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Hiroyuki Kakinuma
Observed names:
H. KAKINUMA,
H. Kakinuma,
Hiroyuki KAKINUMA
Institution:
Taisho Pharmaceutical (Japan)
Observed institutions:
Tokyo Institute of Technology,
Taisho Pharmaceutical (Japan),
Japan Tobacco (Japan),
Eisai (Japan),
Yokohama City University,
University of Sheffield
show all 6
ORCID:
0000-0002-2490-2530
Observed ORCID:
0000-0002-2490-2530
OpenAlex ID:
A5038079325
(1 S )-1,5-Anhydro-1-[5-(4-ethoxybenzyl)-2-methoxy-4-methylphenyl]-1-thio- d -glucitol (TS-071) is a Potent, Selective Sodium-Dependent Glucose Cotransporter 2 (SGLT2) Inhibitor for Type 2 Diabetes Treatment
2010
·
Hiroyuki Kakinuma
, Takahiro Oi
, et al.
·
Journal of Medicinal Chemistry
·
163
Development of a Method for Evaluating Drug-Likeness and Ease of Synthesis Using a Data Set in Which Compounds Are Assigned Scores Based on Chemists' Intuition
2003
·
Yuji Takaoka
, Yutaka Endo
, et al.
·
Journal of Chemical Information and Computer Sciences
·
99
Pyrazole and Isoxazole Derivatives as New, Potent, and Selective 20-Hydroxy-5,8,11,14-eicosatetraenoic Acid Synthase Inhibitors
2003
·
Toshio Nakamura
, Masakazu Sato
, et al.
·
Journal of Medicinal Chemistry
·
78
Imidazole derivatives as new potent and selective 20-HETE synthase inhibitors
2003
·
Toshio Nakamura
, Hiroyuki Kakinuma
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
69
In vitro abzyme evolution to optimize antibody recognition for catalysis
2001
·
Naoko Takahashi
, Hiroyuki Kakinuma
, et al.
·
Nature Biotechnology
·
65
Synthesis and Antifungal Activity of Novel Thiazole-Containing Triazole Antifungals. II. Optically Active ER-30346 and Its Derivatives.
1998
·
Akihiko TSURUOKA
, Yumiko KAKU
, et al.
·
Chemical and Pharmaceutical Bulletin
·
50
PDF
Synthesis and Antifungal Activity of Novel Thiazole-Containing Triazole Antifungals.
1997
·
Akihiko TSURUOKA
, Yumiko KAKU
, et al.
·
Chemical and Pharmaceutical Bulletin
·
35
PDF
A Novel Route for Chiral Synthesis of the Triazole Antifungal ER-30346.
1998
·
Yumiko KAKU
, Akihiko TSURUOKA
, et al.
·
Chemical and Pharmaceutical Bulletin
·
30
PDF
Discovery of Aryloxyphenyl–Heptapeptide Hybrids as Potent and Selective Matrix Metalloproteinase-2 Inhibitors for the Treatment of Idiopathic Pulmonary Fibrosis
2022
·
Tomoki Takeuchi
, Masato Hayashi
, et al.
·
Journal of Medicinal Chemistry
·
27
Discovery of TP0597850: A Selective, Chemically Stable, and Slow Tight-Binding Matrix Metalloproteinase-2 Inhibitor with a Phenylbenzamide–Pentapeptide Hybrid Scaffold
2023
·
Tomoki Takeuchi
, Yusaku Nomura
, et al.
·
Journal of Medicinal Chemistry
·
23
Design and synthesis of 1H-pyrazolo[3,4-c]pyridine derivatives as a novel structural class of potent GPR119 agonists
2016
·
Daisuke Matsuda
, Yohei Kobashi
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
20
Selective chemotherapeutic strategies using catalytic antibodies: a common pro-moiety for antibody-directed abzyme prodrug therapy
2002
·
Hiroyuki Kakinuma
, Ikuo Fujii
, et al.
·
Journal of Immunological Methods
·
20
Novel 3H-[1,2,3]triazolo[4,5-c]pyridine derivatives as GPR119 agonists: Synthesis and structure-activity/solubility relationships
2017
·
Daisuke Matsuda
, Yohei Kobashi
, et al.
·
Bioorganic & Medicinal Chemistry
·
18
Improved generation of catalytic antibodies by MRL/MPJ-lpr/lpr autoimmune mice
2000
·
Naoko Takahashi
, Hiroyuki Kakinuma
, et al.
·
Journal of Immunological Methods
·
17
Discovery of potent, low-absorbable sodium-dependent glucose cotransporter 1 (SGLT1) inhibitor SGL5213 for type 2 diabetes treatment
2018
·
Shoichi Kuroda
, Yohei Kobashi
, et al.
·
Bioorganic & Medicinal Chemistry
·
16
Efficient screening for catalytic antibodies using a short transition‐state analog and detailed characterization of selected antibodies
1999
·
Naoko Takahashi
, Hiroyuki Kakinuma
, et al.
·
European Journal of Biochemistry
·
16
PDF
Comparison of phosphonate transition state analogs for inducing catalytic antibodies and evaluation of key structural factors by an ab initio study
1999
·
Hiroyuki Kakinuma
, Kazuko Shimazaki
, et al.
·
Tetrahedron
·
15
Glycosyltransfer mechanism of α-glucosyltransferase from Protaminobacter rubrum
1998
·
Hiroyuki Kakinuma
, Hideya Yuasa
, et al.
·
Carbohydrate Research
·
15
Discovery of a potent, low-absorbable sodium-dependent glucose cotransporter 1 (SGLT1) inhibitor (TP0438836) for the treatment of type 2 diabetes
2018
·
Shoichi Kuroda
, Yohei Kobashi
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
14
High-resolution Crystal Structure of the Fab-fragments of a Family of Mouse Catalytic Antibodies with Esterase Activity
2003
·
Sergey N. Ruzheinikov
, Tatyana A. Muranova
, et al.
·
Journal of Molecular Biology
·
14
Discovery of novel 2-[(4-hydroxy-6-oxo-2,3-dihydro-1H-pyridine-5-carbonyl)amino]acetic acid derivatives as HIF prolyl hydroxylase inhibitors for treatment of renal anemia
2018
·
Makoto Hamada
, Tetsuo Takayama
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
13
Design, synthesis and biological evaluation of novel 7-azaspiro[3.5]nonane derivatives as GPR119 agonists
2018
·
Daisuke Matsuda
, Madoka Kawamura
, et al.
·
Bioorganic & Medicinal Chemistry
·
13
Structure–activity relationships of novel piperazines as antagonists for the melanocortin-4 receptor
2006
·
Dai Nozawa
, Taketoshi Okubo
, et al.
·
Bioorganic & Medicinal Chemistry
·
13
Lead identification of novel tetrahydroimidazo[1,2-a]pyridine-5-carboxylic acid derivative as a potent heparanase-1 inhibitor
2022
·
Yudai Imai
, Daisuke Wakasugi
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
12
Directed evolution governed by controlling the molecular recognition between an abzyme and its haptenic transition–state analog
2004
·
Naoko Takahashi-Ando
, Hiroyuki Kakinuma
, et al.
·
Journal of Immunological Methods
·
10
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Works count:
55
Citation count:
947
H-index:
16
I10-index:
26
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