Details Top

Internal ID UUID6440036d5741e346519309
Scientific name Simarouba amara
Authority Aubl.
First published in Hist. Pl. Guiane : 860 (1775)

Ethnobotanical Use Top

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General Uses Top

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Common products:
- Light‑colored heartwood and sapwood marketed as “amara” or “marupá” timber for interior finishes, furniture, veneer, plywood and pulp.
- Seed kernels yielding a non‑drying oil processed into industrial soap and lubricant feedstocks.
- Bark and young shoots providing hydrolyzable tannins employed in leather tanning.

Industrial and craft applications:
- Wood chips and sawdust are used in kraft pulp mills for papermaking and in the production of particleboard and medium‑density fiberboard (MDF); they are also converted to charcoal for domestic fuel.
- The seed oil is saponified to produce solid and liquid soaps and may be esterified for biodegradable lubricants.

Colorants and tanning:
- Extracts from the bark contain hydrolyzable tannins with a phenolic content suitable for leather‑tanning processes, imparting a light tan colour to finished hides.

Wood and fiber:
- The species produces a low‑density wood (specific gravity 0.33–0.44 g cm⁻³) with a cellulose content of about 45–55 % and a lignin proportion of 20–25 %. This composition yields a pulp with good brightness and moderate tensile strength, making the timber suitable for interior paneling, doors, crates and lightweight furniture rather than exterior construction.

Properties relevant to use:
- Wood: moderate shrinkage, low durability against insects, but good workability and low moisture uptake.
- Seed oil: high proportion of unsaturated fatty acids (oleic and linoleic acids) with a low iodine value (≈ 100 g I₂ 100 g⁻¹), indicating low drying capacity; the oil’s acid value meets ISO 660 specifications for industrial soaps.
- Tannins: hydrolyzable tannins rich in gallic acid derivatives, conferring high binding capacity for protein fibers in leather.

Standards and regulation:
- Brazil’s ABNT NBR 7190 (Timber Structures) governs the grading and design values for construction timber; Simarouba amara timber is classified in the “light‑wood” category for interior applications.
- The seed oil used in soap production conforms to ISO 660 (Animal and vegetable fats and oils – Determination of acid value) and relevant national cosmetic regulations (e.g., ANVISA – Brazil) for raw material purity.

Sustainability and sourcing:
- Simarouba amara is a fast‑growing pioneer species that readily colonizes secondary forest gaps in the Amazon basin, allowing selective harvesting without forest conversion. Plantations in Brazil and Colombia operate under Forest Stewardship Council (FSC) or Programme for the Endorsement of Forest Certification (PEFC) schemes, providing chain‑of‑custody certification for timber and seed‑oil products.

Synonyms Top

Scientific name Authority First published in
Pistacia americana Mill. Gard. Dict. ed. 8 : n.º 7 (1768)
Zwingera amara Willd. Sp. Pl., ed. 4 , 2: 569 (1799)
Simarouba amara var. opaca Engl. Nat. Pflanzenfam. 3(4): 213 (1896)
Simarouba amara var. puberula Cuatrec. Revista Acad. Colomb. Ci. Exact. 8: 466 (1952)
Quassia alatifolia Stokes Bot. Mat. Med. 2: 491 (1812)
Quassia dioica O.Berg Mater. Med. : 355 (1778)
Quassia officinalis Rich. Actes Soc. Hist. Nat. Paris 1: 108 (1792)
Quassia simaruba L.f. Suppl. Pl. : 234 (1782)
Quassia simarouba W.Wright Trans. Roy. Soc. Edinburgh 2: 80, nom. illegit. 1790 ; cf. D.J. Mabberley in Taxon, 30(1): 12. 1981
Simarouba opaca Radlk. ex F.Boas Beih. Bot. Centralbl. 29(1): 332 (1913)
Simarouba amara var. typica Cronquist Bull. Torrey Bot. Club 71: 229 (1944)

Common names Top

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Language Common/alternative name
Spanish simarouba amara var. opaca
Spanish simarouba amara var. typica
Spanish simarouba opaca
Spanish zwingera amara
Arabic قصب مر/ سماروبه
Hindi लक्ष्मी तरु
Indonesian marupa
Malayalam ലക്ഷ്മിതരു

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
  • Northern America
    • Mexico
      • Mexico Central
      • Mexico Gulf
      • Mexico Southeast
      • Mexico Southwest
  • Southern America
    • Brazil
      • Brazil North
      • Brazil Northeast
      • Brazil Southeast
      • Brazil West-central
    • Caribbean
      • Leeward Islands
      • Southwest Caribbean
      • Trinidad-Tobago
      • Windward Islands
    • Central America
      • Belize
      • Costa Rica
      • El Salvador
      • Guatemala
      • Honduras
      • Nicaragua
      • Panamá
    • 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-0000492139
UNII 1XP13GJA11
Tropicos 29400090
INPN 630675
KEW urn:lsid:ipni.org:names:814124-1
The Plant List kew-2580434
PFAF Simarouba amara
Open Tree Of Life 452697
Observations.org 209618
NCBI Taxonomy 101569
IUCN Red List 61966243
IPNI 814124-1
iNaturalist 291679
GBIF 7329602
Freebase /m/0g59rtq
EPPO SMBAM
Elurikkus 616735
USDA GRIN 33956
Wikipedia Simarouba_amara

Genomes (via NCBI) Top

Below is displayed the reference genome only!
If you wish to browse all genomes for this plant click here.
Accession Assembly
Name Level Submitter Released Coverage Size
GCA_056153145.1 Sam_ufg Scaffold Universidade Federal de Goias 2026-03-19 36 272.91 Mb

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
Linking Anthropogenic Landscape Perturbation to Herbivory and Pathogen Leaf Damage in Tropical Tree Communities Pablo-Rodríguez JL, Bravo-Monzón ÁE, Montiel-González C, Benítez-Malvido J, Álvarez-Betancourt S, Ramírez-Sánchez O, Oyama K, Arena-Ortiz ML, Alvarez-Añorve MY, Avila-Cabadilla LD Plants (Basel) 13-Nov-2023
PMCID:PMC10675074
doi:10.3390/plants12223839
PMID:38005736
Plant sex influences on riparian communities and ecosystems Scheuerell RP, LeRoy CJ Ecol Evol 12-Jul-2023
PMCID:PMC10337289
doi:10.1002/ece3.10308
PMID:37449021
Transcriptomic Evidence Reveals Low Gelatinous Layer Biosynthesis in Neolamarckia cadamba after Gravistimulation Qaseem MF, Wang K, Yang H, Zhao S, Li H, Wu AM Int J Mol Sci 23-Dec-2022
PMCID:PMC9820806
doi:10.3390/ijms24010268
PMID:36613711
Natural products in cosmetics Liu JK Nat Prod Bioprospect 28-Nov-2022
PMCID:PMC9702281
doi:10.1007/s13659-022-00363-y
PMID:36437391
Large differences in leaf cuticle conductance and its temperature response among 24 tropical tree species from across a rainfall gradient Slot M, Nardwattanawong T, Hernández GG, Bueno A, Riederer M, Winter K New Phytol 06-Aug-2021
PMCID:PMC9290923
doi:10.1111/nph.17626
PMID:34270792
Climate change may induce connectivity loss and mountaintop extinction in Central American forests Baumbach L, Warren DL, Yousefpour R, Hanewinkel M Commun Biol 15-Jul-2021
PMCID:PMC8282624
doi:10.1038/s42003-021-02359-9
PMID:34267317
Mega-dams and extreme rainfall: Disentangling the drivers of extensive impacts of a large flooding event on Amazon Forests Oliveira WL, Medeiros MB, Moser P, Simon MF PLoS One 12-Feb-2021
PMCID:PMC7880702
doi:10.1371/journal.pone.0245991
PMID:33578410
Trees as net sinks for methane (CH4) and nitrous oxide (N2O) in the lowland tropical rain forest on volcanic Réunion Island Machacova K, Borak L, Agyei T, Schindler T, Soosaar K, Mander Ü, Ah‐Peng C New Phytol 18-Nov-2020
PMCID:PMC7894294
doi:10.1111/nph.17002
PMID:33058184
Emerging paradigms of viral diseases and paramount role of natural resources as antiviral agents Sagaya Jansi R, Khusro A, Agastian P, Alfarhan A, Al-Dhabi NA, Arasu MV, Rajagopal R, Barcelo D, Al-Tamimi A Sci Total Environ 07-Nov-2020
PMCID:PMC7833357
doi:10.1016/j.scitotenv.2020.143539
PMID:33234268
S N/A Saunders Comprehensive Veterinary Dictionary 16-Oct-2020
PMCID:PMC9771675
doi:10.1016/B978-0-7020-7463-9.50027-6
Dataset of permanent plots of trees with dbh >10cm in Mashpi rainforest biodiversity reserve, a remnant of the Chocó forest in Northern Ecuador Toasa G, Morochz C, Oleas NH Data Brief 12-Jun-2020
PMCID:PMC7327807
doi:10.1016/j.dib.2020.105845
PMID:32637474
Gentiana lutea Extract Modulates Ceramide Synthesis in Primary and Psoriasis-Like Keratinocytes Gendrisch F, Nováčková A, Sochorová M, Haarhaus B, Vávrová K, Schempp CM, Wölfle U Molecules 16-Apr-2020
PMCID:PMC7221824
doi:10.3390/molecules25081832
PMID:32316273
Janzen-Connell effects shape gene flow patterns and realized fitness in the tropical dioecious tree Spondias purpurea (ANACARDIACEAE) Cristóbal-Pérez EJ, Fuchs EJ, Olivares-Pinto U, Quesada M Sci Rep 12-Mar-2020
PMCID:PMC7067871
doi:10.1038/s41598-020-61394-4
PMID:32165645
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
How does bark contribution to postural control change during tree ontogeny? A study of six Amazonian tree species Lehnebach R, Alméras T, Clair B J Exp Bot 13-Feb-2020
PMCID:PMC7210755
doi:10.1093/jxb/eraa070
PMID:32052058

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 / Indolonaphthyridine alkaloids
6H-Indolo[3,2,1-de][1,5]naphthyridin-6-one, 5-hydroxy- 135735549 Click to see C1=CC=C2C(=C1)C3=C4N2C(=O)C(=CC4=NC=C3)O 236.22 unknown https://doi.org/10.1016/S0031-9422(00)86773-4
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Quassinoids
[(1S,4R,5R,6R,7S,8R,11R,13S,17S,18S,19R)-4,5,17-Trihydroxy-6,14,18-trimethyl-9,16-dioxo-3,10-dioxapentacyclo[9.8.0.01,7.04,19.013,18]nonadec-14-en-8-yl] 2-hydroxy-2-methylbutanoate 12310232 Click to see 494.50 unknown https://doi.org/10.1016/0378-8741(88)90126-2
[(1S,4R,5R,6R,7S,8R,11R,17S,18S)-4,5,17-trihydroxy-6,14,18-trimethyl-9,16-dioxo-3,10-dioxapentacyclo[9.8.0.01,7.04,19.013,18]nonadec-14-en-8-yl] 2-methylbutanoate 118701210 Click to see 478.50 unknown https://doi.org/10.1016/0378-8741(88)90126-2
2'-Acetylglaucarubinone 303910 Click to see 536.60 unknown https://doi.org/10.1016/0378-8741(88)90126-2
Ailanthinone 428489 Click to see CCC(C)C(=O)OC1C2C(C(C3(C4C2(CO3)C(CC5C4(C(C(=O)C=C5C)O)C)OC1=O)O)O)C 478.50 unknown https://doi.org/10.1016/0378-8741(88)90126-2
Glaucarubinone 441796 Click to see CCC(C)(C(=O)OC1C2C(C(C3(C4C2(CO3)C(CC5C4(C(C(=O)C=C5C)O)C)OC1=O)O)O)C)O 494.50 unknown https://doi.org/10.1016/0378-8741(88)90126-2
Holacanthone 158475 Click to see 436.50 unknown https://doi.org/10.1016/0378-8741(88)90126-2
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(13alpha,14beta,17alpha)-Lanosta-7,24-dien-3-one 163012852 Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC3C2=CCC4C3(CCC(=O)C4(C)C)C)C)C 424.70 unknown https://doi.org/10.1021/NP060214F
(2S)-6-methyl-2-[(5S,9R,10R,13S,14S,17S)-4,4,10,13,14-pentamethyl-3-oxo-1,2,5,6,9,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-17-yl]hept-5-enal 162931931 Click to see 438.70 unknown https://doi.org/10.1016/S0031-9422(00)89027-5
(5R,10S,13S,14S,17S)-17-[(2R,4S)-4-[(2S)-3,3-dimethyloxiran-2-yl]-4-hydroxybutan-2-yl]-4,4,10,13,14-pentamethyl-1,2,5,6,7,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-3-one 162890208 Click to see 456.70 unknown https://doi.org/10.1021/NP060214F
(5R,9S,10R,13S,14S,17S)-17-[(2R,4R)-4-[(2S)-3,3-dimethyloxiran-2-yl]-4-hydroxybutan-2-yl]-4,4,10,13,14-pentamethyl-1,2,5,6,9,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-3-one 162983975 Click to see 456.70 unknown https://doi.org/10.1021/NP060214F
(5S,9R,10R,13S,14S,17S)-4,4,10,13,14-pentamethyl-17-[(2S)-6-methylhept-5-en-2-yl]-1,2,5,6,9,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-3-one 124902223 Click to see 424.70 unknown https://doi.org/10.1016/S0031-9422(00)89027-5
17-[4-(3,3-Dimethyloxiran-2-yl)-4-hydroxybutan-2-yl]-4,4,10,13,14-pentamethyl-1,2,5,6,7,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-3-one 162890207 Click to see CC(CC(C1C(O1)(C)C)O)C2CCC3(C2(CCC4=C3CCC5C4(CCC(=O)C5(C)C)C)C)C 456.70 unknown https://doi.org/10.1021/NP060214F
17-[4-(3,3-Dimethyloxiran-2-yl)-4-hydroxybutan-2-yl]-4,4,10,13,14-pentamethyl-1,2,5,6,9,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-3-one 3691820 Click to see 456.70 unknown https://doi.org/10.1021/NP060214F
6-Methyl-2-(4,4,10,13,14-pentamethyl-3-oxo-1,2,5,6,9,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-17-yl)hept-5-enal 162931929 Click to see 438.70 unknown https://doi.org/10.1016/S0031-9422(00)89027-5
Butyrospermone 4205159 Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC3C2=CCC4C3(CCC(=O)C4(C)C)C)C)C 424.70 unknown https://doi.org/10.1021/NP060214F
https://doi.org/10.1016/S0031-9422(00)89027-5
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids / Limonoids
(1S,2R,5R,11R,12R,15R,16R)-16-[(2S)-2-[(2R)-3,3-dimethyloxiran-2-yl]-2,3-dihydrofuran-4-yl]-2,6,6,11-tetramethyl-7-oxapentacyclo[13.3.1.01,15.02,12.05,11]nonadec-9-ene-3,8-dione 162902038 Click to see CC1(C2CC(=O)C3(C(C2(C=CC(=O)O1)C)CCC45C3(C4)CCC5C6=COC(C6)C7C(O7)(C)C)C)C 480.60 unknown https://doi.org/10.1021/NP060214F
[(1R,2R,3S,8R,10R,11R,15R,16S)-3-acetyloxy-15-[(2S)-2-[(2R)-3,3-dimethyloxiran-2-yl]-5-oxo-2H-furan-4-yl]-2,7,7,11,16-pentamethyl-5-oxo-6-oxatetracyclo[9.7.0.02,8.012,16]octadec-12-en-10-yl] acetate 163034084 Click to see 598.70 unknown https://doi.org/10.1021/NP060214F
[(1S,2R,3R,5R,10S,11R,12R,15R,16R)-10-acetyloxy-16-[(2S)-2-[(2R)-3,3-dimethyloxiran-2-yl]-5-oxo-2H-furan-4-yl]-2,6,6,11-tetramethyl-8-oxo-7-oxapentacyclo[13.3.1.01,15.02,12.05,11]nonadecan-3-yl] acetate 163073289 Click to see 598.70 unknown https://doi.org/10.1021/NP060214F
[(1S,2R,3R,5R,11R,12R,13R,15S,16R)-3-acetyloxy-16-[(2S)-2-[(2S)-3,3-dimethyloxiran-2-yl]-5-oxo-2H-furan-4-yl]-2,6,6,11-tetramethyl-8-oxo-7-oxapentacyclo[13.3.1.01,15.02,12.05,11]nonadec-9-en-13-yl] (E)-2-methylbut-2-enoate 162859985 Click to see 636.80 unknown https://doi.org/10.1021/NP060214F
[10-acetyloxy-16-[2-(3,3-dimethyloxiran-2-yl)-5-oxo-2H-furan-4-yl]-2,6,6,11-tetramethyl-8-oxo-7-oxapentacyclo[13.3.1.01,15.02,12.05,11]nonadecan-3-yl] acetate 73238336 Click to see 598.70 unknown https://doi.org/10.1021/NP060214F
[3-acetyloxy-15-[2-(3,3-dimethyloxiran-2-yl)-5-oxo-2H-furan-4-yl]-2,7,7,11,16-pentamethyl-5-oxo-6-oxatetracyclo[9.7.0.02,8.012,16]octadec-12-en-10-yl] acetate 73238339 Click to see 598.70 unknown https://doi.org/10.1021/NP060214F
[3-acetyloxy-16-[2-(3,3-dimethyloxiran-2-yl)-5-oxo-2H-furan-4-yl]-2,6,6,11-tetramethyl-8-oxo-7-oxapentacyclo[13.3.1.01,15.02,12.05,11]nonadec-9-en-13-yl] 2-methylbut-2-enoate 73238338 Click to see 636.80 unknown https://doi.org/10.1021/NP060214F
16-[2-(3,3-Dimethyloxiran-2-yl)-2,3-dihydrofuran-4-yl]-2,6,6,11-tetramethyl-7-oxapentacyclo[13.3.1.01,15.02,12.05,11]nonadec-9-ene-3,8-dione 73238335 Click to see 480.60 unknown https://doi.org/10.1021/NP060214F
> Organic acids and derivatives / Carboxylic acids and derivatives / Carboxylic acid derivatives / Alpha,beta-unsaturated carboxylic esters / Enoate esters
(1S,2R,5R,11R,12R,15R)-2,6,6,11-tetramethyl-7-oxapentacyclo[13.3.1.01,15.02,12.05,11]nonadec-9-ene-3,8-dione 16086564 Click to see 342.50 unknown https://doi.org/10.1021/NP060214F
2,6,6,11-Tetramethyl-7-oxapentacyclo[13.3.1.01,15.02,12.05,11]nonadec-9-ene-3,8-dione 73238340 Click to see 342.50 unknown https://doi.org/10.1021/NP060214F

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