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Ondetia linearis

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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 UUID643fd01f74d29576773964
Scientific name Ondetia linearis
Authority Benth.
First published in Hooker's Icon. Pl. 12: t. 1112 (1872)

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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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-0000096394
Tropicos 2720014
KEW urn:lsid:ipni.org:names:235195-1
The Plant List gcc-52539
Open Tree Of Life 182172
NCBI Taxonomy 313933
IPNI 235195-1
iNaturalist 590781
GBIF 3103320
EOL 5120164

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)!
If you wish to see all the related articles click here.
Title Authors Publication Released IDs
Structures, Occurrences and Biosynthesis of 11,12,13-Tri-nor-Sesquiterpenes, an Intriguing Class of Bioactive Metabolites Coca-Ruíz V, Suárez I, Aleu J, Collado IG Plants (Basel) 14-Mar-2022
PMCID:PMC8949605
doi:10.3390/plants11060769
PMID:35336651
Constituents of Xerolekia speciosissima (L.) Anderb. (Inuleae), and Anti-Inflammatory Activity of 7,10-Diisobutyryloxy-8,9-epoxythymyl Isobutyrate Kłeczek N, Malarz J, Gierlikowska B, Kiss AK, Stojakowska A Molecules 23-Oct-2020
PMCID:PMC7660698
doi:10.3390/molecules25214913
PMID:33114240
Eremophilanolides, eudesmanolides, guaianolides and other constituents from Ondetia linearis C. Zdero, F. Bohlmann Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)97819-1

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
(3aR,4aR,5S,8aS,9aR)-8a-hydroxy-4a,5-dimethyl-3-methylidene-3a,4,5,6,9,9a-hexahydrobenzo[f][1]benzofuran-2-one 14357594 Click to see CC1CC=CC2(C1(CC3C(C2)OC(=O)C3=C)C)O 248.32 unknown https://doi.org/10.1016/S0031-9422(00)97819-1
(3aR,4aR,5S,8R,8aR,9aR)-8,8a-dihydroxy-4a,5-dimethyl-3-methylidene-3a,4,5,6,7,8,9,9a-octahydrobenzo[f][1]benzofuran-2-one 14357585 Click to see CC1CCC(C2(C1(CC3C(C2)OC(=O)C3=C)C)O)O 266.33 unknown https://doi.org/10.1016/S0031-9422(00)97819-1
(3aR,4aR,5S,8R,8aR,9aR)-8a-chloro-8-hydroxy-4a,5-dimethyl-3-methylidene-3a,4,5,6,7,8,9,9a-octahydrobenzo[f][1]benzofuran-2-one 14357590 Click to see CC1CCC(C2(C1(CC3C(C2)OC(=O)C3=C)C)Cl)O 284.78 unknown https://doi.org/10.1016/S0031-9422(00)97819-1
(3aR,4aR,5S,9aR)-4a,5-dimethyl-3-methylidene-3a,4,5,6,9,9a-hexahydrobenzo[f][1]benzofuran-2,7-dione 14357592 Click to see CC1CC(=O)C=C2C1(CC3C(C2)OC(=O)C3=C)C 246.30 unknown https://doi.org/10.1016/S0031-9422(00)97819-1
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Eudesmanolides, secoeudesmanolides, and derivatives
(3aR,4aR,8aR,9aR)-6-hydroxy-5,8a-dimethyl-3-methylidene-4,4a,7,8,9,9a-hexahydro-3aH-benzo[f][1]benzofuran-2-one 163105617 Click to see CC1=C(CCC2(C1CC3C(C2)OC(=O)C3=C)C)O 248.32 unknown https://doi.org/10.1016/S0031-9422(00)97819-1
(3aR,6R,8aR,9aR)-6-hydroxy-5,8a-dimethyl-3-methylidene-4,6,7,8,9,9a-hexahydro-3aH-benzo[f][1]benzofuran-2-one 14357562 Click to see CC1=C2CC3C(CC2(CCC1O)C)OC(=O)C3=C 248.32 unknown https://doi.org/10.1016/S0031-9422(00)97819-1
2alpha-Hydroxyalantolactone 125733 Click to see CC1CC(CC2(C1=CC3C(C2)OC(=O)C3=C)C)O 248.32 unknown https://doi.org/10.1016/S0031-9422(00)97819-1
Ivalin 65156 Click to see CC12CC(CC(=C)C1CC3C(C2)OC(=O)C3=C)O 248.32 unknown https://doi.org/10.1016/S0031-9422(00)97819-1
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones / Cyclohexenones
(4aR,5S,8S)-8-hydroxy-4a,5-dimethyl-3,4,5,6,7,8-hexahydronaphthalen-2-one 11735705 Click to see CC1CCC(C2=CC(=O)CCC12C)O 194.27 unknown https://doi.org/10.1016/S0031-9422(00)97819-1
(4aS,5S,7S,8aS)-7,8a-dihydroxy-4a,5-dimethyl-5,6,7,8-tetrahydro-1H-naphthalen-2-one 14357600 Click to see CC1CC(CC2(C1(C=CC(=O)C2)C)O)O 210.27 unknown https://doi.org/10.1016/S0031-9422(00)97819-1
> Organoheterocyclic compounds / Naphthofurans
(1R,3R,7R,9R,10S,12S,14S)-9-hydroxy-1,14-dimethyl-4-methylidene-6,11-dioxatetracyclo[7.5.0.03,7.010,12]tetradecan-5-one 14357596 Click to see CC1CC2C(O2)C3(C1(CC4C(C3)OC(=O)C4=C)C)O 264.32 unknown https://doi.org/10.1016/S0031-9422(00)97819-1
(1S,3R,6R,7R,9R,10R,11R,13R)-11-hydroxy-6,9,10-trimethyl-4,14-dioxatetracyclo[7.5.0.01,13.03,7]tetradecan-5-one 14357583 Click to see CC1C2CC3(C(C(CC4C3(O4)CC2OC1=O)O)C)C 266.33 unknown https://doi.org/10.1016/S0031-9422(00)97819-1
(1S,3R,7R,9R,10S,12S,13R)-12-hydroxy-9,10-dimethyl-6-methylidene-4,14-dioxatetracyclo[7.5.0.01,13.03,7]tetradecan-5-one 14357578 Click to see CC1CC(C2C3(C1(CC4C(C3)OC(=O)C4=C)C)O2)O 264.32 unknown https://doi.org/10.1016/S0031-9422(00)97819-1
(1S,3R,7R,9R,10S,13R)-9,10-dimethyl-6-methylidene-4,14-dioxatetracyclo[7.5.0.01,13.03,7]tetradecan-5-one 14357574 Click to see CC1CCC2C3(C1(CC4C(C3)OC(=O)C4=C)C)O2 248.32 unknown https://doi.org/10.1016/S0031-9422(00)97819-1
(1S,3R,9R,10R,13R)-6-(hydroxymethyl)-9,10-dimethyl-4,14-dioxatetracyclo[7.5.0.01,13.03,7]tetradec-6-en-5-one 162909783 Click to see CC1CCC2C3(C1(CC4=C(C(=O)OC4C3)CO)C)O2 264.32 unknown https://doi.org/10.1016/S0031-9422(00)97819-1
> Uncategorized
2-[(1aS,4R,4aS,6S,8aR)-4,4a-dimethyl-1a,2,3,4,5,6,7,8-octahydronaphtho[1,8a-b]oxiren-6-yl]prop-2-enoic acid 163055935 Click to see CC1CCC2C3(C1(CC(CC3)C(=C)C(=O)O)C)O2 250.33 unknown https://doi.org/10.1016/S0031-9422(00)97819-1

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