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Rumex thianschanicus

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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 UUID644055d430fc3853655230
Scientific name Rumex thianschanicus
Authority Losinsk.
First published in Fl. URSS 5: 716 (1936)

Description Top

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Synonyms Top

No known synonyms.

Common names Top

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Language Common/alternative name
Chinese 天山酸模

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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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • Xinjiang
    • Middle Asia
      • Kazakhstan
      • Kirgizstan
      • Tadzhikistan
      • Turkmenistan
      • Uzbekistan
    • Western Asia
      • Afghanistan
      • Iran

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001246267
Tropicos 50136093
The Plant List tro-50136093
Open Tree Of Life 5920128
NCBI Taxonomy 1786038
IPNI 697559-1
iNaturalist 993397
GBIF 4035491
EOL 2876375

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
Antiulcer Activity of Anthraquinone–Flavonoid Complex of Rumex tianschanicus Losinsk Seitimova GA, Shokan AK, Tolstikova TG, Zhukova NA, Korulkin DY, Kudrina NO, Litvinenko YA, Meduntseva ND, Terletskaya NV, Kulmanov TE Molecules 03-Mar-2023
PMCID:PMC10005188
doi:10.3390/molecules28052347
PMID:36903594
Pest categorisation of potato virus X (non‐EU isolates) Bragard C, Dehnen‐Schmutz K, Gonthier P, Jacques M, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Thulke H, van der Werf W, Civera AV, Yuen J, Zappalà L, Candresse T, Lacomme C, Bottex B, Oplaat C, Roenhorst A, Schenk M, Di Serio F EFSA J 09-Jan-2020
PMCID:PMC7008906
doi:10.2903/j.efsa.2020.5937
PMID:32626491
Crop wild relatives of Kazakhstani Tien Shan: Flora, vegetation, resources Sitpayeva GT, Kudabayevа GM, Dimeyeva LA, Gemejiyeva NG, Vesselova PV Plant Divers 31-Oct-2019
PMCID:PMC7046504
doi:10.1016/j.pld.2019.10.003
PMID:32140634
Chemical composition of the hybrid Rumex K-1 M. A. Omarova, N. A. Artamonova, G. M. Chasovitina Springer Science and Business Media LLC 14-Mar-2006
doi:10.1007/BF02329587

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 / Fluorenes
8-hydroxy-7,9-dimethoxy-11,11-dimethyl-10,10a-dihydro-4bH-benzo[b]fluoren-5-one 73047888 Click to see CC1(C2CC3=C(C(=C(C=C3C(=O)C2C4=CC=CC=C41)OC)O)OC)C 338.40 unknown https://doi.org/10.1007/BF02329587
> Benzenoids / Pyrenes / Benzopyrenes
Hypericin 3663 Click to see CC1=CC(=O)C2=C(C3=C(C=C(C4=C3C5=C2C1=C6C(=CC(=O)C7=C(C8=C(C=C(C4=C8C5=C67)O)O)O)C)O)O)O 504.40 unknown https://doi.org/10.1007/BF02329587
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
Sabinol 94147 Click to see CC(C)C12CC1C(=C)C(C2)O 152.23 unknown https://doi.org/10.1007/BF02329587
> Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids / Carotenoids / Carotenes
all-trans-alpha-Carotene 4369188 Click to see CC1=C(C(CCC1)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2C(=CCCC2(C)C)C)C)C 536.90 unknown https://doi.org/10.1007/BF02329587
alpha-Carotene 6419725 Click to see CC1=C(C(CCC1)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2C(=CCCC2(C)C)C)C)C 536.90 unknown https://doi.org/10.1007/BF02329587
Beta-Carotene 5280489 Click to see CC1=C(C(CCC1)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2=C(CCCC2(C)C)C)C)C 536.90 unknown https://doi.org/10.1007/BF02329587
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
(2R,3R,4S,5R,6R)-2-[(2S,3S,4R,6S)-6-[(2R,3S,4R,6S)-4-hydroxy-6-[(2R,3R,4R,6S)-4-methoxy-6-[(2R,3S,4S,6R)-4-methoxy-2-methyl-6-[(1S,2R,7S,10R,11S,14R,15R,16R,19S)-10,14,16-trimethyl-17,20,21-trioxahexacyclo[14.4.1.01,14.02,11.05,10.015,19]henicos-4-en-7-yl]oxan-3-yl]oxy-2-methyloxan-3-yl]oxy-2-methyloxan-3-yl]oxy-4-methoxy-2-methyloxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 15939579 Click to see CC1C(C(CC(O1)C2CCC3(C4CCC5(C6C7COC6(OC5(C4CC=C3C2)O7)C)C)C)OC)OC8CC(C(C(O8)C)OC9CC(C(C(O9)C)OC1CC(C(C(O1)C)OC1C(C(C(C(O1)CO)O)O)O)OC)O)OC 1055.20 unknown https://doi.org/10.1007/BF02329587
> Organoheterocyclic compounds / Dihydrofurans / Furanones / Butenolides
Ascorbic Acid 54670067 Click to see C(C(C1C(=C(C(=O)O1)O)O)O)O 176.12 unknown https://doi.org/10.1007/BF02329587
> Organoheterocyclic compounds / Tetrapyrroles and derivatives / Chlorins
methyl (21S,22S)-16-ethenyl-11-ethyl-12,17,21,26-tetramethyl-4-oxo-22-[3-oxo-3-[(E)-3,7,11,15-tetramethylhexadec-2-enoxy]propyl]-7,23,24,25-tetrazahexacyclo[18.2.1.15,8.110,13.115,18.02,6]hexacosa-1(23),2(6),5(26),7,9,11,13,15,17,19-decaene-3-carboxylate 6326752 Click to see CCC1=C(C2=CC3=C(C(=C(N3)C=C4C(C(C(=N4)C5=C6C(=C(C(=N6)C=C1N2)C)C(=O)C5C(=O)OC)CCC(=O)OCC=C(C)CCCC(C)CCCC(C)CCCC(C)C)C)C)C=C)C 871.20 unknown https://doi.org/10.1007/BF02329587
methyl (3R,21S,22S)-16-ethenyl-11-ethyl-12,17,21,26-tetramethyl-4-oxo-22-[3-oxo-3-[(E,7R,11R)-3,7,11,15-tetramethylhexadec-2-enoxy]propyl]-7,23,24,25-tetrazahexacyclo[18.2.1.15,8.110,13.115,18.02,6]hexacosa-1(23),2(6),5(26),7,9,11,13,15,17,19-decaene-3-carboxylate 5459387 Click to see CCC1=C(C2=CC3=C(C(=C(N3)C=C4C(C(C(=N4)C5=C6C(=C(C(=N6)C=C1N2)C)C(=O)C5C(=O)OC)CCC(=O)OCC=C(C)CCCC(C)CCCC(C)CCCC(C)C)C)C)C=C)C 871.20 unknown https://doi.org/10.1007/BF02329587

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