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Clematis terniflora

Clematis terniflora - Unknown
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Author: Public Domain - WikiMedia
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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID644011e4cc6ca768023591
Scientific name Clematis terniflora
Authority DC.
First published in Syst. Nat. 1: 137 (1817)

Description Top

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No description added yet. Help us by writing one.

Synonyms Top

Scientific name Authority First published in
Clematis dioscoreifolia H.Lév. & Vaniot Repert. Spec. Nov. Regni Veg. 7: 339 (1909)
Clematis maximowicziana Franch. & Sav. Enum. Pl. Jap. 2: 261 (1878)
Clematis paniculata Thunb. Trans. Linn. Soc. London 2: 337. 1794 [1 May 1794]
Clematis paniculata var. denticulata Nakai Handb. Kor. Manch. For. 110 1939
Clematis recta f. lancifolia Nakai J. Coll. Sci. Imp. Univ. Tokyo 26(1): 10 1909
Clematis terniflora f. denticulata (Nakai) W.Lee Lin. Fl. Koreae : 327 (1996)
Clematis terniflora var. denticulata (Nakai) U.C.La Fl. Coreana 2: 234 (1996)
Clematis terniflora var. lancifolia (Nakai) U.C.La Fl. Coreana 2: 234 (1996)
Clematis dioscoreifolia var. robusta (Carrière) Rehder J. Arnold Arbor. 26: 70 1945
Clematis flammula var. robusta Carrière Rev. Hort. 46: 465 1874
Clematis maximowicziana var. robusta (Carrière) Nakai Bull. Natl. Sci. Mus. Tokyo 33: 7 1953
Clematis paniculata var. dioscoreifolia (H.Lév. & Vaniot) Rehder J. Arnold Arbor. 1: 195 1920
Clematis terniflora var. robusta (Carrière) Tamura Acta Phytotax. Geobot. 15: 18 1953
Clematis terniflora var. koreana (Nakai) Tamura Acta Phytotax. Geobot. 15: 18 1953
Clematis recta var. koreana Nakai J. Coll. Sci. Imp. Univ. Tokyo 26(1): 9. 1909 [8 Feb 1909]

Common names Top

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Language Common/alternative name
English sweet autumn virginsbower
Bulgarian трицветен повет
Indonesian kerisih luruh manis
Japanese キイセンニンソウ
Japanese クレマティス・テルニフローラ
Japanese 仙人草
Japanese センニンソウ
Swedish stor vippklematis
Chinese 黄药子
Chinese 铜脚威灵仙
Chinese 小叶力刚
Chinese 铜威灵
Chinese 圆锥铁线莲
Chinese 蟹珠眼草
Chinese 圓錐鐵線蓮

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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Name Authority First published in
Clematis terniflora var. garanbiensis (Hay.) M.C.Chang Fl. Reipubl. Popularis Sin. 28: 170 (1980)
Clematis terniflora var. manshurica (Rupr.) Ohwi Acta Phytotax. Geobot. 7: 43 1938

Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

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Sow seeds at 20°C, expecting germination within 3 months without further temperature treatment.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • China North-central
      • China South-central
      • China Southeast
      • Inner Mongolia
      • Manchuria
    • Eastern Asia
      • Japan
      • Korea
      • Nansei-shoto
      • Ogasawara-Shoto
      • Taiwan
    • Russian Far East
      • Amur
      • Khabarovsk
      • Primorye
  • Northern America
    • Eastern Canada
      • Ontario
    • North-central U.S.A.
      • Illinois
      • Kansas
      • Minnesota
      • Missouri
      • Nebraska
      • Oklahoma
    • Northeastern U.S.A.
      • Connecticut
      • Indiana
      • Massachusetts
      • New Hampshire
      • New Jersey
      • New York
      • Ohio
      • Pennsylvania
      • Vermont
      • West Virginia
    • South-central U.S.A.
      • Texas
    • Southeastern U.S.A.
      • Alabama
      • Arkansas
      • Florida
      • Georgia
      • Kentucky
      • Louisiana
      • Maryland
      • Mississippi
      • North Carolina
      • South Carolina
      • Tennessee
      • Virginia

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000610758
Florida Plant Atlas 1360
Flora of Alabama 3037
Canadensys 8463
USDA Plants CLTE4
UConn 113
Tropicos 27100907
KEW urn:lsid:ipni.org:names:710123-1
The Plant List kew-2726804
Missouri Botanical Garden 286181
Open Tree Of Life 21289
NCBI Taxonomy 231663
Nature Serve 2.146692
IPNI 710123-1
iNaturalist 62776
GBIF 3033546
Freebase /m/03d3c_7
EPPO CLVMX
EOL 594682
Calflora (Californian flora) 8709
USDA GRIN 316251
Wikipedia Clematis_terniflora

Genomes (via NCBI) Top

No reference genome is available on NCBI yet. We are constantly monitoring for new data.

Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
If you wish to see all the related articles click here.
Title Authors Publication Released IDs
Anti-Inflammatory Effects of Clematis terniflora Leaf on Lipopolysaccharide-Induced Acute Lung Injury Park JY, Kim MJ, Choi YA, Kim YY, Lee S, Chung JM, Kim SY, Jeong GS, Kim SH Evid Based Complement Alternat Med 09-Jan-2024
PMCID:PMC10791263
doi:10.1155/2024/6653893
PMID:38230250
In Vitro Cytotoxic Potential of Selected Jordanian Flora and Their Associated Phytochemical Analysis Alruwad MI, Sabry MM, Gendy AM, El-Dine RS, El Hefnawy HM Plants (Basel) 12-Apr-2023
PMCID:PMC10142466
doi:10.3390/plants12081626
PMID:37111849
Comparative metabolomic profiling of Arabidopsis thaliana roots and leaves reveals complex response mechanisms induced by a seaweed extract Tran TL, Callahan DL, Islam MT, Wang Y, Arioli T, Cahill D Front Plant Sci 09-Mar-2023
PMCID:PMC10035662
doi:10.3389/fpls.2023.1114172
PMID:36968386
Recent Advances of Polyphenol Oxidases in Plants Zhang S Molecules 25-Feb-2023
PMCID:PMC10004730
doi:10.3390/molecules28052158
PMID:36903403
Pest categorisation of Icerya aegyptiaca Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Miret JA, Justesen AF, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Grégoire J, Malumphy C, Akrivou A, Kertesz V, Papachristos D, MacLeod A EFSA J 09-Jan-2023
PMCID:PMC9827230
doi:10.2903/j.efsa.2023.7739
PMID:36628331
Integrative Proteomic and Phosphoproteomic Analyses Revealed the Regulatory Mechanism of the Response to Ultraviolet B Stress in Clematis ternifloraDC Tao M, Liu S, Liu A, Li Y, Tian J, Yang B, Zhu W ACS Omega 29-Dec-2022
PMCID:PMC9835548
doi:10.1021/acsomega.2c07258
PMID:36643485
Rapid Identification of Paeoniae Radix and Moutan Radicis Cortex Using a SCAR Marker-Based Conventional PCR Assay Kim WJ, Noh S, Choi G, Moon BC Plants (Basel) 27-Oct-2022
PMCID:PMC9653921
doi:10.3390/plants11212870
PMID:36365322
Exogenous gibberellin can effectively and rapidly break intermediate physiological dormancy of Amsonia elliptica seeds Lee SY, Park K, Jang BK, Ji B, Lee H, Baskin CC, Cho JS Front Plant Sci 26-Oct-2022
PMCID:PMC9643720
doi:10.3389/fpls.2022.1043897
PMID:36388572
Stem cambial variants of Taiwan lianas Yang SZ, Chen PH, Chen JJ Bot Stud 24-Sep-2022
PMCID:PMC9509506
doi:10.1186/s40529-022-00358-5
PMID:36153445
Characterization of the complete chloroplast genome of the Helleborus atrorubens Waldst. & Kit. (Ranunculaceae) Shi X, Mao L, Jin L, Ma G Mitochondrial DNA B Resour 07-Sep-2022
PMCID:PMC9467529
doi:10.1080/23802359.2022.2119105
PMID:36106185
Aurantiamide Acetate Ameliorates Lung Inflammation in Lipopolysaccharide-Induced Acute Lung Injury in Mice Fang Z, Fang J, Gao C, Wu Y, Yu W Biomed Res Int 22-Aug-2022
PMCID:PMC9424011
doi:10.1155/2022/3510423
PMID:36046440
Solanum nigrum Linn.: An Insight into Current Research on Traditional Uses, Phytochemistry, and Pharmacology Chen X, Dai X, Liu Y, Yang Y, Yuan L, He X, Gong G Front Pharmacol 16-Aug-2022
PMCID:PMC9424827
doi:10.3389/fphar.2022.918071
PMID:36052142
Plantago asiatica mosaic virus: An emerging plant virus causing necrosis in lilies and a new model RNA virus for molecular research Komatsu K, Hammond J Mol Plant Pathol 20-Jul-2022
PMCID:PMC9452766
doi:10.1111/mpp.13243
PMID:35856603
Foliar and Root Comparative Metabolomics and Phenolic Profiling of Micro-Tom Tomato (Solanum lycopersicum L.) Plants Associated with a Gene Expression Analysis in Response to Short Daily UV Treatments Mannucci A, Santin M, Vanhaelewyn L, Sciampagna MC, Miras-Moreno MB, Zhang L, Lucini L, Quartacci MF, Van Der Straeten D, Castagna A, Ranieri A Plants (Basel) 12-Jul-2022
PMCID:PMC9319050
doi:10.3390/plants11141829
PMID:35890464
UVB Irradiation-Induced Transcriptional Changes in Lignin- and Flavonoid Biosynthesis and Indole/Tryptophan-Auxin-Responsive Genes in Rice Seedlings Kim GE, Kim MS, Sung J Plants (Basel) 20-Jun-2022
PMCID:PMC9229965
doi:10.3390/plants11121618
PMID:35736769

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name PubChem ID Canonical SMILES MW Found in Proof
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides
[(2S,3R,4S,5S,6R)-6-[[(2R,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl] (4aS,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-[(2S,3R,4S,5S)-3-[(2S,3R,4R,5S,6S)-4-[(2S,3R,4S,5R)-5-[(2R,3R,4R,5S,6R)-5-[(2S,3R,4S,5R,6R)-4-[(2S,3R,4R,5S,6R)-3,4-dihydroxy-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-6-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxy-5-hydroxy-3-[(E)-3-(3-hydroxy-4-methoxyphenyl)prop-2-enoyl]oxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydroxyoxan-2-yl]oxy-3,5-dihydroxy-6-methyloxan-2-yl]oxy-4,5-dihydroxyoxan-2-yl]oxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 100928195 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3C(C(OC(C3OC(=O)C=CC4=CC(=C(C=C4)OC)O)OC5C(OC(C(C5O)O)OC6COC(C(C6O)O)OC7C(C(OC(C7O)OC8C(C(COC8OC9CCC1(C(C9(C)C)CCC2(C1CC=C1C2(CCC2(C1CC(CC2)(C)C)C(=O)OC1C(C(C(C(O1)COC1C(C(C(C(O1)CO)OC1C(C(C(C(O1)C)O)O)O)O)O)O)O)O)C)C)C)O)O)C)O)CO)CO)O)O)O)OC1C(C(C(C(O1)CO)O)O)O)O)O)O 2308.40 unknown https://doi.org/10.1248/CPB.46.1891
[(2S,3R,4S,5S,6R)-6-[[(2R,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl] (4aS,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-[(2S,3R,4S,5S)-3-[(2S,3R,4R,5S,6S)-4-[(2S,3R,4S,5R)-5-[(2R,3R,4R,5S,6R)-5-[(2S,3R,4S,5R,6R)-4-[(2S,3R,4R,5S,6R)-3,4-dihydroxy-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-6-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxy-5-hydroxy-6-(hydroxymethyl)-3-[(E)-3-(4-methoxyphenyl)prop-2-enoyl]oxyoxan-2-yl]oxy-3,4-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydroxyoxan-2-yl]oxy-3,5-dihydroxy-6-methyloxan-2-yl]oxy-4,5-dihydroxyoxan-2-yl]oxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 100928196 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3C(C(OC(C3OC(=O)C=CC4=CC=C(C=C4)OC)OC5C(OC(C(C5O)O)OC6COC(C(C6O)O)OC7C(C(OC(C7O)OC8C(C(COC8OC9CCC1(C(C9(C)C)CCC2(C1CC=C1C2(CCC2(C1CC(CC2)(C)C)C(=O)OC1C(C(C(C(O1)COC1C(C(C(C(O1)CO)OC1C(C(C(C(O1)C)O)O)O)O)O)O)O)O)C)C)C)O)O)C)O)CO)CO)O)O)O)OC1C(C(C(C(O1)CO)O)O)O)O)O)O 2292.40 unknown https://doi.org/10.1248/CPB.46.1891
[(2S,3R,4S,5S,6R)-6-[[(2R,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl] (4aS,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-[(2S,3R,4S,5S)-3-[(2S,3R,4R,5S,6S)-4-[(2S,3R,4S,5R)-5-[(2R,3R,4R,5S,6R)-5-[(2S,3R,4S,5R,6R)-4-[(2S,3R,4R,5S,6R)-5-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-3,4-dihydroxy-6-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxy-5-hydroxy-3-[(E)-3-(3-hydroxy-4-methoxyphenyl)prop-2-enoyl]oxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydroxyoxan-2-yl]oxy-3,5-dihydroxy-6-methyloxan-2-yl]oxy-4,5-dihydroxyoxan-2-yl]oxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 100928198 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3C(C(OC(C3OC(=O)C=CC4=CC(=C(C=C4)OC)O)OC5C(OC(C(C5O)O)OC6COC(C(C6O)O)OC7C(C(OC(C7O)OC8C(C(COC8OC9CCC1(C(C9(C)C)CCC2(C1CC=C1C2(CCC2(C1CC(CC2)(C)C)C(=O)OC1C(C(C(C(O1)COC1C(C(C(C(O1)CO)OC1C(C(C(C(O1)C)O)O)O)O)O)O)O)O)C)C)C)O)O)C)O)CO)CO)O)O)O)OC1C(C(C(C(O1)CO)O)O)OC1C(C(C(C(O1)CO)O)O)O)O)O)O 2470.50 unknown https://doi.org/10.1248/CPB.46.1891
[(2S,3R,4S,5S,6R)-6-[[(2R,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl] (4aS,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-[(2S,3R,4S,5S)-3-[(2S,3R,4R,5S,6S)-4-[(2S,3R,4S,5R)-5-[(2R,3R,4R,5S,6R)-5-[(2S,3R,4S,5R,6R)-4-[(2S,3R,4R,5S,6R)-6-[[(2R,3R,4R,5R,6S)-4,5-dihydroxy-6-methyl-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,4-dihydroxy-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-3-[(E)-3-(3-hydroxy-4-methoxyphenyl)prop-2-enoyl]oxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydroxyoxan-2-yl]oxy-3,5-dihydroxy-6-methyloxan-2-yl]oxy-4,5-dihydroxyoxan-2-yl]oxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 100928197 Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OCC3C(C(C(C(O3)OC(=O)C45CCC(CC4C6=CCC7C8(CCC(C(C8CCC7(C6(CC5)C)C)(C)C)OC9C(C(C(CO9)O)O)OC1C(C(C(C(O1)C)O)OC1C(C(C(CO1)OC1C(C(C(C(O1)CO)OC1C(C(C(C(O1)CO)O)OC1C(C(C(C(O1)COC1C(C(C(C(O1)C)O)O)OC1C(C(C(C(O1)CO)O)O)O)OC1C(C(C(C(O1)CO)O)O)O)O)O)OC(=O)C=CC1=CC(=C(C=C1)OC)O)O)O)O)O)O)C)(C)C)O)O)O)CO)O)O)O 2470.50 unknown https://doi.org/10.1248/CPB.46.1891
Clematernoside K 49799267 Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OCC3C(C(C(C(O3)OC(=O)C45CCC(CC4C6=CCC7C8(CCC(C(C8CCC7(C6(CC5)C)C)(C)C)OC9C(C(C(CO9)O)O)OC1C(C(C(C(O1)C)O)OC1C(C(C(CO1)OC1C(C(C(C(O1)CO)OC1C(C(C(C(O1)CO)O)OC1C(C(C(C(O1)COC1C(C(C(C(O1)C)O)O)OC1C(C(C(C(O1)CO)O)O)O)O)O)O)OC(=O)C=CC1=CC(=C(C=C1)OC)O)O)O)O)O)O)C)(C)C)O)O)O)CO)O)O)O 2308.40 unknown https://doi.org/10.1248/CPB.46.1891
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
[(2S,3R,4S,5S,6R)-6-[[(2R,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl] (4aS,6aR,6aS,6bR,8aR,10R,12aR,14bS)-10-[(2S,3R,4S,5S)-3-[(2S,3R,4R,5S,6S)-3,5-dihydroxy-6-methyl-4-[(2S,3R,4R,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-4,5-dihydroxyoxan-2-yl]oxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 162998966 Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OCC3C(C(C(C(O3)OC(=O)C45CCC(CC4C6=CCC7C8(CCC(C(C8CCC7(C6(CC5)C)C)(C)C)OC9C(C(C(CO9)O)O)OC1C(C(C(C(O1)C)O)OC1C(C(C(CO1)O)O)O)O)C)(C)C)O)O)O)CO)O)O)O 1337.50 unknown https://doi.org/10.1248/CPB.46.1891
[(2S,3R,4S,5S,6R)-6-[[(2R,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl] (4aS,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-[(2S,3R,4S,5S)-3-[(2S,3R,4R,5S,6S)-4-[(2S,3R,4S,5R)-5-[(2R,3R,4R,5S,6R)-5-[(2S,3R,4S,5S,6R)-3-[(E)-3-(3,4-dimethoxyphenyl)prop-2-enoyl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydroxyoxan-2-yl]oxy-3,5-dihydroxy-6-methyloxan-2-yl]oxy-4,5-dihydroxyoxan-2-yl]oxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 100928193 Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OCC3C(C(C(C(O3)OC(=O)C45CCC(CC4C6=CCC7C8(CCC(C(C8CCC7(C6(CC5)C)C)(C)C)OC9C(C(C(CO9)O)O)OC1C(C(C(C(O1)C)O)OC1C(C(C(CO1)OC1C(C(C(C(O1)CO)OC1C(C(C(C(O1)CO)O)O)OC(=O)C=CC1=CC(=C(C=C1)OC)OC)O)O)O)O)O)C)(C)C)O)O)O)CO)O)O)O 1852.00 unknown https://doi.org/10.1248/CPB.46.1891
Clematernoside B 49799230 Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OCC3C(C(C(C(O3)OC(=O)C45CCC(CC4C6=CCC7C8(CCC(C(C8CCC7(C6(CC5)C)C)(C)C)OC9C(C(C(CO9)O)O)OC1C(C(C(C(O1)C)O)OC1C(C(C(CO1)OC1C(C(C(C(O1)CO)OC1C(C(C(C(O1)CO)O)OC(=O)C=CC1=CC(=C(C=C1)OC)O)O)O)O)O)O)O)C)(C)C)O)O)O)CO)O)O)O 1837.90 unknown https://doi.org/10.1248/CPB.46.1891
Clematernoside C 49799231 Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OCC3C(C(C(C(O3)OC(=O)C45CCC(CC4C6=CCC7C8(CCC(C(C8CCC7(C6(CC5)C)C)(C)C)OC9C(C(C(CO9)O)O)OC1C(C(C(C(O1)C)O)OC1C(C(C(CO1)OC1C(C(C(C(O1)CO)OC1C(C(C(C(O1)CO)O)O)OC(=O)C=CC1=CC(=C(C=C1)OC)O)O)O)O)O)O)C)(C)C)O)O)O)CO)O)O)O 1837.90 unknown https://doi.org/10.1248/CPB.46.1891
Clematernoside D 49799265 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3C(C(OC(C3OC(=O)C=CC4=CC(=C(C=C4)OC)O)OC5C(OC(C(C5O)O)OC6COC(C(C6O)O)OC7C(C(OC(C7O)OC8C(C(COC8OC9CCC1(C(C9(C)CO)CCC2(C1CC=C1C2(CCC2(C1CC(CC2)(C)C)C(=O)OC1C(C(C(C(O1)COC1C(C(C(C(O1)CO)OC1C(C(C(C(O1)C)O)O)O)O)O)O)O)O)C)C)C)O)O)C)O)CO)CO)O)O)O)O)O)O)O 2162.20 unknown https://doi.org/10.1248/CPB.46.1891
Clematernoside E 49799266 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3C(C(OC(C3OC(=O)C=CC4=CC(=C(C=C4)OC)O)OC5C(OC(C(C5O)O)OC6COC(C(C6O)O)OC7C(C(OC(C7O)OC8C(C(COC8OC9CCC1(C(C9(C)C)CCC2(C1CC=C1C2(CCC2(C1CC(CC2)(C)C)C(=O)OC1C(C(C(C(O1)COC1C(C(C(C(O1)CO)OC1C(C(C(C(O1)C)O)O)O)O)O)O)O)O)C)C)C)O)O)C)O)CO)CO)O)O)O)O)O)O)O 2146.20 unknown https://doi.org/10.1248/CPB.46.1891
Clematichinenoside C 49799271 Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OCC3C(C(C(C(O3)OC(=O)C45CCC(CC4C6=CCC7C8(CCC(C(C8CCC7(C6(CC5)C)C)(C)C)OC9C(C(C(CO9)O)O)OC1C(C(C(C(O1)C)O)OC1C(C(C(CO1)OC1C(C(C(C(O1)CO)O)O)O)O)O)O)C)(C)C)O)O)O)CO)O)O)O 1499.60 unknown https://doi.org/10.1248/CPB.46.1891
Huzhangoside B 49799269 Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OCC3C(C(C(C(O3)OC(=O)C45CCC(CC4C6=CCC7C8(CCC(C(C8CCC7(C6(CC5)C)C)(C)C)OC9C(C(C(CO9)O)O)OC1C(C(C(C(O1)C)O)OC1C(C(C(CO1)O)O)O)O)C)(C)C)O)O)O)CO)O)O)O 1337.50 unknown https://doi.org/10.1248/CPB.46.1891
HuzhangosideB 13880086 Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OCC3C(C(C(C(O3)OC(=O)C45CCC(CC4C6=CCC7C8(CCC(C(C8CCC7(C6(CC5)C)C)(C)C)OC9C(C(C(CO9)O)O)OC1C(C(C(C(O1)C)O)OC1C(C(C(CO1)O)O)O)O)C)(C)C)O)O)O)CO)O)O)O 1337.50 unknown https://doi.org/10.1248/CPB.46.1891
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
5,7-Dihydroxy-2-(4-hydroxyphenyl)-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 5462193 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown https://doi.org/10.1007/S10600-007-0061-X
5,7-Dihydroxy-2-(4-hydroxyphenyl)-3-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxymethyl]oxan-2-yl]oxychromen-4-one 12313332 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)O)O)O)O)O)O 594.50 unknown https://doi.org/10.1007/S10600-007-0061-X
Astragalin 5282102 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown https://doi.org/10.1007/S10600-007-0061-X
Kaempferol-3-O-rutinoside 5318767 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)O)O)O)O)O)O 594.50 unknown https://doi.org/10.1007/S10600-007-0061-X
Rutin 5280805 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O 610.50 unknown https://doi.org/10.1007/S10600-007-0061-X
Vitamin P 5293655 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O 610.50 unknown https://doi.org/10.1007/S10600-007-0061-X
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
[(2R,3S,4S,5R,6S)-6-[(2R,3S,4R,5S,6R)-2-[3,5-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-7-yl]oxy-3,5-dihydroxy-6-methyloxan-4-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate 163189399 Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)O)C4=CC=C(C=C4)O)O)O)OC5C(C(C(C(O5)COC(=O)C=CC6=CC(=C(C=C6)O)O)O)O)O)O 756.70 unknown https://doi.org/10.1007/S10600-007-0061-X
[6-[2-[3,5-Dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-7-yl]oxy-3,5-dihydroxy-6-methyloxan-4-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl 3-(3,4-dihydroxyphenyl)prop-2-enoate 163087003 Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)O)C4=CC=C(C=C4)O)O)O)OC5C(C(C(C(O5)COC(=O)C=CC6=CC(=C(C=C6)O)O)O)O)O)O 756.70 unknown https://doi.org/10.1007/S10600-007-0061-X

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