Intravenous administration of N-(beta-alanyl-L-leucyl-L-alanyl-L-leucyl)doxorubicin (4) induces an acute toxic reaction, killing animals in a few minutes. This results from its positive charge at physiological pH combined with its propensity to form large aggregates in aqueous solutions. Negatively charged N-capped versions of 4 such as the succinyl derivative 5 can be administered by the iv route at more than 10 times the LD(50) of doxorubicin without inducing the acute toxic reaction, and they are active in vivo
Three derivatives of doxorubicin (DOX) were prepared by modifying DOX with succinic anhydride, cisac...
The reversible PEGylation endows antitumor drugs with various fascinating advantages, including prol...
International audienceThe first self-immolative dendritic glucuronide prodrug of doxorubicin was stu...
Oligopeptidic derivatives of anthracyclines unable to penetrate cells were prepared and screened for...
The search for cancer therapies that are more selective for tumor cells and spare normal sensitive c...
Doxorubicin toxicity is generally accepted to be free radical-mediated. N-Substituted dehydroalanine...
A number of lipophilic 14-substituted derivatives of doxorubicin were synthesized through conjugatio...
A pH-sensitive doxorubicin (Dox) prodrug was prepared, and its release in vitro and distribution in ...
Recently, studies on the effects of non-toxic substances on cancer prophylaxis have gained value as ...
In this study, we synthesized the valine (Val)-conjugated amide prodrug of doxorubicin (DOX) by the ...
N4-Dipeptidyl slow-release forms of the anticancer drug ara-C were prepared by acylation of the lith...
Co-delivery of siRNAs and chemotherapeutic drugs to kill tumors have achieved superior tumor growth ...
Design of a new drug entity is usually preceded by analysis of quantitative structure activity (prop...
The acute and chronic cardiotoxicity and cytotoxicity of the novel doxorubicin (DXR) derivative 4'-a...
Doxorubicin (DOX) is a very effective anticancer agent. However, in its pure form, its application i...
Three derivatives of doxorubicin (DOX) were prepared by modifying DOX with succinic anhydride, cisac...
The reversible PEGylation endows antitumor drugs with various fascinating advantages, including prol...
International audienceThe first self-immolative dendritic glucuronide prodrug of doxorubicin was stu...
Oligopeptidic derivatives of anthracyclines unable to penetrate cells were prepared and screened for...
The search for cancer therapies that are more selective for tumor cells and spare normal sensitive c...
Doxorubicin toxicity is generally accepted to be free radical-mediated. N-Substituted dehydroalanine...
A number of lipophilic 14-substituted derivatives of doxorubicin were synthesized through conjugatio...
A pH-sensitive doxorubicin (Dox) prodrug was prepared, and its release in vitro and distribution in ...
Recently, studies on the effects of non-toxic substances on cancer prophylaxis have gained value as ...
In this study, we synthesized the valine (Val)-conjugated amide prodrug of doxorubicin (DOX) by the ...
N4-Dipeptidyl slow-release forms of the anticancer drug ara-C were prepared by acylation of the lith...
Co-delivery of siRNAs and chemotherapeutic drugs to kill tumors have achieved superior tumor growth ...
Design of a new drug entity is usually preceded by analysis of quantitative structure activity (prop...
The acute and chronic cardiotoxicity and cytotoxicity of the novel doxorubicin (DXR) derivative 4'-a...
Doxorubicin (DOX) is a very effective anticancer agent. However, in its pure form, its application i...
Three derivatives of doxorubicin (DOX) were prepared by modifying DOX with succinic anhydride, cisac...
The reversible PEGylation endows antitumor drugs with various fascinating advantages, including prol...
International audienceThe first self-immolative dendritic glucuronide prodrug of doxorubicin was stu...