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Jurinea eriobasis

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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 UUID643fc5d264603473443464
Scientific name Jurinea eriobasis
Authority DC.
First published in Prodr. 6: 675 (1838)

Description Top

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Synonyms Top

Scientific name Authority First published in
Derderia eriobasis (DC.) Jaub. & Spach Ill. Pl. Orient. 2(19-20): 97, t. 179 (1847)
Stechmannia eriobasis (DC.) Soják Novit. Bot. Delect. Seminum Horti Bot. Univ. Carol. Prag. 1962: 48 (1962) (1962)

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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000000397
Tropicos 50295012
KEW urn:lsid:ipni.org:names:226921-1
The Plant List gcc-100377
Open Tree Of Life 3894774
NCBI Taxonomy 1496622
IPNI 226921-1
GBIF 5392466

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
Germacranolides from Jurinea eriobasis A. Rustaiyan, M. Ganji Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(88)80707-6

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
[(1R,2S,4S,6R,9Z,11R)-4-(acetyloxymethyl)-9-(hydroxymethyl)-14-methylidene-13-oxo-5,12-dioxatricyclo[9.3.0.04,6]tetradec-9-en-2-yl] 2-(hydroxymethyl)prop-2-enoate 163045630 Click to see CC(=O)OCC12CC(C3C(C=C(CCC1O2)CO)OC(=O)C3=C)OC(=O)C(=C)CO 422.40 unknown https://doi.org/10.1016/0031-9422(88)80707-6
[(1S,2R,4S,7Z,10S,11R)-8-(acetyloxymethyl)-4-(hydroxymethyl)-12-methylidene-13-oxo-3,14-dioxatricyclo[9.3.0.02,4]tetradec-7-en-10-yl] 2-(hydroxymethyl)prop-2-enoate 162878033 Click to see CC(=O)OCC1=CCCC2(C(O2)C3C(C(C1)OC(=O)C(=C)CO)C(=C)C(=O)O3)CO 422.40 unknown https://doi.org/10.1016/0031-9422(88)80707-6
[(3aR,4S,6Z,10Z,11aR)-6-(acetyloxymethyl)-10-(hydroxymethyl)-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-4-yl] 2-(hydroxymethyl)prop-2-enoate 162922684 Click to see CC(=O)OCC1=CCCC(=CC2C(C(C1)OC(=O)C(=C)CO)C(=C)C(=O)O2)CO 406.40 unknown https://doi.org/10.1016/0031-9422(88)80707-6
[(3aR,4S,6Z,10Z,11aR)-6,10-bis(hydroxymethyl)-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-4-yl] 2-(hydroxymethyl)prop-2-enoate 162878174 Click to see C=C1C2C(CC(=CCCC(=CC2OC1=O)CO)CO)OC(=O)C(=C)CO 364.40 unknown https://doi.org/10.1016/0031-9422(88)80707-6
[(3aR,4S,6Z,10Z,11aR)-6,10-bis(hydroxymethyl)-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-4-yl] 2-methylprop-2-enoate 102090434 Click to see CC(=C)C(=O)OC1CC(=CCCC(=CC2C1C(=C)C(=O)O2)CO)CO 348.40 unknown https://doi.org/10.1016/0031-9422(88)80707-6
[4-(Acetyloxymethyl)-9-(hydroxymethyl)-14-methylidene-13-oxo-5,12-dioxatricyclo[9.3.0.04,6]tetradec-9-en-2-yl] 2-(hydroxymethyl)prop-2-enoate 163045629 Click to see CC(=O)OCC12CC(C3C(C=C(CCC1O2)CO)OC(=O)C3=C)OC(=O)C(=C)CO 422.40 unknown https://doi.org/10.1016/0031-9422(88)80707-6
[6-(Acetyloxymethyl)-10-(hydroxymethyl)-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-4-yl] 2-(hydroxymethyl)prop-2-enoate 162922683 Click to see CC(=O)OCC1=CCCC(=CC2C(C(C1)OC(=O)C(=C)CO)C(=C)C(=O)O2)CO 406.40 unknown https://doi.org/10.1016/0031-9422(88)80707-6
[6,10-Bis(hydroxymethyl)-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-4-yl] 2-(hydroxymethyl)prop-2-enoate 162878173 Click to see C=C1C2C(CC(=CCCC(=CC2OC1=O)CO)CO)OC(=O)C(=C)CO 364.40 unknown https://doi.org/10.1016/0031-9422(88)80707-6
[6,10-Bis(hydroxymethyl)-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-4-yl] 2-methylprop-2-enoate 162993763 Click to see CC(=C)C(=O)OC1CC(=CCCC(=CC2C1C(=C)C(=O)O2)CO)CO 348.40 unknown https://doi.org/10.1016/0031-9422(88)80707-6
[6,10-Bis(hydroxymethyl)-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-4-yl] 2-methylpropanoate 325863 Click to see CC(C)C(=O)OC1CC(=CCCC(=CC2C1C(=C)C(=O)O2)CO)CO 350.40 unknown https://doi.org/10.1016/0031-9422(88)80707-6
Alatolide 5281421 Click to see CC(C)C(=O)OC1CC(=CCCC(=CC2C1C(=C)C(=O)O2)CO)CO 350.40 unknown https://doi.org/10.1016/0031-9422(88)80707-6
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Aryl-phenylketones
Isofunicone 10571422 Click to see CC=CC1=C(C(=O)C(=CO1)C(=O)C2=C(C=C(C=C2OC)O)C(=O)OC)OC 374.30 unknown https://doi.org/10.1016/0031-9422(88)80707-6

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