Hydroxamic acid hybrids: Histone deacetylase inhibitors with anticancer therapeutic potency

Y Pan, H Hou, B Zhou, J Gao, F Gao - European Journal of Medicinal …, 2023 - Elsevier
Histone deacetylases (HDACs), a class of enzymes responsible for the removal of acetyl
functional groups from the lysine residues in the amino-terminal tails of core histones, play a …

Design, synthesis, and biological evaluation of tetrahydroquinoline amphiphiles as membrane-targeting antimicrobials against pathogenic bacteria and fungi

J Liu, H Li, Q He, K Chen, Y Chen, R Zhong, H Li… - European Journal of …, 2022 - Elsevier
The rising prevalence of drug-resistant pathogens is one of the biggest threats to human
health. The development of new antibiotics that can overcome drug resistance is in urgent …

Indenyl-thiazole and indenyl-formazan derivatives: Synthesis, anticancer screening studies, molecular-docking, and pharmacokinetic/molin-spiration properties

GH Alfaifi, TA Farghaly, MH Abdellattif - Plos one, 2023 - journals.plos.org
Two new series of thiazole and formazan linked to 5-Bromo-indan were synthesized, and
their structures were assured based on all possible analytical techniques. The size of the …

A Modular Approach for Accessing 3D Heterocycles via 1,2‐Dicyanation of Planar N‐Heteroarenes

S Pradhan, S Maiti, S Dutta… - Angewandte …, 2024 - Wiley Online Library
The rapid construction of three‐dimensional (3D) heterocyclic frameworks is a key challenge
in contemporary medicinal chemistry. The molecules with three‐dimensional complexity …

[HTML][HTML] Novel tetrahydroquinoline derivatives induce ROS-mediated apoptosis in glioblastoma cells

S Koochakkhani, DSN Branco, AV Alonso… - European Journal of …, 2024 - Elsevier
Abstract Current treatment for Glioblastoma Multiforme (GBM) is not efficient due to its
aggressive nature, tendency to infiltrate surrounding brain tissue, and chemotherapy …

Chemical characterization, antiproliferative activity and molecular docking of bioactive compounds from brown algae Fucus spiralis

B Imane, B Laila, H Fouzia, G Ismail, E Ahmed… - Algal Research, 2022 - Elsevier
Faced with the growing demands for natural products, the marine environment is a potential
source for the discovery of therapeutic compounds. The aim of this study was to evaluate the …

Chemistry and pharmacology of natural catechins from Camellia sinensis as anti-MRSA agents

R Gaur, GH Bao - Current Topics in Medicinal Chemistry, 2021 - ingentaconnect.com
Tea, a worldwide popular beverage rich in polyphenols, contributes to the prevention of
many diseases and thus is beneficial to human health. Tea is a product through processing …

Novel tetrahydroisoquinolines as DHFR and CDK2 inhibitors: synthesis, characterization, anticancer activity and antioxidant properties

EM Sayed, EA Bakhite, R Hassanien, N Farhan, HF Aly… - BMC chemistry, 2024 - Springer
In this study, we synthesized new 5, 6, 7, 8-tetrahydroisoquinolines and 6, 7, 8, 9-
tetrahydrothieno [2, 3-c] isoquinolines based on 4-(N, N-dimethylamino) phenyl moiety as …

The hepatoprotective effect of 4-phenyltetrahydroquinolines on carbon tetrachloride induced hepatotoxicity in rats through autophagy inhibition

MH Abdelgalil, RH Elhammamy, HM Ragab, E Sheta… - Biological Research, 2024 - Springer
Background The liver serves as a metabolic hub within the human body, playing a crucial
role in various essential functions, such as detoxification, nutrient metabolism, and hormone …

Chemo-and Diastereoselective Entries into All-Carbon α-Quaternary Aldehydes via C–C Insertion of 4-Diazoisoquinolin-3-ones into C–CHO Bonds

E Levashova, M Adamchik, G Kantin… - The Journal of Organic …, 2023 - ACS Publications
Herein, we describe a chemo-and diastereoselective formal C–C insertion reaction of 1, 2-
disubstituted 4-diazo-3 (2 H)-isoquinolones and 4-diazoisochroman-3-one into C–CHO …