Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 4 de 4
Filter
Add more filters










Database
Language
Publication year range
2.
Bioorg Med Chem Lett ; 26(12): 2788-2794, 2016 06 15.
Article in English | MEDLINE | ID: mdl-27156775

ABSTRACT

Detailed phytochemical investigation from the root bark of Morus alba resulted in the isolation of eleven new compounds, including seven 2-arylbenzofuran derivatives (morusalfurans A-G), three flavonoids (morusalnols A-C), and one geranylated stilbene (morusibene A), as well as 22 known compounds. The structures of the identified compounds were elucidated based on a comprehensive analysis of spectroscopic data and Mosher's method. Compounds 2, 3, 6-8, 11, 23, 24, and 29 showed potent inhibition of PL in comparison with the positive control treatment (orlistat, IC50=0.012µM), with IC50 values ranging from 0.09 to 0.92µM.


Subject(s)
Enzyme Inhibitors/pharmacology , Lipase/antagonists & inhibitors , Pancreas/drug effects , Plant Bark/chemistry , Plant Extracts/pharmacology , Plant Roots/chemistry , Dose-Response Relationship, Drug , Enzyme Inhibitors/chemistry , Enzyme Inhibitors/isolation & purification , Humans , Lipase/metabolism , Molecular Structure , Pancreas/enzymology , Plant Extracts/chemistry , Plant Extracts/isolation & purification , Structure-Activity Relationship
3.
Int J Rheum Dis ; 16(4): 437-41, 2013 Aug.
Article in English | MEDLINE | ID: mdl-23992265

ABSTRACT

OBJECTIVE: Localized scleroderma (morphea) is a rare autoimmune disease limited to the skin, characterized by cutaneous fibrosing and obstructive vasculopathy. Localized scleroderma may invade into the subcutaneous fat layer and cause permanent functional disability. Because of its rarity, there have been few clinical surveys of patients with localized scleroderma in Korea. The aim of this study was to elucidate the clinical presentation, serological data, and clinical outcomes of localized scleroderma. METHODS: This was a retrospective survey conducted by reviewing available medical records during a 7 year-period from 2004 to 2010 in a single medical center in Jeju Island, South Korea. In total 43 patients with localized scleroderma were included. RESULTS: Localized scleroderma occurred primarily in females (female to male ratio 2.6 : 1.0). Most patients were between 10 and 29 years of age and the mean age at diagnosis was 26.2 years. Plaque (51.2%) and linear morphea (37.2%) were most common. No case was associated with systemic scleroderma (systemic sclerosis). The most common site of plaque morphea was the trunk (47.8%). In the linear type, the most common site was head-neck (52.9%). Fluorescent antinuclear antibody was positive in 23.3% of all cases. Treatment included systemic corticosteroids, colchicine, anti-malarial agents, D-penicillamine or intralesional triamcinolone injection. Clinical improvement, including significant and partial response, was seen in only 62.8% of treated patients. CONCLUSION: Localized scleroderma is a chronic inflammatory condition confined to the skin. In order to exclude other conditions, thorough history taking, physical examination, serologic studies and histopathologic examinations should be conducted.


Subject(s)
Adrenal Cortex Hormones/therapeutic use , Antimalarials/therapeutic use , Colchicine/therapeutic use , Scleroderma, Localized/diagnosis , Scleroderma, Localized/drug therapy , Adolescent , Adult , Child , Female , Humans , Male , Middle Aged , Penicillamine/therapeutic use , Prevalence , Republic of Korea/epidemiology , Retrospective Studies , Scleroderma, Localized/epidemiology , Treatment Outcome , Triamcinolone/therapeutic use , Young Adult
4.
Bioorg Med Chem Lett ; 23(5): 1428-32, 2013 Mar 01.
Article in English | MEDLINE | ID: mdl-23357630

ABSTRACT

Four new lanostane triterpenes, butyl lucidenate P (1), butyl lucidenate D(2) (2), butyl lucidenate E(2) (3) and butyl lucidenate Q (4) along with 11 known compounds (5-15) were isolated from the fruiting bodies of Ganoderma lucidum. Their chemical structures were established mainly by 1D and 2D NMR techniques and mass spectrometry. Their anti-inflammatory activity was evaluated against LPS-induced NO production in macrophage RAW 264.7 cells. Compounds 1, 3, 4, 9, 10 and 15 showed inhibitory potency with IC(50) values of 7.4, 6.4, 4.3, 9.4, 9.2 and 4.5 µM, respectively. Compounds 1, 3 and 15 dose-dependently reduced the LPS-induced iNOS expressions. Preincubation of cell with 1, 3 and 15 significantly suppressed LPS-induced expression of COX-2 protein.


Subject(s)
Anti-Inflammatory Agents/chemistry , Anti-Inflammatory Agents/pharmacology , Nitric Oxide/antagonists & inhibitors , Reishi/chemistry , Triterpenes/chemistry , Triterpenes/pharmacology , Cell Line, Tumor , Cyclooxygenase 2/biosynthesis , Cyclooxygenase 2/metabolism , Enzyme Induction/drug effects , Fruiting Bodies, Fungal/chemistry , Humans , Lipopolysaccharides/pharmacology , Macrophages/drug effects , Macrophages/metabolism , Nitric Oxide/biosynthesis , Nitric Oxide/metabolism , Nitric Oxide Synthase Type II/antagonists & inhibitors , Nitric Oxide Synthase Type II/biosynthesis , Nitric Oxide Synthase Type II/metabolism , Nuclear Magnetic Resonance, Biomolecular
SELECTION OF CITATIONS
SEARCH DETAIL
...