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Activity of 2-aryl-2-(3-indolyl)acetohydroxamates against drug-resistant cancer cells

Authors :
Aksenov, Alexander A.V.
Smirnov, Alexander A.N.
Aksenov, Nicolai N.A.
Aksenova, Inna I.V.
Magedov, Igor I.V.
Reisenauer, Mary Rose
Pendleton, Alexander A.L.
Nguyen, Gina
Johnston, Robert
Rogelj, Snezna
Frolova, Liliya V
Rubin, Michael
De Carvalho, Annelise
Kiss, Robert
Mathieu, Véronique
Lefranc, Florence
Correa, Jaime
Kornienko, Alexander
Cavazos, David D.A.
Brenner, Andrew A.J.
Bryan, Brad B.A.
Aksenov, Alexander A.V.
Smirnov, Alexander A.N.
Aksenov, Nicolai N.A.
Aksenova, Inna I.V.
Magedov, Igor I.V.
Reisenauer, Mary Rose
Pendleton, Alexander A.L.
Nguyen, Gina
Johnston, Robert
Rogelj, Snezna
Frolova, Liliya V
Rubin, Michael
De Carvalho, Annelise
Kiss, Robert
Mathieu, Véronique
Lefranc, Florence
Correa, Jaime
Kornienko, Alexander
Cavazos, David D.A.
Brenner, Andrew A.J.
Bryan, Brad B.A.
Source :
Journal of medicinal chemistry, 58 (5
Publication Year :
2015

Abstract

Many types of tumor, including glioma, melanoma, non-small cell lung, esophageal, and head and neck cancer, among others, are intrinsically resistant to apoptosis induction and poorly responsive to current therapies with proapoptotic agents. In addition, tumors often develop multidrug resistance based on the cellular efflux of chemotherapeutic agents. Thus, novel anticancer agents capable of overcoming these intrinsic or developed tumor resistance mechanisms are urgently needed. We describe a series of 2-aryl-2-(3-indolyl)acetohydroxamic acids that are active against apoptosis-and multidrug-resistant cancer cells as well as glioblastoma neurosphere stemlike cell cultures derived from patients. Thus, the described compounds serve as a novel chemical scaffold for the development of potentially highly effective clinical cancer drugs.<br />SCOPUS: ar.j<br />info:eu-repo/semantics/published

Details

Database :
OAIster
Journal :
Journal of medicinal chemistry, 58 (5
Notes :
No full-text files, English
Publication Type :
Electronic Resource
Accession number :
edsoai.ocn908368315
Document Type :
Electronic Resource