JOURNAL 2388


Organic Communications
VOLUME & ISSUE
Year: 2022 Issue: 2 April-June
PAGES
p.204 - 211
STATISTICS
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AUTHORS
  • Abbas Khaja Mohideen
  • Kasim Mohammed Mustaque
  • Ismail Salim Meeran
  • Annadurai Subramani
  • V. S. Jamal Ahamed
  • Habeebullah Thajudeen
  • Timiri Khudus Shabeer
PDF OF ARTICLE

GRAPHICAL ABSTRACT


ABSTRACT


he reaction of anthranilic acid with proline or pipecolinic methyl ester hydrochloride in presence of 1,1’-Carbonyldiimidazole (CDI) on oil bath heating under solvent-free condition afforded 1,4-benzodiazepine-2,5-dione (BZD) derivatives in moderate to good yields. Operational simplicity, absence of hazardous solvents, utility of an inexpensive coupling reagent (CDI) and mild reaction conditions are the significant advantages of this methodology. The cytotoxic activity of six BZDs were evaluated against HCT15 (Human Colon adenocarcinoma), SKMel2 (Human Skin Melanoma) and SKOV3 (Human Ovarian adenocarcinoma) cell lines. Compound 4b with para substituted chlorine atom showed moderate cytotoxicity against HCT15, SKMel2 and SKOV3 with IC50 values 37.04 ± 1.13, 39.45 ± 0.77 and 36.61 ± 0.10 µg/mL respectively. The comprehensive analysis of the interaction between 4a to 4f with receptor VEGFR-2 kinase, the result shows compound 4b have higher molecular docking score with receptor. These result well matched with the result of cytotoxicity.

KEYWORDS
  • 1,4-Benzodiazepine-2,5-diones
  • solvent-free synthesis
  • cytotoxicity
  • molecular simulation

SUPPORTING INFORMATION


Solvent-free Synthesis, Molecular simulation and Cytotoxicity of 1,4-benzodiazepine2,5-diones
Download File Supporting information- Org. Comm.pdf (479.08 KB)