UGC Approved Journal no 63975(19)

ISSN: 2349-5162 | ESTD Year : 2014
Call for Paper
Volume 11 | Issue 5 | May 2024

JETIREXPLORE- Search Thousands of research papers



WhatsApp Contact
Click Here

Published in:

Volume 6 Issue 5
May-2019
eISSN: 2349-5162

UGC and ISSN approved 7.95 impact factor UGC Approved Journal no 63975

7.95 impact factor calculated by Google scholar

Unique Identifier

Published Paper ID:
JETIRBK06010


Registration ID:
207844

Page Number

55-60

Share This Article


Jetir RMS

Title

Molecular docking and Identification of Anisomeles derived inhibitors against Plasmodium falciparum glutathione s-transferase (PF GST) causing Malaria

Abstract

Malaria is a life-threatening disease caused by Plasmodium parasite that are transmitted to people through the bites of infected female Anopheles mosquitoes. In 2017 there were estimated 219 million cases of malaria in 90 countries and WHO reported that malarial death reached 435000 during the same year. Thus the complexity of the malarial parasite made development of malarial vaccine a difficult task. Hence to combat the situation there is need for several research that can identify more efficient anti-malarial drugs. Medicinal plants has the ability to cure many types of infectious disease and hence the present researchers are pointing towards various plant kingdoms. Anisomeles malabarica is a traditional medicinal plant and has been used as a folk medicine for the treatment of various diseases. The pharmacological studies of Anisomeles malabarica were reported for the use of Antibacterial diseases. The 34 compounds from Anisomeles malabarica were retrieved through several journal surveys. The protein PfGST (plasmodium falciparum glutathione S-transferase) of PDB ID 1OKT is responsible for causing malaria in human. Molecular docking is performed using Argus Lab protocol for these 34 compounds against the protein PfGST. The best docking pose were identified and compared with the docking interactions of the PfGST with synthetic compounds S-Hexylglutathione and Protoporphyrin. Thus the docking results and comparative studies shows that the compounds of Anisomeles malabarica exhibit the best binding interactions than the synthetic compounds interactions.

Key Words

Malaria, Anisomeles malabarica, Antibacterial, Synthetic compounds, Docking, Phytochemical.

Cite This Article

"Molecular docking and Identification of Anisomeles derived inhibitors against Plasmodium falciparum glutathione s-transferase (PF GST) causing Malaria ", International Journal of Emerging Technologies and Innovative Research (www.jetir.org), ISSN:2349-5162, Vol.6, Issue 5, page no.55-60, May-2019, Available :http://www.jetir.org/papers/JETIRBK06010.pdf

ISSN


2349-5162 | Impact Factor 7.95 Calculate by Google Scholar

An International Scholarly Open Access Journal, Peer-Reviewed, Refereed Journal Impact Factor 7.95 Calculate by Google Scholar and Semantic Scholar | AI-Powered Research Tool, Multidisciplinary, Monthly, Multilanguage Journal Indexing in All Major Database & Metadata, Citation Generator

Cite This Article

"Molecular docking and Identification of Anisomeles derived inhibitors against Plasmodium falciparum glutathione s-transferase (PF GST) causing Malaria ", International Journal of Emerging Technologies and Innovative Research (www.jetir.org | UGC and issn Approved), ISSN:2349-5162, Vol.6, Issue 5, page no. pp55-60, May-2019, Available at : http://www.jetir.org/papers/JETIRBK06010.pdf

Publication Details

Published Paper ID: JETIRBK06010
Registration ID: 207844
Published In: Volume 6 | Issue 5 | Year May-2019
DOI (Digital Object Identifier):
Page No: 55-60
Country: -, -, - .
Area: Engineering
ISSN Number: 2349-5162
Publisher: IJ Publication


Preview This Article


Downlaod

Click here for Article Preview

Download PDF

Downloads

0002838

Print This Page

Current Call For Paper

Jetir RMS