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Kenji Sagawa
Observed name:
Kenji SAGAWA
Institution:
Ono Pharmaceutical (Japan)
Observed institutions:
National Institutes of Health,
Ono Pharmaceutical (Japan),
National Cancer Institute,
Kumamoto University
OpenAlex ID:
A5035586802
Spirodiketopiperazine-Based CCR5 Inhibitor Which Preserves CC-Chemokine/CCR5 Interactions and Exerts Potent Activity against R5 Human Immunodeficiency Virus Type 1 In Vitro
2004
·
Kenji Maeda
, Hirotomo Nakata
, et al.
·
Journal of Virology
·
221
Novel Low Molecular Weight Spirodiketopiperazine Derivatives Potently Inhibit R5 HIV-1 Infection through Their Antagonistic Effects on CCR5
2001
·
Kenji Maeda
, Kazuhisa Yoshimura
, et al.
·
Journal of Biological Chemistry
·
125
PDF
The Protein-tyrosine Phosphatase SHP-2 Associates with Tyrosine-phosphorylated Adhesion Molecule PECAM-1 (CD31)
1997
·
Kenji Sagawa
, Teruaki Kimura
, et al.
·
Journal of Biological Chemistry
·
105
PDF
Design, Synthesis, and Biological Evaluation of the Combinatorial Library with a New Spirodiketopiperazine Scaffold. Discovery of Novel Potent and Selective Low-Molecular-Weight CCR5 Antagonists
2006
·
Hiromu Habashita
, Masaya Kokubo
, et al.
·
Journal of Medicinal Chemistry
·
82
Aggregation of the High Affinity IgE Receptor Results in the Tyrosine Phosphorylation of the Surface Adhesion Protein PECAM-1 (CD31)
1997
·
Kenji Sagawa
, William Swaim
, et al.
·
Journal of Biological Chemistry
·
55
PDF
Design and Synthesis of a Highly Selective EP2-Receptor Agonist
2001
·
Kousuke Tani
, Atsushi Naganawa
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
48
Spirodiketopiperazine-based CCR5 antagonists: Lead optimization from biologically active metabolite
2006
·
Rena Nishizawa
, Toshihiko Nishiyama
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
47
Development of a highly selective EP2-receptor agonist. Part 1: identification of 16-hydroxy-17,17-trimethylene PGE2 derivatives
2002
·
Kousuke Tani
, Atsushi Naganawa
, et al.
·
Bioorganic & Medicinal Chemistry
·
22
Discovery of orally available spirodiketopiperazine-based CCR5 antagonists
2010
·
Rena Nishizawa
, Toshihiko Nishiyama
, et al.
·
Bioorganic & Medicinal Chemistry
·
18
Spirodiketopiperazine-based CCR5 antagonists: Improvement of their pharmacokinetic profiles
2009
·
Rena Nishizawa
, Toshihiko Nishiyama
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
17
Development of a highly selective EP2-receptor agonist. Part 2: identification of 16-Hydroxy-17,17-trimethylene 9β-chloro PGF derivatives
2002
·
Kousuke Tani
, Atsushi Naganawa
, et al.
·
Bioorganic & Medicinal Chemistry
·
16
Discovery of 4-[4-({(3R)-1-butyl-3-[(R)-cyclohexyl(hydroxy)methyl]-2,5-dioxo-1,4,9-triazaspiro[5.5]undec-9-yl}methyl)phenoxy]benzoic acid hydrochloride: A highly potent orally available CCR5 selective antagonist
2011
·
Rena Nishizawa
, Toshihiko Nishiyama
, et al.
·
Bioorganic & Medicinal Chemistry
·
11
Spirodiketopiperazine-based CCR5 antagonist: Discovery of an antiretroviral drug candidate
2010
·
Rena Nishizawa
, Toshihiko Nishiyama
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
9
Inhibitory effects of prostaglandin E1.ALPHA.-cyclodextrin (PGE1CD) on dimethylnitrosamine-induced acute liver damage in rats.
1995
·
Akihiko SUZUKI
, Masaichiro HAGINO
, et al.
·
Folia Pharmacologica Japonica
·
5
PDF
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Works count:
15
Citation count:
781
H-index:
11
I10-index:
12
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