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Valeriana rossica

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID64404f90bb435090276612
Scientific name Valeriana rossica
Authority P.A.Smirn.
First published in Raboty Oksk. Biol. Stantsii Nizhnem Novogorode 3(2-3): 9 (1925)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Valeriana dubia subsp. rossica Vorosch.
Valeriana pseudodubia Sumnev. Trudy Biol. Nauchno-Issl. Inst. Tomsk. Gosud. Univ. 2: 53 (1936)
Valeriana spryginii P.A.Smirn. Mem. Mus. Etat Reg. Industr. Centr. 4: 7 (1927)
Valeriana sumneviczii Vorosch. Medicin. Valer. : 124 (1959)

Common names Top

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Language Common/alternative name
Russian Валериана русская

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

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Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001144135
Tropicos 33500658
KEW urn:lsid:ipni.org:names:860135-1
The Plant List tro-33500658
Open Tree Of Life 6061718
Observations.org 141669
IPNI 860135-1
iNaturalist 870649
GBIF 4094805
EOL 5237183
Elurikkus 465650

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
Flavonoids and valepotriates of valerian. III.Valeriana spryginii V. G. Zaitsev, N. S. Fursa, V. A. Zhukov Springer Science and Business Media LLC 22-Nov-2004
doi:10.1007/BF00579162
Phenolic compounds, sterols, and iridoids of valerian. VII. Composition of the phenolic compounds, β-sitosterol, and valepotriates ofValeriana rossica N. S. Fursa Springer Science and Business Media LLC 20-Nov-2004
doi:10.1007/BF00574351

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 / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
4-Hydroxybenzoic acid 135 Click to see C1=CC(=CC=C1C(=O)O)O 138.12 unknown https://doi.org/10.1007/BF00574351
Protocatechuic Acid 72 Click to see 154.12 unknown https://doi.org/10.1007/BF00574351
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Iridoids and derivatives
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/BF00574351
Valtrate 442436 Click to see 422.50 unknown https://doi.org/10.1007/BF00574351
https://doi.org/10.1007/BF00579162
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 Click to see 414.70 unknown https://doi.org/10.1007/BF00574351
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1007/BF00574351
Stigmast-5-en-3-ol 22012 Click to see 414.70 unknown https://doi.org/10.1007/BF00574351
> Organic acids and derivatives / Carboxylic acids and derivatives / Tetracarboxylic acids and derivatives
[(7R,7aS)-4-(acetyloxymethyl)-1-(3-methylbutanoyloxy)spiro[6,7a-dihydro-1H-cyclopenta[c]pyran-7,2'-oxirane]-6-yl] 3-acetyloxy-3-methylbutanoate 137706187 Click to see 480.50 unknown https://doi.org/10.1007/BF00579162
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/BF00579162
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
Chlorogenic Acid 1794427 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown https://doi.org/10.1007/BF00574351
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
Caffeic Acid 689043 Click to see 180.16 unknown https://doi.org/10.1007/BF00574351
> 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/BF00574351
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown https://doi.org/10.1007/BF00574351
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Quercetin 5280343 Click to see 302.23 unknown https://doi.org/10.1007/BF00574351
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
5-Hydroxy-2-(3-hydroxy-4-methoxyphenyl)-7-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxymethyl]oxan-2-yl]oxychromen-4-one 5353588 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC(=C(C=C5)OC)O)O)O)O)O)O)O)O 608.50 unknown https://doi.org/10.1007/BF00574351
5-hydroxy-2-(4-hydroxyphenyl)-7-[(2S,5S)-3,4,5-trihydroxy-6-[[(2R,5R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one 133612286 Click to see 578.50 unknown https://doi.org/10.1007/BF00574351
Apigenin 7-O-glucoside 5280704 Click to see 432.40 unknown https://doi.org/10.1007/BF00574351
Luteolin 7-O-glucoside 5280637 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown https://doi.org/10.1007/BF00574351
Thalictiin 5464455 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O 432.40 unknown https://doi.org/10.1007/BF00574351
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
Diosmetin 5281612 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 300.26 unknown https://doi.org/10.1007/BF00574351

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