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Synthesis, characterizations, biological activities and docking studies of novel dihydroxy derivatives of natural phenolic monoterpenoids containing azomethine linkage.
- Source :
-
Research on Chemical Intermediates . Oct2017, Vol. 43 Issue 10, p5377-5393. 17p. 2 Color Photographs, 7 Diagrams, 3 Charts, 3 Graphs. - Publication Year :
- 2017
-
Abstract
- In the present work, we report the synthesis of six new azomethine linkage containing dihydroxy derivatives of carvacrol, thymol, and eugenol. All the synthesized derivatives have been characterized by spectroscopic techniques and their structures were confirmed by X-ray single crystallography. Synthesized derivatives were screened for anti-oxidant activity using DPPH radical scavenging assay, and anticancer activity by using SRB assay against pancreatic cancer with MIAPaCa-2 and colon cancer with HCT-15 cell lines. The molecular docking studies of all the synthesized derivatives were performed on cyclooxygenases (COX-2) protein enzyme. In the anti-oxidant test, the values of EC indicated that all the compounds show excellent anti-oxidant potency, and similarly the GI values in anticancer tests indicated that most of the compounds possess good anticancer efficacy. The overall docking score suggested that all the synthesized compounds exhibit good binding affinity towards cyclooxygenases (COX-2) protein enzyme. Graphical Abstract: [ABSTRACT FROM AUTHOR]
- Subjects :
- *SCHIFF bases
*ADVANCED glycation end-products
*CARVACROL
*THYMOL
*PHENOLS
Subjects
Details
- Language :
- English
- ISSN :
- 09226168
- Volume :
- 43
- Issue :
- 10
- Database :
- Academic Search Index
- Journal :
- Research on Chemical Intermediates
- Publication Type :
- Academic Journal
- Accession number :
- 125109447
- Full Text :
- https://doi.org/10.1007/s11164-017-2933-4