scholarly journals Six New Triterpenoids from the Aerial Parts of Maytenus diversifolia

2016 ◽  
Vol 11 (8) ◽  
pp. 1934578X1601100 ◽  
Author(s):  
Narumi Anoda ◽  
Mayumi Matsunaga ◽  
Miwa Kubo ◽  
Kenichi Harada ◽  
Yoshiyasu Fukuyama

Five new ursane-type triterpenoids 1-5, and one new oleanane-type triterpenoids 7 were isolated from the MeOH extract of the aerial parts of Maytenus diversifolia. Their structures were elucidated by analyzing spectroscopic data and chemical transformation. Compounds 3 and 5 exhibited significant lethal activity in the brine shrimp lethality test (BST).

Author(s):  
AKM Shahidur Rahman ◽  
AK Azad Chowdhury ◽  
Hossain Reza ◽  
Mohammad Shawkat Ali ◽  
Manzurur Rahman Shah Choudhury ◽  
...  

Solvent partitioning followed by column chromatography of the MeOH extract of the seeds of Swietenia mahagoni afforded two limonoids, swietenolide (compound 1) and 2-hydroxy-3-O-tigloylswietenolide (compound 2), later one is new compound. The compounds were identified by spectroscopic means. The cytotoxic activity of these compounds was assessed by using the conventional brine shrimp lethality bioassay. While both compounds were found to have moderate cytotoxic activity, compound 2 displayed overall more potent activity than compound 1. Key words: Cytotoxic; Limonoid; Swietenia mahagoni; Brine shrimp lethality bioassay DOI: 10.3329/bjpp.v24i1.5729Bangladesh J Physiol Pharmacol 2008; 24(1&2) : 1-6


2017 ◽  
Vol 12 (12) ◽  
pp. 1934578X1701201
Author(s):  
Yuka Imura ◽  
Kenichi Harada ◽  
Miwa Kubo ◽  
Yoshiyasu Fukuyama

Three new bibenzyl compounds, 1-3, were isolated along with the previously known bibenzyls 4-6, one diarylpropanoid 7, and three diarylheptanoids 8-10 from the twigs of Smilax longifolia. The structures of the new compounds were elucidated by analyzing their spectroscopic data and comparing them with those of known compounds. Diarylheptanoid 9 exhibited potent lethality in the brine shrimp lethality test (BST).


2014 ◽  
Vol 8 ◽  
pp. 101-104
Author(s):  
Md Moniruzzaman ◽  
Nayeema Parvin ◽  
Sabina Sultana ◽  
Mohammad Abdullah ◽  
Ataur Rahman Khan ◽  
...  

Assessment of Evolvulus nummularius L. through whole plant extracts (collected in petroleum ether [Pet.E.], chloroform [CHCl3] and methanol [MeOH]) were made against Tribolium castaneum (Hbst.) for insecticidal and insect repellency and against Artemia salina L. for brine shrimp lethality, and the results were promising. The LC50 values against T. castaneum adults for Pet.E. extract were 1.280, 1.220, 1.096 and 1.030?g cm-2; for CHCl3 extract 3.249, 2.990, 2.526 and 2.204?g cm-2; and for MeOH extract 2.925, 1.899, 1.875 and 1.789?g cm-2, respectively for 12, 24, 36 and 48h of exposure. The intensity of activity could be arranged in a descending order: Pet.E. extract> MeOH extract> CHCl3 extract. For repellency, CHCl3 and MeOH extracts offered moderate activity (P <0.01), but the Pet.E. extract did not show efficacy against the beetles. The same extracts responded positively in brine shrimp lethality assay where the LC50 values for Pet.E. extract were 141.553, 98.941, 24.684 and 8.560ppm; for CHCl3 extracts 699.048, 366.663, 326.0039 and 40.114ppm; and for MeOH extracts 2336.982, 1258.605, 355.962 and 137.0589ppm respectively for 12, 18, 24 and 30h of exposure. However, the intensity of activity could be arranged in a descending order: Pet.E. extract> CHCl3 extract> MeOH extract. DOI: http://dx.doi.org/10.3329/jles.v8i0.20153 J. Life Earth Sci., Vol. 8: 101-104, 2013


2014 ◽  
Vol 9 (10) ◽  
pp. 1934578X1400901 ◽  
Author(s):  
Wasana Prapalert ◽  
Dammrong Santiarworn ◽  
Saisunee Liawruangrath ◽  
Boonsom Liawruangrath ◽  
Stephen G. Pyne

A new 1,6-benzoxazocine-5-one alkaloid has been isolated as its butyl acetal derivative (1) along with peristrophine from the n-BuOH and EtOAc fractions of the crude MeOH extract of the aerial parts of Peristrophe lanceolaria growing in Thailand. The structures of these compounds were elucidated on the basis of their spectroscopic data. These compounds were isolated for the first time from P. lanceolaria. The EtOAc and n-BuOH fractions also possessed significant antioxidant activity with IC50 values of 57 and 50 μg/mL, respectively (DPPH method), whereas 1 had an IC50 value of 23 μg/mL.


2018 ◽  
Vol 24 (4) ◽  
pp. 332-339 ◽  
Author(s):  
Mohammad-Reza Delnavazi ◽  
Parisa Saiyarsarai ◽  
Saeedeh Jafari-Nodooshan ◽  
Mahnaz Khanavi ◽  
Saeed Tavakoli ◽  
...  

Background: Stachys lavandulifolia Vahl is a herbaceous plant distributed in the west and south western Asia. Despite of the wide medicinal uses, there are some reports on toxicity potential of this plant. In present study we attempted to evaluate the toxicity and to characterize the cytotoxic principles of S. lavandulifolia. Methods: Brine shrimp lethality test (BSLT) was used to evaluate the general toxicity of the extracts and essential oil obtained from the aerial parts of S. lavandulifolia. Phytochemical constituents of the active extract were investigated using various chromatographic and spectroscopic methods. GC and GC-MS were also used to analyze the plant essential oil. GC and GC-MS were used to analyze the plant essential oil. Cytotoxic activities of the isolated compounds were also evaluated using MTT assay method. Results: In brine shrimp lethality test (BSLT), chloroform extract and the plant essential oil exhibited the most toxicity against Artemia salina larvae (LD50: 121.8±5.6 and 127.6±14.7 µg ml-1, respectively). GC and GC-MS analyses of essential oil led to the characterization of forty compounds of which α-bisabolol (23.85%) and thymol (17.88%) were identified as the main constituents. Nine flavonoids, Pachypodol (1), chrysosplenetin (2), kumatakenin (3), velutin (4), penduletin (5), viscosine (6), chrysoeriol (7), hydroxygenkwanin (8) and apigenin (9) were isolated from the chloroform extract of S. lavandulifolia. Among the isolated compounds, chrysosplenetin (2), a polymethoxylated flavonoid, was found as the most toxic compound toward MDA-MB-23 and HT-29 cells, with IC50 values of 88.23 and 116.50 µg ml-1, respectively. Furthermore, chrysosplenetin (2), kumatakenin (3) and viscosine (6) with selectivity indices of 2.70, 2.59 and 3.33, respectively, showed higher preferential toxicity against MDA-MB-23 cells in comparison with tamoxifen (SI:2.45). Conclusion: This study reports methoxylated flavonoids as compounds which could be involved in toxicity of S. lavandulifolia. The results of MTT assay also suggest some of these compounds as appropriate candidates for anti-cancer drug development research.


Antibiotics ◽  
2021 ◽  
Vol 10 (6) ◽  
pp. 681
Author(s):  
Gugulethu P. Khumalo ◽  
Nicholas J. Sadgrove ◽  
Sandy F. Van Vuuren ◽  
Ben-Erik Van Wyk

Indigenous trade of medicinal plants in South Africa is a multi-million-rand industry and is still highly relevant in terms of primary health care. The purpose of this study was to identify today’s most traded medicinal barks, traditionally and contemporaneously used for dermatological, gastrointestinal, and respiratory tract infections; then, to investigate the antimicrobial activity and toxicity of the respective extracts and interpret outcomes in light of pharmacokinetics. Thirty-one popularly traded medicinal barks were purchased from the Faraday and Kwa Mai-Mai markets in Johannesburg, South Africa. Information on the medicinal uses of bark-based medicines in modern commerce was recorded from randomly selected traders. The minimum inhibitory concentration (MIC) method was used for antimicrobial screening, and brine shrimp lethality was used to determine toxicity. New medicinal uses were recorded for 14 bark species. Plants demonstrating some broad-spectrum activities against tested bacteria include Elaeodendron transvaalense, Erythrina lysistemon, Garcinia livingstonei, Pterocelastrus rostratus, Rapanea melanophloeos, Schotia brachypetala, Sclerocarya birrea, and Ziziphus mucronata. The lowest MIC value of 0.004 mg/mL was observed against Staphylococcus epidermidis for a dichloromethane bark extract of E. lysistemon. The tested medicinal barks were shown to be non-toxic against the Artemia nauplii (brine shrimp) bioassay, except for a methanol extract from Trichilia emetica (69.52% mortality). Bacterial inhibition of bark extracts with minimal associated toxicity is consistent with the safety and valuable use of medicinal barks for local muthi market customers. Antimicrobial outcomes against skin and gastrointestinal pathogens are feasible because mere contact-inhibition is required in vivo; however, MIC values against respiratory pathogens require further explaining from a pharmacokinetics or pharmacodynamics perspective, particularly for ingested rather than smoked therapies.


2008 ◽  
Vol 63 (9-10) ◽  
pp. 658-662 ◽  
Author(s):  
Ghada A. Fawzy ◽  
Hossam M. Abdallah ◽  
Mohamed S. A. Marzouk ◽  
Fathy M. Soliman ◽  
Amany A. Sleem

Seven flavonoids were isolated from the butanol fraction of the methanolic extract of the aerial parts of Cynanchum acutum L. (Asclepiadaceae). All of which have been isolated for the first time from the genus Cynanchum. Their structures were established as quercetin 3-O-β-galacturonopyranoside (1), quercetin 7-O-β-glucopyranoside (2), tamarixtin 3-O-β-galacturonopyranoside (3), kaempferol 3-O-β-galacturonopyranoside (4), 8-hydroxyquercetin 3-O-β-galactopyranoside (5), tamarixtin 3-O-α-rhamnopyranoside (6), and tamarixtin 7-O-α-arabinopyranoside (7) on the basis of their chromatographic properties, chemical and spectroscopic data. The major isolated flavonoids 1, 2 and 3 were found to exhibit significant antioxidant and antidiabetic activities (by measuring blood glucose and insulin levels). This is the first report about the antioxidant and antidiabetic activities of compounds 1 - 3.


2004 ◽  
Vol 59 (3) ◽  
pp. 341-344 ◽  
Author(s):  
Jun Wu ◽  
Si Zhang ◽  
Qingxin Li ◽  
Jianshe Huang ◽  
Zhihui Xiao ◽  
...  

Two new cyclolignan glycosides, (+)-lyoniresinol 3a-O-α-D-galactopyranosyl-(1 → 6)-β -D-glucopyranoside (1) and (+)-lyoniresinol 2a-O-α-D-galactopyranosyl-3a-O-β -D-glucopyranoside (2) were isolated from the aerial parts of Acanthus ilicifolius. Their structure elucidation is based on the analyses of spectroscopic data


2015 ◽  
Vol 18 (2) ◽  
pp. 67-72
Author(s):  
Edwin Fadhly ◽  
Dewi Kusrini ◽  
Enny Fachriyah

Penelitian tentang penapisan fitokimia, isolasi, identifikasi alkaloid dari daun getih-getihan (Rivina humilis L.) serta uji sitotoksisitas dengan metode BSLT telah dilakukan. Isolasi alkaloid diawali dengan maserasi daun Rivina humilis L. dengan pelarut etanol 96%, dilanjutkan penghilangan klorofil dengan menggunakan aquades (1:1). Selanjutnya hasil maserasi tersebut dipartisi dengan pelarut n-heksana, diperoleh ekstrak n-heksana dan ekstrak etanol-air. Ekstrak etanol-air dilakukan isolasi alkaloid hingga diperoleh ekstrak alkaloid berwarna coklat kemerahan sebanyak 0,7323 gram. Pemisahan alkaloid dilakukan dengan metode kromatografi lapis tipis preparatif dan uji kemurniannya menggunakan metode KLT dengan berbagai eluen didapatkan 1 noda pada pita A1. Isolat alkaloid A1 berbentuk padatan putih dan mempunyai titik leleh sebesar 290-292°C. Hasil analisis spektrofotometer UV-Vis memperkirakan bahwa senyawa alkaloid A1 mempunyai struktur dasar indol. Analisis dengan spektofotometer FTIR menunjukkan adanya gugus N-H, O-H, =C-H aromatik, CH2, C=N, C=O, C=C aromatik, dan C-O eter. Sedangkan kromatogram LC-MS menunjukkan puncak tertinggi pada waktu retensi 1,8 menit dan memiliki bobot molekul sebesar 267.27 g/mol. Hasil uji sitotoksik menunjukkan bahwa ekstrak alkaloid mempunyai harga LC50 sebesar 25,439 ppm.


2017 ◽  
Vol 1 (1) ◽  
pp. 19-26
Author(s):  
Enda Mora ◽  
Septi Muharini ◽  
Emrizal Emrizal ◽  
Rahayu Utami ◽  
Mella Silfia Andriani

Telah dilakukan isolasi dan pengujian sitotoksik ekstrak etil asetat kulit batang merantirambai (Shorea acuminata Dyer). Ekstraksi dilakukan dengan maserasi bertingkat dan uji sitotoksikdengan metode Brine Shrimp Lethality Test (BSLT). Isolasi dilakukan dengan kromatografi kolommemakai sistem gradient dan diperoleh senyawa D1, berupa amorf berwarna putih sebanyak18 mg dengan titik leleh 280-282oC. Berdasarkan hasil reaksi dengan reagen Liebermann-Buchard(yaitu warna orange kecoklatan) dan hasil karakterisasi dengan spektroskopi UV, IR, 1H-RMI, dan 13CRMI,maka dapat disimpulkan bahwa senyawa D1 termasuk golongan terpenoid. Dari hasil pengujiansitotoksik ekstrak etil asetat didapatkan nilai LC50 sebesar 3,68 ppm dan dapat dinyatakan bahwaekstrak etil asetat kulit batang meranti rambai memiliki sifat sangat toksik terhadap kematian Artemiasalina Leach.


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