571 (d, J = 8.8 Hz, 2H), 5.999 (s, 2H). QN-S: Rf = 0.61, MP = 170 °C–172 °C, λmax (UV) = 283 nm, IR (KBr) cm−1: 3197 (NH), 3100 (CONH), 1689 (aromatic C C stretching), 760 (p-chloro substitution), 690 (meta di substitution). 1H NMR (400 MHz, DMSO) δ (ppm): 8.775 (s, Ar H), 8.171 (d, J = 8.4 Hz, Ar 2H), 8.061 (d, J = 8.4 Hz, Ar 2H), 7.957 (d, J = 8.8 Hz, Ar 2H), 7.839 (d, J = 8.4 Hz, Ar H), 7.694 (d, J = 8.8 Hz,

Ar 2H), 7.559 (d, J = 1.6 Hz, ArH), 3.367 (s, Torin 1 cell line NH), 1.228 (s, 6H), 7.296 (d, J = 10.4 Hz, 1H). QN-B: Rf = 0.66, MP = 180 °C–183 °C, λmax (UV) – 256 nm, IR (KBr) cm−1: 1521 and 1348 (NO2), 3431 (NH), 3329 (CONH), 3095 (aromatic CH stretching), 1624 (C O), 817 (aromatic meta substitution), 736 (para chloro substitution). 1H NMR (400 MHz, DMSO) δ (ppm): 8.052–8.017 (m, Ar H), 7.626 (d, J = 8 Hz, Ar 1H), 7.378 (d, J = 1.6 Hz, Ar 2H), 7.240–7.314 (m, Ar 5H), 6.949 (d, J = 7.6 Hz, Ar 2H). QN-N3: Rf = 0.64, MP: 160 °C–162 °C, λmax (UV) – 271 nm. IR (KBr) cm−1: 3113, 3100 (NH), 1587 (C C stretching), 1670 (C O). 1H NMR (400 MHz, DMSO) δ (ppm): 8.766 (s, 1H), 8.05 (d, J = 8.4 Hz, Ar 2H), 7.95 (d, J = 8.4 Hz, Ar 2H), 7.67 (d, J = 8 Hz, Ar 2H), 7.837 (d, J = 8 Hz, Ar 2H), 7.56 (d, J = 8.8 Hz, Ar 2H), 7.27 (d, J = 8.4 Hz, Ar 2H), 1.32–0.8

(m, 5H). The comparative results are obtained in in-vitro antioxidant studies; DPPH method, hydrogen peroxidase, nitrous oxide, super oxide, lipid peroxidation and ABTS methods. In DPPH method the quinazoline derivatives formed a reduced diphenyl picryl hydrazine after reduction Romidepsin supplier by donating the electrons in different concentrations.

Super oxide radical method is the reduction of nitro blue tetrazolium to formed formazan by donating the electron. Lipid peroxidation methods occur either through ferryl–perferryl complex or OH radical by Fenton reactions. In hydrogen peroxidase method iron dependent deoxyribose damage was produced in increased concentration. In nitrous oxide method, the synthesized drugs compete with oxygen to react with the nitric oxide to form nitrite ions and thus inhibit the peroxynitrite anions. In ABTS method the synthesized compounds showed TCL a significantly increased radical scavenging activity when increasing the concentration of the (1-(7-chloro-2-(4-chloro-phenyl)-3-N-aryl-quinazoline)-4-one urea) derivatives. The oxidative stress is due to the reactive oxygen species like hydrogen peroxide, super oxide hydrogen radical. It leads to the damage in DNA, lipids and proteins, these have a major role in disease and aging in animals and humans. From the results the new quinazoline derivatives are having a potent antioxidant activity by various antioxidant methods ( Table 2). In-vitro anticancer activity was investigated for all hybrid synthesized compounds to different breast cancer cell lines in different doses and found the concentration required for the 50% cell death (IC50).