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Rumex chalepensis

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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 UUID64404b6159c24040254496
Scientific name Rumex chalepensis
Authority Mill.
First published in Gard. Dict. ed. 8 : n.º 11 (1768)

Description Top

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Synonyms Top

Scientific name Authority First published in
Rumex alveolatus Losinsk. Fl. Turkmen. 2(1): 44 (1937)
Rumex dictyocarpus Boiss. & Buhse Nouv. Mém. Soc. Imp. Naturalistes Moscou 12: 192 (1860)
Rumex drobovii Korovin Key Pl. Envir. Tashkent, ed. Popov 84 (1924).
Rumex foveolatus Losinsk. Fl. URSS 5: 478, 717. 1936
Rumex losinskajae Rech.f. Repert. Spec. Nov. Regni Veg. 48: 164 (1940)

Common names Top

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Language Common/alternative name
Chinese 网果酸模
Chinese 血当归
Chinese 網果酸模

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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No forms added yet.

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
    • Caucasus
      • Transcaucasus
    • China
      • China North-central
      • China South-central
      • China Southeast
      • Xinjiang
    • Middle Asia
      • Kazakhstan
      • Kirgizstan
      • Tadzhikistan
      • Turkmenistan
      • Uzbekistan
    • Western Asia
      • Afghanistan
      • Iran
      • Iraq
      • Lebanon-Syria
      • Turkey

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001100853
Tropicos 26000106
KEW urn:lsid:ipni.org:names:696983-1
The Plant List tro-26000106
Open Tree Of Life 5920120
Observations.org 121585
NCBI Taxonomy 1786032
IPNI 696983-1
iNaturalist 1142414
GBIF 4035494
EOL 2904248
Elurikkus 454990
USDA GRIN 408313
CMAUP NPO16419

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
Ethnobotany for food security and ecological transition: wild food plant gathering and consumption among four cultural groups in Kurram District, NW Pakistan Hussain ST, Muhammad S, Khan S, Hussain W, Pieroni A J Ethnobiol Ethnomed 01-Sep-2023
PMCID:PMC10472554
doi:10.1186/s13002-023-00607-2
PMID:37658453
Ethnobotanical inventory and medicinal perspectives of herbal flora of Shiwalik mountainous range of District Bhimber, Azad Jammu and Kashmir, Pakistan Ishtiaq M, Khanum H, Hussain I, Parveen A, Maqbool M, Thind S, Hussain T, Azeem M, Shabir F, Elansary HO PLoS One 29-Mar-2022
PMCID:PMC8963552
doi:10.1371/journal.pone.0265028
PMID:35349579
Antiviral Activities of Halogenated Emodin Derivatives against Human Coronavirus NL63 Horvat M, Avbelj M, Durán-Alonso MB, Banjanac M, Petković H, Iskra J Molecules 11-Nov-2021
PMCID:PMC8618202
doi:10.3390/molecules26226825
PMID:34833917
Pharmacologic Activities of Plant-Derived Natural Products on Respiratory Diseases and Inflammations Timalsina D, Pokhrel KP, Bhusal D Biomed Res Int 04-Oct-2021
PMCID:PMC8505070
doi:10.1155/2021/1636816
PMID:34646882
Regional trade of medicinal plants has facilitated the retention of traditional knowledge: case study in Gilgit-Baltistan Pakistan Salim MA, Ranjitkar S, Hart R, Khan T, Ali S, Kiran C, Parveen A, Batool Z, Bano S, Xu J J Ethnobiol Ethnomed 28-Jan-2019
PMCID:PMC6348662
doi:10.1186/s13002-018-0281-0
PMID:30691476
Isolation and Identification of the Five Novel Flavonoids from Genipa americana Leaves Silva LM, Alves JS, da Silva Siqueira EM, de Souza Neto MA, Abreu LS, Tavares JF, Porto DL, de Santis Ferreira L, Demarque DP, Lopes NP, Aragão CF, Zucolotto SM Molecules 02-Oct-2018
PMCID:PMC6222654
doi:10.3390/molecules23102521
PMID:30279336
An ethnopharmacological evaluation of Navapind and Shahpur Virkanin district Sheikupura, Pakistan for their herbal medicines Zahoor M, Yousaf Z, Aqsa T, Haroon M, Saleh N, Aftab A, Javed S, Qadeer M, Ramazan H J Ethnobiol Ethnomed 08-May-2017
PMCID:PMC5422909
doi:10.1186/s13002-017-0151-1
PMID:28482859
Winners always win: growth of a wide range of plant species from low to future high CO 2 Temme AA, Liu JC, Cornwell WK, Cornelissen JH, Aerts R Ecol Evol 15-Oct-2015
PMCID:PMC4662314
doi:10.1002/ece3.1687
PMID:26640673
Phytochemical and biological research of Polygoneae medicinal resources Hao DC, Gu XJ, Xiao PG Medicinal Plants 03-Jul-2015
PMCID:PMC7158354
doi:10.1016/B978-0-08-100085-4.00012-8
World Allergy Organization Study on Aerobiology for Creating First Pollen and Mold Calendar With Clinical Significance in Islamabad, Pakistan; A Project of World Allergy Organization and Pakistan Allergy, Asthma & Clinical Immunology Centre of Islamabad Abbas S, Katelaris CH, Singh AB, Raza SM, Khan MA, Rashid M, Abbas M, Ismail M World Allergy Organ J 15-Sep-2012
PMCID:PMC3651178
doi:10.1097/WOX.0b013e31826421c8
PMID:23283209
Anticancer potential of emodin Hsu SC, Chung JG Biomedicine (Taipei) 11-May-2012
PMCID:PMC7104001
doi:10.1016/j.biomed.2012.03.003
PMID:32289000
I.—The constituents of Rumex Ecklonianus Frank Tutin, Hubert William Bentley Clewer Royal Society of Chemistry (RSC) 02-Apr-2004
doi:10.1039/CT9109700001
Flavonoid glycosides and an anthraquinone from Rumex chalepensis. Hasan A, Ahmed I, Jay M, Voirin B Phytochemistry 01-Jul-1995
doi:10.1016/0031-9422(95)00071-E
PMID:7662279

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Alkaloids and derivatives / Harmala alkaloids
Harman 5281404 Click to see CC1=NC=CC2=C1NC3=CC=CC=C23 182.22 unknown via CMAUP database
> Alkaloids and derivatives / Yohimbine alkaloids
Rauniticine 72338 Click to see CC1C2CN3CCC4=C(C3CC2C(=CO1)C(=O)OC)NC5=CC=CC=C45 352.40 unknown via CMAUP database
> Benzenoids / Anthracenes / Anthraquinones
Chrysophanic acid 10208 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=CC=C3O 254.24 unknown via CMAUP database
Physcione 10639 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=C(C=C3O)OC 284.26 unknown via CMAUP database
> Benzenoids / Anthracenes / Anthraquinones / Hydroxyanthraquinones
Emodin 3220 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=C(C=C3O)O 270.24 unknown https://doi.org/10.1016/0031-9422(95)00071-E
> 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 via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
Syringic acid 10742 Click to see COC1=CC(=CC(=C1O)OC)C(=O)O 198.17 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Galloyl esters
Ethyl gallate 13250 Click to see CCOC(=O)C1=CC(=C(C(=C1)O)O)O 198.17 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Vanillic Acid 8468 Click to see COC1=C(C=CC(=C1)C(=O)O)O 168.15 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / p-Hydroxybenzoic acid esters / p-Hydroxybenzoic acid alkyl esters
Ethyl 3,4-Dihydroxybenzoate 77547 Click to see CCOC(=O)C1=CC(=C(C=C1)O)O 182.17 unknown via CMAUP database
> Benzenoids / Phenols / Benzenediols / Catechols
Catechol 289 Click to see C1=CC=C(C(=C1)O)O 110.11 unknown via CMAUP database
> Benzenoids / Phenols / Benzenetriols and derivatives / Pyrogallols and derivatives / 5-unsubstituted pyrrogallols
Pyrogallol 1057 Click to see C1=CC(=C(C(=C1)O)O)O 126.11 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Vwjsnopypvuarg-bpnnxiafsa- 14355560 Click to see CC1CCC2(CCC3(C(=CCC4C3(CC(C5C4(CCC(C5=C)O)C)O)C)C2C1(C)O)C)C(=O)OC 486.70 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzaldehydes / Hydroxybenzaldehydes
Protocatechualdehyde 8768 Click to see C1=CC(=C(C=C1C=O)O)O 138.12 unknown via CMAUP database
> Organoheterocyclic compounds / Indolizidines
Isocorynoxeine 3037448 Click to see COC=C(C1CC2C3(CCN2CC1C=C)C4=CC=CC=C4NC3=O)C(=O)OC 382.50 unknown via CMAUP database
Isomitraphylline 11726520 Click to see CC1C2CN3CCC4(C3CC2C(=CO1)C(=O)OC)C5=CC=CC=C5NC4=O 368.40 unknown via CMAUP database
Isopteropodine 9885603 Click to see CC1C2CN3CCC4(C3CC2C(=CO1)C(=O)OC)C5=CC=CC=C5NC4=O 368.40 unknown via CMAUP database
Mitraphylline 94160 Click to see CC1C2CN3CCC4(C3CC2C(=CO1)C(=O)OC)C5=CC=CC=C5NC4=O 368.40 unknown via CMAUP database
Pteropodine 10429112 Click to see CC1C2CN3CCC4(C3CC2C(=CO1)C(=O)OC)C5=CC=CC=C5NC4=O 368.40 unknown via CMAUP database
Speciophylline 168985 Click to see CC1C2CN3CCC4(C3CC2C(=CO1)C(=O)OC)C5=CC=CC=C5NC4=O 368.40 unknown via CMAUP database
Uncarine F 12304288 Click to see CC1C2CN3CCC4(C3CC2C(=CO1)C(=O)OC)C5=CC=CC=C5NC4=O 368.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
cis-p-Coumaric acid 1549106 Click to see C1=CC(=CC=C1C=CC(=O)O)O 164.16 unknown via CMAUP database
Ferulic acid 445858 Click to see COC1=C(C=CC(=C1)C=CC(=O)O)O 194.18 unknown via CMAUP database
p-Coumaric acid 637542 Click to see C1=CC(=CC=C1C=CC(=O)O)O 164.16 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Cianidanol 9064 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
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/10.1039/CT9109700001
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Quercitrin 5280459 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 448.40 unknown https://doi.org/10.1039/CT9109700001
https://doi.org/10.1016/0031-9422(95)00071-E
Rutin 5280805 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O 610.50 unknown https://doi.org/10.1016/0031-9422(95)00071-E
> Phenylpropanoids and polyketides / Isoflavonoids / Coumestans
1,3-Dihydroxy-8,9-dimethoxy-[1]benzofuro[3,2-c]chromen-6-one 11602329 Click to see COC1=C(C=C2C(=C1)C3=C(O2)C4=C(C=C(C=C4OC3=O)O)O)OC 328.27 unknown https://doi.org/10.1039/CT9109700001

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