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Internal ID UUID643fcb7821716077352383
Scientific name Carphochaete bigelovii
Authority A.Gray
First published in Smithsonian Contr. Knowl. 3(5): 89 (1852)

Description Top

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The species is adapted to dry, rocky soils and is found in desert scrub and grassland habitats. It is a popular ornamental plant, and is used in xeriscaping.

Carphochaete bigelovii, commonly known as Bigelow's bristlehead, is a species of North American flowering plant in the Asteraceae family. It is native to northern Mexico and the southwestern United States, and is adapted to dry, rocky soils. It is a shrub that can reach up to 300 cm (10 feet) tall, and has flower heads with purple disc florets and white lobes around the edge. It is a popular ornamental plant, and is often used in xeriscaping.

Synonyms Top

No known synonyms.

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Language Common/alternative name
English bigelow's bristlehead

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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 Northeast
      • 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-0000046516
USDA Plants CABI6
Tropicos 2709705
KEW urn:lsid:ipni.org:names:189421-1
Open Tree Of Life 4727381
NCBI Taxonomy 2773127
Nature Serve 2.160103
IPNI 189421-1
iNaturalist 160161
GBIF 3143116
Freebase /m/013ccn4m
Wikipedia Carphochaete_bigelovii

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
6-Methoxylated Flavones from Carphochaete bigelovii Barbara Meurer, Tom J. Mabry American Chemical Society (ACS) 17-Mar-2005
doi:10.1021/NP50052A046
Sesquiterpene lactones from Carphochaete bigelovii Barbara Meurer, Fred C. Seaman, Tom J. Mabry Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)82280-3

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 / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
[(3aR,4R,6E,9S,10E,11aR)-9-acetyloxy-6,10-dimethyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-4-yl] (E)-4-hydroxy-2-[[(E)-2-(hydroxymethyl)but-2-enoyl]oxymethyl]but-2-enoate 163044676 Click to see CC=C(CO)C(=O)OCC(=CCO)C(=O)OC1CC(=CCC(C(=CC2C1C(=C)C(=O)O2)C)OC(=O)C)C 518.60 unknown https://doi.org/10.1016/S0031-9422(00)82280-3
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Guaianolides and derivatives
(8-acetyloxy-9-methyl-3,6-dimethylidene-2-oxo-4,5,6a,7,8,9,9a,9b-octahydro-3aH-azuleno[4,5-b]furan-4-yl) 2-[2-(acetyloxymethyl)but-2-enoyloxymethyl]-4-hydroxybut-2-enoate 162943965 Click to see CC=C(COC(=O)C)C(=O)OCC(=CCO)C(=O)OC1CC(=C)C2CC(C(C2C3C1C(=C)C(=O)O3)C)OC(=O)C 560.60 unknown https://doi.org/10.1016/S0031-9422(00)82280-3
(8-acetyloxy-9-methyl-3,6-dimethylidene-2-oxo-4,5,6a,7,8,9,9a,9b-octahydro-3aH-azuleno[4,5-b]furan-4-yl) 4-hydroxy-2-[2-(hydroxymethyl)but-2-enoyloxymethyl]but-2-enoate 162935948 Click to see CC=C(CO)C(=O)OCC(=CCO)C(=O)OC1CC(=C)C2CC(C(C2C3C1C(=C)C(=O)O3)C)OC(=O)C 518.60 unknown https://doi.org/10.1016/S0031-9422(00)82280-3
(8-hydroxy-9-methyl-3,6-dimethylidene-2-oxo-4,5,6a,7,8,9,9a,9b-octahydro-3aH-azuleno[4,5-b]furan-4-yl) 2-[2-(acetyloxymethyl)but-2-enoyloxymethyl]-4-hydroxybut-2-enoate 162933185 Click to see CC=C(COC(=O)C)C(=O)OCC(=CCO)C(=O)OC1CC(=C)C2CC(C(C2C3C1C(=C)C(=O)O3)C)O 518.60 unknown https://doi.org/10.1016/S0031-9422(00)82280-3
[(3aR,4R,6aS,8S,9S,9aR,9bR)-8-acetyloxy-9-methyl-3,6-dimethylidene-2-oxo-4,5,6a,7,8,9,9a,9b-octahydro-3aH-azuleno[4,5-b]furan-4-yl] (E)-2-[[(E)-2-(acetyloxymethyl)but-2-enoyl]oxymethyl]-4-hydroxybut-2-enoate 162943966 Click to see CC=C(COC(=O)C)C(=O)OCC(=CCO)C(=O)OC1CC(=C)C2CC(C(C2C3C1C(=C)C(=O)O3)C)OC(=O)C 560.60 unknown https://doi.org/10.1016/S0031-9422(00)82280-3
[(3aR,4R,6aS,8S,9S,9aR,9bR)-8-acetyloxy-9-methyl-3,6-dimethylidene-2-oxo-4,5,6a,7,8,9,9a,9b-octahydro-3aH-azuleno[4,5-b]furan-4-yl] (E)-4-hydroxy-2-[[(E)-2-(hydroxymethyl)but-2-enoyl]oxymethyl]but-2-enoate 162935950 Click to see CC=C(CO)C(=O)OCC(=CCO)C(=O)OC1CC(=C)C2CC(C(C2C3C1C(=C)C(=O)O3)C)OC(=O)C 518.60 unknown https://doi.org/10.1016/S0031-9422(00)82280-3
[(3aR,4R,6aS,8S,9S,9aR,9bR)-8-hydroxy-9-methyl-3,6-dimethylidene-2-oxo-4,5,6a,7,8,9,9a,9b-octahydro-3aH-azuleno[4,5-b]furan-4-yl] (E)-2-[[(E)-2-(acetyloxymethyl)but-2-enoyl]oxymethyl]-4-hydroxybut-2-enoate 162933186 Click to see CC=C(COC(=O)C)C(=O)OCC(=CCO)C(=O)OC1CC(=C)C2CC(C(C2C3C1C(=C)C(=O)O3)C)O 518.60 unknown https://doi.org/10.1016/S0031-9422(00)82280-3
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
[(E)-2-[[(3aR,4R,9aR,9bR)-6,9-dimethyl-3-methylidene-2-oxo-3a,4,5,7,9a,9b-hexahydroazuleno[4,5-b]furan-4-yl]oxycarbonyl]-4-hydroxybut-2-enyl] (E)-4-hydroxy-2-(hydroxymethyl)but-2-enoate 14779727 Click to see CC1=C2CC=C(C2C3C(C(C1)OC(=O)C(=CCO)COC(=O)C(=CCO)CO)C(=C)C(=O)O3)C 474.50 unknown https://doi.org/10.1016/S0031-9422(00)82280-3
[2-[(6,9-Dimethyl-3-methylidene-2-oxo-3a,4,5,7,9a,9b-hexahydroazuleno[4,5-b]furan-4-yl)oxycarbonyl]-4-hydroxybut-2-enyl] 4-hydroxy-2-(hydroxymethyl)but-2-enoate 162894250 Click to see CC1=C2CC=C(C2C3C(C(C1)OC(=O)C(=CCO)COC(=O)C(=CCO)CO)C(=C)C(=O)O3)C 474.50 unknown https://doi.org/10.1016/S0031-9422(00)82280-3
> 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/10.1021/NP50052A046
Jaceosidin 5379096 Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(O2)C=C(C(=C3O)OC)O)O 330.29 unknown https://doi.org/10.1021/NP50052A046
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
5-Hydroxy-2-(3-hydroxy-4,5-dimethoxyphenyl)-6,7-dimethoxychromen-4-one 183329 Click to see COC1=CC(=CC(=C1OC)O)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)OC)O 374.30 unknown https://doi.org/10.1021/NP50052A046
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/10.1021/NP50052A046
> Phenylpropanoids and polyketides / Macrolides and analogues
(11R,12S,15S)-11-bromo-12,21-dihydroxy-15-(2-hydroxypropan-2-yl)-4,12-dimethyl-7-methylidene-16-oxatricyclo[16.3.1.03,8]docosa-1(21),3,18(22),19-tetraen-17-one 42599771 Click to see CC1=C2CC3=C(C=CC(=C3)C(=O)OC(CCC(C(CCC2C(=C)CC1)Br)(C)O)C(C)(C)O)O 521.50 unknown https://doi.org/10.1016/S0031-9422(00)82280-3

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