Synthesis and antitumor activity of <i>N</i>-acylhydrazones from betulin diacetate

Author:

Myasoyedova Yu. V.1,Belyaeva E. R1,Ishmuratova N. M1,Ishmetova D. V2,Vakhitov V. A2,Ishmuratov G. Yu.1

Affiliation:

1. Ufa Institute of Chemistry, Ufa Federal Research Center, Russian Academy of Sciences

2. Institute of Biochemistry and Genetics, Ufa Federal Research Center, Russian Academy of Sciences

Abstract

Eight new N -acylhydrazones were synthesized from betulin diacetate by its low-temperature ozonolysis to obtain 3β,3,28-diacetoxyoxy-20-oxo-29-norlupan and condensation of the latter with hydrazides of aliphatic and aromatic acids. Cytotoxic activity of the obtained compounds in relation to a number of tumor cells was studied in vitro . Derivatives obtained by condensation of 3β,3,28-diacetoxy-20-oxo-29-norlupan with hydrazides of salicylic, isonicotinic and nicotinic acids showed moderate activity against cell lines of human hepatocellular carcinoma HepG2, human colon cancer HTC-116, leukemia THP-1, acute T-cell leukemia Jurkat.

Publisher

The Russian Academy of Sciences

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