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N-Succinyl-(beta-alanyl-L-leucyl-L-alanyl-L-leucyl)doxorubicin: an extracellularly tumor-activated prodrug devoid of intravenous acute toxicity.

Authors :
UCL
Fernandez, A M
Van Derpoorten, K
Dasnois, L
Lebtahi, K
Dubois, Vincent
Lobl, T J
Gangwar, S
Oliyai, C
Lewis, E R
Shochat, D
Trouet, André
UCL
Fernandez, A M
Van Derpoorten, K
Dasnois, L
Lebtahi, K
Dubois, Vincent
Lobl, T J
Gangwar, S
Oliyai, C
Lewis, E R
Shochat, D
Trouet, André
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