Brief introduction of 2-Methylthiophene

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Chemistry is the experimental and theoretical study of materials on their properties at both the macroscopic and microscopic levels. 554-14-3, Name is 2-Methylthiophene, molecular formula is C5H6S. In an article, author is Singh, Gurjaspreet,once mentioned of 554-14-3, Name: 2-Methylthiophene.

Acetylenic Indole-Encapsulated Schiff Bases: Synthesis, In Silico Studies as Potent Antimicrobial Agents, Cytotoxic Evaluation and Synergistic Effects

A family of pharmacophore acetylenic indole-3-carboxaldehyde (3) and acetylenic indole schiff bases (5a-5i) bearing indole framework were synthesized to afford structurally diverse moieties. Acetylenic indole-3-carboxaldehyde was coupled with various amines to furnish the novel scaffolds 5a-5i. These acetylenic indole Schiff bases (AISB) were synthesized in shorter times under microwave irradiation in comparison to classical reaction conditions. AISB were experimentally characterized by using IR, (HNMR)-H-1, (CNMR)-C-13, X ray crystallographic and mass spectrometric methods. The synthesized compounds showed promising anti-bacterial and anti-fungal properties when tested invitro against six bacterial and seven fungal strains. Among these, hybrids 5a, 5c, 5e and 5g were found to be even more potent than the standard drugs and were more influential against the bacterial than the fungal strains. These more potent compounds were then evaluated for their cytotoxicity by MTT assay on Hek293 and HeLa cells. The synergistic effect of bis-acetylenic compound 5g with kanamycin and amphotericin B has also been scrutinized. Further, the structural and electronic properties of the molecules were investigated theoretically by performing density functional theory (DFT).

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Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles