Pyridine Scaffolds, Phenols and Derivatives of Azo Moiety: Current Therapeutic Perspectives
Пиридиновые каркасы, фенолы и производные азосоединений: современные терапевтические перспективы
2021-08-11
SCID: 54.1/p8y9w9n7
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azo derivativesminimum inhibitory concentration (MIC)phenolic compounds (phenols)pyridinesstructure-activity relationship
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Abstract (AI)
Synthetic heterocyclic compounds have incredible potential against different diseases; pyridines, phenolic compounds and the derivatives of azo moiety have shown excellent antimicrobial, antiviral, antidiabetic, anti-melanogenic, anti-ulcer, anticancer, anti-mycobacterial, anti-inflammatory, DNA binding and chemosensing activities. In the present review, the above-mentioned activities of the nitrogen-containing heterocyclic compounds (pyridines), hydroxyl (phenols) and azo derivatives are discussed with reference to the minimum inhibitory concentration and structure-activity relationship, which clearly indicate that the presence of nitrogen in the phenyl ring; in addition, the hydroxyl substituent and the incorporation of a diazo group is crucial for the improved efficacies of the compounds in probing different diseases. The comparison was made with the reported drugs and new synthetic derivatives that showed recent therapeutic perspectives made in the last five years.
Key Findings
1
Incorporation of a diazo (azo) group is key to increasing the efficacy of compounds for probing different diseases.
2
Presence of hydroxyl substituents (phenolic groups) is crucial for improved therapeutic activity across analyzed compounds.
3
Pyridines, phenolic compounds, and azo derivatives show broad bioactivities including antimicrobial, antiviral, antidiabetic, anti-melanogenic, anti-ulcer, anticancer, anti-mycobacterial, anti-inflammatory, DNA binding and chemosensing.
4
Structure–activity relationships and minimum inhibitory concentration data indicate that nitrogen incorporation into the phenyl ring enhances biological efficacy.
5
The review compares reported drugs and newly synthesized derivatives from the last five years, highlighting recent therapeutic perspectives of these scaffolds.
Research Object
Pyridine, phenol, and azo-derivative small-molecule scaffolds (nitrogen-containing heterocycles, hydroxylated aromatics, and diazo-containing compounds)
Research Subject
Therapeutic bioactivities and structure–activity relationships (antimicrobial, antiviral, antidiabetic, anti-melanogenic, anti-ulcer, anticancer, anti-mycobacterial, anti-inflammatory, DNA-binding and chemosensing activities) and how nitrogen, hydroxyl and diazo substituents modulate efficacy (including MIC comparisons and recent synthetic derivatives)
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2021-08-11
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