Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Svetlana V. Vorona"'
Publikováno v:
ACS Omega, Vol 9, Iss 30, Pp 33000-33010 (2024)
Externí odkaz:
https://doaj.org/article/c8d26fd35d4e4249b09523e9bea272b6
Publikováno v:
ACS omega. 7(47)
P-glycoprotein (P-gp) is found to be of considerable interest for the design of drugs capable of treating chemoresistant tumors. This transporter is an interesting target for which an efficient approach has not yet been developed in terms of computer
Publikováno v:
Chemistry of Heterocyclic Compounds. 57:224-233
The review summarizes the advances in medicinal chemistry of tetrazole biologically active compounds and drugs over the past 15 years. Most of the considered compounds are at present actively studied, are in various stages of clinical trials, or have
Autor:
Tatyana A. Grigoreva, Aleksandra V. Sagaidak, Svetlana V. Vorona, Daria S. Novikova, Vyacheslav G. Tribulovich
Publikováno v:
ACS medicinal chemistry letters. 13(12)
Since the problem of transporter-mediated multidrug resistance of tumor cells is becoming increasingly important in cancer therapy, it is necessary to modulate the activity of efflux transporters of the ABC family, among which P-glycoprotein is the b
Publikováno v:
ChemistrySelect. 4:10846-10850
Autor:
Angelina Romanova, Vyacheslav G. Tribulovich, Svetlana V. Vorona, Aleksandra Sagaidak, Daria S. Novikova, Tatyana A. Grigoreva
Publikováno v:
Bioorganicmedicinal chemistry letters. 30(18)
Chemoresistance is thought to be the cause of low treatment efficacy and mortality in more than 90% of patients with advanced cancer. The activation of drug efflux by P-glycoprotein is the key mechanism of resistance. All known P-gp inhibitors are us
Autor:
Maxim Gureev, Vyacheslav G. Tribulovich, Svetlana V. Vorona, Daria S. Novikova, Tatyana A. Grigoreva, A. V. Garabadzhiu
Publikováno v:
Journal of computer-aided molecular design. 34(1)
Targeting of MDM2-p53 protein–protein interaction is a current approach for the development of potent anticancer agents. The classical pharmacophore hypothesis for the design of such molecules describes the three point binding of a small molecule i