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  1. Article ; Online: Six new iridoid glycosides from the whole plants of

    Gao, Huan-Huan / Qin, Ling-Feng / Zhang, Xu / Yuan, Xiang / Feng, Zi-Ming / Jiang, Jian-Shuang / Zhang, Pei-Cheng / Yang, Ya-Nan

    Journal of Asian natural products research

    2024  Volume 26, Issue 1, Page(s) 112–119

    Abstract: Six new iridoid glycosides were isolated from the ethyl acetate fraction of the whole plants ... ...

    Abstract Six new iridoid glycosides were isolated from the ethyl acetate fraction of the whole plants of
    MeSH term(s) Iridoid Glycosides/pharmacology ; Hedyotis/chemistry ; Antioxidants ; Magnetic Resonance Spectroscopy ; Esters ; Glycosides/pharmacology ; Coumaric Acids
    Chemical Substances Iridoid Glycosides ; Antioxidants ; E-6-O-p-coumaroyl scandoside methyl ester ; Esters ; Glycosides ; Coumaric Acids
    Language English
    Publishing date 2024-01-07
    Publishing country England
    Document type Journal Article
    ZDB-ID 2077926-4
    ISSN 1477-2213 ; 1028-6020
    ISSN (online) 1477-2213
    ISSN 1028-6020
    DOI 10.1080/10286020.2023.2293068
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Six undescribed lavandulylated flavonoids with PTP1B inhibition from the roots of Sophora flavescens.

    Zhang, Xu / Lu, Kai-Zhou / Yang, Ya-Nan / Feng, Zi-Ming / Yuan, Xiang / Jiang, Jian-Shuang / Zhang, Pei-Cheng

    Phytochemistry

    2023  Volume 216, Page(s) 113889

    Abstract: Six undescribed lavandulylated flavonoids (1-6) were isolated from the roots of Sophora flavescens. Remarkably, compounds 1 and 2, which were composed of a flavane unit and a phloroglucinol unit, were the first reported dimers. Compounds 3 and 4 were the ...

    Abstract Six undescribed lavandulylated flavonoids (1-6) were isolated from the roots of Sophora flavescens. Remarkably, compounds 1 and 2, which were composed of a flavane unit and a phloroglucinol unit, were the first reported dimers. Compounds 3 and 4 were the first reported neoflavonoids with lavandulyl units. Compounds 5 and 6 were chalcone with oxidized lavandulyl units. Their structures were fully characterized by cumulative analyses of UV, IR, HRESIMS, NMR and ECD spectroscopic data, along with computational calculations through density functional theory. Compounds 1 and 2 showed significant protein tyrosine phosphatase-1B inhibitory activities with IC
    MeSH term(s) Flavonoids/chemistry ; Sophora flavescens ; Sophora/chemistry ; Plant Extracts/chemistry ; Plant Roots/chemistry
    Chemical Substances Flavonoids ; Plant Extracts
    Language English
    Publishing date 2023-10-09
    Publishing country England
    Document type Journal Article
    ZDB-ID 208884-8
    ISSN 1873-3700 ; 0031-9422
    ISSN (online) 1873-3700
    ISSN 0031-9422
    DOI 10.1016/j.phytochem.2023.113889
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: The tanshinones from the plant of Salvia miltiorrhiza.

    Jiang, Jian-Shuang / Gu, Quan-Chang / Feng, Zi-Ming / Yuan, Xiang / Zhang, Xu / Zhang, Pei-Cheng / Yang, Ya-Nan

    Phytochemistry

    2023  Volume 210, Page(s) 113673

    Abstract: Six undescribed tanshinones, (+)-2-Cl-tanshindiol C (1), (-)-2-Cl-tanshindiol C (2), (+)-tanshinoic acid D (3), (-)-tanshinoic acid D (4), (-)-tanshinoic acid E (5), and (+)-tanshinoic acid E (6), were isolated from the rhizome of Salvia miltiorrhiza ... ...

    Abstract Six undescribed tanshinones, (+)-2-Cl-tanshindiol C (1), (-)-2-Cl-tanshindiol C (2), (+)-tanshinoic acid D (3), (-)-tanshinoic acid D (4), (-)-tanshinoic acid E (5), and (+)-tanshinoic acid E (6), were isolated from the rhizome of Salvia miltiorrhiza Bunge. Their structures were elucidated based on the spectroscopic data (UV, IR, HR-ESI-MS, and NMR). The bioactive assays of all these compounds for the antioxidant activities in cardiomyocytes upon hypoxia stimulation were evaluated. The results suggested that compounds 5 and 6 exhibited good antioxidant activities in cardiomyocytes and the cell survival rates were 46.3% and 57.9% (10
    MeSH term(s) Salvia miltiorrhiza/chemistry ; Antioxidants/pharmacology ; Abietanes/pharmacology ; Abietanes/chemistry ; Rhizome/chemistry ; Plant Roots/chemistry
    Chemical Substances tanshinone (03UUH3J385) ; Antioxidants ; Abietanes
    Language English
    Publishing date 2023-04-06
    Publishing country England
    Document type Journal Article
    ZDB-ID 208884-8
    ISSN 1873-3700 ; 0031-9422
    ISSN (online) 1873-3700
    ISSN 0031-9422
    DOI 10.1016/j.phytochem.2023.113673
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Seventeen undescribed iridoid derivatives with anti-inflammatory effects from Hedyotis diffusa and their structure-activity relationships.

    Qin, Ling-Feng / Gao, Huan-Huan / Zhang, Xu / Yuan, Xiang / Feng, Zi-Ming / Zhang, Pei-Cheng / Jiang, Jian-Shuang / Yang, Ya-Nan

    Phytochemistry

    2023  Volume 217, Page(s) 113904

    Abstract: Seventeen undescribed iridoid derivatives (1-17) and four known compounds (18-21) were isolated from the whole plant of Hedyotis diffusa Willd. Their structures were elucidated based on unambiguous spectroscopic data (UV, IR, HRESIMS, CD, and 1D and 2D ... ...

    Abstract Seventeen undescribed iridoid derivatives (1-17) and four known compounds (18-21) were isolated from the whole plant of Hedyotis diffusa Willd. Their structures were elucidated based on unambiguous spectroscopic data (UV, IR, HRESIMS, CD, and 1D and 2D NMR). It is noteworthy that compounds 1-8, which possess unique long-chain aliphatic acid moiety, were reported for the first time among the iridoid natural products. All compounds were evaluated for their anti-inflammatory activities in lipopolysaccharide-induced RAW 264.7 cells. Compounds 2, 4, and 6 showed significant suppression effects on nitric oxide production, with IC
    MeSH term(s) Iridoids/pharmacology ; Iridoids/chemistry ; Hedyotis/chemistry ; Plant Extracts/chemistry ; Structure-Activity Relationship ; Anti-Inflammatory Agents/pharmacology ; Anti-Inflammatory Agents/chemistry
    Chemical Substances Iridoids ; Plant Extracts ; Anti-Inflammatory Agents
    Language English
    Publishing date 2023-11-04
    Publishing country England
    Document type Journal Article
    ZDB-ID 208884-8
    ISSN 1873-3700 ; 0031-9422
    ISSN (online) 1873-3700
    ISSN 0031-9422
    DOI 10.1016/j.phytochem.2023.113904
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: The tanshinones from the plant of Salvia miltiorrhiza

    Jiang, Jian-Shuang / Gu, Quan-chang / Feng, Zi-Ming / Yuan, Xiang / Zhang, Xu / Zhang, Pei-Cheng / Yang, Ya-Nan

    Phytochemistry. 2023 June, v. 210 p.113673-

    2023  

    Abstract: Six undescribed tanshinones, (+)-2-Cl-tanshindiol C (1), (−)-2-Cl-tanshindiol C (2), (+)-tanshinoic acid D (3), (−)-tanshinoic acid D (4), (−)-tanshinoic acid E (5), and (+)-tanshinoic acid E (6), were isolated from the rhizome of Salvia miltiorrhiza ... ...

    Abstract Six undescribed tanshinones, (+)-2-Cl-tanshindiol C (1), (−)-2-Cl-tanshindiol C (2), (+)-tanshinoic acid D (3), (−)-tanshinoic acid D (4), (−)-tanshinoic acid E (5), and (+)-tanshinoic acid E (6), were isolated from the rhizome of Salvia miltiorrhiza Bunge. Their structures were elucidated based on the spectroscopic data (UV, IR, HR-ESI-MS, and NMR). The bioactive assays of all these compounds for the antioxidant activities in cardiomyocytes upon hypoxia stimulation were evaluated. The results suggested that compounds 5 and 6 exhibited good antioxidant activities in cardiomyocytes and the cell survival rates were 46.3% and 57.9% (10⁻⁵ mol/L), respectively.
    Keywords Salvia miltiorrhiza ; antioxidants ; cardiomyocytes ; cell viability ; hypoxia ; plant biochemistry ; rhizomes ; spectral analysis ; Labiatae ; Isolation and purification ; Tanshinone ; Structural elucidation ; Antioxidant activities
    Language English
    Dates of publication 2023-06
    Publishing place Elsevier Ltd
    Document type Article ; Online
    ZDB-ID 208884-8
    ISSN 1873-3700 ; 0031-9422
    ISSN (online) 1873-3700
    ISSN 0031-9422
    DOI 10.1016/j.phytochem.2023.113673
    Database NAL-Catalogue (AGRICOLA)

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  6. Article ; Online: Bioactive amides from

    Zhang, Xu / Liu, Fu / Feng, Zi-Ming / Jiang, Jian-Shuang / Yang, Ya-Nan / Zhang, Pei-Cheng

    Journal of Asian natural products research

    2021  Volume 23, Issue 3, Page(s) 228–234

    Abstract: One pair of new amides enantiomers ( ...

    Abstract One pair of new amides enantiomers (
    MeSH term(s) Amides/pharmacology ; Fallopia japonica ; Molecular Structure ; Plant Extracts ; Polygonum ; Rhizome
    Chemical Substances Amides ; Plant Extracts
    Language English
    Publishing date 2021-01-18
    Publishing country England
    Document type Journal Article
    ZDB-ID 2077926-4
    ISSN 1477-2213 ; 1028-6020
    ISSN (online) 1477-2213
    ISSN 1028-6020
    DOI 10.1080/10286020.2021.1873298
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: Synthesis of 4-thiosubstituted flavan derivatives and their hypoglycemic activities.

    Zhang, Xu / Yun, Ju-Ping / Yang, Ya-Nan / Feng, Zi-Ming / Jiang, Jian-Shuang / Yuan, Xiang / Liu, Wei / Zhang, Pei-Cheng

    Fitoterapia

    2022  Volume 161, Page(s) 105255

    Abstract: A series of 4-thiosubstituted flavan derivatives (1-44) were designed and synthesized. The target compounds were assayed for inhibitory activity against α-glucosidase in vitro, and the results indicated that all compounds displayed significant effects in ...

    Abstract A series of 4-thiosubstituted flavan derivatives (1-44) were designed and synthesized. The target compounds were assayed for inhibitory activity against α-glucosidase in vitro, and the results indicated that all compounds displayed significant effects in the range of IC
    MeSH term(s) Acarbose/pharmacology ; Animals ; Glycoside Hydrolase Inhibitors/pharmacology ; Hypoglycemic Agents/pharmacology ; Mice ; Molecular Docking Simulation ; Molecular Structure ; Structure-Activity Relationship ; alpha-Glucosidases/metabolism
    Chemical Substances Glycoside Hydrolase Inhibitors ; Hypoglycemic Agents ; alpha-Glucosidases (EC 3.2.1.20) ; Acarbose (T58MSI464G)
    Language English
    Publishing date 2022-07-28
    Publishing country Netherlands
    Document type Journal Article
    ZDB-ID 412385-2
    ISSN 1873-6971 ; 0367-326X
    ISSN (online) 1873-6971
    ISSN 0367-326X
    DOI 10.1016/j.fitote.2022.105255
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: Eight new arnebinol B-based meroterpenoids with planar chirality in the constrained 6/10/5 tricyclic skeleton from Arnebia euchroma and their cytotoxicities.

    Yan, Hai-Wei / Yang, Ya-Nan / Zhang, Xu / Jiang, Jian-Shuang / Yuan, Xiang / Feng, Zi-Ming / Zhang, Pei-Cheng

    Bioorganic chemistry

    2022  Volume 128, Page(s) 106091

    Abstract: Eight new arnebinol B-based meroterpenoids ((-)-1, 2, 3, (-)-5, and 7-10) with a constrained 6/10/5 tricyclic backbone were isolated from the roots of Arnebia euchroma. The planar and steric structures of these new compounds were unambiguously elucidated ...

    Abstract Eight new arnebinol B-based meroterpenoids ((-)-1, 2, 3, (-)-5, and 7-10) with a constrained 6/10/5 tricyclic backbone were isolated from the roots of Arnebia euchroma. The planar and steric structures of these new compounds were unambiguously elucidated by extensive spectroscopic analyses, X-ray diffraction crystallography, and ECD calculations. The predominant relative orientation between H-7 and the Z double bond with a methyl substituent in the rigid 10-membered carbocycle, along with the planar chirality of the Z double bond was analyzed and discussed for the first time. The illustration of the planar chirality derived from the Z double bond should be paid great importance during the structure elucidation on these homologous meroterpenoids. All the isolated meroterpenoids were screened for their cytotoxicities against the HCT-8, PANC-1, HGC-27, HepG2, and PC9 cell lines, and compounds (+)-5 and (-)-5 exhibited the most potent cytotoxicity.
    MeSH term(s) Boraginaceae/chemistry ; Molecular Structure ; Plant Roots/chemistry ; Skeleton ; Terpenes/chemistry ; Terpenes/pharmacology
    Chemical Substances Terpenes ; arnebinol (87064-17-3)
    Language English
    Publishing date 2022-08-19
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 120080-x
    ISSN 1090-2120 ; 0045-2068
    ISSN (online) 1090-2120
    ISSN 0045-2068
    DOI 10.1016/j.bioorg.2022.106091
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article ; Online: The phenolic acids from the plant of Salvia miltiorrhiza.

    Jiang, Jian-Shuang / Gu, Quan-Chang / Feng, Zi-Ming / Yuan, Xiang / Zhang, Xu / Zhang, Pei-Cheng / Yang, Ya-Nan

    Fitoterapia

    2022  Volume 159, Page(s) 105180

    Abstract: Seven new phenolic acids, 7, 8-epiblechnic acid (1), 8-epiblechnic acid 9-ehthyl-9'-methyl ester (2), 9'-ehyl-isolithospermate (3), 9''-methyl-isolithospermate (4), 9'-ethyl-9''-methyl-isolithospermate (5), 9', 9''-dimethyl-isolithospermate (6), ... ...

    Abstract Seven new phenolic acids, 7, 8-epiblechnic acid (1), 8-epiblechnic acid 9-ehthyl-9'-methyl ester (2), 9'-ehyl-isolithospermate (3), 9''-methyl-isolithospermate (4), 9'-ethyl-9''-methyl-isolithospermate (5), 9', 9''-dimethyl-isolithospermate (6), sebesteniod E (7), were isolated from the roots of Salvia miltiorrhiza. Their structures were elucidated by detailed spectroscopic means including UV, IR, HRESIMS, and NMR data spectra. The bioactive assays of compounds 1-7 against neuroprotection activities were determined. The results suggested that compound 4 exhibited a moderate glutamate-induced neuroprotective activity and the cell survival rate was 24.0% (10
    MeSH term(s) Hydroxybenzoates/pharmacology ; Molecular Structure ; Plant Roots ; Salvia miltiorrhiza/chemistry
    Chemical Substances Hydroxybenzoates
    Language English
    Publishing date 2022-03-23
    Publishing country Netherlands
    Document type Journal Article
    ZDB-ID 412385-2
    ISSN 1873-6971 ; 0367-326X
    ISSN (online) 1873-6971
    ISSN 0367-326X
    DOI 10.1016/j.fitote.2022.105180
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article: Enhancement of autophagy flux by isopsoralen ameliorates interleukin-1β-stimulated apoptosis in rat chondrocytes

    Chen, Zhi / Li, Chen / Qian, Yi-Hong / Fu, Yang / Feng, Zi-Ming

    Journal of Asian natural products research. 2020 Feb. 1, v. 22, no. 2

    2020  

    Abstract: Chondrocyte apoptosis contributes to the pathogenesis of cartilage degeneration in osteoarthritis (OA). We found that isopsoralen pretreatment significantly reversed the increase in DNA fragmentation and apoptosis rate, and significantly decreased the ... ...

    Abstract Chondrocyte apoptosis contributes to the pathogenesis of cartilage degeneration in osteoarthritis (OA). We found that isopsoralen pretreatment significantly reversed the increase in DNA fragmentation and apoptosis rate, and significantly decreased the caspase-3 activity and PARP cleavage in IL-1β-treated chondrocytes. Isopsoralen pretreatment markedly inhibited disruption of matrix proteins. Moreover, the expressions of LC3-II and LAMP-1 were markedly increased but the expression of p62/SQSTM1 was remarkably decreased by isopsoralen pretreatment. Importantly, the protective effects of isopsoralen against IL-1β were blocked by pretreatment with autophagy inhibitor 3-MA and bafilomycin A1. These results suggest that isopsoralen ameliorates chondrocyte apoptosis by promoting autophagy flux.
    Keywords DNA fragmentation ; apoptosis ; autophagy ; cartilage ; caspase-3 ; chondrocytes ; enzyme activity ; interleukin-1beta ; osteoarthritis ; pathogenesis ; protective effect ; proteins ; rats
    Language English
    Dates of publication 2020-0201
    Size p. 179-192.
    Publishing place Taylor & Francis
    Document type Article
    ZDB-ID 2077926-4
    ISSN 1477-2213 ; 1028-6020
    ISSN (online) 1477-2213
    ISSN 1028-6020
    DOI 10.1080/10286020.2018.1537265
    Database NAL-Catalogue (AGRICOLA)

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