Hydrophobic moments as physicochemical descriptors in structure-activity relationship studies of P-glycoprotein inhibitors

被引:6
作者
Koenig, Gerhard [1 ]
Chiba, Peter [2 ]
Ecker, Gerhard F. [1 ]
机构
[1] Univ Vienna, Dept Med Chem, Emerging Field Pharmacoinformat, A-1090 Vienna, Austria
[2] Med Univ Vienna, Inst Med Chem, Vienna, Austria
来源
MONATSHEFTE FUR CHEMIE | 2008年 / 139卷 / 04期
基金
奥地利科学基金会;
关键词
computer chemistry; propafenone; multidrug resistance; molecular modeling; antitumor agents;
D O I
10.1007/s00706-007-0819-7
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Lipophilicity is one of the major determining physicochemical descriptors for P- glycoprotein ( P- gp) inhibitory activity. In order to consider lipo-philicity as a space directed property, we apply the concept of hydrophobic moments on a set of propafenone-type inhibitors of P- glycoprotein and use them as descriptors in QSAR analyses. While the 0(th) moment is the sum of the atomic hydrophobicity coefficients, which is a measure for the total hydrophobicity of the molecule, the 1(st) moment ( or hydrophobic dipole) is a measure for the asymmetry of the distribution of hydrophobicities and therefore is analogous to the electrostatic dipole. The use of these hydrophobic dipole moments as independent variables remarkably improved the predictive power of QSAR models obtained.
引用
收藏
页码:401 / 405
页数:5
相关论文
共 50 条
[41]   Nonlinear optical studies and structure-activity relationship of chalcone derivatives with in silico insights [J].
Kar, Swayamsiddha ;
Adithya, K. S. ;
Shankar, Pruthvik ;
Babu, N. Jagadeesh ;
Srivastava, Sailesh ;
Rao, G. Nageswara .
JOURNAL OF MOLECULAR STRUCTURE, 2017, 1139 :294-302
[42]   Semisynthetic Latrunculin Derivatives as Inhibitors of Metastatic Breast Cancer: Biological Evaluations, Preliminary Structure-Activity Relationship and Molecular Modeling Studies [J].
Khanfar, Mohammad A. ;
Youssef, Diaa T. A. ;
El Sayed, Khalid A. .
CHEMMEDCHEM, 2010, 5 (02) :274-285
[43]   Structure-Activity Relationships on Cinnamoyl Derivatives as Inhibitors of p300 Histone Acetyltransferase [J].
Madia, Valentina Noemi ;
Benedetti, Rosaria ;
Barreca, Maria Letizia ;
Ngo, Liza ;
Pescatori, Luca ;
Messore, Antonella ;
Pupo, Giovanni ;
Saccoliti, Francesco ;
Valente, Sergio ;
Mai, Antonello ;
Scipione, Luigi ;
Zheng, Yujun George ;
Tintori, Cristina ;
Botta, Maurizio ;
Cecchetti, Violetta ;
Altucci, Lucia ;
Di Santo, Roberto ;
Costi, Roberta .
CHEMMEDCHEM, 2017, 12 (16) :1359-1368
[44]   Structure-activity relationship mediated molecular insights of DprE1 inhibitors: A Comprehensive Review [J].
Dash, Swagatika ;
Rathi, Ekta ;
Kumar, Avinash ;
Chawla, Kiran ;
Joseph, Alex ;
Kini, Suvarna G. .
JOURNAL OF BIOMOLECULAR STRUCTURE & DYNAMICS, 2024, 42 (12) :6472-6522
[45]   Synthesis, cytotoxicity and structure-activity relationship of indolizinoquinolinedione derivatives as DNA topoisomerase IB catalytic inhibitors [J].
Yu, Qian ;
Yang, Hui ;
Zhu, Teng-Wei ;
Yu, Le -Mao ;
Chen, Jian-Wen ;
Gu, Lian-Quan ;
Huang, Zhi-Shu ;
An, Lin-Kun .
EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2018, 152 :195-207
[46]   Synthesis, biological evaluation and 3D-QSAR studies of new chalcone derivatives as inhibitors of human P-glycoprotein [J].
Parveen, Zahida ;
Brunhofer, Gerda ;
Jabeen, Ishrat ;
Erker, Thomas ;
Chiba, Peter ;
Ecker, Gerhard F. .
BIOORGANIC & MEDICINAL CHEMISTRY, 2014, 22 (07) :2311-2319
[47]   Novel tetramethylpiperidine-substituted phenazines are potent inhibitors of P-glycoprotein activity in a multidrug resistant cancer cell line [J].
VanRensburg, CEJ ;
Anderson, R ;
Joone, G ;
Myer, MS ;
OSullivan, JF .
ANTI-CANCER DRUGS, 1997, 8 (07) :708-713
[48]   Novel Heat Shock Protein 90 Inhibitors Suppress P-Glycoprotein Activity and Overcome Multidrug Resistance in Cancer Cells [J].
Dinic, Jelena ;
Podolski-Renic, Ana ;
Jovanovic, Mirna ;
Musso, Loana ;
Tsakovska, Ivanka ;
Pajeva, Ilza ;
Dallavalle, Sabrina ;
Pesic, Milica .
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2019, 20 (18)
[49]   Flavonoid Dimers as Bivalent Modulators for P-Glycoprotein-Based Multidrug Resistance: Structure-Activity Relationships [J].
Chan, Kin-Fai ;
Zhao, Yunzhe ;
Chow, Toby W. S. ;
Yan, Clare S. W. ;
Ma, Dik Lung ;
Burkett, Brendan A. ;
Wong, Iris L. K. ;
Chow, Larry M. C. ;
Chan, Tak Hang .
CHEMMEDCHEM, 2009, 4 (04) :594-614
[50]   Exploring the Potential of Terpenoids as a Possible Treatment for Cancer: Structure-Activity Relationship and Mechanistic Studies [J].
Singh, Arshdeep ;
Debnath, Rabin ;
Sharma, Anjali ;
Saini, Aniket ;
Seni, Kushal ;
Chawla, Viney ;
Chawla, Pooja A. .
CURRENT MEDICINAL CHEMISTRY, 2024,