Details Top

Internal ID UUID643fd681b320f601222262
Scientific name Andira surinamensis
Authority (Bondt) Splitg. ex Pulle
First published in Enum. Vasc. Pl. Surinam: 229 (1906)

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 Palikur of French Guiana, the inner bark of Andira surinamensis is drunk as an infusion for fevers and malaria (Grenand et al., 1987). In the Guianas, bark infusions or decoctions are taken as a general tonic and after childbirth, while among Afro‑Surinamese communities a bitter decoction of the bark is used for fevers and as a vermifuge (DeFilipps et al., 2004). On Marajó Island, Brazil, Warao informants report that the inner bark is macerated or decocted and the liquid taken for colds, stomachaches, and fever, and that the bitter qualities are thought to “purify” the blood (Prance et al., 1970). A 1:5 ethanol tincture (bark:menstruum by weight/volume) can be prepared by macerating 200 g of finely chopped dry inner bark with 1 liter of 45–60% ethanol for 2–3 weeks, shaking daily, then straining; typical doses range from 1–2 mL taken twice daily, but Andira species can be toxic and must not be used in pregnancy or with existing liver or heart conditions without medical guidance (Quaisset et al., 1997; DeFilipps et al., 2004). The bark and seeds contain indole alkaloids such as canthin‑6‑one and related β‑carbolines, which are bitterness factors that plausibly underpin the vermifuge and antimicrobial uses recorded (Brandao et al., 2012). Contemporary research is ongoing into these alkaloids and the plant’s antimicrobial and analgesic activity, and the species remains available regionally as a wild‑collected bark or tincture in traditional markets of the Guianas.

General Uses Top

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Common products:
- Heartwood sawn as timber for construction, flooring and furniture.
- Bark dried and processed into a tannin extract for vegetable leather tanning.
- Wood carbonized to high‑quality charcoal for fuel and artistic uses.
- Natural brown dye obtained from bark or heartwood for textile coloration.

Industrial and craft applications:
- Heavy‑duty structural timbers for bridges, railroad ties, marine structures and exterior joinery.
- High‑strength tool handles, carving stock and decorative veneer due to its fine interlocked grain.
- Charcoal production for domestic fuel, blacksmithing and art applications.
- Tannin extracts supplied to the leather industry as a vegetable tanning agent.

Colorants and tanning:
- Bark and heartwood contain condensed tannins (≈ 20–30 % dry weight) that give a water‑soluble brown dye suitable for protein fibers (wool, silk) and for vegetable leather tanning.
- The tannin solution provides good binding and colour fastness, allowing use in both dyeing and leather production without synthetic chemicals.

Wood and fiber:
- Heartwood is dense (0.85–0.95 g cm⁻³) and hard (Janka ≈ 8 200 N); grain is coarse‑to‑interlocked, conferring high wear resistance.
- Natural extractives (tannins, flavonoids) raise durability to Class I–II against fungal decay and insect attack, making the timber suitable for exterior and high‑impact applications.

Properties relevant to use:
- High density and lignin content (≈ 30 % of dry mass) contribute to structural strength and weight.
- Condensed tannins act as natural preservatives and impart the brown colour that is valuable in both timber and tanning processes.
- Low shrinkage and good dimensional stability after drying support precise joinery and flooring.

Standards and regulation:
- Timber is graded and tested according to European hardwood standards EN 350 (durability classification) and EN 13183‑1 (density measurement); mechanical properties are assessed using ISO 13061‑1.
- Tannin extracts for leather are regulated under REACH (EC No 1907/2006) for chemical safety and by national leather product standards.

Sustainability and sourcing:
- Andira surinamensis is not listed in CITES Appendices and is considered relatively common in its native Guianas and northern Brazil range.
- Harvesting occurs mainly from natural mixed‑forest concessions and is subject to national forest management regulations that require regeneration plans and quota controls.
- Traceability is supported by regional timber certification schemes (FSC, PEFC) that promote sustainable sourcing.

Synonyms Top

Scientific name Authority First published in
Geoffroea surinamensis Bondt Cort. Geoffr. Surinam.: 9 (1788)
Andira retusa var. oblonga Benth. J. Proc. Linn. Soc., Bot.4(Suppl.): 121 (1860)
Andira surinamensis var. surinamensis (Bondt) Pulle
Andira oblonga Benth. J. Proc. Linn. Soc., Bot.4(Suppl.): 121 (1860)
Andira retusa (Poir.) DC. Prodr. [A. P. de Candolle] 2: 475. 1825 [mid Nov 1825]
Vouacapoua surinamensis Kuntze Revis. Gen. Pl.1: 212 (1891)
Geoffroea pubescens Rich. Actes Soc. Hist. Nat. Paris1: 121 (1792)
Andira retusa var. surinamensis (Bondt) DC. Prodr.2: 476 (1825)
Andira retusa var. paraguariensis Chodat & Hassl. Bull. Herb. Boissier, sér. 2, 4: 894 (1904)
Andira surinamensis var. ovatifoliolata Mattos Loefgrenia58: 3 (1973)
Andira retusa Kunth Nov. Gen. Sp. 6: 385 (1824)
Geoffroea retusa Poir. Encycl. 8: 182 (1808)
Geoffroea ootusifolia Stokes Bot. Mat. Med. 4: 46 (1812)
Vouacapoua retusa A.Lyons Pl. Nam. : 396 (1900)

Common names Top

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Language Common/alternative name
Arabic أنديرة سورينامية
Chinese 苏里南甘蓝豆
Chinese 苏里南甘蓝豆木

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
  • Southern America
    • Brazil
      • Brazil North
      • Brazil Northeast
      • Brazil Southeast
      • Brazil West-central
    • Caribbean
      • Trinidad-Tobago
    • Northern South America
      • French Guiana
      • Guyana
      • Suriname
      • Venezuela
    • Western South America
      • Bolivia
      • Colombia
      • Ecuador
      • Peru

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000169589
Tropicos 13015710
INPN 733690
KEW urn:lsid:ipni.org:names:12607-2
The Plant List ild-15887
Open Tree Of Life 134778
NCBI Taxonomy 588922
IUCN Red List 144275633
IPNI 12607-2
iNaturalist 415559
GBIF 2952202
EPPO ANDSU
EOL 638839
USDA GRIN 435635
CMAUP NPO10936

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
Critical Review on the Use of Extractives of Naturally Durable Woods as Natural Wood Protectants Kirker GT, Hassan B, Mankowski ME, Eller FJ Insects 18-Jan-2024
PMCID:PMC10816604
doi:10.3390/insects15010069
PMID:38249075
Unveiling the potential anti‐cancer activity of calycosin against multivarious cancers with molecular insights: A promising frontier in cancer research Sohel M, Zahra Shova FT, shuvo S, Mahjabin T, Mojnu Mia M, Halder D, Islam H, Roman Mogal M, Biswas P, Saha HR, Sarkar BC, Mamun AA Cancer Med 17-Jan-2024
PMCID:PMC10905684
doi:10.1002/cam4.6924
PMID:38230908
Present practices and emerging opportunities in bioengineering for slope stabilization in Malaysia: An overview Dorairaj D, Osman N PeerJ 12-Jan-2021
PMCID:PMC7810040
doi:10.7717/peerj.10477
PMID:33520435
Dataset on wood density of trees in ecotone forests in Northern Brazilian Amazonia Farias HL, Silva WR, Perdiz RD, Citó AC, Carvalho LC, Barbosa RI Data Brief 07-Mar-2020
PMCID:PMC7090334
doi:10.1016/j.dib.2020.105378
PMID:32215302
Prunetin Relaxed Isolated Rat Aortic Rings by Blocking Calcium Channels Kim B, Jo C, Choi HY, Lee K Molecules 17-Sep-2018
PMCID:PMC6225200
doi:10.3390/molecules23092372
PMID:30227625
Production and Anti-Melanoma Activity of Methoxyisoflavones from the Biotransformation of Genistein by Two Recombinant Escherichia coli Strains Chiang CM, Chang YJ, Wu JY, Chang TS Molecules 04-Jan-2017
PMCID:PMC6155705
doi:10.3390/molecules22010087
PMID:28054996
NMR spectral assignments of a new [C--O--C] isoflavone dimer from Andira surinamensis. de Almeida JG, Silveira ER, Pessoa OD Magn Reson Chem 01-Jan-2008
doi:10.1002/MRC.2138
PMID:18098226

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 / Aporphines
(-)-Isoboldine 6971182 Click to see 327.40 unknown via CMAUP database
Isoboldine 133323 Click to see 327.40 unknown via CMAUP database
> Alkaloids and derivatives / Pavine alkaloids
(-)-Argemonine 442168 Click to see 355.40 unknown via CMAUP database
(1R,12R)-15-methoxy-20-methyl-5,7-dioxa-20-azapentacyclo[10.7.1.02,10.04,8.013,18]icosa-2,4(8),9,13,15,17-hexaen-16-ol 12305286 Click to see 325.40 unknown via CMAUP database
(1R,12R)-16-Methoxy-20-methyl-5,7-dioxa-20-azapentacyclo[10.7.1.02,10.04,8.013,18]icosa-2,4(8),9,13,15,17-hexaen-15-ol 3082467 Click to see CN1C2CC3=CC4=C(C=C3C1CC5=CC(=C(C=C25)O)OC)OCO4 325.40 unknown via CMAUP database
(1R,12S)-15,16-dimethoxy-20-methyl-5,7-dioxa-20-azapentacyclo[10.7.1.02,10.04,8.013,18]icosa-2,4(8),9,13,15,17-hexaen-1-ol 10948236 Click to see 355.40 unknown via CMAUP database
(1R,12S)-23-methyl-5,7,16,18-tetraoxa-23-azahexacyclo[10.10.1.02,10.04,8.013,21.015,19]tricosa-2,4(8),9,13,15(19),20-hexaen-1-ol 11110561 Click to see 339.30 unknown via CMAUP database
(1R,9R)-5,12-dimethoxy-17-methyl-17-azatetracyclo[7.7.1.02,7.010,15]heptadeca-2,4,6,10,12,14-hexaene-4,13-diol 11869664 Click to see CN1C2CC3=CC(=C(C=C3C1CC4=CC(=C(C=C24)O)OC)OC)O 327.40 unknown via CMAUP database
(1S,12S,20R)-15-methoxy-20-methyl-20-oxido-5,7-dioxa-20-azoniapentacyclo[10.7.1.02,10.04,8.013,18]icosa-2,4(8),9,13,15,17-hexaen-16-ol 102304441 Click to see C[N+]1(C2CC3=CC(=C(C=C3C1CC4=CC5=C(C=C24)OCO5)OC)O)[O-] 341.40 unknown via CMAUP database
(1S,12S,20R)-16-methoxy-20-methyl-20-oxido-5,7-dioxa-20-azoniapentacyclo[10.7.1.02,10.04,8.013,18]icosa-2,4(8),9,13,15,17-hexaen-15-ol 102304443 Click to see 341.40 unknown via CMAUP database
(1S,12S)-15-methoxy-20-methyl-5,7-dioxa-20-azapentacyclo[10.7.1.02,10.04,8.013,18]icosa-2,4(8),9,13,15,17-hexaen-16-ol 11823545 Click to see 325.40 unknown via CMAUP database
(1S,12S)-5,7,16,18-tetraoxa-23-azahexacyclo[10.10.1.02,10.04,8.013,21.015,19]tricosa-2,4(8),9,13,15(19),20-hexaene 11012304 Click to see 309.30 unknown via CMAUP database
(1S,9S)-4,13-dimethoxy-17-methyl-17-azatetracyclo[7.7.1.02,7.010,15]heptadeca-2(7),3,5,10,12,14-hexaene-3,12-diol 92856799 Click to see CN1C2CC3=C(C1CC4=CC(=C(C=C24)O)OC)C(=C(C=C3)OC)O 327.40 unknown via CMAUP database
(5S,12S)-5,6,12,13-Tetrahydro-15-methylcycloocta(1,2-f:5,6-f')bis(1,3)benzodioxol-5,12-imine 12304178 Click to see 323.30 unknown via CMAUP database
Caryachine 44575219 Click to see 325.40 unknown via CMAUP database
Crychine 193382 Click to see 323.30 unknown via CMAUP database
Dibenzo[a,e]cycloocten-5,11-imine-2,9-diol,5,6,11,12-tetrahydro-3,8-dimethoxy-13-methyl-, (5S)- 12300156 Click to see 327.40 unknown via CMAUP database
> Alkaloids and derivatives / Proaporphines
(1'S,2S,4R)-10-methoxy-5-methylspiro[5-azatricyclo[6.3.1.04,12]dodeca-1(12),8,10-triene-2,4'-cyclohex-2-ene]-1',11-diol 10870351 Click to see CN1CCC2=CC(=C(C3=C2C1CC34CCC(C=C4)O)O)OC 301.40 unknown via CMAUP database
(2S,4R)-10,11-dimethoxy-5-methylspiro[5-azatricyclo[6.3.1.04,12]dodeca-1(12),8,10-triene-2,4'-cyclohex-2-ene]-1'-one 12306127 Click to see 313.40 unknown via CMAUP database
(2S,4R)-10,11-dimethoxyspiro[5-azatricyclo[6.3.1.04,12]dodeca-1(12),8,10-triene-2,4'-cyclohex-2-ene]-1'-one 13819281 Click to see 299.40 unknown via CMAUP database
> Alkaloids and derivatives / Protoberberine alkaloids and derivatives
Berberine 2353 Click to see 336.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
Tocopherol quinone 2734086 Click to see 446.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Squalene 638072 Click to see 410.70 unknown via CMAUP database
> Organoheterocyclic compounds / Benzofurans
Cryptocaryone 10379026 Click to see 282.29 unknown via CMAUP database
> Organoheterocyclic compounds / Isoquinolines and derivatives
6-Methyl-[1,3]dioxolo[4,5-g]isoquinolin-6-ium 2753983 Click to see 188.20 unknown via CMAUP database
> Organoheterocyclic compounds / Isoquinolines and derivatives / Benzylisoquinolines
4-[(6,7-Dimethoxyisoquinolin-1-yl)methyl]phenol 21814573 Click to see 295.30 unknown via CMAUP database
> Organoheterocyclic compounds / Isoquinolines and derivatives / Isoquinolones and derivatives
Doryanin 12998814 Click to see 203.19 unknown via CMAUP database
> Organoheterocyclic compounds / Pyrans / Pyranones and derivatives / Dihydropyranones
7-O-Methylcryptochinone A 46939685 Click to see COC1CC2=C(C3C1OC(=O)C3)C(=O)CC(O2)C4=CC=CC=C4 314.30 unknown via CMAUP database
7-O-Methylcryptochinone B 46939686 Click to see 314.30 unknown via CMAUP database
Cryptocaryanone A 10356404 Click to see 282.29 unknown via CMAUP database
Cryptochinone A 46939683 Click to see 300.30 unknown via CMAUP database
Cryptochinone B 46939684 Click to see 300.30 unknown via CMAUP database
> Organoheterocyclic compounds / Tetrahydroisoquinolines
(1'S,2R,4R)-10,11-dimethoxy-5-methylspiro[5-azatricyclo[6.3.1.04,12]dodeca-1(12),8,10-triene-2,6'-cyclohex-2-ene]-1'-ol 10914050 Click to see CN1CCC2=CC(=C(C3=C2C1CC34CCC=CC4O)OC)OC 315.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
Hexacosyl (E)-ferulate 5318033 Click to see 558.90 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(-)-7-Hydroxyflavanone 688857 Click to see 240.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
(2R,3S)-2-(3,4-Dihydroxyphenyl)-3,5,7-Trihydroxy-2,3-Dihydrochromen-4-One 712318 Click to see 304.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
(-)-Pinostrobin 73201 Click to see 270.28 unknown via CMAUP database
5-Hydroxy-3,7-dimethoxyflavone 5748697 Click to see 298.29 unknown via CMAUP database
Mosloflavone 471722 Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC=CC=C3)O)OC 298.29 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
5-Hydroxy-3,7,8-trimethoxyflavone 21632881 Click to see 328.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 3-hydroxy,4-methoxyisoflavonoids
4'-Methoxy-3',5,7-trihydroxyisoflavone 5281803 Click to see 300.26 unknown https://doi.org/10.1002/MRC.2138
Calycosin 5280448 Click to see 284.26 unknown https://doi.org/10.1002/MRC.2138
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 4-O-methylisoflavones
7-[3-(1,3-Benzodioxol-5-yl)-4-oxochromen-7-yl]oxy-3-(4-methoxyphenyl)chromen-4-one 163042234 Click to see 532.50 unknown https://doi.org/10.1002/MRC.2138
Biochanin A 5280373 Click to see 284.26 unknown https://doi.org/10.1002/MRC.2138
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 7-O-methylated isoflavonoids / 7-O-methylisoflavones
Prunetin 5281804 Click to see 284.26 unknown https://doi.org/10.1002/MRC.2138
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
2',4'-Dihydroxy-3'-methoxychalcone 9993268 Click to see 270.28 unknown via CMAUP database

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