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Patrinia rupestris

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 UUID64404f7f640b0082378182
Scientific name Patrinia rupestris
Authority (Pall.) Dufr.
First published in Hist. Nat. Valér. : 54 (1811)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Fedia rupestris (Pall.) Vahl Enum. Pl. 2: 22 (1805)
Valeriana rupestris Pall. Reise Russ. Reich. 3: 266 (1776)
Fuisa rupestris (Pall.) Raf. Autik. Bot. 88 1840

Common names Top

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Language Common/alternative name
Arabic كورثل الصخور
Chinese 岩败酱

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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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
  • Asia-temperate
    • China
      • China North-central
      • China South-central
      • China Southeast
      • Inner Mongolia
      • Manchuria
    • Eastern Asia
      • Korea
    • Mongolia
      • Mongolia
    • Russian Far East
      • Amur
      • Khabarovsk
      • Primorye
    • Siberia
      • Altay
      • Buryatiya
      • Chita
      • Irkutsk
      • Krasnoyarsk
      • Tuva
      • West Siberia
      • Yakutskiya

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001143746
Tropicos 33500041
KEW urn:lsid:ipni.org:names:859463-1
The Plant List tro-33500041
Open Tree Of Life 1035977
Observations.org 141979
NCBI Taxonomy 59172
IPNI 859463-1
iNaturalist 601634
GBIF 6058845
EOL 5236669
Elurikkus 575798
USDA GRIN 402002

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
Changes in Competitors, Stress Tolerators, and Ruderals (CSR) Ecological Strategies after the Introduction of Shrubs and Trees in Disturbed Semiarid Steppe Grasslands in Hulunbuir, Inner Mongolia Kim EJ, Lee SH, Kim SH, Park JH, You YH Biology (Basel) 30-Nov-2023
PMCID:PMC10740407
doi:10.3390/biology12121479
PMID:38132305
Secondary succession of shrub-herb communities in the hilly area of Taihang Mountain Liu X, Zhou W, Li X, Zhang Y, Dong W Front Plant Sci 08-Sep-2023
PMCID:PMC10514918
doi:10.3389/fpls.2023.1194083
PMID:37746017
Integrated Network Pharmacology Analysis and In Vitro Validation Revealed the Potential Active Components and Underlying Mechanistic Pathways of Herba Patriniae in Colorectal Cancer Yang H, Cheung MK, Yue GG, Leung PC, Wong CK, Lau CB Molecules 05-Oct-2021
PMCID:PMC8513027
doi:10.3390/molecules26196032
PMID:34641576
Effects of large herbivore grazing on relics of the presumed mammoth steppe in the extreme climate of NE-Siberia Reinecke J, Ashastina K, Kienast F, Troeva E, Wesche K Sci Rep 21-Jun-2021
PMCID:PMC8217226
doi:10.1038/s41598-021-92079-1
PMID:34155242
Chemical Constituents from the Roots of <i>Patrinia Rupestris</i> Xiu‐Ping Yang, Cheng‐Shan Yuan, Zhong‐Jian Jia Wiley 01-May-2015
doi:10.1002/JCCS.200700064
An Overview of Antimicrobial Properties of Different Classes of Phytochemicals Patra AK Dietary Phytochemicals and Microbes 18-Feb-2012
PMCID:PMC7121617
doi:10.1007/978-94-007-3926-0_1
A new iridoid compound from Patrinia rupestris (Pall.) Juss. Qiu DF, Yang XP, Xu YJ, Liu XQ, Liu HL, Yuan CS Nat Prod Res 01-Oct-2011
doi:10.1080/14786419.2010.533667
PMID:21790497

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
[(1R,3R)-1,3-diethoxy-7-(hydroxymethyl)-6-oxo-3,5-dihydro-1H-cyclopenta[c]pyran-4-yl]methyl 3-methylbutanoate 163065747 Click to see 368.40 unknown https://doi.org/10.1080/14786419.2010.533667
Homobaldrinal 49999 Click to see CC(C)CC(=O)OCC1=COC=C2C1=CC=C2C=O 260.28 unknown https://doi.org/10.1002/JCCS.200700064
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Iridoids and derivatives
[(1S,4aS,6S,7R,7aS)-6,7-dihydroxy-1-(3-methylbutanoyloxy)-7-(3-methylbutanoyloxymethyl)-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-4-yl]methyl 3-methylbutanoate 162990086 Click to see 484.60 unknown https://doi.org/10.1080/14786419.2010.533667
[(1S,7R,7aS)-7-(ethoxymethyl)-7-hydroxy-1-(3-methylbutanoyloxy)-6-oxo-1,7a-dihydrocyclopenta[c]pyran-4-yl]methyl 3-methylbutanoate 163077269 Click to see 424.50 unknown https://doi.org/10.1002/JCCS.200700064
[7-(Ethoxymethyl)-7-hydroxy-1-(3-methylbutanoyloxy)-6-oxo-1,7a-dihydrocyclopenta[c]pyran-4-yl]methyl 3-methylbutanoate 163077268 Click to see 424.50 unknown https://doi.org/10.1002/JCCS.200700064
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Ursolic Acid 64945 Click to see 456.70 unknown https://doi.org/10.1002/JCCS.200700064
(16-Hydroxy-4,5,9,9,13,20,20-heptamethyl-23-oxo-24-oxahexacyclo[15.5.2.01,18.04,17.05,14.08,13]tetracosan-10-yl) 3-methylbutanoate 162900102 Click to see 556.80 unknown https://doi.org/10.1002/JCCS.200700064
[(1S,4S,5R,8R,10S,13R,14R,16S,17S,18R)-16-hydroxy-4,5,9,9,13,20,20-heptamethyl-23-oxo-24-oxahexacyclo[15.5.2.01,18.04,17.05,14.08,13]tetracosan-10-yl] 3-methylbutanoate 162900103 Click to see CC(C)CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC(C45C3(CCC6(C4CC(CC6)(C)C)C(=O)O5)C)O)C)C 556.80 unknown https://doi.org/10.1002/JCCS.200700064
3-Oxo-olean-12-en-28-oic acid 12313702 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(=O)C5(C)C)C)C)C2C1)C)C(=O)O)C 454.70 unknown https://doi.org/10.1002/JCCS.200700064
alpha-Amyrenol 225688 Click to see 426.70 unknown https://doi.org/10.1002/JCCS.200700064
Alpha-Amyrin 73170 Click to see 426.70 unknown https://doi.org/10.1002/JCCS.200700064
Oleanonic Acid 12313704 Click to see 454.70 unknown https://doi.org/10.1002/JCCS.200700064
Urs-12-en-28-oic acid, 3-hydroxy-, (3beta)- 220774 Click to see 456.70 unknown https://doi.org/10.1002/JCCS.200700064
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
(3beta,5alpha,8alpha,22e)-Ergosta-6,22-diene-3,5,8-triol 15251535 Click to see 430.70 unknown https://doi.org/10.1002/JCCS.200700064
17-(5,6-Dimethylhept-3-En-2-Yl)-10,13-Dimethyl-2,3,4,9,11,12,14,15,16,17-Decahydro-1H-Cyclopenta(A)Phenanthren-3-Ol 247705 Click to see 396.60 unknown https://doi.org/10.1002/JCCS.200700064
17-(5,6-dimethylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,9,11,12,14,15,16,17-decahydro-1H-cyclopenta[a]phenanthrene-3,5,8-triol 73190110 Click to see 430.70 unknown https://doi.org/10.1002/JCCS.200700064
Ergosterol 444679 Click to see CC(C)C(C)C=CC(C)C1CCC2C1(CCC3C2=CC=C4C3(CCC(C4)O)C)C 396.60 unknown https://doi.org/10.1002/JCCS.200700064
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 Click to see 414.70 unknown https://doi.org/10.1002/JCCS.200700064
(6beta,24R)-6-Hydroxystigmast-4-en-3-one 14769504 Click to see 428.70 unknown https://doi.org/10.1002/JCCS.200700064
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/10.1002/JCCS.200700064
6beta-Hydroxystigmast-4-en-3-one 9823926 Click to see 428.70 unknown https://doi.org/10.1002/JCCS.200700064
beta-Sitosterol 3-O-beta-D-galactopyranoside 296119 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1002/JCCS.200700064
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1002/JCCS.200700064
> Organic acids and derivatives / Carboxylic acids and derivatives / Tetracarboxylic acids and derivatives
[(1S,6S,7R,7aS)-6-acetyloxy-7-(acetyloxymethyl)-7-hydroxy-1-(3-methylbutanoyloxy)-6,7a-dihydro-1H-cyclopenta[c]pyran-4-yl]methyl 3-methylbutanoate 162845792 Click to see 482.50 unknown https://doi.org/10.1002/JCCS.200700064
[6-acetyloxy-7-(acetyloxymethyl)-7-hydroxy-1-(3-methylbutanoyloxy)-6,7a-dihydro-1H-cyclopenta[c]pyran-4-yl]methyl 3-methylbutanoate 13073177 Click to see 482.50 unknown https://doi.org/10.1002/JCCS.200700064
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Aryl-aldehydes
Cyclopenta(c)pyran-7-carboxaldehyde, 4-(ethoxymethyl)- 3062371 Click to see CCOCC1=COC=C2C1=CC=C2C=O 204.22 unknown https://doi.org/10.1002/JCCS.200700064
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
1-Hydroxy-5-methoxyxanthone 86168207 Click to see 242.23 unknown https://doi.org/10.1002/JCCS.200700064
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(+-)-Eriodictyol 11095 Click to see 288.25 unknown https://doi.org/10.1002/JCCS.200700064
Eriodictyol 440735 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)O)O 288.25 unknown https://doi.org/10.1002/JCCS.200700064

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