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Naoya Ono
Institution:
Taisho Pharmaceutical (Japan)
Observed institutions:
Tokyo Institute of Technology,
Taisho Pharmaceutical (Japan),
The University of Texas Southwestern Medical Center
OpenAlex ID:
A5111421399
Amelioration of Collagen-Induced Arthritis by a Novel S1P1 Antagonist with Immunomodulatory Activities
2011
·
Yasuyuki Fujii
, Takehiro Hirayama
, et al.
·
The Journal of Immunology
·
61
PDF
Palladiurn( 0 )-catalysed transfer hydrogenation of alkynes to cis-alkenes with HCO 2 H–NEt 3
1993
·
Kousuke Tani
, Naoya Ono
, et al.
·
Journal of the Chemical Society Chemical Communications
·
48
Eicosanoid Regulation of Vascular Endothelial Growth Factor Expression and Angiogenesis in Microvessel Endothelial Cells
2002
·
Alexander Mezentsev
, Francesca Seta
, et al.
·
Journal of Biological Chemistry
·
38
20-Hydroxyeicosatetraenoic acid (20-HETE): structural determinants for renal vasoconstriction
2003
·
Ming Yu
, Magdalena Alonso-Galicia
, et al.
·
Bioorganic & Medicinal Chemistry
·
32
A highly practical synthesis of natural PGE1, Δ2-trans-PGE1 and 2,2,3,3-tetradehydro-PGE1 via two-component coupling process using zinc-copper reagents
1990
·
Hiromi Tsujiyama
, Naoya Ono
, et al.
·
Tetrahedron Letters
·
32
Effects of TS-022, a newly developed prostanoid DP1 receptor agonist, on experimental pruritus, cutaneous barrier disruptions and atopic dermatitis in mice
2006
·
Iwao Arai
, Akiko Takaoka
, et al.
·
European Journal of Pharmacology
·
20
5-(1,3-Benzothiazol-6-yl)-4-(4-methyl-1,3-thiazol-2-yl)-1H-imidazole derivatives as potent and selective transforming growth factor-β type I receptor inhibitors
2012
·
Hideaki Amada
, Yoshinori Sekiguchi
, et al.
·
Bioorganic & Medicinal Chemistry
·
18
Radical Addition Reactions to Allylstannanes Having Substituents at C-1. Highly Efficient Synthesis of Enantiomerically Pure .alpha.-Alkylcyclopentenones, the Key Component for Synthesis of Prostaglandins by the Two-Component Coupling Process
1994
·
Yukio Yoshida
, Naoya Ono
, et al.
·
The Journal of Organic Chemistry
·
17
Blocking S1P interaction with S1P1 receptor by a novel competitive S1P1-selective antagonist inhibits angiogenesis
2012
·
Yasuyuki Fujii
, Yasuji Ueda
, et al.
·
Biochemical and Biophysical Research Communications
·
16
Design, synthesis, and evaluation of novel 4-thiazolylimidazoles as inhibitors of transforming growth factor-β type I receptor kinase
2012
·
Hideaki Amada
, Yoshinori Sekiguchi
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
16
Conversion of allyl alk-2-ynoates to alk-2-ynoic acids using morpholine and palladium(0)-bis(diphenylphosphino)alkane catalyst; synthesis of 2,2,3,3-tetradehydro PGE1
1994
·
Sentaro Okamoto
, Naoya Ono
, et al.
·
Journal of the Chemical Society Chemical Communications
·
14
Lymphopenia induced by a novel selective S1P1 antagonist structurally unrelated to S1P
2011
·
Yasuyuki Fujii
, Hidenori Ohtake
, et al.
·
Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids
·
13
A highly efficient approach to prostaglandins via radical addition of α side-chains to methylenecyclopentanones. Total synthesis of natural PGE1, limaprost and new prostaglandin derivatives.
1993
·
Naoya Ono
, Yukio Yoshida
, et al.
·
Tetrahedron Letters
·
11
Synthesis of a key intermediate for preparation of 4,5-didehydro prostaglandins containing an allenyl side-chain group via two-component coupling process. Synthesis of enprostil
1994
·
Naoya Ono
, Yasufumi Kawanaka
, et al.
·
Journal of the Chemical Society Chemical Communications
·
10
Synthesis and structure–activity relationships of a new class of selective EP3 receptor agonist, 13,14-didehydro-16-phenoxy analogues of prostaglandin E1
2000
·
Youichi Shimazaki
, Kazuya Kameo
, et al.
·
Bioorganic & Medicinal Chemistry
·
9
A new efficient synthesis of the biologically potent PGD2-analogue ZK118182
1992
·
Sentaro Okamoto
, Satoshi Katayama
, et al.
·
Tetrahedron Asymmetry
·
8
Synthesis and pharmacological activities of 13-Dehydro derivatives of primary prostaglandins
1998
·
Tohru Tanami
, Kazuya Kameo
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
6
Synthesis of the key component for preparation of 6-ketoprostaglandins by a two-component coupling process: synthesis of 6-keto-prostaglandin E 1 , ornoprostil and Δ 2 -trans-6-ketoprostaglandin E 1
1996
·
Yasufumi Kawanaka
, Naoya Ono
, et al.
·
Journal of the Chemical Society Perkin Transactions 1
·
6
Synthesis of Allyl Ester of Prostaglandin E and the Conversion of the Allyl Ester Moiety into Carboxylic Acid by Chemical Method. A Highly Practical Synthesis of Natural PGE1 and Limaprost
1992
·
Naoya Ono
, Mie Tsuboi
, et al.
·
Chemistry Letters
·
4
PDF
Abstract 1357: A Novel Prostaglandin E2 Receptor EP4-Selective Agonist Attenuates Inflammatory Activation of Macrophages in vitro and in vivo
2006
·
Kiyoshi Takayama
, Yasuo Asano
, et al.
·
Circulation
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Works count:
20
Citation count:
379
H-index:
12
I10-index:
14
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