The preparation and biological evaluation of a novel series of dimeric camptothecin derivatives are described. All the new compounds showed a significant ability to inhibit human tumor cell growth with IC50 values ranging from 0.03 to 12.2 ?M. The interference with the activity of the nuclear enzymes topoisomerases has been demonstrated, highlighting the poison effect of one of the obtained byproducts toward topoisomerase I. A moderate antiangiogenic activity has been demonstrated for one of the obtained compounds. Moreover, the effects of four new compounds on caspases activity and ROS generation have been studied on transgenic mouse cell
Despite that 9-substituted camptothecins are promising candidates in cancer therapy, the limited acc...
The design, modeling, synthesis and biological activity evaluation of two hybrid agents formed by 7-...
Despite that 9-substituted camptothecins are promising candidates in cancer therapy, the limited acc...
The preparation and biological evaluation of a novel series of dimeric camptothecin derivatives are ...
In an attempt to synthesize potential anticancer agents acting by inhibition of topoisomerase I (Top...
Camptothecins are cytotoxic agents with a wide spectrum of antitumor activity. The unique mechanism ...
The natural alkaloid camptothecin is the lead compound of a new class of antitumor agents with a uni...
A series of novel 9-substituted camptothecins derived from 9-formylcamptothecin were synthesized. T...
DNA topoisomerase I is recognised as a useful target for antitumour therapy. Camptothecin is the pro...
Twelve novel 20-sulfonylamidine derivatives (9a-9l) of camptothecin (1) were synthesized via a Cu-ca...
[[abstract]]Two compounds having a camptothecin(CPT) analog conjugated to the 4 beta-amino-4'-O deme...
*S Supporting Information ABSTRACT: Twelve novel 20-sulfonylamidine derivatives (9a−9l) of camptothe...
[[abstract]]Two compounds having a camptothecin(CPT) analog conjugated to the 4 beta-amino-4'-O deme...
The design, modeling, synthesis and biological activity evaluation of two hybrid agents formed by 7-...
A number of derivatives of camptothecin with a polyamine chain linked to position 7 of camptothecin ...
Despite that 9-substituted camptothecins are promising candidates in cancer therapy, the limited acc...
The design, modeling, synthesis and biological activity evaluation of two hybrid agents formed by 7-...
Despite that 9-substituted camptothecins are promising candidates in cancer therapy, the limited acc...
The preparation and biological evaluation of a novel series of dimeric camptothecin derivatives are ...
In an attempt to synthesize potential anticancer agents acting by inhibition of topoisomerase I (Top...
Camptothecins are cytotoxic agents with a wide spectrum of antitumor activity. The unique mechanism ...
The natural alkaloid camptothecin is the lead compound of a new class of antitumor agents with a uni...
A series of novel 9-substituted camptothecins derived from 9-formylcamptothecin were synthesized. T...
DNA topoisomerase I is recognised as a useful target for antitumour therapy. Camptothecin is the pro...
Twelve novel 20-sulfonylamidine derivatives (9a-9l) of camptothecin (1) were synthesized via a Cu-ca...
[[abstract]]Two compounds having a camptothecin(CPT) analog conjugated to the 4 beta-amino-4'-O deme...
*S Supporting Information ABSTRACT: Twelve novel 20-sulfonylamidine derivatives (9a−9l) of camptothe...
[[abstract]]Two compounds having a camptothecin(CPT) analog conjugated to the 4 beta-amino-4'-O deme...
The design, modeling, synthesis and biological activity evaluation of two hybrid agents formed by 7-...
A number of derivatives of camptothecin with a polyamine chain linked to position 7 of camptothecin ...
Despite that 9-substituted camptothecins are promising candidates in cancer therapy, the limited acc...
The design, modeling, synthesis and biological activity evaluation of two hybrid agents formed by 7-...
Despite that 9-substituted camptothecins are promising candidates in cancer therapy, the limited acc...