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Tamaulipa azurea

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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 UUID643fd2292e737206769847
Scientific name Tamaulipa azurea
Authority (DC.) R.M.King & H.Rob.
First published in Phytologia 22: 154 (1971)

Description Top

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Synonyms Top

Scientific name Authority First published in
Eupatorium azureum DC. Prodr. 5: 168 (1836)
Eupatorium ageratifolium var. acuminatum Coulter Contr. U.S. Natl. Herb. 1: 39. 1890.
Kyrstenia acuta Greene Leafl. Bot. Observ. Crit. 1: 11 (1903)
Eupatorium ageratifolium var. acuminatum J.M.Coult. Contr. U.S. Natl. Herb. 1: 39 (1890)

Common names Top

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Language Common/alternative name
English blue boneset

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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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Northern America
    • Mexico
      • Mexico Gulf
      • Mexico Northeast
    • South-central U.S.A.
      • Texas

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000121304
USDA Plants TAAZ
Tropicos 2711175
KEW urn:lsid:ipni.org:names:249254-2
The Plant List gcc-82529
Open Tree Of Life 731325
NCBI Taxonomy 506632
Nature Serve 2.153402
IPNI 249254-2
iNaturalist 169551
GBIF 3134596
EOL 503292

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
Seco-labdanes fromTamaulipa azurea and constituents from other eupatorieae C. Zdero, F. Bohlmann, R.M. King Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(91)83025-G
Epi-friedelinol and taraxasterol acetate from Eupatorium azureum X.A. Domínguez, P. Rojas, Ma.Del C. Dueñas Wiarco, S. Escarria Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)84661-0

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 / Sesquiterpenoids
(Z)-5-(furan-3-yl)-2-[2-[(1S)-2,6,6-trimethyl-4-oxocyclohex-2-en-1-yl]ethyl]pent-2-enoic acid 15139552 Click to see CC1=CC(=O)CC(C1CCC(=CCCC2=COC=C2)C(=O)O)(C)C 330.40 unknown https://doi.org/10.1016/0031-9422(91)83025-G
1,4,8-Cycloundecatriene, 2,6,6,9-tetramethyl-, (1E,4E,8E)- 23204 Click to see CC1=CCC(C=CCC(=CCC1)C)(C)C 204.35 unknown https://doi.org/10.1016/0031-9422(91)83025-G
5-(Furan-3-yl)-2-[2-(2,6,6-trimethyl-4-oxocyclohex-2-en-1-yl)ethyl]pent-2-enoic acid 163038916 Click to see CC1=CC(=O)CC(C1CCC(=CCCC2=COC=C2)C(=O)O)(C)C 330.40 unknown https://doi.org/10.1016/0031-9422(91)83025-G
Humulene 5281520 Click to see CC1=CCC(C=CCC(=CCC1)C)(C)C 204.35 unknown https://doi.org/10.1016/0031-9422(91)83025-G
> 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/10.1016/0031-9422(91)83025-G
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/10.1016/0031-9422(91)83025-G
Germacrene D 5317570 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown https://doi.org/10.1016/0031-9422(91)83025-G
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
[(4aR,6aS,6aR,6bR,8aR,12aS,14aS,14bR)-4,4,6a,6b,8a,12,14b-heptamethyl-11-methylidene-1,2,3,4a,5,6,6a,7,8,9,10,12,12a,13,14,14a-hexadecahydropicen-3-yl] acetate 137704689 Click to see CC1C2C3CCC4C5(CCC(C(C5CCC4(C3(CCC2(CCC1=C)C)C)C)(C)C)OC(=O)C)C 468.80 unknown https://doi.org/10.1016/0031-9422(91)83025-G
Lup-20(29)-en-3beta-ol, acetate 323074 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)OC(=O)C)C)C 468.80 unknown https://doi.org/10.1016/0031-9422(91)83025-G
Lupeol acetate 92157 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)OC(=O)C)C)C 468.80 unknown https://doi.org/10.1016/0031-9422(91)83025-G
Taraxasterol acetate 13889352 Click to see CC1C2C3CCC4C5(CCC(C(C5CCC4(C3(CCC2(CCC1=C)C)C)C)(C)C)OC(=O)C)C 468.80 unknown https://doi.org/10.1016/0031-9422(91)83025-G
https://doi.org/10.1016/S0031-9422(00)84661-0
Taraxasterol, acetate 344468 Click to see CC1C2C3CCC4C5(CCC(C(C5CCC4(C3(CCC2(CCC1=C)C)C)C)(C)C)OC(=O)C)C 468.80 unknown https://doi.org/10.1016/0031-9422(91)83025-G
https://doi.org/10.1016/S0031-9422(00)84661-0
> Organoheterocyclic compounds / Pyrans / Pyranones and derivatives / Dihydropyranones
(2R)-2-(furan-3-yl)-5-[2-[(1R)-1-hydroxy-2,6,6-trimethyl-4-oxocyclohex-2-en-1-yl]ethyl]-2,3-dihydropyran-6-one 15139551 Click to see CC1=CC(=O)CC(C1(CCC2=CCC(OC2=O)C3=COC=C3)O)(C)C 344.40 unknown https://doi.org/10.1016/0031-9422(91)83025-G
(2R)-2-(furan-3-yl)-5-[2-[(1S)-2,6,6-trimethyl-4-oxocyclohex-2-en-1-yl]ethyl]-2,3-dihydropyran-6-one 13858019 Click to see CC1=CC(=O)CC(C1CCC2=CCC(OC2=O)C3=COC=C3)(C)C 328.40 unknown https://doi.org/10.1016/0031-9422(91)83025-G
2-(Furan-3-yl)-5-[2-(1-hydroxy-2,6,6-trimethyl-4-oxocyclohex-2-en-1-yl)ethyl]-2,3-dihydropyran-6-one 162939601 Click to see CC1=CC(=O)CC(C1(CCC2=CCC(OC2=O)C3=COC=C3)O)(C)C 344.40 unknown https://doi.org/10.1016/0031-9422(91)83025-G
2-(Furan-3-yl)-5-[2-(2,6,6-trimethyl-4-oxocyclohex-2-en-1-yl)ethyl]-2,3-dihydropyran-6-one 13858017 Click to see CC1=CC(=O)CC(C1CCC2=CCC(OC2=O)C3=COC=C3)(C)C 328.40 unknown https://doi.org/10.1016/0031-9422(91)83025-G

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