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SAR and QSAR in Environmental Research Volume 22, 2011 - Issue 7-8
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Original Articles

Receptor-based QSAR study for a series of 3,3-disubstituted-5-aryl oxindoles and 6-aryl benzimidazol-2-ones derivatives as progesterone receptor inhibitors

J.H. Wang Key Lab of Colloid and Interface Chemistry, Ministry of Education, School of Chemistry and Chemical Engineering, Shandong University, Jinan, Shandong, China
,
Q.Q. Hou Key Lab of Colloid and Interface Chemistry, Ministry of Education, School of Chemistry and Chemical Engineering, Shandong University, Jinan, Shandong, China
,
K. Tang Key Lab of Colloid and Interface Chemistry, Ministry of Education, School of Chemistry and Chemical Engineering, Shandong University, Jinan, Shandong, China
,
X.L. Cheng Key Lab of Colloid and Interface Chemistry, Ministry of Education, School of Chemistry and Chemical Engineering, Shandong University, Jinan, Shandong, China
,
L.H. Dong Northwest Institute of Plateau Biology, Chinese Academy of Sciences, Xining, Qinghai, China
,
Y.J. Liu Key Lab of Colloid and Interface Chemistry, Ministry of Education, School of Chemistry and Chemical Engineering, Shandong University, Jinan, Shandong, China; Northwest Institute of Plateau Biology, Chinese Academy of Sciences, Xining, Qinghai, ChinaCorrespondence[email protected]
&
C.B. Liu Key Lab of Colloid and Interface Chemistry, Ministry of Education, School of Chemistry and Chemical Engineering, Shandong University, Jinan, Shandong, China
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Pages 775-799 | Received 29 Mar 2011, Accepted 09 Sep 2011, Published online: 17 Oct 2011

Citations (7)

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V.K. Vyas, N. Gupta, M. Ghate & S. Patel. (2014) Design, synthesis, pharmacological evaluation and in silico ADMET prediction of novel substituted benzimidazole derivatives as angiotensin II–AT1 receptor antagonists based on predictive 3D QSAR models. SAR and QSAR in Environmental Research 25:2, pages 117-146.
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V.K. Vyas & M. Ghate. (2013) Development of docking-based 3D QSAR models for the design of substituted quinoline derivatives as human dihydroorotate dehydrogenase (hDHODH) inhibitors. SAR and QSAR in Environmental Research 24:8, pages 625-645.
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V. K. Vyas, H. G. Bhatt, P. K. Patel, J. Jalu, C. Chintha, N. Gupta & M. Ghate. (2013) CoMFA and CoMSIA studies on C-aryl glucoside SGLT2 inhibitors as potential anti-diabetic agents. SAR and QSAR in Environmental Research 24:7, pages 519-551.
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Articles from other publishers (4)

Asmaa Saber, El Hassane Anouar, Ghizlane Sebbar, Brahim El Ibrahimi, Mohamed Srhir, Tuncer Hökelek, Joel T. Mague, Lhoussaine El Ghayati, Nada Kheira Sebbar & El Mokhtar Essassi. (2021) New 1,2,3-triazole containing benzimidazolone derivatives: Syntheses, crystal structures, spectroscopic characterizations, Hirshfeld surface analyses, DFT calculations, anti-corrosion property anticipation, and antibacterial activities. Journal of Molecular Structure 1242, pages 130719.
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Udit Chaube & Hardik Bhatt. (2017) 3D-QSAR, molecular dynamics simulations, and molecular docking studies on pyridoaminotropanes and tetrahydroquinazoline as mTOR inhibitors. Molecular Diversity 21:3, pages 741-759.
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Vakhid A. Mamedov, Nataliya A. Zhukova & Oleg G. Sinyashin. (2017) Advances in the synthesis of benzimidazolones via rearrangements of benzodiazepinones and quinoxalin(on)es. Mendeleev Communications 27:1, pages 1-11.
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Vakhid A. Mamedov & Nataliya A. Zhukova. 2017. 1 43 .

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