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Solidago spathulata

Solidago spathulata - 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 UUID643fd37ab056d719597127
Scientific name Solidago spathulata
Authority DC.
First published in Prodr. 5: 339 (1836)

Description Top

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Synonyms Top

Scientific name Authority First published in
Solidago spiciformis Torr. & A.Gray Fl. N. Amer. 2(2): 202 (1842)
Solidago simplex var. spathulata (DC.) Cronquist Intermount. Fl. 5: 244 (1994)
Solidago spathulata subsp. spathulata DC.
Aster candollei Kuntze Revis. Gen. Pl. 1: 315 (1891)
Homopappus spathulatus (DC.) Nutt. Trans. Amer. Philos. Soc. , ser. 2, 7: 332 (1840)

Common names Top

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Language Common/alternative name
English mt. albert goldenrod

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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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
    • Northwestern U.S.A.
      • Oregon
    • Southwestern U.S.A.
      • California

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000132357
Tropicos 2703277
KEW urn:lsid:ipni.org:names:312013-2
The Plant List gcc-93200
Open Tree Of Life 3898811
NCBI Taxonomy 1334110
IPNI 312013-2
iNaturalist 60978
GBIF 5389110
EPPO SOOSP
EOL 1248702
Calflora (Californian flora) 11087
USDA GRIN 448015
Wikipedia Solidago_spathulata
CMAUP NPO9353

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
Expanding and testing fluorescent amplified fragment length polymorphisms for identifying roots of boreal forest plant species Metzler P, La Flèche M, Karst J Appl Plant Sci 08-Apr-2019
PMCID:PMC6476169
doi:10.1002/aps3.1236
PMID:31024780
ChemInform Abstract: POLYACETYLENIC COMPOUNDS. 266. NEW C17 ACETYLENIC COMPOUNDS FROM SOLIDAGO SPATHULATA DC F. BOHLMANN, T. GERKE, R. M. KING, H. ROBINSON Wiley 03-May-2016
doi:10.1002/CHIN.198329359
Effect of an Invasive Plant and Moonlight on Rodent Foraging Behavior in a Coastal Dune Ecosystem Johnson MD, De León YL PLoS One 13-Feb-2015
PMCID:PMC4334550
doi:10.1371/journal.pone.0117903
PMID:25679785
Polyacetylenverbindungen, 266. Neue C<sub>17</sub>‐Acetylenverbindungen aus <i>Solidago spathulata</i> DC Ferdinand Bohlmann, Thomas Gerke, Robert M. King, Harold Ronbinson Wiley 19-Jul-2007
doi:10.1002/JLAC.198319830422

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 alcohol esters
[(2Z,9E,11R)-11-hydroxyheptadeca-2,9,16-trien-4,6-diynyl] acetate 163030873 Click to see CC(=O)OCC=CC#CC#CCC=CC(CCCCC=C)O 300.40 unknown https://doi.org/10.1002/JLAC.198319830422
11-Hydroxyheptadeca-2,9,16-trien-4,6-diynyl acetate 163030872 Click to see CC(=O)OCC=CC#CC#CCC=CC(CCCCC=C)O 300.40 unknown https://doi.org/10.1002/JLAC.198319830422
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Bicyclogermacrane and isolepidozane sesquiterpenoids
(1S,2E,10R)-3,7,11,11-tetramethylbicyclo[8.1.0]undeca-2,6-diene 44583886 Click to see CC1=CCCC(=CC2C(C2(C)C)CC1)C 204.35 unknown https://doi.org/10.1002/CHIN.198329359
(1S,2E,6E,10R)-3,7,11,11-tetramethylbicyclo[8.1.0]undeca-2,6-diene 13894537 Click to see CC1=CCCC(=CC2C(C2(C)C)CC1)C 204.35 unknown https://doi.org/10.1002/JLAC.198319830422
CID 522276 522276 Click to see CC1=CCCC(=CC2C(C2(C)C)CC1)C 204.35 unknown https://doi.org/10.1002/JLAC.198319830422
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
(S,1Z,6Z)-8-Isopropyl-1-methyl-5-methylenecyclodeca-1,6-diene 91723653 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown https://doi.org/10.1002/CHIN.198329359
1,6-Cyclodecadiene, 1-methyl-5-methylene-8-(1-methylethyl)- 91104 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown https://doi.org/10.1002/JLAC.198319830422
Germacrene D 5317570 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown https://doi.org/10.1002/JLAC.198319830422
> Phenylpropanoids and polyketides / Coumarins and derivatives
[(1R,5R)-4,6,6-trimethyl-5-[(2-oxochromen-7-yl)oxymethyl]cyclohex-3-en-1-yl] acetate 162902180 Click to see CC1=CCC(C(C1COC2=CC3=C(C=C2)C=CC(=O)O3)(C)C)OC(=O)C 356.40 unknown https://doi.org/10.1002/JLAC.198319830422
[4,6,6-Trimethyl-5-[(2-oxochromen-7-yl)oxymethyl]cyclohex-3-en-1-yl] acetate 162902179 Click to see CC1=CCC(C(C1COC2=CC3=C(C=C2)C=CC(=O)O3)(C)C)OC(=O)C 356.40 unknown https://doi.org/10.1002/JLAC.198319830422
7-[(5-Hydroxy-2,6,6-trimethylcyclohex-2-en-1-yl)methoxy]chromen-2-one 13965514 Click to see CC1=CCC(C(C1COC2=CC3=C(C=C2)C=CC(=O)O3)(C)C)O 314.40 unknown https://doi.org/10.1002/JLAC.198319830422
7-[[(1R,5R)-5-hydroxy-2,6,6-trimethylcyclohex-2-en-1-yl]methoxy]chromen-2-one 163023486 Click to see CC1=CCC(C(C1COC2=CC3=C(C=C2)C=CC(=O)O3)(C)C)O 314.40 unknown https://doi.org/10.1002/JLAC.198319830422
> 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 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 via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Cirsimaritin 188323 Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC=C(C=C3)O)O)OC 314.29 unknown via CMAUP database
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 via CMAUP database
Genkwanin 5281617 Click to see COC1=CC(=C2C(=C1)OC(=CC2=O)C3=CC=C(C=C3)O)O 284.26 unknown via CMAUP database
Sakuranetin 73571 Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=C(C=C3)O)O 286.28 unknown via CMAUP database

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