Session Details
[27P-am]Organic Chemistry 1
Thu. Mar 27, 2025 8:30 AM - 12:00 PM JST
Thu. Mar 27, 2025 11:30 PM - 3:00 AM UTC
Thu. Mar 27, 2025 11:30 PM - 3:00 AM UTC
Poster (MARINE MESSE FUKUOKA Hall B: Exhibition Room [1F])
[27P-am001S]New synthesis monosubstituted β-carbolines and total synthesis of evollionine A
○Rinya Asano1, Takashi Nishiyama1, Tominari Choshi1 (1. Fukuyama Univ.)
[27P-am002S]Synthesis of novel calothrixin derivatives using two tandem type reaction
○takumi ueda1, Takashi Nishiyama1, Noriyuki Hatae2, Tominari Choshi1 (1. Fukuyama Univ. , 2. Yokohama Univ. of Pharm)
[27P-am003S]Total synthesis of the indolo[3,2-a]carbazole alkaloid racemosin B
○yuta uchida1, takashi nishiyama1, tominari choshi1 (1. Fukuyama Univ.)
[27P-am004S]Synthesis of pyrrolo[2,3-c]carbazole skelton by cyclocarbonylation reaction and apply total synthesis of Dictyodendrin B
○Soma Tsuji1, Takashi Nishiyama1, Toshio Motoyashiki1, Noriyuki Hatae2, Tominari Choshi1 (1. Fukuyama University, 2. Yokohama University of Pharmacy)
[27P-am005S]Total Synthesis of norketoyobyrine and its derivatives
○Hana Bessho1, Shota Mizuno1, Takashi Nishiyama1, Tetsuya Nakamura1, Toshio Motoyashiki1, Noriyuki Hatae2, Tominari Choshi1 (1. Fukuyama univ., 2. Yokohama univ. of pharm)
[27P-am006S]Optimization study of 3-arylisoquinolone synthesis by Reissert-Henze reaction
○Shota Mizuno1, Takashi Nishiyama1, Hana Bessho1, Takaki Yoshiura1, Toshiyuki Hata1, Tetsuya Nakamura1, Toshio Motoyashiki1, Yuzo Hieda1,2, Noriyuki Hatae3, Tominari Choshi1 (1. Fukuyama Univ., 2. Fukuyama Univ. Joint Usage Center, 3. Yokohama univ. of pharm)
[27P-am007]Synthesis of indole-4,7-quinones using tandem reaction and evaluation of antitumor activity
○nishiyama takashi1, daichi kurokawa1, tetsuya nakamura1, toshio motoyashiki1, noriyuki hatae2, tominari choshi1 (1. Pharm. Sci., Fukuyama Univ., 2. Pharm. Sci., Yokohama Univ. Pharm.)
[27P-am008S]Synthesis of (-)-Rancinamycin Ia
○Teru Umaba1, Noboru Hayama1, Hiroki Yoneyama1, Yoshihide Usami1 (1. Osaka Med. & Pharm. Univ.)
[27P-am009S]Synthesis and structure-activity relationships of fentanyl derivatives
○Mizuha Nishimoto1, Hironobu Arita1, Shuntaro Kikukawa1, Tsukasa Tomizawa1, Haruka Sakata1, Masahiko Funada2, Kenichi Tomiyama3, Hidetsugu Tabata4, Kayo Nakamura1, Tetsuta Oshitari4, Hideaki Natsugari5, Hideyo Takahashi1 (1. Pharm. Sci., Tokyo Univ. Sci., 2. Pharm. Sci., Shonan Univ. Med. Sci., 3. National Center of Neurology and Psychiatry, 4. Pharm. Sci., Teikyo Univ., 5. Pharm. Sci., The University of Tokyo)
[27P-am010S]Synthetic studies of Streptonigrin based on gold-catalyzed synthesis of polysubstituted pyridines
○Shuto Kosuge1, Kenji Sugimoto1,2, Yuji Matsuya1 (1. Faculty of Pharm. Sci., Univ. of Toyama, 2. Grad. Sch. Life and Environmental Sci., Kyoto Pref. Univ.)
[27P-am011S]Synthetic Studies on Plakinidine Alkaloids
Kazunari Akita1, ○Seiya Hosoi1, Touma Adachi1, Juri Sakata1, Hidetoshi Tokuyama1 (1. Grad. Sch. Pharm. Sci., Tohoku Univ.)
[27P-am012]Synthetic study on hypocrellutins via regioselective iodocyclization
○Junya Hirai1, Tohru Nagamitsu1 (1. Sch. Pharm., Kitasato Univ.)
[27P-am013S]Synthesis and reactivity analysis of a dispiro-epoxy-γ-lactam
○Hayato Yamaguchi1, Junko Fujimoto1, Kazutada Ikeuchi1,2, Naoki Kanoh1,2, Hiromasa Yokoe3 (1. Sch. Pharm., Hoshi Univ., 2. Inst. Med. Chem., Hoshi Univ., 3. Dep. Pharm. Sci., Yokohama Univ. Pharm.)
[27P-am014S]Synthetic study on PF1140 and deoxy-PF1140
○Ryusuke Suzuki1, Junya Hirai1, Tohru Nagamitsu1 (1. Sch. Pharm., Kitasato Univ.)
[27P-am015]Synthetic study of dalomycin T
Yasutaka Chino1, Ryuto Watanabe1, ○Yusuke Akagi1, Erika Iwasaki1, Toshiya Komatsu1 (1. Fac. Pharm. Sci., Teikyo Heisei Univ.)
[27P-am016]Concise synthesis of mono-chloro dehydroanthophyine derivatives and their antimalarial activity by chelating metal ions
○Hibiki Tomimori1, Naoto Yamasaki1, Yosinori Asakawa1, Hirofumi Yamamoto1 (1. Tokushima Bunri Univ.)
[27P-am017]Expansion of Substrate Scope of the Tandem Oxidation/Cycloaddition Reaction of Phthalans and Shortening the Synthetic Route to Morphine
○Eisaku Ohashi1, Manami Tabata1, Kimihiro Noguchi1, Takeshi Watanabe1, Manato Uchida1, Hiroyuki Yamakoshi1, Seiichi Nakamura1 (1. Grad. Sch. Pharm. Sci., Nagoya City Univ.)
[27P-am018]Construction and biological evaluation of side-chain fluorinated 19-norvitamin D3 chemical library that suppress IL-19 secretion from human keratinocytes.
○sayuri mototani1, fumihiro kawagoe2, hiroki mano3, kaori yasuda3, toshie fujishima1, toshiyuki sakaki3, atsushi kittaka1 (1. Faculty Pharm. Sci., Teikyo Univ., 2. Faculty of Sci. Div., Tokyo Univ of Sci., 3. Faculty of Eng., Toyama Pref Univ.)
[27P-am019S]Construction of 1,5-benzodiazocine skeleton by the palladium-catalyzed cascade cyclization using allylic biscarbonates.
○Mai Yamashita1, Shinya Shiomi1, Masahiro Yoshida1 (1. Faculty of Pharmaceutical Sciences, Tokushima Bunri University)
[27P-am020S]Synthesis of nitrogen-containing seven-membered ring compounds by palladium-catalyzed cascade cyclization of allyl bicarbonates.
○Kaho Hida1, Shiya Shiomi1, Masahiro Yoshida1 (1. Faculty of Pharmaceutical Sciences, Tokushima Bunri University)
[27P-am021S]Development of Novel Benzdiyne Equivalents Bearing Two-Sets of Leaving Groups Activated by Silica Gel or Fluoride Salt
○Yuzuki Watanabe1, Motoki Ito1, Ryo Warita1, Kentaro Nakajima1, Asahi Koshikawa1, Kazuhiro Higuchi1, Shigeo Sugiyama1 (1. Grad. Sch. Pharm. Sci., Meiji Pharmaceutical Univ.)
[27P-am022S][4+2]Cycloaddition of Unsymmetrical Aryne and 3-carbonyl furan derivatives
○Yuki Maeda1, Aoi Nagase1, Yoshimitsu Hashimoto1, Osamu Tamura1, Nobuyoshi Morita1 (1. Showa Pharm. Univ.)
[27P-am023]Synthesis and Application of F-18 Indirect Labeling Reagents Boronic Acid Derivatives 3-[18F]TDBFB
○Yusuke Yagi1,3,4, Hiroyuki Kimura2, Takahiro Higuchi3 (1. Kyoto College of Medical Science, 2. Research Center for Experimental Modeling of Human Disease, Kanazawa University, 3. Comprehensive Heart Failure Center, University Hospital of Würzburg, 4. Grad. Sch. Med. Dent. Pharm. Sci., Okayama Univ.)
[27P-am024S]Synthesis of Indole Derivatives via Diynylindole
○Kaoru Komori1, Yuta Kubota1, Norihiro Tada1, Akichika Itoh1 (1. Gifu Pharm. Univ.)
[27P-am025S]One-pot synthesis of highly-functionalized benzenes via rearrangement of electron-withdrawing groups from the corresponding furan
○Sota Yoshimura1, Takaaki Aijima2, Jin Tokunaga1, Shuji Akai2, Yoshinari Sawama2 (1. Sch. Pharm. Sci., Osaka Univ., 2. Grad. Sch. Pharm. Sci., Osaka Univ.)
[27P-am026S]Catalytic synthesis of nitrogen-containing heterocycles by using oxidative cyclization of diarylamines.
○Kanako Date1, Naho Sato2, Kenji Matsumoto1,2 (1. Grad. Sch. Sci. Eng., Kagoshima Univ., 2. Eng., Kagoshima Univ.)
[27P-am027S]Scope of Oxazole Synthesis via Triple Bond Activation by Gold Catalyst and β-Cation Stabilization by Silyl Group
○Hitomi Chiaki1, Aoi Sano1, Hiroaki Iwaya1, Naho Ishii1, Saki Tanaka1, Kousaku Tanaka, III1, Yoshimitsu Hashimoto1, Osamu Tamura1, Nobuyoshi Morita1 (1. Showa Pharm. Univ.)
[27P-am028]Palladium-Catalyzed Three-Component Coupling of Ynamides: Effect of Substitution on the Carbon atom of Ynamides
○Hideaki Wakamatsu1, Haruki Kubo1, Kana Suzuki1, Yuna Ikoma1, Yuichi Yoshimura1 (1. Tohoku Med. Pharm. Univ.)
[27P-am029S]Development of a continuous-flow Diels–Alder reactions utilizing the ring-opening of benzocyclobutene derivatives
○Tomoki Iwama1, Tsuyoshi Yamada1, Masaru Tanioka1, Yuji Matsuya1 (1. Faculty of Pharm. Sci, Univ. of Toyama)
[27P-am030S]Development of red-light-driven Giese reaction promoted by zinc porphyrin catalyst
○Yoshitatsu Yotsumoto1, Yusuke Okanishi1, Takehiko Yoshimitsu1 (1. Graduate School of Medicine, Dentistry, and Pharmaceutical Sciences, Okayama University)
[27P-am031]Synthesis and analysis of stability of 2-aryldihydropyrimidine-5-ester tautomers, and their anticancer activity
○Yoshio Nishimura1, Takanori Kubo2, Misaki Kamikura1, Yuto Kazama1, Rie Hirono1, Ryota Matsuyama1, Hietsura Cho (1. Sch. Pharm. Sci., Ohu Univ., 2. Fac. Pharm., Yasuda Women's Univ.)
[27P-am032S]Development of new photoreactions utilizing regioselective C–C bond cleavage of benzocyclobutenone
○Yukiko Ikeda1, Masaru Tanioka1, Tsuyoshi Yamada1, Yuji Matsuya1 (1. Faculty of Pharm. Sci., University of Toyama)
[27P-am033]A symmetric total synthesis of mafcheenamines
○yuhzo hieda1,2, Takashi Nishiyama2, Shota Mizuno2, Takayoshi Tsuruga2, Tominari Choshi2 (1. Common Resources Center, Fukuyama University, 2. Faculty of Pharmacy and Pharmaceutical Sciences, Fukuyama University)
[27P-am034S]Synthetic study on bulky quaternary ammoniums bearing phenyl and cyclohexyl groups
○Jinwei You1, Hikaru Fujita1, Munetaka Kunishima1,2 (1. Faculty of Pharmaceutical Sciences, Institute of Medical, Pharmaceutical, and Health Sciences, Kanazawa University, 2. Faculty of Pharmaceutical Sciences, Kobe Gakuin University)
[27P-am035S]Construction of aza-bicyclo[5.4.3]tetradecane core derived Phlegmariurine-A
○Ryosuke Maeda1, Nariyoshi Umekubo1, Satoshi Yokoshima1 (1. Grad. Sch. Pharm. Sci., Nagoya Univ.)
[27P-am036S]Substitution effects in the asymmetric hydrolysis of tropic acid β-lactone analogues with chiral phase-transfer catalysts
Midori Kawasaki1, ○Arisa Yasutomi2, Yuna Hasegawa2, Katsuko Shirai2, Ryuichi Shirai1 (1. Grad. Sch. Pharm. Sci., Doshisha Women's Col., 2. Fac. Pharm. Sci., Doshisha Women's Col.)
[27P-am037]Mechanism Study on the Ring-opening Reactions of 1,6-Anhydroglucopyranose Derivatives Catalyzed by Fluorous Lewis Acid
○Akihiro Yoshida1, Sayaka Kubota1, Miki Namiki1, Ryo Sagara1, Hiroshi Akutsu1, Takashi Yamanoi1 (1. Faculty of Pharmacy and Pharmaceutical Sciences, Josai University)
[27P-am038S]Study of the diastereoselective Petasis reaction forming quaternary asymmetric centers
○Shoichi Hiwatari1, Kyoka Azegami1, Eisuke Saito1, Masaya Sasagawa1, Masahiro Noji1, Motoki Ito1, Kazuhiro Higuchi1, Shigeo Sugiyama1 (1. Meiji Pharm. Univ.)
[27P-am039S]Study of the addition of boronic acids to 1,2-dicarbonyl compounds
○Mio Hiraoka1, Naoki Yoshikawa1, Motoki Ito1, Kazuhiro Higuchi1, Shigeo Sugiyama1 (1. Meiji Pharm. Univ.)
[27P-am040S]Reconstructive formation of Fluorinated Heterocycles from Cyclohexadiones by Cut-to-Fuse Strategy
○Yusuke Yoto1, Yusei Matsumoto1, Hideyasu China2, Kotaro Kikushima1, Toshifumi Dohi1 (1. College of Pharmaceutical Sciences, Ritsumeikan University, 2. Faculty of Pharmaceutical Sciences, Doshisha Women’s College of Liberal Arts)
[27P-am041S]Molecular oxygen-driven sequential oxidative cleavage/heterocycle formation of bicyclo[1.1.0]butylamides
○Takumi Mizumachi1, Tsunayoshi TAKEHARA2, Takeyuki SUZUKI2, Atsushi NAKAYAMA1, Mitsuhiro ARISAWA1, Makoto SAKO1 (1. Grad. Sch. Pharm. Sci., Osaka Univ., 2. SANKEN, Osaka Univ.)
[27P-am042]Computational Study on s-trans mode Diels–Alder reactions
○Yoshimitsu Hashimoto1,2, Dean J. Tantillo2 (1. Showa Pharm. Univ., 2. Dept. Chem. Univ. California Davis)
[27P-am043]Oxidation with peracid made from dimethyl oxalate and hydrogen peroxide based on “aquachemistry”
○Takeshi Sugai1,2, Taku Kitanosono1, Shu Kobayashi1 (1. Grad. Sch. Sci. Univ. Tokyo, , 2. Keio Univ.)
[27P-am044S]Development of a mild hydrogenation of unactivated alkenes using hydrosilane as reducing agent
Takahiro Shirai1, ○Shinnosuke Tani2, Ryo Nakajima1, Takuya Kumamoto1 (1. Grad. Sch. Biomed. Health Sci., Hiroshima Univ., 2. Sch. Pharm. Sci., Hiroshima Univ.)
[27P-am045S]Evaluation of catalytic activity of thioxanthone derivatives in E/Z photoisomerization of fumaric acid diester
○Mei Takagi1, Mayuko Suga1, Masanori Motokawa2, Kayo Nakamura1, Hidetsugu Tabata3, Tetsuta Oshitari3, Hideaki Natsugari4, Hideyo Takahashi1 (1. Pharm. Sci., Tokyo Univ. Sci., 2. GL Sciences Co., Ltd., 3. Pharm. Sci., Teikyo Univ., 4. Pharm. Sci., Tokyo Univ.)
[27P-am046S]Photocatalytic Decyanative Intramolecular Alkylation of Malononitriles
○Yuto Yoshida1, Waka Okada2, Shuichi Nakamura1, Naoki Yasukawa1 (1. Grad. Sch. Eng., Nagoya Institute of Technology, 2. Nagoya Institute of Technology)
[27P-am047S]Development of a Facile Synthetic Method for Dianthranilides
Masahiro Abe1, ○Nami Shoji1, Akiho Mizukami1, Tetsutaro Kimachi1, Kiyofumi Inamoto1 (1. Sch. Pharm. Sci., Mukogawa Women's Univ.)
[27P-am048S]Nitrile Synthesis via Desulfonylative Smiles Rearrangement: Development of Mild Nitrile Synthesis through Structural Optimization
Masahiro Abe1, ○Misaki Furukawa1, Akiho Mizukami1, Tetutaro Kimachi1, Inamoto Kiyofumi1 (1. Sch. Pharm. Sci., Mukogawa Women's Univ.)
[27P-am049]FAB-MS of disulfide-linked cyclic oligopeptides using thioglycerol matrix: Counting of disulfide bonds by [M+n2H+H]+
○Mihoyo Fujitake1, Shinya Harusawa1 (1. Fac. Pharm., Osaka Med. Pharm. Univ.)
[27P-am050]C(sp2)-H arylation reaction to 2-Amino-1-phenylethanol derivatives
○Karin Shigematsu1, Motofumi Miura1, Masaharu Toriyama1 (1. School of Pharmacy, Nihon University)
[27P-am051S]Photoinduced Copper-Catalyzed Intramolecular Radical Cyclization of 1,8-Ene-Ynes
○Ayu Yokoyama1, Kyoka Maeda1, Hikaru Takahashi2, Ryo Murakami1, Fuyuhiko Inagaki1 (1. Grad. Sch. Pharm. Sci., Kobegakuin Univ., 2. Grad. Sch. Pharm.Sci.,Kobegakuin Univ.)
[27P-am052S]Synthesis of isocoumarin derivatives by metal-free coupling-cyclization of ester-containing diaryliodonium(III) salts
○Daichi Kashiwagi1, Elghareeb E. Elboray1, Bae Taeho1, Kotaro Kikushima1, Yasuyuki Kita2, Toshifumi Dohi1,2 (1. College of Pharmaceutical Sciences, Ritsumeikan University,, 2. Research Organization of Science and Technology, Ritsumeikan University)
[27P-am053]Site and regioselective reductive Heck hydroarylation of unactivated alkenes
○Takahiro Shirai1, Yusuke Migitera2, Ryo Nakajima1, Takuya Kumamoto1 (1. Grad. Sch. Biomed. Health Sci., Hiroshima Univ., 2. Sch. Pharm. Sci. Hiroshima Univ.)
[27P-am054S]N-Hydroxyphthalimide-catalyzed chemoselective benzylic C-H oxidation of unprotected arylalkanols
○Amane Nakamura1, Masatoshi Shibuya1 (1. Grad. Sch. Sci., Japan Women's Univ.)
[27P-am055S]Synthesis of pyrrole derivatives by transition metal-free cycloaddition of propargyl amine and acetylene diester
○Akinobu Tamura1, Noriko Fukushima1, Yuya Chikayuki1, Tomofumi Hata1, Takayasu Yamauchi1 (1. Hoshi Univ.)
[27P-am056S]Stereostructural Analysis of Trifluoroacetamide Compounds Utilizing Through-Space-Coupling and Solvent Effects
○Kizuki Watanabe1, Yan Li1, Takenori Kusumi2, Kayo Nakamura1, Hidetsugu Tabata3, Motoo Iida1, Kiriko Hirano4, Tetsuta Oshitari3, Hideaki Natsugari5, Hideyo Takahashi1 (1. Fac. Pharm. Sci., Tokyo Univ. Sci., 2. Fac. Pharm. Sci., Tokushima Univ., 3. Fac. Pharm. Sci., Teikyo Univ., 4. Bruker Japan K.K., 5. Fac. Pharm. Sci., Tokyo Univ.)
[27P-am057S]Crystal structure analysis of Aib peptides with aromatic sulfonamide moiety at the N-terminus.
○yuto hiyama1, Yusuke Saiki1, Shoko Kikkawa1, Hidemasa Hikawa1, Isao Azumaya1 (1. Fac. Pharm. Sci., Toho Univ.)
[27P-am058S]Molecular chiralities in the crystal of Ac3c pentapeptides having a sulfonamide group at N-terminus
○Kazuma Kondo1, Tomokatsu Enda1, Shoko Kikkawa1, Hidemasa Hikawa1, Isao Azumaya1 (1. Fac. Pharm. Sci. Toho Univ.)
[27P-am059]Synthesis of 2-Oxypyritriphyrin(1.2.1) and Redox-Induced Reversible Transformation of its π-Conjugation Circuit.
○Tomoki Yoneda1, Su-Gi Chong2, Saburo Neya3 (1. Dep. of Pharm. Sci. at Narita, International University of Health and Welfare, 2. Institute of Advanced Sciences, Yokohama National Univ., 3. Grad. Sch. of Pharm. Sci. Chiba Univ.)
[27P-am060S]Structural analysis of Fentanyl-Type Antagonist of the μ-Opioid Receptor
○Hironobu Arita1, Shuntaro Kikukawa1, Tsukasa Tomizawa1, Haruka Sakata1, Mizuha Nishimoto1, Masahiko Funada2, Kenichi Tomiyama3, Masaru Hashimoto4, Tomohiko Tasaka5, Hidetsugu Tabata6, Kayo Nakamura1, Tetsuta Oshitari6, Hideaki Natsugari7, Hideyo Takahashi1 (1. Pharm. Sci., Tokyo Univ. Science, 2. Pharm. Sci., Shonan Univ. Medical Sciences, 3. National Center of Neurology and Psychiatry, 4. Agric. Life Sci., Hirosaki Univ., 5. ASC, 6. Pharm. Sci., Teikyo Univ., 7. Grad. Sch. Pharm. Sci., The University of Tokyo.)
[27P-am061S]Synthesis and X-ray crystallographic analysis of aminotriazolamers derived from amino acids
○Ryosuke Tomono1, Chihiro Muraki1, Norihiro Tada1, Akichika Itoh1 (1. Gifu Pharm. Univ.)
[27P-am062S]Synthesis of four-membered ring-fused dibenzoazepine derivatives and analysis of their rotational isomeric behaviour
○Juri Kitagawa1, Yuki Itabashi2, Tsuyoshi Inoue2,3, Kei Ohkubo2, Haruyasu Asahara2,3 (1. Sch. Pharm. Sci., Osaka Univ., 2. OTRI, Osaka Univ. , 3. Grad. Sch. Pharm. Sci., Osaka Univ.)
[27P-am063S]Post-synthetic modification of benzo[a]ullazines
Teru Kawazoe1, ○Yui Yamaguchi1, Hikaru Yanai1, Takashi Matsumoto1 (1. Tokyo Univ. Pharm. Life Sci.)
[27P-am064S]Synthesis and secondary structure analysis of photoreactive peptide
○Motoki Naka1, Tomohiro Umeno1, Hiroyasu Takemoto1, Atsushi Ueda2, Masakazu Tanaka2, Makoto Oba1 (1. Grad. Sch. Med. Sci., Kyoto Prefecture Univ. of Medicine, 2. Grad. Sch. Biomed. Sci., Nagasaki Univ.)
[27P-am065]Selective formation of supramolecular chiral centers by inclusion complexes of dibenzofuran disulfonates with the cavity of γ-cyclodextrin
○Kazutaka Koga1, Yutaka Nakatomi2, Madoka Hase2, Makoto Fukudome2, Tatsuya Takimoto2, De-Qi Yuan2 (1. Fac. Pharm., Daiichi Univ. Pharm., 2. Fac. Pharm. Sci., Kobe Gakuin Univ.)
[27P-am066S]Development of alkynylated purine-pyridone unnatural base pairs
○Wenjue Fan1,2, Hidenori Okamura1,2, Zhuoxin Dong1,2, Giang Hoang Trinh1,2, Fumi Nagatsugi1,2 (1. IMRAM, Tohoku Univ., 2. Grad. Sch. Sci., Tohoku Univ.)
[27P-am067]Development of pinpoint chemical modification methods for DNA or RNA and their applications.
○Hirotaka Murase1,4, Mio Eto1, Jeongsu Lee2,4, Yosuke Taniguchi3,4, Shuhei Imoto1, Shigeki Sasaki2,4 (1. Faculty of Pharm. Sci., Sojo Univ., 2. Grad. School of Pharm. Sci., Nagasaki Int. Univ., 3. Grad. School of Pharm. Sci., Okayama Univ., 4. RINAT Imaging, Inc.)
[27P-am068]Investigation of the relationship between the structure of pharmaceutical development products and toxicity
○Mayuko Yasuda1, Hitomi Yuki1, Teruki Honma1 (1. RIKEN)