DEVELOPMENT OF TDPI INHIBITORS BASED ON DERIVATIVES OF CHROMENE AS POTENTIAL ANTI-CANCER DRUGS



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About the authors

A. A Chepanova

Novosibirsk Institute of Chemical Biology and Fundamental Medicine, SBRAS

Email: arinachepanova@mail.ru
Russian Federation, Novosibirsk

N. S Li-Zhulanov

N. N. Vorozhtsov Novosibirsk Institute of Organic Chemistry, SBRAS; Novosibirsk State University

Russian Federation, Novosibirsk

T. A Kurgina

Novosibirsk Institute of Chemical Biology and Fundamental Medicine, SBRAS

Russian Federation, Novosibirsk

A. L Zakharenko

Novosibirsk Institute of Chemical Biology and Fundamental Medicine, SBRAS

Russian Federation, Novosibirsk

O. D Zakharova

Novosibirsk Institute of Chemical Biology and Fundamental Medicine, SBRAS

Russian Federation, Novosibirsk

K. P Volcho

N. N. Vorozhtsov Novosibirsk Institute of Organic Chemistry, SBRAS; Novosibirsk State University

Russian Federation, Novosibirsk

N. F Salakhutdinov

N. N. Vorozhtsov Novosibirsk Institute of Organic Chemistry, SBRAS; Novosibirsk State University

Russian Federation, Novosibirsk

O. I Lavrik

Novosibirsk Institute of Chemical Biology and Fundamental Medicine, SBRAS; Novosibirsk State University

Russian Federation, Novosibirsk

References

  1. Interthal H et al., The tyrosyl-DNA phosphodiesterase Tdp1 is a member of the phospholipase D superfamily. Proc Natl Acad Sci U S A. 2001;98(21):12009-14.
  2. Kamaletdinova T et al., The Enigmatic Function of PARP1: From PARylation Activity to PAR Readers. Cells. 2019; 8(12),1625;
  3. Li-Zhulanov et al., A Novel Class of Tyrosyl-DNA Phosphodiesterase 1 Inhibitors That Contains the Octahydro-2H-chromen-4-ol Scaffold. Molecules, 2018, 23(10), 2468;

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