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Synthesis and antiproliferative evaluation of some novel quinazolin‐4( 3 H )‐one derivatives
Author(s) -
Salem Marwa Sayed,
AlMabrook Selima Ali Mohamed,
ElHashash Maher Abd ElAziz Mahmoud
Publication year - 2020
Publication title -
journal of heterocyclic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.321
H-Index - 59
eISSN - 1943-5193
pISSN - 0022-152X
DOI - 10.1002/jhet.4096
Subject(s) - quinazolinone , chemistry , moiety , in vitro , bioassay , doxorubicin , mtt assay , combinatorial chemistry , stereochemistry , triazole , cancer cell lines , mcf 7 , cell culture , chelation , biological activity , pharmacology , cancer cell , biochemistry , cancer , human breast , organic chemistry , chemotherapy , medicine , biology , genetics
A series of novel quinazolinone derivatives was designed and synthesized. The antiproliferative activities were evaluated in vitro using MTT assay against hepatocellular carcinoma (HepG‐2) and mammary gland breast cancer (MCF‐7). The preliminary bioassay results demonstrated that tested compounds exhibited antiproliferation with various degrees. Triazole moiety enhanced the activity against the two cell lines when incorporating with quinazolinone moiety in a single molecular framework. Acetohydrazide‐quinazolinone derivative showed strong activity against the two cancer cells comparable to that of doxorubicin. Biological evaluation indicated that all the tested compounds possessed antiproliferative activity with certain degrees.