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Podanthus mitiqui

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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 UUID643fc9acabbe9446629225
Scientific name Podanthus mitiqui
Authority Lindl.
First published in Hort. Brit. : 488 (1830)

Description Top

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Synonyms Top

Scientific name Authority First published in
Ogiera triplinervia Bertero ex DC. Prodr. 5: 501, 546 (1836)
Euxenia mitiqui DC. Prodr. 5: 501 (1836)

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-0000032493
Tropicos 2723313
KEW urn:lsid:ipni.org:names:238927-1
The Plant List gcc-131420
Open Tree Of Life 90377
NCBI Taxonomy 183301
IPNI 238927-1
iNaturalist 715313
GBIF 3093214
USDA GRIN 29031

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
TrypanocidalActivity of Natural Sesquiterpenoids Involves Mitochondrial Dysfunction, ROS Production and Autophagic Phenotype in Trypanosoma cruzi Bombaça AC, Von Dossow D, Barbosa JM, Paz C, Burgos V, Menna-Barreto RF Molecules 28-Oct-2018
PMCID:PMC6278339
doi:10.3390/molecules23112800
PMID:30373326
Postfire responses of the woody flora of Central Chile: Insights from a germination experiment Gómez-González S, Paula S, Cavieres LA, Pausas JG PLoS One 12-Jul-2017
PMCID:PMC5507535
doi:10.1371/journal.pone.0180661
PMID:28704449
Crystal structure of erioflorin isolated from Podanthus mitiqui (L.) Paz C, Ortiz L, Schilde U Acta Crystallogr E Crystallogr Commun 07-Feb-2017
PMCID:PMC5347047
doi:10.1107/S2056989017001700
PMID:28316802
Leaf traits in Chilean matorral: sclerophylly within, among, and beyond matorral, and its environmental determinants Read J, Sanson G, Pérez Trautmann MF Ecol Evol 03-Feb-2016
PMCID:PMC4739351
doi:10.1002/ece3.1970
PMID:26865953
Sesquiterpene lactones of Podanthus mitiqui Maritza Hoeneisen, Mitsuaki Kodama, Shô Itô Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)98569-8
Sesquiterpene lactones of Podanthus mitiqui Maritza Hoeneisen, Mario Sicva, Ferdinand Bohlmann Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)83964-3
Comparative study of ovatifolin antioxidant and growth inhibition activities. Cespedes CL, Hoeneisen M, Bittner M, Becerra J, Silva M J Agric Food Chem 01-Sep-2001
doi:10.1021/JF010351C
PMID:11559118

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/S0031-9422(00)83964-3
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Eudesmanolides, secoeudesmanolides, and derivatives
(6-Hydroxy-5a-methyl-3,9-dimethylidene-2-oxo-3a,4,5,6,7,8,9a,9b-octahydrobenzo[g][1]benzofuran-4-yl) 2-methylbut-2-enoate 434776 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/10.1016/S0031-9422(00)83964-3
[(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/10.1016/S0031-9422(00)83964-3
https://doi.org/10.1021/JF010351C
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
(3aR,4R,6Z,10E,11aR)-4-hydroxy-6-(1-hydroxyethenoxymethyl)-10-methyl-3-methylidene-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-2-one 163044788 Click to see CC1=CC2C(C(CC(=CCC1)COC(=C)O)O)C(=C)C(=O)O2 306.40 unknown https://doi.org/10.1016/S0031-9422(00)83964-3
[(1R,2R,4R,6R,8S,9Z,11R)-4,9-dimethyl-14-methylidene-8-(2-methylprop-2-enoyloxy)-13-oxo-5,12-dioxatricyclo[9.3.0.04,6]tetradec-9-en-2-yl] (Z)-2-methylbut-2-enoate 163018188 Click to see CC=C(C)C(=O)OC1CC2(C(O2)CC(C(=CC3C1C(=C)C(=O)O3)C)OC(=O)C(=C)C)C 430.50 unknown https://doi.org/10.1016/S0031-9422(00)98569-8
[(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/S0031-9422(00)83964-3
[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/S0031-9422(00)98569-8
[4,9-Dimethyl-14-methylidene-8-(2-methylprop-2-enoyloxy)-13-oxo-5,12-dioxatricyclo[9.3.0.04,6]tetradec-9-en-2-yl] 2-methylbut-2-enoate 163018187 Click to see CC=C(C)C(=O)OC1CC2(C(O2)CC(C(=CC3C1C(=C)C(=O)O3)C)OC(=O)C(=C)C)C 430.50 unknown https://doi.org/10.1016/S0031-9422(00)98569-8
4-Hydroxy-6-(1-hydroxyethenoxymethyl)-10-methyl-3-methylidene-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-2-one 163044787 Click to see CC1=CC2C(C(CC(=CCC1)COC(=C)O)O)C(=C)C(=O)O2 306.40 unknown https://doi.org/10.1016/S0031-9422(00)83964-3
4-Hydroxy-6-(hydroxymethyl)-10-methyl-3-methylidene-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-2-one 72656715 Click to see CC1=CC2C(C(CC(=CCC1)CO)O)C(=C)C(=O)O2 264.32 unknown https://doi.org/10.1016/S0031-9422(00)83964-3
Deacetylovatifolin 11108215 Click to see CC1=CC2C(C(CC(=CCC1)CO)O)C(=C)C(=O)O2 264.32 unknown https://doi.org/10.1021/JF010351C
https://doi.org/10.1016/S0031-9422(00)83964-3
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/S0031-9422(00)98569-8
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/10.1021/JF010351C

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