1991
DOI: 10.1021/jm00115a027
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Antineoplastic agents. 219. Isolation and structure of the cell growth inhibitory constituents from the western Pacific marine sponge Axinella sp

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Cited by 175 publications
(60 citation statements)
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“…Critical to any research application of the screen is the remarkably high degree of reproducibility of the screening proflle of a given compound tested repetitively over time (6,13,27). (38,(45)(46)(47)54). Samples of the compounds were provided by George R. Pettit for study in the NCI screen.…”
mentioning
confidence: 99%
“…Critical to any research application of the screen is the remarkably high degree of reproducibility of the screening proflle of a given compound tested repetitively over time (6,13,27). (38,(45)(46)(47)54). Samples of the compounds were provided by George R. Pettit for study in the NCI screen.…”
mentioning
confidence: 99%
“…18 During the 1990s, the US National Cancer Institute led attempts at aquaculture, but these were ultimately unsuccessful. 19 The total synthesis of halichondrin B was achieved by Kishi and colleagues at Harvard in 1992, and Eisai, a Japanese pharmaceutical company, began testing it as an anticancer agent. 20 Biological activity was shown to reside in the macrocyclic lactone C1-C8 moiety, located on the right half of the molecule.…”
Section: Preclinical Development Discovery and Synthesismentioning
confidence: 99%
“…Il fallut attendre 1989 pour line et y détecte une puissante activité antitumorale. Une nouvelle récolte de 220 kg d'éponges est effectuée en 1985, mais ce n'est qu'en 1991 que sont réalisées la purification et l'identification des deux composés actifs (Homohalichondrine B et Halichondrine B), présents à très faibles concentrations [20]. En 1986, D. Uemura et Y. Hirata avaient déjà isolé, à partir de 600 kg de Halichondria okadai (Halichondridae), plusieurs composés cytotoxiques similaires qu'ils avaient nommés halichondrines.…”
Section: Les Halichondrinesunclassified