IRIS publication 43337012
Synthesis, isolation and characterisation of beta-sitosterol and beta-sitosterol oxide derivatives
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TY - JOUR - McCarthy, FO,Chopra, J,Ford, A,Hogan, SA,Kerry, JP,O'Brien, NM,Ryan, E,Maguire, AR - 2005 - May - Organic and Biomolecular Chemistry - Synthesis, isolation and characterisation of beta-sitosterol and beta-sitosterol oxide derivatives - Validated - () - OXIDATION-PRODUCTS CHROMATOGRAPHIC SEPARATION MASS-SPECTROMETRY STEROL SYNTHESIS HIGHER-PLANTS PHYTOSTEROLS CHOLESTEROL RATS OXYPHYTOSTEROLS ATHEROSCLEROSIS - 3 - 3059 - 3065 - beta-Sitosterol is the most prevalent plant cholesterol derivative (phytosterol) and can undergo similar oxidation to cholesterol, leading to beta-sitosterol oxides. The biological impact of phytosterol oxides has only been evaluated in a phytosterol blend (usually of beta-sitosterol, campesterol, stigmasterol and dihydrobrassicasterol). The lack of pure phytosterols, including beta-sitosterol, hinders the collection of significant toxicity data on the individual beta-sitosterol oxides. An efficient synthetic route to multi-gram quantities of pure beta-sitosterol is described here, together with the first syntheses and characterisation of pure beta-sitosterol oxides. - DOI 10.1093/b505069c DA - 2005/05 ER -
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@article{V43337012, = {McCarthy, FO and Chopra, J and Ford, A and Hogan, SA and Kerry, JP and O'Brien, NM and Ryan, E and Maguire, AR }, = {2005}, = {May}, = {Organic and Biomolecular Chemistry}, = {Synthesis, isolation and characterisation of beta-sitosterol and beta-sitosterol oxide derivatives}, = {Validated}, = {()}, = {OXIDATION-PRODUCTS CHROMATOGRAPHIC SEPARATION MASS-SPECTROMETRY STEROL SYNTHESIS HIGHER-PLANTS PHYTOSTEROLS CHOLESTEROL RATS OXYPHYTOSTEROLS ATHEROSCLEROSIS}, = {3}, pages = {3059--3065}, = {{beta-Sitosterol is the most prevalent plant cholesterol derivative (phytosterol) and can undergo similar oxidation to cholesterol, leading to beta-sitosterol oxides. The biological impact of phytosterol oxides has only been evaluated in a phytosterol blend (usually of beta-sitosterol, campesterol, stigmasterol and dihydrobrassicasterol). The lack of pure phytosterols, including beta-sitosterol, hinders the collection of significant toxicity data on the individual beta-sitosterol oxides. An efficient synthetic route to multi-gram quantities of pure beta-sitosterol is described here, together with the first syntheses and characterisation of pure beta-sitosterol oxides.}}, = {DOI 10.1093/b505069c}, source = {IRIS} }
Data as stored in IRIS
AUTHORS | McCarthy, FO,Chopra, J,Ford, A,Hogan, SA,Kerry, JP,O'Brien, NM,Ryan, E,Maguire, AR | ||
YEAR | 2005 | ||
MONTH | May | ||
JOURNAL_CODE | Organic and Biomolecular Chemistry | ||
TITLE | Synthesis, isolation and characterisation of beta-sitosterol and beta-sitosterol oxide derivatives | ||
STATUS | Validated | ||
TIMES_CITED | () | ||
SEARCH_KEYWORD | OXIDATION-PRODUCTS CHROMATOGRAPHIC SEPARATION MASS-SPECTROMETRY STEROL SYNTHESIS HIGHER-PLANTS PHYTOSTEROLS CHOLESTEROL RATS OXYPHYTOSTEROLS ATHEROSCLEROSIS | ||
VOLUME | 3 | ||
ISSUE | |||
START_PAGE | 3059 | ||
END_PAGE | 3065 | ||
ABSTRACT | beta-Sitosterol is the most prevalent plant cholesterol derivative (phytosterol) and can undergo similar oxidation to cholesterol, leading to beta-sitosterol oxides. The biological impact of phytosterol oxides has only been evaluated in a phytosterol blend (usually of beta-sitosterol, campesterol, stigmasterol and dihydrobrassicasterol). The lack of pure phytosterols, including beta-sitosterol, hinders the collection of significant toxicity data on the individual beta-sitosterol oxides. An efficient synthetic route to multi-gram quantities of pure beta-sitosterol is described here, together with the first syntheses and characterisation of pure beta-sitosterol oxides. | ||
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DOI_LINK | DOI 10.1093/b505069c | ||
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