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Rudbeckia subtomentosa

Rudbeckia subtomentosa - 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 UUID643fcad95f6fd195093568
Scientific name Rudbeckia subtomentosa
Authority Pursh
First published in Fl. Amer. Sept. 2: 575 (1813)

Description Top

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Synonyms Top

Scientific name Authority First published in
Centrocarpha subtomentosa Sweet Hort. Brit. 2: 310 (1830)
Rudbeckia tomentosa Ell. Sketch Bot. S. Carolina 2: 453 (1823)
Rudbeckia odorata Nutt. J. Acad. Nat. Sci. Philadelphia vii. (1834) 78

Common names Top

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Language Common/alternative name
English sweet coneflower
Chinese 香金光菊

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

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
  • Northern America
    • North-central U.S.A.
      • Illinois
      • Iowa
      • Kansas
      • Minnesota
      • Missouri
      • Oklahoma
      • Wisconsin
    • Northeastern U.S.A.
      • Connecticut
      • Indiana
      • Massachusetts
      • Michigan
      • New York
    • South-central U.S.A.
      • Texas
    • Southeastern U.S.A.
      • Arkansas
      • Kentucky
      • Louisiana
      • Mississippi
      • North Carolina
      • Tennessee

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000041666
USDA Plants RUSU
Tropicos 2725478
KEW urn:lsid:ipni.org:names:30275611-2
The Plant List gcc-140296
Missouri Botanical Garden 277591
Open Tree Of Life 36537
NCBI Taxonomy 52307
Nature Serve 2.147034
IPNI 30275611-2
iNaturalist 168207
GBIF 3114221
WisFlora 4909
EOL 467875
USDA GRIN 416345
Wikipedia Rudbeckia_subtomentosa

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
Terpenoid-Mediated Targeting of STAT3 Signaling in Cancer: An Overview of Preclinical Studies Khan F, Pandey P, Verma M, Upadhyay TK Biomolecules 07-Feb-2024
PMCID:PMC10886526
doi:10.3390/biom14020200
PMID:38397437
In vitro Ploidy Manipulation for Crop Improvement Touchell DH, Palmer IE, Ranney TG Front Plant Sci 03-Jun-2020
PMCID:PMC7284393
doi:10.3389/fpls.2020.00722
PMID:32582252
Studies on Chemical Composition and Antioxidant Activity of Rudbeckia triloba Moldovan Z, Buleandră M, Oprea E, Mînea Z J Anal Methods Chem 27-Nov-2017
PMCID:PMC5723952
doi:10.1155/2017/3407312
PMID:29279786
Targeting Apoptosis Pathways in Cancer with Alantolactone and Isoalantolactone Rasul A, Khan M, Ali M, Li J, Li X ScientificWorldJournal 27-Oct-2013
PMCID:PMC3826378
doi:10.1155/2013/248532
PMID:24288468
Sesquiterpene lactones and lignanes from Rudbeckia species Marta Vasquez, Leovigildo Quijano, Frank R. Fronczek, Francisco A. Macias, Lowell E. Urbatsch, Patricia B. Cox, Nikolaus H. Fischer Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(90)85117-X
Antimycobacterial eudesmanolides from Inula helenium and Rudbeckia subtomentosa. Cantrell CL, Abate L, Fronczek FR, Franzblau SG, Quijano L, Fischer NH Planta Med 01-May-1999
doi:10.1055/S-1999-14001
PMID:10364842
Ambrosanolides and other constituents of two rudbeckia species. Gutiérrez AB, Herz W Planta Med 01-Jun-1990
doi:10.1055/S-2006-960962
PMID:17221423

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
beta-CARYOPHYLLENE OXIDE 1742210 Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C 220.35 unknown https://doi.org/10.1016/0031-9422(90)85117-X
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1016/0031-9422(90)85117-X
Caryophyllene epoxide 14350 Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C 220.35 unknown https://doi.org/10.1016/0031-9422(90)85117-X
Caryophyllene,alpha + beta mixt. 5354499 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1016/0031-9422(90)85117-X
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
beta-Selinene 442393 Click to see CC(=C)C1CCC2(CCCC(=C)C2C1)C 204.35 unknown https://doi.org/10.1016/0031-9422(90)85117-X
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Ambrosanolides and secoambrosanolides
(8-hydroxy-5-methyl-1-methylidene-2-oxo-4,5,5a,6,7,8,9,9a-octahydro-3aH-azuleno[6,5-b]furan-8a-yl)methyl acetate 4555530 Click to see CC1CC2C(CC3(C1CCC3O)COC(=O)C)C(=C)C(=O)O2 308.40 unknown https://doi.org/10.1055/S-2006-960962
(9-acetyloxy-6-methyl-3-methylidene-2-oxo-4,5,6,6a,7,8,9,9b-octahydro-3aH-azuleno[4,5-b]furan-9a-yl)methyl acetate 101526919 Click to see CC1CCC2C(C3(C1CCC3OC(=O)C)COC(=O)C)OC(=O)C2=C 350.40 unknown https://doi.org/10.1016/0031-9422(90)85117-X
[8a-(hydroxymethyl)-5-methyl-1-methylidene-2-oxo-4,5,5a,6,7,8,9,9a-octahydro-3aH-azuleno[6,7-b]furan-8-yl] acetate 73816673 Click to see CC1CC2C(CC3(C1CCC3OC(=O)C)CO)C(=C)C(=O)O2 308.40 unknown https://doi.org/10.1055/S-2006-960962
Rudmollin 196467 Click to see CC1CC2C(CC3(C1CCC3O)CO)C(=C)C(=O)O2 266.33 unknown https://doi.org/10.1055/S-2006-960962
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Eudesmanolides, secoeudesmanolides, and derivatives
(3aR,8aR,9aR)-5,8a-dimethyl-3-methylene-3a,4,7,8,9,9a-hexahydrobenzo[f]benzofuran-2,6-dione 474519 Click to see CC1=C2CC3C(CC2(CCC1=O)C)OC(=O)C3=C 246.30 unknown https://doi.org/10.1055/S-1999-14001
(3aS,5aR,9aS,9bS)-5a,9-Dimethyl-3-methylene-3a,4,5,5a,9a,9b-hexahydronaphtho[1,2-b]furan-2(3H)-one 14467711 Click to see CC1=CC=CC2(C1C3C(CC2)C(=C)C(=O)O3)C 230.30 unknown https://doi.org/10.1016/0031-9422(90)85117-X
(3aS,5aS,9aS,9bS)-5a,9-dimethyl-3-methylidene-4,5,9a,9b-tetrahydro-3aH-benzo[g][1]benzofuran-2-one 14467712 Click to see CC1=CC=CC2(C1C3C(CC2)C(=C)C(=O)O3)C 230.30 unknown https://doi.org/10.1016/0031-9422(90)85117-X
(3aS,5aS,9bS)-5a,9-dimethyl-3-methylidene-4,5,8,9b-tetrahydro-3aH-benzo[g][1]benzofuran-2-one 162847338 Click to see CC1=C2C3C(CCC2(C=CC1)C)C(=C)C(=O)O3 230.30 unknown https://doi.org/10.1016/0031-9422(90)85117-X
5,8a-dimethyl-3-methylidene-2H,3H,3aH,4H,6H,7H,8H,8aH,9H,9aH-naphtho[2,3-b]furan-2-one 315677 Click to see CC1=C2CC3C(CC2(CCC1)C)OC(=O)C3=C 232.32 unknown https://doi.org/10.1055/S-1999-14001
5,8a-Dimethyl-3-methylidene-3a,4,7,8,9,9a-hexahydrobenzo[f][1]benzofuran-2,6-dione 13889963 Click to see CC1=C2CC3C(CC2(CCC1=O)C)OC(=O)C3=C 246.30 unknown https://doi.org/10.1055/S-1999-14001
5a,9-dimethyl-3-methylidene-4,5,8,9b-tetrahydro-3aH-benzo[g][1]benzofuran-2-one 14486974 Click to see CC1=C2C3C(CCC2(C=CC1)C)C(=C)C(=O)O3 230.30 unknown https://doi.org/10.1016/0031-9422(90)85117-X
6-Hydroxy-5a-methyl-3,9-dimethylidenedecahydronaphtho[1,2-b]furan-2(3h)-one 98958 Click to see CC12CCC3C(C1C(=C)CCC2O)OC(=O)C3=C 248.32 unknown https://doi.org/10.1016/0031-9422(90)85117-X
Alloalantolactone 474518 Click to see CC1=C2CC3C(CC2(CCC1)C)OC(=O)C3=C 232.32 unknown https://doi.org/10.1055/S-1999-14001
Reynosin 482788 Click to see CC12CCC3C(C1C(=C)CCC2O)OC(=O)C3=C 248.32 unknown https://doi.org/10.1016/0031-9422(90)85117-X
Santamarine 188297 Click to see CC1=CCC(C2(C1C3C(CC2)C(=C)C(=O)O3)C)O 248.32 unknown https://doi.org/10.1016/0031-9422(90)85117-X
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
(3aS,6E,11aR)-6,10-dimethyl-3-methylidene-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-2-one 133640194 Click to see CC1=CCCC(=CC2C(CC1)C(=C)C(=O)O2)C 232.32 unknown https://doi.org/10.1016/0031-9422(90)85117-X
(6,10-Dimethyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-8-yl) 2-methylbut-2-enoate 162912179 Click to see CC=C(C)C(=O)OC1CC(=CC2C(CCC(=C1)C)C(=C)C(=O)O2)C 330.40 unknown https://doi.org/10.1016/0031-9422(90)85117-X
Costunolide 5281437 Click to see CC1=CCCC(=CC2C(CC1)C(=C)C(=O)O2)C 232.32 unknown https://doi.org/10.1016/0031-9422(90)85117-X
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/0031-9422(90)85117-X
24-Ethylcholest-5-en-3beta-ol 22012 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/0031-9422(90)85117-X
Stigmasterol 5280794 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1016/0031-9422(90)85117-X
> Phenylpropanoids and polyketides / Coumarins and derivatives
Coumarin 323 Click to see C1=CC=C2C(=C1)C=CC(=O)O2 146.14 unknown https://doi.org/10.1055/S-2006-960962
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Eupatorin 97214 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)OC)O)O 344.30 unknown https://doi.org/10.1016/0031-9422(90)85117-X

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