scholarly journals Isolation and Characterization of Alkyl Peroxy Radical Scavenging Compound from Leaves of Laurus nobilis

2002 ◽  
Vol 25 (1) ◽  
pp. 102-108 ◽  
Author(s):  
Hye Won Kang ◽  
Kwang Won Yu ◽  
Woo Jin Jun ◽  
Ih Seop Chang ◽  
Sang Bae Han ◽  
...  
2021 ◽  
Vol 38 (1) ◽  
pp. 1-5
Author(s):  
Md Arifur Rahman ◽  
Ahmed Abu Rus’d ◽  
Md Enamul Haque

Sonneratia apetala (S. apetala) (Lythraceae) has been investigated for the isolation and characterization of antimicrobial compounds and evaluation of their biological activities. The chloroform extract of the stem bark and different partitionate of the chloroform extracts i.e. Petroleum ether soluble fraction (PESF), Ethyl acetate soluble fraction(EASF), Methanol soluble fraction(MSF) and aqueous soluble fractions (ASF) were subjected to different chromatographic techniques to isolate secondary metabolites. Successive chromatographic separation and purification yielded a total of two compounds identified and characterized as Taraxerone(1) and 5,8-dihydroxy- 6-methoxy-4,9-dioxo-1,3,4,9-tetrahydronaphthol[2,3-c]furan-1-yl acetate (2) by extensive proton NMR spectrum (1H-NMRspectrum) analysis. The different partitionate like PESF, EASF, MESF and ASF were subjected to screen their antimicrobial properties against some selected Gram positive and Gram negative bacteria and fungi, brine shrimp lethality and antioxidant activities. The maximum zone of inhibition of chloroform extract was found against Pseudomonas sp. (16mm). All fractions showed more activity against Gram negative bacteria then Gram positive bacteria. In the brine shrimp lethality bioassay, among all extracts, the petroleum ether and ethyl acetate soluble fraction showed significant lethality having the LC50 value of 7.72 μg/ml. The antioxidant activity was evaluated in terms of determination of free radical scavenging activity (DPPH assay). Among all the extracts of S. apetala the highest free radical scavenging activity showed by (Methanol soluble fraction) MESF with IC50 value 18.0 μg/ml. Bangladesh J Microbiol, Volume 38, Number 1, June 2021, pp 1-5


2019 ◽  
Vol 2 (2) ◽  
Author(s):  
Isaac John Umaru

Objective: This investigation involves the extraction, isolation, and characterization of chemical constituents from a Barringtonia family plant, Barringtonia asiatica followed by Antibacterial, cytotoxicity and evaluation of its antioxidant principles. Methods: The dried stem-bark powders were subjected to sequential soaking with polar and nonpolar solvents and extraction using rota-vap. Dichloromethane extract reveals the presence of significant amount of phytochemicals. The dichloromethane extract was subjected to isolation using column chromatographic analysis with solvents such as, dichloromethane, chloroform, hexane, ethyl acetate and methanol. Further, the isolated compound was subjected to thin layer chromatography technique and spectral analysis such as infrared, 1H-NMR, 13C-NMR, FT-IR, and mass spectroscopy. The antibacterial using agar disc method. Results: The compound was isolated in hexane: ethyl acetate (9:1) and dichloromethane: ethyl acetate in the solvent system in the ratio of 9:1 and 7:3, respectively using column chromatographic technique. On the basis of phytochemical, chromatographic, and spectral analysis, the isolated compounds were identified as Nerolidiol and Heneicosane. Conclusion: This compound was isolated for the first time from the stem-bark of Barringtonia asiatica. The in vitro antioxidant assay of isolated compounds has shown a dose-dependent increase in free radical scavenging activity using DPPH, the antibacterial and artemia salina cytotoxicity testing showed a significant result. The chromatographic separation led to the isolation of Nerolidiol (1) and Heneicosane (2). Their structures were determined by 1H-NMR, 13CNMR, IR and MS data analysis as well as by comparison of their data with the published values.


2018 ◽  
Vol 1 (4) ◽  
pp. 46 ◽  
Author(s):  
Siripat Ngoennet ◽  
Yasuhiro Nishikawa ◽  
Takashi Hibino ◽  
Rungaroon Waditee-Sirisattha ◽  
Hakuto Kageyama

This report provides a broadly applicable and cost-effective method for the purification of mycosporine-like amino acids (MAAs) from cyanobacteria. As MAAs are known to have multiple bioactivities for health and beauty, a universal isolation method of MAAs from biomass is attractive. In particular, the biomass of photosynthetic microorganisms such as cyanobacteria is of interest as a natural source of useful compound production, because of their photoautotrophic property. The method presented here is applicable for the isolation of mycosporine-2-glycine (M2G), which is a rare MAA produced in a halotolerant cyanobacterium. This method also allowed for the isolation of two of the most common MAAs, shinorine (SHI) and porphyra-334 (P334). A three-step separation process using low pressure liquid chromatography yielded purified MAAs, which were characterized by nuclear magnetic resonance (NMR) and liquid chromatography-mass spectrometry (LC/MS) analyses. The purified MAAs exhibited free radical scavenging activity in the 2,2′-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid) (ABTS) assay. The experimental parameters obtained in this report may allow for a scale-up of the MAA purification process for future industrial applications.


2000 ◽  
Vol 31 (2) ◽  
pp. 149-149 ◽  
Author(s):  
T Tozaki ◽  
H Kakoi ◽  
S Mashima ◽  
K Hirota ◽  
T Hasegawa ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document