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Abstract

QSAR, HQSAR and GRIND Studies on a Set of Heterocyclic Propafenone-Type Inhibitors of P-Glycoprotein

1
Department of Medicinal Chemistry, University of Vienna, Althanstraße 14, A-1090, Vienna, Austria
2
Department of Drug and Natural Product Synthesis, University of Vienna, Althanstraße 14, A-1090, Vienna, Austria
*
Author to whom correspondence should be addressed.
Sci. Pharm. 2009, 77(7), 201; https://doi.org/10.3797/scipharm.oephg.21.PO-02
Submission received: 16 April 2009 / Accepted: 16 April 2009 / Published: 16 April 2009

Abstract

P-Glycoprotein (P-gp) is a member of the ABC (ATP binding cassette) super-family of transport proteins, which in addition to their physiological role in tissue protection, actively extrude a large variety of therapeutically administered drugs from the malignant cells and thus are responsible for multiple drug resistance (MDR) in cancer patients [1]. Since the discovery of P-gp more than 30 years ago many studies have shown that MDR can be reversed by the use of inhibitors, often denoted as MDR modulators.

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MDPI and ACS Style

JABEEN, I.; PLAGENS, B.; HOLZER, W.; ECKER, G.F. QSAR, HQSAR and GRIND Studies on a Set of Heterocyclic Propafenone-Type Inhibitors of P-Glycoprotein. Sci. Pharm. 2009, 77, 201. https://doi.org/10.3797/scipharm.oephg.21.PO-02

AMA Style

JABEEN I, PLAGENS B, HOLZER W, ECKER GF. QSAR, HQSAR and GRIND Studies on a Set of Heterocyclic Propafenone-Type Inhibitors of P-Glycoprotein. Scientia Pharmaceutica. 2009; 77(Posters (PO)):201. https://doi.org/10.3797/scipharm.oephg.21.PO-02

Chicago/Turabian Style

JABEEN, I., B. PLAGENS, W. HOLZER, and G. F. ECKER. 2009. "QSAR, HQSAR and GRIND Studies on a Set of Heterocyclic Propafenone-Type Inhibitors of P-Glycoprotein" Scientia Pharmaceutica 77, Posters (PO): 201. https://doi.org/10.3797/scipharm.oephg.21.PO-02

APA Style

JABEEN, I., PLAGENS, B., HOLZER, W., & ECKER, G. F. (2009). QSAR, HQSAR and GRIND Studies on a Set of Heterocyclic Propafenone-Type Inhibitors of P-Glycoprotein. Scientia Pharmaceutica, 77(Posters (PO)), 201. https://doi.org/10.3797/scipharm.oephg.21.PO-02

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