scholarly journals Sterol and triterpenoids from Hygrophila schulli Buch.-Ham.

2018 ◽  
Vol 44 (2) ◽  
pp. 319-321
Author(s):  
Md Abu Suflan ◽  
Fatema Begum ◽  
Mohammad Rashedul Haque ◽  
Choudhury Mamood Hasan ◽  
Mohammad Abdur Rashid

The methanol extract of whole plants of Hygrophila schulli Buch.-Ham. was subjected to repeated chromatographic separation and purification processes to isolate its chemical constituents. A total of three compounds were isolated which have been characterized as stigmasterol, lupeol and lup-20(29)-ene-3β,23- diol on the basis of 1H NMR spectral evidence and confirmed by comparing with published data, as well as co-TLC in case of stigmasterol and lupeol. This is the first report of lup-20(29)-ene-3β,23-diol from this plant.

2017 ◽  
Vol 55 (2) ◽  
pp. 188
Author(s):  
Nguyen Thi Mai

From the methanol extract of Bischofia javanica leaves, five compounds including 5'-b-D-glucopyranosyloxyjasmonic acid methyl ester (1), 2-(4-hydroxy-3-methoxyphenyl)ethyl-O-β-D-glucopyranoside (2), hexyl-O-β-D-glucopyranoside (3), friedelan-3-one (4), and gallic acid (5) were isolated. Their structures were elucidated by NMR spectra as well as in comparison with previous reported data. This is the first report of 1 and 2 from Bischofia javanica.


2016 ◽  
Vol 19 (2) ◽  
pp. 166-169 ◽  
Author(s):  
Bidyut Kanti Datta ◽  
Tahamina Iasmin ◽  
Mohammad A Rashid

Repeated chromatographic separation and purification of the n-hexane-ethyl acetate (3:1) extract of aerial parts of Polygonum viscosum provided a flavonoid- ternatin (1) and two steroids- stigmasterol (2) and stigmasta-4,22-dien-3-one (3). The structure of these compounds were determined on the basis of extensive NMR and other spectroscopic techniques and comparison with published data. The identity of steroids 2 and 3 was confirmed by co-TLC with authentic sample.Bangladesh Pharmaceutical Journal 19(2): 166-169, 2016


2018 ◽  
Vol 20 (2) ◽  
pp. 213-220
Author(s):  
Akhtaruzzaman Chowdhury ◽  
Md Ashraful Alam ◽  
Md Shafiullah Shajib ◽  
Mohammad Abdullah Al Mansur ◽  
Mohammad A Rashid

This article focuses on the chemical constituents and protection of biodiversity through plantation of saplings of Corypha taliera Roxb., a critically endangered plant of Bangladesh. Until 2010, the tree in the campus of University of Dhaka, used to be considered as the lone surviving species in the world in nature. Succesive chromatographic separation and purification of the methanol extract of air dried flowers of C. taliera provided β-sitosterol (1), β-amyrin (2), and betulinic acid (3) for the first time from its flowers. The structures of these purified compounds were established by extensive spectroscopic analysis and comparison of spectral data with published values as well as co-TLC with authentic samples. On the other hand, 500 mature seeds were sown in seed beds in the Medicinal Plant Garden of Faculty of Pharmacy, University of Dhaka, and Azimpur Government Officers' Quarter premises. After 40 days, the root was first seen to grow in its habitat and 85 days later the shoot developed up to 2.5 cm in height. The rate of germination was found to be 89-93%. The produced saplings were later on planted in different places of Bangladesh for conservation of the plant and protection of biodiversity by ex situ arrangement.Bangladesh Pharmaceutical Journal 20(2): 213-220, 2017


2021 ◽  
Vol 50 (4) ◽  
pp. 1191-1194
Author(s):  
- Md Moniruzzaman ◽  
Md Ruhul Kuddus ◽  
Md Al Amin Sikder ◽  
AM Sarwaruddin Chowdhury ◽  
Mohammad A Rashid

The study was carried out to investigate the composition of natural compounds of methanol extract of leaf and stem bark of Stereospermum suaveolens (Roxb.) DC by repeated chromatographic separation and purification processes over silica gel. The phytochemical investigation resulted in the isolation of a total of three compounds, which were identified as stigmasterol (1), β-amyrin (2) and 4-methoxycinnamic acid (3). The chemical structures of the isolated compounds were elucidated by analyses of their physical properties, acquired 1H NMR data and comparison with published reports. Among these, compounds 2 and 3 are first report of their isolation from this plant species. Bangladesh J. Bot. 50(4): 1191-1194, 2021 (December)


2017 ◽  
Vol 15 (2) ◽  
pp. 155-159 ◽  
Author(s):  
Md Mubarak Hossain ◽  
Faiza Tahia ◽  
Md Abdullah Al Mansur ◽  
Mohammad A Rashid

Four coumarin derivatives were isolated from the methanol extract of stem bark of Murraya koenigii (Linn.) Spreng. Extensive spectroscopic studies, including high field NMR analyses allowed to identify these compounds as meranzin hydrate (1), epoxyosthol (2), isomeranzin (3) and murracarpin (4). The identity of the compounds was confirmed by comparison with published data as well as co-TLC with authentic samples. This is the first report of occurrence of meranzin hydrate (1), epoxyosthol (2) and isomeranzin (3) from M. koenigii.Dhaka Univ. J. Pharm. Sci. 15(2): 155-159, 2016 (December)


2015 ◽  
Vol 13 (1) ◽  
pp. 31-36 ◽  
Author(s):  
Fatema Begum ◽  
Mohammad Rashedul Haque ◽  
Kazi Sharmin Nahar ◽  
Mohammad Abdur Rashid

The methanol extract of leaves and bark of Stereospermum suaveolens has been subjected to repeated-chromatographic separation and purification processes to isolate the secondary metabolites. A total of seven compounds have been isolated from the plant, which were identified as fridelin (1), ?-sitosterone (stigmast-5- en-3-one) (2), stigmasterol (3), 3,4-dimethoxy cis-caffeic acid (4), 3?-friedelanol (5), ?-amyrone (6) and glyceryl tricaprate (7). The structures of the isolated compounds were elucidated by extensive NMR studies. DOI: http://dx.doi.org/10.3329/dujps.v13i1.21857 Dhaka Univ. J. Pharm. Sci. 13(1): 31-36, 2014 (June)


2021 ◽  
Vol 13 (3) ◽  
pp. 71-78
Author(s):  
Quoc Luan Ngo ◽  
Thao Cuong Ta ◽  
Thi Manh Huynh Tran ◽  
Minh Dan Le ◽  
Khac Khong Minh Ngo ◽  
...  

This study is aimed to screen the biological activities and chemical composition to find evidences for potential medicinal applications of Centrostachys aquatica in the Mekong Delta. Crude methanol extract and subextracts in n-hexane, ethyl acetate, and acetone from Centrostachys aquatica were tested bioactivities. The methanol extract, n-hexane and ethyl acetate subextracts exhibited antimicrobial activity with corresponding MIC values of 200, 100 and 200 µg/mL, respectively. The ethyl acetate subextract was inhibited cytotoxicity against cancer cell line LU-1 with IC50 of 27.66 µg/mL. None of the  extracts showed antioxidant ability. Three known secondary metabolites including oleanolic acid (1), 20(E)-hydroxy-b-ecdysone (2), and b-spinasterol (3) were isolated for the first time from the bioactive (ethyl acetate) subextract of Centrostachys aquatica. Their structures were elucidated by modern spectra as MS, NMR and comparison with published data.


2021 ◽  
Vol 11 ◽  
Author(s):  
Charina Worarat ◽  
Wilart Pompimon ◽  
Phansuang Udomputtimekakul ◽  
Sukee Sukdee ◽  
Punchavee Sombutsiri ◽  
...  

Background: Although the chemical constituents and biological activities of a large number of plants in the Croton genus have been studied, there are still recently discovered plants to be investigated. Objective: 1. To investigate the anti-bacterial, anti-HIV1-RT, and cytotoxicity activities of crude extracts from these plants. 2. To investigate the chemical constituents of Croton fluviatilis, Croton acutifolius, and Croton thorelii. Method: The anti-bacterial, anti-HIV1-RT, and cytotoxicity of the three plants were evaluated by standard techniques. Extraction, separation, and purification of extracts from the three plants were undertaken. Results: The ethyl acetate extract of C. fluviatilis showed low anti-bacterial activity against E. aerogenes, E. coli 0157: H7, and P. mirabilis, together with the ethyl acetate extract of C. acutifolius displayed low anti-bacterial activity against E. aerogenes, while all the crude extracts of C. thorelii were inactive. The ethyl acetate extracts of C. thorelii, and C. fluviatilis showed strong inhibited HIV1-RT, whereas the ethyl acetate extract of C. acutifolius, and the hexane extract of C. fluviatilis displayed moderate inhibited HIV1-RT. Cytotoxic properties of three Croton plants were specific to KKU-M213, MDA-MB-231, A-549, and MMNK-1. Especially, the ethyl acetate extract of C. acutifolius exhibited strong cytotoxic activities against MDA-MB-231, A-549, and MMNK-1. Furthermore, the ethyl acetate extract of C. thorelii showed high cytotoxic activities against KKU-M213, and MDA-MB-231. Compounds 1, and 4 were found in C. fluviatilis. Compounds 2 and 4 were also found in C. acutifolius. Moreover, compound 3 was only found in C. thorelii. Conclusion: The present study revealed that the three Croton species are good sources of flavonoid compounds and further investigation of the chemical constituents from these plants may prove to be fruitful to discover more active compounds to be tested as potential medicines.


2011 ◽  
Vol 6 (2) ◽  
pp. 1934578X1100600 ◽  
Author(s):  
Phan Van Kiem ◽  
Nguyen Xuan Cuong ◽  
Nguyen Xuan Nhiem ◽  
Dan Thi Thuy Hang ◽  
Nguyen Hoai Nam ◽  
...  

One new megastigmane glycoside, ficalloside (1), and eleven known compounds, were isolated from methanol extract of Ficus callosa leaves by repeated column chromatography. Their structures were established on the basis of spectral and chemical evidence. The antioxidant activities of these compounds were measured using the oxygen radical absorbance capacity (ORAC) assay. Compound 8 exhibited potent antioxidant activity of 10.6 μM trolox equivalents at the concentration of 2 μM. At this concentration, compounds 4-7 and 9-12 showed significant antioxidant activity with ranging of 2.1~6.1 μM trolox equivalents.


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