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Internal ID UUID643fc61b1cc4f170523323
Scientific name Cirsium carolinianum
Authority (Walter) Fernald & B.G.Schub.
First published in Rhodora 50: 229 (1948)

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Synonyms Top

Scientific name Authority First published in
Carduus glutinosus L.C.Beck Bot. North. Middle States : 173 (1833)
Cnicus glutinosus Bigelow Fl. Boston., ed. 2 : 291 (1824)
Carduus carolinianus Walter Fl. Carol. : 195 (1788)
Cirsium flaccidum Petr. Beih. Bot. Centralbl. 35: 543 (1917)
Cirsium flaccidum Small
Carduus flaccidum Small Fl. S.E. U.S. 1307, 1341 (1903)

Common names Top

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Language Common/alternative name
English soft thistle

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Northern America
    • North-central U.S.A.
      • Illinois
      • Missouri
      • Oklahoma
    • Northeastern U.S.A.
      • Indiana
      • Ohio
    • South-central U.S.A.
      • Texas
    • Southeastern U.S.A.
      • Alabama
      • Arkansas
      • Georgia
      • Kentucky
      • Louisiana
      • Mississippi
      • North Carolina
      • South Carolina
      • Tennessee

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000002583
Flora of Alabama 642
USDA Plants CICA7
Tropicos 2725626
KEW urn:lsid:ipni.org:names:58975-2
The Plant List gcc-102487
Open Tree Of Life 3894747
NCBI Taxonomy 1308047
Nature Serve 2.142605
IPNI 58975-2
iNaturalist 129675
GBIF 3112872
Freebase /m/013d7jz2
EOL 468267
USDA GRIN 449876
Wikipedia Cirsium_carolinianum
CMAUP NPO25943

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 CentralĀ®) and other sources (DOI number only)!
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Title Authors Publication Released IDs
Aplotaxene epoxide from Cirsium hypoleucum Ferdinand Bohlmann, Wolf-Rainer Abraham Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(81)85199-0

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 / Fatty Acyls / Fatty acid esters / Wax esters / Wax monoesters
Hexacosyl tetracosanoate 5315798 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCOC(=O)CCCCCCCCCCCCCCCCCCCCCCC 733.30 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Octatriacontanol 13847926 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCO 551.00 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
(3aS,6aR,9aR,9bS)-6,9-dimethylidene-3a,4,5,6a,7,8,9a,9b-octahydro-3H-azuleno[4,5-b]furan-2-one 162406238 Click to see C=C1CCC2CC(=O)OC2C3C1CCC3=C 218.29 unknown https://doi.org/10.1016/0031-9422(81)85199-0
6,9-dimethylidene-3a,4,5,6a,7,8,9a,9b-octahydro-3H-azuleno[4,5-b]furan-2-one 162909853 Click to see C=C1CCC2CC(=O)OC2C3C1CCC3=C 218.29 unknown https://doi.org/10.1016/0031-9422(81)85199-0
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Guaianolides and derivatives
Dehydrocostus lactone, (-)- 73174 Click to see C=C1CCC2C(C3C1CCC3=C)OC(=O)C2=C 230.30 unknown https://doi.org/10.1016/0031-9422(81)85199-0
Dehydrocostuslactone 4426320 Click to see C=C1CCC2C(C3C1CCC3=C)OC(=O)C2=C 230.30 unknown https://doi.org/10.1016/0031-9422(81)85199-0
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Shikimic acids and derivatves
Shikimic acid 8742 Click to see C1C(C(C(C=C1C(=O)O)O)O)O 174.15 unknown via CMAUP database
> Organoheterocyclic compounds / Benzodioxanes / Phenylbenzodioxanes / Phenylbenzo-1,4-dioxanes
Kielcorin 13834128 Click to see COC1=C(C=CC(=C1)C2C(OC3=C4C(=CC(=C3O2)OC)C(=O)C5=CC=CC=C5O4)CO)O 436.40 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
1,3-dihydroxy-5-methoxy-9H-xanthen-9-one 12026489 Click to see COC1=CC=CC2=C1OC3=CC(=CC(=C3C2=O)O)O 258.23 unknown via CMAUP database
3,4,5-Trihydroxy-9H-xanthen-9-one 46209537 Click to see C1=CC2=C(C(=C1)O)OC3=C(C2=O)C=CC(=C3O)O 244.20 unknown via CMAUP database
4-Hydroxy-2,3-dimethoxyxanthone 378690 Click to see COC1=C(C(=C2C(=C1)C(=O)C3=CC=CC=C3O2)O)OC 272.25 unknown via CMAUP database
Gentisein 5281635 Click to see C1=CC2=C(C=C1O)C(=O)C3=C(C=C(C=C3O2)O)O 244.20 unknown via CMAUP database
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
hyperinol A 16081994 Click to see CC1C2C3(CCC1=C)CCC4(C2(CCC5C4(CCC6C5(CCC(C6(C)C)O)C)C)OC3=O)C 454.70 unknown via CMAUP database
hyperinol B 16081995 Click to see CC1C2C3(CCC4(C2(CCC5C4(CCC6C5(CCC(C6(C)C)O)C)C)OC3=O)C)C(CC1=C)O 470.70 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
3,4-Dihydroxy-trans-cinnamic acid tetracosyl ester 5320239 Click to see CCCCCCCCCCCCCCCCCCCCCCCCOC(=O)C=CC1=CC(=C(C=C1)O)O 516.80 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin 5280443 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 270.24 unknown https://doi.org/10.1016/0031-9422(81)85199-0
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Isorhamnetin 5281654 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 316.26 unknown via CMAUP database
Kaempferol 5280863 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown via CMAUP database
Myricetin 5281672 Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O 318.23 unknown via CMAUP database
Quercetin 5280343 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 302.23 unknown via CMAUP database
Rhamnetin 5281691 Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)O)C3=CC(=C(C=C3)O)O)O 316.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
Hispidulin 5281628 Click to see COC1=C(C2=C(C=C1O)OC(=CC2=O)C3=CC=C(C=C3)O)O 300.26 unknown https://doi.org/10.1016/0031-9422(81)85199-0

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