Quantitative Structure-Activity Relationship and Docking Studies on a Series of Oxadiazole and Triazole Substituted Naphthyridines as HIV-1 Integrase Inhibitors

By  

Letters in Drug Design & Discovery, Vol. 14, Iss. 1, 2017-01 ,pp. : 10-27

Bentham Science Publishers

Access to resources Recommend Favorite

3D-QSAR Studies on a Series of 2,4-Thiazolidinedione Derivatives: A Self- Organizing Molecular Field Analysis Approach to Design Novel PTP 1B Inhibitors

By  

Medicinal Chemistry, Vol. 9, Iss. 6, 2013-01 ,pp. : 828-845

Bentham Science Publishers

Access to resources Recommend Favorite

Advances in the molecular modeling and quantitative structure–activity relationship-based design for antihistamines

By Galvez Jorge   Galvez-Llompart Maria   Zanni Riccardo   Garcia-Domenech Ramon  

Expert Opinion on Drug Discovery, Vol. 8, Iss. 3, 2013-03 ,pp. : 305-317

Informa Healthcare

Access to resources Recommend Favorite

Symmetry-based inhibitors of HIV-1 protease. Design, synthesis and preliminary structure-activity studies of acylated 2,3-diamino-1-hydroxypropanes and 2,4 diamino-1-hydroxybutanes

By Marastoni M.   Bazzaro M.   Bortolotti F.   Salvadori S.   Tomatis R.  

European Journal of Medicinal Chemistry, Vol. 34, Iss. 7, 1999-07 ,pp. : 651-657

Elsevier

Access to resources Recommend Favorite

Combined Three Dimensional Quantitative Structure Activity Relationships (3D-QSAR) Modeling and Molecular Docking Studies on Naphthoquinone Analogs as Proteasome Inhibitors

By  

Letters in Drug Design & Discovery, Vol. 10, Iss. 2, 2013-02 ,pp. : 129-144

Bentham Science Publishers

Access to resources Recommend Favorite