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Kei Takedomi
Observed name:
K. Takedomi
Institution:
Tanabe Pharma Corporation (Japan)
Observed institutions:
Japan Biological Informatics Consortium,
Tanabe Research Laboratories,
Tanabe Pharma Corporation (Japan),
National Institute of Advanced Industrial Science and Technology,
Yokohama City University,
The University of Osaka
show all 6
ORCID:
0000-0001-8792-9688
Observed ORCID:
0000-0001-8792-9688
OpenAlex ID:
A5080362763
Classification of Chemical Compounds by Protein−Compound Docking for Use in Designing a Focused Library
2005
·
Yoshifumi Fukunishi
, Yoshiaki Mikami
, et al.
·
Journal of Medicinal Chemistry
·
42
Discovery of Novel Pyrazole-Based Selective Aldosterone Synthase (CYP11B2) Inhibitors: A New Template to Coordinate the Heme-Iron Motif of CYP11B2
2018
·
Ryo Sakakibara
, Wataru Sasaki
, et al.
·
Journal of Medicinal Chemistry
·
24
Discovery of a pyrazolo[1,5-a]pyrimidine derivative (MT-3014) as a highly selective PDE10A inhibitor via core structure transformation from the stilbene moiety
2019
·
Yuuki Koizumi
, Yoshihito Tanaka
, et al.
·
Bioorganic & Medicinal Chemistry
·
16
Combination of Virtual Screening and High Throughput Gene Profiling for Identification of Novel Liver X Receptor Modulators
2008
·
Jie-Fei Cheng
, James Zapf
, et al.
·
Journal of Medicinal Chemistry
·
14
Discovery of SPH3127: A Novel, Highly Potent, and Orally Active Direct Renin Inhibitor
2022
·
Daisuke Iijima
, Hiroshi Sugama
, et al.
·
Journal of Medicinal Chemistry
·
13
Discovery of Apararenone (MT-3995) as a Highly Selective, Potent, and Novel Nonsteroidal Mineralocorticoid Receptor Antagonist
2022
·
Toru Iijima
, Makoto Katoh
, et al.
·
Journal of Medicinal Chemistry
·
13
Discovery and structure–activity relationship studies of indole derivatives as liver X receptor (LXR) agonists
2007
·
Farid Bakir
, Sunil Kher
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
13
Discovery of 2-[(E)-2-(7-Fluoro-3-methylquinoxalin-2-yl)vinyl]-6-pyrrolidin-1-yl-N-(tetrahydro-2H-pyran-4-yl)pyrimidin-4-amine Hydrochloride as a Highly Selective PDE10A Inhibitor
2018
·
Yoichi Kadoh
, Haruko Miyoshi
, et al.
·
Chemical and Pharmaceutical Bulletin
·
10
PDF
Prediction of the binding affinity of compounds with diverse scaffolds by MP-CAFEE
2013
·
Okimasa Okada
, Hiroshi Yamashita
, et al.
·
Biophysical Chemistry
·
5
Discovery of Novel 2-Carbamoyl Morpholine Derivatives as Highly Potent and Orally Active Direct Renin Inhibitors
2022
·
Daisuke Iijima
, Hiroshi Sugama
, et al.
·
ACS Medicinal Chemistry Letters
·
3
Effect of Water Molecules on the Activating S810L Mutation of the Mineralocorticoid Receptor
2021
·
Kei Takedomi
, Masateru Ohta
, et al.
·
Journal of Chemical Information and Modeling
·
2
PDF
Generation of novel respiratory syncytial virus vaccine candidate antigens that can induce high levels of prefusion-specific antibodies
2024
·
Rima Matsuyama-Ito
, Tomoharu Hogiri
, et al.
·
Journal of Bioscience and Bioengineering
Discovery of Pyrazolo[1,5-a]pyrimidine Derivative as a Highly Selective PDE10A Inhibitor
2019
·
K. Takedomi
, Y. Koizumi
·
Worldwide Protein Data Bank
Discovery of a Novel PDE10A Inhibitor as Highly Effective for Schizophrenia
2017
·
Yoichi Kadoh
, Takehiko Matsumura
, et al.
·
日本薬学会年会要旨集(CD-ROM)
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Works count:
14
Citation count:
155
H-index:
8
I10-index:
8
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