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Erythrina cochleata

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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 UUID643fd5f1ca8e2392000834
Scientific name Erythrina cochleata
Authority Standl.
First published in Contr. U.S. Natl. Herb.30: 179 (1919)

Description Top

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Synonyms Top

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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
  • Southern America
    • Central America
      • Costa Rica
    • Northern South America
      • Venezuela
    • Western South America
      • Colombia

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000165884
Tropicos 13009257
KEW urn:lsid:ipni.org:names:96572-2
The Plant List ild-12310
Open Tree Of Life 3921529
NCBI Taxonomy 2590690
IUCN Red List 151999996
IPNI 96572-2
GBIF 5349520
EOL 416397
USDA GRIN 436194

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
Alkaloids in seeds of four Erythrina species Amrik S. Chawla, Fawzia M.J. Redha, Anthony H. Jackson Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)82559-5

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
> Alkaloids and derivatives / Erythrina alkaloids / Erythrinanes
(2R,13bS)-11-methoxy-2,6,8,9-tetrahydro-1H-indolo[7a,1-a]isoquinoline-2,12-diol 21679845 Click to see COC1=C(C=C2C(=C1)CCN3C24CC(C=CC4=CC3)O)O 285.34 unknown https://doi.org/10.1016/S0031-9422(00)82559-5
CID 21679844 21679844 Click to see COC1CC23C(=CCN2CCC4=CC(=C(C=C34)O)O)C=C1 285.34 unknown https://doi.org/10.1016/S0031-9422(00)82559-5
Erysodine 169017 Click to see COC1CC23C(=CCN2CCC4=CC(=C(C=C34)OC)O)C=C1 299.40 unknown https://doi.org/10.1016/S0031-9422(00)82559-5
Erysotrine 442219 Click to see COC1CC23C(=CCN2CCC4=CC(=C(C=C34)OC)OC)C=C1 313.40 unknown https://doi.org/10.1016/S0031-9422(00)82559-5
Erysovine 5317203 Click to see COC1CC23C(=CCN2CCC4=CC(=C(C=C34)O)OC)C=C1 299.40 unknown https://doi.org/10.1016/S0031-9422(00)82559-5
Erythravine 11231853 Click to see COC1=C(C=C2C(=C1)CCN3C24CC(C=CC4=CC3)O)OC 299.40 unknown https://doi.org/10.1016/S0031-9422(00)82559-5
Erythrinan-16-ol, 1,2,6,7-tetradehydro-3,15-dimethoxy-, (3beta)- 622748 Click to see COC1CC23C(=CCN2CCC4=CC(=C(C=C34)OC)O)C=C1 299.40 unknown https://doi.org/10.1016/S0031-9422(00)82559-5

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Contributors Top

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Collections Top

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