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Synthesis, Characterization and Anti-Microbial Evaluation of Substituted Benzo[g]indol-2-one Derivatives


Affiliations
1 Department of Pharmaceutical Chemistry, J.K.K. Nataraja College of Pharmacy, Komarapalayam-638183 Tamil Nadu, India
2 Department of Pharmaceutical Chemistry, J.K.K. Nattraja College of Pharmacy, Komarapalayam-638183, Tamil Nadu, India
     

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Indole derivatives (Isatin) are potential synthons, for building synthetically a variety of chemical systems known for their broader biological and pharmacological applications. In the present investigation, title compounds (V1-V5) were synthesized by the condensation reaction of 3-[(2)-(phenyl methylidene) hydrazono]-1, 3-dihydro-2H-benzo[g]indol-2-one (IV) with different aryl aldehydes, as such reactions are not reported so far. The synthesized compounds were characterized by IR, 1H NMR and MASS spectroscopy. They were screened for their antimicrobial potential against bacterial strains i.e., Bacillus subtilis, Staphylococcus aureus, Escherichia coli, Proteus vulgaris and fungal strains i.e., Candida albicans and Yeast. Compound V5 (Nitro) was more potent anti- microbial agent against both bacteria [Gram (+Ve) and Gram (-Ve) organisms] followed by compound V4 (Chloro) and V2 (4-Methoxy).

Keywords

Isatin, Aryl Aldehydes, Antimicrobial Activity, Bacillus subtilis, Candida albicans.
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  • Synthesis, Characterization and Anti-Microbial Evaluation of Substituted Benzo[g]indol-2-one Derivatives

Abstract Views: 241  |  PDF Views: 0

Authors

M. Vijayabaskaran
Department of Pharmaceutical Chemistry, J.K.K. Nataraja College of Pharmacy, Komarapalayam-638183 Tamil Nadu, India
G. Lakshmi
Department of Pharmaceutical Chemistry, J.K.K. Nattraja College of Pharmacy, Komarapalayam-638183, Tamil Nadu, India
M. Senthilraja
Department of Pharmaceutical Chemistry, J.K.K. Nattraja College of Pharmacy, Komarapalayam-638183, Tamil Nadu, India
P. Sivakumar
Department of Pharmaceutical Chemistry, J.K.K. Nattraja College of Pharmacy, Komarapalayam-638183, Tamil Nadu, India
P. Vaijayanthimala
Department of Pharmaceutical Chemistry, J.K.K. Nattraja College of Pharmacy, Komarapalayam-638183, Tamil Nadu, India
P. Perumal
Department of Pharmaceutical Chemistry, J.K.K. Nattraja College of Pharmacy, Komarapalayam-638183, Tamil Nadu, India

Abstract


Indole derivatives (Isatin) are potential synthons, for building synthetically a variety of chemical systems known for their broader biological and pharmacological applications. In the present investigation, title compounds (V1-V5) were synthesized by the condensation reaction of 3-[(2)-(phenyl methylidene) hydrazono]-1, 3-dihydro-2H-benzo[g]indol-2-one (IV) with different aryl aldehydes, as such reactions are not reported so far. The synthesized compounds were characterized by IR, 1H NMR and MASS spectroscopy. They were screened for their antimicrobial potential against bacterial strains i.e., Bacillus subtilis, Staphylococcus aureus, Escherichia coli, Proteus vulgaris and fungal strains i.e., Candida albicans and Yeast. Compound V5 (Nitro) was more potent anti- microbial agent against both bacteria [Gram (+Ve) and Gram (-Ve) organisms] followed by compound V4 (Chloro) and V2 (4-Methoxy).

Keywords


Isatin, Aryl Aldehydes, Antimicrobial Activity, Bacillus subtilis, Candida albicans.