scholarly journals ISOLATION AND CHARACTERISATION OF BERGENIN FROM ETHYL ACETATE EXTRACT OF FLUEGGEA VIROSA LEAVES

2020 ◽  
Vol 45 (6) ◽  
Author(s):  
C. T. Agber ◽  
T. A. Tor-Anyii ◽  
J. O. Igoli ◽  
J. V. Anyam

Bergenin is an important constituent of Flueggea virosa (Euphorbiaceae), a tropical plant with several traditional uses. While there are numerous reports on the isolation and characterization of bergenin, a rapid, high-throughput, readily accessible method for the isolation and characterization of the compound locally has not been reported. Isocratic elution of ethyl acetate extract via vacuum liquid chromatography (VLC) with methanol produced a white amorphous solid (100 mg), which was successfully isolated from 250 g of the plant. On the basis of spectral data (1H, C NMR, COSY, HSQC and HMBC) and comparison with literature reports, the structure of this solid was shown to be bergenin, a dihydroisocoumarin derivative of glucopyranosyl gallic acid.

2018 ◽  
Vol 10 (1) ◽  
pp. 87
Author(s):  
Doni Eko Saputra ◽  
Nestri Handayani ◽  
Muhammad Widyo Wartono

<p>Chemical isolation and identificationof root bark of <em>Calophyllumsoulattri</em>Burm. f. have been conducted. Isolation was conducted by maceration with ethyl acetate as solvent. Ethyl acetate extract was separated and purified by vacuum liquid chromatography and flash chromatography which was guided by thin layer chromatography to obtain yellowish white solid. Isolated compounds were determined by spectroscopy methods such as UV, FTIR, <sup>1</sup>H NMR, <sup>13</sup>C NMR, DEPT, HSQC, HMBC and were compared to the references. Based on the analysis result it’s known that the compounds are the mixture of?-sitosterol and stigmasterol.</p>


2016 ◽  
Vol 10 (1) ◽  
pp. 87
Author(s):  
Doni Eko Saputra ◽  
Nestri Handayani ◽  
Muhammad Widyo Wartono

<p>Chemical isolation and identificationof root bark of <em>Calophyllumsoulattri</em>Burm. f. have been conducted. Isolation was conducted by maceration with ethyl acetate as solvent. Ethyl acetate extract was separated and purified by vacuum liquid chromatography and flash chromatography which was guided by thin layer chromatography to obtain yellowish white solid. Isolated compounds were determined by spectroscopy methods such as UV, FTIR, <sup>1</sup>H NMR, <sup>13</sup>C NMR, DEPT, HSQC, HMBC and were compared to the references. Based on the analysis result it’s known that the compounds are the mixture of?-sitosterol and stigmasterol.</p>


Author(s):  
Yuri Pratiwi Utami ◽  
Imrawati Imrawati ◽  
Abd Rasyid

ISOLASI DAN KARAKTERISASI EKSTRAK ETANOL DAUN LEILEM (Clerodendrum minahassae Teijsm dan Binn.) DENGAN METODE SPEKTROFOTOMETRIISOLATION AND CHARACTERIZATION ETHANOL EXTRACT OF LEILEM LEAVES (Clerodendrum minahassae Teijsm and Binn) WITH METHODS SPECTROPHOTOMETRICYuri Pratiwi Utami1), Imrawati1), Abd.Rasyid.D1)1)Program studi sarjana farmasi, Sekolah Tinggi Ilmu Farmasi MakassarJl. Perintis Kemerdekaan KM.13,7 Daya telp/fax. 0411-583190 Makassar [email protected] leaf (Clerodendrum minahassae Teijsm .And Binn.) have been reported in traditional medicine for the treatment of various deseases such as stomatch ache and ascariasis. In Minahassa, leilem leaf generally consumed as vegetables. The present study revealed that leilem leaf can inhibit the growth of escherhia coli because of the presence of flavonoid that can demage bacterial cell membranes. This study at characterization of isolated compounds from ethanol extract of leilem leaves (Clerodendrum minahassae Teijsm and Binn). Extraction was done maceration using 70% ethanol with the percentage of rendement was 10,19%. The phytochemical analysis of ethanol extract of leilem leaves showed a positive result of alkoloid, flavonoid, streroid and tanin. The ethyl acetate extract was selected and 2 grams of it was taken to continued to second conventional column chromatography and 5 fractions were obtained. Fraction 2 was choosen and continued to preparative and result 2 isolates. Isolate 2 that showed one spot on tlc with rf 0,66. Was continued for spectrofotometri uv-vis and ftir analysis. The spectrophotometer uv-vis maximum wavalength at 269,0 nm and 333,0 nm. The ftir data indicated the presence of functional O-H, C-H, C=C and C-O which is suspected ad flavonoid.Keywords : Isolation, Characterization, leilem leaf (Clerodendrum minahassae Teijsm and Binn)ABSTRAKDaun leilem (Clerodendrum minahassae Teijsm dan Binn.) dilaporkan yaitu sebagai obat tradisional untuk menyembuhkan beberapa penyakit, seperti sakit perut dan Ascariasis. Daun leilem biasanya dikonsumsi sebagai sayuran oleh masyarakat di Minahasa. Penelitian ini bertujuan untuk mengetahui profil (karakter) senyawa yang diisolasi dari ekstrak etanol daun leilem (Clerodendrum minahassae Teijsm dan Binn.) ekstrak diperoleh dari proses maserasi menggunakan pelarut etanol 70% dengan persen rendamen 10,19%. Hasil uji kandungan kimia ekstrak etanol daun leilem positif mengandung alkaloid, flavonoid, steroid dan tanin. Ekstrak etil astetat dipilih dan diambil 2 gram dilanjutkan untuk dilakukan pemisahan menggunakan komatografi kolom konvensional dan menghasilkan 5 fraksi. Fraksi 3 dipilih dilanjutkan kromatografi kolom konvensional kedua dan didapatkan 5 fraksi. Fraksi 2 dipilih dan dilanjutkan ketahapan kromatgrafi lapis tipis preparatif dan menghasilkan 2 isolat. Isolat 2 yang menunjukkan 1 noda tunggal pada profil KLT dengan niliai Rf 0,66 dilanjutkan untuk dianalisis dengan spektofometri UV-Vis dan FT-IR. Hasil analisis spektrofotometri UV-Vis isolat 2 mempunyai serapan maksimal pada panjang gelombang 269,0 nm dan 333,0 nm-1. Data FT-IR menunjukkan adanya gugus fungsi O-H, C-H, C=C dan C-O yang diduga merupakan senyawa flavonoid. Kata kunci: Isolasi, karakteriksasi, Daun Leilem(Clerodendrum minahassae Teijsm and Binn). 


2019 ◽  
Vol 1 (1) ◽  
pp. 40-44
Author(s):  
Hilda Amanda

Euphorbia plant, Euphorbia thymifolia Linn, is one the Euphorbiaceae families that still need to be developed due to its benefits. An effort to be able to use this plant maximumly is by studying the active component in the plant. This study aims to isolate and characterize phenolic compound in euphorbia plant extract using ethyl acetate. 500 gram of euphorbia plant (Patikan Cina) powder was macerated using methanol. Then, the macerated extract was evaporated to eliminate excess solvent and as a result, a solvent-free extract was obtained. Next, the result was partitioned with a solution of methanol : ethyl acetate (1:1) in order to get methanol and ethyl acetate extracts. The ethyl acetate extract of the partition was evaporated to get concentrated ethyl acetate extract. Next, it was isolated in a vacuum liquid and gravitational column chromatography to get pure isolate. Silica gel 60 (0.040 – 0.063 mm) and n-hexane motion phase were used in the separation of concentrated ethyl acetate in vacuum liquid chromatography. There were 16 fractions produced from the yield. Then the fractions were put in TLC. With silica gel 60 (0.2 – 0.5 mm) mesh and n-hexane mobile phase, ethyl acetate gave 5 fractions in gravitational column chromatography and fraction 3 produced a single spot. UV and IR spectroscopy were used to determine the constituents in the isolate. From UV spectrum, max is 268.97 nm. While IR data shows the presence O-H group in 3521.38 cm-1, C – H (alkane) presents at wave number 2926.45 cm-1 reinforced by the appearance of 5 other alkanes absorption at 2857.00 cm-1, 1447.31 cm-1, 1370.18 cm-1, 868.774 cm-1 and 757.887 cm-1 wavelengths. There is also C = O (carbonyl) groups in wave number 1693.19 cm-1. The identification of structures based on UV and IR spectra data has shown that the isolate is a phenolic compound.


2018 ◽  
Vol 54 (2C) ◽  
pp. 278
Author(s):  
Ton Nu Lien Huong

This research focuses on the isolation and characterization of eight natural compounds fromthe ethyl acetate extract of Scoparia dulcis L. collected in An Giang province, Vietnam. Sixflavonoid compounds: apigenin (1), luteolin (2), baicalein (3), oroxylin A (4), oroxylin A 7-O-β-D-glucoside (5) and vitexin (6) along with two nitrogen-containing compounds: 2,4-dihydroxy-1,4-benzoxazin-3-one (7) and uracil (8) were successfully isolated via the methods of naturalproduct extraction. The structures of these compounds were elucidated base on 1D-NMR and2D-NMR spectral data as well as MS and compared with those in the authentic reports. Thisstudy contributed new results to the phytochemical examination of Scoparia dulcis Linn.growing in Vietnam with the presence of the first isolated compounds as (3), (4), (5), (7) and (8).


2017 ◽  
Vol 3 (1) ◽  
pp. 79-87
Author(s):  
Alfindah Rusanti ◽  
Dede Sukandar ◽  
Tarso Rudiana ◽  
Adawiah Adawiah

The research characterization of cytotoxic fraction against P-388 leukemia murine cells from the extract honje (Etlingera elatior) seed have been reported. This research lead to isolated and characterization of cytotoxic compounds against P-388 leukemia murine cells from the extract E. elantior seed. The extract of E. elantior seed was maserated by methanol, n-hexane, and ethyl acetate, respectively and estimated their cytotoxic activity against P-388 leukemia murine cell with 3- (4, 5-dimetiltiazol-2-yl) -2,5-difeniltetrazolium bromide (MTT) assay guided toxicity test against of shrimp Artemia salina Leach. Brine shirmp Lethality Test (BSLT) method. The active extracts will be separated by fractionation using column chromatography, radial chromatography, and for analyzing the purity of isolate will estimate by HPLC. The chemical structure of pure isolate will be identified by spectroscopies data UV Vis, FTIR, NMR and MS. The ethyl acetate extract from honje seed have cytotoxic activity by leukemia P-388 cell  with IC50 19.21 µg/mL. The compound toxic as cytotoxicagainst P-388 leukemia murine cells is flavonoid compouds their is resveratrol, lapachol, apigenin, methylated chrysin, 6,2’-dihydroxyflavanone, 3-hydroxy-3,4’-dymethoxyflavone and 4’-hydroxy-5,7-dimethoxyflavanone.DOI: http://dx.doi.org/10.15408/jkv.v0i0.3640


2019 ◽  
Vol 15 ◽  
pp. 1339-1346
Author(s):  
Sven Götz ◽  
Andreas Schneider ◽  
Arne Lützen

The preparative resolution of a trifunctionalized C 3-symmetrical chiral cyclotriveratrylene derivative was achieved via high-performance liquid chromatography (HPLC) on a chiral stationary phase. This approach is a promising alternative to the previously reported resolution through formation of diastereomeric esters because it involves fewer synthetic steps and is less prone to thermal (re)racemization. During these studies an intermediate saddle conformer could also be isolated and characterized by 1H and 13C NMR spectroscopy. The HPLC separation method was further developed in order to allow investigations on the racemization behavior of the cyclotriveratrylene derivative.


Author(s):  
Sharmila Tirumale ◽  
Nazir Wani

Objective: This study evaluated the Chaetomium cupreum extracts as biocontrol agents against four plant pathogenic fungi (Cladosporium cladosporioides, Fusarium oxysporum, Phomopsis azadirachtae, and Rhizoctonia solani).Method: The antifungal activity of n-butanol and ethyl acetate extracts of C. cupreum was evaluated against plant pathogenic fungi using food poison method.Result: In n-butanol extract, the percentage inhibition of mycelial growth against C. cladosporoides was 88.3±0.1, F. oxysporum was 59.4±0.2, R. solani was 56.2±0.9, and P. azadirachtae was 52.0±0.1at 0.25 mg/ml, respectively. In ethyl acetate extract, the percentage inhibition of mycelial growth against C. cladosporoides was 86.0±0.5, F. oxysporum was 66.4±0.1, P. azadirachtae was 55.2±0.9, and R. solani was 52.0±0.1 at 0.25 mg/ml, respectively.Conclusion: It was found that n-butanol extract is more effective than ethyl acetate extract of C. cupreum. Future studies will focus on the purification and characterization of compounds of C. cupreum and their biocontrol capacity with the mechanism for plant pathological applications.


Sign in / Sign up

Export Citation Format

Share Document