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Molecular-Docking Study of the Interaction of Anti-Inflammatory N-Aroyl-Substituted Halo(H)Anthranilic Acid Amides and Hydrazides with Cyclooxygenase 1
Andryukov K., Korkodinova L.
Synthesis, Docking, and Anticoagulant Activity of New Factor-Xa Inhibitors in a Series of Pyrrolo[3,2,1-ij]Quinoline-1,2-Diones
Medvedeva S., Potapov A., Gribkova I., Katkova E., Sulimov V., Shikhaliev K.
Facile One-Pot Synthesis Methodology for Nitrogen-Containing Heterocyclic Derivatives of 3,5-Disubstituted 4,5-Dihydro-1H-Pyrazole, Their Biological Evaluation and Molecular Docking Studies
Upadhyay S., Tripathi A., Paliwal S., Saraf S.
Assessment of 5-substituted Isatin as Surface Recognition Group: Design, Synthesis, and Antiproliferative Evaluation of Hydroxamates as Novel Histone Deacetylase Inhibitors
Singh A., Raghuwanshi K., Patel V., Jain D., Veerasamy R., Dixit A., Rajak H.
Synthesis, Antimicrobial and In Silico EGFR Inhibitory Activity Evaluation of Sulfonylamino Pyrrolidine Derivatives
Kumar B., Prasad A., Reddy P., Ravindranath L.
Peptide Derivatives of 1,2-Dihydro-3-Methyl-2-Oxoquinoxaline-6-Carboxylic Acid: Synthesis and Evaluation of Antimicrobial, Antifungal and Antiviral Potential
Chaudhary S., Kumar S., Tarazi H.
Theoretical and Experimental in vitro Antifungal and Antitumor Activities of Organotin(IV) Derivatives of 3-(4-nitrophenyl)-2-methylacrylic acid
Muhammad N., Shah N., Ali S., Elahi S., Rehman W., Shujah S., Khan M., Wadood A., Ghufran M., Rashid U.
DNA Binding Mode and Affinity of Antitumor Drugs of 2-aroylbenzofuran-3-ols: Molecular Dynamics Simulation Study
Sargolzaei M., Nikoofard H., Afshar M.
Free Radical Scavenging and Cytotoxic Properties of Acylated and Non-Acylated Kaempferol Glycosides from Stenochlaena Palustris: a Perspective on Their Structure – Activity Relationships
Chear N., Fauzi A., Khaw K., Choi S., Yaacob N., Lai C.
Design of New Uracil Derivatives Possessing Inhibitory Activity with Respect to Reverse Transcriptase of HIV-1 Mutant K103N/Y181C
Pechinskii S., Kuregyan A., Ozerov A., Novikov M.
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