Back to Search Start Over

Total synthesis and evaluation of 22-(3-azidobenzoyloxy)methyl epothilone C for photoaffinity labeling of beta-tubulin.

Authors :
Hutt OE
Inagaki J
Reddy BS
Nair SK
Reiff EA
Henri JT
Greiner JF
VanderVelde DG
Chiu TL
Amin EA
Himes RH
Georg GI
Source :
Bioorganic & medicinal chemistry letters [Bioorg Med Chem Lett] 2009 Jun 15; Vol. 19 (12), pp. 3293-6. Date of Electronic Publication: 2009 Apr 22.
Publication Year :
2009

Abstract

The total synthesis of 22-(3-azidobenzoyloxy)methyl epothilone C is described as a potential photoaffinity probe to elucidate the beta-tubulin binding site. A sequential Suzuki-aldol-Yamaguchi macrolactonization strategy was utilized employing a novel derivatized C1-C6 fragment. The C22-functionalized analog exhibited good activity in microtubule assembly assays, but cytotoxicity was significantly reduced. Molecular modeling simulations indicated that excessive steric bulk in the C22 position is accommodated by the large hydrophobic pocket of the binding site. Photoaffinity labeling studies were inconclusive suggesting non-specific labeling.

Details

Language :
English
ISSN :
1464-3405
Volume :
19
Issue :
12
Database :
MEDLINE
Journal :
Bioorganic & medicinal chemistry letters
Publication Type :
Academic Journal
Accession number :
19428248
Full Text :
https://doi.org/10.1016/j.bmcl.2009.04.077