山下　泰信

2008-2012　　慶應義塾大学　薬学部　薬科学科　学士　（薬科学）
2012-2014　　慶應義塾大学大学院　薬学研究科　修士　（薬科学）
2014-2017　　慶應義塾大学大学院　薬学研究科　博士　（薬科学）

2015.04-2017.03　　日本学術振興会特別研究員(DC2)
2017.04-2017.07　　次世代天然物化学技術研究組合
2017.08-2018.03　　ドイツ・Bielefeld大学特別研究員(ONE FLOW PROJECT)
2018.03-2019.12　　ドイツ・Bielefeld大学特別研究員 (フンボルト財団)
2020.01-                  大阪大学産業科学研究所助教
2022.04 –                 理化学研究所客員研究員

1. Cancer-Cell-Selective Targeting by Arylcyclopropylamine-Vorinostat Conjugates
   Yosuke Ota, Yukihiro Itoh, Takashi Kurohara, Ritesh Singh, Elghareeb E. Elboray, Chenliang Hu, Farzad Zamani, Anirban Mukherjee, Yuri Takada, Yasunobu Yamashita, Mie Morita, Mano Horinaka, Yoshihiro Sowa, Mitsuharu Masuda, Toshiyuki Sakai, Takayoshi Suzuki.
   ACS Med. Chem. Lett. 2022, 13, 1568–1573.
2. Medicinal Chemistry Research on Targeting Epigenetic Complexes
   Yuri Takada, Yasunobu Yamashita, Yukihiro Itoh, Takayoshi Suzuki 
   J. Synth. Org. Chem. Jpn. 2022, 80, 664-675.
3. Selective degradation of histone deacetylase 8 mediated by a proteolysis targeting chimera (PROTAC)
   Jiranan Chotitumnavee, Yasunobu Yamashita, Yukari Takahashi, Yuri Takada, Tetsuya Iida, Makoto Oba, Yukihiro Itoh, Takayoshi Suzuki
   Chem. Commun. 2022, 58, 4635-4638. 
4. Identification of novel histone deacetylase 6-selective inhibitors bearing 3,3,3-trifluorolactic amide (TFLAM) motif as a zinc binding group.
   Takashi Kurohara, Keita Tanaka, Daisuke Takahashi, Satoshi Ueda, Yasunobu Yamashita, Yuri Takada, Hirokazu Takeshima, Shengwang Yu, Yukihiro Itoh, Koji Hase, Takayoshi Suzuki 
   ChemBioChem 2021, 22, 3158-3163.
5. Identification of Potent and Selective Inhibitors of Fat Mass Obesity Associated Protein Using a Fragment-Merging Approach.
   Muthuraj Prakash, Yukihiro Itoh, Yoshie Fujiwara,Yukari Takahashi, Yuri Takada, Paolo Mellini, Elghareeb E. Elboray, Mitsuhiro Terao, Yasunobu Yamashita, Chika Yamamoto, Takao Yamaguchi, Masayuki Kotoku, Yuki Kitao, Ritesh Singh, Rohini Roy, Satoshi Obika, Makoto Oba, Dan Ohtan Wang, and Takayoshi Suzuki
   J. Med. Chem. 2021, 64, 15810–15824.
6. Design, Synthesis, and Biological Evaluation of Lysine Demethylase 5C Degraders.
   Tetsuya Iida, Yukihiro Itoh, Yukari Takahashi, Yasunobu Yamashita,　Takashi Kurohara,　Yuka Miyake, Makoto Oba, Takayoshi Suzuki.
   ChemMedChem 2021, 16, in press.
7. Learning about enzyme stability against organic co-solvents from structural insight by ion mobility mass spectrometry.
   Jens Sproß, Yasunobu Yamashita, Harald Gröger
   ChemBioChem, 2020, 21, 1968-1971.
8. Metalloprotein-catalyzed click reaction for In situ generation of a potent inhibitor.
   Yuka Miyake, Yukihiro Itoh, Yoshinori Suzuma, Hidehiko Kodama, Takashi Kurohara, Yasunobu Yamashita, Remy Narozny, Yutaro Hanatani, Shusaku Uchida, Takayoshi Suzuki
   ACS Catal., 2020, 10, 5383-5392.
9. Chemical modification-mediated optimization of bronchodilatory activity of mepenzolate, a muscarinic receptor antagonist with anti-inflammatory activity.
   Yasunobu Yamashita, Ken-Ichiro Tanaka, Naoki Yamakawa, Teita Asano, Yuki Kanda, Ayaka Takafuji, Masahiro Kawahara, Mitsuko Takenaga, Yoshifumi Fukunishi, Tohru Mizushima
   Bioorg. Med. Chem., 2019, 27, 3339-3346.
10. An asymmetric organocatalytic aldol reaction of a hydrophobic aldehyde in aqueous medium running in flow mode
    Lukas Schober, Shahilan Ratnam, Yasunobu Yamashita, Niklas Adebar, Matthias Pieper, Albrecht Berkessel, Volker Hessel, Harald Gröger
    Synthesis, 2019, 51, 1178-1184.
11. Identification of mepenzolate derivatives with long-acting bronchodilatory activity.
    Ken-Ichiro Tanaka, Naoki Yamakawa Yasunobu Yamashita, Teita Asano, Yuki Kanda, Ayaka Takafuji, Masahiro Kawahara, Mitsuko Takenaga, Yoshifumi Fukunishi, Tohru Mizushima
    Frontiers in Pharmacology, 2018, 9, 344.
12. Prediction of protein-compound binding energies from known activity data: docking-score-based method and its applications
    Yoshifumi Fukunishi, Yasunobu Yamashita, Tadaaki Mashimo, Haruki Nakamura
    Mol. Inf., 2018, 37, 1700120.
13. Short-step syntheses of naturally occurring polyoxygenated aromatics based on site-selective
    Yasunobu Yamashita, Alan Biard, Kengo Hanaya, Mitsuru Shoji, Takeshi Sugai
    Biosci. Biotechnol. Biochem., 2017, 81, 1279-1284.
14. Preparation of (R)-3-hydroxy-N-methylpiperidine, a synthetic key intermediate of (R)-mepenzolate, based on the lipase-catalyzed resolution of the racemic form.
    Yasunobu Yamashita, Kengo Hanaya, Mitsuru Shoji, Takeshi Sugai
    Heterocycles, 2017, 95, 370-379.
15. Simple synthesis of sakuranetin and selinone via common intermediate, utilizing complementary regioselectivity in the deacetylation of naringenin triacetate.
    Yasunobu Yamashita, Kengo Hanaya, Mitsuru Shoji, Takeshi Sugai
    Chem. Pharm. Bull., 2016, 64, 961-965.
16. Ex situ enantioconvergent approaches for effective use of undesired isomers: stereochemical convergence of substrates with multiple chiral centers and recycling of decarboxylated byproduct.
    Yasunobu Yamashita, Tohru Kurihara, Takanobu Horiguchi, Atsushi Miki, Mitsuru Shoji, Takeshi Sugai, Kengo Hanaya
    Synthesis, 2016, 48, 2191-2200.
17. Recent advances for synthesis of scyphostatin and utilization of oxabicyclo[2.2.1]heptane toward ethyl shikimate.
    Kazuaki Kuwata, Yasunobu Yamashita, Kengo Hanaya, Takeshi Sugai, Tohru Mizushima, Mitsuru Shoji
    Studies in Natural Products Chemistry, 2016, 47, 387.
18. Superiority of pulmonary administration of mepenzolate bromide over other routes as treatment for chronic obstructive pulmonary disease.
    Ken-Ichiro Tanaka, Shota Kurotsu, Teita Asano, Naoki Yamakawa, Daisuke Kobayashi, Yasunobu Yamashita, Hiroshi Yamazaki, Tomoaki Ishihara, Hiroshi Watanabe, Toru Maruyama, Hidekazu Suzuki, Tohru Mizushima
    Scientific Report, 2014, 4, 1.
19. Synthesis and biological comparison of enantiomers of mepenzolate bromide, a muscarinic receptor antagonist with bronchodilatory and anti-inflammatory activity.
    Yasunobu Yamashita, Ken-Ichiro Tanaka, Teita Asano, Naoki Yamakawa, Daisuke Kobayashi, Tomoaki Ishihara, Kengo Hanaya, Mitsuru Shoji, Takeshi Sugai, Mitsuhito Wada, Tadaaki Mashimo, Yoshifumi Fukunishi, Tohru Mizushima
    Bioorg. Med. Chem., 2014, 22, 3488-3497.
20. Structure-activity relationship of celecoxib and rofecoxib for the membrane permeabilizing activity.
    Naoki Yamakawa, Koichiro Suzuki, Yasunobu Yamashita, Takashi Katsu, Kengo Hanaya, Mitsuru Shoji, Takeshi Sugai, Tohru Mizushima
    Bioorg. Med. Chem., 2014, 22, 2529.
21. Mepenzolate bromide displays beneficial effects in a mouse model of chronic obstructive pulmonary disease.
    Ken-Ichiro Tanaka, Tomoaki Ishihara, Toshifumi Sugizaki, Daisuke Kobayashi, Yasunobu Yamashita, Kayoko Tahara, Naoki Yamakawa, Kumiko Iijima, Kaoru Mogushi, Hiroshi Tanaka, Keizo Sato, Hidekazu Suzuki, Tohru Mizushima
    Nat. Commun., 2013, 4, 2686.
22. Prostaglandin E₁-encapsulated nanoparticles improve walking activity in an experimental rat model of intermittent claudication.
    Tomoaki Ishihara, Yasunobu Yamashita, Naoko Takasaki, Shuhei Yamamoto, Erika Hayashi, Kayoko Tahara, Mitsuko Takenaga, Naoki Yamakawa, Tsutomu Ishihara, Tadashi Kasahara, Tohru Mizushima
    J. Pharm. Pharmacol., 2013, 65, 1187.
23. Chemo-enzymatic enantioconvergent approach toward ethyl shikimate from ethyl 5-hydroxy-3,4-isopropylidenedioxycyclohex-1-enecarboxylate.
    Yasunobu Yamashita, Kengo Hanaya, Takeshi Sugai, Tohru Mizushima, Mitsuru Shoji
    Tetrahedron, 2013, 69, 6527-6532.

1. “Recent progress on small molecules targeting epigenetic complexes” Yukihiro Itoh, Yuri Takada, Yasunobu Yamashita Takayoshi Suzuki. Curr. Opin. Chem. Biol. 2022, 67, 102130.
2. Yasunobu Yamashita, Harald Gröger, in Science of Synthesis: Dual Catalysis in Organic Synthesis (Hrsg.: G. A. Molander), Vol. 2, Thieme, Stuttgart, 2019, chapter 2.5, p. 339-364.

1. Tohru Mizushima, Yasunobu Yamashita, Naoki Yamakawa
   Quinuclidine Derivative.
   PCT Int. Appl. (2016) No. WO2016140136.
2. 細貝 知直、山下 泰信、室屋 裕佐、鈴木 孝禎
   電子ビーム照射装置及び電子ビーム照射方法
   特願2022-046567

1. 2015年３月　日本薬学会 第 135 年会優秀発表賞
2. 2018年５月　アレキサンダー・フォン・フンボルト財団　ポストドクトラルフェロー
3. 2022年 有機合成化学協会 味の素研究企画賞

1. 山下泰信　μ-オピオイド受容体選択的蛍光プローブを用いた１分子イメージング ファルマシア　2020, 56, 955.

日本薬学会、日本化学会、有機合成化学協会