Literature DB >> 27141229

3-D structural interactions and quantitative structural toxicity studies of tyrosine derivatives intended for safe potent inflammation treatment.

Ayarivan Puratchikody1, Dharmaraj Sriram2, Appavoo Umamaheswari1, Navabshan Irfan1.   

Abstract

BACKGROUND: Drugs that inhibit cyclooxygenase-2 (COX-2) while sparing cyclooxygenase-1 (COX-1) represent a new attractive therapeutic development and offer new perspective for further use of COX-2 inhibitors. Intention of this work is to develop safer, selective COX-2 inhibitors that do not produce harmful effects.
RESULTS: A series of 55 tyrosine derivatives were designed for evaluation as selective COX-2 inhibitors and investigated by in silico for their anti-inflammatory activities using C-Docker. The results of docking study showed that 35 molecules were found to selectively inhibit the enzyme COX-2. These molecules formed stable π hydrophobic and additional van der Waals interactions in the active site side pocket of COX-2. The molecules selected from docking studies were examined through ADMET descriptors and Osiris property explorer to find its safety profile as well. The tyrosine derivatives containing toxic fragments were eliminated.
CONCLUSION: The results conclude that out of 55, 19 molecules possessed best binding energy (< -3.333 kcal/mol) and these molecules had more selective and safer COX-2 inhibitor profile compared to the standard celecoxib.Graphical abstract3-D structural interactions of COX-2 inhibiting tyrosine derivatives.

Entities:  

Keywords:  ADMET descriptors; Anti-inflammatory; Docking; Osiris; Tyrosine derivatives

Year:  2016        PMID: 27141229      PMCID: PMC4852405          DOI: 10.1186/s13065-016-0169-9

Source DB:  PubMed          Journal:  Chem Cent J        ISSN: 1752-153X            Impact factor:   4.215


  19 in total

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6.  Structural requirements for potential HIV-integrase inhibitors identified using pharmacophore-based virtual screening and molecular dynamics studies.

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7.  Inhibition of HERG potassium channels by celecoxib and its mechanism.

Authors:  Roman V Frolov; Irina I Ignatova; Satpal Singh
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8.  Synthesis and structural properties of 2-((10-alkyl-10H-phenothiazin-3-yl)methylene)malononitrile derivatives; a combined experimental and theoretical insight.

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Journal:  Chem Cent J       Date:  2016-03-15       Impact factor: 4.215

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  4 in total

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2.  Design and virtual screening of novel fluoroquinolone analogs as effective mutant DNA GyrA inhibitors against urinary tract infection-causing fluoroquinolone resistant Escherichia coli.

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3.  Design and green synthesis of novel quinolinone derivatives of potential anti-breast cancer activity against MCF-7 cell line targeting multi-receptor tyrosine kinases.

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4.  An in-silico evaluation of different bioactive molecules of tea for their inhibition potency against non structural protein-15 of SARS-CoV-2.

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  4 in total

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