S
Suresh Panthee
Researcher at Teikyo University
Publications - 58
Citations - 815
Suresh Panthee is an academic researcher from Teikyo University. The author has contributed to research in topics: Staphylococcus aureus & Antimicrobial. The author has an hindex of 13, co-authored 50 publications receiving 546 citations. Previous affiliations of Suresh Panthee include University of Tokyo & Tribhuvan University.
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Journal ArticleDOI
Reveromycin A biosynthesis uses RevG and RevJ for stereospecific spiroacetal formation.
Shunji Takahashi,Atsushi Toyoda,Yasuyo Sekiyama,Hiroshi Takagi,Toshihiko Nogawa,Masakazu Uramoto,Ryuichiro Suzuki,Hiroyuki Koshino,Takuto Kumano,Suresh Panthee,Tohru Dairi,Jun Ishikawa,Haruo Ikeda,Yoshiyuki Sakaki,Hiroyuki Osada +14 more
TL;DR: This work comprehensively describes the spiroacetal formation involved in the biosynthesis of reveromycin A, which inhibits bone resorption and bone metastases of tumor cells by inducing apoptosis in osteoclasts and provides insights into the creation of a variety of biologically active spiro acetal compounds for drug leads.
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Lysobacter species: a potential source of novel antibiotics.
Suresh Panthee,Suresh Panthee,Hiroshi Hamamoto,Hiroshi Hamamoto,Atmika Paudel,Atmika Paudel,Kazuhisa Sekimizu,Kazuhisa Sekimizu +7 more
TL;DR: The structural diversity, activity and biosynthesis of lysobacterial antibiotics are summarized and the importance of Lysobacter species for antibiotic production is highlighted.
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Advantages of the Silkworm As an Animal Model for Developing Novel Antimicrobial Agents
TL;DR: It is proposed that the utilization of silkworm infection model will facilitate the discovery of novel therapeutically effective antimicrobial agents, and the silkworm antibiotic screening model is very effective for identifying novel antibiotics.
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Development of a high-throughput strategy for discovery of potent analogues of antibiotic lysocin E
Hiroaki Itoh,Kotaro Tokumoto,Takuya Kaji,Atmika Paudel,Suresh Panthee,Hiroshi Hamamoto,Kazuhisa Sekimizu,Masayuki Inoue +7 more
TL;DR: A high-throughput one-bead-on-compound method for the synthesis and screening lysocin E derivatives, with several hits being more active than the parent compound, to efficiently decipher biologically crucial residues and identify potentially useful agents for the treatment of infectious diseases.
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Unified Total Synthesis of Polyoxins J, L, and Fluorinated Analogues on the Basis of Decarbonylative Radical Coupling Reactions.
Haruka Fujino,Masanori Nagatomo,Atmika Paudel,Suresh Panthee,Hiroshi Hamamoto,Kazuhisa Sekimizu,Masayuki Inoue +6 more
TL;DR: The unified total synthesis of 1’a, 1 b, and their artificial analogues 1c and 1d with trifluorothymine and fluorouracil structures with high applicability was reported.