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Persicaria ferruginea

Persicaria ferruginea - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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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 UUID6440030540c3e253870177
Scientific name Persicaria ferruginea
Authority (Wedd.) Soják
First published in Preslia 46: 153 (1974)

Description Top

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Synonyms Top

Scientific name Authority First published in
Polygonum ferrugineum Wedd. Ann. Sci. Nat., Bot. , sér. 3, 13: 252 (1849)
Polygonum gummifera Wedd. Ann. Sci. Nat., Bot. , sér. 3, 13: 252 (1849)
Polygonum spectabile Mart. ex Meisn. Prodr. [A. P. de Candolle] 14(1): 119. 1856 [mid Oct 1856]
Polygonum spectabile var. minor Chodat Bull. Herb. Boissier 7, App. 1: 62. 1899

Common names Top

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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
  • Northern America
    • Mexico
      • Mexico Gulf
      • Mexico Northeast
      • Mexico Southeast
  • Southern America
    • Brazil
      • Brazil North
      • Brazil Northeast
      • Brazil South
      • Brazil Southeast
      • Brazil West-central
    • Caribbean
      • Cuba
      • Dominican Republic
      • Haiti
    • Central America
      • Costa Rica
      • El Salvador
      • Guatemala
      • Honduras
      • Nicaragua
    • Northern South America
      • French Guiana
      • Venezuela
    • Southern South America
      • Argentina Northeast
      • Paraguay
      • Uruguay
    • Western South America
      • Bolivia
      • Colombia
      • Peru

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000488041
Tropicos 100362558
INPN 883752
KEW urn:lsid:ipni.org:names:694968-1
The Plant List kew-2571939
Open Tree Of Life 478827
NCBI Taxonomy 487993
IPNI 694968-1
iNaturalist 866172
GBIF 4035927

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
Alpinetin: A Review of Its Pharmacology and Pharmacokinetics Zhao G, Tong Y, Luan F, Zhu W, Zhan C, Qin T, An W, Zeng N Front Pharmacol 04-Feb-2022
PMCID:PMC8854656
doi:10.3389/fphar.2022.814370
PMID:35185569
An Update on Phytochemicals and Pharmacological Activities of the Genus Persicaria and Polygonum Seimandi G, Álvarez N, Stegmayer MI, Fernández L, Ruiz V, Favaro MA, Derita M Molecules 01-Oct-2021
PMCID:PMC8512787
doi:10.3390/molecules26195956
PMID:34641500
Medicinal Plants for the Treatment of Local Tissue Damage Induced by Snake Venoms: An Overview from Traditional Use to Pharmacological Evidence Félix-Silva J, Silva-Junior AA, Zucolotto SM, Fernandes-Pedrosa MD Evid Based Complement Alternat Med 21-Aug-2017
PMCID:PMC5585606
doi:10.1155/2017/5748256
PMID:28904556
Checklist of vascular plants of the Department of Ñeembucú, Paraguay Egea JD, Peña-Chocarro M, Espada C, Knapp S PhytoKeys 30-Jan-2012
PMCID:PMC3281576
doi:10.3897/phytokeys.9.2279
PMID:22371688
Detection of antifungal compounds in Polygonum ferrugineum Wedd. extracts by bioassay-guided fractionation. Some evidences of their mode of action. López SN, Furlan RL, Zacchino SA J Ethnopharmacol 18-Nov-2011
doi:10.1016/J.JEP.2011.09.038
PMID:22001591
An unusual homoisoflavanone and a structurally-related dihydrochalcone from Polygonum ferrugineum (Polygonaceae). López SN, Sierra MG, Gattuso SJ, Furlán RL, Zacchino SA Phytochemistry 01-Oct-2006
doi:10.1016/J.PHYTOCHEM.2006.06.018
PMID:16884749

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
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
5-Hydroxy-7-methoxy-2-phenylchroman-4-one 73201 Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=CC=C3)O 270.28 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.06.018
https://doi.org/10.1016/J.JEP.2011.09.038
5-Hydroxy-7-methoxyflavanone 4101463 Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=CC=C3)O 270.28 unknown https://doi.org/10.1016/J.JEP.2011.09.038
https://doi.org/10.1016/J.PHYTOCHEM.2006.06.018
Pinostrobin 6950539 Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=CC=C3)O 270.28 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.06.018
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
(2S)-7-hydroxy-5,8-dimethoxy-2-phenyl-2,3-dihydrochromen-4-one 86311127 Click to see COC1=C2C(=O)CC(OC2=C(C(=C1)O)OC)C3=CC=CC=C3 300.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.06.018
https://doi.org/10.1016/J.JEP.2011.09.038
7-Hydroxy-5,8-dimethoxyflavanone 23786424 Click to see COC1=C2C(=O)CC(OC2=C(C(=C1)O)OC)C3=CC=CC=C3 300.30 unknown https://doi.org/10.1016/J.JEP.2011.09.038
https://doi.org/10.1016/J.PHYTOCHEM.2006.06.018
> Phenylpropanoids and polyketides / Homoisoflavonoids / Homoisoflavans / Homoisoflavanones
(3R)-5,7-dihydroxy-3-[(S)-hydroxy(phenyl)methyl]-6-methoxy-2,3-dihydrochromen-4-one 26235906 Click to see COC1=C(C2=C(C=C1O)OCC(C2=O)C(C3=CC=CC=C3)O)O 316.30 unknown https://doi.org/10.1016/J.JEP.2011.09.038
https://doi.org/10.1016/J.PHYTOCHEM.2006.06.018
5,7-Dihydroxy-3-(hydroxy-phenyl-methyl)-6-methoxy-chroman-4-one 45360194 Click to see COC1=C(C2=C(C=C1O)OCC(C2=O)C(C3=CC=CC=C3)O)O 316.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.06.018
https://doi.org/10.1016/J.JEP.2011.09.038
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxy-dihydrochalcones
(2R,3S)-3-hydroxy-2-(hydroxymethyl)-3-phenyl-1-(2,4,6-trihydroxy-3-methoxyphenyl)propan-1-one 163045803 Click to see COC1=C(C=C(C(=C1O)C(=O)C(CO)C(C2=CC=CC=C2)O)O)O 334.30 unknown https://doi.org/10.1016/J.JEP.2011.09.038
https://doi.org/10.1016/J.PHYTOCHEM.2006.06.018
3-Hydroxy-2-(hydroxymethyl)-3-phenyl-1-(2,4,6-trihydroxy-3-methoxyphenyl)propan-1-one 101418808 Click to see COC1=C(C=C(C(=C1O)C(=O)C(CO)C(C2=CC=CC=C2)O)O)O 334.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.06.018
https://doi.org/10.1016/J.JEP.2011.09.038
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
1-(2,4-Dihydroxy-6-methoxyphenyl)-3-phenylprop-2-en-1-one 154102 Click to see COC1=CC(=CC(=C1C(=O)C=CC2=CC=CC=C2)O)O 270.28 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.06.018
https://doi.org/10.1016/J.JEP.2011.09.038
2-Propen-1-one, 1-(2,6-dihydroxy-3,4-dimethoxyphenyl)-3-phenyl-, (E)-; (2E)-1-(2,6-Dihydroxy-3,4-dimethoxyphenyl)-3-phenyl-2-propen-1-one 179543 Click to see COC1=C(C(=C(C(=C1)O)C(=O)C=CC2=CC=CC=C2)O)OC 300.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.06.018
https://doi.org/10.1016/J.JEP.2011.09.038
6'-Hydroxy-2',4'-dimethoxychalcone 242589 Click to see COC1=CC(=C(C(=C1)OC)C(=O)C=CC2=CC=CC=C2)O 284.31 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.06.018
https://doi.org/10.1016/J.JEP.2011.09.038
Cardamonin 641785 Click to see COC1=CC(=CC(=C1C(=O)C=CC2=CC=CC=C2)O)O 270.28 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.06.018
https://doi.org/10.1016/J.JEP.2011.09.038
Flavokawain B 5356121 Click to see COC1=CC(=C(C(=C1)OC)C(=O)C=CC2=CC=CC=C2)O 284.31 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.06.018
https://doi.org/10.1016/J.JEP.2011.09.038
Pashanone 6254251 Click to see COC1=C(C(=C(C(=C1)O)C(=O)C=CC2=CC=CC=C2)O)OC 300.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.06.018
https://doi.org/10.1016/J.JEP.2011.09.038

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