Potent and selective inhibitors of glutathione S-transferase omega 1 that impair cancer drug resistance
…, V Fernandez-Vega, P Hodder, H Rosen…
Index: Tsuboi, Katsunori; Bachovchin, Daniel A.; Speers, Anna E.; Spicer, Timothy P.; Fernandez-Vega, Virneliz; Hodder, Peter; Rosen, Hugh; Cravatt, Benjamin F. Journal of the American Chemical Society, 2011 , vol. 133, # 41 p. 16605 - 16616
Full Text: HTML
Citation Number: 36
Abstract
Glutathione S-transferases (GSTs) are a superfamily of enzymes that conjugate glutathione to a wide variety of both exogenous and endogenous compounds for biotransformation and/or removal. Glutathione S-tranferase omega 1 (GSTO1) is highly expressed in human cancer cells, where it has been suggested to play a role in detoxification of chemotherapeutic agents. Selective inhibitors of GSTO1 are, however, required to test the ...
Related Articles:
[Adamczyk, Maciej; Fishpaugh, Jeffrey R.; Heuser, Kevin J.; Ramp, John M.; Reddy, Rajarathnam E.; Wong, Martin Tetrahedron, 1998 , vol. 54, # 13 p. 3093 - 3112]
[Gavande, Navnath; Kim, Hye-Lim; Doddareddy, Munikumar R.; Johnston, Graham A. R.; Chebib, Mary; Hanrahan, Jane R. ACS Medicinal Chemistry Letters, 2013 , vol. 4, # 4 p. 402 - 407]