Isolation of Oleanolic Acid from Parinari curatellifolia (Planch Ex. Benth) Stem Bark and Evaluation of its Anticonvulsant and Sedative activities in Rodents

2019 ◽  
Vol 3 (1) ◽  
pp. 17-21 ◽  
Author(s):  
Halilu Mshelia ◽  
◽  
Chinenye Ugwah-Oguejiofor ◽  
Natasha October ◽  
Kabiru Abubakar ◽  
...  
2014 ◽  
Vol 9 (6) ◽  
pp. 1934578X1400900
Author(s):  
Zelalem Yibralign Desta ◽  
Runner R. T. Majinda
Keyword(s):  
2D Nmr ◽  

Three new isoflavonoids, 5,7-dihydroxy-2′,4′-dimethoxy-5′-(3-methylbut-2-enyl) isoflavanone (erycaffra A) (1), 5,7-dihydroxy-2′,4′-dimethoxy-5′-(2-hydroxy-3-methylbut-3-enyl)isoflavanone (erycaffra B) (2), and 5,7-dihydroxy-6,8-di-(2-hydroxy-3-methylbut-3-enyl)isoflavone (erycaffra C) (3), were isolated from the stem bark of E. caffra Thunb., along with eight known compounds, namely, alpinumisoflavone (4), isoerysenegalensein E (5), β-amyrin (6), oleanolic acid (7), octacosyl- E-ferulate (8), triacontyl-4-hydroxycinnamate (9), n-tetracosyl p-coumarate (10) and octacosan-1-ol (11). The structures were determined on the basis of spectroscopic (1D, 2D-NMR) and MS data and by comparison with literature values.


2010 ◽  
Vol 5 (2) ◽  
pp. 1934578X1000500 ◽  
Author(s):  
Faryal Vali Mohammad ◽  
Viqar Uddin Ahmad ◽  
Mushtaq Noorwala ◽  
Nordin HJ. Lajis

Phytochemical investigation of the stem bark of Pometia pinnata resulted in the isolation of a new triterpenoidal saponin. The structure of the new compound, pometin (1), was established as 3-O-[β-D-glucopyranosyl-(1→2)-β-D-glucopyranosyl-(1→3)-β-D-glucopyranosyl]-oleanolic acid based on 1D and 2D-NMR analysis including COSY, 2D J-resolved, HMQC, HMBC correlations and chemical transformations.


2011 ◽  
Vol 89 (10) ◽  
pp. 1277-1282 ◽  
Author(s):  
Guang-Chun Gao ◽  
Zhong-Xian Lu ◽  
Shu-Hong Tao ◽  
Si Zhang ◽  
Fa-Zuo Wang ◽  
...  

Four new triterpenoid saponins, Catunaroside E (1; 3-O-{β-D-glucopyranosyl-(1→2)-[β-D-glucopyranosyl-(1→3)]-β-D-glucopyranosyl}-siaresinolic acid), Catunaroside F (2; 3-O-{α-L-rhamnopyranosyl-(1→2)-[β-D-glucopyranosyl-(1→3)]-β-D-glucopyranosyl}-28-O-(β-D-glucopyranosyl)-oleanolic acid), Catunaroside G (3; 3-O-[α-L-rhamnopyranosyl-(1→2)-β-D-glucopyranosyl]- 28-O-(β-D-glucopyranosyl)-siaresinolic acid), and Catunaroside H (4; 3-O-{β-D-glucopyranosyl-(1→2)-[β-D-glucopyranosyl-(1→3)]-β-D-glucopyranosyl}-28-O-(β-D-glucopyranosyl)-siaresinolic acid), and the known triterpenoid saponin Mussaendoside J (5), were isolated from the stem bark of Catunaregam spinosa . Their structures were elucidated on the basis of their spectral data and chemical evidence.


2021 ◽  
Vol 18 (2) ◽  
pp. 103-112
Author(s):  
Babasoji P. Omoniwa ◽  
Kunle Okaiyeto ◽  
David O. Omoniwa ◽  
Olumuyiwa A. Olorunyomi

Parinari curatellifolia and other Parinari species are used traditionally in many parts of Africa as a remedy for malaria among other diseases. To ascertain this folkloric claim, the antiplasmodial potential of ethanol extract of Parinari curatellifolia stem bark (EEPCSB) and n-hexane extract of Parinari curatellifolia stem bark (HEPCSB) on Plasmodium falciparum was studied. Parasites were grown in a 96-well plate containing Roswell Park Memorial Institute-1640. The wells were grouped into: control (untreated), artemether-treated, EEPCSB-treated and HEPCSBtreated groups. Treatments were administered to the tune of 10, 20, 40 and 80 μg/ml. Parasitemia was observed by microscopy after 24, 48 and 72h of incubation. EEPCSB and HEPCSB elicited dose and duration-dependent reduction (p<0.05) in parasitemia when compared with the untreated group. The recorded percentage parasite inhibition by the extracts was lower (p<0.05) when compared with artemether. There was no difference (p>0.05) in plasmodium lactate dehydrogenase activity of EEPCSB-treated and artemether-treated groups. Findings from this study show that extracts of P. curatellifolia stem bark, especially EEPCSB, demonstrated excellent inhibitory activities against P. falciparum and can be a good source of compounds for the development of novel antimalarial drugs. Keywords: Parinari curatellifolia; Extracts; Plasmodium falciparum; Parasitemia; Antiplasmodial


Plants ◽  
2021 ◽  
Vol 11 (1) ◽  
pp. 19
Author(s):  
Souleymane Fofana ◽  
Moussa Ouédraogo ◽  
Rafaèle Calvo Esposito ◽  
Windbedema Prisca Ouedraogo ◽  
Cédric Delporte ◽  
...  

The objective of this study was to carry out a systematic review of the substances isolated from the African medicinal plant Erythrina senegalensis, focusing on compounds harboring activities against cancer models detailed in depth herein at both in vitro and in vivo preclinical levels. The review was conducted through Pubmed and Google Scholar. Nineteen out of the forty-two secondary metabolites isolated to date from E. senegalensis displayed interesting in vitro and/or in vivo antitumor activities. They belonged to alkaloid (Erysodine), triterpenes (Erythrodiol, maniladiol, oleanolic acid), prenylated isoflavonoids (senegalensin, erysenegalensein E, erysenegalensein M, alpinumisoflavone, derrone, warangalone), flavonoids (erythrisenegalone, senegalensein, lupinifolin, carpachromene) and pterocarpans (erybraedine A, erybraedine C, phaseollin). Among the isoflavonoids called “erysenegalensein”, only erysenealenseins E and M have been tested for their anticancerous properties and turned out to be cytotoxic. Although the stem bark is the most frequently used part of the plant, all pterocarpans were isolated from roots and all alkaloids from seeds. The mechanisms of action of its metabolites include apoptosis, pyroptosis, autophagy and mitophagy via the modulation of cytoplasmic proteins, miRNA and enzymes involved in critical pathways deregulated in cancer. Alpinumisoflavone and oleanolic acid were studied in a broad spectrum of cancer models both in vitro and in preclinical models in vivo with promising results. Other metabolites, including carpachromen, phaseollin, erybraedin A, erysenegalensein M and maniladiol need to be further investigated, as they display potent in vitro effects.


1985 ◽  
Vol 23 (12) ◽  
pp. 2925-2928 ◽  
Author(s):  
P Waterman
Keyword(s):  

1996 ◽  
Vol 59 (10) ◽  
pp. 1002-1002 ◽  
Author(s):  
Yanwen Guo ◽  
Bilo Diallo ◽  
Mondher Jaziri ◽  
Renée Vanhaelen-Fastré, ◽  
Maurice Vanhaelen ◽  
...  
Keyword(s):  

Planta Medica ◽  
2009 ◽  
Vol 75 (09) ◽  
Author(s):  
CM Strüh ◽  
S Jäger ◽  
CM Schempp ◽  
T Jakob ◽  
A Scheffler ◽  
...  

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