Quinazolinone and quinazoline derivatives: recent structures with potent antimicrobial and cytotoxic activities

E Jafari, MR Khajouei, F Hassanzadeh… - Research in …, 2016 - journals.lww.com
The heterocyclic compounds have a great importance in medicinal chemistry. One of the
most important heterocycles in medicinal chemistry are quinazolines possessing wide …

[HTML][HTML] Advances in synthesis and biological activities of quinazoline scaffold analogues: A review

SNM Boddapati, HB Bollikolla, KG Bhavani… - Arabian Journal of …, 2023 - Elsevier
Creating effective, ecologically friendly, and commercially viable synthetic routes is crucial in
the design and synthesis of organic substances. Quinazoline, a heterocyclic compound with …

An overview on the synthetic urease inhibitors with structure-activity relationship and molecular docking

W Yang, Q Feng, Z Peng, G Wang - European Journal of Medicinal …, 2022 - Elsevier
Urease is a kind of enzyme which could be found in various bacteria, fungi, plants, and
algae, which can quickly catalyze the hydrolysis of urea into ammonia and carbon dioxide …

Design, synthesis and Molecular modeling study of certain EGFR inhibitors with a quinazolinone scaffold as anti-hepatocellular carcinoma and Radio-sensitizers

WM Ghorab, SA El-Sebaey, MM Ghorab - Bioorganic chemistry, 2023 - Elsevier
A set of novel N-substituted-2-((4-oxo-3-phenyl-3, 4-dihydroquinazolin-2-yl) thio) acetamide
3–16 were designed and synthesized from 2-mercapto-3-phenylquinazolinone 2. The …

Synthesis, spectroscopic characterization, antimicrobial evaluation and molecular docking study of novel triazine-quinazolinone based hybrids

M Dinari, F Gharahi, P Asadi - Journal of Molecular Structure, 2018 - Elsevier
Abstract A new series of 1, 3, 5-triazine incorporating aromatic quinazolinone moieties as a
potential antimicrobial agents is reported. The first chlorine group of the cyanuric chloride (1) …

Antimicrobial, anticancer and immunomodulatory potential of new quinazolines bearing benzenesulfonamide moiety

MM Ghorab, AS Alqahtani, AM Soliman… - Future Medicinal …, 2023 - Taylor & Francis
Sulfonamides are privileged candidates with potent anti-methicillin-resistant Staphylococcus
aureus (MRSA) activity and could replenish the MRSA antibiotic pipeline. The initial …

[HTML][HTML] Transition metal-free synthesis of 2-aryl quinazolines via alcohol dehydrogenation

P Hima, M Vageesh, M Tomasini, A Poater, R Dey - Molecular Catalysis, 2023 - Elsevier
We report here a transition metal-free synthesis of quinazoline derivatives starting from 2-
aminobenzyl alcohols and aryl amides via an alcohol dehydrogenation strategy promoted …

Design, synthesis and molecular modeling study of certain quinazolinone derivatives targeting poly (ADP-ribose) polymerase 1 (PARP-1) enzyme as anti-breast …

WM Ghorab, SA El-Sebaey, MM Ghorab - Journal of Molecular Structure, 2023 - Elsevier
A novel two series of S-alkylated quinazolinones 4–10 and N-alkylated quinazolinones 11–
17 was designed and synthesized as potential PARP-1 inhibitors. Quinazolinone scaffold …

Actinoquinazolinone, a New Quinazolinone Derivative from a Marine Bacterium Streptomyces sp. CNQ-617, Suppresses the Motility of Gastric Cancer Cells

S Pulat, DA Kim, PF Hillman, DC Oh, H Kim, SJ Nam… - Marine Drugs, 2023 - mdpi.com
A HPLC-UV guided fractionation of the culture broth of Streptomyces sp. CNQ-617 has led to
the isolation of a new quinazolinone derivative, actinoquinazolinone (1), as well as two …

Ultrasound mediated efficient synthesis of new 4-oxoquinazolin-3 (4H)-yl) furan-2-carboxamides as potent tyrosinase inhibitors: Mechanistic approach through …

NC Dige, PG Mahajan, H Raza, M Hassan… - Bioorganic …, 2019 - Elsevier
We have carried out the synthesis of new 4-oxoquinazolin-3 (4H)-yl) furan-2-carboxamide
derivatives by the reaction between isatoic anhydride, 2-furoic hydrazide and substituted …