Composition containing ohioensins f as a polytrichastrum alpinum-derived novel compound for preventing or treating arteriosclerosis
A technology of arteriosclerosis and composition, applied in the field of compositions for preventing or treating inflammatory diseases, to achieve the effect of treating and preventing arteriosclerosis or inflammatory diseases
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Embodiment 1
[0067] Embodiment 1: Preparation of pseudoblond moss (Polytrichastrum alpinum) extract
[0068] Pseudoblond moss (Polytrichastrum alpinum (Hedw.) G.L.Sm.) was personally collected in Sejong base (S62 ° 13.3) of Antarctic King George Island (King George Island) in January, 2003 by one of the inventors of the present invention (J.H.Yim). ',W58°47.0') on the Barton Peninsula (Barton Peninsular).
[0069] The collected dry sample (50 g) of Polytrichastrum alpinum (Hedw.) G.L.Sm. was extracted with methanol (1 L×2) for 24 hours, then concentrated under reduced pressure to obtain 4.7 g of crude MeOHextract.
Embodiment 2
[0070] Example 2: Isolation of the benzonaphthoxanthone-series compound philodendron F from Pseudomonas blondii
[0071] After loading 4.7 g of the crude methanol extract of Physcomitrella blondii prepared in Example 1 on C18 functionalized silica gel flash column chromatography (C18functionalized silica gel flash column chromatography, 3x15cm, Aldrich), the 4.7 g of the crude extract of Physcomitrella blondii prepared in the above-mentioned example 1 was sequentially mixed in every 400 mL of water. 20%, 40%, 60%, 70%, 80%, 90%, and 100% (v / v) methanol mixed solvents were respectively injected to obtain fractionated products. Then inject the fractionated product eluted with 80% aqueous methanol into a semi-preparative reverse-phase (semi-preparative reverse-phase) high-performance liquid chromatography (HPLC), and for water (0.1% formic acid (formic acid) ) using a mixed solvent of acetonitrile (CH3CN) at a concentration of 40 to 60% for about 27 minutes to isolate the compoun...
experiment example 1
[0072] Experimental Example 1: Cell Culture
[0073] The vascular smooth muscle cell line MOVAS-1 was purchased from the American Standard Biological Collection (ATCC) (Rockville, MD), and was prepared in the presence of 200 mg / ml G418 (a kind of aminoglycoside antibiotics), 100 IU / ml penicillin, and 100 mg / ml chain Mycin and 10% fetal bovine serum (FBS) (Carlsbad, CA) in DMEM medium (Carlsbad, CA) were maintained at 37°C and 5% CO2. In the case of subculture, the cells were divided with 0.125% trypsin containing 0.01M ethylenediaminetetraacetic acid (EDTA). The cells used in this experiment were subcultured from the first to the sixth time. All All experiments were carried out with the same configuration of MOVAS-1 in a single donor. Mononuclear macrophages (THP-1) (ATCC), a human myelomonocytic cell line, were used for the cell adhesion assay of MOVAS-1. These cells were cultured in RPMI1640 (one type of medium) containing 2 mM L-glutamine, 100 µg / ml streptomycin, 100 IU / m...
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