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Kazunari Nakao · SciRah

Researcher profile · Semantic Scholar

Kazunari Nakao

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Kazunari Nakao — researcher profile on SciRah

h-index: 12
Works: 35
Citations: 468

Most-cited papers

CJ-023,423, a Novel, Potent and Selective Prostaglandin EP4 Receptor Antagonist with Antihyperalgesic Properties
Kazunari Nakao, A. Murase, Hiroyuki Ohshiro, Takako Okumura +6 more
2007Journal of Pharmacology and Experimental Therapeutics118 citations
Semantic Scholar
Effect of prostanoid EP4 receptor antagonist, CJ-042,794, in rat models of pain and inflammation.
A. Murase, Takako Okumura, Ayano Sakakibara, Hiroko Tonai-Kachi +2 more
2008European Journal of Pharmacology53 citations
Semantic Scholar
Novel imidazole compounds as a new series of potent, orally active inhibitors of 5-lipoxygenase.
T. Mano, R. Stevens, K. Ando, Kazunari Nakao +5 more
2003Bioorganic & Medicinal Chemistry45 citations
Semantic Scholar
Efficient synthesis of [6-chloro-2-(4-chlorobenzoyl)-1H-indol-3-yl]-acetic acid, a novel COX-2 inhibitor.
S. Caron, E. Vazquez, R. Stevens, Kazunari Nakao +2 more
2003Journal of Organic Chemistry44 citations
Semantic Scholar
In vitro pharmacological characterization of CJ-042794, a novel, potent, and selective prostaglandin EP(4) receptor antagonist.
A. Murase, Yasuhito Taniguchi, Hiroko Tonai-Kachi, Kazunari Nakao +1 more
2008Life Science40 citations
Semantic Scholar
The novel Nrf2 inducer TFM‐735 ameliorates experimental autoimmune encephalomyelitis in mice
Chika Higashi, Atsuko Kawaji, Naoto Tsuda, M. Hayashi +8 more
2017European Journal of Pharmacology37 citations
Semantic Scholar
Optimization of imidazole 5-lipoxygenase inhibitors and selection and synthesis of a development candidate.
T. Mano, R. Stevens, K. Ando, M. Kawai +7 more
2005Chemical and pharmaceutical bulletin21 citations Open access
Semantic Scholar
A synthesis of the tetraene fragment of calyculins as its antipodal form
J. Matsubara, Kazunari Nakao, Y. Hamada, T. Shioiri
199219 citations
Semantic Scholar
Discovery of AAT-008, a novel, potent, and selective prostaglandin EP4 receptor antagonist.
Y. Okumura, T. Yamagishi, S. Nukui, Kazunari Nakao
2017Bioorganic & Medicinal Chemistry Letters18 citations Open access
Semantic Scholar
Pharmacological characterization of a novel potent, selective, and orally active phosphodiesterase 10A inhibitor, PDM‐042 [(E)‐4‐(2‐(2‐(5,8‐dimethyl‐[1,2,4]triazolo[1,5‐a]pyrazin‐2‐yl)vinyl)‐6‐(pyrrolidin‐1‐yl)pyrimidin‐4‐yl)morpholine] in rats: potential for the treatment of schizophrenia
Keita Arakawa, S. Maehara, Natsuko Yuge, M. Ishikawa +4 more
2016Pharmacology Research & Perspectives15 citations Open access
Semantic Scholar
Pharmacological separation between peripheral and central functions of cyclooxygenase-2 with CIAA, a novel cyclooxygenase-2 inhibitor.
Takako Okumura, Y. Murata, M. Hizue, Tomomi Matsuura +6 more
2006European Journal of Pharmacology13 citations
Semantic Scholar
Discovery of novel aminobenzisoxazole derivatives as orally available factor IXa inhibitors.
Isao Sakurada, Toshiya Endo, K. Hikita, Tomokazu Hirabayashi +18 more
2017Bioorganic & Medicinal Chemistry Letters12 citations Open access
Semantic Scholar
Synthesis of 2-acylindole-3-acetic acids: a novel base-mediated indole synthesis
Kazunari Nakao, Y. Murata, Hiroki Koike, Chikara Uchida +4 more
200311 citations
Semantic Scholar
Total Synthesis of Avellanins A and B, New Fungal Metabolites from Hamigera avellanea with Pressor Effect
Kazunari Nakao, Y. Hamada, T. Shioiri
19897 citations Open access
Semantic Scholar
Dopamine D1 signaling involvement in the effects of the phosphodiesterase 10A inhibitor, PDM‐042 on cognitive function and extrapyramidal side effect in rats
Keita Arakawa, Kazunari Nakao, S. Maehara
2017Behavioural Brain Research5 citations
Semantic Scholar
Characterization of Binding Affinity of CJ-023,423 for Human Prostanoid EP4 Receptor
A. Murase, Kazunari Nakao, Junji Takada
2008Pharmacology5 citations
Semantic Scholar
Efficient Synthesis of 4-(3-Fluoro-5-{[4-(2-methyl-1H-imidazol-1-yl)benzyl]oxy}phenyl)tetrahydro-2H-pyran-4-carboxamide, a Novel 5-Lipoxygenase Inhibitor
T. Mano, R. Stevens, Kazunari Nakao, Y. Okumura +3 more
20044 citations
Semantic Scholar
Pharmacological characterization of a novel potent, selective, and orally active phosphodiesterase 2A inhibitor, PDM-631.
S. Maehara, Keita Arakawa, K. Hoshida, Hiroshi Nagasue +3 more
2017European Journal of Pharmacology2 citations
Semantic Scholar
Synthesis of 2‐Acylindole‐3‐acetic Acids: A Novel Base‐Mediated Indole Synthesis.
Kazunari Nakao, Y. Murata, Hiroki Koike, C. Uchida +4 more
20031 citations
Semantic Scholar
(1) Immunopharmacological Characterization of Potent, Selective and Orally Available RORγt Inhibitors for Treatment of Autoimmune Diseases
J. Masuda, T. Takeuchi, Chinatsu Tomizawa, Atsuko Kawaji +6 more
20150 citations Open access
Semantic Scholar
N-sulfonylaminofeniletil-2-phenoxyacetamide substituted compounds.
T. Hanazawa, Misato Hirano, Tadashi Inoue, Satoshi Nahayama +3 more
20060 citations
Semantic Scholar
N-substituted-2-sulfonylaminophenylethyl phenoxyacetamidverbindungen
T. Hanazawa, Misato Hirano, Tadashi Inoue, Satoshi Nahayama +3 more
20060 citations
Semantic Scholar
Composes a base de n-sulfonylaminophenylethyl-2-phenoxy acetamide substitues
T. Hanazawa, Misato Hirano, Tadashi Inoue, S. Nagayama +3 more
20060 citations
Semantic Scholar
aryl or heteroarylamidverbindungen ortho-substituted
Hiroki Koike, Yuka Matsumoto, T. Yamagishi, Y. Okumura +1 more
20050 citations
Semantic Scholar
Aryl compounds heteroaryl amide ortho.
Hiroki Koike, Yuka Matsumoto, Kazunari Nakao, Y. Okumura +1 more
20050 citations
Semantic Scholar
Substituted N-sulfonylaminobenzyl-2-phenoxyacetamidverbindungen
Tadashi Inoue, S. Nagayama, Kazunari Nakao
20050 citations
Semantic Scholar
Composes methylaryl- ou heteroarylamides substitues
Hiroki Koike, Yuka Matsumoto, T. Yamagishi, K. Kon-i +2 more
20050 citations
Semantic Scholar
Efficient Synthesis of 4‐(3‐Fluoro‐5‐{ [4‐(2‐methyl‐1H‐imidazol‐1‐yl)benzyl] oxy}phenyl)tetrahydro‐2H‐pyran‐4‐carboxamide, a Novel 5‐Lipoxygenase Inhibitor.
T. Mano, W. StevensRodney, Kazunari Nakao, Y. Okumura +3 more
20050 citations
Semantic Scholar
Substituted methylaryl- or heteroarylamideverbindingen.
Hiroki Koike, Yuka Matsumoto, T. Yamagishi, K. Kana +2 more
20050 citations
Semantic Scholar
Composes de n-sulfonylaminobenzyl-2-phenoxy acetamide substitue
Tadashi Inoue, S. Nagayama, Kazunari Nakao
20050 citations
Semantic Scholar
Sammenföjede aryl or heteroaryl compounds as anti-inflammatory and analgesic agents
Naomi Uneo, Kazunari Nakao, Y. Okumura, Miyako Matsumizu +7 more
20010 citations
Semantic Scholar
Tetrazolylalkylindol compounds as anti-inflammatory and analgesic agents
Kazunari Nakao, R. Stevens
20000 citations
Semantic Scholar
Biciclocarbonil indole compounds as anti-inflammatory / analgesic agents and as inhibitors of cox-2.
S. Hayashi, R. Stevens, Kazunari Nakao
20000 citations
Semantic Scholar
Tetrazolylalkyl-indole derivatives as anti-inflammatory and analgesic agents
Kazunari Nakao, R. Stevens
20000 citations
Semantic Scholar
2,3-substituted indole compounds as inhibitors of cox-2.
Kazunari Nakao, W. Stevens, K. Kawamura, C. Uchida +2 more
19980 citations
Semantic Scholar

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Y. Okumura×11
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Y. Okumura — researcher profile on SciRah
R. Stevens×8
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Hiroki Koike×8
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Hiroki Koike — researcher profile on SciRah
K. Kawamura×6
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×5

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A. Murase — researcher profile on SciRah

Takako Okumura×5

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T. Yamagishi×5

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Tadashi Inoue×5

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Tadashi Inoue — researcher profile on SciRah

Junji Takada×4

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Junji Takada — researcher profile on SciRah

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T. Mano — researcher profile on SciRah

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Yuka Matsumoto×4

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