A Cytotoxic and Hepatoprotective Agent from Withania somnifera and Biological evaluation of its Ester Derivatives

Detailed chemical investigation of Withania somnifera roots resulted in the isolation and identification of a cytotoxic and hepatoprotective agent, palmitic acid (1), which was converted to eight semi-synthetic ester derivatives 2–9. t-Butyl palmitate (8) and amyl palmitate (9) were 4–6 times more active than 1 against adherent and suspension colon cancer cell lines. Interestingly, palmitic acid (1) and its ester derivatives 2–9 also showed hepatoprotective activity which is being reported for the first time.

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An Immunomodulator from Terminalia Arjuna and Biological Evaluation of its Derivatives

Natural Product Communications ◽

10.1177/1934578x0800300613 ◽

2008 ◽

Vol 3 (6) ◽

pp. 1934578X0800300 ◽

Cited By ~ 2

Author(s):

Mohit Saxena ◽

Sachidanand Yadav ◽

Dhyaneshwar U. Bawankule ◽

Santosh K. Srivastava ◽

Anirban Pal ◽

...

Keyword(s):

Biological Evaluation ◽

Chemical Investigation ◽

Terminalia Arjuna ◽

Immunomodulatory Effects ◽

Immunosuppressive Activity ◽

Isolation And Identification ◽

First Time ◽

Synthetic Derivatives ◽

Detailed Chemical

Detailed chemical investigation of Terminalia arjuna bark resulted in the isolation and identification of an immunomodulatory constituent, arjunic acid (1), which was converted into seven semi-synthetic derivatives (2–8). All the test compounds in 0.1, 1 and 10 μg/mL concentrations exhibited immunomodulatory effects in a dose dependant manner. 2- O-Lauroyl arjunic acid (3) and 2- O-palmitoyl arjunic acid (4) exhibited immunostimulatory response at all the tested concentrations, while arjunic acid (1), 2,3-di- O-acetyl arjunic acid (2), 2,3-di -O-benzoyl arjunic acid (6), and 2- O-p-anisoyl arjunic acid (7) exhibited immunostimulatory responses at lower doses, whereas at higher concentrations they exhibited immunosuppressive activity. Only 2,3-di- O-palmitoyl arjunic acid (5) showed immunosuppressive activity at all the concentrations; this is being reported for the first time.

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A New Colchicinoid from Colchicum tauri, an Unexplored Meadow Saffron Native to Jordan

Natural Product Communications ◽

10.1177/1934578x0600100203 ◽

2006 ◽

Vol 1 (2) ◽

pp. 1934578X0600100 ◽

Cited By ~ 3

Author(s):

Feras Q. Alali ◽

Amani S. Ma'aya'h ◽

Ahmad Alkofahi ◽

Amjad Qandil ◽

Chen Li ◽

...

Keyword(s):

Brine Shrimp ◽

2D Nmr ◽

Biological Evaluation ◽

Preparative Hplc ◽

Low Resolution ◽

Isolation And Identification ◽

Brine Shrimp Lethality ◽

Chromatographic Techniques ◽

General Toxicity ◽

First Time

This study reports the isolation, characterization, and biological evaluation of constituents of Colchicum tauri Siehe ex Stef. (Colchicaceae), an unexplored Colchicum species native to Jordan. Methanolic extraction, crude alkaloid fractionation, and separation using several different chromatographic techniques (open columns, preparative TLC, and semi-preparative HPLC), as directed by the brine shrimp lethality test (BST), resulted in the isolation and identification of nine compounds: (-)-colchicine (1), (-)-2-demethylcolchicine (2), (-)-3-demethylcolchicine (3), (-)-demecolcine (4), (-)- N-methyldemecolcine (5), (-)-3-demethyl- N-methyldemecolcine (6), β-lumicolchicine (7), 3-demethyl-β-lumicolchicine (8), and apigenin (9). Compounds 1–5 and 7–8 were isolated for the first time from this species, while compound (6) represents a new colchicinoid. The structure elucidations were achieved using a series of spectroscopic and spectrometric techniques, principally 1D-NMR (1H, and 13C), 2D-NMR (COSY, ROESY, HMBC, and HSQC), and low resolution EI-MS. All compounds were tested for general toxicity using the BST, and compounds 1 and 4 were found to be the most potent, with LC50 values of 2.5 and 8.1 μg/mL, respectively.

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Antirheumatoid Arthritis Activities and Chemical Compositions of Phenolic Compounds-Rich Fraction fromUrtica atrichocaulis, an Endemic Plant to China

Evidence-based Complementary and Alternative Medicine ◽

10.1155/2012/818230 ◽

2012 ◽

Vol 2012 ◽

pp. 1-10 ◽

Cited By ~ 2

Author(s):

Mengyue Wang ◽

Ke Li ◽

Yuxiao Nie ◽

Yingfang Wei ◽

Xiaobo Li

Keyword(s):

Phenolic Compounds ◽

Chemical Constituents ◽

Biological Evaluation ◽

Chemical Compositions ◽

Endemic Plant ◽

Isolation And Identification ◽

Phenolic Components ◽

Phenolic Constituents ◽

Cotton Pellet ◽

First Time

Urtica atrichocaulis, an endemic plant to China, is commonly used to treat rheumatoid arthritis even though its pharmaceutical activities and chemical constituents were not studied. Herein, we reported our investigations on the chemical compositions of the phenolic compounds-rich fraction fromU. atrichocaulis(TFUA) and their antirheumatoid arthritis activities. We found that the TFUA significantly inhibited the adjuvant-induced rats arthritis, carrageenin-induced rats paw edema, cotton pellet-induced mice granuloma, and the acetic acid-induced mice writhing response. Our phytochemical investigations on the TFUA resulted in the first-time isolation and identification of 17 phenolic constituents and a bis (5-formylfurfuryl) ether. The extensive HPLC analysis also revealed the chemical compositions of TFUA. Our further biological evaluation of the main phenolic components, individually and collectively, indicated that the antirheumatoid arthritis activities of TFUA were the combined effect of multiple phenolic constituents.

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The Volatile Phytochemistry of Seven Native American Aromatic Medicinal Plants

Plants ◽

10.3390/plants10061061 ◽

2021 ◽

Vol 10 (6) ◽

pp. 1061

Author(s):

Sims K. Lawson ◽

Prabodh Satyal ◽

William N. Setzer

Keyword(s):

Native American ◽

Medicinal Plants ◽

Essential Oil ◽

Essential Oils ◽

Palmitic Acid ◽

Methyl Salicylate ◽

Chromatographic Techniques ◽

Germacrene D ◽

First Time ◽

Gaultheria Procumbens

As part of our evaluation of essential oils derived from Native American medicinal plants, we have obtained the essential oils of Agastache foeniculum (Pursch) Kuntze (Lamiaceae), Gaultheria procumbens L. (Ericaceae), Heliopsis helianthoides (L.) Sweet (Asteraceae), Liatris spicata (L.) Willd. (Asteraceae), Pycnanthemum incanum (L.) Michx. (Lamiaceae), Smallanthus uvedalia (L.) Mack. ex Mack. (Asteraceae), and Verbena hastata L. (Verbenaceae) by hydrodistillation. The essential oils were analyzed by gas chromatographic techniques. The essential oil of A. foeniculum was dominated by estragole (88–93%), while methyl salicylate (91%) dominated the G. procumbens essential oil. Germacrene D was the major component in H. helianthoides (42%) and L. spicata (24%). 1,8-Cineole (31%) and α-terpineol (17%) were the main compounds in P. incanum essential oil. The essential oil of S. uvedalia showed α-pinene (24%), perillene (15%), and β-caryophyllene (17%) as major components. Verbena hastata essential oil was rich in 1-octen-3-ol (up to 29%) and palmitic acid (up to 22%). Four of these essential oils, H. helianthoides, L. spicata, P. incanum, and V. hastata, are reported for the first time. Additionally, the enantiomeric distributions of several terpenoid components have been determined.

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Revealing the constituents of Egypt’s oldest beer using infrared and mass spectrometry

Scientific Reports ◽

10.1038/s41598-019-52877-0 ◽

2019 ◽

Vol 9 (1) ◽

Cited By ~ 1

Author(s):

Mohamed A. Farag ◽

Moamen M. Elmassry ◽

Masahiro Baba ◽

Renée Friedman

Keyword(s):

Large Scale ◽

Beer Brewing ◽

Chemical Signatures ◽

Chemical Determination ◽

Materials Used ◽

High Level ◽

Beer Production ◽

First Time ◽

Detailed Chemical

Abstract Previous studies have shown that the Ancient Egyptians used malted wheat and barley as the main ingredients in beer brewing, but the chemical determination of the exact recipe is still lacking. To investigate the constituents of ancient beer, we conducted a detailed IR and GC-MS based metabolite analyses targeting volatile and non-volatile metabolites on the residues recovered from the interior of vats in what is currently the world’s oldest (c. 3600 BCE) installation for large-scale beer production located at the major pre-pharaonic political center at Hierakonpolis, Egypt. In addition to distinguishing the chemical signatures of various flavoring agents, such as dates, a significant result of our analysis is the finding, for the first time, of phosphoric acid in high level probably used as a preservative much like in modern beverages. This suggests that the early brewers had acquired the knowledge needed to efficiently produce and preserve large quantities of beer. This study provides the most detailed chemical profile of an ancient beer using modern spectrometric techniques and providing evidence for the likely starting materials used in beer brewing.

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Mammalian Arginase Inhibitory Activity of Methanolic Extracts and Isolated Compounds from Cyperus Species

Molecules ◽

10.3390/molecules26061694 ◽

2021 ◽

Vol 26 (6) ◽

pp. 1694

Author(s):

Kamel Arraki ◽

Perle Totoson ◽

Alain Decendit ◽

Andy Zedet ◽

Justine Maroilley ◽

...

Keyword(s):

Inhibitory Activity ◽

Methanolic Extract ◽

Significant Inhibition ◽

Isolation And Identification ◽

Vasorelaxant Effect ◽

Methanolic Extracts ◽

Phytochemical Investigation ◽

Ic50 Values ◽

First Time

Polyphenolic enriched extracts from two species of Cyperus, Cyperus glomeratus and Cyperus thunbergii, possess mammalian arginase inhibitory capacities, with the percentage inhibition ranging from 80% to 95% at 100 µg/mL and 40% to 64% at 10 µg/mL. Phytochemical investigation of these species led to the isolation and identification of two new natural stilbene oligomers named thunbergin A-B (1–2), together with three other stilbenes, trans-resveratrol (3), trans-scirpusin A (4), trans-cyperusphenol A (6), and two flavonoids, aureusidin (5) and luteolin (7), which were isolated for the first time from C.thunbergii and C. glomeratus. Structures were established on the basis of the spectroscopic data from MS and NMR experiments. The arginase inhibitory activity of compounds 1–7 was evaluated through an in vitro arginase inhibitory assay using purified liver bovine arginase. As a result, five compounds (1, 4–7) showed significant inhibition of arginase, with IC50 values between 17.6 and 60.6 µM, in the range of those of the natural arginase inhibitor piceatannol (12.6 µM). In addition, methanolic extract from Cyperus thunbergii exhibited an endothelium and NO-dependent vasorelaxant effect on thoracic aortic rings from rats and improved endothelial dysfunction in an adjuvant-induced arthritis rat model.

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Studies on the Chemical Diversities of Secondary Metabolites Produced by Neosartorya fischeri via the OSMAC Method

Molecules ◽

10.3390/molecules23112772 ◽

2018 ◽

Vol 23 (11) ◽

pp. 2772 ◽

Cited By ~ 5

Author(s):

You-Min Ying ◽

Lu Huang ◽

Ting Tian ◽

Cui-Yu Li ◽

Shi-Lei Wang ◽

...

Keyword(s):

Secondary Metabolites ◽

Cancer Cell Line ◽

2D Nmr ◽

Natural Occurrence ◽

Fungal Metabolites ◽

Isolation And Identification ◽

Late Step ◽

Neosartorya Fischeri ◽

The One ◽

First Time

The One Strain Many Compounds (OSMAC) method was applied to explore the chemical diversities of secondary metabolites produced by Neosartorya fischeri NRRL 181. Four pyripyropenes 1–4, eight steroids 5–11, and four prenylated indole alkaloids 12–15, were obtained from the fungus cultured in petri dishes containing potato dextrose agar (PDA). 1,7,11-trideacetylpyripyropene A (1) and 1,11-dideacetyl pyripyropene A (2) were obtained and spectroscopically characterized (1D, 2D NMR, and HR-ESI-MS) from a natural source for the first time. It offered a sustainable source of these two compounds, which were usually used as starting materials in preparing pyripyropene derivatives. In addition, as compared with all the other naturally occurring pyripyropenes, 1 and 2 possessed unique acetylation patterns that did not follow the established late-step biosynthetic rules of pyripyropenes. The natural occurrence of 1 and 2 in the fungus implied that the timing and order of hydroxylation and acetylation in the late-step biosynthetic pathway of pyripyropenes remained to be revealed. The isolation and identification of 1–15 indicated that the OSMAC method could remarkably alter the metabolic profile and enrich the chemical diversities of fungal metabolites. Compounds 1–4 exhibited no obvious cytotoxicity against the triple-negative breast cancer cell line MDA-MB-231 as compared with taxol.

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The Hepatoprotective Effect of Ethanol Extract of Syzygium campanulatum (Korth) and Syzygium aromaticum (L) Leaf on Male Wistar Rat (Rattus Norvegicus) was Induced by Paracetamol

JURNAL ILMU KEFARMASIAN INDONESIA ◽

10.35814/jifi.v15i2.517 ◽

2017 ◽

Vol 15 (2) ◽

pp. 196

Author(s):

Much Ilham Novalisa Aji Wibowo ◽

Nur Aeni ◽

Zidna Mazayatul Huda ◽

Nunuk Aries Nurulita

Keyword(s):

Wistar Rats ◽

Ethanolic Extract ◽

Ethanol Extract ◽

Hepatoprotective Activity ◽

Group Iv ◽

Control Group ◽

Syzygium Aromaticum ◽

Male Wistar Rats ◽

Hepatoprotective Agent ◽

Better Than

Syzygium campanulatum and Syzygium aromaticum contains antioxidant components suchas flavonoids, phenolic, and terpenoids. May have hepatoprotective properties in reducing SGPT and SGOT activity. This research wants to determine the potency of hepatoprotective of ethanolic extract of Syzygium campanulatum (Korth) and Syzygium aromaticum leaf compared with curcuma tablets. This research uses 24 male Wistar rats divided into 6 groups: I, II, III (as a normal, induction, and compared control), group IV, V, VI were treated 105, 210, and 420 mg/kg BW respectively. The study was conducted for 9 days. After 7 days of treatment, treated groups were exposed by hepatotoxic dose of paracetamol (2000 mg/kg BW). The SGPT and SGOT activity of all groups was measured by enzimatic assay. The result can be concluded that Syzygium campanulatum extract was found to be active as hepatoprotective agent with 210 mg/kg BW dosage (SGPT 21.76 ± 3.98 U/L and SGOT 7.32±6.74U/L) as eff ective as with the curcuma tablets (SGPT 23.91 ± 4.41 U/L and SGOT 14.12±5.37 U/L) and the hepatoprotective activity of Syzygium campanulatum extract at a dosage 420 mg/kg BW better than curcuma tablets (SGPT 12.43 ± 6.51 U/L and SGOT 6.64 ± 5.88 U/L). While the hepatoprotec Syzygium campanulatum and Syzygium aromaticum contains antioxidant components such as flavonoids, phenolic, and terpenoids.May have hepatoprotective properties in reducing SGPT and SGOT activity. This research wants to determine the potency of hepatoprotective of ethanolic extract of Syzygium campanulatum (Korth) and Syzygium aromaticum leaf compared with curcuma tablets. This research uses 24 male Wistar rats divided into 6 groups: I, II, III (as a normal, induction, and compared control), group IV, V, VI were treated 105, 210, and 420 mg/kg BW respectively. The study was conducted for 9 days. After 7 days of treatment, treated groups were exposed by hepatotoxic dose of paracetamol (2000 mg/kg BW). The SGPT and SGOT activity of all groups was measured by enzimatic assay. The result can be concluded that Syzygium campanulatum extract was found to be active as hepatoprotective agent with 210 mg/kg BW dosage (SGPT 21.76 ± 3.98 U/L and SGOT 7.32±6.74U/L) as eff ective as with the curcuma tablets (SGPT 23.91 ± 4.41 U/L and SGOT 14.12±5.37 U/L) and the hepatoprotective activity of Syzygium campanulatum extract at a dosage 420 mg/kg BW better than curcuma tablets (SGPT 12.43 ± 6.51 U/L and SGOT 6.64 ± 5.88 U/L). While the hepatoprotective activity of Syzygium aromaticum extracts eff ective as with curcuma tablets at all dosage variation.

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Isolation and Identification of Vibrio cholerae causes Epidemic cholera 2007 in Iraq by Rapid Method (Immunochromatographic one step rapid visual test) and comparing it with the traditional Bacterlogical Methods

Baghdad Science Journal ◽

10.21123/bsj.8.1.29-34 ◽

2011 ◽

Vol 8 (1) ◽

pp. 29-34

Author(s):

Baghdad Science Journal

Keyword(s):

Vibrio Cholerae ◽

Rapid Method ◽

Fast Method ◽

Visual Test ◽

Cultural Characteristics ◽

Isolation And Identification ◽

One Step ◽

Anti Body ◽

First Time ◽

Cultural Media

This study was for searching for Cholera Bacteria serotype which causes epidemiology Cholera in the 2007 in a fast method which contains (Rapid Visual Test) (Crystal V.C.) which was used for the first time in Iraq to diagnosis of Cholera Bacteria & compared with the traditional bacteriology method. The Cholera disease is one of the most dangerous epidemiological diseases which lead to death with a percentage of (50 – 70) % in the severe cases for untreated patients . For this purpose, 100 samples of stool from the patients from a (13) hospitals in Baghdad Governorate in the period from August to the end of December. The Cholera was diagnosis in two methods, 1st method was the fast method using the nitrocellulose which is coated with anti-body of Cholera Bacteria .The results was compared with the 2nd method which depends on the cultural characteristics of the cultural media, also the bacteria was diagnosis using the biochemical inspects by the system of API 20E in addition to the using of antisera to specify serotype& sub-serotype ( Monovalent, Polyvalent(O1) . Also, the relation between the disease & the months in the year in which the disease appear was studied. The results show the ability to isolate & identifecate (78) isolate for the serotype (01) in the fast method ( Rapid Visual Test ) ( Crystal V-C ) , & after the bacteriology inspects on these (78) isolate the all isolates were belongs for Cholera Bacteria of the serotype (01) till the sub-serotype , all the (78) isolates were belongs to the sub-serotype (Inaba). The results show, the most infection was in September (36) , & October (22).

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Evaluation of hepatoprotective potential of aqueous extract of Withania somnifera in albino rats

International Journal of Basic & Clinical Pharmacology ◽

10.18203/2319-2003.ijbcp20210477 ◽

2021 ◽

Vol 10 (3) ◽

pp. 255

Author(s):

Monica Sharma ◽

Anand Gaur ◽

Pinki Vishwakarma ◽

Raj Kumar Goel ◽

K. K. Saxena

Keyword(s):

Aqueous Extract ◽

Withania Somnifera ◽

Work Force ◽

Hepatoprotective Activity ◽

Albino Rats ◽

Standard Drug ◽

Hepatic Diseases ◽

Organ Systems ◽

Herbal Plant ◽

Biochemical Examination

Background: Hepatic diseases are a major cause of morbidity and disability of work force throughout the world. The treatment of hepatic diseases with standard drugs poses the risk of toxicity on various organ systems. Withania somnifera, a herbal plant has been claimed to be effective in the treatment of various types of hepatic conditions. The present study was undertaken to explore the hepatoprotective activity of aqueous extract of Withania somnifera (AEWS) in experimentally induced hepatotoxicity in albino rats.Methods: The study was commenced after obtaining approval from institutional animal ethical committee using AEWS leaves in Albino wistar rats (150-200 gm) of either sex. The hepatoprotective activity was evaluated using biochemical examination. The animals were divided into five groups of six animals each. In each experiment, first group was given normal saline (1 ml/kg/day), second group was injected with toxin CCl4 (1 ml/kg) i.p only once to produce hepatotoxicity, third and fourth groups were given Withania somnifera orally (500 mg/kg and 1000 mg/kg) (respectively), as a single dose per orally every morning and fifthgroup was given standard drug Liv-52 (1 mg/kg).Results: Aqueous extract of Withania somnifera leaves in oral dose exhibited significant hepatoprotective effect in all models used in this study.Conclusions: It can be concluded from our study that aqueous extract of Withania somnifera leaves possesses hepatoprotective activity.

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