noThe duocarmycins belong to a class of agent that has fascinated scientists for over four decades. Their exquisite potency, unique mechanism of action, and efficacy in multidrug-resistant tumour models makes them attractive to medicinal chemists and drug hunters. However, despite great advances in fine-tuning biological activity through structure-activity relationship studies (SARS), no duocarmycin-based therapeutic has reached clinical approval. In this review, we provide an overview of the most promising strategies currently used and include both tumour-targeted prodrug approaches and antibody-directed technologies
: Antibody-drug conjugates (ADCs) constitute a relatively new group of anticancer agents, whose firs...
Herkömmliche Zytostatika greifen vornehmlich in den Zellzyklus ein und somit werden Zellen mit hoher...
ABSTRACT Cancer is one of the leading causes of death worldwide. With the increase in life expectanc...
The duocarmycins and (+)-CC-1065 are amongst the most potent antitumour antibiotics discovered to da...
Synthetic analogues of the DNA-alkylating cytotoxins of the duocarmycin class have been extensively ...
It is accepted that neoplastic diseases are related to gene alteration or oncogene activation. In pa...
The duocarmycins are a family of natural products first described in 1978 with the discovery of CC-1...
While the global cancer burden is still high with 10 million people being diagnosed with cancer and ...
Antibody–drug conjugates (ADCs) that are currently on the market or in clinical trials are predomina...
The CC-1065 and duocarmycin family of compounds are ultrapotent antitumour antibiotics which demonst...
Background: Dual-targeting in cancer treatment by a single drug is an unconventional approach in rel...
The duocarmycins are potent antitumor agents with potential for use in the development of antibody–d...
The duocarmycins are potent antitumor agents with potential for use in the development of antibody–d...
A library of duocarmycin bioprecursors based on the CPI and CBI scaffolds was synthesized and used t...
The series of four dimers derived from head to tail coupling of the two enantiomers of the duocarmyc...
: Antibody-drug conjugates (ADCs) constitute a relatively new group of anticancer agents, whose firs...
Herkömmliche Zytostatika greifen vornehmlich in den Zellzyklus ein und somit werden Zellen mit hoher...
ABSTRACT Cancer is one of the leading causes of death worldwide. With the increase in life expectanc...
The duocarmycins and (+)-CC-1065 are amongst the most potent antitumour antibiotics discovered to da...
Synthetic analogues of the DNA-alkylating cytotoxins of the duocarmycin class have been extensively ...
It is accepted that neoplastic diseases are related to gene alteration or oncogene activation. In pa...
The duocarmycins are a family of natural products first described in 1978 with the discovery of CC-1...
While the global cancer burden is still high with 10 million people being diagnosed with cancer and ...
Antibody–drug conjugates (ADCs) that are currently on the market or in clinical trials are predomina...
The CC-1065 and duocarmycin family of compounds are ultrapotent antitumour antibiotics which demonst...
Background: Dual-targeting in cancer treatment by a single drug is an unconventional approach in rel...
The duocarmycins are potent antitumor agents with potential for use in the development of antibody–d...
The duocarmycins are potent antitumor agents with potential for use in the development of antibody–d...
A library of duocarmycin bioprecursors based on the CPI and CBI scaffolds was synthesized and used t...
The series of four dimers derived from head to tail coupling of the two enantiomers of the duocarmyc...
: Antibody-drug conjugates (ADCs) constitute a relatively new group of anticancer agents, whose firs...
Herkömmliche Zytostatika greifen vornehmlich in den Zellzyklus ein und somit werden Zellen mit hoher...
ABSTRACT Cancer is one of the leading causes of death worldwide. With the increase in life expectanc...