Date of Publication
12-12-1996
Document Type
Master's Thesis
Degree Name
Master of Science in Chemistry
Subject Categories
Chemistry
College
College of Science
Department/Unit
Chemistry
Thesis Adviser
Consolacion Y. Ragasa
Defense Panel Chair
Gerardo C. Janairo
Defense Panel Member
Jaime Raul O. Janairo
Marissa G. Noel
Abstract/Summary
Hyptis suaveolens afforded suaveolic acid, suaveolol and ursolic acid from the CHCl3 extract. The structures of suaveolic acid and suaveolol were identified by comparison of their 1H nmr spectral data with those found in the literature,11 while the structure of ursolic acid was identified by 1H nmr spectroscopy and FT-IR.Antimicrobial test conducted on suaveolol, suaveolic acid and ursolic acid using the paper disc diffusion method indicated that they are inactive against the bacteria Escherichia coli, Pseudomonas aeruginosa, Staphylococcus aureus, and Bacillus subtilis. However, it showed zones of inhibition against the fungi Candida albicans at a concentration of 100 ug/ml.Argemone mexicana afforded four interesting secondary metabolites from its CHCl3 extract: norchelerythrine, norsanguinarine, chelamine and sitosterol-B-D-glycoside. The separation was achieved by repeated gravity column chromatography (dry packing) and recrystallization. The structures of the compounds were elucidated by (1H, 13C, COSY) nmr, spectroscopy, and mass spectrometry.
Abstract Format
html
Language
English
Format
Accession Number
TG02530
Shelf Location
Archives, The Learning Commons, 12F Henry Sy Sr. Hall
Physical Description
108 leaves
Keywords
Lamiaceae--Analysis; Terpenes--Spectra; Extracts; Medicinal plants; Plants, Useful
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Recommended Citation
Maliwat, L. P. (1996). Antifungal terpenes from Hyptis suaveolens and alkaloids and saponin from Argemone mexicana. Retrieved from https://animorepository.dlsu.edu.ph/etd_masteral/1742