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Carpesium triste

Carpesium triste - Unknown
Part: Unknown
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 UUID643fc70a955ed647509111
Scientific name Carpesium triste
Authority Maxim.
First published in Bull. Acad. Imp. Sci. Saint-Pétersbourg xix. (1874) 479.

Description Top

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Synonyms Top

Scientific name Authority First published in
Carpesium manshuricum Kitam. Acta Phytotax. Geobot. 4: 71 (1935)
Carpesium pseudotracheliifolium Y.Ling Contr. Inst. Bot. Natl. Acad. Peiping 2: 482 (1934)
Carpesium triste var. manshuricum (Kitam.) Kitam. Memoirs of the College of Science, Kyoto Imperial University. Series B. Biology 13: 280 1937
Carpesium tristiforme Hand.-Mazz. Oesterr. Bot. Z. 83: 236 (1934)

Common names Top

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Language Common/alternative name
Japanese ミヤマヤブタバコ
Chinese 地朝阳
Chinese 暗花金挖耳
Chinese 东北金挖耳

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Carpesium triste var. sinense Diels Botanische Jahrbucher fur Systematik, Pflanzengeschichte und Pflanzengeographie 29(5): 615 1901

Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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No germination or propagation data was added yet.

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
      • Manchuria
      • Xinjiang
    • Eastern Asia
      • Japan
      • Korea
      • Taiwan
    • Russian Far East
      • Kuril Islands
      • Primorye
    • Siberia
      • Altay

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000011220
Tropicos 2700363
KEW urn:lsid:ipni.org:names:189367-1
The Plant List gcc-110878
Open Tree Of Life 792531
Observations.org 148466
NCBI Taxonomy 1161924
IPNI 189367-1
iNaturalist 508465
GBIF 3094832
EOL 6265331

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
In Vitro Multiplication and Rooting of Plum Rootstock ‘Saint Julien’ (Prunus domestica subsp. insititia) under Fluorescent Light and Different LED Spectra Nacheva L, Dimitrova N, Koleva-Valkova L, Stefanova M, Ganeva T, Nesheva M, Tarakanov I, Vassilev A Plants (Basel) 27-May-2023
PMCID:PMC10255918
doi:10.3390/plants12112125
PMID:37299104
Effect of LED Lighting on Physical Environment and Microenvironment on In Vitro Plant Growth and Morphogenesis: The Need to Standardize Lighting Conditions and Their Description Barceló-Muñoz A, Barceló-Muñoz M, Gago-Calderon A Plants (Basel) 25-Dec-2021
PMCID:PMC8747321
doi:10.3390/plants11010060
PMID:35009064
Antiprostate Cancer Activity of Ineupatolide Isolated from Carpesium cernuum L. Huang YS, Mao JX, Zhang L, Guo HW, Yan C, Chen M Biomed Res Int 29-Apr-2021
PMCID:PMC8105106
doi:10.1155/2021/5515961
PMID:33996996
Application of Light-Emitting Diodes for Improving the Nutritional Quality and Bioactive Compound Levels of Some Crops and Medicinal Plants Jung WS, Chung IM, Hwang MH, Kim SH, Yu CY, Ghimire BK Molecules 09-Mar-2021
PMCID:PMC7963184
doi:10.3390/molecules26051477
PMID:33803168
Physiological and Proteomic Insights Into Red and Blue Light-Mediated Enhancement of in vitro Growth in Scrophularia kakudensis—A Potential Medicinal Plant Manivannan A, Soundararajan P, Park YG, Jeong BR Front Plant Sci 20-Jan-2021
PMCID:PMC7855028
doi:10.3389/fpls.2020.607007
PMID:33552100
6,8-Dihy­droxy-8a-methyl-3,5-dimethyl­idenedeca­hydro­naphtho­[2,3-b]furan-2(3H)-one Liu TT, Wu HB, Wang WS Acta Crystallogr Sect E Struct Rep Online 31-Oct-2012
PMCID:PMC3515328
doi:10.1107/S160053681204425X
PMID:23284548
New Acyclic 12‐Hydroxygeranylgeraniol‐Derived Diterpenoids from the Seeds of <i>Carpesium triste</i> Xue Gao, Zhan‐Xin Zhang, Zhong‐Jian Jia Wiley 29-Oct-2008
doi:10.1002/HLCA.200890206
Cytotoxic germacranolides and acyclic diterpenoides from the seeds of Carpesium triste. Gao X, Lin CJ, Jia ZJ J Nat Prod 01-May-2007
doi:10.1021/NP0700570
PMID:17432904
Sesquiterpene lactones from Carpesium triste var. manshuricum Mi Ran Kim, Bo Ram Suh, Jae Gil Kim, Young Ho Kim, Dae Keun Kim, Dong Cheul Moon Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(99)00173-9

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 / Diterpenoids
[(2Z,6E)-8-hydroxy-2-[(4R)-4-[(2S,4R)-4-hydroxy-5,5-dimethyloxolan-2-yl]pentyl]-6-methylocta-2,6-dienyl] acetate 163019683 Click to see CC(CCCC(=CCCC(=CCO)C)COC(=O)C)C1CC(C(O1)(C)C)O 382.50 unknown https://doi.org/10.1002/HLCA.200890206
[8-Hydroxy-2-[4-(4-hydroxy-5,5-dimethyloxolan-2-yl)pentyl]-6-methylocta-2,6-dienyl] acetate 74396882 Click to see CC(CCCC(=CCCC(=CCO)C)COC(=O)C)C1CC(C(O1)(C)C)O 382.50 unknown https://doi.org/10.1002/HLCA.200890206
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Acyclic diterpenoids
(2E,6E,11S,12R)-3,7,11,15-tetramethylhexadeca-2,6,14-triene-1,12-diol 16681369 Click to see CC(CCCC(=CCCC(=CCO)C)C)C(CC=C(C)C)O 308.50 unknown https://doi.org/10.1021/NP0700570
[(2E,11S,12R)-7-(acetyloxymethyl)-12-hydroxy-3,11,15-trimethylhexadeca-2,6,14-trienyl] acetate 162897873 Click to see CC(CCCC(=CCCC(=CCOC(=O)C)C)COC(=O)C)C(CC=C(C)C)O 408.60 unknown https://doi.org/10.1021/NP0700570
[(2E,6Z,11S,12R)-7-(acetyloxymethyl)-12-hydroxy-3,11,15-trimethylhexadeca-2,6,14-trienyl] acetate 16681371 Click to see CC(CCCC(=CCCC(=CCOC(=O)C)C)COC(=O)C)C(CC=C(C)C)O 408.60 unknown https://doi.org/10.1021/NP0700570
[(2Z,5E,7R)-7-hydroxy-2-[(E)-6-hydroxy-4-methylhex-4-enylidene]-6,10-dimethylundeca-5,9-dienyl] acetate 25147192 Click to see CC(=CCC(C(=CCCC(=CCCC(=CCO)C)COC(=O)C)C)O)C 364.50 unknown https://doi.org/10.1002/HLCA.200890206
[(2Z,5E,7R)-7-hydroxy-6,10-dimethyl-2-[(E)-4-methyl-6-oxohex-4-enylidene]undeca-5,9-dienyl] acetate 102522532 Click to see CC(=CCC(C(=CCCC(=CCCC(=CC=O)C)COC(=O)C)C)O)C 362.50 unknown https://doi.org/10.1002/HLCA.200890206
[(2Z,6R,7R,9S)-7,9-dihydroxy-2-[(E)-6-hydroxy-4-methylhex-4-enylidene]-6,10-dimethylundec-10-enyl] acetate 163027953 Click to see CC(CCCC(=CCCC(=CCO)C)COC(=O)C)C(CC(C(=C)C)O)O 382.50 unknown https://doi.org/10.1002/HLCA.200890206
[(2Z,6S,7R)-7-hydroxy-2-[(E)-6-hydroxy-4-methylhex-4-enylidene]-6,10-dimethylundec-9-enyl] acetate 16681370 Click to see CC(CCCC(=CCCC(=CCO)C)COC(=O)C)C(CC=C(C)C)O 366.50 unknown https://doi.org/10.1021/NP0700570
[(2Z,6S)-2-[(E)-6-hydroxy-4-methylhex-4-enylidene]-6,10-dimethyl-7-oxoundec-9-enyl] acetate 162920816 Click to see CC(CCCC(=CCCC(=CCO)C)COC(=O)C)C(=O)CC=C(C)C 364.50 unknown https://doi.org/10.1021/NP0700570
[(E,2Z,6R,7S)-7,10-dihydroxy-2-[(E)-6-hydroxy-4-methylhex-4-enylidene]-6,10-dimethylundec-8-enyl] acetate 162904747 Click to see CC(CCCC(=CCCC(=CCO)C)COC(=O)C)C(C=CC(C)(C)O)O 382.50 unknown https://doi.org/10.1002/HLCA.200890206
[2-(6-Hydroxy-4-methylhex-4-enylidene)-6,10-dimethyl-7-oxoundec-9-enyl] acetate 72740032 Click to see CC(CCCC(=CCCC(=CCO)C)COC(=O)C)C(=O)CC=C(C)C 364.50 unknown https://doi.org/10.1021/NP0700570
[7-(Acetyloxymethyl)-12-hydroxy-3,11,15-trimethylhexadeca-2,6,14-trienyl] acetate 73307149 Click to see CC(CCCC(=CCCC(=CCOC(=O)C)C)COC(=O)C)C(CC=C(C)C)O 408.60 unknown https://doi.org/10.1021/NP0700570
[7-Hydroxy-2-(6-hydroxy-4-methylhex-4-enylidene)-6,10-dimethylundec-9-enyl] acetate 73307148 Click to see CC(CCCC(=CCCC(=CCO)C)COC(=O)C)C(CC=C(C)C)O 366.50 unknown https://doi.org/10.1021/NP0700570
[7-Hydroxy-2-(6-hydroxy-4-methylhex-4-enylidene)-6,10-dimethylundeca-5,9-dienyl] acetate 74396883 Click to see CC(=CCC(C(=CCCC(=CCCC(=CCO)C)COC(=O)C)C)O)C 364.50 unknown https://doi.org/10.1002/HLCA.200890206
[7-Hydroxy-6,10-dimethyl-2-(4-methyl-6-oxohex-4-enylidene)undeca-5,9-dienyl] acetate 162943198 Click to see CC(=CCC(C(=CCCC(=CCCC(=CC=O)C)COC(=O)C)C)O)C 362.50 unknown https://doi.org/10.1002/HLCA.200890206
[7,10-Dihydroxy-2-(6-hydroxy-4-methylhex-4-enylidene)-6,10-dimethylundec-8-enyl] acetate 74396881 Click to see CC(CCCC(=CCCC(=CCO)C)COC(=O)C)C(C=CC(C)(C)O)O 382.50 unknown https://doi.org/10.1002/HLCA.200890206
[7,9-Dihydroxy-2-(6-hydroxy-4-methylhex-4-enylidene)-6,10-dimethylundec-10-enyl] acetate 74396938 Click to see CC(CCCC(=CCCC(=CCO)C)COC(=O)C)C(CC(C(=C)C)O)O 382.50 unknown https://doi.org/10.1002/HLCA.200890206
3,7,11,15-Tetramethylhexadeca-2,6,14-triene-1,12-diol 73307147 Click to see CC(CCCC(=CCCC(=CCO)C)C)C(CC=C(C)C)O 308.50 unknown https://doi.org/10.1021/NP0700570
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
[(3aR,4R,5R,6R,10R,11R,11aS)-4,10-dihydroxy-6,10-dimethyl-5-(3-methylbutanoyloxy)-3-methylidene-2,9-dioxo-3a,4,5,6,7,8,11,11a-octahydrocyclodeca[b]furan-11-yl] (2R)-2-methylbutanoate 162996225 Click to see CCC(C)C(=O)OC1C2C(C(C(C(CCC(=O)C1(C)O)C)OC(=O)CC(C)C)O)C(=C)C(=O)O2 482.60 unknown https://doi.org/10.1021/NP0700570
[(3aR,4R,5R,6R,10R,11R,11aS)-4,10-dihydroxy-6,10-dimethyl-5-(3-methylbutanoyloxy)-3-methylidene-2,9-dioxo-3a,4,5,6,7,8,11,11a-octahydrocyclodeca[b]furan-11-yl] 2-methylbutanoate 16681336 Click to see CCC(C)C(=O)OC1C2C(C(C(C(CCC(=O)C1(C)O)C)OC(=O)CC(C)C)O)C(=C)C(=O)O2 482.60 unknown https://doi.org/10.1021/NP0700570
[(3aR,4R,5R,6R,10R,11R,11aS)-5,10-dihydroxy-6,10-dimethyl-3-methylidene-11-(2-methylpropanoyloxy)-2,9-dioxo-3a,4,5,6,7,8,11,11a-octahydrocyclodeca[b]furan-4-yl] 2-methylpropanoate 16681337 Click to see CC1CCC(=O)C(C(C2C(C(C1O)OC(=O)C(C)C)C(=C)C(=O)O2)OC(=O)C(C)C)(C)O 454.50 unknown https://doi.org/10.1021/NP0700570
[(3aS,4R,6R,10S,11R,11aS)-10-hydroxy-6,10-dimethyl-3-methylidene-11-(2-methylpropanoyloxy)-2,5-dioxo-3a,4,6,7,8,9,11,11a-octahydrocyclodeca[b]furan-4-yl] (Z)-2-methylbut-2-enoate 16681334 Click to see CC=C(C)C(=O)OC1C2C(C(C(CCCC(C1=O)C)(C)O)OC(=O)C(C)C)OC(=O)C2=C 450.50 unknown https://doi.org/10.1021/NP0700570
[10-Hydroxy-6,10-dimethyl-3-methylidene-11-(2-methylpropanoyloxy)-2,5-dioxo-3a,4,6,7,8,9,11,11a-octahydrocyclodeca[b]furan-4-yl] 2-methylbut-2-enoate 73307128 Click to see CC=C(C)C(=O)OC1C2C(C(C(CCCC(C1=O)C)(C)O)OC(=O)C(C)C)OC(=O)C2=C 450.50 unknown https://doi.org/10.1021/NP0700570
[10-Hydroxy-6,10-dimethyl-3-methylidene-11-(2-methylpropanoyloxy)-2,5-dioxo-3a,4,6,7,8,9,11,11a-octahydrocyclodeca[b]furan-4-yl] 2-methylpropanoate 162964996 Click to see CC1CCCC(C(C2C(C(C1=O)OC(=O)C(C)C)C(=C)C(=O)O2)OC(=O)C(C)C)(C)O 438.50 unknown https://doi.org/10.1021/NP0700570
[4,10-Dihydroxy-6,10-dimethyl-3-methylidene-11-(2-methylpropanoyloxy)-2,9-dioxo-3a,4,5,6,7,8,11,11a-octahydrocyclodeca[b]furan-5-yl] 2-methylpropanoate 162952224 Click to see CC1CCC(=O)C(C(C2C(C(C1OC(=O)C(C)C)O)C(=C)C(=O)O2)OC(=O)C(C)C)(C)O 454.50 unknown https://doi.org/10.1021/NP0700570
[4,10-Dihydroxy-6,10-dimethyl-3-methylidene-11-(2-methylpropanoyloxy)-2,9-dioxo-3a,4,5,6,7,8,11,11a-octahydrocyclodeca[b]furan-5-yl] 3-methylbutanoate 73307129 Click to see CC1CCC(=O)C(C(C2C(C(C1OC(=O)CC(C)C)O)C(=C)C(=O)O2)OC(=O)C(C)C)(C)O 468.50 unknown https://doi.org/10.1021/NP0700570
[4,10-Dihydroxy-6,10-dimethyl-5-(3-methylbutanoyloxy)-3-methylidene-2,9-dioxo-3a,4,5,6,7,8,11,11a-octahydrocyclodeca[b]furan-11-yl] 2-methylbutanoate 73307130 Click to see CCC(C)C(=O)OC1C2C(C(C(C(CCC(=O)C1(C)O)C)OC(=O)CC(C)C)O)C(=C)C(=O)O2 482.60 unknown https://doi.org/10.1021/NP0700570
[5,10-Dihydroxy-6,10-dimethyl-3-methylidene-11-(2-methylpropanoyloxy)-2,9-dioxo-3a,4,5,6,7,8,11,11a-octahydrocyclodeca[b]furan-4-yl] 2-methylpropanoate 73307131 Click to see CC1CCC(=O)C(C(C2C(C(C1O)OC(=O)C(C)C)C(=C)C(=O)O2)OC(=O)C(C)C)(C)O 454.50 unknown https://doi.org/10.1021/NP0700570
4beta,8alpha-Dihydroxy-5beta-isobutyryloxy-9beta(3-methylbutyryloxy)-3-oxogermacran-7beta,12alpha-olide 16681335 Click to see CC1CCC(=O)C(C(C2C(C(C1OC(=O)CC(C)C)O)C(=C)C(=O)O2)OC(=O)C(C)C)(C)O 468.50 unknown https://doi.org/10.1021/NP0700570
incaspitolide A 44423080 Click to see CC1CCCC(C(C2C(C(C1=O)OC(=O)C(C)C)C(=C)C(=O)O2)OC(=O)C(C)C)(C)O 438.50 unknown https://doi.org/10.1021/NP0700570
incaspitolide D 44423088 Click to see CC1CCC(=O)C(C(C2C(C(C1OC(=O)C(C)C)O)C(=C)C(=O)O2)OC(=O)C(C)C)(C)O 454.50 unknown https://doi.org/10.1021/NP0700570
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
[(1R,2S,3R,7R,8S,9R,11S,13S)-1,9-dihydroxy-9,13-dimethyl-8-(3-methylbutanoyloxy)-4-methylidene-5-oxo-6,14-dioxatricyclo[9.2.1.03,7]tetradecan-2-yl] (Z)-2-methylbut-2-enoate 162937825 Click to see CC=C(C)C(=O)OC1C2C(C(C(CC3CC(C1(O3)O)C)(C)O)OC(=O)CC(C)C)OC(=O)C2=C 480.50 unknown https://doi.org/10.1016/S0031-9422(99)00173-9
[(1S,2S,3R,7R,8S,9R,11R,13S)-1,9-dihydroxy-9,13-dimethyl-2-[(Z)-2-methylbut-2-enoyl]oxy-4-methylidene-5-oxo-6,14-dioxatricyclo[9.2.1.03,7]tetradecan-8-yl] (2R)-2-methylbutanoate 162882576 Click to see CCC(C)C(=O)OC1C2C(C(C3(C(CC(O3)CC1(C)O)C)O)OC(=O)C(=CC)C)C(=C)C(=O)O2 480.50 unknown https://doi.org/10.1016/S0031-9422(99)00173-9
[1,9-Dihydroxy-9,13-dimethyl-2-(2-methylbut-2-enoyloxy)-4-methylidene-5-oxo-6,14-dioxatricyclo[9.2.1.03,7]tetradecan-8-yl] 2-methylbutanoate 71440321 Click to see CCC(C)C(=O)OC1C2C(C(C3(C(CC(O3)CC1(C)O)C)O)OC(=O)C(=CC)C)C(=C)C(=O)O2 480.50 unknown https://doi.org/10.1016/S0031-9422(99)00173-9
[1,9-Dihydroxy-9,13-dimethyl-8-(3-methylbutanoyloxy)-4-methylidene-5-oxo-6,14-dioxatricyclo[9.2.1.03,7]tetradecan-2-yl] 2-methylbut-2-enoate 72679662 Click to see CC=C(C)C(=O)OC1C2C(C(C(CC3CC(C1(O3)O)C)(C)O)OC(=O)CC(C)C)OC(=O)C2=C 480.50 unknown https://doi.org/10.1016/S0031-9422(99)00173-9
Angelic acid [(3aR,4S,5S,6S,8R,10R,11S,11aR)-dodecahydro-2-oxo-3-methylene-5,10-dihydroxy-6,10-dimethyl-5,8-epoxy-11-(1-oxo-3-methylbutoxy)cyclodeca[b]furan]-4-yl ester 60198107 Click to see CC=C(C)C(=O)OC1C2C(C(C(CC3CC(C1(O3)O)C)(C)O)OC(=O)CC(C)C)OC(=O)C2=C 480.50 unknown https://doi.org/10.1016/S0031-9422(99)00173-9
Ineupatolide 21603602 Click to see CCC(C)C(=O)OC1C2C(C(C3(C(CC(O3)CC1(C)O)C)O)OC(=O)C(=CC)C)C(=C)C(=O)O2 480.50 unknown https://doi.org/10.1016/S0031-9422(99)00173-9

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