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Ursinia saxatilis

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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 UUID643fcf7888b28629361406
Scientific name Ursinia saxatilis
Authority N.E.Br.
First published in Bull. Misc. Inform. Kew 1894: 355 (1894)

Description Top

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Synonyms Top

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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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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Africa
    • Southern Africa
      • Cape Provinces
      • Free State
      • Kwazulu-Natal
      • Lesotho
      • Northern Provinces
      • Swaziland

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000090634
Tropicos 2722016
KEW urn:lsid:ipni.org:names:257142-1
The Plant List gcc-46920
Open Tree Of Life 7597314
IPNI 257142-1
iNaturalist 595920
GBIF 3089039
EOL 6276585

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)!
Title Authors Publication Released IDs
Four guaianolides, a eudesmanolide and a germacranolide from Ursinia saxatilis Ferdinand Bohlmann, Naleen Borthakur, Jasmin Jakupovic, Joachim Pickard Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(82)80141-6

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 / Fatty Acyls / Fatty acid esters
(9-Hydroxy-3,6,9-trimethyl-2-oxo-3,3a,4,5,9a,9b-hexahydroazuleno[4,5-b]furan-4-yl) 2-methylbutanoate 162951949 Click to see CCC(C)C(=O)OC1CC(=C2C=CC(C2C3C1C(C(=O)O3)C)(C)O)C 348.40 unknown https://doi.org/10.1016/0031-9422(82)80141-6
(9-Hydroxy-3,6,9-trimethyl-2-oxo-3,3a,4,5,9a,9b-hexahydroazuleno[4,5-b]furan-4-yl) 3-methylbutanoate 162895428 Click to see CC1C2C(CC(=C3C=CC(C3C2OC1=O)(C)O)C)OC(=O)CC(C)C 348.40 unknown https://doi.org/10.1016/0031-9422(82)80141-6
[(3R,3aR,4S,9S,9aS,9bS)-9-hydroxy-3,6,9-trimethyl-2-oxo-3,3a,4,5,9a,9b-hexahydroazuleno[4,5-b]furan-4-yl] (2R)-2-methylbutanoate 162951950 Click to see CCC(C)C(=O)OC1CC(=C2C=CC(C2C3C1C(C(=O)O3)C)(C)O)C 348.40 unknown https://doi.org/10.1016/0031-9422(82)80141-6
[(3R,3aR,4S,9S,9aS,9bS)-9-hydroxy-3,6,9-trimethyl-2-oxo-3,3a,4,5,9a,9b-hexahydroazuleno[4,5-b]furan-4-yl] 3-methylbutanoate 162895429 Click to see CC1C2C(CC(=C3C=CC(C3C2OC1=O)(C)O)C)OC(=O)CC(C)C 348.40 unknown https://doi.org/10.1016/0031-9422(82)80141-6
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Eudesmanolides, secoeudesmanolides, and derivatives
(1S,3R,7R,9R,10S,12R)-1,10-dimethyl-6-methylidene-4,11-dioxatetracyclo[7.5.0.03,7.010,12]tetradec-13-en-5-one 102059812 Click to see CC12CC3C(CC1C4(C(O4)C=C2)C)C(=C)C(=O)O3 246.30 unknown https://doi.org/10.1016/0031-9422(82)80141-6
1,10-Dimethyl-6-methylidene-4,11-dioxatetracyclo[7.5.0.03,7.010,12]tetradec-13-en-5-one 163011296 Click to see CC12CC3C(CC1C4(C(O4)C=C2)C)C(=C)C(=O)O3 246.30 unknown https://doi.org/10.1016/0031-9422(82)80141-6
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
(5-Acetyloxy-6,10-dimethyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-9-yl) acetate 163031545 Click to see CC1=CCC(C(=CC2C(CC1OC(=O)C)C(=C)C(=O)O2)C)OC(=O)C 348.40 unknown https://doi.org/10.1016/0031-9422(82)80141-6
[(3aS,5R,6E,9S,10E,11aS)-5-acetyloxy-6,10-dimethyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-9-yl] acetate 163031547 Click to see CC1=CCC(C(=CC2C(CC1OC(=O)C)C(=C)C(=O)O2)C)OC(=O)C 348.40 unknown https://doi.org/10.1016/0031-9422(82)80141-6
[(3aS,5S,6E,9S,10E,11aR)-5-acetyloxy-6,10-dimethyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-9-yl] acetate 163031546 Click to see CC1=CCC(C(=CC2C(CC1OC(=O)C)C(=C)C(=O)O2)C)OC(=O)C 348.40 unknown https://doi.org/10.1016/0031-9422(82)80141-6
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Lup-20(29)-en-3-ol, (3beta)- 521518 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1016/0031-9422(82)80141-6
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1016/0031-9422(82)80141-6
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(82)80141-6
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(82)80141-6
> Organoheterocyclic compounds / Heteroaromatic compounds
2-[(E)-5-(furan-3-yl)-2-methylpent-2-enyl]-4-methylfuran 15558825 Click to see CC1=COC(=C1)CC(=CCCC2=COC=C2)C 230.30 unknown https://doi.org/10.1016/0031-9422(82)80141-6
2-[5-(Furan-3-yl)-2-methylpent-2-enyl]-4-methylfuran 85786007 Click to see CC1=COC(=C1)CC(=CCCC2=COC=C2)C 230.30 unknown https://doi.org/10.1016/0031-9422(82)80141-6
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(3R,3aS,9aR,9bR)-9a-hydroxy-3,6,9-trimethyl-3a,4,5,9b-tetrahydro-3H-azuleno[4,5-b]furan-2,7-dione 162976899 Click to see CC1C2CCC(=C3C(=O)C=C(C3(C2OC1=O)O)C)C 262.30 unknown https://doi.org/10.1016/0031-9422(82)80141-6
9a-hydroxy-3,6,9-trimethyl-3a,4,5,9b-tetrahydro-3H-azuleno[4,5-b]furan-2,7-dione 13818989 Click to see CC1C2CCC(=C3C(=O)C=C(C3(C2OC1=O)O)C)C 262.30 unknown https://doi.org/10.1016/0031-9422(82)80141-6

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