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Podanthus ovatifolius

Podanthus ovatifolius - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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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 UUID643fcdb7dafdc010852460
Scientific name Podanthus ovatifolius
Authority Lag.
First published in Gen. Sp. Pl. : 24 (1816)

Description Top

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Synonyms Top

Scientific name Authority First published in
Podanthus gratus D.Don ex Sweet Hort. Brit. : 353 (1830)
Ogiera triplinervia Spreng. Syst. Veg. 3: 674 (1826)
Baccharis chilensis Weinm. Syll. Pl. Nov. ii. (1828) 21
Euxenia grata Cham. Horae Phys. Berol. 75. t. 16 (1820) (1820)
Euxenia ovalifolia Kuntze Revis. Gen. Pl. 1: 338 (1891)

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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000074903
Tropicos 2723314
KEW urn:lsid:ipni.org:names:238928-1
The Plant List gcc-31612
Open Tree Of Life 7605433
IPNI 238928-1
iNaturalist 623453
GBIF 3093210
USDA GRIN 29032

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
Anti-inflammatory Activity Vino Daniel Springer Berlin Heidelberg 12-Mar-2015
doi:10.1007/978-3-642-27728-3_42-1
Sesquiterpene lactones from Podanthus ovatifolius Sarah Gnecco, J.Philip Poyser, Mario Silva, Peter G. Sammes‡, Thomas W. Tyler Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(73)80456-X

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
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
(3R,3aS,10aR,10bR)-3a,6,9-trimethyl-3-propan-2-yl-2,3,4,5,7,8,10a,10b-octahydro-1H-benzo[e]azulene 23426489 Click to see CC1=CC2C3CCC(C3(CCC(=C2CC1)C)C)C(C)C 272.50 unknown https://doi.org/10.1016/0031-9422(73)80456-X
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Eudesmanolides, secoeudesmanolides, and derivatives
[(3aR,4R,5aR,6R,9aS,9bR)-6-hydroxy-5a-methyl-3,9-dimethylidene-2-oxo-3a,4,5,6,7,8,9a,9b-octahydrobenzo[g][1]benzofuran-4-yl] (Z)-2-methylbut-2-enoate 60125946 Click to see CC=C(C)C(=O)OC1CC2(C(CCC(=C)C2C3C1C(=C)C(=O)O3)O)C 346.40 unknown https://doi.org/10.1007/978-3-642-27728-3_42-1
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
(4-Hydroxy-10-methyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-6-yl)methyl acetate 3487854 Click to see CC1=CC2C(C(CC(=CCC1)COC(=O)C)O)C(=C)C(=O)O2 306.40 unknown https://doi.org/10.1016/0031-9422(73)80456-X
(8-Acetyloxy-4,9-dimethyl-14-methylidene-13-oxo-5,12-dioxatricyclo[9.3.0.04,6]tetradec-9-en-2-yl) 2-methylprop-2-enoate 161572 Click to see CC1=CC2C(C(CC3(C(O3)CC1OC(=O)C)C)OC(=O)C(=C)C)C(=C)C(=O)O2 390.40 unknown https://doi.org/10.1016/0031-9422(73)80456-X
[(1R,2R,4R,6R,8S,9Z,11S)-4,9-dimethyl-14-methylidene-2-(2-methylprop-2-enoyloxy)-13-oxo-5,12-dioxatricyclo[9.3.0.04,6]tetradec-9-en-8-yl] 2-methylprop-2-enoate 162993268 Click to see CC1=CC2C(C(CC3(C(O3)CC1OC(=O)C(=C)C)C)OC(=O)C(=C)C)C(=C)C(=O)O2 416.50 unknown https://doi.org/10.1016/0031-9422(73)80456-X
[(1R,2R,4R,6R,8S,9Z,11S)-8-acetyloxy-4,9-dimethyl-14-methylidene-13-oxo-5,12-dioxatricyclo[9.3.0.04,6]tetradec-9-en-2-yl] 2-methylprop-2-enoate 162994475 Click to see CC1=CC2C(C(CC3(C(O3)CC1OC(=O)C)C)OC(=O)C(=C)C)C(=C)C(=O)O2 390.40 unknown https://doi.org/10.1016/0031-9422(73)80456-X
[(1S,2R,4S,6R,8S,9Z,11S)-8-hydroxy-4,9-dimethyl-14-methylidene-13-oxo-5,12-dioxatricyclo[9.3.0.04,6]tetradec-9-en-2-yl] 2-methylprop-2-enoate 163010380 Click to see CC1=CC2C(C(CC3(C(O3)CC1O)C)OC(=O)C(=C)C)C(=C)C(=O)O2 348.40 unknown https://doi.org/10.1016/0031-9422(73)80456-X
[(3aR,4R,6Z,10E,11aS)-4-hydroxy-10-methyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-6-yl]methyl acetate 163024454 Click to see CC1=CC2C(C(CC(=CCC1)COC(=O)C)O)C(=C)C(=O)O2 306.40 unknown https://doi.org/10.1016/0031-9422(73)80456-X
[4,9-Dimethyl-14-methylidene-2-(2-methylprop-2-enoyloxy)-13-oxo-5,12-dioxatricyclo[9.3.0.04,6]tetradec-9-en-8-yl] 2-methylprop-2-enoate 162608 Click to see CC1=CC2C(C(CC3(C(O3)CC1OC(=O)C(=C)C)C)OC(=O)C(=C)C)C(=C)C(=O)O2 416.50 unknown https://doi.org/10.1016/0031-9422(73)80456-X
Deacetylovatifolin 11108215 Click to see CC1=CC2C(C(CC(=CCC1)CO)O)C(=C)C(=O)O2 264.32 unknown https://doi.org/10.1007/978-3-642-27728-3_42-1
Erioflorin 5382553 Click to see CC1=CC2C(C(CC3(C(O3)CC1O)C)OC(=O)C(=C)C)C(=C)C(=O)O2 348.40 unknown https://doi.org/10.1016/0031-9422(73)80456-X
Erioflorin acetate 5281443 Click to see CC1=CC2C(C(CC3(C(O3)CC1OC(=O)C)C)OC(=O)C(=C)C)C(=C)C(=O)O2 390.40 unknown https://doi.org/10.1016/0031-9422(73)80456-X
Erioflorin methacrylate 5281444 Click to see CC1=CC2C(C(CC3(C(O3)CC1OC(=O)C(=C)C)C)OC(=O)C(=C)C)C(=C)C(=O)O2 416.50 unknown https://doi.org/10.1016/0031-9422(73)80456-X
Ovatifolin 5281492 Click to see CC1=CC2C(C(CC(=CCC1)COC(=O)C)O)C(=C)C(=O)O2 306.40 unknown https://doi.org/10.1016/0031-9422(73)80456-X
https://doi.org/10.1007/978-3-642-27728-3_42-1

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