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Fleischmannia hymenophylla

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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 UUID643fce2db0eaf446171171
Scientific name Fleischmannia hymenophylla
Authority (Klatt) R.M.King & H.Rob.
First published in Phytologia 19: 203 (1970)

Description Top

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Synonyms Top

Scientific name Authority First published in
Eupatorium valerianum Standl. Publ. Field Columb. Mus., Bot. Ser. 18: 1474 (1938)
Fleischmannia valeriana (Standl.) R.M.King & H.Rob. Phytologia 19: 206 (1970)
Eupatorium hymenophyllum Klatt Bull. Soc. Roy. Bot. Belgique 31: 190 (1892)
Eupatorium hymenophyllum Klatt ex T.Durand & Pittier Bull. Soc. Roy. Bot. Belgique 31: 190. 1893 [1892 publ 1893]

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

Area

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© OpenStreetMap
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-0000079016
Tropicos 2711389
KEW urn:lsid:ipni.org:names:105092-2
The Plant List gcc-35611
Open Tree Of Life 7603559
IPNI 105092-2
iNaturalist 925532
GBIF 5399645
CMAUP NPO19943

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
Diterpenes from Fleischmannia hymenophylla and Brickellia laciniata J. Jakupovic, F. Tsichritzis, G. Tamayo-Castillo, V. Castro, F. Bohlmann, E. Boldt Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)98080-4

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
> Benzenoids / Benzene and substituted derivatives / Acetophenones
(-)-Usnic Acid 442614 Click to see CC1=C(C(=C2C(=C1O)C3(C(=CC(=C(C3=O)C(=O)C)O)O2)C)C(=O)C)O 344.30 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
Orsellinic acid 68072 Click to see CC1=CC(=CC(=C1C(=O)O)O)O 168.15 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / p-Hydroxybenzoic acid esters / p-Hydroxybenzoic acid alkyl esters
Methyl Haematommate 591773 Click to see CC1=CC(=C(C(=C1C(=O)OC)O)C=O)O 210.18 unknown via CMAUP database
Methyl Orsellinate 76658 Click to see CC1=CC(=CC(=C1C(=O)OC)O)O 182.17 unknown via CMAUP database
> Benzenoids / Phenols / Benzenediols / Resorcinols
Orcinol 10436 Click to see CC1=CC(=CC(=C1)O)O 124.14 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans
Sesamin 72307 Click to see C1C2C(COC2C3=CC4=C(C=C3)OCO4)C(O1)C5=CC6=C(C=C5)OCO6 354.40 unknown https://doi.org/10.1016/S0031-9422(00)98080-4
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Acyclic diterpenoids
(E)-(7R,11R)-3,7,11,15-tetramethylhexadec-2-ene-1-ol 145386 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C 296.50 unknown https://doi.org/10.1016/S0031-9422(00)98080-4
3,7,11,15-Tetramethyl-2-hexadecen-1-OL 5366244 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C 296.50 unknown https://doi.org/10.1016/S0031-9422(00)98080-4
Phytol 5280435 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C 296.50 unknown https://doi.org/10.1016/S0031-9422(00)98080-4
> Organoheterocyclic compounds / Lactones / Delta valerolactones
5,9,13-Trimethyl-15-oxo-16-oxatetracyclo[11.3.1.01,10.04,9]heptadecane-5-carboxylic acid 14396715 Click to see CC12CCC3C4(CCCC(C4CCC3(C1)OC(=O)C2)(C)C(=O)O)C 334.40 unknown https://doi.org/10.1016/S0031-9422(00)98080-4
> Phenylpropanoids and polyketides / Depsides and depsidones
Atranorin 68066 Click to see CC1=CC(=C(C(=C1C(=O)OC2=C(C(=C(C(=C2)C)C(=O)OC)O)C)O)C=O)O 374.30 unknown via CMAUP database
Divaricatic acid 371610 Click to see CCCC1=C(C(=CC(=C1)OC)O)C(=O)OC2=CC(=C(C(=C2)O)C(=O)O)CCC 388.40 unknown via CMAUP database
Lecanoric Acid 99613 Click to see CC1=CC(=CC(=C1C(=O)OC2=CC(=C(C(=C2)C)C(=O)O)O)O)O 318.28 unknown via CMAUP database

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