Structure-activity relationships of antimalarial indolo[3,2-c]quinolines [1, 2]
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Pharmacology,General Medicine
Reference8 articles.
1. Mechanism of action of amodiaquine. Synthesis of its indoloquinoline analog
2. CM Industries (1977) French Pat 2,327,783; June 17, 1977
3. 2,4,7-Triamino-6-ortho-substituted Arylpteridines. A New Series of Potent Antimalarial Agents
4. The chemotherapy of rodent malaria XLIII. Indolo (3,2-c)quinoline-N-oxides
5. The chemotherapy of rodent malaria
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1. Indoloquinoline Alkaloids as Antimalarials: Advances, Challenges, and Opportunities;ChemMedChem;2024-07-04
2. Palladium‐catalyzed dual C–H activation of N‐phenyl‐1H‐indole‐3‐carboxamides for the synthesis of 5,11‐dihydro‐6H‐indolo[3,2‐c]quinolin‐6‐ones;Journal of the Chinese Chemical Society;2023-12
3. A Compilation of Synthetic Strategies to Access the Most Utilized Indoloquinoline Motifs;Chemistry – An Asian Journal;2022-02-21
4. Synthesis of indolo- and benzothieno[3,2-c]quinolines via POCl3 mediated tandem cyclization of o-alkynylisocyanobenzenes derived from o-alkynyl-N-phenylformamides;New Journal of Chemistry;2022
5. Role of basic aminoalkyl chains in the lead optimization of Indoloquinoline alkaloids;European Journal of Medicinal Chemistry;2022-01
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