Acridones circumvent P-glycoprotein-associated multidrug resistance (MDR) in cancer cells
VS Gopinath, P Thimmaiah, KN Thimmaiah
Index: Gopinath, Vadiraj S.; Thimmaiah, Padma; Thimmaiah, Kuntebommanahalli N. Bioorganic and Medicinal Chemistry, 2008 , vol. 16, # 1 p. 474 - 487
Full Text: HTML
Citation Number: 22
Abstract
Multidrug resistance (MDR) mediated by overexpression of MDR1 P-glycoprotein (P-gp) is one of the best characterized transporter-mediated barriers to successful chemotherapy in cancer patients. Chemosensitizers are the agents that increase the sensitivity of multidrug- resistant cells to the toxic influence of previously less effective drugs. In an attempt to find such vital chemosensitizers, a series of N10-substituted-2-chloroacridone analogous (1– ...
Related Articles:
Regioselective copper-catalysed amination of halobenzoic acids using aromatic amines
[Maradolla, Mohan Babu; Mandha, Amaravathi; Garimella, Chandra Mouli Journal of Chemical Research, 2007 , # 10 p. 587 - 589]
Regioselective copper-catalysed amination of halobenzoic acids using aromatic amines
[Maradolla, Mohan Babu; Mandha, Amaravathi; Garimella, Chandra Mouli Journal of Chemical Research, 2007 , # 10 p. 587 - 589]
Preparation and antiinflammatory properties of some 5-(2-anilinophenyl) tetrazoles
[Juby,P.F. et al. Journal of Medicinal Chemistry, 1968 , vol. 11, # 1 p. 111 - 117]