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Dysphania procera

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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 UUID644022a65fb86353343655
Scientific name Dysphania procera
Authority (Hochst. ex Moq.) Mosyakin & Clemants
First published in J. Bot. Res. Inst. Texas 2: 429 (2008)

Description Top

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Synonyms Top

Scientific name Authority First published in
Chenopodium procerum Hochst. ex Moq. Prodr. 13(2): 75 (1849)
Chenopodium suberifolium Murr Bull. Herb. Boissier II, 4: 990 1904

Common names Top

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Language Common/alternative name
German chenopodium procerum
Vietnamese chenopodium procerum

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
  • Africa
    • East Tropical Africa
      • Kenya
      • Tanzania
      • Uganda
    • Northeast Tropical Africa
      • Ethiopia
      • Sudan
    • South Tropical Africa
      • Angola
      • Malawi
      • Mozambique
      • Zambia
      • Zimbabwe
    • West-central Tropical Africa
      • Burundi
      • Rwanda
      • Zaïre

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000743795
KEW urn:lsid:ipni.org:names:77099587-1
The Plant List kew-2896054
Open Tree Of Life 3944404
NCBI Taxonomy 2570626
IPNI 77099587-1
iNaturalist 931726
GBIF 7610852

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, Ethnopharmacology, and Phytochemistry of Medicinal Plants Used for Treating Human Diarrheal Cases in Rwanda: A Review Gahamanyi N, Munyaneza E, Dukuzimana E, Tuyiringire N, Pan CH, Komba EV Antibiotics (Basel) 09-Oct-2021
PMCID:PMC8532704
doi:10.3390/antibiotics10101231
PMID:34680811
Chemical Structure and Biological Activities of Secondary Metabolites from Salicornia europaea L. Kim S, Lee EY, Hillman PF, Ko J, Yang I, Nam SJ Molecules 13-Apr-2021
PMCID:PMC8069253
doi:10.3390/molecules26082252
PMID:33924656
Sephadex® LH-20, Isolation, and Purification of Flavonoids from Plant Species: A Comprehensive Review Mottaghipisheh J, Iriti M Molecules 10-Sep-2020
PMCID:PMC7570886
doi:10.3390/molecules25184146
PMID:32927822
Resurrection of the genus Botrydium Spach (Chenopodiaceae), with a description of four new species from China, Peru and Burundi Zhang M, Zhu G Plant Divers 07-Dec-2016
PMCID:PMC6112192
doi:10.1016/j.pld.2016.10.005
PMID:30159484
Ethnobotanical survey of medicinal plant species used by communities around Mabira Central Forest Reserve, Uganda Tugume P, Kakudidi EK, Buyinza M, Namaalwa J, Kamatenesi M, Mucunguzi P, Kalema J J Ethnobiol Ethnomed 13-Jan-2016
PMCID:PMC4712608
doi:10.1186/s13002-015-0077-4
PMID:26762159
Fruit and Seed Anatomy of Chenopodium and Related Genera (Chenopodioideae, Chenopodiaceae/Amaranthaceae): Implications for Evolution and Taxonomy Sukhorukov AP, Zhang M PLoS One 23-Apr-2013
PMCID:PMC3633980
doi:10.1371/journal.pone.0061906
PMID:23626750
Antifungal constituents of Chenopodium procerum Chantal Bergeron, Andrew Marston, Etienne Hakizamungu, Kurt Hostettmann Informa UK Limited 19-Nov-2007
doi:10.3109/13880209509055209

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
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
Pygmol 14167388 Click to see CC12CCCC(C1C(C(CC2)C(C)(C)O)O)(C)O 256.38 unknown https://doi.org/10.3109/13880209509055209
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
5,7-Dihydroxy-2-(3-hydroxy-4-methoxyphenyl)-3-(((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-((((2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyltetrahydro-2H-pyran-2-yl)oxy)methyl)tetrahydro-2H-pyran-2-yl)oxy)-4H-chromen-4-one 5320020 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)OC)O)O)O)O)O)O)O 624.50 unknown https://doi.org/10.3109/13880209509055209
Narcissin 5481663 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)OC)O)O)O)O)O)O 624.50 unknown https://doi.org/10.3109/13880209509055209
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
Dihydrowogonin 11491431 Click to see COC1=C(C=C(C2=C1OC(CC2=O)C3=CC=CC=C3)O)O 286.28 unknown https://doi.org/10.3109/13880209509055209
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
5,7,2'-Trihydroxy-6-methoxyisoflavone 5491551 Click to see COC1=C(C2=C(C=C1O)OC=C(C2=O)C3=CC=CC=C3O)O 300.26 unknown https://doi.org/10.3109/13880209509055209
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 7-O-methylated isoflavonoids / 7-O-methylisoflavones
Irilin A 5491550 Click to see COC1=C(C(=C2C(=C1)OC=C(C2=O)C3=CC=CC=C3O)O)OC 314.29 unknown https://doi.org/10.3109/13880209509055209

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