2010
DOI: 10.1016/j.fct.2010.05.057
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Amelioration of cisplatin induced nephrotoxicity by PTY: A herbal preparation

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Cited by 27 publications
(24 citation statements)
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References 39 publications
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“…Among these, various compounds of herbal origin have been tested (Nagwani and Tripathi, 2010;Nitha and Janardhanan, 2008;Sohn et al, 2009a, b). These are notably issued from traditional Chinese medicine remedies that benefit from long-term use probably justifying their safety.…”
Section: Introductionmentioning
confidence: 99%
“…Among these, various compounds of herbal origin have been tested (Nagwani and Tripathi, 2010;Nitha and Janardhanan, 2008;Sohn et al, 2009a, b). These are notably issued from traditional Chinese medicine remedies that benefit from long-term use probably justifying their safety.…”
Section: Introductionmentioning
confidence: 99%
“…These pharmacological approaches have mainly focused on discovering compounds of natural origin (Nagwani & Tripathi, 2010;Nitha & Janardhanan, 2008;Sohn et al, 2009), notably issuing from Traditional Chinese Medicine (TCM) remedies.…”
Section: Introductionmentioning
confidence: 99%
“…The oxidative conversion of 3,9-dimethoxypterocarpan (11) to 3, 9-dimethoxypterocarpan-6a-ol (12) is carried out using lead tetra acetate-aqueous acetic acid. The conversion of tuberosin (6) to yield 1a-hydroxytuberosone (7) is achieved from sodium periodate after many attempts with Fremy'salt, thallium(III) triperchlorate, and thallium (III) triflouro acetate were unsuccessful to produce the desired compound, (7). The further transformations to 3-O-methyldeoxytuberosin (4a) from deoxytuberosin (4), 3-O-methylanhydrotuberosin (8a) from anhydrotuberosin (8) and vice versa (8a to 8) is mimicked using methyl iodide for the methylation step in an analogy to the biogenesis of 3-O-methylpterocarpan and 3-O-methylpterocarpene from pterocarpan and pterocarpene, whereas boron tribromide [59] (Hazard!)…”
Section: Resultsmentioning
confidence: 99%
“…To the isoflavan-4-ol dissolved in dichloromethane (20 mL) was added glacial acetic acid (1.0 mL) and RM refluxed at water bath for 1 h. Solvent evaporated under vacuum to yield a solid, which was PLC purified to give deoxytuberosin (4) Tuberosin (6) to 1a-hydroxytuberosone (7). To tuberosin (6, 30 mg), excess sodium periodate (20 mg) in water (50 mL) was added and stirred for 10 h. The light-brown mixture evaporated to 1/3 volume, extracted with diethyl ether (2 Â 25 mL), dried over anhydrous sodium sulfate and concentrated to an oily mass, which was purified by PLC to give 1a-hydroxytuberosone, identical to natural sample (7,22 1a-Hydroxytuberosone (7) to tuberosin (6). A mixture of 1a-hydroxytuberosone (7, 10 mg), Zn-dust (20 mg) and glacial acetic acid (4.0 mL) was vigorously stirred at RT for 2 h and 3-O-Methylanhydrotuberosin (8a) to anhydrotuberosin (8).…”
Section: Methodsmentioning
confidence: 99%
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