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Ferula communis subsp. linkii

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You are now on a "subspecies" page! Please be sure to also check the "species" page for compounds!

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 UUID644023b0d142a036375517
Scientific name Ferula communis subsp. linkii
Authority (Webb) Reduron & Dobignard
First published in Index Syn. Fl. Afrique N. 2: 95 (2011)

Description Top

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Common names Top

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Varieties (abbr. var.) 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-0000749310
KEW urn:lsid:ipni.org:names:77115477-1
The Plant List kew-2903905
IPNI 77115477-1
GBIF 8205771

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
Eight carotane sesquiterpenes from Ferula linkii Jesús G. Diaz, Braulio M. Fraga, Antonio G. González, Pedro Gónzalez, Melchor G. Hernández Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)84095-9
Carotdiol esters from Ferula linkii Braulio M. Fraga, M.G. Hernández, Jesús G. Diaz Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)97818-X
Sesquiterpene esters and sesquiterpene coumarin ethers from Ferula linkii-TF A.G. González, Jesus G. Díaz, L.Arancibia López, E. Valencia, P.Pérez De Paz, J.Bermejo Barrera Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(93)85291-X
Carotane sesquiterpenes from Ferula linkii Jesus G. Diaz, Braulio M. Fraga, Antonio G. González, Melchor G. Hernandez, Aurea Perales Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)81572-1
Antinociceptive, anti-inflammatory and antipyretic effects of lapidin, a bicyclic sesquiterpene. Valencia E, Feria M, Díaz JG, González A, Bermejo J Planta Med 01-Oct-1994
doi:10.1055/S-2006-959517
PMID:7997463

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 / Fatty Acyls / Fatty acid esters
[(2aS,5R,7aR)-2-acetyloxy-5-hydroxy-2a,7a-dimethyl-5-propan-2-yl-2,3,4,5a,6,7-hexahydro-1aH-azuleno[6,7-b]oxiren-6-yl] (Z)-2-methylbut-2-enoate 54608030 Click to see CC=C(C)C(=O)OC1CC2(C(O2)C(C3(C1C(CC3)(C(C)C)O)C)OC(=O)C)C 394.50 unknown https://doi.org/10.1016/S0031-9422(00)84095-9
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols / Long-chain fatty alcohols
(3S,8R)-heptadeca-1,9-dien-4,6-diyne-3,8-diol 131954651 Click to see CCCCCCCC=CC(C#CC#CC(C=C)O)O 260.40 unknown https://doi.org/10.1016/0031-9422(93)85291-X
Falcarindiol 5281148 Click to see CCCCCCCC=CC(C#CC#CC(C=C)O)O 260.40 unknown https://doi.org/10.1016/0031-9422(93)85291-X
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(6,8a-dihydroxy-3a,6-dimethyl-1-propan-2-yl-2,3,4,5,7,8-hexahydro-1H-azulen-5-yl) 2-methylbut-2-enoate 3492049 Click to see CC=C(C)C(=O)OC1CC2(CCC(C2(CCC1(C)O)O)C(C)C)C 338.50 unknown https://doi.org/10.1016/0031-9422(93)85291-X
[(1S,3aS,5S,6S,8aR)-6,8a-dihydroxy-3a,6-dimethyl-1-propan-2-yl-2,3,4,5,7,8-hexahydro-1H-azulen-5-yl] (Z)-2-methylbut-2-enoate 1777035 Click to see CC=C(C)C(=O)OC1CC2(CCC(C2(CCC1(C)O)O)C(C)C)C 338.50 unknown https://doi.org/10.1016/S0031-9422(00)81572-1
1,8-dihydroxy-3a,6-dimethyl-1-propan-2-yl-3,7,8,8a-tetrahydro-2H-azulen-4-one 14239510 Click to see CC1=CC(=O)C2(CCC(C2C(C1)O)(C(C)C)O)C 252.35 unknown https://doi.org/10.1016/0031-9422(93)85291-X
Ferutidin 10172562 Click to see CC1=CCC2(CCC(C2C(C1)OC(=O)C3=CC=C(C=C3)OC)(C(C)C)O)C 372.50 unknown https://doi.org/10.1016/S0031-9422(00)84095-9
Lapidin 11872435 Click to see CC=C(C)C(=O)OC1CC(=CC(=O)C2(C1C(CC2)(C(C)C)O)C)C 334.40 unknown https://doi.org/10.1055/S-2006-959517
https://doi.org/10.1016/0031-9422(93)85291-X
Lapidine 6440625 Click to see CC=C(C)C(=O)OC1CC(=CC(=O)C2(C1C(CC2)(C(C)C)O)C)C 334.40 unknown https://doi.org/10.1055/S-2006-959517
https://doi.org/10.1016/0031-9422(93)85291-X
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
[(3R,3aS,5R,8aR)-3a-hydroxy-6,8a-dimethyl-3-propan-2-yl-1,2,3,4,5,8-hexahydroazulen-5-yl] 3,4-dimethoxybenzoate 14313704 Click to see CC1=CCC2(CCC(C2(CC1OC(=O)C3=CC(=C(C=C3)OC)OC)O)C(C)C)C 402.50 unknown https://doi.org/10.1016/S0031-9422(00)97818-X
[(3R,3aS,5R,8aR)-3a-hydroxy-6,8a-dimethyl-3-propan-2-yl-1,2,3,4,5,8-hexahydroazulen-5-yl] acetate 14313702 Click to see CC1=CCC2(CCC(C2(CC1OC(=O)C)O)C(C)C)C 280.40 unknown https://doi.org/10.1016/S0031-9422(00)97818-X
> 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(93)85291-X
> Organoheterocyclic compounds / Benzodioxoles
[1-(7-methoxy-1,3-benzodioxol-5-yl)-1-[(E)-2-methylbut-2-enoyl]oxypropan-2-yl] 2-hydroxy-2-methyl-3-[(E)-2-methylbut-2-enoyl]oxybutanoate 14313719 Click to see CC=C(C)C(=O)OC(C)C(C)(C(=O)OC(C)C(C1=CC2=C(C(=C1)OC)OCO2)OC(=O)C(=CC)C)O 506.50 unknown https://doi.org/10.1016/0031-9422(93)85291-X
Laserine 102571636 Click to see CC=C(C)C(=O)OC(C)C(C1=CC2=C(C(=C1)OC)OCO2)OC(=O)C(=CC)C 390.40 unknown https://doi.org/10.1016/0031-9422(93)85291-X
> Phenylpropanoids and polyketides / Coumarins and derivatives
7-[[(1S,4aR,6S,8aS)-6-hydroxy-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]methoxy]chromen-2-one 21627903 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(93)85291-X
Colladonin 375430 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(93)85291-X
Nevskin 495442 Click to see CC1(C2CCC(C(C2(CCC1O)C)COC3=CC4=C(C=C3)C=CC(=O)O4)(C)O)C 400.50 unknown https://doi.org/10.1016/0031-9422(93)85291-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(93)85291-X
Scoparone 8417 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)OC 206.19 unknown https://doi.org/10.1016/0031-9422(93)85291-X
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins
Isoscopoletin 69894 Click to see COC1=C(C=C2C=CC(=O)OC2=C1)O 192.17 unknown https://doi.org/10.1016/0031-9422(93)85291-X
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Scopoletin 5280460 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)O 192.17 unknown https://doi.org/10.1016/0031-9422(93)85291-X

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