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Journal ArticleDOI

Design, Synthesis, and Antifungal Evaluation of Neocryptolepine Derivatives against Phytopathogenic Fungi.

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TLDR
The designed assemblage possesses several benefits with a high-profile of variation in synthesized molecules, the ease of synthesis and good cost-effectiveness of commercially available synthetic reagents, all of which have highlighted the potential worth of compound 24 as a new and highly efficient agricultural fungicide.
Abstract
Neocryptolepine is an alkaloid isolated from traditional African herbal medicine Cryptolepis sanguinolenta, and its broad spectrum of biological activities has been illuminated in past decades. In this study, neocryptolepine and its derivatives (1-49) were designed and synthesized from economical and readily available starting materials. Their structures were confirmed by proton nuclear magnetic resonance, carbon nuclear magnetic resonance, and mass spectrometry. The synthesized compounds were screened for their antifungal profile against six agriculturally important fungi Rhizoctonia solani, Botrytis cinerea (B. cinerea), Fusarium graminearum, Mycosphaerella melonis, Sclerotinia sclerotiorum, and Magnaporthe oryzae. The results of in vitro assay revealed that compounds 5, 21, 24, 35, 40, 45, and 47 presented remarkable antifungal activity against the fungi tested with EC50 values lower than 1 μg/mL. Significantly, compound 24 displayed the most effective inhibitory potency against B. cinerea (EC50 = 0.07 μg/mL), and the data from in vivo experiments revealed that compound 24 demonstrated comparable protective activity with the positive control boscalid. Preliminary mechanism studies indicated that compound 24 showed impressive spore germination inhibitory effectiveness and lower cytotoxicity than azoxystrobin, imparted on normal function of the cell membrane and cell wall, and arrested the normal function of the nucleus. Besides the excellent inhibitory activity against agriculturally important phytopathogenic fungi tested, the designed assemblage possesses several benefits with a high profile of variation in synthesized molecules, the ease of synthesis, and good cost-effectiveness of commercially available synthetic reagents, all of these have highlighted the potential worth of compound 24 as a new and highly efficient agricultural fungicide.

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Journal ArticleDOI

Design, Synthesis, and Antifungal Evaluation of Cryptolepine Derivatives against Phytopathogenic Fungi.

TL;DR: In this paper, the antifungal properties of cryptolepine derivatives were evaluated against four agriculturally important fungi Rhizoctonia solani, Botrytis cinerea, Fusarium graminearum, and Sclerotinia sclerotiorum.
Journal ArticleDOI

Design, Synthesis, and Structure-Activity Relationship of Quinazolinone Derivatives as Potential Fungicides.

TL;DR: In this paper, the authors designed and synthesized eight series of quinazolinone derivatives and evaluated their anti-phytopathogenic fungal activity in vitro and in vivo.
Journal ArticleDOI

Discovery of Novel Pyrazole Carboxylate Derivatives Containing Thiazole as Potential Fungicides.

TL;DR: Inspired by commercially established fluxapyroxad as the lead compound of novel efficient antifungal ingredients, novel pyrazole carboxylate derivatives containing a flexible thiazole backbone were successfully designed, synthesized, and detected for their in vitro and in vivo biological activities against eight agricultural fungi as discussed by the authors.
Journal ArticleDOI

Design, Synthesis, Antibacterial, Antifungal and Anticancer Evaluations of Novel β-Pinene Quaternary Ammonium Salts

TL;DR: In this paper, six novel β-pinene quaternary ammonium (β-PQA) salts were synthesized and evaluated in vitro for their antifungal, antibacterial and anticancer activities.
Journal ArticleDOI

Recent advances for alkaloids as botanical pesticides for use in organic agriculture

TL;DR: Alkaloids are the most basic organic compounds involved in crucial physiological activities and are widely found in plants, animals and microorganisms and contribute to the anti-inflammatory, anti-tumor, and anti-cancer activities.
References
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Journal ArticleDOI

Antifungal efficacy of thymol, carvacrol, eugenol and menthol as alternative agents to control the growth of food-relevant fungi.

TL;DR: In this paper, the antifungal activity of thymol, carvacrol, eugenol and menthol against 11 food-decaying fungi was examined in terms of minimum inhibitory concentration (MIC) and minimum fungicidal concentration (MFC) using microdilution method in 96 multi-well microtiter plates.
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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.
Journal ArticleDOI

New alkaloids from Cryptolepis sanguinolenta

TL;DR: In this article, the root bark extract of the African medicinal plant, Cryptolepis sanguinolenta (Lindl.) Schlechter (Periplocaceae), and its structures elucidated on the basis of spectral evidence.
Journal ArticleDOI

Secondary metabolites of fluorescent pseudomonads in biocontrol of phytopathogens for sustainable agriculture

TL;DR: The objective of this review is to describe and assess the roles of secondary metabolites produced by fluorescent pseudomonads in controlling the phytopathogens and enhancing the plant health.
Journal ArticleDOI

Synthesis and antiplasmodial activity of aminoalkylamino-substituted neocryptolepine derivatives.

TL;DR: A series of chloro- and aminoalkylamino-substituted neocryptolepine derivatives were synthesized and evaluated as antiplasmodial agents, finding the most efficient compounds showed antiplAsmodial activities in the nanomolar range.
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