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Hidehisa Iwata
Hidehisa Iwata
Takeda Pharmaceutical Company
Verified email at takeda.com
Title
Cited by
Cited by
Year
Structure of the Bacillus subtilis quorum-sensing peptide pheromone ComX
M Okada, I Sato, SJ Cho, H Iwata, T Nishio, D Dubnau, Y Sakagami
Nature chemical biology 1 (1), 23-24, 2005
2052005
Structure-Based Approach for the Discovery of Pyrrolo[3,2-d]pyrimidine-Based EGFR T790M/L858R Mutant Inhibitors
S Sogabe, Y Kawakita, S Igaki, H Iwata, H Miki, DR Cary, T Takagi, ...
ACS medicinal chemistry letters 4 (2), 201-205, 2013
1392013
A BET family protein degrader provokes senolysis by targeting NHEJ and autophagy in senescent cells
M Wakita, A Takahashi, O Sano, TM Loo, Y Imai, M Narukawa, H Iwata, ...
Nature communications 11 (1), 1935, 2020
1382020
Design, synthesis, and evaluation of 5-methyl-4-phenoxy-5H-pyrrolo[3,2-d]pyrimidine derivatives: Novel VEGFR2 kinase inhibitors binding to inactive kinase …
Y Oguro, N Miyamoto, K Okada, T Takagi, H Iwata, Y Awazu, H Miki, ...
Bioorganic & medicinal chemistry 18 (20), 7260-7273, 2010
1132010
Discovery of N-[5-({2-[(cyclopropylcarbonyl)amino]imidazo[1,2-b]pyridazin-6-yl}oxy)-2-methylphenyl]-1,3-dimethyl-1H-pyrazole-5-carboxamide (TAK-593), a …
N Miyamoto, N Sakai, T Hirayama, K Miwa, Y Oguro, H Oki, K Okada, ...
Bioorganic & medicinal chemistry 21 (8), 2333-2345, 2013
742013
Design and synthesis of novel pyrimido[4,5-b]azepine derivatives as HER2/EGFR dual inhibitors
Y Kawakita, M Seto, T Ohashi, T Tamura, T Yusa, H Miki, H Iwata, ...
Bioorganic & medicinal chemistry 21 (8), 2250-2261, 2013
692013
Structure-based design, synthesis, and evaluation of imidazo[1,2-b]pyridazine and imidazo[1,2-a]pyridine derivatives as novel dual c-Met and VEGFR2 kinase …
S Matsumoto, N Miyamoto, T Hirayama, H Oki, K Okada, M Tawada, ...
Bioorganic & medicinal chemistry 21 (24), 7686-7698, 2013
682013
Structure-based discovery of cellular-active allosteric inhibitors of FAK
N Tomita, Y Hayashi, S Suzuki, Y Oomori, Y Aramaki, Y Matsushita, ...
Bioorganic & medicinal chemistry letters 23 (6), 1779-1785, 2013
602013
Vacuolin‐1 inhibits autophagy by impairing lysosomal maturation via PIK fyve inhibition
O Sano, K Kazetani, M Funata, Y Fukuda, J Matsui, H Iwata
FEBS letters 590 (11), 1576-1585, 2016
522016
Discovery and characterization of novel allosteric FAK inhibitors
M Iwatani, H Iwata, A Okabe, RJ Skene, N Tomita, Y Hayashi, Y Aramaki, ...
European Journal of Medicinal Chemistry 61, 49-60, 2013
522013
Design, synthesis, and evaluation of novel VEGFR2 kinase inhibitors: Discovery of [1,2,4]triazolo[1,5-a]pyridine derivatives with slow dissociation kinetics
Y Oguro, DR Cary, N Miyamoto, M Tawada, H Iwata, H Miki, A Hori, ...
Bioorganic & medicinal chemistry 21 (15), 4714-4729, 2013
502013
Design and Synthesis of Pyrrolo[3,2-d]pyrimidine Human Epidermal Growth Factor Receptor 2 (HER2)/Epidermal Growth Factor Receptor (EGFR) Dual Inhibitors …
Y Kawakita, H Banno, T Ohashi, T Tamura, T Yusa, A Nakayama, H Miki, ...
Journal of Medicinal Chemistry 55 (8), 3975-3991, 2012
422012
Biochemical characterization of TAK-593, a novel VEGFR/PDGFR inhibitor with a two-step slow binding mechanism
H Iwata, S Imamura, A Hori, MS Hixon, H Kimura, H Miki
Biochemistry 50 (5), 738-751, 2011
422011
A Novel Inhibitor of c-Met and VEGF Receptor Tyrosine Kinases with a Broad Spectrum of In Vivo Antitumor Activities
Y Awazu, K Nakamura, A Mizutani, Y Kakoi, H Iwata, S Yamasaki, ...
Molecular cancer therapeutics 12 (6), 913-924, 2013
302013
A back-to-front fragment-based drug design search strategy targeting the DFG-out pocket of protein tyrosine kinases
H Iwata, H Oki, K Okada, T Takagi, M Tawada, Y Miyazaki, S Imamura, ...
ACS medicinal chemistry letters 3 (4), 342-346, 2012
302012
Design, synthesis, and evaluation of imidazo[1,2-b]pyridazine derivatives having a benzamide unit as novel VEGFR2 kinase inhibitors
N Miyamoto, Y Oguro, T Takagi, H Iwata, H Miki, A Hori, S Imamura
Bioorganic & medicinal chemistry 20 (24), 7051-7058, 2012
292012
Biochemical characterization of a novel type-II VEGFR2 kinase inhibitor: comparison of binding to non-phosphorylated and phosphorylated VEGFR2
H Iwata, S Imamura, A Hori, MS Hixon, H Kimura, H Miki
Bioorganic & medicinal chemistry 19 (18), 5342-5351, 2011
262011
Feedback activation of AMPK-mediated autophagy acceleration is a key resistance mechanism against SCD1 inhibitor-induced cell growth inhibition
A Ono, O Sano, K Kazetani, T Muraki, K Imamura, H Sumi, J Matsui, ...
PLoS One 12 (7), e0181243, 2017
242017
Anti‐angiogenic and anti‐tumor effects of TAK‐593, a potent and selective inhibitor of vascular endothelial growth factor and platelet‐derived growth factor receptor tyrosine …
Y Awazu, A Mizutani, Y Nagase, S Tsuchiya, K Nakamura, Y Kakoi, ...
Cancer science 104 (4), 486-494, 2013
212013
A novel pyrrolo[3, 2‐d]pyrimidine derivative, as a vascular endothelial growth factor receptor and platelet‐derived growth factor receptor tyrosine kinase inhibitor …
Y Awazu, A Mizutani, Y Nagase, H Iwata, Y Oguro, H Miki, S Imamura, ...
Cancer science 103 (5), 939-944, 2012
212012
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