Synthesis and evaluation of novel benzophenone-thiazole derivatives as potent VEGF-A inhibitors
A series of 2-(4-benzoyl-phenoxy)-N-(4-phenyl-thiazol-2-yl)-acetamides (10a–n) were synthesized by multistep reaction sequence and all the compounds were well characterized for structural elucidation. The in vitro cytotoxicity of compounds 10a–n was evaluated against EAC and DLA cell lines using try...
Saved in:
Published in: | European journal of medicinal chemistry Vol. 87; pp. 274 - 283 |
---|---|
Main Authors: | , , , , , |
Format: | Journal Article |
Language: | English |
Published: |
France
Elsevier Masson SAS
24-11-2014
|
Subjects: | |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Summary: | A series of 2-(4-benzoyl-phenoxy)-N-(4-phenyl-thiazol-2-yl)-acetamides (10a–n) were synthesized by multistep reaction sequence and all the compounds were well characterized for structural elucidation. The in vitro cytotoxicity of compounds 10a–n was evaluated against EAC and DLA cell lines using trypan blue dye exclusion method. Further MTT assay and LDH release assay, followed by in vivo studies on murine model were also evaluated. The compound 10h with a methyl and fluoro groups at benzophenone moiety and methoxy group at phenyl ring was in a leading position to exhibit the promising antiproliferative effect through translational VEGF-A inhibition.
A series of 2-(4-benzoyl-phenoxy)-N-(4-phenyl-thiazol-2-yl)-acetamides were synthesized and characterized, further all the new compounds were tested for their anticancer activity. [Display omitted]
•Novel benzophenone-thiazole derivatives were synthesized.•In-vitro cytotoxicity of 10a–n was evaluated against EAC and DLA cell lines.•10h with methyl, fluoro and methoxy groups was in a leading position among 10a–n.•In-vivo studies are conducted on murine models.•Compound 10h exhibits the promising antiproliferative effect. |
---|---|
Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0223-5234 1768-3254 |
DOI: | 10.1016/j.ejmech.2014.09.069 |