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Lamium galeobdolon subsp. galeobdolon

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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
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Details Top

Internal ID UUID643fe04bcb20f304816687
Scientific name Lamium galeobdolon subsp. galeobdolon
First published in Unknown

Description Top

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Common names Top

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Language Common/alternative name
English lamium galeobdolon galeobdolon
Spanish lamium galeobdolon galeobdolon
Bulgarian lamium galeobdolon galeobdolon
French lamium galeobdolon galeobdolon
Italian lamium galeobdolon galeobdolon
Russian lamium galeobdolon galeobdolon

Varieties (abbr. var.) 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

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000222513
INPN 137072
Flora of Italy 4500
KEW urn:lsid:ipni.org:names:77168576-1
Open Tree Of Life 470556
NCBI Taxonomy 1080049
GBIF 7308052

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)!
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Title Authors Publication Released IDs
Benzoxazinoids and iridoid glucosides from four Lamium species. Alipieva KI, Taskova RM, Evstatieva LN, Handjieva NV, Popov SS Phytochemistry 01-Dec-2003
doi:10.1016/J.PHYTOCHEM.2003.08.001
PMID:14630008

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
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
(1S,4aR,5R,7S,7aR)-7-methyl-1-[(2R,3S,4R,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,5,6,7a-tetrahydrocyclopenta[c]pyran-4a,5,7-triol 162989826 Click to see CC1(CC(C2(C1C(OC=C2)OC3C(C(C(C(O3)CO)O)O)O)O)O)O 364.34 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.08.001
[(1S,4aR,5R,7S,7aS)-4a,5-dihydroxy-7-methyl-1-[(2R,3S,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,5,6,7a-tetrahydrocyclopenta[c]pyran-7-yl] acetate 162894616 Click to see CC(=O)OC1(CC(C2(C1C(OC=C2)OC3C(C(C(C(O3)CO)O)O)O)O)O)C 406.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.08.001
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(2S)-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-1,4-benzoxazin-3-one 101615954 Click to see C1=CC=C2C(=C1)NC(=O)C(O2)OC3C(C(C(C(O3)CO)O)O)O 327.29 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.08.001

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