Monogalactosyldiacylglyceride and its preparation method and use
A technology of lactosyl diacylglycerol and its use, which is applied in the field of preparation of monogalactosyl diacylglyceride
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Embodiment 1
[0033] Example 1: Extraction preparation and structural identification of monogalactosyldiacylglyceride
[0034] Take 2000g of Hijiki, extract with 10 times the volume of 75% ethanol under reflux for 2h, repeat 3 times. Combine the extracts, filter and concentrate until there is no alcohol smell, extract 3 times with an equal volume of ethyl acetate, combine the extracts, concentrate to obtain 33.26 g of extract. The extract was dissolved in ethyl acetate, mixed with 41g 200-300 mesh silica gel H, and subjected to silica gel column chromatography, using dichloromethane-methanol as a solvent for gradient elution, wherein dichloromethane-methanol (v / v 95:5 ) to elute the resulting components, and then through Sephadex LH-20 gel column chromatography (dichloromethane-methanol 1:1) and silica gel column chromatography to obtain a mixture of monogalactosyl diacylglycerides (MGDG) , measure its 1 H-NMR spectrum and 13 C-NMR spectrum (such as figure 1 and 2 shown).
[0035] accor...
Embodiment 2
[0039] Example 2: Activation of PPARα and PPARγ by MGDG
[0040] Transcriptional activation of PPARα and PPARγ was detected using a dual-luciferase reporter gene assay. 293T cells were inoculated in 96-well plates with DMEM medium (10% FBS, without antibiotics). After 8-12 hours, the cells grew to about 60%. Without changing the medium, the plasmid was directly transfected according to the instructions of lipo2000. The total amount of plasmid was 0.075 g / well (0.05 μg PPRE, 0.005 μg internal control pRL-TK and 0.02 μg PPARα / γ). The amount of lipo2000 used was 2.5 times the mass of the transfected plasmid (2.5*0.075L=0.1875 μL / well). The plasmid and lipo2000 were mixed in 25 μL / well optim medium in advance. After 12 hours of transfection, the positive drug (the positive drug for PPARγ is rosiglitazone at a concentration of 1 μM, and the positive drug for PPARα is WY14643 at a concentration of 10 μM) and the MGDG obtained in Example 1 were added. 24 hours after adding the dru...
Embodiment 3
[0041] Example 3: Activation of MD1-MD6 on PPARα and PPARγ
[0042] The transcriptional activation of PPARα and PPARγ was detected by dual-luciferase reporter gene analysis technology, and the specific method was the same as that in Example 2. The drugs added are MD1-MD6 prepared in Example 1. The results are shown in Table 2.
[0043] Table 2 Activation of PPARα / γ by MD1~MD6
[0044]
[0045]
[0046] Note: Compared with the blank group, "*"P<0.05; "**"P<0.01; "***"P<0.001.
[0047] The results showed that the above compounds could activate PPARα and / or PPARγ to varying degrees. In particular, MD5 (compound of formula (II)) exhibited significant PPARα / γ dual agonism.
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