Cultivation Factors That Affect Amyloid-β Aggregation Inhibitory Activity in Perilla frutescens var. crispa
Keiya Shimamori, Tomohiko Nambu, Daiki Kawamata, Masahiro Kuragano, Naoki Nishishita, Toshifumi Iimori, Shinya Yamanaka, Koji Uwai, Kiyotaka Tokuraku
Foods 12, 486 (2023).
71) Microwave-assisted synthesis and formation mechanism of fluorescent carbon dots from starch
Hisahiko Shibata, Mina Abe, Kazuya Sato, Koji Uwai, Kiyotaka Tokuraku, Toshifumi Iimori
Carbohydrate Polymer Technologies and Applications, 3, Article number 100218 (2022).
70) Chemical analysis of amyloid β aggregation inhibitors derived from Geranium thunbergii
Kenji Kubo, Hikaru Watanabe, Hiroyuki Kumeta, Tomoyasu Aizawa, Chigusa Seki, Hiroto Nakano, Kiyotaka Tokuraku,
Koji Uwai
Bioorg. Med. Chem., 68, 116840 (2022).
69) New small gamma-turn type N-primary amino terminal tripeptide organocatalyst for solvent-free
asymmetric aldol reaction of various ketones with aldehydes
R. Thiyagarajan, Z. Begum, C. Seki, Y. Okuyama, E. Kwon, K. Uwai, M. Tokiwa, S. Tokiwa, M. Takeshita, H. Nakan
RSC Advances,11(61), 38925 - 38932 (2021).
68) Simple amino silyl ether organocatalyst for asymmetric hetero Diels–Alder reaction of isatins with enones
Parasuraman, D. Ganesan, Z. Begum, C. Seki, Y. Okuyama, E. Kwon, K. Uwai, M. Tokiwa, S. Tokiwa, M. Takeshita, Nakano,
CHIRALITY,33 (8),454- 464 (2021).
67) Farm use of calcium hydroxide as an effective barrier against pathogens
Shinji Matsuzaki, Kento Azuma, Xuguang Lin, Masahiro Kuragano, Koji Uwai, Shinya Yamanaka, Kiyotaka Tokuraku
Scientific Reports, 11, Article number 7941 (2021).
66) Simple primary β-amino alcohols as organocatalysts for the asymmetric Michael addition of β-keto esters to nitroalkenes
Zubeda Begum, Haruka Sannabe, Chigusa Seki, Yuko Okuyama, Eunsang Kwon, Koji Uwai, Michio Tokiwa, Suguru
Tokiwa, Mitsuhiro Takeshita and Hiroto Nakano,
RSC Advances. 1, 203-209 (2021).
65) Simple organocatalyst component system for asymmetric hetero Diels–Alder reaction of isatins with enones
Perumalsamy Parasuraman, Zubeda Begum, Madhu Chennapuram, Chigusa Seki, Yuko Okuyama, Eunsang Kwon, Koji
Uwai, Michio Tokiwa, Suguru Tokiwa, Mitsuhiro Takeshita and Hiroto Nakano,
RSC Advances. 10, 17486-17491 (2020).
64)Daurichromenic Acid from the Chinese Traditional Medicinal Plant Rhododendron dauricum Inhibits Sphingomyelin Synthase and Aβ Aggregation
Hadya Virupaksha Deepak, Mahadeva M. Swamy, Yuta Murai, Yoshiko Suga, Masaki Anetai, Takuro Yo, Masahiro
Kuragano, Koji Uwai, Kiyotaka Tokuraku, Kenji Monde
Molecules 25, 4077 (2020).
63)Evaluation of amyloid β42 aggregation inhibitory activity of commercial dressings by a microliter-scale high-throughput screening system using quantum-dot nanoprobes
Masahiro Kuragano, Wataru Yoshinari, Xuguang Lin, Keiya Shimamori, Koji Uwai and Kiyotaka Tokuraku
Foods 9, 825 (2020).
62)Design of calcium hydroxide–based granules for livestock sanitation
Shinya Yamanaka, Shuya Hirano, Koji Uwai, Kiyotaka Tokuraku
Case Studies in Chemical and Environmental Engineering 2, 100005 (2020).
61)Sugar Based γ-Amino Alcohol Organocatalyst for Asymmetric Michael Addition of β-Keto Esters with Nitroolefins
D. Ganesan, M. Chennapuram, Z. Begum, C. Seki, Y. Okuyama, E. Kwon, K. Uwai, M. Tokiwa, S. Tokiwa, M.Takeshita, and H. Nakano
Heterocycles,98 (11), 1536 ~ 1545 (2019)
60)2-Azanorbornane-Based Amino Alcohol Organocatalysts for Asymmetric Michael Reaction of β-Keto Esters with Nitroolefins
R. Togashi, M. Chennapuram, C. Seki, Y. Okuyama, E. Kwon, K. Uwai, M. Tokiwa, M. Takeshita, H. Nakano
Eur J. Org. Chem,2019 (24),3882 ~ 3889 (2019)
59)An automated microliter-scale high-throughput screening system (MSHTS) for real-time monitoring of protein aggregation using quantum-dot nanoprobes
Sasaki, R., Tainaka, R., Ando, Y., Hashi, Y., Virupaksha D.H., Suga, Y., Murai, Y, Anetai, M., Monde, K., Ota, K., Ito, I.,
Kikuchi, H., Oshima, Y., Endo, Y., Nakao, H., Sakono, M., Uwai, K., and Tokuraku, K.
Scientific Reports 9, Article number 2587 (2019).
57)Amino Amide Organocatalysts for Asymmetric Michael Addition of β-Keto Esters with β-Nitroolefins
Isiaka A. Owolabi, Madhu Chennapuram, Chigusa Seki, Yuko Okuyama, Eunsang Kwon, Koji Uwai, Michio Tokiwa,
Mitsuhiro Takeshita, Hiroto Nakano
Bulletin of the Chemical Society, Japan, 92, 696-701 (2019).
56)Rosmarinic acid is a novel inhibitor for Hepatitis B virus replication targeting viral epsilon RNA-polymerase interaction
Yuta Tsukamoto, Sotaro Ikeda, Koji Uwai, Riho Taguchi, Kazuaki Chayama, Takemasa Sakaguchi, Ryo Narita, Wan-Ling
Yao, Fumihiko Takeuchi, Yukie Otakaki, Koichi Watashi, Takaji Wakita, Hiroki Kato, Takashi Fujita
PLOS ONE,13 (5), e0197664 (2018).
55)New Hybrid-type Squaramide-Fused Amino Alcohol Organocatalyst for Enantioselective Domino Michael Addition/Cyclization Reaction of Oxoindolines with Cyclic 1,3-DiketonesMadhu Chennapuram,
Isiaka Alade Owolabi, Chigusa Seki, Yuko Okuyama, Eunsang Kwon, Koji Uwai, Michio Tokiwa, Mitsuhiro Takeshita, and
Hiroto Nakano
ACS OMEGA,3 (9), 11718-11726 (2018).
54)A new type of amino amide organocatalyzed enantioselective crossed aldol reaction of ketones with aromatic aldehydes Isiaka A. Owolabi, U.V.Subba Reddy, Madhu Chennapuram, Chigusa Seki, Yuko Okuyama, Eunsang Kwon, Koji Uwai, Michio Tokiwa, Mitsuhiro Takeshita, Hiroto Nakano
Tetrahedron,74 (36), 4705-4711 (2018).
53)Structure–activity relations of rosmarinic acid derivatives for the amyloid β aggregation inhibition and antioxidant properties
R. Taguchi, K. Hatayama, T. Takahashi, T. Hayashi, Y. Sato, D. Sato, K. Ohta, H. Nakano, C. Seki, Y. Endo, K. Tokuraku, K. Uwai
Eur. J. Med. Chem., 138, 1066-1075 (2017).
52) Hybrid-Type Squaramide-Fused Amino Alcohol Organocatalysts for Enantioselective Diels–Alder Reactions of 3-Hydroxy-2-Pyridones with Maleimides
Madhu Chennapuram, U. V. Subba Reddy, Chigusa Seki, Yuko Okuyama, Eunsang Kwon, Koji Uwai, Michio Tokiwa, Mitsuhiro Takeshita and Hiroto Nakano
European Journal of Organic Chemistry, 2017, 4633-4641 (2017).
51)A Diamino Alcohol Catalyzed Enantioselective Crossed Aldol Reaction of Acetaldehyde with Isatins – A Concise Total Synthesis of Antitumor Agents
U. V. Subba Reddy, Madhu Chennapuram, Kento Seki, Chigusa Seki, Bheemreddy Anusha, Eunsang Kwon, Yuko Okuyama, Koji Uwai, Michio Tokiwa, Mitsuhiro Takeshita, Hiroto Nakano
European Journal of Organic Chemistry, 2017, 3847-3885 (2017).
50)Hybrid-Type Squaramide-Fused Amino Alcohol Organocatalysts for Enantioselective Nitro-Aldol Reaction of Nitromethane with Isatins
Madhu Chennapuram, U. V. Subba Reddy, Chigusa Seki, Yuko Okuyama, Eunsang Kwon, Koji Uwai, Michio Tokiwa, Mitsuhiro Takeshita and Hiroto Nakano
European Journal of Organic Chemistry, 2017, 1638-1646 (2017).
49)T. Takahashi, U.V. S. Reddy, Y. Kohari, C. Seki, T. Furuyama, N. Kobayashi, Y. Okuyama, E. Kwon, K. Uwai, M. Tokiwa, M. Takeshita, H. Nakano
Simple primary β-amino alcohol catalyzed enantioselective Diels-Alder reaction of 3-hydroxy-2-pyridones
Tetrahedron Letters, 57 (51), 5771-5776 (2016)
48) A. Ogasawara, U.V. S. Reddy, C. Seki, Y. Okuyama, K. Uwai, M. Tokiwa, M. Takeshita, H. Nakano
2-Azanorbornane-based amine organocatalyst for enantioselective aldol reaction of isatins with ketones
Tetrahedron: Asymmetry, 27(20-21), 1062-1068 (2016)
47)J. Kimura, U. V. S. Reddy, Y. Kohari, C. Seki, Y. Mawatari, K. Uwai, Y. Okuyama, E. Kwon, M. Tokiwa, M. Takeshita, T. Iwasa and H. Nakano
Simple Primary Amino Amide Organocatalyst for Enantioselective Aldol Reactions of Isatins with Ketones
Eur. J. Org. Chem., 2016, 3748-3756 (2016)
46)M Galaqin, K Uwai, M Yuguchi, T Iwasa
Simultaneous analysis of major ingredients of Gardenia fruit by HPLC-MS/TQMS method
Mongolian J. Chem.17, 34-37(2016)
45) K. Sano, Y. Kohari, H. Nakano, C. Seki, M. Takeshita, M. Tokiwa, Y. Hirose, K. Uwai
Lipase-Catalyzed Domino Michael-Aldol Reaction of 2-Methyl-1,3-Cycloalkanedione and Methyl Vinyl Ketone for the Synthesis of Bicyclic Compounds
Synthetic Communications, 46 (1), 46-54 (2016).
44)J. Kumagai, T. Otsuki, U. V. Subba Reddy, Y. Kohari, C. Seki, K. Uwai, Y. Okuyama, E. Kwon, M. Tokiwa, M. Takeshita,
H. Nakano
Chiral primary amino alcohol organobase catalysts for the asymmetric Diels-Alder reactions of anthrones with maleimides
Tetrahedron: Asymmetry, 26 (24), 1423-1439 (2015).
43)T. Otsuki, J. Kumagai, Y. Kohari, Y. Okuyama, E. Kwon, C. Seki, K. Uwai, Y. Mawatari, N. Kobayashi, T.o Iwasa, M.
Tokiwa, M. Takeshita, A. Maeda, A. Hashimoto, K. Turuga, H. Nakano
Silyloxy Amino Alcohol Organocatalyst for Enantioselective 1,3-Dipolar Cycloaddition of Nitrones to α,β- Unsaturated Aldehydes
Eur. J. Org. Chem., 2015 (33), 7292-7300 (2015).
42) J. Kumagai, Y. Kohari, C. Seki, K. Uwai, Y. Okuyama, E. Kwon, H. Nakano
Chiral Primary Amino Amide Alcohol Organocatalyst for the Asymmetric Michael Addition of 4-Hydroxycoumarin with α,β-Unsaturated Ketones
Heterocycles, 90 (2), 1124-1134 (2015).
41) T. Ogara; T. Takahashi, H. Yasui, K. Uwai, K. Tokuraku
Evaluation of the effects of amyloid- beta aggregation from seaweed extracts by a microliter-scale high-throughput screening system with a quantum dot nanoprobe
J. Biosci. Bioeng.,120 (1), 45-50 (2015).
40)Y. Kohari, Y. Okuyama, E. Kwon, T. Furuyama, N. Kobayashi, T. Otuki, J. Kumagai, C. Seki, K. Uwai, G. Dai, T. Iwasa, H. Nakano
Enantioselective Diels-Alder Reaction of 1,2-Dihydropyridines with Aldehydes using beta-Amino Alcohol Organocatalyst
J. Org. Chem., 79 (20), 9500-9511 (2014).
39) K. Uwai, Y. Okuyama, H. Nakano,, K. Furukawa, E. Hiroshima, H. Azuma, M. Watanabe, T. Matsumoto, M. Tokiwa, M. Takeshita,
Biotransformation of organic compounds in vivo using larvae of beetles (Allomyrina dichotoma) as biocatalysts
Biocat. Agric. Biotech. 3 (4), 129-133 (2014).
38) J. Kumagai, Y. Kohari, C. Seki, K. Uwai, Y. Okuyama, E. Kwon, H. Nakano
Chiral Primary Amino Amide Alcohol Organocatalyst for the Asymmetric Michael Addition of 4-Hydroxycoumarin with α,β-Unsaturated Ketones
Heterocycles, 90 (2), 1124-1134 (2014).
37)Y. Ishigaki, H. Tanaka, H. Akama, T. Ogara, K. Uwai, K. Tokuraku
A Microliter-scale High-throughput Screening System with Quantum-dot Nanoprobes for Amyloid-β aggregation Inhibitors
PLoS ONE 8(8): e72992. doi:10.1371/journal.pone.0072992
36) K. Sano, S. Saito, Y. Kohari, H. Nakano, Y. Hirose, M. Tokiwa, M. Takeshita, K. Uwai
Development of a Novel Method for Warfarin Synthesis via Lipase-Catalyzed Stereoselective Michael Reaction
Heterocycles, 87 (6), 1269-1278 (2013)
35)N. D. M. R. Hutabarat, C. Seki, T. Shimizu, M. Hirama, Y. Kohari, H. Nakano, K. Uwai, N. Takano, E. Kwon, H. Matsuyama
Highly Enantioselective Synthesis of Isoquinuclidine by Diels-Alder Reaction of 1,2-Dihydropyridine Utilizing Chiral Bisoxazoline-Cu(II) Complex
Heterocycles, 86 (1), 203-217 (2012)
34)Y. Sakuta, Y. Kohari, N. D. M. R. Hutabarat, K. Uwai, E. Kwon, Y. Okuyama, C. Seki, H. Matsuyama, N. Takano, M. Tokiwa, M. Takeshita, H. Nakano
Chiral primary Amino Silyl Ether Organocatalyst for the Enantioselective Diels-Alder Reaction of 1,2-Dihydropyridines with Aldehydes
Heterocycles, 86 (2), 1379-1389 (2012)
33)T. Hayashi, K. Uwai, E. Sasaki, K. Sasaki, Y. Iwabuchi, H. Agatsuma, T. Suzuki
Compatibility of heparin sodium in intravenous line with nicardipine injected from a side tube via T-shape stopcock
Jpn. J. Pharm. Health Care Sci., 38 (11), 679-387 (2012):平成25年度日本医療薬学会 論文賞受賞
32)C. Seki, M. Hirama, T. Sato, S. Takeda, Y. Kohari, K. Ishigaki, M. Ohuchi, K. Yokoi, H. Nakano, K. Uwai, N. Takano, K. Umemura, H. Matsuyama
One Step Synthesis of Optically Active Diazabicyclo[3.3.0]octanones or Diazabicyclo[4.3.0]nonanones by Asymmetric Conjugate Addition of Cyclic Hydrazine
Heterocycles, 85 (5), 1045-1052 (2012)
31)C. Seki, M. Hirama, N.D.M. R. Hutabarat, J. Takada, C. Suttibut, H. Takahashi, T. Takaguchi, Y. Kohari, H. Nakano, K. Uwai, N. Takano, M. Yasui, Y. Okuyama, M. Takeshita, H. Matsuyama
Asymmetric synthesis of isoquinuclidines by DielseAlder reaction of 1,2-dihydropyridine utilizing a chiral Lewis acid catalyst
Tetrahedron, 68 (6), 1774-1781 (2012)
30)M. Hirama, C. Suttibut, N. D. M. R. Hutabarat, C. Seki, N. Sakuta, T. Tsuchiya, Y. Kohari, H. Nakano, K. Uwai, N. Takano, M. Yasui, Y. Okuyama, K. Osone, M. Takeshita, H. Matsuyama
Asymmetric Synthesis of Isoquinuclidine by Diels-Alder Reaction of 1,2-Dihydropyridine and Chiral Dienophile Utilizing a Chiral Lewis Acid
Heterocycles, 84 (1), 377-384 (2012)
29)C. Suttibut, Y. Kohari, K. Igarashi, H. Nakano, M. Hirama, C. Seki, H. Matsuyama, K. Uwai, N. Takano, Y Okuyama, K. Osone, M. Takeshita, E. Kwon
A highly enantioselective Diels–Alder reaction of 1,2-dihydropyridine using a simple β-amino alcohol organocatalyst for a practical synthetic methodology of oseltamivir intermediate
Tetrahedron Lett., 52 (37), 4745-4748 (2011)
28) 吉川真一,鈴木美,村田亮,吉田進,上井幸司,鈴木常義、竹下光弘
ロキソプロフェンナトリウム錠後発医薬品の単回投与での臨床効果
ペインクリニック,31(5), 635-640(2010).
27) S. Yoshikawa, R. Murata, S. Shida, K. Uwai, T. Suzuki, S. Katsumata, M. Takeshita
Evaluation of correlation between dissolution rates of loxoprofen tablets and their surface morphology observed by scanning electron microscope and atomic force microscope.
Chem. Pharm. Bull., 58(1), 34-37 (2010).
26)S. Masuda, R. Oka, K. Uwai, Y. Matsuda, T. Shiraishi, Y. Nakagawa, T. Shoji, C. Mihara, M. Takeshita, K. Ozawa
Development of clinical application for a nutritional prescription support system for total parenteral/enteral nutrition.
Yakugaku Zasshi, 129 (9), 1077-1086 (2009).
25) Y. Nishiuchi, H. Nakano, Y. Araki, R Sato, R. Fujita, K. Uwai, M. Takeshita
Reactivity and efficient recycling of a chiral Pd-BINAP catalyst for catalytic asymmetric Diels-Alder reaction in ionic liquid.
Heterocycles, 77(2), 1323-1331 (2009).
24)Y. Okuyama, H. Nakano, Y. Watanabe, M. Makabe, M. Takeshita, K. Uwai, C. Kabuto, E. Kwon
Organocatalitic activity of 4-hydroxy-prolinamide alchol with different noncovalent coordination sites in asymmetric Michael and direct aldol reactions.
Tetrahedron Lett., 50, 193-197 (2009).
23)H. Nakano, Y. Nishiuchi, K. Takahashi, R. Fujita, K. Uwai, M. Takeshita
Chiral cationic Pd-phosphinooxazolidine catalysts for a highly efficient asymmetric diels-alder reaction in ionic liquids.
Heterocycles, 76(1), 381-390 (2008).
22) Y. Osanai, S. Kanno, K. Uwai, M. Takeshita, M. Ishikawa
Inhibitory effect of octylcaffeate on lipopolysaccharaide-induced nitric oxide production in macrophages.
Pharmacometrics, 75 (1/2), 19-24 (2008).
21) K. Uwai, Y. Osanai, T. Imaizumi, S. Kanno, M. Takeshita, M. Ishikawa
Inhibitory effect of the alkyl side chain of caffeic acid analogues on lipopolysaccharide-induced nitric oxide production in RAW264.7 macrophages.
Bioorg. Med, Chem., 16, 7795-7803 (2008).
20)S. Kanno, T. Ohtake, Y. Osanai, K. Kurauchi, M. Ujibe, K. Uwai, M. Takeshita, S. Satoh, M. Ishikawa
Trimidox-induced apoptosis is mediated through induction of p53 in NALM-6 cells.
J. Pharmacol. Sci., 106(3), 521-524 (2008).
19)K. Uwai, N. Konno, Y. Yasuta, M. Takeshita
Electronic effects of para-substituon on acetophenones in the reaction of rat liver 3α-hydroxysteroid dehydrogenase.
Bioorg. Med. Chem., 16, 1084-1089 (2008).
18)R. Oka,K. Uwai, T. Toyoguchi, T.i Shiraishi, Y. Nakagawa, M. Takeshita
Stability of magnesium oxide products kept in single-dose packages.
Jpn. J. Pharm. Health Care Sci., 33 (12), 1013-1019 (2007).
17)S. Kanno, K. Kakuta, Y. Kitajima, Y. Osanai, K. Kurauchi, T. Ohtake, M. Ujibe, K. Uwai, M. Takeshita, M. Ishikawa
Inhibitory effect of trimidox on lipopolysaccharide-induced nitric oxide production in RAW 264.7 macrophages.
J. Pharmacol. Sci., 104(3), 278-281 (2007).
16)S. Kanno, M. Kakuta, Y. Kitajima,Y. Osanai, K. Kurauchi, T. Ohtake, M. Ujibe, K. Uwai, M. Takeshita, M. Ishikawa
Preventive effect of trimidox on oxidative stress in U937 cell line.
Biol. Pharm. Bull., 30(5), 994-998 (2007).
15) S. Kanno, K. Uwai, A. Tomizawa, T. Hiura, Y. Osanai, M. Ujibe, M. Takeshita, T. Ohtake, K. Kimura, M. Ishikawa
Trimidox induces apoptosis via cytochrome c release in NALM-6 human B cell leukemia cells.
Basic and Clinical Pharmacology and Toxicology, 98 (1), 44-50 (2006).
14) M. Ujibe, S. Kanno, Y. Osanai, K. Koiwai, T. Ohtake, K. Kimura, K. Uwai, M. Takeshita, M. Ishikawa
Octylcaffeate induced apoptosis in human leukemia U937 cells.
Biol. Pharm. Bull., 28 (12), 2338-2341 (2005).
13)K. Uwai, N. Konno, S. Kitamura, S. Ohta, M. Takeshita
Purification and characterization of rat liver enzyme catalyzing stereoselective reduction of acetylpyridines.
Chirality, 17 (8), 494-500 (2005).
12)K. Uwai, M. Tani, Y. Ohtake, S. Abe, A. Maruko, T. Chiba, Y. Hamaya, Y. Ohkubo, M. Takeshita
Photodegradation products of propranolol: the structures and pharmacological studies.
Life Sci, 78, 357-365 (2005).
11)M. Takeshita, T. Chiba, K. Uwai, K. Hisamichi, N. Sasaki, Y. Hamaya
Photostability of naftopidil.
Jpn. J. Pharm. Health Care Sci., 31. 464-469 (2005).
10)K. Uwai, H. Uchiyama, S. Sakurada, C. Kabuto, M. Takeshita
Syntheses and receptor-binding study of derivatives of the opioid antagonist naltrexone.
Bioorg. Med. Chem., 12, 417-421 (2004).
9)M. Völkert, K. Uwai, A. Tebbe, B. Popkirova, M. Wagner, J. Kuhlmann, H. Waldmann
Synthesis and biological activity of photoactivatable N-Ras-peptides and proteins.
J. Am. Chem. Soc., 125, 12749-12758 (2003).
8)K. Uwai, H. Sato, N. Kazakami, H. Matsuzaki, M. Takeshita
Synthesis and reduction of (S)-(-)-nicotine-N’-oxide and N,N’-dioxides by rat liver S-9 fraction.
Arkivoc, 8, 211-219 (2003).
7) J. Kuhlmann, A. Tebbe, M. Völkert, M. Wagner, K. Uwai, H. Waldmann
Photoactivatable synthetic Ras proteins: "baits" for the identification of plasma-membrane-bound binding partners of Ras.
Angew. Chem. Int. Ed., 41(14), 2546-2550 (2002).
6)K. Uwai, K. Ohashi, Y. Takaya, Y. Oshima, K. Furukawa, K.,Yamagata, T. Ohmura, S. Okuyama
Virol A, a toxic polyacetylenic alcohol of Cicuta virosa, inhibits the GABA-induced Cl-current in the rat hippocampal CA1 Neurons.
Brain Research, 889, 174-180 (2001).
5)K. Uwai, K. Ohashi, Y. Takaya, T. Ohta, T. Tadano, K. Kisara, K. Shibusawa, R. Sakakibara, Y. Oshima
Exploring the structural basis of neurotoxicity in C17-polyacetylenes isolated from water hemlock.
J. Med. Chem., 43, 4508-4515 (2000).
4) K. Uwai, Y. Oshima, T. Sugihara, T. Ohta
Syntheses and stereochemical assignment of toxic C17-polyacetylenic alcohols, virols A, B, and C, isolated from water hemlock (Cicuta virosa).
Tetrahedron, 55, 9469-9480 (1999).
3)T. Ohta, K. Uwai, R. Kikuchi, S. Nozoe, Y. Oshima, K. Sasaki, F. Yoshizaki
Absolute stereochemistry of cicutoxin and related toxic polyacetylenic alcohols from Cicuta virosa.
Tetrahedron, 55, 12087-12098 (1999).
2) Y. Takaya, H. Tasaka, T. Chiba, K. Uwai, M. Tanitsu, H.-S. Kim, Y. Wataya, M. Miura, M. Takeshita, Y. Oshima
New type of feburifugine analogues, bearing a quinolizine moiety, show potent antimalarial activity against Plasmodium malaria parasite.
J. Med. Chem., 42, 3163-3166(1999).
1)K. Hiroya, K. Uwai, K. Ogasawara
Enantio- and diastereocontrolled synthesis of epibatidine analogues.
Chem. Pharm. Bull., 43, 901-903 (1995).