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Parthenium fruticosum

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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 UUID643fc910e76da960776905
Scientific name Parthenium fruticosum
Authority Less. ex Schltdl. & Cham.
First published in Linnaea 5: 152. 1830.

Description Top

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Synonyms Top

Scientific name Authority First published in
Parthenium parviceps S.F.Blake Contr. U.S. Natl. Herb. 22: 607 (1924)
Parthenium fruticosum var. fruticosum Less. ex Schltdl. & Cham. 1830
Parthenium fruticosum var. trilobatum Rollins Contr. Gray Herb. 172: 31 (1950)

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
  • Northern America
    • Mexico
      • Mexico Gulf
      • Mexico Northeast
      • Mexico Southeast

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000027417
Tropicos 2726981
KEW urn:lsid:ipni.org:names:236506-1
The Plant List gcc-126500
Open Tree Of Life 5794483
IUCN Red List 163587450
IPNI 236506-1
iNaturalist 274029
GBIF 3086796
USDA GRIN 315275

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
Tetracyclic triterpenes from Parthenium fruticosum Cecilia Matsubara, Alfonso Romo de Vivar Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)80784-0
The sesquiterpene lactone chemistry of the genus Parthenium (compositae) Eloy Rodriguez, Hirosuke Yoshioka, Tom J. Mabry Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)89954-9
Pseudoguaianolides from Parthenium fruticosum Alfredo Ortega, Emma Maldonado Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(86)88027-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
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
(1S,3R,8R,11S,12S,14S,15R,16R)-14-hydroxy-15-[(2S,5S)-5-hydroxy-2,6,6-trimethyloxan-2-yl]-7,7,12,16-tetramethylpentacyclo[9.7.0.01,3.03,8.012,16]octadecan-6-one 101321354 Click to see CC1(C2CCC3C4(CC(C(C4(CCC35C2(C5)CCC1=O)C)C6(CCC(C(O6)(C)C)O)C)O)C)C 472.70 unknown https://doi.org/10.1016/S0031-9422(00)80784-0
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Ambrosanolides and secoambrosanolides
(6a-hydroxy-6-methyl-3-methylidene-2,9-dioxo-4,5,6,7,8,9b-hexahydro-3aH-azuleno[4,5-b]furan-9a-yl)methyl 2-methylpropanoate 163004374 Click to see CC1CCC2C(C3(C1(CCC3=O)O)COC(=O)C(C)C)OC(=O)C2=C 350.40 unknown https://doi.org/10.1016/0031-9422(86)88027-X
(6a-hydroxy-6-methyl-3-methylidene-2,9-dioxo-4,5,6,7,8,9b-hexahydro-3aH-azuleno[4,5-b]furan-9a-yl)methyl acetate 162961335 Click to see CC1CCC2C(C3(C1(CCC3=O)O)COC(=O)C)OC(=O)C2=C 322.40 unknown https://doi.org/10.1016/0031-9422(86)88027-X
(9-Acetyloxy-6a-hydroxy-6-methyl-3-methylidene-2-oxo-3a,4,5,6,7,8,9,9b-octahydroazuleno[4,5-b]furan-9a-yl)methyl acetate 14165784 Click to see CC1CCC2C(C3(C1(CCC3OC(=O)C)O)COC(=O)C)OC(=O)C2=C 366.40 unknown https://doi.org/10.1016/0031-9422(86)88027-X
(9a-hydroxy-6a-methyl-3-methylidene-2,9-dioxo-4,5,6,7,8,9b-hexahydro-3aH-azuleno[4,5-b]furan-6-yl)methyl 2-methylpropanoate 163046166 Click to see CC(C)C(=O)OCC1CCC2C(C3(C1(CCC3=O)C)O)OC(=O)C2=C 350.40 unknown https://doi.org/10.1016/S0031-9422(00)89954-9
(9a-Methyl-3-methylidene-2,9-dioxo-3a,4,5,6,6a,7,8,9b-octahydroazuleno[4,5-b]furan-6-yl)methyl 2-methylpropanoate 162963230 Click to see CC(C)C(=O)OCC1CCC2C(C3(C1CCC3=O)C)OC(=O)C2=C 334.40 unknown https://doi.org/10.1016/0031-9422(86)88027-X
https://doi.org/10.1016/S0031-9422(00)89954-9
[(3aR,6R,6aR,9aR,9bS)-9a-methyl-3-methylidene-2,9-dioxo-3a,4,5,6,6a,7,8,9b-octahydroazuleno[4,5-b]furan-6-yl]methyl 2-methylpropanoate 162963231 Click to see CC(C)C(=O)OCC1CCC2C(C3(C1CCC3=O)C)OC(=O)C2=C 334.40 unknown https://doi.org/10.1016/S0031-9422(00)89954-9
[(3aS,6R,6aS,9aR,9bS)-9a-hydroxy-6a-methyl-3-methylidene-2,9-dioxo-4,5,6,7,8,9b-hexahydro-3aH-azuleno[4,5-b]furan-6-yl]methyl 2-methylpropanoate 163046167 Click to see CC(C)C(=O)OCC1CCC2C(C3(C1(CCC3=O)C)O)OC(=O)C2=C 350.40 unknown https://doi.org/10.1016/S0031-9422(00)89954-9
[(3aS,6S,6aR,9aS,9bR)-6a-hydroxy-6-methyl-3-methylidene-2,9-dioxo-4,5,6,7,8,9b-hexahydro-3aH-azuleno[4,5-b]furan-9a-yl]methyl 2-methylpropanoate 163004375 Click to see CC1CCC2C(C3(C1(CCC3=O)O)COC(=O)C(C)C)OC(=O)C2=C 350.40 unknown https://doi.org/10.1016/0031-9422(86)88027-X
[(3aS,6S,6aR,9aS,9bR)-6a-hydroxy-6-methyl-3-methylidene-2,9-dioxo-4,5,6,7,8,9b-hexahydro-3aH-azuleno[4,5-b]furan-9a-yl]methyl acetate 101306775 Click to see CC1CCC2C(C3(C1(CCC3=O)O)COC(=O)C)OC(=O)C2=C 322.40 unknown https://doi.org/10.1016/S0031-9422(00)80784-0
https://doi.org/10.1016/0031-9422(86)88027-X
[(3aS,6S,6aR,9S,9aS,9bR)-6a,9-dihydroxy-6-methyl-3-methylidene-2-oxo-3a,4,5,6,7,8,9,9b-octahydroazuleno[4,5-b]furan-9a-yl]methyl acetate 14165786 Click to see CC1CCC2C(C3(C1(CCC3O)O)COC(=O)C)OC(=O)C2=C 324.40 unknown https://doi.org/10.1016/0031-9422(86)88027-X
[(3aS,6S,6aR,9S,9aS,9bR)-9-acetyloxy-6a-hydroxy-6-methyl-3-methylidene-2-oxo-3a,4,5,6,7,8,9,9b-octahydroazuleno[4,5-b]furan-9a-yl]methyl acetate 101306774 Click to see CC1CCC2C(C3(C1(CCC3OC(=O)C)O)COC(=O)C)OC(=O)C2=C 366.40 unknown https://doi.org/10.1016/0031-9422(86)88027-X
[(3aS,6S,6aS,9aR,9bR)-9a-methyl-3-methylidene-2,9-dioxo-3a,4,5,6,6a,7,8,9b-octahydroazuleno[4,5-b]furan-6-yl]methyl 2-methylpropanoate 101603212 Click to see CC(C)C(=O)OCC1CCC2C(C3(C1CCC3=O)C)OC(=O)C2=C 334.40 unknown https://doi.org/10.1016/0031-9422(86)88027-X
Tetraneurin A 174868 Click to see CC(=O)OCC1CCC2C(C3(C1(CCC3=O)O)C)OC(=O)C2=C 322.40 unknown https://doi.org/10.1016/0031-9422(86)88027-X
Tetraneurin D 579318 Click to see CC1CCC2C(C3(C1(CCC3O)O)COC(=O)C)OC(=O)C2=C 324.40 unknown https://doi.org/10.1016/0031-9422(86)88027-X
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(10S,13R,14R,16S,17R)-16-hydroxy-17-[(2S)-5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-4,4,10,13,14-pentamethyl-1,2,5,6,7,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-3-one 193673 Click to see CC1(C2CCC3=C(C2(CCC1=O)C)CCC4(C3(CC(C4C5(CCC(O5)C(C)(C)O)C)O)C)C)C 472.70 unknown https://doi.org/10.1016/S0031-9422(00)80784-0
(20S,24R)-Incanilin 139067831 Click to see CC1(C2CCC3=C(C2(CCC1=O)C)CCC4(C3(CC(C4C5(CCC(O5)C(C)(C)O)C)O)C)C)C 472.70 unknown https://doi.org/10.1016/S0031-9422(00)80784-0
(5R,10S,13R,14R,16S,17R)-16-hydroxy-17-[(2R,5S)-5-hydroxy-2,6,6-trimethyloxan-2-yl]-4,4,10,13,14-pentamethyl-1,2,5,6,7,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-3-one 101321353 Click to see CC1(C2CCC3=C(C2(CCC1=O)C)CCC4(C3(CC(C4C5(CCC(C(O5)(C)C)O)C)O)C)C)C 472.70 unknown https://doi.org/10.1016/S0031-9422(00)80784-0
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
[(1R,2S,9R,10R,11S)-11-acetyloxy-6-(hydroxymethyl)-2-methyl-7-oxo-8,14-dioxatetracyclo[7.4.1.01,10.05,9]tetradec-5-en-10-yl]methyl acetate 162844988 Click to see CC1CCC2=C(C(=O)OC23C4(C1(O3)CCC4OC(=O)C)COC(=O)C)CO 380.40 unknown https://doi.org/10.1016/0031-9422(86)88027-X
[11-Acetyloxy-6-(hydroxymethyl)-2-methyl-7-oxo-8,14-dioxatetracyclo[7.4.1.01,10.05,9]tetradec-5-en-10-yl]methyl acetate 162844987 Click to see CC1CCC2=C(C(=O)OC23C4(C1(O3)CCC4OC(=O)C)COC(=O)C)CO 380.40 unknown https://doi.org/10.1016/0031-9422(86)88027-X

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