Non-classical antifolates. Part 2: Synthesis, biological evaluation, and molecular modeling study of some new 2,6-substituted-quinazolin-4-ones

A new series of 2,6-substituted-quinazolin-4-ones was designed, synthesized, and evaluated for their in vitro DHFR inhibition, antimicrobial, and antitumor activities. Compounds 22, 33–37, 39–43, and 45 proved to be active DHFR inhibitors with IC 50 range of 0.4–1.0 μM. Compound 18 showed broad-spec...

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Veröffentlicht in:Bioorganic & medicinal chemistry 2010-04, Vol.18 (8), p.2849-2863
Hauptverfasser: Al-Omary, Fatmah A.M., Abou-zeid, Laila A., Nagi, Mahmoud N., Habib, El-Sayed E., Abdel-Aziz, Alaa A.-M., El-Azab, Adel S., Abdel-Hamide, Sami G., Al-Omar, Mohamed A., Al-Obaid, Abdulrahman M., El-Subbagh, Hussein I.
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Sprache:eng
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