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Reseda villosa

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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 UUID643fffca57e01147788211
Scientific name Reseda villosa
Authority Coss.
First published in Bull. Soc. Bot. France 6: 392 (1859)

Description Top

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Synonyms Top

Scientific name Authority First published in
Reseda sudanica A.Chev. Compt. Rend. Intern. Cong. Bot. : 273 (1900)

Common names Top

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Language Common/alternative name
Arabic بليحاء شعرية

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
    • Northeast Tropical Africa
      • Chad
    • Northern Africa
      • Algeria
      • Libya
      • Morocco
      • Western Sahara
    • West Tropical Africa
      • Mali
      • Mauritania
      • Niger

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000462414
Tropicos 50004905
KEW urn:lsid:ipni.org:names:715662-1
The Plant List kew-2525712
PaleoBotany 16589
Open Tree Of Life 409198
NCBI Taxonomy 415837
IPNI 715662-1
GBIF 3916548

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
Monofloral Honeys as a Potential Source of Natural Antioxidants, Minerals and Medicine Mărgăoan R, Topal E, Balkanska R, Yücel B, Oravecz T, Cornea-Cipcigan M, Vodnar DC Antioxidants (Basel) 25-Jun-2021
PMCID:PMC8300703
doi:10.3390/antiox10071023
PMID:34202118
Climatic Zone and Soil Properties Determine the Biodiversity of the Soil Bacterial Communities Associated to Native Plants from Desert Areas of North-Central Algeria Bona E, Massa N, Toumatia O, Novello G, Cesaro P, Todeschini V, Boatti L, Mignone F, Titouah H, Zitouni A, Lingua G, Vuolo F, Gamalero E Microorganisms 23-Jun-2021
PMCID:PMC8303931
doi:10.3390/microorganisms9071359
PMID:34201731
The role of Nucularia perrinii Batt. (Chenopodiaceae) in the camel-based Sahrawi social-ecological system Volpato G, Di Nardo A J Ethnobiol Ethnomed 08-Feb-2017
PMCID:PMC5299638
doi:10.1186/s13002-017-0141-3
PMID:28179025
Comparative antioxidant activity of two Algerian Reseda species Djemaa Berrehal, Assia Khalfallah, Soumeya Bencharif-Betina, Zahia Kabouche, Nassira Kacem, Ahmed Kabouche, Claude-Alain Calliste, Jean-Luc Duroux Springer Science and Business Media LLC 06-Jul-2010
doi:10.1007/S10600-010-9643-0

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
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
3,5-Dihydroxy-2-(4-hydroxyphenyl)-7-(2,4,5-trihydroxy-6-methyloxan-3-yl)oxychromen-4-one 163016846 Click to see CC1C(C(C(C(O1)O)OC2=CC(=C3C(=C2)OC(=C(C3=O)O)C4=CC=C(C=C4)O)O)O)O 432.40 unknown https://doi.org/10.1007/S10600-010-9643-0
3,5-dihydroxy-2-(4-hydroxyphenyl)-7-[(2R,3R,4S,5R,6S)-2,4,5-trihydroxy-6-methyloxan-3-yl]oxychromen-4-one 163016847 Click to see CC1C(C(C(C(O1)O)OC2=CC(=C3C(=C2)OC(=C(C3=O)O)C4=CC=C(C=C4)O)O)O)O 432.40 unknown https://doi.org/10.1007/S10600-010-9643-0
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-dihydroxyphenyl)-5-hydroxy-3-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-7-[(2R,3R,4S,5S,6R)-2,4,5-trihydroxy-6-methyloxan-3-yl]oxychromen-4-one 163046841 Click to see CC1C(C(C(C(O1)O)OC2=CC(=C3C(=C2)OC(=C(C3=O)OC4C(C(C(C(O4)CO)O)O)O)C5=CC(=C(C=C5)O)O)O)O)O 610.50 unknown https://doi.org/10.1007/S10600-010-9643-0
2-(3,4-Dihydroxyphenyl)-5-hydroxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-7-(2,4,5-trihydroxy-6-methyloxan-3-yl)oxychromen-4-one 163046840 Click to see CC1C(C(C(C(O1)O)OC2=CC(=C3C(=C2)OC(=C(C3=O)OC4C(C(C(C(O4)CO)O)O)O)C5=CC(=C(C=C5)O)O)O)O)O 610.50 unknown https://doi.org/10.1007/S10600-010-9643-0
5-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-3-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-7-[(2R,3R,4S,5S,6R)-2,4,5-trihydroxy-6-methyloxan-3-yl]oxychromen-4-one 162888844 Click to see CC1C(C(C(C(O1)O)OC2=CC(=C3C(=C2)OC(=C(C3=O)OC4C(C(C(C(O4)CO)O)O)O)C5=CC(=C(C=C5)O)OC)O)O)O 624.50 unknown https://doi.org/10.1007/S10600-010-9643-0
5-Hydroxy-2-(4-hydroxy-3-methoxyphenyl)-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-7-(2,4,5-trihydroxy-6-methyloxan-3-yl)oxychromen-4-one 162888843 Click to see CC1C(C(C(C(O1)O)OC2=CC(=C3C(=C2)OC(=C(C3=O)OC4C(C(C(C(O4)CO)O)O)O)C5=CC(=C(C=C5)O)OC)O)O)O 624.50 unknown https://doi.org/10.1007/S10600-010-9643-0
5-Hydroxy-2-(4-hydroxyphenyl)-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-7-(2,4,5-trihydroxy-6-methyloxan-3-yl)oxychromen-4-one 162948315 Click to see CC1C(C(C(C(O1)O)OC2=CC(=C3C(=C2)OC(=C(C3=O)OC4C(C(C(C(O4)CO)O)O)O)C5=CC=C(C=C5)O)O)O)O 594.50 unknown https://doi.org/10.1007/S10600-010-9643-0
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
5-hydroxy-2-(4-hydroxyphenyl)-3,7-bis[[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy]chromen-4-one 11444588 Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)OC4C(C(C(C(O4)C)O)O)O)C5=CC=C(C=C5)O)O)O)O)O 578.50 unknown https://doi.org/10.1007/S10600-010-9643-0
Lespedin;Lespenephryl 12305415 Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)OC4C(C(C(C(O4)C)O)O)O)C5=CC=C(C=C5)O)O)O)O)O 578.50 unknown https://doi.org/10.1007/S10600-010-9643-0

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Collections Top

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