Quinazolines and quinazolinones as ubiquitous structural fragments in medicinal chemistry: An update on the development of synthetic methods and pharmacological …

I Khan, S Zaib, S Batool, N Abbas, Z Ashraf… - Bioorganic & medicinal …, 2016 - Elsevier
Nitrogen-rich heterocycles, particularly quinazolines and quinazolinones, represent a
unique class of diversified frameworks displaying a broad spectrum of biological functions …

1, 3, 4-Oxadiazole: an emerging scaffold to inhibit the thymidine phosphorylase as an anticancer agent

A Murmu, P Banjare, BW Matore… - Current Medicinal …, 2024 - benthamdirect.com
Thymidine phosphorylase (TP), also referred to as “platelet-derived endothelial cell growth
factor” is crucial to the pyrimidine salvage pathway. TP reversibly transforms thymidine into …

2-(4-Fluorophenyl)-quinazolin-4 (3H)-one as a novel tyrosinase inhibitor: Synthesis, inhibitory activity, and mechanism

R Wang, WM Chai, Q Yang, MK Wei, Y Peng - Bioorganic & Medicinal …, 2016 - Elsevier
(4-Fluorophenyl)-quinazolin-4 (3H)-one (FQ) was synthesized, and its structure was
identified with 1 H nuclear magnetic resonance (1 H NMR), 13 C nuclear magnetic …

Biological activity of quinazolinones

AA Radwan, FK Alanazi - Quinazolinone and Quinazoline …, 2020 - books.google.com
The chemical structure of quinazolinones includes benzene ring fused with 2-pyrimidinone
(1), 4-pyrimidinone (2) or 2, 4-pyrimidinedione (3) ring, and are named as quinazolin-2 (1H) …

Dihydroquinazolin-4(1H)-one derivatives as novel and potential leads for diabetic management

O Babatunde, S Hameed, U Salar, S Chigurupati… - Molecular Diversity, 2021 - Springer
Abstract A variety of dihydroquinazolin-4 (1 H)-one derivatives (1–37) were synthesized via
“one-pot” three-component reaction scheme by treating aniline and different aromatic …

Newly designed quinazolinone derivatives as novel tyrosinase inhibitor: synthesis, inhibitory activity, and mechanism

Y Huang, J Yang, Y Chi, C Gong, H Yang, F Zeng… - Molecules, 2022 - mdpi.com
We synthesized a series of quinazolinone derivates as tyrosinase inhibitors and evaluated
their inhibition constants. We synthesized 2-(2, 6-dimethylhepta-1, 5-dien-1-yl) quinazolin-4 …

Recent discovery of non-nucleobase thymidine phosphorylase inhibitors targeting cancer

H Bera, S Chigurupati - European Journal of Medicinal Chemistry, 2016 - Elsevier
Abstract Thymidine phosphorylase (TP, EC 2.4. 2.4), an enzyme involved in pyrimidine
salvage pathway, is identical to platelet-derived endothelial cell growth factor (PD-ECGF) …

[HTML][HTML] Enzyme inhibitory and anti-cancer properties of Moringa peregrina

SFA Albaayit - Vitae, 2024 - scielo.org.co
Background: Moringa peregrina is widely used in the traditional medicine of the Arabian
Peninsula to treat various ailments, because it has many pharmacologically active …

Thymidine phosphorylase and prostrate cancer cell proliferation inhibitory activities of synthetic 4-hydroxybenzohydrazides: In vitro, kinetic, and in silico studies

S Javaid, SM Saad, H Zafar, R Malik, KM Khan… - Plos one, 2020 - journals.plos.org
Over-expression of thymidine phosphorylase (TP) plays a key role in many pathological
complications, including angiogenesis which leads to cancer cells proliferation. Thus in …

Natural compounds as angiogenic enzyme thymidine phosphorylase inhibitors: In vitro biochemical inhibition, mechanistic, and in silico modeling studies

S Javaid, M Shaikh, N Fatima, MI Choudhary - PloS one, 2019 - journals.plos.org
Natural flora is the richest source of novel therapeutic agents due to their immense chemical
diversity and novel biological properties. In this regard, eighteen natural products belonging …