Erythrina velutina - Unknown
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Internal ID UUID643fd8cad2380541569547
Scientific name Erythrina velutina
Authority Willd.
First published in Neue Schriften Ges. Naturf. Freunde Berlin3: 426 (1801)

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Synonyms Top

Scientific name Authority First published in
Erythrina aculeatissima Desf. Tabl. École Bot.: 191 (1804)
Corallodendron velutinum (Willd.) Kuntze Revis. Gen. Pl.1: 173 (1891)
Chirocalyx velutinus (Willd.) Walp. Flora36: 148 (1853)
Erythrina splendida Diels Biblioth. Bot.29: 96 (1937)
Erythrina aurantiaca Ridl. J. Linn. Soc., Bot.27: 30 (1890)
Erythrina velutina f. aurantiaca (Ridl.) Krukoff Brittonia3: 329 (1939)

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Language Common/alternative name
Persian فردوسی برزیلی
Armenian Իլենի թավշանման
Portuguese mulungu
Portuguese suinã

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Distribution (via POWO/KEW) Top

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Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000181214
Tropicos 13009331
INPN 629669
KEW urn:lsid:ipni.org:names:494616-1
The Plant List ild-2737
Open Tree Of Life 959917
Observations.org 198694
NCBI Taxonomy 1076878
IPNI 96663-2
iNaturalist 327720
GBIF 5349685
Freebase /m/0bh8z9_
EPPO ERZVE
EOL 644484
Elurikkus 524586
USDA GRIN 15772
Wikipedia Erythrina_velutina

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 influence of exotic and native plants on illnesses with physical and spiritual causes in the semiarid region of Piauí, Northeast of Brazil da Silva PH, Ferreira Júnior WS, Zank S, do Nascimento AL, de Abreu MC J Ethnobiol Ethnomed 26-Feb-2024
PMCID:PMC10895823
doi:10.1186/s13002-024-00667-y
PMID:38409039
Non-thermal plasma (NTP) treatment of Trigonella foenum-graecum L. seeds stimulates the sprout growth and the production of nutraceutical compounds Motrescu I, Lungoci C, Ciolan MA, Jităreanu G BMC Plant Biol 06-Jan-2024
PMCID:PMC10770889
doi:10.1186/s12870-023-04710-0
PMID:38183006
More than 17,000 tree species are at risk from rapid global change Boonman CC, Serra-Diaz JM, Hoeks S, Guo WY, Enquist BJ, Maitner B, Malhi Y, Merow C, Buitenwerf R, Svenning JC Nat Commun 02-Jan-2024
PMCID:PMC10761716
doi:10.1038/s41467-023-44321-9
PMID:38167693
Plant parentage influences the type of timber use by traditional peoples of the Brazilian Caatinga Pedrosa KM, Ramos MB, La Torre-Cuadros MD, Lopes SD PLoS One 17-Oct-2023
PMCID:PMC10581497
doi:10.1371/journal.pone.0286434
PMID:37847702
From Plants to Psycho-Neurology: Unravelling the Therapeutic Benefits of Bioactive Compounds in Brain Disorders Grosso C, Santos M, Barroso MF Antioxidants (Basel) 11-Aug-2023
PMCID:PMC10451187
doi:10.3390/antiox12081603
PMID:37627598
A Comprehensive Review on the Biological, Agricultural and Pharmaceutical Properties of Secondary Metabolites Based-Plant Origin Elshafie HS, Camele I, Mohamed AA Int J Mol Sci 07-Feb-2023
PMCID:PMC9959544
doi:10.3390/ijms24043266
PMID:36834673
Biological Evaluation of Valeriana Extracts from Argentina with Potent Cholinesterase Inhibition for the Treatment of Neurodegenerative Disorders and Their Comorbidities—The Case of Valeriana carnosa Sm. (Caprifoliaceae) Studied in Mice Marcucci C, Rademacher M, Kamecki F, Pastore V, Bach HG, Ricco RA, Wagner ML, Knez D, Gobec S, Colettis N, Marder M Pharmaceuticals (Basel) 16-Jan-2023
PMCID:PMC9861714
doi:10.3390/ph16010129
PMID:36678626
LC-HRMS/MS-Based Metabolomics Approaches Applied to the Detection of Antifungal Compounds and a Metabolic Dynamic Assessment of Orchidaceae Lima GS, Lima NM, Roque JV, de Aguiar DV, Oliveira JV, dos Santos GF, Chaves AR, Vaz BG Molecules 16-Nov-2022
PMCID:PMC9692279
doi:10.3390/molecules27227937
PMID:36432039
Unravelling the fungal darkness in a tropical cave: richness and the description of one new genus and six new species Alves VC, Lira RA, Lima JM, Barbosa RN, Bento DM, Barbier E, Bernard E, Souza-Motta CM, Bezerra JD Fungal Syst Evol 01-Nov-2022
PMCID:PMC9875697
doi:10.3114/fuse.2022.10.06
PMID:36741552
Multifunctional role of natural products for the treatment of Parkinson’s disease: At a glance Rahman MM, Wang X, Islam MR, Akash S, Supti FA, Mitu MI, Harun-Or-Rashid M, Aktar MN, Khatun Kali MS, Jahan FI, Singla RK, Shen B, Rauf A, Sharma R Front Pharmacol 06-Oct-2022
PMCID:PMC9590378
doi:10.3389/fphar.2022.976385
PMID:36299886
Non-target molecular network and putative genes of flavonoid biosynthesis in Erythrina velutina Willd., a Brazilian semiarid native woody plant Chacon DS, Santos MD, Bonilauri B, Vilasboa J, da Costa CT, da Silva IB, Torres TD, de Araújo TF, Roque AD, Pilon AC, Selegatto DM, Freire RT, Reginaldo FP, Voigt EL, Zuanazzi JA, Scortecci KC, Cavalheiro AJ, Lopes NP, Ferreira LD, dos Santos LV, Fontes W, de Sousa MV, Carvalho PC, Fett-Neto AG, Giordani RB Front Plant Sci 08-Sep-2022
PMCID:PMC9493460
doi:10.3389/fpls.2022.947558
PMID:36161018
Allelopathy and Allelochemicals of Leucaena leucocephala as an Invasive Plant Species Kato-Noguchi H, Kurniadie D Plants (Basel) 24-Jun-2022
PMCID:PMC9269122
doi:10.3390/plants11131672
PMID:35807624
In-silico Studies Calculated a New Chitin Oligomer Binding Site Inside Vicilin: A Potent Antifungal and Insecticidal Agent Saeed A, Rafiq Z, Imran M, Saeed Q, Saeed MQ, Ali Z, Iqbal RK, Hussain S, Khaliq B, Mehmood S, Akrem A Dose Response 16-Jun-2022
PMCID:PMC9208065
doi:10.1177/15593258221108280
PMID:35734395
Meleagrin Isolated from the Red Sea Fungus Penicillium chrysogenum Protects against Bleomycin-Induced Pulmonary Fibrosis in Mice Elhady SS, Goda MS, Mehanna ET, Elfaky MA, Koshak AE, Noor AO, Bogari HA, Malatani RT, Abdelhameed RF, Wahba AS Biomedicines 18-May-2022
PMCID:PMC9138525
doi:10.3390/biomedicines10051164
PMID:35625905
Diversity of Useful Plants in Cabo Verde Islands: A Biogeographic and Conservation Perspective Duarte MC, Gomes I, Catarino S, Brilhante M, Gomes S, Rendall A, Moreno Â, Fortes AR, Ferreira VS, Baptista I, Dinis H, Romeiras MM Plants (Basel) 15-May-2022
PMCID:PMC9144021
doi:10.3390/plants11101313
PMID:35631738

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,3R,4S,5S,6R)-2-[[(2R,13bS)-2,12-dimethoxy-2,6,8,9-tetrahydro-1H-indolo[7a,1-a]isoquinolin-11-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 162994861 Click to see COC1CC23C(=CCN2CCC4=CC(=C(C=C34)OC)OC5C(C(C(C(O5)CO)O)O)O)C=C1 461.50 unknown https://doi.org/10.1016/J.BMCL.2008.10.111
[(2R,13bS)-11-hydroxy-2-methoxy-2,6,8,9-tetrahydro-1H-indolo[7a,1-a]isoquinolin-12-yl] hydrogen sulfate 53237199 Click to see COC1CC23C(=CCN2CCC4=CC(=C(C=C34)OS(=O)(=O)O)O)C=C1 365.40 unknown https://doi.org/10.1248/CPB.59.564
19-Methoxy-5,7-dioxa-13-azapentacyclo[11.7.0.0^{1,16}.0^{2,10}.0^{4,8}]icosa-2(10),3,8,15,17-pentaene 12308897 Click to see COC1CC23C(=CCN2CCC4=CC5=C(C=C34)OCO5)C=C1 297.30 unknown https://doi.org/10.1016/J.BMCL.2008.10.111
19-Methoxy-5,7-dioxa-13-azapentacyclo[11.7.0.01,16.02,10.04,8]icosa-2,4(8),9,15,17-pentaen-14-one 73812404 Click to see COC1CC23C(=CC(=O)N2CCC4=CC5=C(C=C34)OCO5)C=C1 311.30 unknown https://doi.org/10.1016/J.BMCL.2008.10.111
2-[(2,12-dimethoxy-2,6,8,9-tetrahydro-1H-indolo[7a,1-a]isoquinolin-11-yl)oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 3792560 Click to see COC1CC23C(=CCN2CCC4=CC(=C(C=C34)OC)OC5C(C(C(C(O5)CO)O)O)O)C=C1 461.50 unknown https://doi.org/10.1016/J.BMCL.2008.10.111
https://doi.org/10.1016/J.BMCL.2008.06.002
2,11,12-trimethoxy-2,6,8,9-tetrahydro-1H-indolo[7a,1-a]isoquinoline 3472080 Click to see COC1CC23C(=CCN2CCC4=CC(=C(C=C34)OC)OC)C=C1 313.40 unknown https://doi.org/10.1016/J.BMCL.2008.10.111
8-Oxoerythraline 21599256 Click to see COC1CC23C(=CC(=O)N2CCC4=CC5=C(C=C34)OCO5)C=C1 311.30 unknown https://doi.org/10.1016/J.BMCL.2008.10.111
Erymelanthine 44570488 Click to see COC1CC23C(=CCN2CCC4=CN=C(C=C34)C(=O)OC)C=C1 312.40 unknown https://doi.org/10.1016/J.BMCL.2008.10.111
Erysodine 169017 Click to see COC1CC23C(=CCN2CCC4=CC(=C(C=C34)OC)O)C=C1 299.40 unknown https://doi.org/10.1016/J.BMCL.2008.10.111
Erysotrine 442219 Click to see COC1CC23C(=CCN2CCC4=CC(=C(C=C34)OC)OC)C=C1 313.40 unknown https://doi.org/10.1016/J.BMCL.2008.10.111
Erysovine 5317203 Click to see COC1CC23C(=CCN2CCC4=CC(=C(C=C34)O)OC)C=C1 299.40 unknown https://doi.org/10.1016/J.BMCL.2008.10.111
Erythraline 5317205 Click to see COC1CC23C(=CCN2CCC4=CC5=C(C=C34)OCO5)C=C1 297.30 unknown https://doi.org/10.1016/J.BMCL.2008.10.111
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/J.BMCL.2008.10.111
Grycoerysodine 44570487 Click to see COC1CC23C(=CCN2CCC4=CC(=C(C=C34)OC)OC5C(C(C(C(O5)CO)O)O)O)C=C1 461.50 unknown https://doi.org/10.1016/J.BMCL.2008.06.002
methyl 2-methoxy-2,6,8,9-tetrahydro-1H-indolo[7a,1-a][2,6]naphthyridine-12-carboxylate 13491128 Click to see COC1CC23C(=CCN2CCC4=CN=C(C=C34)C(=O)OC)C=C1 312.40 unknown https://doi.org/10.1016/J.BMCL.2008.10.111
> 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/10.1016/J.BMCL.2008.10.111
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 3-prenylated flavans / 3-prenylated flavanones
4'-Methylsigmoidin B 21721826 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/10.1016/S0031-9422(96)00529-8
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/10.1016/S0031-9422(96)00529-8
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
Hesperetin 3'-methyl ether 14466294 Click to see COC1=C(C=C(C=C1)C2CC(=O)C3=C(C=C(C=C3O2)O)O)OC 316.30 unknown https://doi.org/10.1016/S0305-1978(00)00077-6
> Phenylpropanoids and polyketides / Isoflavonoids / Furanoisoflavonoids / Pterocarpans
Phaseollidin 119268 Click to see CC(=CCC1=C(C=CC2=C1OC3C2COC4=C3C=CC(=C4)O)O)C 324.40 unknown https://doi.org/10.1016/S0305-1978(00)00077-6
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 7-O-methylated isoflavonoids
(3R)-3-(2,4-dihydroxyphenyl)-7-methoxy-6-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one 102445438 Click to see CC(=CCC1=CC2=C(C=C1OC)OCC(C2=O)C3=C(C=C(C=C3)O)O)C 354.40 unknown https://doi.org/10.1016/S0031-9422(96)00529-8

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