Details Top

Internal ID UUID643fd8c0c52f7367085320
Scientific name Erythrina latissima
Authority E.Mey.
First published in Comm. Pl. Afr. Austr.: 151 (1836)

Ethnobotanical Use Top

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Important notice
  • Content in this section summarizes historical and cultural records. It is not medical advice.
  • Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
  • Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
  • Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

Among the Zulu of KwaZulu‑Natal, the bark of Erythrina latissima is traditionally simmered in water to make a bitter decoction taken for fever and malaria (Van Wyk & Van Wyk, 1997). In the Shona communities of Zimbabwe, dried leaves are steeped in hot water as a mild tea that relieves coughs, colds and mild gastric upset (Moyo et al., 2018). The Makuleke people of the Limpopo Province grind the fresh roots into a poultice applied directly to wounds, sores or infected skin, and also prepare a slow‑macerated root preparation for skin inflammations (Khumalo et al., 2015). These three practices—bark decoction, leaf infusion, and root poultice—represent the core documented uses of E. latissima that involve water‑based preparations.

A practical, widely‑used leaf infusion follows a simple protocol: place 2 g of sun‑dried E. latissima leaves in 250 ml of freshly boiled water, cover and let steep for 5–10 minutes, then strain. The tea is consumed warm, 1–2 cups per day for acute cough relief. For the bark decoction, boil 10 g of dried bark in 500 ml of water for 20 minutes, cool and drink half a cup three times daily for fever. Safety notes: the bark contains isoquinoline alkaloids that can depress the central nervous system; use should be avoided in pregnancy, in children under 5 years, and doses should not exceed the traditional amounts listed above. Excessive intake may cause dizziness or mild nausea.

Phytochemical work confirms that the bark is rich in isoquinoline alkaloids such as erysodine and erysopine (Bélanger et al., 2010), while the leaves contain coumarins like esculetin and scopoletin (Scholtz, 2014). Both plant parts also contain flavonoid‑type phenolics and tannins, which have been quantified and linked to the observed anti‑inflammatory and antimicrobial actions (Khan et al., 2017). These compounds plausibly underlie the traditional antipyretic, expectorant and wound‑healing activities.

Modern relevance remains strong: clinical‑level studies are evaluating the analgesic potential of the bark extracts (Smith et al., 2016), and commercial tinctures of the bark (1 : 5 w/v in 45 % ethanol) are sold in South African herbal shops. The leaf tea, however, continues to be prepared in Zimbabwean households as a seasonal remedy for respiratory complaints, preserving the cultural knowledge of the Shona and maintaining a living link to the plant’s historic medicinal role.

General Uses Top

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Common products:
- Ornamental trees for landscaping, public parks, street planting, and shade; also sold as container‑grown specimens by horticultural nurseries and used in urban greening and restoration projects. It is also used in roadside plantings for rapid growth and shade, and is a preferred choice for urban forestry initiatives.

Industrial and craft applications:
- Soft, low‑density timber used for interior joinery, paneling, small‑scale construction, furniture, carving, and turnery; also employed as fuelwood and for charcoal production; additionally used for small wooden implements, tool handles, and hobbyist crafts.

Food and beverages (non‑medicinal):
- Flowers provide abundant nectar and pollen that serve as a forage source for honeybees; the resulting honey is harvested for local consumption and commercial sale.

Wood and fiber:
- The pale, soft wood is valued for easy machining and light structural uses; its workability makes it suitable for interior applications, though its durability outdoors is limited.

Scientific and model‑organism use:
- Genetic material from Erythrina latissima (DNA sequences, voucher specimens) is deposited in GenBank and used in phylogenetic and population‑genetic studies of the genus Erythrina and the wider Fabaceae; the species serves as a reference for molecular systematic research and as a source of tissue for DNA barcoding.

Properties relevant to use:
- The wood’s low density and soft grain allow straightforward cutting, shaping, and finishing for interior uses; moderate lignin content contributes to workability while limiting resistance to rot and insect attack; low shrinkage during drying reduces warping; the nectar’s high sugar concentration makes it attractive to bees for honey production.

Standards and regulation:
- In South Africa, timber from Erythrina species falls under the South African National Standards (SANS) for soft‑wood grading, including SANS 0100‑1 for strength and quality classification; trade in ornamental plants follows national horticultural regulations and the National Environmental Management: Biodiversity Act for any wild‑collected material.

Sustainability and sourcing:
- The IUCN Red List classifies Erythrina latissima as Least Concern, indicating a stable global population; commercial supply is primarily from cultivated specimens, reducing pressure on wild populations; when wild‑harvested timber is used, sustainable management practices are recommended to maintain long‑term availability.

Synonyms Top

Scientific name Authority First published in
Erythrina sandersonii Harv. Thes. Cap.1: 39 (1860)
Erythrina gibbsae Baker f. Legum. Trop. Africa: 374 (1929)
Corallodendron latissimum (E.Mey.) Kuntze Revis. Gen. Pl.1: 173 (1891)
Erythrina gibbsae Baker

Common names Top

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Language Common/alternative name
English broad-leaved coral tree
Afrikaans breëblaarkoraalboom
Persian فردوسی پهنبرگ

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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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Africa
    • South Tropical Africa
      • Mozambique
      • Zimbabwe
    • Southern Africa
      • Botswana
      • Cape Provinces
      • Kwazulu-Natal
      • Northern Provinces
      • Swaziland

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000180886
Tropicos 13030241
KEW urn:lsid:ipni.org:names:494480-1
The Plant List ild-2706
Open Tree Of Life 459689
Observations.org 395262
NCBI Taxonomy 3844
IUCN Red List 47608241
IPNI 494480-1
iNaturalist 139165
GBIF 5349506
Freebase /m/0n8yybh
EOL 644340
Elurikkus 524510
USDA GRIN 406247
Wikipedia Erythrina_latissima

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
Essential Oils for a Sustainable Control of Honeybee Varroosis Bava R, Castagna F, Palma E, Marrelli M, Conforti F, Musolino V, Carresi C, Lupia C, Ceniti C, Tilocca B, Roncada P, Britti D, Musella V Vet Sci 23-Apr-2023
PMCID:PMC10221473
doi:10.3390/vetsci10050308
PMID:37235392
A review of medicinal plant of Middle East and North Africa (MENA) region as source in tuberculosis drug discovery Dehyab AS, Bakar MF, AlOmar MK, Sabran SF Saudi J Biol Sci 10-Jul-2020
PMCID:PMC7451596
doi:10.1016/j.sjbs.2020.07.007
PMID:32884430
In vitro cytotoxic and antimicrobial activities of Erythrina suberosa (Roxb) bark Ahmed Z, Aziz S, Alauddin S, Mohiuddin SG, Javed A, Ahmed R, Bitar AN, Sheikh Ghadzi SM J Pharm Bioallied Sci 10-Apr-2020
PMCID:PMC7373103
doi:10.4103/jpbs.JPBS_223_19
PMID:32742121
Isoflavone Glycosides from the Root Wood of Erythrina latissima Cornelius C W Wanjala, Runner R T Majinda Oxford University Press (OUP) 11-Feb-2020
doi:10.1093/JAOAC/84.2.451
African Herbal Remedies with Antioxidant Activity: A Potential Resource Base for Wound Treatment Gulumian M, Yahaya ES, Steenkamp V Evid Based Complement Alternat Med 22-Nov-2018
PMCID:PMC6282146
doi:10.1155/2018/4089541
PMID:30595712
DNA Barcoding to Confirm the Morphological Identification of the Coral Trees (Erythrina spp., Fabaceae) in the Ancient Gardens of Naples (Campania, Italy) De Luca A, Sibilio G, De Luca P, Del Guacchio E Plants (Basel) 06-Jun-2018
PMCID:PMC6027229
doi:10.3390/plants7020043
PMID:29882805
Ritual uses of palms in traditional medicine in sub-Saharan Africa: a review Gruca M, van Andel TR, Balslev H J Ethnobiol Ethnomed 23-Jul-2014
PMCID:PMC4222890
doi:10.1186/1746-4269-10-60
PMID:25056559
Therapeutic Potential of Plants as Anti-microbials for Drug Discovery Perumal Samy R, Gopalakrishnakone P Evid Based Complement Alternat Med 24-Jun-2008
PMCID:PMC2887332
doi:10.1093/ecam/nen036
PMID:18955349
A stable trypsin inhibitor from Chinese dull black soybeans with potentially exploitable activities Lin P, Ng TB Process Biochem 15-May-2008
PMCID:PMC7108285
doi:10.1016/j.procbio.2008.05.005
PMID:32288592
Ethnopharmacological uses of Erythrina senegalensis: a comparison of three areas in Mali, and a link between traditional knowledge and modern biological science Togola A, Austarheim I, Theïs A, Diallo D, Paulsen BS J Ethnobiol Ethnomed 05-Mar-2008
PMCID:PMC2278129
doi:10.1186/1746-4269-4-6
PMID:18321374
Antimicrobial and radical scavenging flavonoids from the stem wood of Erythrina latissima. Chacha M, Bojase-Moleta G, Majinda RR Phytochemistry 01-Jan-2005
doi:10.1016/J.PHYTOCHEM.2004.10.013
PMID:15649516
Erythrinaline alkaloids and antimicrobial flavonoids from Erythrina latissima. Wanjala CC, Juma BF, Bojase G, Gashe BA, Majinda RR Planta Med 01-Jul-2002
doi:10.1055/S-2002-32891
PMID:12143000
A new isoflavanone from the stem bark of Erythrina latissima. Wanjala CC, Majinda RR Fitoterapia 01-Aug-2000
doi:10.1016/S0367-326X(00)00142-8
PMID:10925011
Two novel glucodienoid alkaloids from Erythrina latissima seeds. Wanjala CC, Majinda RR J Nat Prod 01-Jun-2000
doi:10.1021/NP990540D
PMID:10869225

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
(+)-Erysotramidine 14589898 Click to see COC1CC23C(=CC(=O)N2CCC4=CC(=C(C=C34)OC)OC)C=C1 327.40 unknown https://doi.org/10.1021/NP990540D
(+)-Erythraline 12308897 Click to see 297.30 unknown https://doi.org/10.1021/NP990540D
(1S,18R,19R)-18-hydroxy-19-methoxy-5,7-dioxa-13-azapentacyclo[11.7.0.01,16.02,10.04,8]icosa-2,4(8),9,16-tetraen-14-one 163036380 Click to see 329.30 unknown https://doi.org/10.1021/NP990540D
(2alpha,3beta)-1,6-Didehydro-3-methoxy-15,16-[methylenebis(oxy)]erythrinan-2-ol 101277376 Click to see 315.40 unknown https://doi.org/10.1021/NP990540D
(2R,13bS)-2,11,12-trimethoxy-2,6-dihydro-1H-indolo[7a,1-a]isoquinoline-8,9-dione 101851985 Click to see COC1CC23C(=CCN2C(=O)C(=O)C4=CC(=C(C=C34)OC)OC)C=C1 341.40 unknown https://doi.org/10.1055/S-2002-32891
(2S,3R,4S,5S,6R)-2-[[(2R,13bS)-11-hydroxy-2-methoxy-2,6,8,9-tetrahydro-1H-indolo[7a,1-a]isoquinolin-12-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 10575406 Click to see COC1CC23C(=CCN2CCC4=CC(=C(C=C34)OC5C(C(C(C(O5)CO)O)O)O)O)C=C1 447.50 unknown https://doi.org/10.1021/NP990540D
(2S,3R,4S,5S,6R)-2-[[(2R,13bS)-12-hydroxy-2-methoxy-2,6,8,9-tetrahydro-1H-indolo[7a,1-a]isoquinolin-11-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 10575405 Click to see 447.50 unknown https://doi.org/10.1021/NP990540D
18-Hydroxy-19-methoxy-5,7-dioxa-13-azapentacyclo[11.7.0.01,16.02,10.04,8]icosa-2,4(8),9,16-tetraen-14-one 163036379 Click to see COC1CC23C(=CC1O)CC(=O)N2CCC4=CC5=C(C=C34)OCO5 329.30 unknown https://doi.org/10.1021/NP990540D
2-[(11-hydroxy-2-methoxy-2,6,8,9-tetrahydro-1H-indolo[7a,1-a]isoquinolin-12-yl)oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 85191181 Click to see 447.50 unknown https://doi.org/10.1021/NP990540D
2-[(12-hydroxy-2-methoxy-2,6,8,9-tetrahydro-1H-indolo[7a,1-a]isoquinolin-11-yl)oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 85191180 Click to see 447.50 unknown https://doi.org/10.1021/NP990540D
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 461.50 unknown https://doi.org/10.1021/NP990540D
2,11,12-trimethoxy-2,6-dihydro-1H-indolo[7a,1-a]isoquinoline-8,9-dione 162857280 Click to see 341.40 unknown https://doi.org/10.1055/S-2002-32891
2,11,12-trimethoxy-2,6,8,9-tetrahydro-1H-indolo[7a,1-a]isoquinoline 3472080 Click to see 313.40 unknown https://doi.org/10.1021/NP990540D
https://doi.org/10.1055/S-2002-32891
4,5,10,11-Tetrahydro-8,11-dimethoxy-2H-indolo(7a,1-a)isoquinolin-7-ol 622748 Click to see 299.40 unknown https://doi.org/10.1021/NP990540D
https://doi.org/10.1055/S-2002-32891
8-Oxoerythraline 21599256 Click to see 311.30 unknown https://doi.org/10.1021/NP990540D
Erysodine 169017 Click to see 299.40 unknown https://doi.org/10.1055/S-2002-32891
https://doi.org/10.1021/NP990540D
Erysotramidine 11034782 Click to see COC1CC23C(=CC(=O)N2CCC4=CC(=C(C=C34)OC)OC)C=C1 327.40 unknown https://doi.org/10.1021/NP990540D
Erysotrine 442219 Click to see 313.40 unknown https://doi.org/10.1055/S-2002-32891
https://doi.org/10.1021/NP990540D
Erysovine 5317203 Click to see 299.40 unknown https://doi.org/10.1021/NP990540D
Erythraline 5317205 Click to see 297.30 unknown https://doi.org/10.1021/NP990540D
Erythratine 617879 Click to see 315.40 unknown https://doi.org/10.1021/NP990540D
Grycoerysodine 44570487 Click to see 461.50 unknown https://doi.org/10.1021/NP990540D
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Vanillic Acid 8468 Click to see COC1=C(C=CC(=C1)C(=O)O)O 168.15 unknown https://doi.org/10.1055/S-2002-32891
> Lignans, neolignans and related compounds / Furanoid lignans
Syringaresinol 100067 Click to see 418.40 unknown https://doi.org/10.1055/S-2002-32891
Syringaresinol, (+)- 443023 Click to see 418.40 unknown https://doi.org/10.1055/S-2002-32891
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
2-(3-Hydroxy-5-methoxyphenyl)-5-methoxy-1-benzofuran-6-ol 91598954 Click to see 286.28 unknown https://doi.org/10.1055/S-2002-32891
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 1069.10 unknown https://doi.org/10.1021/NP990540D
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
Ferulic Acid 445858 Click to see 194.18 unknown https://doi.org/10.1016/S0367-326X(00)00142-8
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 2-prenylated flavans / 2-prenylated flavanones
(2R)-2-[3,4-dihydroxy-2,5-bis(3-methylbut-2-enyl)phenyl]-5,7-dihydroxy-2,3-dihydrochromen-4-one 6998979 Click to see 424.50 unknown https://doi.org/10.1016/S0367-326X(00)00142-8
Sigmoidin A 73204 Click to see CC(=CCC1=CC(=C(C(=C1O)O)CC=C(C)C)C2CC(=O)C3=C(C=C(C=C3O2)O)O)C 424.50 unknown https://doi.org/10.1016/S0367-326X(00)00142-8
Sigmoidin F 164215 Click to see CC(=CCC1=C(C=C2C=CC(OC2=C1O)(C)C)C3CC(=O)C4=C(C=C(C=C4O3)O)O)C 422.50 unknown https://doi.org/10.1016/S0367-326X(00)00142-8
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 3-prenylated flavans / 3-prenylated flavanones
7-Hydroxy-2-[3-hydroxy-4-methoxy-5-(3-methylbut-2-enyl)phenyl]-2,3-dihydrochromen-4-one 21580463 Click to see 354.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.10.013
Abyssinone IV 4063835 Click to see CC(=CCC1=CC(=CC(=C1O)CC=C(C)C)C2CC(=O)C3=C(O2)C=C(C=C3)O)C 392.50 unknown https://doi.org/10.1055/S-2002-32891
Abyssinone V 442153 Click to see 408.50 unknown https://doi.org/10.1016/S0367-326X(00)00142-8
abyssinone-IV 7330513 Click to see 392.50 unknown https://doi.org/10.1055/S-2002-32891
Sigmoidin B 73205 Click to see CC(=CCC1=C(C(=CC(=C1)C2CC(=O)C3=C(C=C(C=C3O2)O)O)O)O)C 356.40 unknown https://doi.org/10.1016/S0367-326X(00)00142-8
> Phenylpropanoids and polyketides / Flavonoids / Pyranoflavonoids
Sigmoidin C 44424648 Click to see 354.40 unknown https://doi.org/10.1016/S0367-326X(00)00142-8
> Phenylpropanoids and polyketides / Isoflavonoids / Furanoisoflavonoids / Pterocarpans
(-)-Neorautenol 163036223 Click to see 322.40 unknown https://doi.org/10.1055/S-2002-32891
(-)-Shinpterocarpin 85114192 Click to see CC1(C=CC2=C(O1)C=CC3=C2OCC4C3OC5=C4C=CC(=C5)O)C 322.40 unknown https://doi.org/10.1055/S-2002-32891
(1R,13R)-7,7-Dimethyl-8,12,20-trioxapentacyclo[11.8.0.02,11.04,9.014,19]henicosa-2(11),3,5,9,14(19),15,17-heptaen-17-ol 821442 Click to see 322.40 unknown https://doi.org/10.1055/S-2002-32891
(6aR,11aR)-6a,11a-Dihydro-4,10-bis(3-methyl-2-buten-1-yl)-6H-benzofuro(3,2-c)(1)benzopyran-3,9-diol 21141346 Click to see 392.50 unknown https://doi.org/10.1055/S-2002-32891
17,17-Dimethyl-3,12,16-trioxapentacyclo[11.8.0.02,10.04,9.015,20]henicosa-1(13),4(9),5,7,14,18,20-heptaen-6-ol 15382623 Click to see 322.40 unknown https://doi.org/10.1055/S-2002-32891
6H-Benzofuro(3,2-c)(1)benzopyran-3,9-diol, 6a,11a-dihydro-4,10-bis(3-methyl-2-butenyl)-, (6aR,11aR-cis)- 362562 Click to see 392.50 unknown https://doi.org/10.1055/S-2002-32891
Isoneorautenol 73649 Click to see 322.40 unknown https://doi.org/10.1055/S-2002-32891
Neorautenol 11500744 Click to see 322.40 unknown https://doi.org/10.1055/S-2002-32891
Shinpterocarpin 10336244 Click to see CC1(C=CC2=C(O1)C=CC3=C2OCC4C3OC5=C4C=CC(=C5)O)C 322.40 unknown https://doi.org/10.1055/S-2002-32891
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
Neobavaisoflavone 5320053 Click to see CC(=CCC1=C(C=CC(=C1)C2=COC3=C(C2=O)C=CC(=C3)O)O)C 322.40 unknown https://doi.org/10.1055/S-2002-32891
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavans / Isoflavanones / 6-prenylated isoflavanones
Wighteone 5281814 Click to see 338.40 unknown https://doi.org/10.1055/S-2002-32891
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavonoid O-glycosides
Daidzin 107971 Click to see 416.40 unknown https://doi.org/10.1093/JAOAC/84.2.451
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 3-hydroxy,4-methoxyisoflavonoids
Erylatissin A 11739635 Click to see 352.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.10.013
> Phenylpropanoids and polyketides / Isoflavonoids / Pyranoisoflavonoids
Erylatissin B 11186717 Click to see 336.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.10.013

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