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Oxylobus arbutifolius

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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 UUID643fd18105d6f283793095
Scientific name Oxylobus arbutifolius
Authority A.Gray
First published in Proc. Amer. Acad. Arts xv. 26 (1879)

Description Top

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Synonyms Top

Scientific name Authority First published in
Oxylobus trinervius (Moc. ex DC.) A.Gray Proc. Amer. Acad. Arts 15: 26 (1880)
Carelia arbutifolia Kuntze Revis. Gen. Pl. 1: 325 (1891)
Phania arbutifolia DC. Prodr. 5: 115 (1836)
Ageratum arbutifolium Kunth Nov. Gen. Sp. 4(15): 117 (ed. fol.) (1818)
Oxylobus subglabrus R.M.King & H.Rob. Phytologia 27: 385 (1974)
Phania trinervia Moc. ex DC. Prodr. 5: 115 (1836)
Stevia arbutifolia Willd. ex DC. Prodr. 5: 115 (1836)

Common names Top

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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 Central
      • Mexico Gulf
      • Mexico Southwest

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000115972
Tropicos 2716027
KEW urn:lsid:ipni.org:names:236232-1
The Plant List gcc-77396
Open Tree Of Life 7624431
NCBI Taxonomy 2773129
IPNI 236232-1
iNaturalist 279731
GBIF 5393432

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
Constituents of the genus Oxylobus Ferdinand Bohlmann, Lievy Hartono, Christa Zdero, Jasmin Jakupovic Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)83200-8

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 / Phenol ethers
(2R)-2-[4-methyl-2-(2-methylpropoxy)phenyl]-2-(2-methylpropoxymethyl)oxirane 162919328 Click to see CC1=CC(=C(C=C1)C2(CO2)COCC(C)C)OCC(C)C 292.40 unknown https://doi.org/10.1016/S0031-9422(00)83200-8
4-Methyl-2-(2-methylpropoxy)-1-[3-(2-methylpropoxy)prop-1-en-2-yl]benzene 14543618 Click to see CC1=CC(=C(C=C1)C(=C)COCC(C)C)OCC(C)C 276.40 unknown https://doi.org/10.1016/S0031-9422(00)83200-8
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Eudesmanolides, secoeudesmanolides, and derivatives
5a,9-dimethyl-3-methylidene-4,5,6,7,8,9b-hexahydro-3aH-benzo[g][1]benzofuran-2-one 3478505 Click to see CC1=C2C3C(CCC2(CCC1)C)C(=C)C(=O)O3 232.32 unknown https://doi.org/10.1016/S0031-9422(00)83200-8
Arbusculin B 161442 Click to see CC1=C2C3C(CCC2(CCC1)C)C(=C)C(=O)O3 232.32 unknown https://doi.org/10.1016/S0031-9422(00)83200-8
beta-Cyclocostunolide 442192 Click to see CC12CCCC(=C)C1C3C(CC2)C(=C)C(=O)O3 232.32 unknown https://doi.org/10.1016/S0031-9422(00)83200-8
Critonilide 325063 Click to see CC12CCCC(=C)C1C3C(CC2)C(=C)C(=O)O3 232.32 unknown https://doi.org/10.1016/S0031-9422(00)83200-8
> 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/S0031-9422(00)83200-8
(3R,3aS,6E,10E,11aS)-3,6,10-trimethyl-3a,4,5,8,9,11a-hexahydro-3H-cyclodeca[b]furan-2-one 14164874 Click to see CC1C2CCC(=CCCC(=CC2OC1=O)C)C 234.33 unknown https://doi.org/10.1016/S0031-9422(00)83200-8
3,6,10-trimethyl-3a,4,5,8,9,11a-hexahydro-3H-cyclodeca[b]furan-2-one 102769 Click to see CC1C2CCC(=CCCC(=CC2OC1=O)C)C 234.33 unknown https://doi.org/10.1016/S0031-9422(00)83200-8
Costunolide 5281437 Click to see CC1=CCCC(=CC2C(CC1)C(=C)C(=O)O2)C 232.32 unknown https://doi.org/10.1016/S0031-9422(00)83200-8
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
4-[3-(3,5-Dihydroxyphenyl)-4-hydroxy-6-[2-(4-hydroxyphenyl)ethenyl]-2,3-dihydro-1-benzofuran-2-yl]benzene-1,3-diol 73802098 Click to see C1=CC(=CC=C1C=CC2=CC(=C3C(C(OC3=C2)C4=C(C=C(C=C4)O)O)C5=CC(=CC(=C5)O)O)O)O 470.50 unknown https://doi.org/10.1016/S0031-9422(00)83200-8

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