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Eucnide bartonioides

Eucnide bartonioides - 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 UUID64401bb8a88fc373295467
Scientific name Eucnide bartonioides
Authority Zucc.
First published in in Del. Sem. Hort. Bot. Monac. Coll. 1844 (1844).

Description Top

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Synonyms Top

Scientific name Authority First published in
Mentzelia bartonioides (Zucc.) Lehm. Index Seminum (HBG, Hamburgensis) 1850: 6 (1850)
Mentzelia gronoviifolia Fisch. & C.A.Mey. Index Seminum (LE, Petropolitanus) 10: 54 (1845)
Microsperma bartonioides Walp. Repert. Bot. Syst. 5: 777 (1846)

Common names Top

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Language Common/alternative name
English yellow stingbush
Chinese 岩荨麻
Chinese 巖蕁麻

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Eucnide bartonioides var. edwardsiana B.L.Turner Phytologia 94: 306 (2012)

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

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-0000681144
USDA Plants EUBA3
Tropicos 18900196
KEW urn:lsid:ipni.org:names:545110-1
The Plant List kew-2802723
Open Tree Of Life 935368
NCBI Taxonomy 86880
Nature Serve 2.132157
IPNI 545111-1
iNaturalist 81986
GBIF 2874728
EOL 589441

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
Iridoid glycosides from Eucnide bartonioides Veronica Rodriguez, Jan Schripsema, Søren Rosendal Jensen Elsevier BV 04-Mar-2003
doi:10.1016/S0031-9422(97)00162-3

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
methyl 3-ethenyl-4-(2-hydroxyethyl)-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydro-2H-pyran-5-carboxylate 14488075 Click to see COC(=O)C1=COC(C(C1CCO)C=C)OC2C(C(C(C(O2)CO)O)O)O 390.40 unknown https://doi.org/10.1016/S0031-9422(97)00162-3
NCGC00384878-01_C17H26O10_2H-Pyran-5-carboxylic acid, 3-ethenyl-2-(beta-D-glucopyranosyloxy)-3,4-dihydro-4-(2-hydroxyethyl)-, methyl ester, (2S,3R,4S)- 14488076 Click to see COC(=O)C1=COC(C(C1CCO)C=C)OC2C(C(C(C(O2)CO)O)O)O 390.40 unknown https://doi.org/10.1016/S0031-9422(97)00162-3
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
5-Hydroxyloganin 101713109 Click to see CC1C(CC2(C1C(OC=C2C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O)O)O 406.40 unknown https://doi.org/10.1016/S0031-9422(97)00162-3
8-Epiloganin 10548420 Click to see CC1C(CC2C1C(OC=C2C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O)O 390.40 unknown https://doi.org/10.1016/S0031-9422(97)00162-3
Loganin 87691 Click to see CC1C(CC2C1C(OC=C2C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O)O 390.40 unknown https://doi.org/10.1016/S0031-9422(97)00162-3
methyl (1S,4aR,6S,7R,7aR)-4a,6-dihydroxy-7-methyl-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,6,7,7a-tetrahydro-1H-cyclopenta[c]pyran-4-carboxylate 162877720 Click to see CC1C(CC2(C1C(OC=C2C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O)O)O 406.40 unknown https://doi.org/10.1016/S0031-9422(97)00162-3
methyl 4a,6-dihydroxy-7-methyl-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,6,7,7a-tetrahydro-1H-cyclopenta[c]pyran-4-carboxylate 73800781 Click to see CC1C(CC2(C1C(OC=C2C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O)O)O 406.40 unknown https://doi.org/10.1016/S0031-9422(97)00162-3
Methyl 6-hydroxy-7-methyl-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-4-carboxylate 601562 Click to see CC1C(CC2C1C(OC=C2C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O)O 390.40 unknown https://doi.org/10.1016/S0031-9422(97)00162-3
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(3S,4R,4aS)-4-ethenyl-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4,4a,5,6-tetrahydro-3H-pyrano[3,4-c]pyran-8-one 354447 Click to see C=CC1C2CCOC(=O)C2=COC1OC3C(C(C(C(O3)CO)O)O)O 358.34 unknown https://doi.org/10.1016/S0031-9422(97)00162-3
(7Alpha-Hydroxy)-Morroniside 21593530 Click to see CC1C2C(CC(O1)O)C(=COC2OC3C(C(C(C(O3)CO)O)O)O)C(=O)OC 406.40 unknown https://doi.org/10.1016/S0031-9422(97)00162-3
[(4aS,8S,8aS)-1-methyl-3-oxo-8-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4,4a,8,8a-tetrahydro-1H-pyrano[3,4-c]pyran-5-yl] acetate 6325484 Click to see CC1C2C(CC(=O)O1)C(=COC2OC3C(C(C(C(O3)CO)O)O)O)OC(=O)C 404.40 unknown https://doi.org/10.1016/S0031-9422(97)00162-3
4-ethenyl-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4,4a,5,6-tetrahydro-3H-pyrano[3,4-c]pyran-8-one 581257 Click to see C=CC1C2CCOC(=O)C2=COC1OC3C(C(C(C(O3)CO)O)O)O 358.34 unknown https://doi.org/10.1016/S0031-9422(97)00162-3
CID 12312977 12312977 Click to see CC1C2C(CC(O1)O)C(=COC2OC3C(C(C(C(O3)CO)O)O)O)C(=O)OC 406.40 unknown https://doi.org/10.1016/S0031-9422(97)00162-3
Kingiside 12304884 Click to see CC1C2C(CC(=O)O1)C(=COC2OC3C(C(C(C(O3)CO)O)O)O)C(=O)OC 404.40 unknown https://doi.org/10.1016/S0031-9422(97)00162-3
methyl (4aS,8aS)-3-hydroxy-1-methyl-8-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,3,4,4a,8,8a-hexahydropyrano[3,4-c]pyran-5-carboxylate 138107798 Click to see CC1C2C(CC(O1)O)C(=COC2OC3C(C(C(C(O3)CO)O)O)O)C(=O)OC 406.40 unknown https://doi.org/10.1016/S0031-9422(97)00162-3
methyl 1-methyl-3-oxo-8-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4,4a,8,8a-tetrahydro-1H-pyrano[3,4-c]pyran-5-carboxylate 12304883 Click to see CC1C2C(CC(=O)O1)C(=COC2OC3C(C(C(C(O3)CO)O)O)O)C(=O)OC 404.40 unknown https://doi.org/10.1016/S0031-9422(97)00162-3
Sweroside 161036 Click to see C=CC1C2CCOC(=O)C2=COC1OC3C(C(C(C(O3)CO)O)O)O 358.34 unknown https://doi.org/10.1016/S0031-9422(97)00162-3

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