Evidence map›Paper›PMID 31384818›Full record

ArticleBMC chemistry2019

In silico design and synthesis of targeted rutin derivatives as xanthine oxidase inhibitors.

Neelam Malik, Priyanka Dhiman, Anurag Khatkar

Abstract read
In one paragraph

Article in BMC chemistry, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

10 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Identification ofMetabolites · 2024
    Article
  8. Review
  9. Article
  10. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Neelam Malik1Faculty, Department of Pharmaceutical Sciences, M.D. University, Rohtak, 124001 India.
Priyanka Dhiman1Faculty, Department of Pharmaceutical Sciences, M.D. University, Rohtak, 124001 India.
Anurag Khatkar2Laboratory for Preservation Technology and Enzyme Inhibition Studies, Department of Pharmaceutical Sciences, M.D. University, Rohtak, Haryana India.ORCID 0000-0002-0856-3620

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundXanthine oxidase is an important enzyme of purine catabolism pathway and has been associated directly in pathogenesis of gout and indirectly in many pathological conditions like cancer, diabetes and metabolic syndrome. In this research rutin, a bioactive flavonoid was explored to determine the capability of itself and its derivatives to inhibit xanthine oxidase.

objectiveTo develop new xanthine oxidase inhibitors from natural constituents along with antioxidant potential.

methodIn this report, we designed and synthesized rutin derivatives hybridized with hydrazines to form hydrazides and natural acids to form ester linkage with the help of molecular docking. The synthesized compounds were evaluated for their antioxidant and xanthine oxidase inhibitory potential.

resultsThe enzyme kinetic studies performed on rutin derivatives showed a potential inhibitory effect on XO ability in competitive manner with IC

conclusionTaking advantage of molecular docking, this hybridization of two natural constituent could lead to desirable xanthine oxidase inhibitors with improved activity.

Indexed as

AntioxidantMolecular dockingRutinXanthine oxidase

Identifiers

PMID31384818
PMCPMC6661775

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.