نتایج جستجو برای: epothilones

تعداد نتایج: 208  

Journal: :Organic letters 2005
Tanja Gaich Johann Mulzer

[reaction: see text] A short synthesis of epothilone B and D is reported. The key step for generating the C12-13-trisubstituted Z-double bond uses a ring-closing metathesis reaction of a disiloxane to form a nine-membered silicon-tethered ring.

2014
Hong Zhang Fan An Li Tang Rongguo Qiu

The epothilones are a class of microtubule inhibitors that exhibit a strong antitumor activity. UTD2 is a novel epothilone analog generated by genetic manipulation of the polyketide biosynthetic gene cluster. This study investigated the effects of UTD2 on the actin cytoskeleton and its critical regulators, and the signaling pathways which are essential for cell motility, growth and survival in ...

Journal: :Chembiochem : a European journal of chemical biology 2001
K C Nicolaou K Namoto J Li A Ritzén T Ulven M Shoji D Zaharevitz R Gussio D L Sackett R D Ward A Hensler T Fojo P Giannakakou

With some members in clinical trials, the epothilones command attention as potential anticancer agents of considerable promise. In addition to several naturally occurring substances, an impressive array of epothilone analogues has been constructed and biologically evaluated. 2] We have previously reported the apartialo construction of two 12,13-cyclopropyl epothilone A analogues. Their structur...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 1998
T C Chou X G Zhang A Balog D S Su D Meng K Savin J R Bertino S J Danishefsky

A new class of 16-membered macrolides, the epothilones (Epos), has been synthesized and evaluated for antitumor potential in vitro and in vivo. Recent studies in these and other laboratories showed that epothilones and paclitaxel (paclitaxel) share similar mechanisms of action in stabilizing microtubule arrays as indicated by binding-displacement studies, substitution for paclitaxel in paclitax...

Journal: :Proceedings of the National Academy of Sciences 2001

Journal: :DEStech Transactions on Engineering and Technology Research 2018

Journal: :Clinical cancer research : an official journal of the American Association for Cancer Research 2000
L A Martello H M McDaid D L Regl C P Yang D Meng T R Pettus M D Kaufman H Arimoto S J Danishefsky A B Smith S B Horwitz

Recently, three natural products have been identified, the epothilones, eleutherobin, and discodermolide, whose mechanism of action is similar to that of Taxol in that they stabilize microtubules and block cells in the mitotic phase of the cell cycle. In this report, we have compared and contrasted the effects of these new agents in Taxol-sensitive and -resistant cell lines. We also have taken ...

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