Study on synergistic mechanism of pangolin in high temperature sand-fried processing / 中草药

Objective Traditional raw pangolin products are not used as medicine, which can only be used as medicine after processing. Therefore, the processing mechanism of high temperature sand-fried pangolin was studied. Methods The changes of liposolubility and protein composition of pangolin before and after processing were analyzed by TLC and Nano LC-Q Exactive Orbitrap MS. Meanwhile, the simulation processing of cyclic dipeptides, which were significantly increased during processing, was performed. The activity of L-serine-L-tyrosine cyclic dipeptide was screened. Results The results showed that there was no significant change in fat-soluble components, significant decrease in polypeptides and significant increase in cyclic dipeptides after the sand-fried processing of pangolin. The formation of cyclic dipeptides was mainly related to the heating of the processing. At low temperature, the N-terminal of the linear peptide could be cycled to form L-shaped cyclic dipeptides. At high temperature, the N-terminal and C-terminal of the linear peptide could be rapidly cycled to form cyclic dipeptides. L-serine-L-tyrosine cyclic dipeptide could prolong coagulation time and increase the proliferation rate of mammary epithelial cells and the expression of genes related to milk protein synthesis in dairy cows. It also had significant analgesic activity, which was consistent with the traditional efficacy of pangolin. Conclusion These results suggested that large amounts of L-serine-L-tyrosine cyclic dipeptide produced by the processing of pangolin may be one of the material bases for enhancing the processing efficiency of pangolin. It was of great significance for revealing the material basis of pharmacodynamics of pangolin, searching for alternative resources and protecting pangolin.

Study on chemical constituents of sponge Mycale sp.from the South China Sea / 药学实践杂志

Objective To investigate the chemical constituents of marine sponge Mycale sp.collected from the South China Sea.Methods The ethyl acetate extract of the marine sponge Mycale sp.was separated and purified by repeated column chromatography on silica gel, Sephadex LH-20 and reversed-phase high-performance liquid chromatography (RP-HPLC).The structures of these compounds were identified by means of various modern spectroscopic techniques and comparison with their physicochemical properties to reported data.The tumor cell growth inhibitory activities of these compounds against human breast cancer cell lines MCF-7 and human lung cancer cell lines PC9 were tested by Cell Counting Kit-8 (CCK-8) method.Results Ten compounds were isolated and identified as cyclo-(Pro-Ile)(1),cyclo-(Pro-Leu)(2),cyclo-(Ile-Leu)(3),cyclo-(Phe-Pro)(4),cyclo-(Phe-Val)(5),cyclo-(Phe-Leu)(6),cyclo-(Phe-Ile)(7), 2′-deoxythymidine (8), thymine (9), 5-hydroxy-3,4-dimethyl-5-pentyl-2(5H)-furanone (10).These compounds showed weak tumor cell growth inhibitory activities toward cells MCF-7 and PC9 in vitro.Conclusion Compounds 1, 2, 4, 5, 6, 7 and 10 were isolated from the sponge Mycale sp.for the first time.It is the first time to report the antitumor activity evaluation for compounds 1~10.

Isolation and identification of the chemical constituents from stems and leaves of Arachis hypogaea L / 中国药学杂志

OBJECTIVE: To study the chemical constituents from the stems and leaves of Arachis hypogaea L. METHODS: Various column chromatographic techniques were used to separate and purify the chemical constituents and their structures were elucidated by spectral analysis. RESULTS: Fifteen compounds were isolated and identified as 4,9-dihydroxy-3-methothxy-coumestan(I), 3-hydroxy-9-dimethothxycoumestan (II), 3-isopropyl-pyrrolopiperazine-2,5-dione(III), 3-isobutylpyrrol-opiperazine-2,5-dione(IV), uracil(V), thymine(VI), thymidine(VH), L-(-)-phenylalanine(VI), nicotinic acid(IX), 2-furancarboxylic acid(X), ferulic acid (XI), vanillic acid(XII), 2-hydroxybenzoic acid(XIII), amber acid(XIV), and methyl hydrogen succinate(XV). CONCLUSION: The compounds I-IX are isolated from Arachis hypogaea L. for the first time.

Cyclic dipeptides in actinomycete Brevibacterium sp. associated with sea cucumber Apostichopus japonicus Selenka: Isolation and identification / 第二军医大学学报

Objective To investigate the secondary metabolites of actinomycete Brevibacterium sp. associated with the sea cucumber Apostichopus japonicus Selenka. Methods The ethyl acetate extract of the actinomycete was purified by repeated column chromatography on silica gel, Sephadex LH-20, and high-performance liquid chromatography (HPLC) to obtain pure compounds; and the compound structures were elucidated by spectroscopic analysis (nuclear magnetic resonance, NMR; mass spectrometry, MS) and the results were compared with the previously reported data. Results Seven compounds were isolated: cyclo-(L-Pro-L-Phe) (1), cyclo-(L-Pro-L-Met) (2), cyclo-(L-Pro-L-Tyr) (3), cyclo-(L-Pro-L-Val) (4), cyclo-(L-Pro-L-Pro) (5), cyclo-(L-Val-Gly) (6), and cyclo-(L-Pro-L-Leu) (7). Conclusion This is the first report on the secondary metabolites of microorganisms associated with the sea cucumber Apostichopus japonicus Selenka, and all the seven compounds have been reported from the actinomycete Brevibacterium sp. for the first time.