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Valeriana eriophylla

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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 UUID64404f9077e12589152865
Scientific name Valeriana eriophylla
Authority Utkin
First published in Bot. Mater. Gerb. Glavn. Bot. Sada R.S.F.S.R. 4: 124 (1923)

Description Top

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Synonyms Top

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Common names Top

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Language Common/alternative name
Armenian Կատվախոտ բրդատերև

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-0001144120
Tropicos 33500635
KEW urn:lsid:ipni.org:names:859776-1
Open Tree Of Life 6061633
Observations.org 124541
IPNI 859776-1
iNaturalist 777935
GBIF 8270703
Elurikkus 654064

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
Phenolic compounds of the epigeal part and iridoids of the hypogeal part of valerian. VI. Flavonoids and valepotriates ofValeriana eriophylla andV. cardamines N. S. Fursa, S. D. Trzhetsinskii, V. G. Zaitsev, Yu. N. Gorbunov Springer Science and Business Media LLC 21-Nov-2004
doi:10.1007/BF00579496
Further investigations of valepotriates in the Valerianaceae. Chavadej S, Becker H, Weberling F Pharm Weekbl Sci 23-Aug-1985
doi:10.1007/BF02097255
PMID:4047916

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 / Monoterpenoids / Iridoids and derivatives
[(4aR,7R,7aS)-6-acetyloxy-1-(3-methylbutanoyloxy)spiro[4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-7,2'-oxirane]-4-yl]methyl 3-methylbutanoate 137796089 Click to see CC(C)CC(=O)OCC1=COC(C2C1CC(C23CO3)OC(=O)C)OC(=O)CC(C)C 424.50 unknown https://doi.org/10.1007/BF00579496
Didrovaltrate 65689 Click to see CC(C)CC(=O)OCC1=COC(C2C1CC(C23CO3)OC(=O)C)OC(=O)CC(C)C 424.50 unknown https://doi.org/10.1007/BF00579496
Isovaltrate 92275 Click to see CC(C)CC(=O)OCC1=COC(C2C1=CC(C23CO3)OC(=O)C)OC(=O)CC(C)C 422.50 unknown https://doi.org/10.1007/BF02097255
Valtrate 442436 Click to see CC(C)CC(=O)OC1C=C2C(C13CO3)C(OC=C2COC(=O)C)OC(=O)CC(C)C 422.50 unknown https://doi.org/10.1007/BF00579496
> Organic acids and derivatives / Carboxylic acids and derivatives / Tetracarboxylic acids and derivatives
Acevaltrate 65717 Click to see CC(C)CC(=O)OC1C2C(=CC(C23CO3)OC(=O)CC(C)(C)OC(=O)C)C(=CO1)COC(=O)C 480.50 unknown https://doi.org/10.1007/BF00579496
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin 5280443 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 270.24 unknown https://doi.org/10.1007/BF00579496
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol 5280863 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown https://doi.org/10.1007/BF00579496
Quercetin 5280343 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 302.23 unknown https://doi.org/10.1007/BF00579496

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