The total synthesis of 22-(3-azidobenzoyloxy)methyl epothilone C is described as a potential photoaffinity probe to elucidate the β-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
Epothilones are a new class of microtubule depolymerization inhibitors, which inhibit the growth of ...
Deaza-epothilone C, which incorporates a thiophene moiety in place of the thiazole heterocycle in th...
AbstractBackground: The epothilones are natural substances that are potently cytotoxic, having an al...
The total synthesis of 22-(3-azidobenzoyloxy)methyl epothilone C is described as a potential photoaf...
Three photaffinity labeled derivatives of epothilone D were prepared by total synthesis, using effic...
Photoaffinity labeling with an epothilone A photoprobe led to the identification of the β-tubulin pe...
This is the peer reviewed version of the following article: Entwistle, R. A., Rizk, R. S., Cheng, D....
A green fluorescent 12-aza-epothilone (azathilone) derivative has been prepared through the attachme...
Epothilones are macrocyclic bacterial natural products with potent microtubule-stabilizing and antip...
The preparation and biological evaluation of a novel series of dimeric epothilone A derivatives (1-6...
26 p.-6 fig.2 tab.12-Aza-epothilones (azathilones) incorporating quinoline side chains and bearing ...
36 p.-6 fig.+ 9 p.-2 fig.-4 tab. (support. inf.)The binding of epothilones to dimeric tubulin and to...
AbstractThe potent epothilone tubulin polymerization promoters have been studied extensively by synt...
Microtubule ligands such as taxanes and epothilones have emerged as broadly applied chemotherapeutic...
12-Aza-epothilones (azathilones) incorporating quinoline side chains and bearing different N12-subst...
Epothilones are a new class of microtubule depolymerization inhibitors, which inhibit the growth of ...
Deaza-epothilone C, which incorporates a thiophene moiety in place of the thiazole heterocycle in th...
AbstractBackground: The epothilones are natural substances that are potently cytotoxic, having an al...
The total synthesis of 22-(3-azidobenzoyloxy)methyl epothilone C is described as a potential photoaf...
Three photaffinity labeled derivatives of epothilone D were prepared by total synthesis, using effic...
Photoaffinity labeling with an epothilone A photoprobe led to the identification of the β-tubulin pe...
This is the peer reviewed version of the following article: Entwistle, R. A., Rizk, R. S., Cheng, D....
A green fluorescent 12-aza-epothilone (azathilone) derivative has been prepared through the attachme...
Epothilones are macrocyclic bacterial natural products with potent microtubule-stabilizing and antip...
The preparation and biological evaluation of a novel series of dimeric epothilone A derivatives (1-6...
26 p.-6 fig.2 tab.12-Aza-epothilones (azathilones) incorporating quinoline side chains and bearing ...
36 p.-6 fig.+ 9 p.-2 fig.-4 tab. (support. inf.)The binding of epothilones to dimeric tubulin and to...
AbstractThe potent epothilone tubulin polymerization promoters have been studied extensively by synt...
Microtubule ligands such as taxanes and epothilones have emerged as broadly applied chemotherapeutic...
12-Aza-epothilones (azathilones) incorporating quinoline side chains and bearing different N12-subst...
Epothilones are a new class of microtubule depolymerization inhibitors, which inhibit the growth of ...
Deaza-epothilone C, which incorporates a thiophene moiety in place of the thiazole heterocycle in th...
AbstractBackground: The epothilones are natural substances that are potently cytotoxic, having an al...