IN VITRO ANTI-MICROBIAL ACTIVITY OF (1R,3aR,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bR)-3a,5a,5b,8,8,11a-hexamethyl-1-prop-1- en-2-yl 1,2,3,4,5,6,7,7A,9,10,11,11B,12,13,13A,13B hexadecahydrocyclopenta[a]chrysen-9-ol ISOLATED FROM METHANOLIC LEAF EXTRACT OF ANDROGRAPHIS ECHIOIDES
Authors: Gurupriya S* and Cathrine L

ABSTRACT
Objective: The present study was designed to evaluate the in vitro antimicrobial activity of (1R,3aR,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bR)-3a,5a,5b,8,8,11a-hexamethyl-1-prop-1-en-2- yl1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-ol (Lupeol) isolated from methanolic leaf extract of Andrographis echioides. Methods: The anti microbial activity was determined by using the disc diffusion method against selected pathogens. The isolation was done using chromatography techniques. Isolated compound was subjected to spectral analysis. Structural elucidation was carried out by Interpretation of spectral data. The pure isolated compound from methanolic leaf extract of Andrographis echioides was confirmed to be (1R,3aR,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bR)-3a,5a,5b,8,8,11a-hexamethyl-1-prop-1-en-2-yl- 1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-ol. Results: The obtained results indicated that the isolated compound (1R,3aR,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bR)-3a,5a,5b,8,8,11a-hexamethyl-1-prop-1-en-2-yl- 1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-ol was more efficient against selected pathogens at higher concentration. The antimicrobial potential of methanolic leaf extract of isolated compound from Andrographis echioides determined on the basis of mean diameter of zone of inhibition around the disc in millimeters. The isolated compound (1R,3aR,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bR)-3a,5a,5b,8,8,11a-hexamethyl-1-prop-1-en-2-yl- 1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-ol exhibited antibacterial activity against Escherichia coli, Staphylococcus aureus and Enterococcus aerogenes, Pseudomonas aeruginosa ,Proteus vulgaris and anti-fungal activity against Candida albicans, Candida tropicalis, Aspergillus flavus, Aspergillus niger and Candida vulgaris. Conclusion: The isolated compound (1R,3aR,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bR)-3a,5a,5b,8,8,11ahexamethyl- 1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13bhexadecahydrocyclopenta[ a]chrysen-9-ol showed good anti-bacterial and anti-fungal activity against selected pathogens. Keywords: Andrographis echioides, leaves, anti-bacterial, anti-fungal, Isolated compound
Publication date: 01/09/2020
    https://ijbpas.com/pdf/2020/July/MS_IJBPAS_2020_50451.pdf
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https://doi.org/10.31032/IJBPAS/2020/9.7.5045