We describe the preparation of a series of hybrid molecules containing a combretastatin A-4 moiety and a pironetin analogue fragment linked by an ester spacer of variable length. The cytotoxic activities of these compounds have been measured and the relationship between the structure and cytotoxicity is discussed. Some of the tested compounds showed cytotoxicity values of the same order of magnitude as those of the parental molecules, combretastatin A-4 and pironetin, and were less toxic than the latter for normal cells
The preparation of several new truncated analogues of the natural dihydropyrone pironetin is describ...
The preparation of four new analogues of the natural pyrone pironetin, known to bind to α-tubulin, i...
Thirteen methylpyrazoline analogs (1a-m) of combretastatin A-4 (CA-4, 2) were synthesized. The trans...
We here describe the preparation of a series of hybrid molecules containing a combretastatin A-4 moi...
We describe the preparation of a series of hybrid molecules containing a combretastatin A-4 moiety a...
We here report an investigation of the interactions with tubulin of two types of molecules of a hybr...
We here report the synthesis of a series of 12 hybrid molecules composed of a colchicine moiety and ...
The preparation of four new lipophilic analogues of the natural pyrone pironetin is described. The n...
We here report the synthesis of a series of 12 hybrid molecules composed of a colchicine moiety and ...
The preparation of a series of pironetin analogues with simplified structure is described. Their cyt...
We here report the synthesis of a series of 12 hybrid molecules composed of a colchicine moiety and ...
A series of new analogs of combretastatin A-4 (CA-4, 1) with the A or B-ring replaced by a 3-oxo-2,3...
A new series of combretastatin analogues with B-ring modifications were synthesized and evaluated fo...
ombretastatin derivs., such as I [R1, R2, R3, R4 = H, OH, OMe, OCH2O, NO2, F, Cl, Br, OPO3H2, OCH2OP...
The stereospecific synthesis of nine trans-combretastatin analogs (5 - 13) is described. The trans g...
The preparation of several new truncated analogues of the natural dihydropyrone pironetin is describ...
The preparation of four new analogues of the natural pyrone pironetin, known to bind to α-tubulin, i...
Thirteen methylpyrazoline analogs (1a-m) of combretastatin A-4 (CA-4, 2) were synthesized. The trans...
We here describe the preparation of a series of hybrid molecules containing a combretastatin A-4 moi...
We describe the preparation of a series of hybrid molecules containing a combretastatin A-4 moiety a...
We here report an investigation of the interactions with tubulin of two types of molecules of a hybr...
We here report the synthesis of a series of 12 hybrid molecules composed of a colchicine moiety and ...
The preparation of four new lipophilic analogues of the natural pyrone pironetin is described. The n...
We here report the synthesis of a series of 12 hybrid molecules composed of a colchicine moiety and ...
The preparation of a series of pironetin analogues with simplified structure is described. Their cyt...
We here report the synthesis of a series of 12 hybrid molecules composed of a colchicine moiety and ...
A series of new analogs of combretastatin A-4 (CA-4, 1) with the A or B-ring replaced by a 3-oxo-2,3...
A new series of combretastatin analogues with B-ring modifications were synthesized and evaluated fo...
ombretastatin derivs., such as I [R1, R2, R3, R4 = H, OH, OMe, OCH2O, NO2, F, Cl, Br, OPO3H2, OCH2OP...
The stereospecific synthesis of nine trans-combretastatin analogs (5 - 13) is described. The trans g...
The preparation of several new truncated analogues of the natural dihydropyrone pironetin is describ...
The preparation of four new analogues of the natural pyrone pironetin, known to bind to α-tubulin, i...
Thirteen methylpyrazoline analogs (1a-m) of combretastatin A-4 (CA-4, 2) were synthesized. The trans...