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Antimalarial Activity of Tri- and Tetra-Substituted Anilino Pyrazoles
by
Basilico, Nicoletta
, Lusardi, Matteo
, Rotolo, Chiara
, Spallarossa, Andrea
, Parapini, Silvia
in
Antimalarials - pharmacology
/ antiplasmodial activity
/ Cancer therapies
/ Case management
/ Cervical cancer
/ Chemical tests and reagents
/ Chloroquine - pharmacology
/ Crizotinib
/ Disease prevention
/ Enzymes
/ Health aspects
/ Indicators and Reagents
/ Insecticides
/ Malaria
/ Melanoma
/ Plasmodium falciparum
/ pyrazoles
/ Pyrimethamine
/ regioselective synthesis
/ Structure-Activity Relationship
/ structure–activity relationships
/ Vaccines
2023
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Antimalarial Activity of Tri- and Tetra-Substituted Anilino Pyrazoles
by
Basilico, Nicoletta
, Lusardi, Matteo
, Rotolo, Chiara
, Spallarossa, Andrea
, Parapini, Silvia
in
Antimalarials - pharmacology
/ antiplasmodial activity
/ Cancer therapies
/ Case management
/ Cervical cancer
/ Chemical tests and reagents
/ Chloroquine - pharmacology
/ Crizotinib
/ Disease prevention
/ Enzymes
/ Health aspects
/ Indicators and Reagents
/ Insecticides
/ Malaria
/ Melanoma
/ Plasmodium falciparum
/ pyrazoles
/ Pyrimethamine
/ regioselective synthesis
/ Structure-Activity Relationship
/ structure–activity relationships
/ Vaccines
2023
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Antimalarial Activity of Tri- and Tetra-Substituted Anilino Pyrazoles
by
Basilico, Nicoletta
, Lusardi, Matteo
, Rotolo, Chiara
, Spallarossa, Andrea
, Parapini, Silvia
in
Antimalarials - pharmacology
/ antiplasmodial activity
/ Cancer therapies
/ Case management
/ Cervical cancer
/ Chemical tests and reagents
/ Chloroquine - pharmacology
/ Crizotinib
/ Disease prevention
/ Enzymes
/ Health aspects
/ Indicators and Reagents
/ Insecticides
/ Malaria
/ Melanoma
/ Plasmodium falciparum
/ pyrazoles
/ Pyrimethamine
/ regioselective synthesis
/ Structure-Activity Relationship
/ structure–activity relationships
/ Vaccines
2023
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Antimalarial Activity of Tri- and Tetra-Substituted Anilino Pyrazoles
Journal Article
Antimalarial Activity of Tri- and Tetra-Substituted Anilino Pyrazoles
2023
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Overview
Pyrazole core represents a privilege scaffold in medicinal chemistry; a number of pyrazole compounds are endowed with various pharmacological activities in different therapeutic areas including antimalarial treatment. Supported by this evidence, a series of 5-anilino-3-(hetero)arylpyrazoles were evaluated for their antiplasmodial activity in in vitro assays. The compounds were synthesized according to regioselective and versatile protocols that combine active methylene reagents, aryl isothiocyanates and (substituted)hydrazines. The considered derivatives 2 allowed the definition of consistent structure–activity relationships and compounds 2b,e,k,l were identified as the most interesting derivatives of the series showing micromolar IC50 values against chloroquine-sensitive and chloroquine-resistant Plasmodium strains. Additionally, the most active anilino-pyrazoles did not show any cytotoxicity against tumor and normal cells and were predicted to have favorable drug-like and pharmacokinetic properties.
Publisher
MDPI AG,MDPI
Subject
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