Journal of Medicinal Chemistry 1975-11-01

A lapachol derivative active against mouse lymphocytic leukemia P-388.

M da Consolação, F Linardi, M M de Oliveira, M R Sampaio

Index: J. Med. Chem. 18(11) , 1159-61, (1975)

Full Text: HTML

Abstract

Lapachol [2-hydroxy-3-(3-methyl-2-butenyl)-1,4-naphthoquinone] and its analogs [2-(3,7-dimethyl-2,6-octadienyl)-3-hydroxy-1,4-naphthoquinone and 2-(3,3-dibromo-2-propenyl)-3-hydroxy-1,4-naphthoquinone] have been described, among almost a hundred synthesized analogs, as active against rat tumor Walker 256 carcinosarcoma. The acetylglucosylation of lapachol results in a compound which extends lapachol activity becoming effective against mouse lymphocytic leukemia P-388. When mice inoculated with 10(6) leukemic cells were treated with the drug during 9 days, their life span increased 80% over the control animals. Identification spectral data (uv, ir, 1H NMR, and MS) of the compound obtained by synthesis are given.

Related Compounds

Structure Name/CAS No. Articles
5-Chloro-2-thiophenecarbaldehyde Structure 5-Chloro-2-thiophenecarbaldehyde
CAS:7283-96-7