Polyphenols: A concise overview on the chemistry, occurrence, and human health

A Durazzo, M Lucarini, EB Souto, C Cicala… - Phytotherapy …, 2019 - Wiley Online Library
This review gives an updated picture of each class of phenolic compounds and their
properties. The most common classification implies the subdivision of phenolics in two main …

A comprehensive review of monoamine oxidase inhibitors as Anti-Alzheimer's disease agents: A review

S Manzoor, N Hoda - European journal of medicinal chemistry, 2020 - Elsevier
Monoamine oxidases (MAO-A and MAO-B) are mammalian flavoenzyme, which catalyze the
oxidative deamination of several neurotransmitters like norepinephrine, dopamine, tyramine …

Multi-objective de novo drug design with conditional graph generative model

Y Li, L Zhang, Z Liu - Journal of cheminformatics, 2018 - Springer
Recently, deep generative models have revealed itself as a promising way of performing de
novo molecule design. However, previous research has focused mainly on generating …

From oxiranes to oligomers: Architectures of US FDA approved pharmaceuticals containing oxygen heterocycles

MD Delost, DT Smith, BJ Anderson… - Journal of Medicinal …, 2018 - ACS Publications
Oxygen heterocycles are the second most common type of heterocycles that appear as
structural components of US Food and Drug Administration (FDA) approved …

Site-selective cross-coupling of polyhalogenated arenes and heteroarenes with identical halogen groups

V Palani, MA Perea, R Sarpong - Chemical reviews, 2021 - ACS Publications
Methods to functionalize arenes and heteroarenes in a site-selective manner are highly
sought after for rapidly constructing value-added molecules of medicinal, agrochemical, and …

A Strategy for Accessing Trifluoromethyl Carbinol-Containing Chromones from o-Hydroxyaryl Enaminones and Trifluoroacetaldehyde/Ketone Derivatives

S Pan, M Song, L Zuo, X Geng… - The Journal of Organic …, 2023 - ACS Publications
Herein, we present a practical strategy for the direct construction of structurally diverse
trifluoromethyl carbinol-containing compounds, especially CF3-substituted tertiary alcohol …

Synthetic heterocyclic candidates as promising α-glucosidase inhibitors: An overview

M Dhameja, P Gupta - European journal of medicinal chemistry, 2019 - Elsevier
Abstract α-Glucosidase enzyme inhibition is an effective therapeutic decorum in the
treatment of type 2 diabetes mellitus. Since 1990, three α-glucosidase inhibitors are known …

Toward the generation of 2-amino-3-formyl difunctionalized chromones via Pd-enabled rearrangement strategy

Q Tong, RF Xiu, JH Chen, Y Zhang, BD Cui… - ACS …, 2023 - ACS Publications
Accomplished herein is a rearrangement strategy for the highly efficient assembly of
synthetically cumbersome while medicinally significant 2-amino-3-formyl chromones via …

AI-aided design of novel targeted covalent inhibitors against SARS-CoV-2

B Tang, F He, D Liu, F He, T Wu, M Fang, Z Niu, Z Wu… - Biomolecules, 2022 - mdpi.com
The drug repurposing of known approved drugs (eg, lopinavir/ritonavir) has failed to treat
SARS-CoV-2-infected patients. Therefore, it is important to generate new chemical entities …

Agarwood induction: current developments and future perspectives

CS Tan, NM Isa, I Ismail, Z Zainal - Frontiers in plant science, 2019 - frontiersin.org
Agarwood is a resinous part of the non-timber Aquilaria tree, which is a highly valuable
product for medicine and fragrance purposes. To protect the endangered Aquilaria species …