Novel quinazoline-1,2,3-triazole hybrids with anticancer and MET kinase targeting properties.
Ontology highlight
ABSTRACT: Oncogenic activation of receptor tyrosine kinases (RTKs) such as MET is associated with cancer initiation and progression. We designed and synthesized a new series of quinazoline derivatives bearing 1,2,3-triazole moiety as targeted anticancer agents. The MET inhibitory effect of synthesized compounds was assessed by homogeneous time-resolved fluorescence (HTRF) assay and western blot analysis. Sulforhodamine B assay was conducted to examine the antiproliferative effects of synthetic compounds against 6 cancer cell lines from different origins including MET-dependent AsPC-1, EBC-1 and MKN-45 cells and also Mia-Paca-2, HT-29 and K562 cells. The growth inhibitory effect of compounds in a three-dimensional spheroid culture was examined by acid phosphatase (APH) assay, while apoptosis inductio
SUBMITTER: Mortazavi M
PROVIDER: S-EPMC10482942 | biostudies-literature | 2023 Sep
REPOSITORIES: biostudies-literature
ACCESS DATA