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Internal ID UUID64404f9041eeb777051227
Scientific name Valeriana amurensis
Authority P.A.Smirn. ex Kom.
First published in Izv. Bot. Sada Akad. Nauk S.S.S.R. 30: 214 (1931 publ. 1932)

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Synonyms Top

Scientific name Authority First published in
Valeriana sambucifolia subsp. amurensis (P.Smirn. ex Kom.) H.Hara J. Fac. Sci. Univ. Tokyo, Sect. 3, Bot. 6(7): 387 1956
Valeriana officinalis var. incisa Nakai ex Mori Enum. Pl. Corea 333 1922
Valeriana amurensis f. leiocarpa H.Hara J. Jap. Bot. 17(3): 127 1941

Common names Top

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Language Common/alternative name
Chinese 缬草
Chinese 蜘蛛香
Chinese 黑水缬草

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Varieties (abbr. var.) 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
  • Asia-temperate
    • China
      • Manchuria
    • Eastern Asia
      • Korea
    • Russian Far East
      • Amur
      • Khabarovsk
      • Primorye

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001144115
Tropicos 33500625
KEW urn:lsid:ipni.org:names:859584-1
The Plant List tro-33500625
PFAF Valeriana amurensis
Open Tree Of Life 245959
Observations.org 123282
NCBI Taxonomy 323660
IPNI 859584-1
iNaturalist 777883
GBIF 4095377
Elurikkus 465768
USDA GRIN 423580

Genomes (via NCBI) Top

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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
Network pharmacology-based approach to elucidate the pharmacologic mechanisms of natural compounds from Dictyostelium discoideum for Alzheimer's disease treatment Patil N, Dhariwal R, Mohammed A, Wei LS, Jain M Heliyon 06-Apr-2024
PMCID:PMC11033062
doi:10.1016/j.heliyon.2024.e28852
PMID:38644825
Phytochemical Investigation of Equisetum arvense and Evaluation of Their Anti-Inflammatory Potential in TNFα/INFγ-Stimulated Keratinocytes Jeong SY, Yu HS, Ra MJ, Jung SM, Yu JN, Kim JC, Kim KH Pharmaceuticals (Basel) 16-Oct-2023
PMCID:PMC10609812
doi:10.3390/ph16101478
PMID:37895949
Neuroprotective Iridoids and Lignans from Valeriana amurensis Ye M, Lin X, Wang Q, Yang B, Wang C Molecules 01-Aug-2023
PMCID:PMC10421132
doi:10.3390/molecules28155793
PMID:37570763
An Effective Chromatography Process for Simultaneous Purification and Separation of Total Lignans and Flavonoids from Valeriana amurensis Zhang M, Yang B, Ye M, Chen J, Liu Y, Wang C Molecules 06-Dec-2022
PMCID:PMC9741226
doi:10.3390/molecules27238598
PMID:36500691
Therapeutic potential of plant iridoids in depression: a review Kou Y, Li Z, Yang T, Shen X, Wang X, Li H, Zhou K, Li L, Xia Z, Zheng X, Zhao Y Pharm Biol 27-Oct-2022
PMCID:PMC9621214
doi:10.1080/13880209.2022.2136206
PMID:36300881
The potential of Valeriana as a traditional Chinese medicine: traditional clinical applications, bioactivities, and phytochemistry Li J, Li X, Wang C, Zhang M, Ye M, Wang Q Front Pharmacol 21-Sep-2022
PMCID:PMC9534556
doi:10.3389/fphar.2022.973138
PMID:36210806
Ginsenoside and Its Therapeutic Potential for Cognitive Impairment Feng H, Xue M, Deng H, Cheng S, Hu Y, Zhou C Biomolecules 16-Sep-2022
PMCID:PMC9496100
doi:10.3390/biom12091310
PMID:36139149
Biotic Elicitors in Adventitious and Hairy Root Cultures: A Review from 2010 to 2022 Alcalde MA, Perez-Matas E, Escrich A, Cusido RM, Palazon J, Bonfill M Molecules 17-Aug-2022
PMCID:PMC9416168
doi:10.3390/molecules27165253
PMID:36014492
Improving galegine production in transformed hairy roots of Galega officinalis L. via elicitation Khezri M, Asghari Zakaria R, Zare N, Johari-Ahar M AMB Express 03-Jun-2022
PMCID:PMC9166927
doi:10.1186/s13568-022-01409-7
PMID:35657528
Plant Species of Sub-Family Valerianaceae—A Review on Its Effect on the Central Nervous System Das G, Shin HS, Tundis R, Gonçalves S, Tantengco OA, Campos MG, Acquaviva R, Malfa GA, Romano A, Robles JA, Clores MQ, Patra JK Plants (Basel) 22-Apr-2021
PMCID:PMC8144999
doi:10.3390/plants10050846
PMID:33922184
Pharmacognostical Sources of Popular Medicine To Treat Alzheimer’s Disease Kalász H, Ojha S, Tekes K, Szőke É, Mohanraj R, Fahim M, Adeghate E, Adem A Open Med Chem J 16-Feb-2018
PMCID:PMC5827296
doi:10.2174/1874104501812010023
PMID:29515678
Compounds from the Roots and Rhizomes of Valeriana amurensis Protect against Neurotoxicity in PC12 Cells Wang Q, Wang C, Zuo Y, Wang Z, Yang B, Kuang H Molecules 18-Dec-2012
PMCID:PMC6268518
doi:10.3390/molecules171215013
PMID:23250029
Phenolic compounds of the epigeal part of valerian. II. Composition of the phenolic compounds ofValeriana amurensis N. S. Fursa Springer Science and Business Media LLC 20-Nov-2004
doi:10.1007/BF00566097

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/BF00566097
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
(1S,3R,4R,5S)-3-[(E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy-1,4,5-trihydroxycyclohexane-1-carboxylic acid 7067333 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/BF00566097
3-{[3-(3,4-Dihydroxyphenyl)prop-2-enoyl]oxy}-1,4,5-trihydroxycyclohexane-1-carboxylic acid 348159 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/BF00566097
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/BF00566097
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
3-(3,4-Dihydroxyphenyl)Prop-2-Enoic Acid 2518 Click to see 180.16 unknown https://doi.org/10.1007/BF00566097
Caffeic Acid 689043 Click to see 180.16 unknown https://doi.org/10.1007/BF00566097
> 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/BF00566097
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/BF00566097
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol 5280863 Click to see 286.24 unknown https://doi.org/10.1007/BF00566097
Quercetin 5280343 Click to see 302.23 unknown https://doi.org/10.1007/BF00566097
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Apigenin 7-O-glucoside 5280704 Click to see 432.40 unknown https://doi.org/10.1007/BF00566097
> 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/BF00566097

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