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Erythrina speciosa

Erythrina speciosa - Unknown
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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 UUID643fd75c5ad05078945038
Scientific name Erythrina speciosa
Authority Andrews
First published in Bot. Repos.7: t. 443 (1807)

Description Top

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Erythrina speciosa is a tree that is native to Brazil but can also be found in Africa and India due to cultivation. It is known for its unique pollination method by hummingbirds.

Synonyms Top

Scientific name Authority First published in
Micropteryx reticulata (C.Presl) Walp. Linnaea23: 741 (1851)
Erythrina poianthes Brot. Trans. Linn. Soc. London 14(2): 342. 1824 [15 Nov 1824]
Stenotropis berteroi Hassk. Retzia1: 183 (1855)
Erythrina poianthes var. subinermis Lindl. Edwards's Bot. Reg.19: t. 1617 (1833)
Corallodendron reticulatum (C.Presl) Kuntze Revis. Gen. Pl.1: 173 (1891)
Erythrina reticulata C.Presl Symb. Bot.2: 22 (1834)
Erythrina poyanthes Brot. ex Tilloch & Taylor Philos. Mag. J.61: 465 (1823)
Erythrina speciosa var. rosea N.F.Mattos Loefgrenia21: 1 (1967)

Common names Top

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Language Common/alternative name
English ivory coral tree
Arabic حمرية جميلة
Chinese 象牙花

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

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
  • Southern America
    • Brazil
      • Brazil Northeast
      • Brazil South
      • Brazil Southeast
      • Brazil West-central

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000174141
Tropicos 13030281
KEW urn:lsid:ipni.org:names:494588-1
The Plant List ild-20251
Open Tree Of Life 848216
NCBI Taxonomy 132442
IUCN Red List 177827429
IPNI 494588-1
iNaturalist 427620
GBIF 5349528
Freebase /m/04y5p1v
EOL 640418
USDA GRIN 15766
Wikipedia Erythrina_speciosa
CMAUP NPO10350

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
Helicobacter pylori infection in humans and phytotherapy, probiotics, and emerging therapeutic interventions: a review Liu M, Gao H, Miao J, Zhang Z, Zheng L, Li F, Zhou S, Zhang Z, Li S, Liu H, Sun J Front Microbiol 10-Jan-2024
PMCID:PMC10806011
doi:10.3389/fmicb.2023.1330029
PMID:38268702
Flavonoids with Anti-Herpes Simplex Virus Properties: Deciphering Their Mechanisms in Disrupting the Viral Life Cycle Šudomová M, Hassan ST Viruses 29-Nov-2023
PMCID:PMC10748012
doi:10.3390/v15122340
PMID:38140581
Tensor methods in data analysis of chromatography/mass spectroscopy-based plant metabolomics Guo L, Yu H, Li Y, Zhang C, Kharbach M Plant Methods 21-Nov-2023
PMCID:PMC10662285
doi:10.1186/s13007-023-01105-y
PMID:37990220
Partial Characterization of Lectins Purified from the Surco and Vara (Furrow and Rod) Varieties of Black Phaseolus vulgaris Valadez-Vega C, Lugo-Magaña O, Betanzos-Cabrera G, Villagómez-Ibarra JR Molecules 02-Dec-2022
PMCID:PMC9741355
doi:10.3390/molecules27238436
PMID:36500537
Diversity of Legumes in the Cashew Agroforestry System in East Timor (Southeast Asia) Guterres L, Duarte MC, Catarino S, Roxo G, Barnabé J, Sebastiana M, Monteiro F, Romeiras MM Foods 03-Nov-2022
PMCID:PMC9655503
doi:10.3390/foods11213503
PMID:36360115
Raffinose family oligosaccharides (RFOs): role in seed vigor and longevity Salvi P, Varshney V, Majee M Biosci Rep 04-Oct-2022
PMCID:PMC9547172
doi:10.1042/BSR20220198
PMID:36149314
Adsorption of the First-Line Covid Treatment Analgesic onto Activated Carbon from Residual Pods of Erythrina Speciosa Georgin J, Franco DS, Netto MS, Manzar MS, Zubair M, Meili L, Piccilli DG, Silva LF Environ Manage 10-Sep-2022
PMCID:PMC9463666
doi:10.1007/s00267-022-01716-6
PMID:36087146
Flavonoids-Rich Plant Extracts Against Helicobacter pylori Infection as Prevention to Gastric Cancer Ivyna de Araújo Rêgo R, Guedes Silvestre GF, Ferreira de Melo D, Albino SL, Pimentel MM, Silva Costa Cruz SB, Silva Wurzba SD, Rodrigues WF, Goulart de Lima Damasceno BP, Cançado Castellano LR Front Pharmacol 31-Aug-2022
PMCID:PMC9470917
doi:10.3389/fphar.2022.951125
PMID:36120379
Seed Longevity in Legumes: Deeper Insights Into Mechanisms and Molecular Perspectives Ramtekey V, Cherukuri S, Kumar S, V. SK, Sheoran S, K. UB, K. BN, Kumar S, Singh AN, Singh HV Front Plant Sci 27-Jul-2022
PMCID:PMC9364935
doi:10.3389/fpls.2022.918206
PMID:35968115
Unravelling the paradox in physically dormant species: elucidating the onset of dormancy after dispersal and dormancy-cycling Jaganathan GK Ann Bot 23-Jun-2022
PMCID:PMC9445591
doi:10.1093/aob/mcac084
PMID:35737935
Natural compounds based chemotherapeutic against Chagas disease and leishmaniasis: mitochondrion as a strategic target Lazarin-Bidóia D, Garcia FP, Ueda-Nakamura T, Silva SD, Nakamura CV Mem Inst Oswaldo Cruz 30-Mar-2022
PMCID:PMC8970591
doi:10.1590/0074-02760220396
PMID:35352776
Flavonoids Target Human Herpesviruses That Infect the Nervous System: Mechanisms of Action and Therapeutic Insights Šudomová M, Berchová-Bímová K, Mazurakova A, Šamec D, Kubatka P, Hassan ST Viruses 13-Mar-2022
PMCID:PMC8949561
doi:10.3390/v14030592
PMID:35336999
Pest categorisation of Maconellicoccus hirsutus Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, Sven Magnusson C, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Civera AV, Yuen J, Zappalà L, Gregoire J, Malumphy C, Antonatos S, Kertesz V, Maiorano A, Papachristos D, MacLeod A EFSA J 11-Jan-2022
PMCID:PMC8749475
doi:10.2903/j.efsa.2022.7024
PMID:35035580
Mobile forms of carbon in trees: metabolism and transport Dominguez PG, Niittylä T Tree Physiol 20-Sep-2021
PMCID:PMC8919412
doi:10.1093/treephys/tpab123
PMID:34542151
Natural and Historical Heritage of the Lisbon Botanical Gardens: An Integrative Approach with Tree Collections Cunha AR, Soares AL, Brilhante M, Arsénio P, Vasconcelos T, Espírito-Santo D, Duarte MC, Romeiras MM Plants (Basel) 04-Jul-2021
PMCID:PMC8309379
doi:10.3390/plants10071367
PMID:34371570

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
Erysodine 169017 Click to see COC1CC23C(=CCN2CCC4=CC(=C(C=C34)OC)O)C=C1 299.40 unknown https://doi.org/10.3987/R-1984-03-0453
Erysovine 5317203 Click to see COC1CC23C(=CCN2CCC4=CC(=C(C=C34)O)OC)C=C1 299.40 unknown https://doi.org/10.3987/R-1984-03-0453
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/10.3987/R-1984-03-0453
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
dimethyl (2S,3R,4S,4aR,6aR,6bS,8aS,12aS,14aR,14bR)-2-hydroxy-4,6a,6b,11,11,14b-hexamethyl-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene-4,8a-dicarboxylate 101630395 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C(=O)OC)OC6C(C(C(C(O6)CO)O)O)O)O)C)C)C2C1)C)C(=O)OC)C 692.90 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(2S,3R,4S,4aS,6aR,6bS,8aS,12aS,14aR,14bR)-2,3-dihydroxy-4,6a,6b,11,11,14b-hexamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene-4,8a-dicarboxylic acid 462205 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C(=O)O)O)O)C)C)C2C1)C)C(=O)O)C 502.70 unknown via CMAUP database
(4aS,6aR,6aS,6bR,8aR,9S,10R,11S,12aR,14bR)-10,11-dihydroxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 93492873 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1)C)C(=O)O)C 488.70 unknown via CMAUP database
Bayogenin 12305221 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1)C)C(=O)O)C 488.70 unknown via CMAUP database
Medicagenic acid 65048 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C(=O)O)O)O)C)C)C2C1)C)C(=O)O)C 502.70 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(1S,7abeta)-Hexahydro-2alpha-[(beta-D-glucopyranosyl)oxy]-3beta-(hydroxymethyl)-1H-pyrrolizine-1alpha,7alpha-diol 21576629 Click to see C1CN2C(C(C(C2C1O)O)OC3C(C(C(C(O3)CO)O)O)O)CO 351.35 unknown via CMAUP database
[(8aalpha)-Octahydro-1beta,6alpha,7beta-trihydroxyindolizin]-8alpha-yl beta-D-glucopyranoside 10089286 Click to see C1CN2CC(C(C(C2C1O)OC3C(C(C(C(O3)CO)O)O)O)O)O 351.35 unknown via CMAUP database
> Organoheterocyclic compounds / Indolizidines
6-epi-Castanospermine 184806 Click to see C1CN2CC(C(C(C2C1O)O)O)O 189.21 unknown via CMAUP database
Castanospermine 54445 Click to see C1CN2CC(C(C(C2C1O)O)O)O 189.21 unknown via CMAUP database
Rel-(1R,6R,7S,8S,8aS)-octahydroindolizine-1,6,7,8-tetraol 13959480 Click to see C1CN2CC(C(C(C2C1O)O)O)O 189.21 unknown via CMAUP database
> Organoheterocyclic compounds / Piperidines
3-Epi-fagomine 10290867 Click to see C1CNC(C(C1O)O)CO 147.17 unknown via CMAUP database
Fagomine 72259 Click to see C1CNC(C(C1O)O)CO 147.17 unknown via CMAUP database
> Organoheterocyclic compounds / Pyrrolidines
2-Pyrrolidinemethanol, 3-hydroxy-, (2R,3S)- 11073391 Click to see C1CNC(C1O)CO 117.15 unknown via CMAUP database
> Organoheterocyclic compounds / Pyrrolizidines
(1R,2S,3S,7R,8R)-3-(hydroxymethyl)-2,3,5,6,7,8-hexahydro-1H-pyrrolizine-1,2,7-triol 21576628 Click to see C1CN2C(C(C(C2C1O)O)O)CO 189.21 unknown via CMAUP database
(1R,2S,3S,7S,8R)-3-(hydroxymethyl)-2,3,5,6,7,8-hexahydro-1H-pyrrolizine-1,2,7-triol 21576627 Click to see C1CN2C(C(C(C2C1O)O)O)CO 189.21 unknown via CMAUP database
(1S,2R,3R,7S,7aR)-3-Hydroxymethyl-1,2,7-trihydroxypyrrolizidine 453575 Click to see C1CN2C(C(C(C2C1O)O)O)CO 189.21 unknown via CMAUP database
(1S,2R,3R,7S,8S)-3-(hydroxymethyl)-2,3,5,6,7,8-hexahydro-1H-pyrrolizine-1,2,7-triol 14164813 Click to see C1CN2C(C(C(C2C1O)O)O)CO 189.21 unknown via CMAUP database
3-(Hydroxymethyl)-1,2,7-trihydroxypyrrolizidine 72360 Click to see C1CN2C(C(C(C2C1O)O)O)CO 189.21 unknown via CMAUP database
3,7a-Diepialexine 189605 Click to see C1CN2C(C(C(C2C1O)O)O)CO 189.21 unknown via CMAUP database
Australine 442628 Click to see C1CN2C(C(C(C2C1O)O)O)CO 189.21 unknown via CMAUP database
> 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/10.3987/R-1984-03-0453
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
2'-Methoxy-3',4',7-trihydroxyisoflavone 101785462 Click to see COC1=C(C=CC(=C1O)O)C2=COC3=C(C2=O)C=CC(=C3)O 300.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 3-hydroxy,4-methoxyisoflavonoids
Koparin 5318834 Click to see COC1=C(C(=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)O)O)O 300.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 4-O-methylisoflavones
Afrormosin 5281704 Click to see COC1=CC=C(C=C1)C2=COC3=CC(=C(C=C3C2=O)OC)O 298.29 unknown via CMAUP database

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