Zobrazeno 1 - 10
of 263
pro vyhledávání: '"Hideo Kigoshi"'
Publikováno v:
ACS Omega, Vol 4, Iss 5, Pp 8598-8613 (2019)
Externí odkaz:
https://doaj.org/article/b59bd02160604b189e54b31cccdbee9d
Autor:
Haruna Ebisu, Kana Shintani, Takumi Chinen, Yoko Nagumo, Shuya Shioda, Taisei Hatanaka, Akira Sakakura, Ichiro Hayakawa, Hideo Kigoshi, Takeo Usui
Publikováno v:
Frontiers in Pharmacology, Vol 11 (2021)
α/β-Tubulin inhibitors that alter microtubule (MT) dynamics are commonly used in cancer therapy, however, these inhibitors also cause severe side effects such as peripheral neuropathy. γ-Tubulin is a possible target as antitumor drugs with low sid
Externí odkaz:
https://doaj.org/article/538758ef14db4b708215884f46c3aa3d
Autor:
Takayuki Ohyoshi, Yiwen Zhao, Kei Akemoto, Takuma Ishihara, Ayaka Taniguchi, Menghua Zhang, Hideo Kigoshi
Publikováno v:
Bulletin of the Chemical Society of Japan. 95:1242-1249
Publikováno v:
Journal of Natural Products. 85:2082-2089
Publikováno v:
Journal of Natural Products. 85:1850-1860
A structure revision of trichomide D has been achieved by its total synthesis. The sterically hindered peptide sequence was successfully prepared using not only a conventional amidation with EDCI but also coupling with an Fmoc-protected amino acid ch
Publikováno v:
Organic Letters. 24:4635-4639
A strategy for constructing a tricyclo[4.3.1.0
Autor:
Hideo Kigoshi
Publikováno v:
Journal of Synthetic Organic Chemistry, Japan. 80:70-73
Publikováno v:
Bulletin of the Chemical Society of Japan. 94:1922-1930
The total synthesis of the piperazic acid-containing antibiotic cyclic peptide, hytramycin V, has been achieved. Unexpected cleavage of the peptide bond was observed during the synthesis of a penta...
Publikováno v:
Supramolecular Chemistry. 33:194-201
New squalene receptors bearing open-chain polyether ligands (SQ-diEG, SQ-triEG, SQ-tetraEG) were synthesised. The stoichiometries and association constants (Ka) for the interactions between these squalene receptors and representative alkaline earth m
Publikováno v:
Bulletin of the Chemical Society of Japan. 94:1179-1184
Aplysiasecosterol A, a 9,11-secosteroid, has a unique tricyclic γ-diketone skeleton including a hemiacetal. The concise and efficient synthesis of the tricyclic core was developed by using pseudo-d...