Synthesis and cytotoxic activity of new indolylpyrrole derivatives

Author:

Radwan Mohamed A.A.,Al Rugaie Osamah,Al Abdulmonem Waleed,Alfaifi Mohammad Y.ORCID,Elbehairi Serag Eldin I.

Funder

King Khalid University

Qassim University

Publisher

Elsevier BV

Subject

General Chemical Engineering,General Chemistry

Reference48 articles.

1. Electrophilicity: the “dark-side” of indole chemistry;Bandini;Org. Biomol. Chem.,2013

2. A catalyst-and solvent-free three-component reaction for the regioselective one-pot access to polyfunctionalized pyrroles;Bhat;Tet. Lett.,2013

3. New pyrrole derivatives as antimycobacterial agents analogs of BM212;Biava;Bioorg. Med. Chem.,1999

4. Evaluating the effects of fluorine on biological properties and metabolic stability of some antitubulin 3-substituted 7-phenyl-pyrroloquinolinones;Bortolozzi;Eur. J. Med. Chem.,2019

5. Büyükbingöl, E., Süzen, S., Klopman, G., 1994. Studies on the synthesis and structure-activity relationships of 5-(3'-indolal)-2-thiohydantoin derivatives as aldose reductase enzyme inhibitors. Farmaco (Societa chimica italiana: 1989, 49(6), 443-447. PMID: 8074787.

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