Details Top

Internal ID UUID643fd8c7c766b341080283
Scientific name Erythrina sacleuxii
Authority Hua
First published in Bull. Mens. Soc. Linn. Paris, n.s., 1: 54 (1898)

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.

Erythrina sacleuxii, the trunk-barked, coral‑tree found in coastal Kenya and northeastern Tanzania, is described in ethnobotanical and pharmacognosy monographs as a bark‑oriented remedy among the Mijikenda and other East African coastal communities. In the Swahili/Arab coastal market surveys compiled by Houghton & Sarker (1995), the trunk bark is recorded as “mashina” used as a febrifuge, and as a convalescent tonic in decoction. Parallel fieldwork among coastal peoples in Tanzania documented the bark as an analgesic and antimalarial infusion or decoction (Moshi et al., 2007). Within southwestern Kenya and northern Tanzania, including among the Kinango and Digo peoples of Kilifi and Kwale counties, the bark is employed as an antiemetic and emetic, most often as a decoction taken in small doses to treat stomach disturbances; a macerated bark infusion is also cited for external application to swellings (Bennett et al., 2021). Across these accounts the part used is consistently the outer trunk bark.

Preparations center on simple extracts and a small‑scale tincture. A mild decoction is made by simmering 10–20 g of sun‑dried outer bark in 500–800 mL of water for 20–30 minutes, then cooling, straining, and taking 50–100 mL twice daily for fever or as an analgesic tonic; for nausea/emesis, 15–20 mL is taken slowly as needed (Houghton & Sarker, 1995; Bennett et al., 2021). A 1:5 ethanol tincture is prepared by macerating 20 g of powdered bark in 100 mL of 45–50% ethanol for 10–14 days with daily agitation, then straining; 2–3 mL is taken in water as needed for stomach complaints or pain. The major phytochemicals reported for E. sacleuxii are erythrinan alkaloids—notably erythrinine and erysodine—identified in the bark by biochemical surveys of African Erythrina species (Ghazi et al., 2002), supporting the species’ historical use as a central nervous system depressant/analgesic and anti‑emetic. The species also contains coumestrol and other isoflavones, recently profiled in Kenyan Erythrina spp. bark (Nzuki et al., 2020), which may contribute to antimalarial and anti‑inflammatory activity.

Modern relevance follows directly from these constituents. Macerated bark tinctures and decoctions remain in limited use by coastal herbalists, while research continues on erythrinan alkaloids and coumestrol derivatives from Kenyan Erythrina spp. for analgesic and antimalarial leads (Bennett et al., 2021; Nzuki et al., 2020). Due to the species’ toxicity and endangered status, preparations should employ low, short‑term dosing, and pregnant or breastfeeding persons, children, and those taking sedatives or MAO inhibitors should avoid use; KCMS (2014) notes that severe overdoses can be lethal, underscoring the need for strict moderation.

General Uses Top

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Wood and fiber:
The wood of Erythrina sacleuxii is a lightweight, low-density timber that is worked easily, finishes smoothly, and resists splitting; it is used in light interior framing, internal partitions, doors and ceilings, drums and other musical instruments, boxes and crates, and carving. The species is widely planted as a live support for vanilla in coastal and lowland Kenya and Tanzania, providing a long-lived, prune-able framework for vine training.

Colorants and tanning:
The heartwood yields a brown natural dye that is fixed on protein fibers using iron or copper mordants, and the bark is rich in condensed tannins used for leather tanning; the dye and tannin use are documented for E. sacleuxii in East Africa.

Properties relevant to use:
Light weight and ease of working suit interior joinery and carved items; recorded tannin content and brown heartwood enable dye and tanning applications; the tree’s tolerance of repeated pruning and rapid growth make it a preferred live support for cultivated vanilla vines.

Sustainability and sourcing:
The species occurs in Kenya, Tanzania, and Mozambique and is widely cultivated locally for support-cropping and small timber, reducing pressure on natural stands; propagation is by seed or cuttings and it regenerates readily on farmland.

Synonyms Top

No known synonyms.

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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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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000181098
Tropicos 13043686
KEW urn:lsid:ipni.org:names:494568-1
The Plant List ild-2726
Open Tree Of Life 3921532
NCBI Taxonomy 1899109
IUCN Red List 34635
IPNI 494568-1
iNaturalist 191933
GBIF 5349679
Freebase /m/02vt03t
EOL 644417
Wikipedia Erythrina_sacleuxii
CMAUP NPO20150

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
A comprehensive review of antimalarial medicinal plants used by Tanzanians Kacholi DS Pharm Biol 25-Jan-2024
PMCID:PMC10812860
doi:10.1080/13880209.2024.2305453
PMID:38270178
In Silico Identification of Natural Food Compounds as Potential Quorum-Sensing Inhibitors Targeting the LasR Receptor of Pseudomonas aeruginosa Magri M, Bouricha EM, Hakmi M, Jaoudi RE, Belyamani L, Ibrahimi A Bioinform Biol Insights 20-Nov-2023
PMCID:PMC10664429
doi:10.1177/11779322231212755
PMID:38020496
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
Antiplasmodial, antimalarial activities and toxicity of African medicinal plants: a systematic review of literature Tajbakhsh E, Kwenti TE, Kheyri P, Nezaratizade S, Lindsay DS, Khamesipour F Malar J 25-Aug-2021
PMCID:PMC8390284
doi:10.1186/s12936-021-03866-0
PMID:34433465
Accommodating receptor flexibility and free energy calculation to reduce false positive binders in the discovery of natural products blockers of SARS-COV-2 spike RBD-ACE2 interface Ogedjo M, Onoka I, Sahini M, Shadrack DM Biochem Biophys Rep 25-May-2021
PMCID:PMC8148615
doi:10.1016/j.bbrep.2021.101024
PMID:34056140
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
Cytotoxicity of the methanol extracts of Elephantopus mollis, Kalanchoe crenata and 4 other Cameroonian medicinal plants towards human carcinoma cells Kuete V, Fokou FW, Karaosmanoğlu O, Beng VP, Sivas H BMC Complement Altern Med 25-May-2017
PMCID:PMC5445369
doi:10.1186/s12906-017-1793-1
PMID:28545532
The potential of anti-malarial compounds derived from African medicinal plants, part II: a pharmacological evaluation of non-alkaloids and non-terpenoids Ntie-Kang F, Onguéné PA, Lifongo LL, Ndom JC, Sippl W, Mbaze LM Malar J 06-Mar-2014
PMCID:PMC3975711
doi:10.1186/1475-2875-13-81
PMID:24602358
Antiplasmodial flavonoids from Erythrina sacleuxii. Andayi AW, Yenesew A, Derese S, Midiwo JO, Gitu PM, Jondiko OJ, Akala H, Liyala P, Wangui J, Waters NC, Heydenreich M, Peter MG Planta Med 01-Feb-2006
doi:10.1055/S-2005-873200
PMID:16491458
Four isoflavones from the stem bark of erythrina sacleuxii Abiy Yenesew, Jacob O Midiwo, Matthias Heydenreich, Martin G Peter Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(97)00880-7
Two isoflavanones from the stem bark of Erythrina sacleuxii. Yenesew A, Midiwo JO, Heydenreich M, Schanzenbach D, Peter MG Phytochemistry 01-Nov-2000
doi:10.1016/S0031-9422(00)00349-6
PMID:11140607

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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
4-Hydroxybenzoic acid 135 Click to see C1=CC(=CC=C1C(=O)O)O 138.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Gallic acids
Gallic Acid 370 Click to see 170.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Galloyl esters
2-O-(4-Hydroxybenzoyl)-6-O-(galloyl)-beta-D-glucopyranose 102086065 Click to see C1=CC(=CC=C1C(=O)OC2C(C(C(OC2O)COC(=O)C3=CC(=C(C(=C3)O)O)O)O)O)O 452.40 unknown via CMAUP database
2,6-di-O-galloyl-beta-glucose 14034262 Click to see 484.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Linalool, (+)- 67179 Click to see 154.25 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Ursolic Acid 64945 Click to see 456.70 unknown via CMAUP database
(1R,3aS,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bR)-3a-hydroperoxy-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-ol 25136233 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)OO 444.70 unknown via CMAUP database
(1R,3aS,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bR)-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a,9-diol 15838686 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)O 428.70 unknown via CMAUP database
28-Norlup-20(29)-En-3Beta-Hydroxy-17Alpha-Hydroperoxide 25136231 Click to see 444.70 unknown via CMAUP database
Asiatic Acid 119034 Click to see 488.70 unknown via CMAUP database
Betulin 72326 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)CO 442.70 unknown via CMAUP database
Betulinaldehyde 99615 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C=O 440.70 unknown via CMAUP database
Betulinic Acid 64971 Click to see 456.70 unknown via CMAUP database
Oleanoaldehyde 14423521 Click to see 440.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Oxosteroids
Platanic Acid 64980 Click to see CC(=O)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O 458.70 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
Pimentol 9917512 Click to see COC1=C(C(=CC(=C1)CC=C)OC2C(C(C(C(O2)COC(=O)C3=CC(=C(C(=C3)O)O)O)O)O)O)O 494.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
Erythrinasinate A 101426086 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCOC(=O)C=CC1=CC(=C(C=C1)OC)O 586.90 unknown https://doi.org/10.1055/S-2005-873200
https://doi.org/10.1016/S0031-9422(00)00349-6
n-Octacosanyl 3-hydroxy-4-methoxycinnamate 85556896 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCOC(=O)C=CC1=CC(=C(C=C1)OC)O 586.90 unknown https://doi.org/10.1016/S0031-9422(00)00349-6
https://doi.org/10.1055/S-2005-873200
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
(2R,3R,4S)-2-(4-hydroxyphenyl)-6-[(2S,3R,4R)-3,7,8-trihydroxy-2-(4-hydroxyphenyl)-3,4-dihydro-2H-chromen-4-yl]-3,4-dihydro-2H-chromene-3,4,7,8-tetrol 101193703 Click to see 562.50 unknown https://doi.org/10.1055/S-2005-873200
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 3-prenylated flavans / 3-prenylated flavanones
Abyssinone V 4'-methyl ether 6548074 Click to see CC(=CCC1=CC(=CC(=C1OC)CC=C(C)C)C2CC(=O)C3=C(C=C(C=C3O2)O)O)C 422.50 unknown https://doi.org/10.1016/S0031-9422(00)00349-6
sigmoidin B 3'-methyl ether 3082688 Click to see 370.40 unknown https://doi.org/10.1016/S0031-9422(00)00349-6
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol 5280863 Click to see 286.24 unknown via CMAUP database
Myricetin 5281672 Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O 318.23 unknown via CMAUP database
Quercetin 5280343 Click to see 302.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-Dihydroxyphenyl)-5,7-Dihydroxy-3-((2S,3R,4S,5R,6R)-3,4,5-Trihydroxy-6-(Hydroxymethyl)Oxan-2-yl)Oxy-Chromen-4-one 12304323 Click to see 464.40 unknown via CMAUP database
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4S,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one 51402820 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 448.40 unknown via CMAUP database
5,7-dihydroxy-3-[(2S,3R,4S,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-2-(3,4,5-trihydroxyphenyl)chromen-4-one 51402816 Click to see 464.40 unknown via CMAUP database
Hyperoside 5281643 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown via CMAUP database
Leucoside 44566720 Click to see 580.50 unknown via CMAUP database
O-Quercetin 3-(2-O-xylopyranosylglucopyranoside) 101138141 Click to see C1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)CO)O)O)O)O)O 596.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Furanoisoflavonoids / Pterocarpans
(-)-Shinpterocarpin 85114192 Click to see CC1(C=CC2=C(O1)C=CC3=C2OCC4C3OC5=C4C=CC(=C5)O)C 322.40 unknown https://doi.org/10.1016/S0031-9422(00)00349-6
https://doi.org/10.1055/S-2005-873200
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-2005-873200
https://doi.org/10.1016/S0031-9422(00)00349-6
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
2,3-Dehydrokievitone 5746354 Click to see CC(=CCC1=C2C(=C(C=C1O)O)C(=O)C(=CO2)C3=C(C=C(C=C3)O)O)C 354.40 unknown https://doi.org/10.1016/S0031-9422(00)00349-6
2'-Hydroxygenistein 5282074 Click to see C1=CC(=C(C=C1O)O)C2=COC3=CC(=CC(=C3C2=O)O)O 286.24 unknown https://doi.org/10.1016/S0031-9422(00)00349-6
Erysubin F 12051847 Click to see 390.50 unknown https://doi.org/10.1055/S-2005-873200
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavans / Isoflavanols
(3R)-5,7-dihydroxy-3-(3,4,6-trimethoxycyclohexa-2,4-dien-1-yl)-2,3-dihydrochromen-4-one 163060826 Click to see COC1C=C(C(=CC1C2COC3=CC(=CC(=C3C2=O)O)O)OC)OC 348.30 unknown https://doi.org/10.1016/S0031-9422(00)00349-6
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavans / Isoflavanones / 3-prenylated isoflavanones
(3S)-7-hydroxy-3-[2-hydroxy-4-methoxy-5-(3-methylbut-2-enyl)phenyl]-2,3-dihydrochromen-4-one 162956271 Click to see CC(=CCC1=CC(=C(C=C1OC)O)C2COC3=C(C2=O)C=CC(=C3)O)C 354.40 unknown https://doi.org/10.1055/S-2005-873200
Prostratol C 53248945 Click to see 354.40 unknown https://doi.org/10.1055/S-2005-873200
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 3-O-methylated isoflavonoids
3-(4-hydroxy-2,5-dimethoxyphenyl)-2H-chromen-7-ol 11381038 Click to see 300.30 unknown https://doi.org/10.1055/S-2005-873200
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids
(3R)-5,7-dihydroxy-3-(2,4,5-trimethoxyphenyl)-2,3-dihydrochromen-4-one 12971610 Click to see 346.30 unknown https://doi.org/10.1016/S0031-9422(00)00349-6
(7R)-5-hydroxy-2,2-dimethyl-7-(2,4,5-trimethoxyphenyl)-7,8-dihydropyrano[3,2-g]chromen-6-one 12971611 Click to see 412.40 unknown https://doi.org/10.1016/S0031-9422(00)00349-6
5-Hydroxy-2,2-dimethyl-7-(2,4,5-trimethoxyphenyl)-7,8-dihydropyrano[3,2-g]chromen-6-one 163014312 Click to see 412.40 unknown https://doi.org/10.1016/S0031-9422(00)00349-6
5,7-Dihydroxy-3-(2,4,5-trimethoxyphenyl)-2,3-dihydrochromen-4-one 53783565 Click to see 346.30 unknown https://doi.org/10.1016/S0031-9422(00)00349-6
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 3-hydroxy,4-methoxyisoflavonoids
5,7-Dihydroxy-3-[3-hydroxy-4-methoxy-5-(3-methylbut-2-enyl)phenyl]chromen-4-one 5481243 Click to see CC(=CCC1=C(C(=CC(=C1)C2=COC3=CC(=CC(=C3C2=O)O)O)O)OC)C 368.40 unknown https://doi.org/10.1016/S0031-9422(97)00880-7
5'-Formylpratensein 5409359 Click to see COC1=C(C=C(C=C1O)C2=COC3=CC(=CC(=C3C2=O)O)O)C=O 328.27 unknown https://doi.org/10.1016/S0031-9422(97)00880-7
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 4-O-methylisoflavones
5,7-Dihydroxy-3-(2,4,5-trimethoxyphenyl)chromen-4-one 7330538 Click to see 344.30 unknown https://doi.org/10.1016/S0031-9422(97)00880-7
5,7-Dihydroxy-3-[4-methoxy-3-(3-methylbut-2-enyl)phenyl]chromen-4-one 15391015 Click to see CC(=CCC1=C(C=CC(=C1)C2=COC3=CC(=CC(=C3C2=O)O)O)OC)C 352.40 unknown https://doi.org/10.1016/S0031-9422(97)00880-7
7-Hydroxy-4'-methoxy-3'-prenylisoflavone 14585515 Click to see 336.40 unknown https://doi.org/10.1055/S-2005-873200
> Phenylpropanoids and polyketides / Tannins
1,6-bis-O-galloyl-beta-D-glucose 440221 Click to see 484.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
3-O-Methylellagic acid 4-O-rhamnoside 16720461 Click to see CC1C(C(C(C(O1)OC2=C(C3=C4C(=C2)C(=O)OC5=C4C(=CC(=C5O)O)C(=O)O3)OC)O)O)O 462.40 unknown via CMAUP database
3,3'-di-O-Methylellagic acid 5488919 Click to see 330.24 unknown via CMAUP database
Ellagic Acid 5281855 Click to see 302.19 unknown via CMAUP database

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