A landmark in drug discovery based on complex natural product synthesis

Despite their outstanding antitumour activity in mice, the limited supply from the natural sources has prevented drug discovery/development based on intact halichondrins. We achieved a total synthesis of C52-halichondrin-B amine (E7130) on a >10 g scale with >99.8% purity under GMP conditions....

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Detalles Bibliográficos
Autores principales: Kawano, Satoshi, Ito, Ken, Yahata, Kenzo, Kira, Kazunobu, Abe, Takanori, Akagi, Tsuyoshi, Asano, Makoto, Iso, Kentaro, Sato, Yuki, Matsuura, Fumiyoshi, Ohashi, Isao, Matsumoto, Yasunobu, Isomura, Minetaka, Sasaki, Takeo, Fukuyama, Takashi, Miyashita, Yusuke, Kaburagi, Yosuke, Yokoi, Akira, Asano, Osamu, Owa, Takashi, Kishi, Yoshito
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6572832/
https://www.ncbi.nlm.nih.gov/pubmed/31209263
http://dx.doi.org/10.1038/s41598-019-45001-9

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6572832/
https://www.ncbi.nlm.nih.gov/pubmed/31209263
http://dx.doi.org/10.1038/s41598-019-45001-9

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