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Rei Okamoto
Observed name:
Okamoto, Rei
Institution:
Tri-Institutional Therapeutics Discovery Institute
Observed institutions:
Tohoku University,
Tri-Institutional Therapeutics Discovery Institute,
Takeda (Japan)
OpenAlex ID:
A5111956018
Small molecule inhibition of cGAS reduces interferon expression in primary macrophages from autoimmune mice
2017
·
Jessica Vincent
, Carolina Adura
, et al.
·
Nature Communications
·
395
PDF
Development of human cGAS-specific small-molecule inhibitors for repression of dsDNA-triggered interferon expression
2019
·
Lodoe Lama
, Carolina Adura
, et al.
·
Nature Communications
·
315
PDF
Antimalarial proteasome inhibitor reveals collateral sensitivity from intersubunit interactions and fitness cost of resistance
2018
·
Laura A. Kirkman
, Wenhu Zhan
, et al.
·
Proceedings of the National Academy of Sciences
·
103
PDF
Simple Construction of Bicyclo[4.3.0]nonane, Bicyclo[3.3.0]octane, and Related Benzo Derivatives by Palladium-Catalyzed Cycloalkenylation
2002
·
Masahiro Toyota
, Andivelu Ilangovan
, et al.
·
Organic Letters
·
65
Development of a Highly Selective Plasmodium falciparum Proteasome Inhibitor with Anti‐malaria Activity in Humanized Mice
2021
·
Wenhu Zhan
, Hao Zhang
, et al.
·
Angewandte Chemie International Edition
·
46
Novel Pure αVβ3 Integrin Antagonists That Do Not Induce Receptor Extension, Prime the Receptor, or Enhance Angiogenesis at Low Concentrations
2019
·
Jihong Li
, Yoshiyuki Fukase
, et al.
·
ACS Pharmacology & Translational Science
·
40
PDF
Toward the Total Synthesis of (±)-Andrastin C
2012
·
Rei Okamoto
, Kazutaka Takeda
, et al.
·
The Journal of Organic Chemistry
·
31
Publisher Correction: Small molecule inhibition of cGAS reduces interferon expression in primary macrophages from autoimmune mice
2017
·
Jessica Vincent
, Carolina Adura
, et al.
·
Nature Communications
·
26
PDF
Discovery and characterization of selective human sphingomyelin synthase 2 inhibitors
2017
·
Ryutaro Adachi
, Kazumasa Ogawa
, et al.
·
European Journal of Medicinal Chemistry
·
26
Design, Synthesis, and Optimization of Macrocyclic Peptides as Species-Selective Antimalaria Proteasome Inhibitors
2022
·
Hao Zhang
, John Ginn
, et al.
·
Journal of Medicinal Chemistry
·
25
PDF
Selective Phenylimidazole-Based Inhibitors of the Mycobacterium tuberculosis Proteasome
2019
·
Wenhu Zhan
, Hao-Chi Hsu
, et al.
·
Journal of Medicinal Chemistry
·
22
Macrocyclic Peptides that Selectively Inhibit the Mycobacterium tuberculosis Proteasome
2021
·
Hao Zhang
, Hao-Chi Hsu
, et al.
·
Journal of Medicinal Chemistry
·
19
Structure–Activity Relationship Studies of Antimalarial Plasmodium Proteasome Inhibitors─Part II
2023
·
Hao Zhang
, John Ginn
, et al.
·
Journal of Medicinal Chemistry
·
18
PDF
Discovery of 3,5-Diphenyl-4-methyl-1,3-oxazolidin-2-ones as Novel, Potent, and Orally Available Δ-5 Desaturase (D5D) Inhibitors
2017
·
Jun Fujimoto
, Rei Okamoto
, et al.
·
Journal of Medicinal Chemistry
·
18
Discovery of 1,8-naphthyridin-2-one derivative as a potent and selective sphingomyelin synthase 2 inhibitor
2020
·
Takafumi Yukawa
, Takashi Nakahata
, et al.
·
Bioorganic & Medicinal Chemistry
·
11
Structure‐Based Design, Synthesis, and Biological Evaluation of Imidazo[4,5‐b]pyridin‐2‐one‐Based p38 MAP Kinase Inhibitors: Part 1
2019
·
Akira Kaieda
, Masashi Takahashi
, et al.
·
ChemMedChem
·
10
Whole Cell Active Inhibitors of Mycobacterial Lipoamide Dehydrogenase Afford Selectivity over the Human Enzyme through Tight Binding Interactions
2021
·
John Ginn
, Xiuju Jiang
, et al.
·
ACS Infectious Diseases
·
8
Development of a Highly Selective Plasmodium falciparum Proteasome Inhibitor with Anti‐malaria Activity in Humanized Mice
2021
·
Wenhu Zhan
, Hao Zhang
, et al.
·
Angewandte Chemie
·
6
Structure‐Based Design, Synthesis, and Biological Evaluation of Imidazo[4,5‐b]Pyridin‐2‐one‐Based p38 MAP Kinase Inhibitors: Part 2
2019
·
Akira Kaieda
, Masashi Takahashi
, et al.
·
ChemMedChem
·
6
Ti(III)-induced radical cyclization. A stereoselective entry to the perhydrobenzo[e]indene unit of new protein farnesyltransferase inhibitors, andrastins A–D
2004
·
Masahiro Toyota
, Rei Okamoto
, et al.
·
Tetrahedron Letters
·
6
Structure–Activity Relationship Study of Antimalarial Asparagine-Derived Proteasome Inhibitors
2026
·
Hao Zhang
, Daqiang Li
, et al.
·
ACS Omega
CCDC 1968615: Experimental Crystal Structure Determination
2020
·
Yukawa, Takafumi
, Nakahata, Takashi
, et al.
·
The Cambridge Structural Database
CCDC 1519191: Experimental Crystal Structure Determination
2017
·
Fujimoto, Jun
, Okamoto, Rei
, et al.
·
The Cambridge Structural Database
Ti(III)‐Induced Radical Cyclization. A Stereoselective Entry to the Perhydrobenzo[e]indene Unit of New Protein Farnesyltransferase Inhibitors, Andrastins A—D.
2005
·
Masahiro Toyota
, Rei Okamoto
, et al.
·
ChemInform
Simple Construction of Bicyclo[4.3.0]nonane, Bicyclo[3.3.0]octane, and Related Benzo Derivatives by Palladium‐Catalyzed Cycloalkenylation.
2003
·
Masahiro Toyota
, Andivelu Ilangovan
, et al.
·
ChemInform
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Works count:
25
Citation count:
1,196
H-index:
14
I10-index:
16
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