A hydroxypropionic acid compound and its preparation method and medical application
A technology of hydroxypropionic acid and compounds, applied in the field of medicine, to achieve the effects of convenient and easy-to-obtain raw material sources, favorable industrialization, and simple preparation steps
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Embodiment 1
[0023] Example 1 :The preparation and structure identification of the compound of formula (I)
[0024] 1.1 Experimental equipment and materials
[0025] NMR spectrum was measured by Bruker AV-400 nuclear magnetic resonance spectrometer (δ is ppm, TMS is internal standard, J is Hz); MS spectrum is measured by Agilent G3250AA LC / MSD TOF electrospray time-of-flight mass spectrometer; Rotary evaporator uses Heidolph, Germany; the circulating condensate pump adopts Japan's EYELA; the analytical balance adopts the pioneer manufactured by Ohaus Instrument (Shanghai) Co., Ltd. Sephadex (Pharmadex LH-20) for column chromatography was purchased from Amphamacia Biotechnology (China) Co., Ltd.; ODS reversed-phase materials were purchased from Merck; column-layer silica gel and thin-layer chromatography silica gel plates were Produced by Qingdao Ocean Chemical Plant. The elution solvents for chromatography are industrially pure solvents or chemically pure solvents that have been re-evaporated...
Embodiment 2
[0039] Example 2 :Detection of the ability of compounds of formula (I) to scavenge 1,1-diphenyl-dipicrylhydrazine (DPPH) free radicals
[0040] 2.1 Experimental principle and experimental purpose
[0041] DPPH is a relatively stable lipid free radical, with a free electron on its N, and its ethanol solution is purple. Scanning at the full wavelength shows that it has a maximum absorption peak at 517nm. After adding antioxidants, DPPH captures an electron to pair with free electrons, the purple fades and becomes a colorless substance, and the absorption peak at 517nm disappears. The degree of fading has a quantitative relationship with the number of electrons it accepts. That is, the absorption value of DPPH decreases when it is redox, and the lower the absorbance, the stronger its antioxidant effect. According to this principle, the ability of the sample to provide hydrogen atoms, scavenge free radicals, and resist oxidation can be measured.
[0042] 2.2 Methods and results
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