Geraea canescens - Unknown
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Internal ID UUID643fd1c91b459621263449
Scientific name Geraea canescens
Authority Torr. & A.Gray
First published in Proc. Amer. Acad. Arts i. (1847) 49

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Synonyms Top

Scientific name Authority First published in
Encelia eriocephala A.Gray Proc. Amer. Acad. Arts viii. (1873) 657.
Geraea canescens var. canescens Torr. & A.Gray
Simsia canescens A.Gray Mem. Amer. Acad. Arts , ser. 2, 4(1): 85 (1849)
Geraea canescens var. paniculata S.F.Blake Proc. Amer. Acad. Arts 49: 357 (1913)

Common names Top

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Language Common/alternative name
English hairy desertsunflower

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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
    • Mexico
      • Mexico Northwest
    • Southwestern U.S.A.
      • Arizona
      • California
      • Nevada
      • Utah

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000118208
UNII CN87J0WK6J
USDA Plants GECA2
Tropicos 2710246
KEW urn:lsid:ipni.org:names:208833-1
The Plant List gcc-79545
Open Tree Of Life 864185
NCBI Taxonomy 41582
Nature Serve 2.156262
IPNI 208833-1
iNaturalist 77248
GBIF 3091936
Freebase /m/03c13t6
EPPO GEECA
EOL 468480
Calflora (Californian flora) 3792
USDA GRIN 452886
Wikipedia Geraea_canescens

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)!
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Title Authors Publication Released IDs
Warming puts the squeeze on photosynthesis – lessons from tropical trees Dusenge ME, Way DA J Exp Bot 30-May-2017
PMCID:PMC5447882
doi:10.1093/jxb/erx114
Honey bees preferentially consume freshly-stored pollen Carroll MJ, Brown N, Goodall C, Downs AM, Sheenan TH, Anderson KE PLoS One 21-Apr-2017
PMCID:PMC5400263
doi:10.1371/journal.pone.0175933
PMID:28430801
Benzofurans and methylated flavonoids of Geraea (Asteraceae) Peter Proksch, Aristotelis Mitsakos, Jutta Bodden, Eckhard Wollenweber Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)81697-0
New dihydroflavonols from enceliopsis and geraea. Proksch P, Breuer M, Mitsakos A, Budzikiewicz H Planta Med 01-Aug-1987
doi:10.1055/S-2006-962731
PMID:17269037

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
> Benzenoids / Benzene and substituted derivatives / Acetophenones
1-[(2S)-6-hydroxy-2-prop-1-en-2-yl-2,3-dihydro-1-benzofuran-5-yl]ethanone 12838730 Click to see CC(=C)C1CC2=CC(=C(C=C2O1)O)C(=O)C 218.25 unknown https://doi.org/10.1016/S0031-9422(00)81697-0
6-Hydroxytremetone 186059 Click to see CC(=C)C1CC2=CC(=C(C=C2O1)O)C(=O)C 218.25 unknown https://doi.org/10.1016/S0031-9422(00)81697-0
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
[(2S,3R,4S,5S,6R)-2-[[(1S,4aR,7R,7aR)-4-formyl-4a-hydroxy-7-methyl-5,6,7,7a-tetrahydro-1H-cyclopenta[c]pyran-1-yl]oxy]-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl] (E)-3-(4-hydroxyphenyl)prop-2-enoate 101677404 Click to see CC1CCC2(C1C(OC=C2C=O)OC3C(C(C(C(O3)CO)O)O)OC(=O)C=CC4=CC=C(C=C4)O)O 506.50 unknown https://doi.org/10.1016/S0031-9422(00)81697-0
> Organoheterocyclic compounds / Benzofurans
(1R)-1-(6-methoxy-2-prop-1-en-2-yl-1-benzofuran-5-yl)ethanol 162991174 Click to see CC(C1=C(C=C2C(=C1)C=C(O2)C(=C)C)OC)O 232.27 unknown https://doi.org/10.1016/S0031-9422(00)81697-0
1-(6-Methoxy-2-prop-1-en-2-yl-1-benzofuran-5-yl)ethanol 101316766 Click to see CC(C1=C(C=C2C(=C1)C=C(O2)C(=C)C)OC)O 232.27 unknown https://doi.org/10.1016/S0031-9422(00)81697-0
1-[5-(1-Hydroxyethyl)-6-methoxy-1-benzofuran-2-yl]ethanone 162933419 Click to see CC(C1=C(C=C2C(=C1)C=C(O2)C(=O)C)OC)O 234.25 unknown https://doi.org/10.1016/S0031-9422(00)81697-0
1-[5-[(1R)-1-hydroxyethyl]-6-methoxy-1-benzofuran-2-yl]ethanone 162933420 Click to see CC(C1=C(C=C2C(=C1)C=C(O2)C(=O)C)OC)O 234.25 unknown https://doi.org/10.1016/S0031-9422(00)81697-0
Euparin 119039 Click to see CC(=C)C1=CC2=CC(=C(C=C2O1)O)C(=O)C 216.23 unknown https://doi.org/10.1016/S0031-9422(00)81697-0
Euparin methyl ether 182181 Click to see CC(=C)C1=CC2=CC(=C(C=C2O1)OC)C(=O)C 230.26 unknown https://doi.org/10.1016/S0031-9422(00)81697-0
Euparone 104654 Click to see CC(=O)C1=CC2=CC(=C(C=C2O1)O)C(=O)C 218.20 unknown https://doi.org/10.1016/S0031-9422(00)81697-0
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
[(2R,3S)-5,7-dihydroxy-2-(4-hydroxyphenyl)-8-methoxy-4-oxo-2,3-dihydrochromen-3-yl] acetate 163106724 Click to see CC(=O)OC1C(OC2=C(C1=O)C(=CC(=C2OC)O)O)C3=CC=C(C=C3)O 360.30 unknown https://doi.org/10.1055/S-2006-962731
[(2S,3R)-5,7-dihydroxy-2-(4-hydroxyphenyl)-8-methoxy-4-oxo-2,3-dihydrochromen-3-yl] (Z)-2-methylbut-2-enoate 162908251 Click to see CC=C(C)C(=O)OC1C(OC2=C(C1=O)C(=CC(=C2OC)O)O)C3=CC=C(C=C3)O 400.40 unknown https://doi.org/10.1055/S-2006-962731
3',4',5,7-Tetrahydroxy-3,8-dimethoxyflavone 5748553 Click to see COC1=C(C=C(C2=C1OC(=C(C2=O)OC)C3=CC(=C(C=C3)O)O)O)O 346.30 unknown https://doi.org/10.1016/S0031-9422(00)81697-0
4'-Hydroxywogonin 5322078 Click to see COC1=C(C=C(C2=C1OC(=CC2=O)C3=CC=C(C=C3)O)O)O 300.26 unknown https://doi.org/10.1016/S0031-9422(00)81697-0
5,7,4'-Trihydroxy-3,8-dimethoxyflavone 13983738 Click to see COC1=C(C=C(C2=C1OC(=C(C2=O)OC)C3=CC=C(C=C3)O)O)O 330.29 unknown https://doi.org/10.1016/S0031-9422(00)81697-0
Gossypetin 3,8,3'-trimethyl ether 5386961 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(O2)C(=C(C=C3O)O)OC)OC)O 360.30 unknown https://doi.org/10.1016/S0031-9422(00)81697-0

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