Synthesis and biological activity of 2-arylaminonicotinic acid hydrazide derivatives

Mikhalev, A. I.; Falaleeva, L. B.; Шрамм, Н. И.; Polukhina, L. M.; Zalesov, V. S.; Pershin, G. N.

doi:10.1007/bf00765715

Cited by 3 publications

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“…The derivatives of hydrazides always show higher biological activities than amides; consequently, they are considered as an ideal and fully qualified alternative to amides. Hydrazide derivatives have been found as ubiquitous building blocks in fungicides, which exhibit antituberculosis, , antidepressant, insecticidal, anticonvulsant, antiviral, , anti-inflammatory, , anticancer, antifungal, − antibacterial, − and other − properties. For instance, RH-5849 is the first nonsteroidal ecdysone agonist that exhibited admirable activity against Drosophila via stimulating the ecdysteroid receptors (EcR) and inducing the molt of larva .…”

Section: Introductionmentioning

confidence: 99%

Synthesis, Structure–Activity Relationship, and Mechanism of a Series of Diarylhydrazide Compounds as Potential Antifungal Agents

Liu

et al. 2023

J. Agric. Food Chem.

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A series of simple diarylhydrazide derivatives (45 examples) were well-designed, prepared, and screened for their antifungal activities both in vitro and in vivo. Bioassay results suggested that all designed compounds had significant activity against Alternaria brassicae (EC 50 = 0.30−8.35 μg/mL). Among of them, 2c, as the highest activity compound, could effectively inhibit the growth of plant pathogens Pyricularia oryza, Fusarium solani, Alternaria solani, Alternaria brassicae, and Alternaria alternate and was more potent than carbendazim and thiabendazole. 2c showed almost 100% protection at 200 μg/mL in vivo activity against A. solani in tomato. Moreover, 2c did not affect the germination of cowpea seed and the growth of normal human hepatocytes. The preliminary mechanistic exploration documented that 2c could result in the abnormal morphology and irregular structure of the cell membrane, destroy the function of mitochondria, increase the reactive oxygen species, and inhibit the proliferation of hypha cell. The above results manifested that target compound 2c could be a potential fungicidal candidate against phytopathogenic diseases for its excellent fungicidal activities.

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Section: Introductionmentioning

confidence: 99%

Synthesis, Structure–Activity Relationship, and Mechanism of a Series of Diarylhydrazide Compounds as Potential Antifungal Agents

Liu

et al. 2023

J. Agric. Food Chem.

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“…They exhibited antimicrobial activity. It was shown [7] that 2-anisidinonicotinic acid hydrazide and its arylidene derivatives possessed antituberculosis and anticonvulsant activity.…”

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Synthesis and pharmacological activity of 2-arylaminonicotinic acid β-(3-carboxypropionyl)hydrazides

et al. 2011

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“…Previous research showed that hydrazides of 2-arylaminonicotinic acids exhibit antimicrobial activity; the hydrazide of 2-anisidinonicotinic acid, anticonvulsant activity [1,2]. b-(3-Carboxypropionyl)hydrazides of 2-arylaminonicotinic acids include compounds that exhibit procoagulation and antimicrobial activity.…”

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confidence: 99%

Synthesis, anticoagulant, antimicrobial, and antifungal activity of β-anthraniloylhydrazides of 2-arylaminonicotinic acids

Konshin¹,

Efremov²,

Syropyatov³

et al. 2011

Pharm Chem J

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Synthesis and biological activity of 2-arylaminonicotinic acid hydrazide derivatives

Cited by 3 publications

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Synthesis, Structure–Activity Relationship, and Mechanism of a Series of Diarylhydrazide Compounds as Potential Antifungal Agents

Synthesis, Structure–Activity Relationship, and Mechanism of a Series of Diarylhydrazide Compounds as Potential Antifungal Agents

Synthesis and pharmacological activity of 2-arylaminonicotinic acid β-(3-carboxypropionyl)hydrazides

Synthesis, anticoagulant, antimicrobial, and antifungal activity of β-anthraniloylhydrazides of 2-arylaminonicotinic acids

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