Design, synthesis and biological activities of novel 5-isopropyl-2-methylphenolhydrazide-based sulfonamide derivatives
Sulfonamides have enormous importance in biological sciences. In the present investigation, the fundamental energetic group, hydrazide-based sulfonamide, has been incorporated into a naturally occurring phenolic monoterpenoid, carvacrol (5-isopropyl-2-methylphenol) moiety, with the aim of combining...
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Veröffentlicht in: | Research on chemical intermediates 2017-04, Vol.43 (4), p.2241-2252 |
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Hauptverfasser: | , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
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Zusammenfassung: | Sulfonamides have enormous importance in biological sciences. In the present investigation, the fundamental energetic group, hydrazide-based sulfonamide, has been incorporated into a naturally occurring phenolic monoterpenoid, carvacrol (5-isopropyl-2-methylphenol) moiety, with the aim of combining the active groups in order to generate more potent antimicrobial and anti-oxidant agents. Series of hydrazide-based sulfonamide derivatives (
IV a
–
g
) have been synthesized and characterized by modern sophisticated techniques such as
1
H NMR,
13
C NMR and LC–MS. The newly synthesized derivatives were screened for their antimicrobial activities against three fungal (
Aspergillus niger
,
A. flavus
and
A. fumigatus
) and three bacterial (
Escherichia coli
,
Staphylococcus aureus
and
Bacillus subtilis
) species, of which compounds
IVc
and
IVd
were found to have good antifungal activity and compounds
IVd
and
IVg
exhibited decent antibacterial activities. antioxidant activity was performed by DPPH radical scavenging assay. Compound
IVd
has been found to be more active in comparison to standard ascorbic acid and compounds
IVa
,
IVb
, and
IVc
demonstrated excellent antioxidant activity.
Graphical Abstract |
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ISSN: | 0922-6168 1568-5675 |
DOI: | 10.1007/s11164-016-2759-5 |