Non-steroidal anti-inflammatory drugs: Recent advances in the use of synthetic COX-2 inhibitors

M Ahmadi, S Bekeschus, KD Weltmann… - RSC Medicinal …, 2022 - pubs.rsc.org
Cyclooxygenase (COX) enzymes comprise COX-1 and COX-2 isoforms and are responsible
for prostaglandin production. Prostaglandins have critical roles in the inflammation pathway …

2-Aminobenzothiazoles in anticancer drug design and discovery

G Huang, T Cierpicki, J Grembecka - Bioorganic chemistry, 2023 - Elsevier
Cancer is one of the major causes of mortality and morbidity worldwide. Substantial
research efforts have been made to develop new chemical entities with improved anticancer …

Design, synthesis, and biological evaluation of novel EGFR inhibitors containing 5-chloro-3-hydroxymethyl-indole-2-carboxamide scaffold with apoptotic …

FAM Mohamed, HAM Gomaa, OM Hendawy, AT Ali… - Bioorganic …, 2021 - Elsevier
New EGFR inhibitor series of fifteen 5-chloro-3-hydroxymethyl-indole-2-carboxamide
derivatives has been designed, synthesized, and tested for antiproliferative activity against a …

New benzothiazole hybrids as potential VEGFR-2 inhibitors: design, synthesis, anticancer evaluation, and in silico study

MM Al-Sanea, A Hamdi, AAB Mohamed… - Journal of enzyme …, 2023 - Taylor & Francis
A new series of 2-aminobenzothiazole hybrids linked to thiazolidine-2, 4-dione 4a–e, 1, 3, 4-
thiadiazole aryl urea 6a–d, and cyanothiouracil moieties 8a–d was synthesised. The in vitro …

Synthesis and anticancer evaluation of novel indole based arylsulfonylhydrazides against human breast cancer cells

A Gaur, MN Peerzada, NS Khan, I Ali, A Azam - ACS omega, 2022 - ACS Publications
A series of novel indole based sulfonohydrazide derivatives (5a–k) containing morpholine
heterocyclic ring were synthesized through multistep chemical reactions. The target …

EGFR-targeted pentacyclic triterpene analogues for glioma therapy

HI Ciftci, MO Radwan, B Sever, AK Hamdy… - International Journal of …, 2021 - mdpi.com
Glioma, particularly its most malignant form, glioblastoma multiforme (GBM), is the most
common and aggressive malignant central nervous system tumor. The drawbacks of the …

Recent advances in nitrogen-containing heterocyclic compounds as receptor tyrosine kinase inhibitors for the treatment of cancer: biological activity and structural …

KT Jha, A Shome, PA Chawla - Bioorganic Chemistry, 2023 - Elsevier
Erratic cell proliferation is the initial symptom of cancer, which can eventually metastasize to
other organs. Before cancer becomes metastatic, its spread is triggered by pro-angiogenic …

Synthesis of new bioactive indolyl-1, 2, 4-triazole hybrids as dual inhibitors for EGFR/PARP-1 targeting breast and liver cancer cells

MF Youssef, MS Nafie, EE Salama, ATA Boraei… - ACS …, 2022 - ACS Publications
Cancer is the most severe disease worldwide. Every year, tens of millions of people are
diagnosed with cancer, and over half of those people will ultimately die from the disease …

Unveiling the chemistry of 1, 3, 4‐oxadiazoles and thiadiazols: A comprehensive review

VK Gour, S Yahya, M Shahar Yar - Archiv der Pharmazie, 2024 - Wiley Online Library
Oxadiazoles and thiadiazoles are malleable heterocycles that have recently generated
major interest in the field of medicinal chemistry. Compounds based on these moieties have …

Design, synthesis and investigation of the mechanism of action underlying anti-leukemic effects of the quinolinequinones as LY83583 analogs

HI Ciftci, N Bayrak, M Yıldız, H Yıldırım, B Sever… - Bioorganic …, 2021 - Elsevier
Literature conclusively shows that one of the quinolinequinone analogs (6-anilino-5, 8-
quinolinequinone), referred to as LY83583 hereafter, an inhibitor of guanylyl cyclase, was …