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Journal ArticleDOI

A new approach to the synthesis of benzofuro[3,2-b]quinolines, benzothieno[3,2-b]quinolines and indolo[3,2-b]quinolines†

Stanislav Radl, +2 more
- 01 Jul 2000 - 
- Vol. 37, Iss: 4, pp 855-862
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TLDR
In this article, a new method for preparation of quindoline 2 and its O and S analogs was presented, which represents a new way of preparation of the quinoline.
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This article is published in Journal of Heterocyclic Chemistry.The article was published on 2000-07-01. It has received 32 citations till now. The article focuses on the topics: Benzofuran & Benzothiophene.

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Citations
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Journal ArticleDOI

Synthesis and evaluation of quindoline derivatives as G-quadruplex inducing and stabilizing ligands and potential inhibitors of telomerase.

TL;DR: The results revealed that the introduction of electron-donating groups such as substituted amino groups at the C-11 position of quindoline significantly improved the inhibitory effect on telomerase activity.
Journal ArticleDOI

Indoloquinolines as Scaffolds for Drug Discovery

TL;DR: An overview of the potential of indoloquinolines as scaffolds in drug discovery is presented by reviewing the in vitro and in vivo biological activities of natural and synthetic analogues, as well as the proposed mechanisms of action and structure-activity relationships.
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Isolation, Biological Activities and Synthesis of Indoloquinoline Alkaloids: Cryptolepine, Isocryptolepine and Neocryptolepine

TL;DR: This review describes the isolation, brief biological activities and various synthetic methodologies developed during recent years for the preparation of this important class of alkaloids, with special emphasis on preparation and properties of cryptolepine 1, isocryptolepine 2 and neocryptolespine 3.
Journal ArticleDOI

Substituted indoloquinolines as new antifungal agents.

TL;DR: Comparison of MICs of a number of 2-substituted indoloquinolines designed to increase potency and expand the antifungal spectrum of cryptolepine shows them to be comparable to Amphotericin B and Ketoconazole.
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Facile and convenient syntheses of 6,11-dihydro-5H-indeno[1,2-c]isoquinolin- 5-ones and 6,11-dihydro-5H-indolo[3,2-c]isoquinolin-5-one.

TL;DR: The synthesis of 6,11-dihydro-5H-indeno[1,2-c]isoquinolin-5-ones from the base-promoted condensation reaction of homophthalic anhydride and 2-(bromomethyl)-benzonitrile and a convenient method for the synthesis of indolo[3,2 -c]isalquinolinones are described.
References
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Journal ArticleDOI

In Vitro and in Vivo Antiplasmodial Activity of Cryptolepine and Related Alkaloids from Cryptolepis sanguinolenta

TL;DR: Three different extracts and four alkaloids from the root bark of Cryptolepis sanguinolenta have been assessed in vitro against Plasmodium falciparum D-6, K-1, and W-2 (chloroquine-resistant strains) and showed a strong antiplasmodial activity.
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Constituents of West African Medicinal Plants XX: Quindoline from Cryptolepis sanguinolenta

TL;DR: An ethanol extract of the roots of Cryptolepis sanguinolenta afforded, after partitioning and chromatography, the alkaloids quindoline and CSA-3, and the structural elucidation of C SA-3 is currently in progress.
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Die Konstitution des Alkaloids Cryptolepin

TL;DR: In this paper, die Konstitution des Alkaloids Cryptolepin was aufgeklart und im Zusammenhang damit bewiesen, dass das zuerst von Fichter synthetisierte Chindolinsystem [Indolo-3′,2′:2,3-chinolin] auch in Naturprodukten vorkommen kann.
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Antimalarial Activity of Cryptolepine and Some Other Anhydronium Bases

TL;DR: Eight naturally occurring anhydronium bases and the synthetic quaternary compound Nb‐methylharmalane were tested against Plasmodium falciparum in vitro and Cryptolepine found to have moderate antimalarial activity; parasitaemia was suppressed by 80% at 50 mg/kg/day.
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