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Brickellia baccharidea

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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 UUID643fd2e880759262337168
Scientific name Brickellia baccharidea
Authority A.Gray
First published in Smithsonian Contr. Knowl. 3(5): 87 (1852)

Description Top

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Synonyms Top

Scientific name Authority First published in
Coleosanthus baccharideus Kuntze Revis. Gen. Pl. 1: 328 (1891)

Common names Top

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Language Common/alternative name
English resinleaf brickellbush

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
    • Mexico
      • Mexico Northwest
    • South-central U.S.A.
      • New Mexico
      • Texas
    • Southwestern U.S.A.
      • Arizona

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000127680
USDA Plants BRBA2
Tropicos 2712683
KEW urn:lsid:ipni.org:names:186197-1
The Plant List gcc-88677
Open Tree Of Life 3899963
NCBI Taxonomy 1550803
Nature Serve 2.140566
IPNI 186197-1
iNaturalist 159428
GBIF 5388450
Freebase /m/013cctxs
EOL 467833
Wikipedia Brickellia_baccharidea

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
Sulfated and 6-methoxyflavonoids from Brickellia baccharidea (compositae) Barbara N. Timmermann, Shirley A. Graham, Tom J. Mabry Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)98581-9

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
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Eupatin 5317287 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C(=C(C=C3O2)OC)OC)O)O)O 360.30 unknown https://doi.org/10.1016/S0031-9422(00)98581-9
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-dihydroxyphenyl)-5-hydroxy-6,7-dimethoxy-3-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 162936705 Click to see COC1=C(C(=C2C(=C1)OC(=C(C2=O)OC3C(C(C(C(O3)CO)O)O)O)C4=CC(=C(C=C4)O)O)O)OC 508.40 unknown https://doi.org/10.1016/S0031-9422(00)98581-9
2-(3,4-Dihydroxyphenyl)-5-hydroxy-6,7-dimethoxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 14630676 Click to see COC1=C(C(=C2C(=C1)OC(=C(C2=O)OC3C(C(C(C(O3)CO)O)O)O)C4=CC(=C(C=C4)O)O)O)OC 508.40 unknown https://doi.org/10.1016/S0031-9422(00)98581-9
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-6-methoxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 11968829 Click to see COC1=C(C2=C(C=C1O)OC(=C(C2=O)OC3C(C(C(C(O3)CO)O)O)O)C4=CC(=C(C=C4)O)O)O 494.40 unknown https://doi.org/10.1016/S0031-9422(00)98581-9
2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-6-methoxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 14134315 Click to see COC1=C(C2=C(C=C1O)OC(=C(C2=O)OC3C(C(C(C(O3)CO)O)O)O)C4=CC(=C(C=C4)O)O)O 494.40 unknown https://doi.org/10.1016/S0031-9422(00)98581-9
Patuletin 3-O-beta-D-galactoside 5320434 Click to see COC1=C(C2=C(C=C1O)OC(=C(C2=O)OC3C(C(C(C(O3)CO)O)O)O)C4=CC(=C(C=C4)O)O)O 494.40 unknown https://doi.org/10.1016/S0031-9422(00)98581-9
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
Centaureidin 5315773 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(O2)C=C(C(=C3O)OC)O)OC)O 360.30 unknown https://doi.org/10.1016/S0031-9422(00)98581-9
Desmethoxycentaureidin 5469524 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(O2)C=C(C(=C3O)OC)O)O 330.29 unknown https://doi.org/10.1016/S0031-9422(00)98581-9
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/S0031-9422(00)98581-9
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Artemetin 5320351 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C(=C(C=C3O2)OC)OC)O)OC)OC 388.40 unknown https://doi.org/10.1016/S0031-9422(00)98581-9
Casticin 5315263 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C(=C(C=C3O2)OC)OC)O)OC)O 374.30 unknown https://doi.org/10.1016/S0031-9422(00)98581-9
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/S0031-9422(00)98581-9
Salvigenin 161271 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)OC)O 328.30 unknown https://doi.org/10.1016/S0031-9422(00)98581-9

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