Back to Search
Start Over
N-Succinyl-(beta-alanyl-L-leucyl-L-alanyl-L-leucyl)doxorubicin: an extracellularly tumor-activated prodrug devoid of intravenous acute toxicity.
- Source :
- Journal of medicinal chemistry, Vol. 44, no. 22, p. 3750-3 (2001)
- Publication Year :
- 2001
-
Abstract
- 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.
Details
- Database :
- OAIster
- Journal :
- Journal of medicinal chemistry, Vol. 44, no. 22, p. 3750-3 (2001)
- Notes :
- English
- Publication Type :
- Electronic Resource
- Accession number :
- edsoai.on1130585826
- Document Type :
- Electronic Resource