Modified 5-fluorouracil: Uridine phosphorylase inhibitor


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Resumo

5-Fluorouracil (5-FU) is a medication widely used in chemotherapy to treat various types of cancer. Being a substrate for the reverse reaction catalyzed by uridine phosphorylase (UPase), 5-FU serves as a promising prototype molecule (molecular scaffold) for the design of a selective UPase inhibitor that enhances the antitumor activity of 5-FU and exhibits intrinsic cytostatic effects on cancer cells. The chemical formula of the new compound, which binds to the uracil-binding site and, in the presence of a phosphate anion, to the phosphate-binding site of UPase, is proposed and investigated by molecular simulation methods.

Sobre autores

A. Lashkov

Shubnikov Institute of Crystallography of Federal Scientific Research Centre “Crystallography and Photonics”

Autor responsável pela correspondência
Email: alashkov83@gmail.com
Rússia, Leninskii pr. 59, Moscow, 119333

A. Shchekotikhin

Gause Institute of New Antibiotics

Email: alashkov83@gmail.com
Rússia, ul. Bol’shaya Pirogovskaya 11, Moscow, 119021

A. Shtil

Blokhin Russian Cancer Research Center

Email: alashkov83@gmail.com
Rússia, Kashirskoe sh. 23, Moscow, 115478

S. Sotnichenko

Shubnikov Institute of Crystallography of Federal Scientific Research Centre “Crystallography and Photonics”

Email: alashkov83@gmail.com
Rússia, Leninskii pr. 59, Moscow, 119333

A. Mikhailov

Shubnikov Institute of Crystallography of Federal Scientific Research Centre “Crystallography and Photonics”

Email: alashkov83@gmail.com
Rússia, Leninskii pr. 59, Moscow, 119333

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