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Elegia microcarpa

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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 UUID644034805bd75297904271
Scientific name Elegia microcarpa
Authority (Kunth) Moline & H.P.Linder
First published in Syst. Bot. 30: 772 (2005)

Description Top

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Synonyms Top

Scientific name Authority First published in
Chondropetalum microcarpum (Kunth) Pillans Trans. Roy. Soc. South Africa 16: 303 (1928)
Dovea microcarpa Kunth Enum. Pl. 3: 459 (1841)
Dovea rigens Mast. Beibl. Bot. Jahrb. Syst. 66: 7 (1900)

Common names Top

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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-0000917710
KEW urn:lsid:ipni.org:names:77107898-1
The Plant List kew-463058
Open Tree Of Life 553300
NCBI Taxonomy 311265
IPNI 77107898-1
iNaturalist 584424
GBIF 6312123
EOL 1122889

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
The composition, geography, biology and assembly of the coastal flora of the Cape Floristic Region Grobler BA, Cowling RM PeerJ 11-Aug-2021
PMCID:PMC8364326
doi:10.7717/peerj.11916
PMID:34447627
Variations in flavonoid patterns within the genus Chondropetalum (restionaceae) Jeffrey B. Harborne, Marian Boardley, H. Peter Lindert Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)83536-0

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
Kaempferol 5280863 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown https://doi.org/10.1016/S0031-9422(00)83536-0
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides
5,7-Dihydroxy-2-(4-hydroxy-3,5-dimethoxyphenyl)-3-(3,4,5-trihydroxyoxan-2-yl)chromen-4-one 162994952 Click to see COC1=CC(=CC(=C1O)OC)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)C4C(C(C(CO4)O)O)O 462.40 unknown https://doi.org/10.1016/S0031-9422(00)83536-0
5,7-dihydroxy-2-(4-hydroxy-3,5-dimethoxyphenyl)-3-[(2S,3R,4R,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one 163020492 Click to see COC1=CC(=CC(=C1O)OC)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)C4C(C(C(C(O4)CO)O)O)O 492.40 unknown https://doi.org/10.1016/S0031-9422(00)83536-0
5,7-dihydroxy-2-(4-hydroxy-3,5-dimethoxyphenyl)-3-[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]chromen-4-one 162994953 Click to see COC1=CC(=CC(=C1O)OC)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)C4C(C(C(CO4)O)O)O 462.40 unknown https://doi.org/10.1016/S0031-9422(00)83536-0
5,7-Dihydroxy-2-(4-hydroxy-3,5-dimethoxyphenyl)-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one 68893416 Click to see COC1=CC(=CC(=C1O)OC)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)C4C(C(C(C(O4)CO)O)O)O 492.40 unknown https://doi.org/10.1016/S0031-9422(00)83536-0
5,7-Dihydroxy-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)-2-(3,4,5-trihydroxyphenyl)chromen-4-one 162978104 Click to see CC1C(C(C(C(O1)C2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C(=C4)O)O)O)O)O)O 448.40 unknown https://doi.org/10.1016/S0031-9422(00)83536-0
5,7-dihydroxy-3-[(2S,3R,4R,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-2-(3,4,5-trihydroxyphenyl)chromen-4-one 162845008 Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)C4C(C(C(C(O4)CO)O)O)O 464.40 unknown https://doi.org/10.1016/S0031-9422(00)83536-0
5,7-dihydroxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]-2-(3,4,5-trihydroxyphenyl)chromen-4-one 162978105 Click to see CC1C(C(C(C(O1)C2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C(=C4)O)O)O)O)O)O 448.40 unknown https://doi.org/10.1016/S0031-9422(00)83536-0
5,7-Dihydroxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-2-(3,4,5-trihydroxyphenyl)chromen-4-one 162845007 Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)C4C(C(C(C(O4)CO)O)O)O 464.40 unknown https://doi.org/10.1016/S0031-9422(00)83536-0
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
myricetin 3-O-beta-D-glucopyranoside 5318606 Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O 480.40 unknown https://doi.org/10.1016/S0031-9422(00)83536-0
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Artemexitin 44259710 Click to see COC1=CC(=CC(=C1O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC 346.30 unknown https://doi.org/10.1016/S0031-9422(00)83536-0

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