Journal of Organic Chemistry 2008-01-18

Synthesis and evaluation of derrubone and select analogues.

Jedidiah M Hastings, M Kyle Hadden, Brian S J Blagg

文献索引:J. Org. Chem. 73(2) , 369-73, (2008)

全文:HTML全文

摘要

Recently, we reported that the natural product derrubone exhibits Hsp90 inhibitory activity. Due to its unique architectural scaffold and proposed rapid assembly, the synthesis of this natural product was pursued with the aim of identifying structure--activity relationships. Synthesis of the natural product was accomplished in eight highly convergent steps, which led to a facile method for the construction of related compounds. Biological evaluation of derrubone and its analogues identified several compounds that exhibit low micromolar inhibitory activity against breast and colon cancer cell lines.


相关化合物

  • 3,4-亚甲二氧基苯乙...

相关文献:

Enzymatic nitrile hydrolysis catalyzed by nitrilase ZmNIT2 from maize. An unprecedented ß-hydroxy functionality enhanced amide formation. Mukherjee C, et al.

[Tetrahedron 62(26) , 6150-54, (2006)]

Seized methamphetamine samples with unique profiles of stable nitrogen isotopic composition documented by stable isotope ratio mass spectrometry. Iwata YT, et al.

[Forensic Toxicol. 28(2) , 119-123, (2010)]

更多文献...