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Mentzelia lindheimeri

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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 UUID6440479028e4e738579161
Scientific name Mentzelia lindheimeri
Authority Urb. & Gilg
First published in Nova Acta Acad. Caes. Leop.-Carol. German. Nat. Cur. 76: 54 (1900)

Description Top

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Synonyms Top

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Common names Top

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Language Common/alternative name
English lindheimer's blazingstar

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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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001073567
USDA Plants MELI3
Tropicos 18900021
KEW urn:lsid:ipni.org:names:157455-2
The Plant List tro-18900021
Open Tree Of Life 3900093
Nature Serve 2.151055
IPNI 157455-2
iNaturalist 165316
GBIF 5331431
EOL 486820

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)!
Title Authors Publication Released IDs
Iridoid mono- and di-glycosides in Mentzelia Søren Rosendal Jensen, Carl Bjarne Mikkelsen, Bent Juhl Nielsen Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(81)85221-1

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
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-[[(1R,2R,4S,5S,6R,10S)-5-hydroxy-10-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-7-yl]methoxy]oxane-3,4,5-triol 162964814 Click to see C1=C(C2C(C3C(C2O)O3)C(O1)OC4C(C(C(C(O4)CO)O)O)O)COC5C(C(C(C(O5)CO)O)O)O 524.50 unknown https://doi.org/10.1016/0031-9422(81)85221-1
(2S,3R,4S,5S,6R)-2-[[(1R,2R,4S,5S,6R,10S)-5-hydroxy-7-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 162966338 Click to see C1=C(C2C(C3C(C2O)O3)C(O1)OC4C(C(C(C(O4)CO)O)O)O)CO 362.33 unknown https://doi.org/10.1016/0031-9422(81)85221-1
2-[[5-Hydroxy-7-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 162966337 Click to see C1=C(C2C(C3C(C2O)O3)C(O1)OC4C(C(C(C(O4)CO)O)O)O)CO 362.33 unknown https://doi.org/10.1016/0031-9422(81)85221-1

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