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tephrosia purpurea/nekrose

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ArtikelKlinische VersuchePatente
10 Ergebnisse
Tephrosia purpurea (L.) Pers., commonly known as "sarpunkha" and "wild indigo", is being used in traditional systems of medicine to treat liver disorders, spleen and kidney. In the present study, a validated High Performance Thin Layer Chromatography (HPTLC) method was
CONTEXT. Tephrosia toxicaria is currently known as Tephrosia sinapou (Buc'hoz) A. Chev. (Fabaceae) and is a source of compounds such as flavonoids that inhibit inflammatory pain. OBJECTIVE To investigate the analgesic effect and mechanisms of the ethyl acetate extract of T. sinapou in inflammatory

Periacinar liver fibrosis caused by Tephrosia cinerea in sheep.

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Tephrosia cinerea has been associated with ascites and liver fibrosis in sheep in Brazil. The dried plant was fed ad libitum to three sheep for 55-80 days. Three additional sheep were used as controls. All the treated sheep presented with hypoalbuminemia and increased γ-glutamyltransferase and

Evaluation of hepatoprotective activity of aerial parts of Tephrosia purpurea L. and stem bark of Tecomella undulata.

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BACKGROUND The aerial parts of Tephrosia purpurea (L.) pers. (Fabaceae) and stem bark of Tecomella undulata seem. (Bignoniaceae) are used for liver disorders in the traditional system of medicine. OBJECTIVE To evaluate the hepatoprotective activity of aerial parts of Tephrosia purpurea and stem bark

Hepatoprotective activity of Tephrosia purpurea against arsenic induced toxicity in rats.

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OBJECTIVE The present study was conducted to evaluate the hepatoprotective activity of Tephrosia purpurea (TP) against sodium arsenite (NaAsO2) induced sub-acute toxicity in rats. METHODS Twenty four wistar albino rats of either sex were randomly divided into three groups. Group II and III were

Ameliorative Effect of Tephrosia Purpurea in Arsenic-induced Nephrotoxicity in Rats.

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OBJECTIVE The present investigation was conducted to evaluate the nephroprotective activity of Tephrosia purpurea (TPE) against arsenic-induced toxicity. METHODS Twenty four number of wistar rats were equally divided into three groups. Sodium arsenite (10 mg/kg) was orally given to group I for 28

Anti-inflammatory Flavanones and Flavones from Tephrosia linearis.

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Phytochemical analysis of a methanol-dichloromethane (1:1) extract of the aerial parts of Tephrosialinearis led to the isolation of 18 compounds. Seven of these, namely, lineaflavones A-D (1-4), 6-methoxygeraldone (5), 8″-acetylobovatin (6), and

Isoflavones from the seedpods of Tephrosia vogelii and pyrazoisopongaflavone with anti-inflammatory effects

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Phytochemical investigation of Tephrosia vogelii seedpods led to the isolation of twelve compounds: vogelisoflavone A (1), vogelisoflavone B (2), isopongaflavone (3), onogenin, luteolin, 4',7-dihydroxy-3'-methoxyflavanone, trans-p-hydroxycinnamic acid, tephrosin, 2-methoxygliricidol,

Synergistic anti-inflammatory activities of a new flavone and other flavonoids from Tephrosia hildebrandtii vatke.

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A new flavone, named hildeflavone (1) along with 7 other known flavonoids were isolated from the aerial parts of Tephrosia hildebrandtii Vatke. Their characterisation was based on NMR and MS data analysis. The anti-inflammatory properties of the crude extract, isolated compounds and
BACKGROUND Tephrosia apollinea (Delile) DC (Leguminosae) has been used in folk medicine in Arabian countries to treat inflammatory disorders. The plant has been described to treat swelling, bone fracture, bronchitis, cough, earache and wounds. OBJECTIVE the current study aims to evaluate the
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