Collect. Czech. Chem. Commun.
1990, 55, 296-306
https://doi.org/10.1135/cccc19900296
Use of QSAR in design of antiinflammatory fluorinated arylalkanoic acids
Miroslav Kuchař, Jaroslava Grimová, Václav Rejholec, Hana Tomková, Magda Jelínková and Jiří Holubek
Research Institute for Pharmacy and Biochemistry, 130 60 Prague 3
Crossref Cited-by Linking
- Liao Weike, Xu Chen, Ji Xiaohui, Hu Gang, Ren Lixiang, Liu Yajing, Li Ruijuan, Gong Ping, Sun Tiemin: Design and optimization of novel 4-(2-fluorophenoxy)quinoline derivatives bearing a hydrazone moiety as c-Met kinase inhibitors. European Journal of Medicinal Chemistry 2014, 87, 508. <https://doi.org/10.1016/j.ejmech.2014.09.095>
- Duffy J C, Dearden J C, Rostron C: A Qsar Study Of Anti-Inflammatory N-Arylanthranilic Acids. Journal of Pharmacy and Pharmacology 2011, 48, 883. <https://doi.org/10.1111/j.2042-7158.1996.tb05993.x>
- Bubert Christian, Woo L. W. Lawrence, Sutcliffe Oliver B., Mahon Mary F., Chander Surinder K., Purohit Atul, Reed Michael J., Potter Barry V. L.: Synthesis of Aromatase Inhibitors and Dual Aromatase Steroid Sulfatase Inhibitors by Linking an Arylsulfamate Motif to 4‐(4H‐1,2,4‐triazol‐4‐ylamino)benzonitrile: SAR, Crystal Structures, in vitro and in vivo Activities. ChemMedChem 2008, 3, 1708. <https://doi.org/10.1002/cmdc.200800164>
- Michaelidou A. S., Hadjipavlou-Litina D.: Nonsteroidal Anti-Inflammatory Drugs (NSAIDs): A Comparative QSAR Study. Chem. Rev. 2005, 105, 3235. <https://doi.org/10.1021/cr040708m>
- Brown Steven D., Bear Robert S., Blank Thomas B.: Chemometrics. Anal. Chem. 1992, 64, 22. <https://doi.org/10.1021/ac00036a002>
