Synthesis, docking study, and in-vitro anti-cancer evaluation of new triazole derivatives of flufenamic acid-Reference-Cited by-同舟云学术

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Synthesis, docking study, and in-vitro anti-cancer evaluation of new triazole derivatives of flufenamic acid

Published:2021-05 Issue: Volume: Page:
ISSN:2214-7853
Container-title:Materials Today: Proceedings
language:en
Short-container-title:Materials Today: Proceedings

Author:

Al-Bayati Ammar I.,Razzak Mahmood Ammar A.,Tahtamouni Lubna H.^ORCID,Al-Mazaydeh Zainab A.,Rammaha Majdoleen S.,Al-bayati Rheda I.,Alsoubani Fatima

Publisher

Elsevier BV

Subject

General Medicine

Reference33 articles.

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2. Advancements in development’s of the heterocyclic nucleoside for treatments of the cancer - a review;Mirzas;Nucleotides Nucleic Acids,2019

3. The importance of heterocyclic compounds in anti-cancer drug design;Pearce;Drug Discov. World,2017

4. Facile synthesis of indole heterocyclic compounds based micellar nano anti-cancer drugs;Ali;RSC Adv.,2018

5. Recent advances in various biological potential;Daoudi;Moroccan J. Heterocycl. Chem.,2020

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1. In silico investigations of triazole -trimethoxyphenyl hybrids as anti-proliferative agents against adenocarcinomic human alveolar basal epithelial cells (A549): DFT, QSAR and Molecular Docking Approaches;2024-03-01

2. Design, synthesis, and biological evaluation of new celecoxib analogs as apoptosis inducers and cyclooxygenase‐2 inhibitors;Archiv der Pharmazie;2022-08-17

3. Synthesis, docking study, and structure activity relationship of novel anti-tumor 1, 2, 4 triazole derivatives incorporating 2-(2, 3- dimethyl aminobenzoic acid) moiety;Pharmacia;2022-05-11

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