1.Chemical constituents from Hydrangea paniculata.
Jing SHI ; Jingzhi YANG ; Chuangjun LI ; Dongming ZHANG
China Journal of Chinese Materia Medica 2010;35(22):3007-3009
In order to study the chemical constituents of the plant of Hydrangea paniculata and provide reference for the study of the bioactive substances, we isolated nine compounds from the dried branches of H. paniculata. Their structures were determined by application of spectroscopic (NMR, MS) and chemical methods. These compounds were identified as skimmin (1), isotachioside (2), 8-methoxy-7-O-beta-D-glucopyranosyloxy coumarin glycoside (3), scopolin (4), 1-(alpha-L-rhamnosyl-(1 --> 6) -O-beta-D-glucopyranosyloxy) - 3, 4, 5-trimethoxybenzene (5), apiosylskimmin (6), umbelliferone (7), scopoletin (8), 7-hydroxy-8-methoxycoumarin (9). Compounds 1 - 7 were isolated from H. paniculata for the first time.
Drugs, Chinese Herbal
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analysis
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isolation & purification
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Hydrangea
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chemistry
2.Study on chemical constituents from leaves of Tripterygium wilfordii.
Xu CAO ; Chuangjun LI ; Jingzhi YANG ; Baixing WEI ; Yongming LUO ; Dongming ZHANG
China Journal of Chinese Materia Medica 2011;36(8):1028-1031
In order to study the chemical constituents of the leaves of Tripterygium wilfordii and provide references for the bio-active study, we isolated nine compounds from the dried leaves of Tripterygium wilfordii. Their structures were determined by application of spectroscopic (NMR, MS) and chemical methods. These compounds were isolated and identified as (+)-lyoniresinol (1), (+)-isolariciresinol (2), burselignan (3), dibutyl phthalate (4), cyclo-(S-Pro-R-Phe) (5), cyclo-(S-Pro-R-Leu) (6), cyclo-(S-Pro-S-Ile) (7), 3-hydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)-1-propanone (8) and daucosterol (9). Compounds 1-3, 5-8 were isolated from this plant for the first time.
Anisoles
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chemistry
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isolation & purification
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Dibutyl Phthalate
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chemistry
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isolation & purification
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Lignin
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chemistry
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isolation & purification
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Magnetic Resonance Imaging
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methods
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Mass Spectrometry
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methods
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Naphthalenes
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chemistry
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isolation & purification
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Naphthols
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chemistry
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isolation & purification
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Peptides, Cyclic
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chemistry
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isolation & purification
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Plant Extracts
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chemistry
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isolation & purification
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Plant Leaves
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chemistry
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Sitosterols
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chemistry
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isolation & purification
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Tripterygium
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chemistry
3.Chemical constituents of Clausena lansium.
Qing ZHAO ; Chuangjun LI ; Jingzhi YANG ; Dongming ZHANG
China Journal of Chinese Materia Medica 2010;35(8):997-1000
OBJECTIVETo study the chemical constituents of the leaf of Clausena lansium (Lour.) Skeels.
METHODThe compounds were isolated by various chromatographic techniques and their structures were elucidated by their physicochemical properties and the analysis of their spectroscopic data.
RESULTSeven compounds were isolated and identified as corchoionoside C (1), 1'-O-beta-D-glucopyranosyl (2R,3S)-3-hydroxynodakenetin (2), quercetin-3-O-robinobioside (3), rutin (4), quercetin-3-O-scillabioside (5), keampferol-3-O-alpha-L-rhamnopyranosyl(1-->2) [alpha-L-rhamnopyranosyl(1-->6)]-beta-D-glucopyranoside (6), mauritianin (7).
CONCLUSIONCompounds 1-7 were isolated from the genus Clausena for the first time.
Chemical Phenomena ; Chromatography, High Pressure Liquid ; Clausena ; chemistry ; Organic Chemicals ; analysis ; chemistry
4.Chemical constituents from Sarcandra glabra.
Chao WANG ; Liping ZHU ; Jingzhi YANG ; Chuangjun LI ; Dongming ZHANG
China Journal of Chinese Materia Medica 2010;35(6):714-717
OBJECTIVETo study the chemical constituents of the plant of Sarcandra glabra and provide reference for the study of the bioactive substances.
METHODThe compounds were isolated from the EtOH extract by various chromatographic methods and their structures were elucidated by their physico-chemical properties and the analysis of their spectral data.
RESULTNine compounds were isolated and identified as isoscopletin (1), syringaresinol monoside (2), styraxjaponoside B (3), 5-O-caffeoylshikimic acid (4), shizukanolide E (5), isoastilbin (6), neoisoastilbin (7), astilbin (8), neoastilbin (9).
CONCLUSIONCompounds 1-7 were isolated from S. glabra for the first time.
Cholestenones ; analysis ; Drugs, Chinese Herbal ; analysis ; chemistry ; Flavonoids ; analysis ; Flavonols ; analysis ; Furans ; analysis ; Lignans ; analysis ; Magnoliopsida ; chemistry ; Plant Bark ; chemistry ; Plant Stems ; chemistry ; Shikimic Acid ; analogs & derivatives ; analysis
5.Sequential immunization with SARS-CoV-2 vaccines
Weiwei SONG ; Qiang XU ; Zunyang KE ; Chuangjun QIU ; Zhongming LI ; Yu WANG
Chinese Journal of Microbiology and Immunology 2022;42(6):456-463
Sequential immunization is one of the special means to solve the shortage of vaccines, respond to SARS-CoV-2 variants and improve the efficacy of vaccines in the current pandemic period. This article mainly reviewed five sequential immunization strategies using the vaccines authorized by World Health Organization: priming with inactivated vaccine and boosting with recombinant protein vaccine, vector vaccine or mRNA vaccine; priming with vector vaccine and boosting with mRNA vaccine; prime-boost immunization with mRNA vaccines produced by different manufactures. Results of the related studies showed that heterologous sequential immunization strategies were safe and effective, and higher immunogenicity and efficacy could be achieved by sequential immunization. In addition, sequential immunization could provide certain protective effects against SARS-CoV-2 variants.
6.Two new phenylpropanoid glycosides from the aerial parts of.
Chuangfeng ZHANG ; Jian ZHOU ; Jingzhi YANG ; Chuangjun LI ; Jie MA ; Dan ZHANG ; Dongming ZHANG
Acta Pharmaceutica Sinica B 2016;6(6):564-567
Two new phenylpropanoid glycosides named cuneataside E () and cuneataside F (), were isolated from the aerial parts of(Dum. Cours.) G. Don, whose structures wereandisomer, respectively. Their structures were elucidated on the basis of comprehensive spectroscopic analysis (UV, IR, HR-ESI-MS, 1D and 2D NMR). Inbioassays at 10 μmol/L, compoundshowed moderate hepatoprotective activity against-acetyl--aminophenol (APAP)-induced toxicity in HeG2 cells.