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J Med Chem ; 18(11): 1159-61, 1975 Nov.
Article in English | MEDLINE | ID: mdl-1177264

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.


Subject(s)
Antineoplastic Agents/chemical synthesis , Leukemia, Experimental/drug therapy , Naphthoquinones/chemical synthesis , Animals , Antineoplastic Agents/therapeutic use , Carcinoma 256, Walker/drug therapy , Mice , Mice, Inbred C57BL , Mice, Inbred DBA , Naphthoquinones/therapeutic use , Rats
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