Molecular structure investigation and Biological Evaluation of Michael Adducts Derived from Dimedone
- Publication Type
- Original research
- Authors
- Assem Barakat , Abdullah M. Al-Majid Mohammad Shahidul Islam Vijay H. Masand M. Iqbal Choudhary , Ismail Warad , Sammer Yousuf
- Ismail Warad
- Ismail Warad
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Trimolecular salt Michael adducts 2a–c were synthesized in excellent
yields up to 92 % via one-pot multicomponent reactions in an aqueous medium. The
chemical structures of compounds 2a–c were characterized by X-ray single-crystal
diffraction techniques. Calculations of the density functional theory for the synthesized
compound were performed. The stability of the products was deduced by
TGA analysis. Compounds 2a–c were screened in vitro for different bio-assays such
as thymidine phosphorylase inhibition assay, urease inhibition assay, b-glucuronidase
inhibition assays and cytotoxicity against PC-3 and HeLa cell lines.
Journal
- Title
- Res Chem Intermed
- Publisher
- Springer Netherlands
- Publisher Country
- United States of America
- Publication Type
- Both (Printed and Online)
- Volume
- 42
- Year
- 2016
- Pages
- 4041-4053