Erythrina costaricensis - Unknown
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Internal ID UUID643fd5f1d8d45842846998
Scientific name Erythrina costaricensis
Authority Micheli
First published in Bull. Herb. Boissier2: 445 (1894)

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Synonyms Top

Scientific name Authority First published in
Erythrina costaricensis var. panamensis (Standl.) Croat Fl. Barro Colorado Is.: 471 (1978)
Erythrina colombiana Krukoff Brittonia3: 325 (1939)
Erythrina panamensis Standl. J. Washington Acad. Sci.17: 10 (1927)

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Varieties (abbr. var.) 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
      • Honduras
      • Panamá
    • Western South America
      • Colombia

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000165885
Tropicos 13009263
KEW urn:lsid:ipni.org:names:96578-2
The Plant List ild-12311
Open Tree Of Life 337220
NCBI Taxonomy 466222
IUCN Red List 144288384
IPNI 96578-2
iNaturalist 633646
GBIF 5349770
EOL 416396
USDA GRIN 436195

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
Structure-dependent activity of plant natural products against methicillin-resistant Staphylococcus aureus Moreno Cardenas C, Çiçek SS Front Microbiol 15-Aug-2023
PMCID:PMC10463185
doi:10.3389/fmicb.2023.1234115
PMID:37649631
Phylogenetic distribution and evolutionary dynamics of nod and T3SS genes in the genus Bradyrhizobium Teulet A, Gully D, Rouy Z, Camuel A, Koebnik R, Giraud E, Lassalle F Microb Genom 12-Aug-2020
PMCID:PMC7643967
doi:10.1099/mgen.0.000407
PMID:32783800
Antimicrobial Isoflavones and Derivatives from Erythrina (Fabaceae): Structure Activity Perspective (Sar & Qsar) on Experimental and Mined Values Against Staphylococcus aureus Sadgrove NJ, Oliveira TB, Khumalo GP, van Vuuren SF, van Wyk BE Antibiotics (Basel) 30-Apr-2020
PMCID:PMC7277434
doi:10.3390/antibiotics9050223
PMID:32365905
Seedling responses to salinity of 26 Neotropical tree species De Sedas A, González Y, Winter K, Lopez OR AoB Plants 25-Nov-2019
PMCID:PMC6876892
doi:10.1093/aobpla/plz062
PMID:31788179
High-quality permanent draft genome sequence of Bradyrhizobium sp. Tv2a.2, a microsymbiont of Tachigali versicolor discovered in Barro Colorado Island of Panama Tian R, Parker M, Seshadri R, Reddy T, Markowitz V, Ivanova N, Pati A, Woyke T, Baeshen MN, Baeshen NA, Kyrpides N, Reeve W Stand Genomic Sci 17-May-2015
PMCID:PMC4511254
doi:10.1186/s40793-015-0006-0
PMID:26203338
A Genomic Encyclopedia of the Root Nodule Bacteria: assessing genetic diversity through a systematic biogeographic survey Reeve W, Ardley J, Tian R, Eshragi L, Yoon JW, Ngamwisetkun P, Seshadri R, Ivanova NN, Kyrpides NC Stand Genomic Sci 09-Feb-2015
PMCID:PMC4322651
doi:10.1186/1944-3277-10-14
PMID:25685260
Variability within the 10-Year Pollen Rain of a Seasonal Neotropical Forest and Its Implications for Paleoenvironmental and Phenological Research Haselhorst DS, Moreno JE, Punyasena SW PLoS One 08-Jan-2013
PMCID:PMC3540050
doi:10.1371/journal.pone.0053485
PMID:23320089
Three new isoflavanones from Erythrina costaricensis. Tanaka H, Hattori H, Oh-Uchi T, Sato M, Sako M, Tateishi Y, Rizwani GH Nat Prod Res 01-Jan-2009
doi:10.1080/14786410802292286
PMID:19662573
Synchronous Pulsed Flowering: Analysis of the Flowering Phenology in Juncus (Juncaceae) Michalski SG, Durka W Ann Bot 19-Sep-2007
PMCID:PMC2759248
doi:10.1093/aob/mcm206
PMID:17881343
Erythrina Alkaloids. X. Isolation and Characterization of Erysonine and Other Liberated Alkaloids Karl Folkers, John Shavel, Frank Koniuszy American Chemical Society (ACS) 19-Mar-2005
doi:10.1021/JA01851A016
Case of Localized Recombination in 23S rRNA Genes from Divergent Bradyrhizobium Lineages Associated with Neotropical Legumes Parker MA Appl Environ Microbiol 01-May-2001
PMCID:PMC92839
doi:10.1128/AEM.67.5.2076-2082.2001
PMID:11319084

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
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/10.1021/JA01851A016
Erysonine 442218 Click to see COC1=C(C=C2CCN3CC=C4C3(C2=C1)CC(C=C4)O)O 285.34 unknown https://doi.org/10.1021/JA01851A016
> Phenylpropanoids and polyketides / Isoflavonoids / Furanoisoflavonoids / Pterocarpans
(6aS,11aS)-9-methoxy-11a-methyl-10-(3-methylbut-2-enyl)-6H-[1]benzofuro[3,2-c]chromene-3,6a-diol 163187873 Click to see CC(=CCC1=C(C=CC2=C1OC3(C2(COC4=C3C=CC(=C4)O)O)C)OC)C 368.40 unknown https://doi.org/10.1080/14786410802292286
9-methoxy-11a-methyl-10-(3-methylbut-2-enyl)-6H-[1]benzofuro[3,2-c]chromene-3,6a-diol 163023575 Click to see CC(=CCC1=C(C=CC2=C1OC3(C2(COC4=C3C=CC(=C4)O)O)C)OC)C 368.40 unknown https://doi.org/10.1080/14786410802292286
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavans / Isoflavanones / 3-prenylated isoflavanones
(3S)-5,7-dihydroxy-3-[3-hydroxy-4-methoxy-5-(3-methylbut-2-enyl)phenyl]-6-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one 163045258 Click to see CC(=CCC1=C(C(=CC(=C1)C2COC3=C(C2=O)C(=C(C(=C3)O)CC=C(C)C)O)O)OC)C 438.50 unknown https://doi.org/10.1080/14786410802292286
(7R)-5-hydroxy-7-[3-hydroxy-4-methoxy-5-(3-methylbut-2-enyl)phenyl]-2,2-dimethyl-7,8-dihydropyrano[3,2-g]chromen-6-one 162863734 Click to see CC(=CCC1=C(C(=CC(=C1)C2COC3=C(C2=O)C(=C4C=CC(OC4=C3)(C)C)O)O)OC)C 436.50 unknown https://doi.org/10.1080/14786410802292286
(7S)-5-hydroxy-7-(8-hydroxy-2,2-dimethylchromen-6-yl)-2,2-dimethyl-7,8-dihydropyrano[3,2-g]chromen-6-one 163193063 Click to see CC1(C=CC2=C(O1)C(=CC(=C2)C3COC4=C(C3=O)C(=C5C=CC(OC5=C4)(C)C)O)O)C 420.50 unknown https://doi.org/10.1080/14786410802292286
5-Hydroxy-7-(8-hydroxy-2,2-dimethylchromen-6-yl)-2,2-dimethyl-7,8-dihydropyrano[3,2-g]chromen-6-one 101448021 Click to see CC1(C=CC2=C(O1)C(=CC(=C2)C3COC4=C(C3=O)C(=C5C=CC(OC5=C4)(C)C)O)O)C 420.50 unknown https://doi.org/10.1080/14786410802292286
5-Hydroxy-7-[3-hydroxy-4-methoxy-5-(3-methylbut-2-enyl)phenyl]-2,2-dimethyl-7,8-dihydropyrano[3,2-g]chromen-6-one 101448019 Click to see CC(=CCC1=C(C(=CC(=C1)C2COC3=C(C2=O)C(=C4C=CC(OC4=C3)(C)C)O)O)OC)C 436.50 unknown https://doi.org/10.1080/14786410802292286
5,7-Dihydroxy-3-[3-hydroxy-4-methoxy-5-(3-methylbut-2-enyl)phenyl]-6-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one 101448020 Click to see CC(=CCC1=C(C(=CC(=C1)C2COC3=C(C2=O)C(=C(C(=C3)O)CC=C(C)C)O)O)OC)C 438.50 unknown https://doi.org/10.1080/14786410802292286
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavans / Isoflavanones / 6-prenylated isoflavanones
(2S)-4-hydroxy-6-(4-hydroxyphenyl)-2-(2-hydroxypropan-2-yl)-9-(3-methylbut-2-enyl)-2,3-dihydrofuro[3,2-g]chromen-5-one 162842930 Click to see CC(=CCC1=C2C(=C(C3=C1OC=C(C3=O)C4=CC=C(C=C4)O)O)CC(O2)C(C)(C)O)C 422.50 unknown https://doi.org/10.1080/14786410802292286
4-Hydroxy-6-(4-hydroxyphenyl)-2-(2-hydroxypropan-2-yl)-9-(3-methylbut-2-enyl)-2,3-dihydrofuro[3,2-g]chromen-5-one 195652 Click to see CC(=CCC1=C2C(=C(C3=C1OC=C(C3=O)C4=CC=C(C=C4)O)O)CC(O2)C(C)(C)O)C 422.50 unknown https://doi.org/10.1080/14786410802292286

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