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Isao Yasumatsu
Observed names:
I Yasumatsu,
Isao YASUMATSU
Institution:
Daiichi Sankyo RD Novare (Japan)
Observed institutions:
Konan University,
Fuji Chemical Industries (Japan),
Daiichi-Sankyo (Japan),
Technology Research Association for Next generation natural products chemistry,
Daiichi Sankyo RD Novare (Japan)
ORCID:
0009-0000-9865-4835
Observed ORCID:
0009-0000-9865-4835
OpenAlex ID:
A5032517716
Novel orally bioavailable EZH1/2 dual inhibitors with greater antitumor efficacy than an EZH2 selective inhibitor
2017
·
Daisuke Honma
, Osamu Kanno
, et al.
·
Cancer Science
·
147
PDF
Mechanisms of action and resistance in histone methylation-targeted therapy
2024
·
Makoto Yamagishi
, Yuta Kuze
, et al.
·
Nature
·
129
PDF
Discovery and structure-guided fragment-linking of 4-(2,3-dichlorobenzoyl)-1-methyl-pyrrole-2-carboxamide as a pyruvate kinase M2 activator
2017
·
Yumi Matsui
, Isao Yasumatsu
, et al.
·
Bioorganic & Medicinal Chemistry
·
31
Discovery of DS79932728: A Potent, Orally Available G9a/GLP Inhibitor for Treating β-Thalassemia and Sickle Cell Disease
2020
·
Katsushi Katayama
, Ken Ishii
, et al.
·
ACS Medicinal Chemistry Letters
·
30
Discovery of novel histone lysine methyltransferase G9a/GLP (EHMT2/1) inhibitors: Design, synthesis, and structure-activity relationships of 2,4-diamino-6-methylpyrimidines
2020
·
Katsushi Katayama
, Ken Ishii
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
28
Discovery of Novel Pyrido-pyridazinone Derivatives as FER Tyrosine Kinase Inhibitors with Antitumor Activity
2019
·
Toru Taniguchi
, Hiroaki Inagaki
, et al.
·
ACS Medicinal Chemistry Letters
·
27
Discovery of imidazo[1,2-b]pyridazines as IKKβ inhibitors. Part 2: Improvement of potency in vitro and in vivo
2010
·
Hiroki Shimizu
, Isao Yasumatsu
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
22
Quantitative Structure‐activity Relationship (QSAR) Models for Docking Score Correction
2016
·
Yoshifumi Fukunishi
, Satoshi Yamasaki
, et al.
·
Molecular Informatics
·
21
PDF
Discovery of imidazo[1,2-b]pyridazine derivatives as IKKβ inhibitors. Part 1: Hit-to-lead study and structure–activity relationship
2010
·
Hiroki Shimizu
, Shinji Tanaka
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
21
A novel inhibitor stabilizes the inactive conformation of MAPK-interacting kinase 1
2018
·
Yumi Matsui
, Isao Yasumatsu
, et al.
·
Acta Crystallographica Section F Structural Biology Communications
·
18
PDF
Synthesis, activity, and their relationships of 2,4-diaminonicotinamide derivatives as EGFR inhibitors targeting C797S mutation
2023
·
Hideaki Kageji
, Takayuki Momose
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
10
Flexibility and Cell Permeability of Cyclic Ras-Inhibitor Peptides Revealed by the Coupled Nosé–Hoover Equation
2021
·
Kei Moritsugu
, Koh Takeuchi
, et al.
·
Journal of Chemical Information and Modeling
·
9
Design and Synthesis of Carboxylate Inhibitors for Matrix Metalloproteinases.
2001
·
Tetsunori FUJISAWA
, Shin-ichi KATAKURA
, et al.
·
Chemical and Pharmaceutical Bulletin
·
7
PDF
Stabilities of internal rU-dG and rG-dT pairs in RNA/DNA hybrids.
1997
·
N Sugimoto
, I Yasumatsu
, et al.
·
PubMed
·
5
Antitumor effects of novel highly hydrophilic and non-ATP-competitive MEK1/2 inhibitor, SMK-17
2011
·
Masaki Kiga
, Fumie Tanzawa
, et al.
·
Anti-Cancer Drugs
·
3
A New Concept for the Design of Antisense Oligonucleotides Based on Nucleic Acid Thermostability
2001
·
Naoki Sugimoto
, Isao Yasumatsu
·
Anti-Cancer Agents in Medicinal Chemistry
·
3
Discovery of a potent, selective, and orally available EGFR C797S mutant inhibitor (DS06652923) with in vivo antitumor activity
2024
·
Hideaki Kageji
, Takayuki Momose
, et al.
·
Bioorganic & Medicinal Chemistry
·
2
Optimization of Novel Pyrido-pyridazinone Derivatives as FER Tyrosine Kinase Inhibitors, Leading to the Potent DS08701581
2024
·
Toru Taniguchi
, Isao Yasumatsu
, et al.
·
ACS Medicinal Chemistry Letters
·
2
PDF
Discovery of Forvisirvat (DS-7830a/SP-624), a Brain-Penetrant Sirtuin 6 Activator Derived from Griseofulvin with Antidepressant-Like Effects
2026
·
Yasuyuki Ogawa
, Keiji Saito
, et al.
·
ACS Medicinal Chemistry Letters
PDF
Durable Clinical Impacts and Mechanisms of Action and Resistance in EZH1/2-Targeting Epigenetic Therapy
2022
·
Makoto Yamagishi
, Yuta Kuze
, et al.
·
Blood
Abstract B133: Antitumor effects of novel high-hydrophilic and non-ATP-competitive MEK1/2 inhibitor SMK-17.
2011
·
Masaki Kiga
, Fumie Tanzawa
, et al.
·
Molecular Cancer Therapeutics
ChemInform Abstract: Design and Synthesis of Carboxylate Inhibitors for Matrix Metalloproteinases.
2002
·
Tetsunori Fujisawa
, Shin‐ichi Katakura
, et al.
·
ChemInform
Specific Effect of Rare Earth Ions on the Binding between a Ribozyme and a Substrate-The Analysis by Using a Surface Plasmon Resonance
1996
·
Tatsuo Ohmichi
, Isao Yasumatsu
, et al.
·
希土類 = Rare earths
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Works count:
23
Citation count:
515
H-index:
10
I10-index:
11
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