New iridal-type triterpenoid analogues with 6/5/6-fused carbon skeleton from the rhizomes of Belamcanda chinensis
Five new iridal-type triterpenoid derivatives with 6/5/6 tricyclic ring skeleton (1–5) were obtained from the rhizomes of Belamcanda chinensis. Their structures were determined on the basis of detailed spectroscopic data and ECD calculation. Compounds 1–5 possessed the same 6/5/6-fused carbon skelet...
Ausführliche Beschreibung
Gespeichert in:
| Autor*in: |
Li, Jiayuan [verfasserIn] |
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| Format: |
E-Artikel |
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| Sprache: |
Englisch |
| Erschienen: |
2022transfer abstract |
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| Übergeordnetes Werk: |
Enthalten in: MASE-EGTI: An agent-based simulator for environmental land change - Coelho, Cássio Giorgio Couto ELSEVIER, 2021, the journal of the study of medicinal plants, Amsterdam [u.a.] |
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| Übergeordnetes Werk: |
volume:157 ; year:2022 ; pages:0 |
| Links: |
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| DOI / URN: |
10.1016/j.fitote.2021.105040 |
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ELV056819889 |
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| 520 | |a Five new iridal-type triterpenoid derivatives with 6/5/6 tricyclic ring skeleton (1–5) were obtained from the rhizomes of Belamcanda chinensis. Their structures were determined on the basis of detailed spectroscopic data and ECD calculation. Compounds 1–5 possessed the same 6/5/6-fused carbon skeleton as Belamchinenin A, which further enriched this kind of iridals. In vitro bioassay, compounds 2 and 3 exhibited 51.95 and 54.52% inhibitory activities, respectively, against Fe2+/cysteine-induced liver microsomal lipid peroxidation at a concentration of 10 μM. A putative biogenetic pathway for compounds 1–5 was proposed. | ||
| 520 | |a Five new iridal-type triterpenoid derivatives with 6/5/6 tricyclic ring skeleton (1–5) were obtained from the rhizomes of Belamcanda chinensis. Their structures were determined on the basis of detailed spectroscopic data and ECD calculation. Compounds 1–5 possessed the same 6/5/6-fused carbon skeleton as Belamchinenin A, which further enriched this kind of iridals. In vitro bioassay, compounds 2 and 3 exhibited 51.95 and 54.52% inhibitory activities, respectively, against Fe2+/cysteine-induced liver microsomal lipid peroxidation at a concentration of 10 μM. A putative biogenetic pathway for compounds 1–5 was proposed. | ||
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10.1016/j.fitote.2021.105040 doi /cbs_pica/cbs_olc/import_discovery/elsevier/einzuspielen/GBV00000000001836.pica (DE-627)ELV056819889 (ELSEVIER)S0367-326X(21)00215-X DE-627 ger DE-627 rakwb eng 690 004 VZ 43.03 bkl Li, Jiayuan verfasserin aut New iridal-type triterpenoid analogues with 6/5/6-fused carbon skeleton from the rhizomes of Belamcanda chinensis 2022transfer abstract nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Five new iridal-type triterpenoid derivatives with 6/5/6 tricyclic ring skeleton (1–5) were obtained from the rhizomes of Belamcanda chinensis. Their structures were determined on the basis of detailed spectroscopic data and ECD calculation. Compounds 1–5 possessed the same 6/5/6-fused carbon skeleton as Belamchinenin A, which further enriched this kind of iridals. In vitro bioassay, compounds 2 and 3 exhibited 51.95 and 54.52% inhibitory activities, respectively, against Fe2+/cysteine-induced liver microsomal lipid peroxidation at a concentration of 10 μM. A putative biogenetic pathway for compounds 1–5 was proposed. Five new iridal-type triterpenoid derivatives with 6/5/6 tricyclic ring skeleton (1–5) were obtained from the rhizomes of Belamcanda chinensis. Their structures were determined on the basis of detailed spectroscopic data and ECD calculation. Compounds 1–5 possessed the same 6/5/6-fused carbon skeleton as Belamchinenin A, which further enriched this kind of iridals. In vitro bioassay, compounds 2 and 3 exhibited 51.95 and 54.52% inhibitory activities, respectively, against Fe2+/cysteine-induced liver microsomal lipid peroxidation at a concentration of 10 μM. A putative biogenetic pathway for compounds 1–5 was proposed. Ni, Gang oth Liu, Yanfei oth Wang, Renzhong oth Yu, Dequan oth Enthalten in Elsevier Science Coelho, Cássio Giorgio Couto ELSEVIER MASE-EGTI: An agent-based simulator for environmental land change 2021 the journal of the study of medicinal plants Amsterdam [u.a.] (DE-627)ELV007030444 volume:157 year:2022 pages:0 https://doi.org/10.1016/j.fitote.2021.105040 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U SSG-OLC-UMW SSG-OLC-ARC SSG-OLC-TEC SSG-OLC-MAT SSG-OLC-FOR 43.03 Methoden der Umweltforschung und des Umweltschutzes VZ AR 157 2022 0 |
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10.1016/j.fitote.2021.105040 doi /cbs_pica/cbs_olc/import_discovery/elsevier/einzuspielen/GBV00000000001836.pica (DE-627)ELV056819889 (ELSEVIER)S0367-326X(21)00215-X DE-627 ger DE-627 rakwb eng 690 004 VZ 43.03 bkl Li, Jiayuan verfasserin aut New iridal-type triterpenoid analogues with 6/5/6-fused carbon skeleton from the rhizomes of Belamcanda chinensis 2022transfer abstract nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Five new iridal-type triterpenoid derivatives with 6/5/6 tricyclic ring skeleton (1–5) were obtained from the rhizomes of Belamcanda chinensis. Their structures were determined on the basis of detailed spectroscopic data and ECD calculation. Compounds 1–5 possessed the same 6/5/6-fused carbon skeleton as Belamchinenin A, which further enriched this kind of iridals. In vitro bioassay, compounds 2 and 3 exhibited 51.95 and 54.52% inhibitory activities, respectively, against Fe2+/cysteine-induced liver microsomal lipid peroxidation at a concentration of 10 μM. A putative biogenetic pathway for compounds 1–5 was proposed. Five new iridal-type triterpenoid derivatives with 6/5/6 tricyclic ring skeleton (1–5) were obtained from the rhizomes of Belamcanda chinensis. Their structures were determined on the basis of detailed spectroscopic data and ECD calculation. Compounds 1–5 possessed the same 6/5/6-fused carbon skeleton as Belamchinenin A, which further enriched this kind of iridals. In vitro bioassay, compounds 2 and 3 exhibited 51.95 and 54.52% inhibitory activities, respectively, against Fe2+/cysteine-induced liver microsomal lipid peroxidation at a concentration of 10 μM. A putative biogenetic pathway for compounds 1–5 was proposed. Ni, Gang oth Liu, Yanfei oth Wang, Renzhong oth Yu, Dequan oth Enthalten in Elsevier Science Coelho, Cássio Giorgio Couto ELSEVIER MASE-EGTI: An agent-based simulator for environmental land change 2021 the journal of the study of medicinal plants Amsterdam [u.a.] (DE-627)ELV007030444 volume:157 year:2022 pages:0 https://doi.org/10.1016/j.fitote.2021.105040 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U SSG-OLC-UMW SSG-OLC-ARC SSG-OLC-TEC SSG-OLC-MAT SSG-OLC-FOR 43.03 Methoden der Umweltforschung und des Umweltschutzes VZ AR 157 2022 0 |
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10.1016/j.fitote.2021.105040 doi /cbs_pica/cbs_olc/import_discovery/elsevier/einzuspielen/GBV00000000001836.pica (DE-627)ELV056819889 (ELSEVIER)S0367-326X(21)00215-X DE-627 ger DE-627 rakwb eng 690 004 VZ 43.03 bkl Li, Jiayuan verfasserin aut New iridal-type triterpenoid analogues with 6/5/6-fused carbon skeleton from the rhizomes of Belamcanda chinensis 2022transfer abstract nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Five new iridal-type triterpenoid derivatives with 6/5/6 tricyclic ring skeleton (1–5) were obtained from the rhizomes of Belamcanda chinensis. Their structures were determined on the basis of detailed spectroscopic data and ECD calculation. Compounds 1–5 possessed the same 6/5/6-fused carbon skeleton as Belamchinenin A, which further enriched this kind of iridals. In vitro bioassay, compounds 2 and 3 exhibited 51.95 and 54.52% inhibitory activities, respectively, against Fe2+/cysteine-induced liver microsomal lipid peroxidation at a concentration of 10 μM. A putative biogenetic pathway for compounds 1–5 was proposed. Five new iridal-type triterpenoid derivatives with 6/5/6 tricyclic ring skeleton (1–5) were obtained from the rhizomes of Belamcanda chinensis. Their structures were determined on the basis of detailed spectroscopic data and ECD calculation. Compounds 1–5 possessed the same 6/5/6-fused carbon skeleton as Belamchinenin A, which further enriched this kind of iridals. In vitro bioassay, compounds 2 and 3 exhibited 51.95 and 54.52% inhibitory activities, respectively, against Fe2+/cysteine-induced liver microsomal lipid peroxidation at a concentration of 10 μM. A putative biogenetic pathway for compounds 1–5 was proposed. Ni, Gang oth Liu, Yanfei oth Wang, Renzhong oth Yu, Dequan oth Enthalten in Elsevier Science Coelho, Cássio Giorgio Couto ELSEVIER MASE-EGTI: An agent-based simulator for environmental land change 2021 the journal of the study of medicinal plants Amsterdam [u.a.] (DE-627)ELV007030444 volume:157 year:2022 pages:0 https://doi.org/10.1016/j.fitote.2021.105040 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U SSG-OLC-UMW SSG-OLC-ARC SSG-OLC-TEC SSG-OLC-MAT SSG-OLC-FOR 43.03 Methoden der Umweltforschung und des Umweltschutzes VZ AR 157 2022 0 |
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10.1016/j.fitote.2021.105040 doi /cbs_pica/cbs_olc/import_discovery/elsevier/einzuspielen/GBV00000000001836.pica (DE-627)ELV056819889 (ELSEVIER)S0367-326X(21)00215-X DE-627 ger DE-627 rakwb eng 690 004 VZ 43.03 bkl Li, Jiayuan verfasserin aut New iridal-type triterpenoid analogues with 6/5/6-fused carbon skeleton from the rhizomes of Belamcanda chinensis 2022transfer abstract nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Five new iridal-type triterpenoid derivatives with 6/5/6 tricyclic ring skeleton (1–5) were obtained from the rhizomes of Belamcanda chinensis. Their structures were determined on the basis of detailed spectroscopic data and ECD calculation. Compounds 1–5 possessed the same 6/5/6-fused carbon skeleton as Belamchinenin A, which further enriched this kind of iridals. In vitro bioassay, compounds 2 and 3 exhibited 51.95 and 54.52% inhibitory activities, respectively, against Fe2+/cysteine-induced liver microsomal lipid peroxidation at a concentration of 10 μM. A putative biogenetic pathway for compounds 1–5 was proposed. Five new iridal-type triterpenoid derivatives with 6/5/6 tricyclic ring skeleton (1–5) were obtained from the rhizomes of Belamcanda chinensis. Their structures were determined on the basis of detailed spectroscopic data and ECD calculation. Compounds 1–5 possessed the same 6/5/6-fused carbon skeleton as Belamchinenin A, which further enriched this kind of iridals. In vitro bioassay, compounds 2 and 3 exhibited 51.95 and 54.52% inhibitory activities, respectively, against Fe2+/cysteine-induced liver microsomal lipid peroxidation at a concentration of 10 μM. A putative biogenetic pathway for compounds 1–5 was proposed. Ni, Gang oth Liu, Yanfei oth Wang, Renzhong oth Yu, Dequan oth Enthalten in Elsevier Science Coelho, Cássio Giorgio Couto ELSEVIER MASE-EGTI: An agent-based simulator for environmental land change 2021 the journal of the study of medicinal plants Amsterdam [u.a.] (DE-627)ELV007030444 volume:157 year:2022 pages:0 https://doi.org/10.1016/j.fitote.2021.105040 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U SSG-OLC-UMW SSG-OLC-ARC SSG-OLC-TEC SSG-OLC-MAT SSG-OLC-FOR 43.03 Methoden der Umweltforschung und des Umweltschutzes VZ AR 157 2022 0 |
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10.1016/j.fitote.2021.105040 doi /cbs_pica/cbs_olc/import_discovery/elsevier/einzuspielen/GBV00000000001836.pica (DE-627)ELV056819889 (ELSEVIER)S0367-326X(21)00215-X DE-627 ger DE-627 rakwb eng 690 004 VZ 43.03 bkl Li, Jiayuan verfasserin aut New iridal-type triterpenoid analogues with 6/5/6-fused carbon skeleton from the rhizomes of Belamcanda chinensis 2022transfer abstract nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Five new iridal-type triterpenoid derivatives with 6/5/6 tricyclic ring skeleton (1–5) were obtained from the rhizomes of Belamcanda chinensis. Their structures were determined on the basis of detailed spectroscopic data and ECD calculation. Compounds 1–5 possessed the same 6/5/6-fused carbon skeleton as Belamchinenin A, which further enriched this kind of iridals. In vitro bioassay, compounds 2 and 3 exhibited 51.95 and 54.52% inhibitory activities, respectively, against Fe2+/cysteine-induced liver microsomal lipid peroxidation at a concentration of 10 μM. A putative biogenetic pathway for compounds 1–5 was proposed. Five new iridal-type triterpenoid derivatives with 6/5/6 tricyclic ring skeleton (1–5) were obtained from the rhizomes of Belamcanda chinensis. Their structures were determined on the basis of detailed spectroscopic data and ECD calculation. Compounds 1–5 possessed the same 6/5/6-fused carbon skeleton as Belamchinenin A, which further enriched this kind of iridals. In vitro bioassay, compounds 2 and 3 exhibited 51.95 and 54.52% inhibitory activities, respectively, against Fe2+/cysteine-induced liver microsomal lipid peroxidation at a concentration of 10 μM. A putative biogenetic pathway for compounds 1–5 was proposed. Ni, Gang oth Liu, Yanfei oth Wang, Renzhong oth Yu, Dequan oth Enthalten in Elsevier Science Coelho, Cássio Giorgio Couto ELSEVIER MASE-EGTI: An agent-based simulator for environmental land change 2021 the journal of the study of medicinal plants Amsterdam [u.a.] (DE-627)ELV007030444 volume:157 year:2022 pages:0 https://doi.org/10.1016/j.fitote.2021.105040 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U SSG-OLC-UMW SSG-OLC-ARC SSG-OLC-TEC SSG-OLC-MAT SSG-OLC-FOR 43.03 Methoden der Umweltforschung und des Umweltschutzes VZ AR 157 2022 0 |
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MASE-EGTI: An agent-based simulator for environmental land change |
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New iridal-type triterpenoid analogues with 6/5/6-fused carbon skeleton from the rhizomes of Belamcanda chinensis |
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New iridal-type triterpenoid analogues with 6/5/6-fused carbon skeleton from the rhizomes of Belamcanda chinensis |
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Li, Jiayuan |
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MASE-EGTI: An agent-based simulator for environmental land change |
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10.1016/j.fitote.2021.105040 |
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690 004 |
| title_sort |
new iridal-type triterpenoid analogues with 6/5/6-fused carbon skeleton from the rhizomes of belamcanda chinensis |
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New iridal-type triterpenoid analogues with 6/5/6-fused carbon skeleton from the rhizomes of Belamcanda chinensis |
| abstract |
Five new iridal-type triterpenoid derivatives with 6/5/6 tricyclic ring skeleton (1–5) were obtained from the rhizomes of Belamcanda chinensis. Their structures were determined on the basis of detailed spectroscopic data and ECD calculation. Compounds 1–5 possessed the same 6/5/6-fused carbon skeleton as Belamchinenin A, which further enriched this kind of iridals. In vitro bioassay, compounds 2 and 3 exhibited 51.95 and 54.52% inhibitory activities, respectively, against Fe2+/cysteine-induced liver microsomal lipid peroxidation at a concentration of 10 μM. A putative biogenetic pathway for compounds 1–5 was proposed. |
| abstractGer |
Five new iridal-type triterpenoid derivatives with 6/5/6 tricyclic ring skeleton (1–5) were obtained from the rhizomes of Belamcanda chinensis. Their structures were determined on the basis of detailed spectroscopic data and ECD calculation. Compounds 1–5 possessed the same 6/5/6-fused carbon skeleton as Belamchinenin A, which further enriched this kind of iridals. In vitro bioassay, compounds 2 and 3 exhibited 51.95 and 54.52% inhibitory activities, respectively, against Fe2+/cysteine-induced liver microsomal lipid peroxidation at a concentration of 10 μM. A putative biogenetic pathway for compounds 1–5 was proposed. |
| abstract_unstemmed |
Five new iridal-type triterpenoid derivatives with 6/5/6 tricyclic ring skeleton (1–5) were obtained from the rhizomes of Belamcanda chinensis. Their structures were determined on the basis of detailed spectroscopic data and ECD calculation. Compounds 1–5 possessed the same 6/5/6-fused carbon skeleton as Belamchinenin A, which further enriched this kind of iridals. In vitro bioassay, compounds 2 and 3 exhibited 51.95 and 54.52% inhibitory activities, respectively, against Fe2+/cysteine-induced liver microsomal lipid peroxidation at a concentration of 10 μM. A putative biogenetic pathway for compounds 1–5 was proposed. |
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New iridal-type triterpenoid analogues with 6/5/6-fused carbon skeleton from the rhizomes of Belamcanda chinensis |
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https://doi.org/10.1016/j.fitote.2021.105040 |
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Ni, Gang Liu, Yanfei Wang, Renzhong Yu, Dequan |
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