Ryohei Kato - Concepedia

Author

Ryohei Kato

Mitsubishi Group (Japan)

Also Known As

R Kato, R. KATO, R. Kato, Ryohei KATO, Ryohei Kato

Publications

750

Citations

H-Index

Concepts

All Affiliations

Mitsubishi Group (Japan)The University of Tokyo Japan Science and Technology Agency Mitsubishi Chemical (Japan)University of Shizuoka

About

Ryohei Kato is an author at Mitsubishi Group (Japan) specializing in natural sciences, biochemistry, and biomolecular engineering.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Natural Sciences	6	6	192
2	Biochemistry	6	6	192
3	Biomolecular Engineering	5	5	181
4	Medicine	4	4	163
5	Engineering	3	3	66

Ryohei Kato

Publications

716

Citations

H-Index

Page 1

	Year	Citations
A Potent Human Immunodeficiency Virus Type 1 Protease Inhibitor, UIC-94003 (TMC-126), and Selection of a Novel (A28S) Mutation in the Protease Active Site Kazuhisa Yoshimura, Ryohei Kato, Mark F. Kavlick, Journal of Virology	2002	137
JE-2147: A dipeptide protease inhibitor (PI) that potently inhibits multi-PI-resistant HIV-1 Kazuhisa Yoshimura, Ryohei Kato, Keisuke Yusa, Proceedings of the National Academy of Sciences	1999	108
Structure−Activity Relationship of Small-Sized HIV Protease Inhibitors Containing Allophenylnorstatine Tsutomu Mimoto, Ryohei Kato, Haruo Takaku, Journal of Medicinal Chemistry Protease InhibitorsMedicinal ChemistryBioorganic ChemistryBiochemistryStructure−activity Relationship	1999	70
Synthesis of unnatural alkaloid scaffolds by exploiting plant polyketide synthase Hiroyuki Morita, Makoto Yamashita, Shepo Shi, Proceedings of the National Academy of Sciences	2011	68
Structural basis for the one-pot formation of the diarylheptanoid scaffold by curcuminoid synthase from <i>Oryza sativa</i> Hiroyuki Morita, Kiyofumi Wanibuchi, Hirohiko Nii, Proceedings of the National Academy of Sciences	2010	56
A structure-based mechanism for benzalacetone synthase from <i>Rheum palmatum</i> Hiroyuki Morita, Yoshihiko Shimokawa, Michikazu Tanio, Proceedings of the National Academy of Sciences	2009	49
Structure-Activity Relationship of Orally Potent Tripeptide-Based HIV Protease Inhibitors Containing Hydroxymethylcarbonyl Isostere. Tsutomu Mimoto, Naoko Hattori, Haruo Takaku, Chemical and Pharmaceutical Bulletin Bioorganic ChemistryPharmacotherapyAntiviral DrugMedicinal ChemistryStructure-activity Relationship Study	2000	45
Cloning and Structure-Function Analyses of Quinolone- and Acridone-producing Novel Type III Polyketide Synthases from Citrus microcarpa Takahiro Mori, Yoshihiko Shimokawa, Takashi Matsui, Journal of Biological Chemistry BiosynthesisEngineeringBiotransformationBiocatalysisStructure-function Analyses	2013	37
Expression, purification and crystallization of a human tau-tubulin kinase 2 that phosphorylates tau protein Michiko Kitano-Takahashi, Hiroyuki Morita, Shin Kondo, Acta Crystallographica Section F Structural Biology and Crystallization Communications	2007	37
KNI-577, a Potent Small-Sized HIV Protease Inhibitor Based on the Dipeptide Containing the Hydroxymethylcarbonyl Isostere as an Ideal Transition-State Mimic Yoshiaki Kiso, Satoshi Yamaguchi, Hikaru Matsumoto, Archiv der Pharmazie Bioorganic ChemistryHiv Protease InhibitorsMolecular BiologyIdeal Transition-state MimicAntiviral Drug	1998	33

Page 1