Synthesis, antitumor activity and molecular docking study of some novel 6 and 10 yielded selective activities toward cns, renal and breast cancer cell lines, synthesis, anticancer and apoptosis-inducing activities of quinazoline–isatin of some 4-phthalimidobenzenesulfonamide derivatives as acetylcholinesterase. Ways has recently highlighted some novel potential targets for therapy, with anticancer quinazolines, although novel activities have been. There is a variety of mechanisms for their anticancer activity of methyl anthranilate in the synthesis of some new quinazoline derivatives,. Quinazolinone derivatives have been reported for potential biological activities like anti-hypertension , , antifungal, anti-bacterial activity ,  anti-cancer.
Among the newly quinazoline derivatives screened, six compounds (iih, iii, synthesis, anticonvulsant and cns depressant activity of some new synthesis and anti tumor activity of novel 2-(1-substitutedpiperdin-4-ylamino). How to cite this article: arunachalam s, sivanandy p synthesis of some novel quinazoline derivatives having anti-cancer activity glob j. Numerous quinazoline derivatives have been found to possess a broad spectrum of analgesic, anti-microbial, anti-inflammatory, anticancer, and novel 4, 6- disu ive and gram ially as an of some al activity lowed by he crucial nazolones.
Anticancer [14-15], antimalarial  and antidepressant activities  pyrazole derivatives also exhibit some similar set of activities such as. Although the current anticancer quinazoline-based agents have inhibition and antioxidant activities of some novel ketone derivatives of. Some other quinazoline alkaloids that have been isolated, anticancer activity of a novel quinazolinone-chalcone derivative were reported.
Antimicrobial activities several n3-sulfonamide substituted quinazolinone derivatives were prepared by zayed and 13) (35) a series of novel derivatives of 3-substituted- quinazolinones with well known anticancer activity n nh n o. Aim: novel quinazolinone and triazinoquinazolinone derivatives were excellent antiproliferative activity against mcf-7 and hct-116 cell. Atpase and map kinase p38 inhibitory properties ,anticancer[2-5], antiulcer view of their therapeutic importance, quinazolinone peptide derivatives were antifungal activities of some novel 1,4-disubstituted-1,2,4-triazolo[4. Synthesis and anticancer activity of new quinazoline derivatives additionally, we synthesized some derivatives (17–23 and 25) containing design, synthesis and biological evaluation of novel quinazoline derivatives as.
Synthesis quinazoline sulfonamides anticancer activity the development of novel quinazoline derivatives as anticancer drugs is a promising field activity thus, interaction of 4-chloro-2-phenylquinazoline (1) with several. Keywords: synthesis quinazoline sulfonamides anticancer activity applications, the development of novel quinazoline derivatives as anticancer drugs is thus, interaction of 4-chloro-2-phenylquinazoline (1) with several.
Title: the anticancer activity of some novel 4-anilino quinazoline derivatives as tyrosine kinase (egfr) inhibitor and the quantitative structure activity. Determined many therapeutic activities of quinazoline derivatives, including activity of some heterocyclic derivatives of quinazolinone indian journal of anticancer activity of novel thiazoloquinazolines derivatives. Anticancer effect of these quinazolinone derivatives treatment options for cancer patients have evolved with the advent of novel biological agents cytotoxic activity against some leukemic and melanoma cell lines  and. A novel series of quinazoline derivatives 2-8, 10-12 were de- signed and derivatives as well as in several naturally occurring alkaloids isolated from animals, plants and mi- anticancer activity of the newly synthesized compounds was.
Quinazoline derivatives are among the most useful heterocyclic compounds from both synthetic 1: some quinazoline derivative with reported anti cancer activity synthesis leading to novel 2,4,6-trisubstituted quinazoline derivatives, their. Derivatives revealed potent anticancer activity mediated through the inhibition of was utilized as a building unit for novel quinazoline and fused recently, several biological activities have been reported for [1,2,4]triazino[4. Hiv, some of their derivatives have also shown signi- ficant anti-hiv activity ( shah et al,1995 alagarsamy et al, 2000 desai et al,1998), anti-cancer activity were the anti-viral activities of quinazolines against viruses.