Design, synthesis, docking, ADMET studies, and anticancer evaluation of new 3-methylquinoxaline derivatives as VEGFR-2 inhibitors and apoptosis inducers

MM Alanazi, IH Eissa, NA Alsaif… - Journal of Enzyme …, 2021 - Taylor & Francis
Vascular endothelial growth factor receptor-2 (VEGFR-2) plays a critical role in cancer
angiogenesis. Inhibition of VEGFR-2 activity proved effective suppression of tumour …

Discovery of new quinoxaline-based derivatives as anticancer agents and potent VEGFR-2 inhibitors: Design, synthesis, and in silico study

MM Alanazi, H Elkady, NA Alsaif, AJ Obaidullah… - Journal of Molecular …, 2022 - Elsevier
VEGFR-2 is one of the most vital targets for the treatment of solid tumors. This work
represents synthetic approaches of new set of quinoxaline-based derivatives having …

Brønsted acid-promoted synthesis of common heterocycles and related bio-active and functional molecules

S Ponra, KC Majumdar - RSC advances, 2016 - pubs.rsc.org
Various heterocyclic systems based on natural and unnatural biologically active products
were synthesized by Brønsted acid-promoted cyclization. We have made an attempt to …

DABCO-Catalyzed DMSO-Promoted Sulfurative 1,2-Diamination of Phenylacetylenes with Elemental Sulfur and o-Phenylenediamines: Access to Quinoxaline-2 …

TMC Tran, ND Lai, TTT Bui, DH Mac, TTT Nguyen… - Organic …, 2023 - ACS Publications
The oxidative amination of alkynes typically requires transition metal catalysts and strong
oxidants. Herein, we alternatively utilize DABCO as a sulfur-activating catalyst to achieve the …

Discovery of new 3-methylquinoxalines as potential anti-cancer agents and apoptosis inducers targeting VEGFR-2: design, synthesis, and in silico studies

MM Alanazi, A Elwan, NA Alsaif… - Journal of Enzyme …, 2021 - Taylor & Francis
There is an urgent need to design new anticancer agents that can prevent cancer cell
proliferation even with minimal side effects. Accordingly, two new series of 3 …

New [1,2,4]triazolo[4,3-c]quinazolines as intercalative Topo II inhibitors: Design, synthesis, biological evaluation, and in silico studies

AA Gaber, M Sobhy, A Turky, WM Eldehna… - Plos one, 2023 - journals.plos.org
Fifteen quinazoline derivatives were designed and synthesized as DNA intercalators. The
cytotoxicity of the designed members was assessed against HCT-116 and HepG2 cancer …

Experimental and theoretical investigations for novel 6-nitroquinoxaline-2, 3‑dione derivatives: Synthesis, characterization, DFT calculations, ADME analysis, hirshfeld …

Y Seqqat, H El Monfalouti, S Laaraj, JT Mague… - Journal of Molecular …, 2025 - Elsevier
This work describes the synthesis of eight different 6-nitro-1, 4-disubstituted-quinoxaline-2, 3‑
dione derivatives (4a-h). The starting material, 6-nitroquinoxaline-2, 3‑dione 3 was prepared …

Efficient synthesis of 2-phenyl-3-substituted furo/thieno [2, 3-b] quinoxalines via Sonogashira coupling reaction followed by iodocyclization and subsequent palladium …

T Besharati-Seidani, A Keivanloo, B Kaboudin… - RSC …, 2016 - pubs.rsc.org
In this paper, we report the successful synthesis of new 2-phenyl-3-substituted furo/thieno [2,
3-b] quinoxaline derivatives from 2-chloro-3-methoxyquinoxaline and 2-chloro-3 …

Facile Synthesis of Quinoxaline-2-thiol and Quinoxaline from α-Oxosulfines and o-Arylenediamines

J Dong, Y Chen, X Huang - Synthesis, 2022 - thieme-connect.com
A series of quinoxaline-2-thiols and quinoxalines were prepared in moderate to good yields
from various phenacyl sulfoxides bearing 1-methyl-1H-tetrazole and o-arylenediamines. The …

Synthesis and pharmacological applications of certain quinoxaline analogues: A review

SK Subran, P Paira - Current Bioactive Compounds, 2017 - ingentaconnect.com
Background: Quinoxaline is versatile ring systems which possesses a wide range of
physicochemical and biological activities. This heterocyclic nucleus is becoming an …