Recent development of VEGFR small molecule inhibitors as anticancer agents: A patent review (2021–2023)

J Zeng, Q Deng, Z Chen, S Yan, Q Dong, Y Zhang… - Bioorganic …, 2024 - Elsevier
VEGFR, a receptor tyrosine kinase inhibitor (TKI), is an important regulatory factor that
promotes angiogenesis and vascular permeability. It plays a significant role in processes …

A patent review of anticancer CDK2 inhibitors (2017–present)

MA Said, MA Abdelrahman… - Expert Opinion on …, 2022 - Taylor & Francis
Introduction The success of the CDK4/6 inhibitor Ibrance™(Palbociclib) as an anticancer
agent inspired and directed more efforts toward the discovery of selective cyclin-dependent …

Discovery and optimization of 2, 3-diaryl-1, 3-thiazolidin-4-one-based derivatives as potent and selective cytotoxic agents with anti-inflammatory activity

AM Shawky, FA Almalki, AN Abdalla… - European Journal of …, 2023 - Elsevier
Several studies have indicated the potential therapeutic outcomes of combining selective
COX-2 inhibitors with tubulin-targeting anticancer agents. In the current study, a novel series …

Novel 4-(piperazin-1-yl) quinolin-2 (1H)-one bearing thiazoles with antiproliferative activity through VEGFR-2-TK inhibition

A Hassan, M Badr, HA Hassan, D Abdelhamid… - Bioorganic & Medicinal …, 2021 - Elsevier
Abstract A new series of 2-(4-(2-oxo-1, 2-dihydroquinolin-4-yl) piperazin-1-yl)-N-(4-
phenylthiazol-2-yl) acetamide derivatives were synthesized and evaluated for anticancer …

Phytochemical, Cytotoxic, and Antimicrobial Evaluation of Tribulus terrestris L., Typha domingensis Pers., and Ricinus communis L.: Scientific Evidences for …

A Khalid, AS Algarni, HE Homeida… - Evidence‐Based …, 2022 - Wiley Online Library
Many medicinal plants have been utilized for centuries despite the lack of scientific evidence
of their therapeutic effects. This study evaluated the phytochemical and dual biological …

Discovery of new pyrimidopyrrolizine/indolizine-based derivatives as P-glycoprotein inhibitors: Design, synthesis, cytotoxicity, and MDR reversal activities

AM Shawky, AN Abdalla, NA Ibrahim… - European Journal of …, 2021 - Elsevier
Targeting P-glycoprotein (P-gp, ABCB1 transporter), which plays an essential role in multi-
drug resistance (MDR) in cancers, with new cytotoxic agents is a promising strategy in …

[HTML][HTML] Evaluation of the effects of a dasatinib-containing, self-emulsifying, drug delivery system on HT29 and SW420 human colorectal carcinoma cells, and MCF7 …

RA Baghdadi, AN Abdalla, MAS Abourehab… - Journal of Taibah …, 2024 - Elsevier
Cancer is the second leading cause of death worldwide, following cardiovascular disease. 1
This complicated illness can result from a variety of spatiotemporal alterations in cellular …

Bioactive fluorenes. Part IV: Design, synthesis, and a combined in vitro, in silico anticancer and antibacterial evaluation of new fluorene-heterocyclic sulfonamide …

EM Hussein, MS Malik, RI Alsantali, BH Asghar… - Journal of Molecular …, 2021 - Elsevier
A series of new fluorene-heterocyclic sulfonamide conjugates were designed and
synthesized as potential anticancer agents. In the design of the conjugates, heterocyclic ring …

Co-Inhibition of P-gp and Hsp90 by an Isatin-Derived Compound Contributes to the Increase of the Chemosensitivity of MCF7/ADR-Resistant Cells to Doxorubicin

AN Abdalla, M Di Stefano, G Poli, T Tuccinardi, A Bader… - Molecules, 2021 - mdpi.com
Breast cancer is a complex and multi-drug resistant (MDR) disease, which could result in the
failure of many chemotherapeutic clinical agents. Discovering effective molecules from …

Therapeutic Potential of Acanthospermum hispidum: A Comprehensive Analysis of Its Antimicrobial, Antioxidant, and Anticancer Properties

EH Moglad, AA Alnoor, NM Eltayeb… - Journal of …, 2024 - Wiley Online Library
Acanthospermum hispidum DC. is a plant with extensive traditional use in folk medicine for
treatment of various infections in Sudan including jaundice, stomach discomfort …