In the current study we prepared cost-effective adsorbents based on ajwa date pits to remove Cu(II) ions from aqueous medium. Adsorbents were studied using scanning electron microscopy (SEM), FT-IR, and Brunauer-Emmett-Teller (BET) methods to characterize the surface functionalities, morphology, pore size, and particle size. The concentration of Cu(II) ions in the studied samples was determined by atomic adsorption spectrometry technique (AAS). Adsorption method was performed sequentially in a batch system followed by optimization by studying the numerous conditions, for instance the initial amounts of Cu(II) ions, dosages of the adsorbent, contact time, and pH of the solution. The ideal pH observed for maximum adsorption capacity was ~6.5. Langmuir and Freundlich isotherm models correctly predicted the investigation results, with the maximum monolayer adsorption capacities for Cu(II) ions at 328 K being 1428.57 mg/g (treated ajwa date pits, TADP) and 1111.1 mg/g for as produced ajwa date pits (ADP). It was revealed that TADP possess greater adsorption capability than ADP. Recovery investigations revealed that the saturated adsorbents eluted the maximum metal with 0.1 M HCl. Cu(II) ions adsorption was observed to be reduced by 80–89% after the second regeneration cycle. For the raw and chemically processed ajwa date pits adsorbent, the Langmuir model performed significantly better than the Freundlich model. The results demonstrated that the adsorbent made from ajwa date pits could be an economical and environmentally friendly alternative for removing Cu(II) ion pollutant from aqueous media.

Spirooxindole is a promising chemo therapeutic agent. Possible targets include cancers of the liver, prostate, lung, stomach, colon, and breast. Here, we demonstrate a one-pot three-component reaction via a [3 + 2] cycloaddition/ring contraction sequence of a dipolarophile (activated alkene) with in situ-generated azomethine ylide (1,3-dipoles) without the use of any catalyst. The reaction provides efficient access to synthetically useful and biologically important spirooxindoles in high yield (69–94%) with high diastereoselectivity. The synthesized compounds were subjected to cytotoxicity evaluation using colorectal cancer (HCT-116), hepatocellular carcinoma (HepG2), and prostate cancer (PC-3) cells. Compounds 4i, 4j, and 4k showed potent cytotoxic activity and high selectivity against HCT-116 cells when compared to cisplatin. Meanwhile compound 4d retained high cytotoxic activity and selectivity against HepG2 and PC-3 cells in comparison to cisplatin. The mechanism of compound 4d was further studied using phosphodiesterase 1 enzyme and showed 74.2% inhibitory activity. A possible binding mode for compound 4d to PDE-1 was investigated by molecular modeling using OpenEye software. Pose predictions for the active compounds were demonstrated by ROCS alignments. Compound 4d has a special geometry and differs from other active compounds.