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Ferula loscosii

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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 UUID64401c397b5bc613597952
Scientific name Ferula loscosii
Authority Willk.
First published in Index Seminum (PRC, Pragensis) 1882: [5] (1882)

Description Top

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Synonyms Top

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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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000686668
Tropicos 1703469
KEW urn:lsid:ipni.org:names:842369-1
The Plant List kew-2808522
Open Tree Of Life 214836
NCBI Taxonomy 371365
IPNI 842369-1
iNaturalist 1149838
GBIF 6027025

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)!
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Title Authors Publication Released IDs
Recent and ancient evolutionary events shaped plant elemental composition of edaphic endemics: a phylogeny‐wide analysis of Iberian gypsum plants Palacio S, Cera A, Escudero A, Luzuriaga AL, Sánchez AM, Mota JF, Pérez‐Serrano Serrano M, Merlo ME, Martínez‐Hernández F, Salmerón‐Sánchez E, Mendoza‐Fernández AJ, Pérez‐García FJ, Montserrat‐Martí G, Tejero P New Phytol 13-Jul-2022
PMCID:PMC9545410
doi:10.1111/nph.18309
PMID:35704043
Environmental isolation explains Iberian genetic diversity in the highly homozygous model grass Brachypodium distachyon Marques I, Shiposha V, López-Alvarez D, Manzaneda AJ, Hernandez P, Olonova M, Catalán P BMC Evol Biol 15-Jun-2017
PMCID:PMC5472904
doi:10.1186/s12862-017-0996-x
PMID:28619047
Pre-Holocene Origin for the Coronopus navasii Disjunction: Conservation Implications from Its Long Isolation Martín-Hernanz S, G. Fernández de Castro A, Moreno-Saiz JC, Valcárcel V PLoS One 27-Jul-2016
PMCID:PMC4963129
doi:10.1371/journal.pone.0159484
PMID:27463521
Range expansion of a selfing polyploid plant despite widespread genetic uniformity Voss N, Eckstein RL, Durka W Ann Bot 22-Jun-2012
PMCID:PMC3400446
doi:10.1093/aob/mcs117
PMID:22730022
A new coumarin from Ferula loscosii and the correct structure of coladonin Mariano Pinar, Benjamín Rodríguez Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(77)80109-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 lactones
Umbelliprenin 1781413 Click to see CC(=CCCC(=CCCC(=CCOC1=CC2=C(C=C1)C=CC(=O)O2)C)C)C 366.50 unknown https://doi.org/10.1016/0031-9422(77)80109-X
> Phenylpropanoids and polyketides / Coumarins and derivatives
[(2R,4aR,5R,8aS)-1,1,4a-trimethyl-6-methylidene-5-[(2-oxochromen-7-yl)oxymethyl]-3,4,5,7,8,8a-hexahydro-2H-naphthalen-2-yl] 3-methylbutanoate 163019101 Click to see CC(C)CC(=O)OC1CCC2(C(C1(C)C)CCC(=C)C2COC3=CC4=C(C=C3)C=CC(=O)O4)C 466.60 unknown https://doi.org/10.1016/0031-9422(77)80109-X
[(2R,4aS,5R,8aS)-1,1,4a-trimethyl-6-methylidene-5-[(2-oxochromen-7-yl)oxymethyl]-3,4,5,7,8,8a-hexahydro-2H-naphthalen-2-yl] acetate 7213590 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC(=C)C2COC3=CC4=C(C=C3)C=CC(=O)O4)C 424.50 unknown https://doi.org/10.1016/0031-9422(77)80109-X
[1,1,4a-trimethyl-6-methylidene-5-[(2-oxochromen-7-yl)oxymethyl]-3,4,5,7,8,8a-hexahydro-2H-naphthalen-2-yl] 3-methylbutanoate 163019100 Click to see CC(C)CC(=O)OC1CCC2(C(C1(C)C)CCC(=C)C2COC3=CC4=C(C=C3)C=CC(=O)O4)C 466.60 unknown https://doi.org/10.1016/0031-9422(77)80109-X
[1,1,4a-trimethyl-6-methylidene-5-[(2-oxochromen-7-yl)oxymethyl]-3,4,5,7,8,8a-hexahydro-2H-naphthalen-2-yl] acetate 3703209 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC(=C)C2COC3=CC4=C(C=C3)C=CC(=O)O4)C 424.50 unknown https://doi.org/10.1016/0031-9422(77)80109-X
7-[(6-hydroxy-5,5,8a-trimethyl-2-methylidene-decahydronaphthalen-1-yl)methoxy]-2H-chromen-2-one 495441 Click to see CC1(C2CCC(=C)C(C2(CCC1O)C)COC3=CC4=C(C=C3)C=CC(=O)O4)C 382.50 unknown https://doi.org/10.1016/0031-9422(77)80109-X
7-[[(1R,4aS,6R,8aR)-6-hydroxy-5,5,8a-trimethyl-2-methylene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]methoxy]-1-benzopyran-2-one 7067264 Click to see CC1(C2CCC(=C)C(C2(CCC1O)C)COC3=CC4=C(C=C3)C=CC(=O)O4)C 382.50 unknown https://doi.org/10.1016/0031-9422(77)80109-X
7-[[(1R,4aS,6R,8aS)-6-hydroxy-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]methoxy]chromen-2-one 7002461 Click to see CC1(C2CCC(=C)C(C2(CCC1O)C)COC3=CC4=C(C=C3)C=CC(=O)O4)C 382.50 unknown https://doi.org/10.1016/0031-9422(77)80109-X
Polyanthin 1765141 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC(=C)C2COC3=CC4=C(C=C3)C=CC(=O)O4)C 424.50 unknown https://doi.org/10.1016/0031-9422(77)80109-X

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