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机译:螺取代喹唑啉-4-酮抗癌及PDE 5抑制活性的合成与评价
Menia Univ, Chem Dept, Fac Sci, El Minya, Egypt;
Al Azhar Univ, Organ Chem Dept, Fac Pharm, Assiut, Egypt;
Spiro compounds; Cycloadditions; Antitumor agents; Structure elucidation;
机译:ChemInform Abstract: Quinoxaline Chemistry. Part 11. 3‐Phenyl‐2phenoxy‐ and phenoxymethyl‐6(7) or 6,8‐Substituted Quinoxalines and N‐4‐(6(7)‐Substituted or 6,8‐Disubstituted‐3‐phenylquinoxalin‐2‐yl)hydroxy or hydroxymethylbenzoylglutamates. Synthesis and Evaluation of in vitro Anticancer Activity and Enzymatic Inhibitory Activity Against Dihydrofolate Reductase and Thymidylate Synthase.
机译:A facile stereoselective synthesis of dispiro-indeno pyrrolidine/pyrrolothiazole-thiochroman hybrids and evaluation of their antimycobacterial, anticancer and AchE inhibitory activities
机译:Identification of Promising Biofilm Inhibitory and Cytotoxic Quinazolin-4-one Derivatives: Synthesis, Evaluation, Molecular Docking and ADMET Studies
机译:pharmacophore mapping: prediction of BCR–aBL kinase inhibitory activity of α-benzylthio chalcones