Sequoiatones A and B: Novel antitumor metabolites isolated from a redwood endophyte

Citation
Aa. Stierle et al., Sequoiatones A and B: Novel antitumor metabolites isolated from a redwood endophyte, J ORG CHEM, 64(15), 1999, pp. 5479-5484
Citations number
16
Categorie Soggetti
Chemistry & Analysis","Organic Chemistry/Polymer Science
Journal title
JOURNAL OF ORGANIC CHEMISTRY
ISSN journal
00223263 → ACNP
Volume
64
Issue
15
Year of publication
1999
Pages
5479 - 5484
Database
ISI
SICI code
0022-3263(19990723)64:15<5479:SAABNA>2.0.ZU;2-J
Abstract
Sequoiatones A and B were isolated from the fungus Aspergillus parasiticus, an endophytic fungus of the coast redwood, Sequoia sempervirens. The compo unds were isolated from the methanol extract of the mycelial mat of the fun gus when grown in liquid culture for 21 days. The compounds were isolated b ecause of their brine shrimp lethality, which served as an excellent guide for chromatographic purification. Full details of the isolation and charact erization of sequoiatones A and B are provided herein, along with the test results from the NCI human tumor 60 cell-line screen.