Isolation, Identification and quantitative analysis of Ellagic acid: a tannin compound from Helicteres isora

@inproceedings{Joshi2016IsolationIA,
  title={Isolation, Identification and quantitative analysis of Ellagic acid: a tannin compound from Helicteres isora},
  author={Ridhi Joshi and Ramraj Meena and Rishi Kesh Meena and Vidya Patni},
  year={2016}
}
ARTICLE INFO: Article history: Received: 26 July 2016 Received in revised form: 10 August 2016 Accepted: 18 August 2016 Available online: 30September 2016 

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References

SHOWING 1-10 OF 27 REFERENCES

Antibacterial and antifungal evaluation of some chalcogen bearing ligands , their transition and non-transition metal complexes

ARTICLE INFO: Article history: Received: 20 June2015 Received in revised form: 30 July 2015 Accepted: 15 August 2015 Available online: 30 September 2015

Studies on the Constituents of Fruits of Helicteres isora L.

Three new compounds; 4'-O-β-D-glucopyranosyl rosmarinic acid (2), 4,4'-O-di-β-D-glucopyranosyl rosmarinic acid(3) and 2R-O-(4'-O-β-D-glucopyranosyl caffeoyl)-3-(4-hydroxyphenyl) lactic acid named as

Screening and Quantitation of Phytochemicals and Nutritional Components of the Fruit and Bark of Helicteres Isora

Helicteres isora is a medium sized tree abundantly found in the hil ls and forests, well known for its use in traditional medicine. The fruit and bark are said to possess several medicinal values.

Antioxidant activity and free radical scavenging capacity of phenolic extracts from Helicteres isora L. and Ceiba pentandra L.

The potential of multiple antioxidant activity of samples can be further evidenced by inhibition of reactive oxygen mediated erythrocyte cell lysis and metal ion chelating activity.

Influence of Helicteres isora L . Bark Extracts on Glycaemic Control and Renoprotective Activity in Streptozotocin-induced Diabetic Rats *

The results indicate a prolonged action in reduction of blood glucose by Helicteres isora and are probably mediated through enhanced secretion of insulin from the β-cells of Langerhans or through extra pancreatic mechanism.

Free radical scavenging reactions and phytochemical analysis of triphala, an ayurvedic formulation

When triphala was tested for superoxide radical scavenging activity, it was observed that in addition to reacting with superoxideradical, it also inhibited uric acid formation, indicative of xanthine oxidase enzyme inhibitory activity.

Inhibitory effects of indonesian plant extracts on reverse transcriptase of an RNA Tumour Virus (I)

Indonesian medicinal plants extracts tested for inhibitory activity on avian myeloblastosis virus showed no appreciable cytotoxicity at concentrations where over 90% of RT activity was inhibited.

Plant drug analysis : a thin layer chromatography atlas

Screening of Unknown Commercial Drugs and Thin-Layer Chromatography Analysis of Herbal Drug Mixtures for Pungent-Tasting Principles.

Low concentrations of quercetin and ellagic acid synergistically influence proliferation, cytotoxicity and apoptosis in MOLT-4 human leukemia cells.

The interaction of ellagic acid and quercetin demonstrated an enhanced anticarcinogenic potential of polyphenol combinations, which was not based solely on the additive effect of individual compounds, but rather on synergistic biochemical interactions.

The effects of dietary ellagic acid on rat hepatic and esophageal mucosal cytochromes P450 and phase II enzymes.

It is demonstrated that EA causes a decrease in total hepatic P450 with a significant effect on hepatics P450 2E1, increases some hepatic phase II enzyme activities [GST, NAD-(P)H:QR and UDPGT] and decreases hepatic mEH expression, and inhibits the catalytic activity of some P450 isozymes in vitro.