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1.
Rev. bras. farmacogn ; 27(2): 214-219, Mar.-Apr. 2017. tab, graf
Article in English | LILACS | ID: biblio-843812

ABSTRACT

ABSTRACT This study assesses the anti-arthritic effect of the affinin-enriched (spilanthol, main alkamide) hexane extract from the roots of Heliopsis longipes (A. Gray) S.F. Blake, Asteraceae, on a Freund adjuvant-induced arthritis model in rodents. The extract was orally administered at a dose of 2, 6.6, or 20 mg/kg; a significant edema-inhibitory activity in the acute and chronic phases was observed with a dose of 2 and 20 mg/kg, respectively. The extract showed higher anti-inflammatory and anti-arthritic effects than the reference drug phenylbutazone (80 mg/kg). Moreover, the extract prevented the occurrence of secondary lesions associated to this pharmacological model.

2.
Electron. j. biotechnol ; 11(4): 2-3, Oct. 2008. ilus, tab
Article in English | LILACS | ID: lil-531932

ABSTRACT

Chiral diarylmethanols are versatile building blocks for the preparation of biologically active substances, but they are difficult to obtain in enantiopure form. We used Nocardia corallina B-276 for the oxidative kinetic resolution of (+/-)-4-(chlorophenyl)phenylmethanol, 1. Two experimental methods were used: 1) Suspension of cells in a phosphate buffer solution and 2) Cells in the culture media, in a 3-L bioreactor. After 36 hrs using the first method, the ketone/alcohol ratio was 56/44 and the unoxidized alcohol had an enantiomeric ratio of 93/7, predominating the R-alcohol.


Subject(s)
Bacteria, Aerobic , Biologic Oxidation , Bioreactors , Gram-Positive Bacteria , Methanol , Biotransformation , Catalysis , Chromatography, High Pressure Liquid
3.
Electron. j. biotechnol ; 10(4): 508-513, oct. 2007. ilus, tab
Article in English | LILACS | ID: lil-504124

ABSTRACT

The esterification of phenylpropanoid and hydrophenylpropanoid acids, catalyzed by candida antarctica lipase B (CAL-B), with several alcohols has demonstrated that the substitution pattern on the aromatic ring has a very significant influence on the reactivity of the carboxyl group due, mainly, to electronic effects, when compared to the unsaturated acids with the hydrogenated acids. It is also clear that in the saturated acids there still remain some unclear effects related to the aromatic substituents.


Subject(s)
Esterification , Phenylpropionates/metabolism , Lipase/metabolism , Catalysis , Chromatography, High Pressure Liquid , Candida/enzymology , Enzymes, Immobilized/metabolism , Enzymes, Immobilized/chemistry , Phenylpropionates/chemistry , Lipase/chemistry , Solvents
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