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Erythrina berteroana

Erythrina berteroana - 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 UUID643fd8b2874d7677692529
Scientific name Erythrina berteroana
Authority Urb.
First published in Symb. Antill.5: 370 (1908)

Description Top

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Synonyms Top

Scientific name Authority First published in
Erythrina neglecta Krukoff & Moldenke Phytologia1: 287 (1939)

Common names Top

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Language Common/alternative name
Arabic حمرية برتروانية
guc patsua
Malayalam എറിത്രിന ബെർട്ടെറോന

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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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Northern America
    • Mexico
      • Mexico Gulf
      • Mexico Southeast
      • Mexico Southwest
  • Southern America
    • Caribbean
      • Cuba
      • Dominican Republic
      • Haiti
      • Puerto Rico
    • Central America
      • Belize
      • Costa Rica
      • El Salvador
      • Guatemala
      • Honduras
      • Nicaragua
      • Panamá
    • Northern South America
      • Venezuela
    • Western South America
      • Colombia
      • Ecuador
      • Peru

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000180543
Tropicos 13009248
INPN 629665
KEW urn:lsid:ipni.org:names:96559-2
The Plant List ild-2674
Open Tree Of Life 3921474
NCBI Taxonomy 1471844
IUCN Red List 204910065
IPNI 96559-2
iNaturalist 289892
GBIF 5349775
EPPO ERZBE
EOL 644105
USDA GRIN 15733
Wikipedia Erythrina_berteroana

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
Multiscale predictors of small tree survival across a heterogeneous tropical landscape Helmer EH, Kay S, Marcano-Vega H, Powers JS, Wood TE, Zhu X, Gwenzi D, Ruzycki TS PLoS One 15-Mar-2023
PMCID:PMC10016699
doi:10.1371/journal.pone.0280322
PMID:36920898
Browse from Three Tree Legumes Increases Forage Production for Cattle in a Silvopastoral System in the Southwest Amazon Dablin L, Lewis SL, Milliken W, Monro A, Lee MA Animals (Basel) 17-Dec-2021
PMCID:PMC8698037
doi:10.3390/ani11123585
PMID:34944360
Microstructural Surface Properties of Drifting Seeds—A Model for Non-Toxic Antifouling Solutions Clasen A, Kesel AB Biomimetics (Basel) 13-May-2019
PMCID:PMC6630564
doi:10.3390/biomimetics4020037
PMID:31105222
Ethnopharmacological Field Study of Three Q'eqchi Communities in Guatemala Vargas JM, Andrade-Cetto A Front Pharmacol 06-Nov-2018
PMCID:PMC6240767
doi:10.3389/fphar.2018.01246
PMID:30483122
Higher agrobiodiversity is associated with improved dietary diversity, but not child anthropometric status, of Mayan Achí people of Guatemala Luna-González DV, Sørensen M Public Health Nutr 03-Apr-2018
PMCID:PMC10260805
doi:10.1017/S1368980018000617
PMID:29611490
Wild edible plant knowledge, distribution and transmission: a case study of the Achí Mayans of Guatemala Turreira-García N, Theilade I, Meilby H, Sørensen M J Ethnobiol Ethnomed 16-Jun-2015
PMCID:PMC4474567
doi:10.1186/s13002-015-0024-4
PMID:26077151
Alkaloid-Bearing Plants and Their Contained Alkaloids. 1957-1968 R. Melville, J. J. Willaman, Hui-Lin Li JSTOR 27-Nov-2007
doi:10.2307/4117899
Studies of alkaloids in foliage of <i>Erythrina berteroana</i> and <i>E. poeppigiana</i>: Detection of β‐erythroidine in goats milk M. Soto‐Hernandez, A. H. Jackson Wiley 07-Mar-2007
doi:10.1002/PCA.2800040302
Studies of <i>Erythrina</i> alkaloids: VII—<sup>13</sup>C NMR spectral studies of some <i>Erythina</i> alkaloids A. S. Chawla, S. Chunchatprasert, A. H. Jackson Wiley 28-May-2005
doi:10.1002/OMR.1270210110
Erythrina alkaloids. Part 6. Isolation and characterisation of alkaloids from Erythrina berteroana seeds and leaves: formation of oxoerythroidines Amrik S. Chawla, Anthony H. Jackson, Peter Ludgate Royal Society of Chemistry (RSC) 26-Apr-2004
doi:10.1039/P19820002903
An Antifungal Isoflavanone and a Structure Revision of a Flavanone from Erythrina berteroana. Maillard M, Hamburger M, Gupta MP, Hostettmann K Planta Med 01-Jun-1989
doi:10.1055/S-2006-962004
PMID:17262415
Isolation, gas chromatography-mass spectrometry, and structures of new alkaloids from Erythrina folkersii Krukoff and Moldenke and Erythrina salviiflora Krukoff and Barneby. Millington DS, Steinman DH, Rinehart KL Jr J Am Chem Soc 20-Mar-1974
doi:10.1021/JA00813A043
PMID:4815761

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Alkaloids and derivatives / Erythrina alkaloids / Erythrinanes
(1S,7R,16R)-16-methoxy-5-oxa-10-azatetracyclo[8.7.0.01,13.02,7]heptadeca-2,12,14-trien-4-one 92642277 Click to see COC1CC23C(=CCN2CCC4C3=CC(=O)OC4)C=C1 273.33 unknown https://doi.org/10.1039/P19820002903
https://doi.org/10.1002/OMR.1270210110
(1S,7R,16R)-16-methoxy-5-oxa-10-azatetracyclo[8.7.0.01,13.02,7]heptadeca-2,12,14-triene-4,11-dione 163191255 Click to see COC1CC23C(=CC(=O)N2CCC4C3=CC(=O)OC4)C=C1 287.31 unknown https://doi.org/10.1039/P19820002903
(1S,7R,16R)-16-methoxy-5-oxa-10-azatetracyclo[8.7.0.01,13.02,7]heptadeca-2,12,14-triene-4,9-dione 163083070 Click to see COC1CC23C(=CCN2C(=O)CC4C3=CC(=O)OC4)C=C1 287.31 unknown https://doi.org/10.1002/OMR.1270210110
(1S,7S,16S)-16-methoxy-5-oxa-10-azatetracyclo[8.7.0.01,13.02,7]heptadeca-2,12-dien-4-one 163018600 Click to see COC1CCC2=CCN3C2(C1)C4=CC(=O)OCC4CC3 275.34 unknown https://doi.org/10.1021/JA00813A043
(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/10.1039/P19820002903
(2R,3S,9S,13bS)-2,11,12-trimethoxy-2,3,5,6,8,9-hexahydro-1H-indolo[7a,1-a]isoquinoline-3,9-diol 162871726 Click to see COC1CC23C(=CC1O)CCN2CC(C4=CC(=C(C=C34)OC)OC)O 347.40 unknown https://doi.org/10.1039/P19820002903
(2R,3S,9S,13bS)-2,12-dimethoxy-2,3,5,6,8,9-hexahydro-1H-indolo[7a,1-a]isoquinoline-3,9,11-triol 162955433 Click to see COC1CC23C(=CC1O)CCN2CC(C4=CC(=C(C=C34)OC)O)O 333.40 unknown https://doi.org/10.1039/P19820002903
11-methoxy-2,6,8,9-tetrahydro-1H-indolo[7a,1-a]isoquinoline-2,12-diol 73823602 Click to see COC1=C(C=C2C(=C1)CCN3C24CC(C=CC4=CC3)O)O 285.34 unknown https://doi.org/10.1039/P19820002903
12-methoxy-2,6,8,9-tetrahydro-1H-indolo[7a,1-a]isoquinoline-2,11-diol 3472079 Click to see COC1=C(C=C2CCN3CC=C4C3(C2=C1)CC(C=C4)O)O 285.34 unknown https://doi.org/10.1039/P19820002903
16-Methoxy-5-oxa-10-azatetracyclo[8.7.0.01,13.02,7]heptadeca-2,12-dien-4-one 163018599 Click to see COC1CCC2=CCN3C2(C1)C4=CC(=O)OCC4CC3 275.34 unknown https://doi.org/10.1021/JA00813A043
16-Methoxy-5-oxa-10-azatetracyclo[8.7.0.01,13.02,7]heptadeca-2,12,14-trien-4-one 4460702 Click to see COC1CC23C(=CCN2CCC4C3=CC(=O)OC4)C=C1 273.33 unknown https://doi.org/10.1039/P19820002903
https://doi.org/10.1002/OMR.1270210110
16-Methoxy-5-oxa-10-azatetracyclo[8.7.0.01,13.02,7]heptadeca-2,12,14-triene-4,11-dione 73823606 Click to see COC1CC23C(=CC(=O)N2CCC4C3=CC(=O)OC4)C=C1 287.31 unknown https://doi.org/10.1039/P19820002903
16-Methoxy-5-oxa-10-azatetracyclo[8.7.0.01,13.02,7]heptadeca-2,12,14-triene-4,9-dione 163083069 Click to see COC1CC23C(=CCN2C(=O)CC4C3=CC(=O)OC4)C=C1 287.31 unknown https://doi.org/10.1002/OMR.1270210110
2,11,12-trimethoxy-2,3,5,6,8,9-hexahydro-1H-indolo[7a,1-a]isoquinoline-3,9-diol 74927724 Click to see COC1CC23C(=CC1O)CCN2CC(C4=CC(=C(C=C34)OC)OC)O 347.40 unknown https://doi.org/10.1039/P19820002903
2,12-dimethoxy-2,3,5,6,8,9-hexahydro-1H-indolo[7a,1-a]isoquinoline-3,9,11-triol 162955432 Click to see COC1CC23C(=CC1O)CCN2CC(C4=CC(=C(C=C34)OC)O)O 333.40 unknown https://doi.org/10.1039/P19820002903
alpha-Erythroidine 441076 Click to see COC1CC23C(=CCN2CCC4C3=CC(=O)OC4)C=C1 273.33 unknown https://doi.org/10.1002/PCA.2800040302
https://doi.org/10.2307/4117899
CID 21679844 21679844 Click to see COC1CC23C(=CCN2CCC4=CC(=C(C=C34)O)O)C=C1 285.34 unknown https://doi.org/10.1039/P19820002903
Erysodine 169017 Click to see COC1CC23C(=CCN2CCC4=CC(=C(C=C34)OC)O)C=C1 299.40 unknown https://doi.org/10.1039/P19820002903
Erysonine 442218 Click to see COC1=C(C=C2CCN3CC=C4C3(C2=C1)CC(C=C4)O)O 285.34 unknown https://doi.org/10.1039/P19820002903
Erysopine 12308892 Click to see COC1CC23C(=CCN2CCC4=CC(=C(C=C34)O)O)C=C1 285.34 unknown https://doi.org/10.1039/P19820002903
Erysovine 5317203 Click to see COC1CC23C(=CCN2CCC4=CC(=C(C=C34)O)OC)C=C1 299.40 unknown https://doi.org/10.1039/P19820002903
https://doi.org/10.1002/PCA.2800040302
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/10.1039/P19820002903
https://doi.org/10.1002/PCA.2800040302
> Organoheterocyclic compounds / Azaspirodecane derivatives
(3'R,5R,8aS)-3'-methoxyspiro[6,7,8,8a-tetrahydro-1H-pyrano[4,3-c]pyridine-5,5'-cyclohexene]-3-one 163046401 Click to see COC1CC2(CC=C1)C3=CC(=O)OCC3CCN2 249.30 unknown https://doi.org/10.1021/JA00813A043
3'-methoxyspiro[6,7,8,8a-tetrahydro-1H-pyrano[4,3-c]pyridine-5,5'-cyclohexene]-3-one 163046400 Click to see COC1CC2(CC=C1)C3=CC(=O)OCC3CCN2 249.30 unknown https://doi.org/10.1021/JA00813A043
> Organoheterocyclic compounds / Indoles and derivatives
(1S,16R)-16-methoxy-5-oxa-10-azatetracyclo[8.7.0.01,13.02,7]heptadeca-2(7),12,14-triene-4,11-dione 21679851 Click to see COC1CC23C4=C(CCN2C(=O)C=C3C=C1)COC(=O)C4 287.31 unknown https://doi.org/10.1039/P19820002903
(1S,16R)-16-methoxy-5-oxa-10-azatetracyclo[8.7.0.01,13.02,7]heptadeca-2(7),12,14-triene-4,9-dione 162961334 Click to see COC1CC23C4=C(CC(=O)N2CC=C3C=C1)COC(=O)C4 287.31 unknown https://doi.org/10.1002/OMR.1270210110
16-Methoxy-5-oxa-10-azatetracyclo[8.7.0.01,13.02,7]heptadeca-2(7),12,14-triene-4,11-dione 73823607 Click to see COC1CC23C4=C(CCN2C(=O)C=C3C=C1)COC(=O)C4 287.31 unknown https://doi.org/10.1039/P19820002903
16-Methoxy-5-oxa-10-azatetracyclo[8.7.0.01,13.02,7]heptadeca-2(7),12,14-triene-4,9-dione 162961333 Click to see COC1CC23C4=C(CC(=O)N2CC=C3C=C1)COC(=O)C4 287.31 unknown https://doi.org/10.1002/OMR.1270210110
6-Methoxy-1,4,6,10,12,13-hexahydro-3H,5H-pyrano[4',3':3,4]pyrido[2,1-i]indol-3-one 410620 Click to see COC1CC23C4=C(CCN2CC=C3C=C1)COC(=O)C4 273.33 unknown https://doi.org/10.1002/OMR.1270210110
https://doi.org/10.1039/P19820002903
beta-ERYTHROIDINE 10074 Click to see COC1CC23C4=C(CCN2CC=C3C=C1)COC(=O)C4 273.33 unknown https://doi.org/10.1002/OMR.1270210110
https://doi.org/10.1039/P19820002903
https://doi.org/10.1002/PCA.2800040302
https://doi.org/10.2307/4117899
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
9-[4,6-Dihydroxy-8,16-bis(4-hydroxyphenyl)-12-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-15-oxatetracyclo[8.6.1.02,7.014,17]heptadeca-2(7),3,5,10(17),11,13-hexaen-9-yl]-8,16-bis(4-hydroxyphenyl)-15-oxatetracyclo[8.6.1.02,7.014,17]heptadeca-2(7),3,5,10(17),11,13-hexaene-4,6,12-triol 75244299 Click to see C1=CC(=CC=C1C2C(C3=C4C(C(OC4=CC(=C3)O)C5=CC=C(C=C5)O)C6=C2C(=CC(=C6)O)O)C7C(C8=C(C=C(C=C8O)O)C9C(OC1=CC(=CC7=C91)OC1C(C(C(C(O1)CO)O)O)O)C1=CC=C(C=C1)O)C1=CC=C(C=C1)O)O 1069.10 unknown https://doi.org/10.1039/P19820002903
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 3-prenylated flavans / 3-prenylated flavanones
5'-Prenylhomoeriodictyol 442457 Click to see CC(=CCC1=C(C(=CC(=C1)C2CC(=O)C3=C(C=C(C=C3O2)O)O)OC)O)C 370.40 unknown https://doi.org/10.1055/S-2006-962004
Sbmet 3082688 Click to see CC(=CCC1=C(C(=CC(=C1)C2CC(=O)C3=C(C=C(C=C3O2)O)O)O)OC)C 370.40 unknown https://doi.org/10.1055/S-2006-962004

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