Satoshi Niizuma - Concepedia

Author

Satoshi Niizuma

Hokkaido University

Also Known As

S. NIIZUMA, Satoshi Niizuma

Publications

462

Citations

H-Index

Concepts

All Affiliations

Hokkaido University Chugai Pharma (United States)

About

Satoshi Niizuma is an author at Hokkaido University specializing in drug discovery, medicine, and pharmacology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	6	6	230
2	Biomolecular Engineering	5	5	392
3	Engineering	2	2	294
4	Natural Sciences	2	2	73
5	Biochemistry	1	1	18

Satoshi Niizuma

Publications

459

Citations

H-Index

Page 1

	Year	Citations
Catalytic asymmetric synthesis of axially chiral biaryls by palladium-catalyzed enantioposition-selective cross-coupling. Tamio Hayashi, Satoshi Niizuma, Takashi Kamikawa, Journal of the American Chemical Society Catalytic Asymmetric SynthesisCross-coupling ReactionEngineeringChiral BiarylsAltmetric Attention Score	1995	196
Design and synthesis of novel benzofurans as a new class of antifungal agents targeting fungal N-myristoyltransferase. Part 3 Ken‐ichi Kawasaki, Miyako Masubuchi, Kenji Morikami, Bioorganic & Medicinal Chemistry Letters BiosynthesisBioorganic ChemistryEngineeringAntifungal AgentAntifungal Agents	2003	98
One-Pot Conversion of α,β-Unsaturated Alcohols into the Corresponding Carbon-Elongated Dienes with a Stable Phosphorus Ylide−BaMnO<sub>4</sub> System. Synthesis of 6‘-Methylene Derivatives of Neplanocin A as Potential Antiviral Nucleosides. New Neplanocin Analogues. 11<sup>1</sup> Satoshi Shuto, Satoshi Niizuma, Akira Matsuda The Journal of Organic Chemistry Bioorganic ChemistryCorresponding Carbon-elongated DienesNatural SciencesMedicineAltmetric Attention Score	1998	55
New Neplanocin Analogues. 12. Alternative Synthesis and Antimalarial Effect of (6‘<i>R</i>)-6‘-<i>C</i>-Methylneplanocin A, a Potent AdoHcy Hydrolase Inhibitor Satoshi Shuto, Noriaki Minakawa, Satoshi Niizuma, Journal of Medicinal Chemistry	2002	33
New neplanocin analogues. 10. The conversion of adenosine to neplanocin A, a carbocyclic nucleoside antibiotic with potent antiviral activity Satoshi Niizuma, Satoshi Shuto, Akira Matsuda Tetrahedron Medicinal ChemistryMedicineDrug DiscoveryAntiviral Drug DevelopmentPotent Antiviral Activity	1997	27
Synthesis and biological activities of a pH-dependently activated water-soluble prodrug of a novel hexacyclic camptothecin analog Jun Ohwada, Sawako Ozawa, Masami Kohchi, Bioorganic & Medicinal Chemistry Letters Medicinal ChemistryPharmaceutical ScienceBiochemistryNatural SciencesMedicine	2009	18
A water soluble prodrug of a novel camptothecin analog is efficacious against breast cancer resistance protein-expressing tumor xenografts Mika Endo, Masanori Miwa, Masako Ura, Cancer Chemotherapy and Pharmacology Water Soluble ProdrugMedicineNovel Camptothecin AnalogBreast CancerTumor Targeting	2009	16
Synthesis of new camptothecin analogs with improved antitumor activities Satoshi Niizuma, Masao Tsukazaki, Hitomi Suda, Bioorganic & Medicinal Chemistry Letters Medicinal ChemistryMedicineNew Camptothecin AnalogsAnti-cancer AgentPharmacology	2009	16

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