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Plantago arborescens

Plantago arborescens - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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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 UUID644002f810adc329876669
Scientific name Plantago arborescens
Authority Poir.
First published in Encycl. 5: 389 (1804)

Description Top

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Synonyms Top

Scientific name Authority First published in
Psyllium arborescens Mirb. Hist. Nat. Pl. , ed. 2, 14: 334 (1800)

Common names Top

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Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Plantago arborescens subsp. maderensis (Decne.) A.Hansen & G.Kunkel Monogr. Biol. Canar. 3: 69 (1972)

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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Sow seeds at 20°C, expecting germination within 3 months without further temperature treatment.

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-0000487689
Tropicos 25200246
KEW urn:lsid:ipni.org:names:684873-1
Open Tree Of Life 217269
Observations.org 120678
NCBI Taxonomy 197793
IUCN Red List 104185163
IPNI 684873-1
iNaturalist 467311
GBIF 7303029
Elurikkus 585321

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
The role of mucilage envelope in the endozoochory of selected plant taxa Kreitschitz A, Haase E, Gorb SN Naturwissenschaften 11-Dec-2020
PMCID:PMC7732809
doi:10.1007/s00114-020-01709-7
PMID:33306163
Antioxidant Capacity of Macaronesian Traditional Medicinal Plants Tavares L, Carrilho D, Tyagi M, Barata D, Serra AT, Duarte CM, Duarte RO, Feliciano RP, Bronze MR, Chicau P, Espírito-Santo MD, Ferreira RB, dos Santos CN Molecules 12-Apr-2010
PMCID:PMC6257369
doi:10.3390/molecules15042576
PMID:20428065
Nuclear DNA Amounts in Macaronesian Angiosperms SUDA J, KYNCL T, FREIOVÁ R Ann Bot 01-Jul-2003
PMCID:PMC4243629
doi:10.1093/aob/mcg104
PMID:12824074
Chemotaxonomy of Plantago. Iridoid glucosides and caffeoyl phenylethanoid glycosides. Rønsted N, Gøbel E, Franzyk H, Jensen SR, Olsen CE Phytochemistry 01-Oct-2000
doi:10.1016/S0031-9422(00)00306-X
PMID:11117882

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 / Iridoid O-glycosides
6-Hydroxy-7-methyl-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-4-carboxylic acid 4430509 Click to see CC1C(CC2C1C(OC=C2C(=O)O)OC3C(C(C(C(O3)CO)O)O)O)O 376.36 unknown https://doi.org/10.1016/S0031-9422(00)00306-X
7-Hydroxy-7-methyl-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-4-carboxylic acid 13878352 Click to see CC1(CCC2C1C(OC=C2C(=O)O)OC3C(C(C(C(O3)CO)O)O)O)O 376.36 unknown https://doi.org/10.1016/S0031-9422(00)00306-X
Mussaenosidic acid 21633105 Click to see CC1(CCC2C1C(OC=C2C(=O)O)OC3C(C(C(C(O3)CO)O)O)O)O 376.36 unknown https://doi.org/10.1016/S0031-9422(00)00306-X
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
6-hydroxy-7-methylidene-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-4-carboxylic acid 73981590 Click to see C=C1C(CC2C1C(OC=C2C(=O)O)OC3C(C(C(C(O3)CO)O)O)O)O 374.34 unknown https://doi.org/10.1016/S0031-9422(00)00306-X
Methyl 7-(hydroxymethyl)-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,6-tetrahydrocyclopenta[c]pyran-4-carboxylate 20979918 Click to see COC(=O)C1=COC(C2=C(CCC12)CO)OC3C(C(C(C(O3)CO)O)O)O 388.40 unknown https://doi.org/10.1016/S0031-9422(00)00306-X
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
[(2R,3R,4R,5R,6R)-6-[2-(3,4-dihydroxyphenyl)ethoxy]-5-hydroxy-2-(hydroxymethyl)-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-3-yl] (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate 4484595 Click to see C1=CC(=C(C=C1CCOC2C(C(C(C(O2)CO)OC(=O)C=CC3=CC(=C(C=C3)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 640.60 unknown https://doi.org/10.1016/S0031-9422(00)00306-X

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