Recent advances in the pharmacological diversification of quinazoline/quinazolinone hybrids

PS Auti, G George, AT Paul - RSC advances, 2020 - pubs.rsc.org
Due to the pharmacological activities of quinazoline and quinazolinone scaffolds, it has
aroused great interest in medicinal chemists for the development of new drugs or drug …

DHFR inhibitors: reading the past for discovering novel anticancer agents

MV Raimondi, O Randazzo, M La Franca, G Barone… - Molecules, 2019 - mdpi.com
Dihydrofolate reductase inhibitors are an important class of drugs, as evidenced by their use
as antibacterial, antimalarial, antifungal, and anticancer agents. Progress in understanding …

Diaryl ether: a privileged scaffold for drug and agrochemical discovery

T Chen, H Xiong, JF Yang, XL Zhu… - Journal of Agricultural …, 2020 - ACS Publications
Diaryl ether (DE) is a functional scaffold existing widely both in natural products (NPs) and
synthetic organic compounds. Statistically, DE is the second most popular and enduring …

Dihydrofolate reductase inhibitors for use as antimicrobial agents

J He, W Qiao, Q An, T Yang, Y Luo - European journal of medicinal …, 2020 - Elsevier
Drug-resistant bacteria pose an increasingly serious threat to mankind all over the world.
However, the currently available clinical treatments do not meet the urgent demand …

Dihydrofolate reductase inhibitors: Patent landscape and phases of clinical development (2001–2021)

K Bhagat, N Kumar, H Kaur Gulati… - Expert Opinion on …, 2022 - Taylor & Francis
Introduction Dihydrofolate reductase (DHFR) plays an important role in the biosynthesis of
amino acid and folic acid. It participates by reducing dihydrofolate to tetrahydrofolate, in the …

Thiadiazole inhibitors: a patent review

KM Dawood, TA Farghaly - Expert opinion on therapeutic patents, 2017 - Taylor & Francis
Introduction: Four isomeric structures of thiadiazole motifs have outstanding
pharmacological inhibitory applications are reported in this review. Thiadiazole nucleus is …

A novel of azo-thiazole moiety alternative for benzidine-based pigments: design, synthesis, characterization, biological evaluation, and molecular docking study

HF Rizk, MA El-Borai, A Ragab… - Polycyclic Aromatic …, 2023 - Taylor & Francis
A new series of coloring compounds (pigments) based on 5-(2-aminothiazol-5-yl) thiazol-2-
amine and 5-(4-aminophenyl) thiazol-2-amine as heterocyclic alternatives for benzidine …

Novel 1, 2, 4-oxadiazole-chalcone/oxime hybrids as potential antibacterial DNA gyrase inhibitors: Design, synthesis, ADMET prediction and molecular docking study

TS Ibrahim, AJ Almalki, AH Moustafa, RM Allam… - Bioorganic …, 2021 - Elsevier
New antibacterial drugs are urgently needed to tackle the rapid rise in multi-drug resistant
bacteria. DNA gyrase is a validated target for the development of new antibacterial drugs …

Synthesis, biological evaluation and molecular modeling study of new (1, 2, 4-triazole or 1, 3, 4-thiadiazole)-methylthio-derivatives of quinazolin-4 (3H)-one as DHFR …

YI El-Gazzar, HH Georgey, SM El-Messery… - Bioorganic …, 2017 - Elsevier
A new series of 2-mercapto-quinazolin-4-one analogues was designed, synthesized and
evaluated for their in vitro DHFR inhibition, antitumor and antimicrobial activity. Compound …

Synthesis, antiviral activity, 3D-QSAR, and interaction mechanisms study of novel malonate derivatives containing quinazolin-4 (3H)-one moiety

M Chen, P Li, D Hu, S Zeng, T Li, L Jin, W Xue… - Bioorganic & Medicinal …, 2016 - Elsevier
A series of novel malonate derivatives containing quinazolin-4 (3 H)-one moiety were
synthesized and evaluated for their antiviral activities against cucumber mosaic virus (CMV) …