Podachaenium eminens - Unknown
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Internal ID UUID643fd35032840276057684
Scientific name Podachaenium eminens
Authority Baill.
First published in Flora 44: 557 (1861)

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Synonyms Top

Scientific name Authority First published in
Zaluzania eminens hort. ex F.T.Hubb. Stand. Cycl. Hort. 2724 (1916), in syn. (1916)
Podachaenium andinum André Rev. Hort. (Paris) 64: 414 (1892)
Dicalymma fragrans Lem. Ill. Hort. ii. (1855) Misc. 37
Podachaenium paniculatum Benth. Vidensk. Meddel. Naturhist. Foren. Kjøbenhavn 1852(5-7): 99. 1853 [1852 publ. 1853]
Ferdinanda eminens Lag. Gen. Sp. Pl. [Lagasca] 31, t. 2. 1816
Podachaenium paniculatum Benth. ex Oerst. 99 1852

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Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Northern America
    • Mexico
      • Mexico Central
      • Mexico Gulf
      • Mexico Northeast
      • Mexico Northwest
      • Mexico Southeast
      • Mexico Southwest
  • Southern America
    • Central America
      • Belize
      • Costa Rica
      • El Salvador
      • Guatemala
      • Honduras
      • Nicaragua
    • Western South America
      • Colombia

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000130918
Tropicos 2701151
KEW urn:lsid:ipni.org:names:238923-1
The Plant List gcc-91802
Open Tree Of Life 931870
NCBI Taxonomy 121888
IUCN Red List 136783867
IPNI 238923-1
iNaturalist 288686
GBIF 3149837
USDA GRIN 29027

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
Natural and Historical Heritage of the Lisbon Botanical Gardens: An Integrative Approach with Tree Collections Cunha AR, Soares AL, Brilhante M, Arsénio P, Vasconcelos T, Espírito-Santo D, Duarte MC, Romeiras MM Plants (Basel) 04-Jul-2021
PMCID:PMC8309379
doi:10.3390/plants10071367
PMID:34371570
Towards Conservation of the Remarkably High Number of Daisy Trees (Asteraceae) in Mexico Redonda-Martínez R, Pliscoff P, Moreira-Muñoz A, Martínez Salas EM, Samain MS Plants (Basel) 12-Mar-2021
PMCID:PMC8000269
doi:10.3390/plants10030534
PMID:33809003
New species and host records of New World, mostly Neotropical, opiine Braconidae (Hymenoptera) reared from flower-infesting, stem-galling, and stem-mining Tephritidae (Diptera) Wharton R, Norrbom AL Zookeys 13-Nov-2013
PMCID:PMC3837405
doi:10.3897/zookeys.349.5914
PMID:24294078
ChemInform Abstract: A Costic Acid Guaianyl Ester and Other Constituents of Podachaenium eminens. A. ORTEGA, R. A. TOSCANO, E. MALDONADO Wiley 24-Jun-2010
doi:10.1002/CHIN.199908196
Anti-Inflammatory properties of Salograviolide A purified from Lebanese plant Centaurea ainetensis Al-Saghir J, Al-Ashi R, Salloum R, Saliba NA, Talhouk RS, Homaidan FR BMC Complement Altern Med 23-Sep-2009
PMCID:PMC2761300
doi:10.1186/1472-6882-9-36
PMID:19775456
Differential enhancement of leukaemia cell differentiation without elevation of intracellular calcium by plant-derived sesquiterpene lactone compounds Kim SH, Danilenko M, Kim TS Br J Pharmacol 25-Aug-2008
PMCID:PMC2597232
doi:10.1038/bjp.2008.319
PMID:18724384
Molecular Targets of Dietary Polyphenols with Anti-inflammatory Properties Yoon JH, Baek SJ Yonsei Med J 31-Oct-2005
PMCID:PMC2562783
doi:10.3349/ymj.2005.46.5.585
PMID:16259055
A costic acid guaianyl ester and other constituents of podachaenium EMINENSfn1fn1Contribution No. 1658 of Instituto de Química, UNAM. Alfredo Ortega, Rubén A.Toscanoand Emma Maldonado Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(98)00309-4
Inhibition of the transcription factor NF-kappa B by sesquiterpene lactones from Podachaenium eminens. Castro V, Murillo R, Klaas CA, Meunier C, Mora G, Pahl HL, Merfort I Planta Med 01-Oct-2000
doi:10.1055/S-2000-8649
PMID:11105560

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
(6,9-dimethyl-3-methylidene-2,7-dioxo-4,5,9a,9b-tetrahydro-3aH-azuleno[4,5-b]furan-8-yl) 2-(4a-methyl-8-methylidene-1,2,3,4,5,6,7,8a-octahydronaphthalen-2-yl)prop-2-enoate 163002494 Click to see CC1=C2C(C3C(CC1)C(=C)C(=O)O3)C(=C(C2=O)OC(=O)C(=C)C4CCC5(CCCC(=C)C5C4)C)C 476.60 unknown https://doi.org/10.1055/S-2000-8649
(9-Hydroxy-6,9-dimethyl-3-methylidene-2,7-dioxo-3a,4,5,8,9a,9b-hexahydroazuleno[4,5-b]furan-8-yl) 2-(4a-methyl-8-methylidene-1,2,3,4,5,6,7,8a-octahydronaphthalen-2-yl)prop-2-enoate 75297592 Click to see CC1=C2C(C3C(CC1)C(=C)C(=O)O3)C(C(C2=O)OC(=O)C(=C)C4CCC5(CCCC(=C)C5C4)C)(C)O 494.60 unknown https://doi.org/10.1055/S-2000-8649
[(3aS,8R,9S,9aS,9bS)-9-hydroxy-6,9-dimethyl-3-methylidene-2,7-dioxo-3a,4,5,8,9a,9b-hexahydroazuleno[4,5-b]furan-8-yl] 2-[(2R,4aR,8aS)-4a-methyl-8-methylidene-1,2,3,4,5,6,7,8a-octahydronaphthalen-2-yl]prop-2-enoate 15828229 Click to see CC1=C2C(C3C(CC1)C(=C)C(=O)O3)C(C(C2=O)OC(=O)C(=C)C4CCC5(CCCC(=C)C5C4)C)(C)O 494.60 unknown https://doi.org/10.1002/CHIN.199908196
[(3aS,8S,9S,9aS,9bS)-9-hydroxy-6,9-dimethyl-3-methylidene-2,7-dioxo-3a,4,5,8,9a,9b-hexahydroazuleno[4,5-b]furan-8-yl] 2-[(2S,4aS,8aR)-4a-methyl-8-methylidene-1,2,3,4,5,6,7,8a-octahydronaphthalen-2-yl]prop-2-enoate 162849057 Click to see CC1=C2C(C3C(CC1)C(=C)C(=O)O3)C(C(C2=O)OC(=O)C(=C)C4CCC5(CCCC(=C)C5C4)C)(C)O 494.60 unknown https://doi.org/10.1055/S-2000-8649
[(3aS,9aS,9bS)-6,9-dimethyl-3-methylidene-2,7-dioxo-4,5,9a,9b-tetrahydro-3aH-azuleno[4,5-b]furan-8-yl] 2-[(2S,4aS,8aR)-4a-methyl-8-methylidene-1,2,3,4,5,6,7,8a-octahydronaphthalen-2-yl]prop-2-enoate 102011241 Click to see CC1=C2C(C3C(CC1)C(=C)C(=O)O3)C(=C(C2=O)OC(=O)C(=C)C4CCC5(CCCC(=C)C5C4)C)C 476.60 unknown https://doi.org/10.1055/S-2000-8649
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Eudesmanolides, secoeudesmanolides, and derivatives
(3aR,5aR,9R,9aS,9bR)-3a,9-dihydroxy-5a,9-dimethyl-3-methylidene-5,6,7,8,9a,9b-hexahydro-4H-benzo[g][1]benzofuran-2-one 15828228 Click to see CC12CCCC(C1C3C(CC2)(C(=C)C(=O)O3)O)(C)O 266.33 unknown https://doi.org/10.1002/CHIN.199908196
https://doi.org/10.1016/S0031-9422(98)00309-4
Santamarine 188297 Click to see CC1=CCC(C2(C1C3C(CC2)C(=C)C(=O)O3)C)O 248.32 unknown https://doi.org/10.1055/S-2000-8649
Sesquiterpene lactone CP-1 331391 Click to see CC1=CCC(C2(C1C3C(CC2)C(=C)C(=O)O3)C)O 248.32 unknown https://doi.org/10.1055/S-2000-8649
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
(6,10-Dimethyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-9-yl) acetate 71437691 Click to see CC1=CCC(C(=CC2C(CC1)C(=C)C(=O)O2)C)OC(=O)C 290.40 unknown https://doi.org/10.1055/S-2000-8649
https://doi.org/10.1016/S0031-9422(98)00309-4
3-Acetoxycostunolide 44409565 Click to see CC1=CCC(C(=CC2C(CC1)C(=C)C(=O)O2)C)OC(=O)C 290.40 unknown https://doi.org/10.1055/S-2000-8649
https://doi.org/10.1016/S0031-9422(98)00309-4
3,4-Epoxydehydroleucodin 10422717 Click to see CC1=C2C(C3C(CC1)C(=C)C(=O)O3)C4(C(C2=O)O4)C 260.28 unknown https://doi.org/10.1002/CHIN.199908196
https://doi.org/10.1016/S0031-9422(98)00309-4
3a-hydroxy-6,10-dimethyl-3-methylidene-5,8,9,11a-tetrahydro-4H-cyclodeca[b]furan-2-one 75012028 Click to see CC1=CCCC(=CC2C(CC1)(C(=C)C(=O)O2)O)C 248.32 unknown https://doi.org/10.1055/S-2000-8649
7-Hydroxycostunolide 5471440 Click to see CC1=CCCC(=CC2C(CC1)(C(=C)C(=O)O2)O)C 248.32 unknown https://doi.org/10.1055/S-2000-8649
Costunolide 5281437 Click to see CC1=CCCC(=CC2C(CC1)C(=C)C(=O)O2)C 232.32 unknown https://doi.org/10.1055/S-2000-8649
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1002/CHIN.199908196
Stigmasterol 5280794 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1002/CHIN.199908196
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
3-Chlorodehydroleucodin 14589124 Click to see CC1=C2C(C3C(CC1)C(=C)C(=O)O3)C(=C(C2=O)Cl)C 278.73 unknown https://doi.org/10.1055/S-2000-8649
8-chloro-6,9-dimethyl-3-methylidene-4,5,9a,9b-tetrahydro-3aH-azuleno[4,5-b]furan-2,7-dione 14589123 Click to see CC1=C2C(C3C(CC1)C(=C)C(=O)O3)C(=C(C2=O)Cl)C 278.73 unknown https://doi.org/10.1055/S-2000-8649
Dehydroachillin 301781 Click to see CC1=C2C(C3C(CC1)C(=C)C(=O)O3)C(=CC2=O)C 244.28 unknown https://doi.org/10.1016/S0031-9422(98)00309-4
https://doi.org/10.1055/S-2000-8649
Dehydroleucodine 73440 Click to see CC1=C2C(C3C(CC1)C(=C)C(=O)O3)C(=CC2=O)C 244.28 unknown https://doi.org/10.1055/S-2000-8649
https://doi.org/10.1016/S0031-9422(98)00309-4
Desacetoxymatricarin 167683 Click to see CC1C2CCC(=C3C(C2OC1=O)C(=CC3=O)C)C 246.30 unknown https://doi.org/10.1002/CHIN.199908196

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