Tetrahydroquinoline: an efficient scaffold as mTOR inhibitor for the treatment of lung cancer
Author:
Affiliation:
1. Department of Pharmaceutical Chemistry, Institute of Pharmacy, Nirma University, Ahmedabad, Gujarat, 382481, India
Abstract
Funder
Nirma University
Publisher
Future Science Ltd
Subject
Drug Discovery,Pharmacology,Molecular Medicine
Link
https://www.future-science.com/doi/pdf/10.4155/fmc-2022-0204
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1. Synthesis, biological screening, and binding mode analysis of some N-substituted tetrahydroquinoline analogs as apoptosis inducers and anticancer agents;Journal of Molecular Structure;2024-12
2. Novel tetrahydroquinoline derivatives induce ROS-mediated apoptosis in glioblastoma cells;European Journal of Pharmaceutical Sciences;2024-09
3. Designing of target‐specific N‐substituted tetrahydroquinoline derivatives as potent mTOR inhibitors via integrated structure‐guided computational approaches;ChemistrySelect;2024-02-14
4. Synthesis of tetrahydroquinolines by gold-catalyzed cascade ring-opening–intramolecular hydroarylation of 2-alkynylazetidines;Tetrahedron;2024-01
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