Myroxylon balsamum - Unknown
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Internal ID UUID643fdeac1b3a7226105104
Scientific name Myroxylon balsamum
Authority Harms
First published in Notizbl. Königl. Bot. Gart. Berlin5: 94 (1908)

Description Top

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It is also valued for its medicinal properties, as the resin is used in traditional medicine to treat various ailments. The tree is native to tropical forests in Mexico, Peru, and Brazil, and can reach heights of up to 45 meters. It has two varieties, known as Tolu balsam tree and Peru balsam tree, which produce different types of resin. The tree has a round crown and yellowish bark with a strong odor. Its leaves are pubescent and have glandular oil dots. The tree blooms after 5 years and produces white flowers with 10 stamens. The fruit is a flat, winged pod that drops in the months of November to January. The wood of M. balsamum is used for various purposes, including flooring, furniture, and construction, and is resistant to fungal decay. The tree is also planted for balsam production in other regions such as West Africa, India, and Sri Lanka. Its resin is used in the production of cosmetics and medicines, and the tree is also valued for its medicinal properties in traditional medicine.

Synonyms Top

Scientific name Authority First published in
Myroxylon balsamum var. balsamum (L.) Harms
Myroxylon balsamum var. pereirae Harms Notizbl. Königl. Bot. Gart. Berlin4: 95 (1908)
Toluifera balsamum L. Sp. Pl.: 384 (1753)
Myroxylon pereirae Klotzsch Bonplandia (Hannover)5: 274 (1857)
Toluifera balsamum var. pereirae (Royle) Baill. Traité Bot. Méd. Phan.: 676 (1883)
Myrospermum pereirae Royle Man. Mat. Med., ed. 2: 414 (1853)
Toluifera pereirae (Royle) Baill. Hist. Pl.2: 383 (1870)
Myroxylon pereirae Royle
Myroxylon balsamum var. punctatum Harms Notizbl. Königl. Bot. Gart. Berlin5: 97 (1908)
Myroxylon punctatum Klotzsch F.G.Hayne, Getreue Darstell. Gew.14: t. 12 (1843)
Myroxylon hanburyanum Klotzsch Bonplandia (Hannover)5: 275 (1857)
Myroxylon sonsouatense (Peeira ex Oerst.) Flueck. & D.Hanb. Pharmacogr.: 179 (1874)
Myrospermum punctatum (Klotzsch) Walp. Repert. Bot. Syst.1: 805 (1843)
Toluifera punctata (Klotzsch) Baill. Hist. Pl.2: 383 (1870)
Myrospermum sonsonatense Pereira ex Oersted Medicinal Plantz il. No. 83 (1880).
Toluifera balsamum var. punctata (Klotzsch) Baill. Traité Bot. Méd. Phan.: 677 (1883)
Myrospermum balsamiferum Ruiz & Pav. Anales Inst. Bot. Cavanilles14: 717 (1956)

Common names Top

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Language Common/alternative name
English balsam of tolu
Spanish árbol de bálsamo
Spanish bálsamo
Spanish bálsamo de tolú
Arabic طاليسفر
Arabic بسان العصافير
Catalan bàlsam del perú
Finnish rohtobalsami
French baumier du pérou
Japanese マメ科
Japanese ペルーバルサム
Japanese トルーバルサムノキ
Polish woniawiec balsamowy
Portuguese bálsamo-de-tolu
Chinese 吐鲁香树
Chinese 香脂豆
Chinese 秘鲁胶树
Chinese 吐鲁胶豆

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

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

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000212074
USDA Plants MYBA3
Tropicos 13003351
INPN 447574
KEW urn:lsid:ipni.org:names:166483-2
The Plant List ild-7152
Open Tree Of Life 354903
NCBI Taxonomy 53906
IUCN Red List 62026528
IPNI 509446-1
iNaturalist 209950
GBIF 5357190
EPPO MYXBA
EOL 702850
USDA GRIN 24873
Wikipedia Myroxylon_balsamum
CMAUP NPO6528

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
Effect of intraspecific seed trait variation on the germination of eight tropical dry forest species Villa-Rivera N, Castellanos-Barliza J, Mondragón-Botero A, Barranco-Pérez W Naturwissenschaften 22-Mar-2024
PMCID:PMC10959815
doi:10.1007/s00114-024-01898-5
PMID:38517488
Use of Essential Oils to Counteract the Phenomena of Antimicrobial Resistance in Livestock Species Lupia C, Castagna F, Bava R, Naturale MD, Zicarelli L, Marrelli M, Statti G, Tilocca B, Roncada P, Britti D, Palma E Antibiotics (Basel) 07-Feb-2024
PMCID:PMC10885947
doi:10.3390/antibiotics13020163
PMID:38391549
Toxicity and Repellency Efficacy of Benzyl Alcohol and Benzyl Benzoate as Eco-Friendly Choices to Control the Red Flour Beetle Tribolium castaneum (Herbst. 1797) Aboelhadid SM, Ibrahium SM, Abdel-Tawab H, Hassan AO, Al-Quraishy S, Saleh FE, Abdel-Baki AA Molecules 23-Nov-2023
PMCID:PMC10707955
doi:10.3390/molecules28237731
PMID:38067462
Safety profile of herbal medicines submitted for marketing authorization in Tanzania: a cross-sectional retrospective study Mssusa AK, Holst L, Kagashe G, Maregesi S J Pharm Policy Pract 20-Nov-2023
PMCID:PMC10658996
doi:10.1186/s40545-023-00661-x
PMID:37986124
In vitro and in silico prediction of antibacterial interaction between essential oils via graph embedding approach Yabuuchi H, Hayashi K, Shigemoto A, Fujiwara M, Nomura Y, Nakashima M, Ogusu T, Mori M, Tokumoto SI, Miyai K Sci Rep 02-Nov-2023
PMCID:PMC10622510
doi:10.1038/s41598-023-46377-5
PMID:37919469
PeruNPDB: the Peruvian Natural Products Database for in silico drug screening Barazorda-Ccahuana HL, Ranilla LG, Candia-Puma MA, Cárcamo-Rodriguez EG, Centeno-Lopez AE, Davila-Del-Carpio G, Medina-Franco JL, Chávez-Fumagalli MA Sci Rep 10-May-2023
PMCID:PMC10170056
doi:10.1038/s41598-023-34729-0
PMID:37165197
Endophytic species of Induratia from coffee and carqueja plants from Brazil and its potential for the biological control of toxicogenic fungi on coffee beans by means of antimicrobial volatiles Gomes AA, Paes SA, Ferreira AP, Pinho DB, de Lourdes Cardeal Z, Menezes HC, Cardoso PG, Pereira OL Braz J Microbiol 04-Jan-2023
PMCID:PMC9944607
doi:10.1007/s42770-022-00887-y
PMID:36598751
Active Compounds with Medicinal Potential Found in Maxillariinae Benth. (Orchidaceae Juss.) Representatives—A Review Lipińska MM, Haliński ŁP, Gołębiowski M, Kowalkowska AK Int J Mol Sci 01-Jan-2023
PMCID:PMC9821772
doi:10.3390/ijms24010739
PMID:36614181
Medicinal Plants from Latin America with Wound Healing Activity: Ethnomedicine, Phytochemistry, Preclinical and Clinical Studies—A Review Salazar-Gómez A, Alonso-Castro AJ Pharmaceuticals (Basel) 31-Aug-2022
PMCID:PMC9505834
doi:10.3390/ph15091095
PMID:36145316
Evaluation of the anti-SARS-CoV-2 properties of essential oils and aromatic extracts Strub DJ, Talma M, Strub M, Rut W, Zmudzinski M, Brud W, Neyts J, Vangeel L, Zhang L, Sun X, Lv Z, Nayak D, Olsen SK, Hilgenfeld R, Jochmans D, Drąg M Sci Rep 20-Aug-2022
PMCID:PMC9392441
doi:10.1038/s41598-022-18676-w
PMID:35987981
A whiff of the future: functions of phenylalanine‐derived aroma compounds and advances in their industrial production Skaliter O, Livneh Y, Agron S, Shafir S, Vainstein A Plant Biotechnol J 30-Jun-2022
PMCID:PMC9398379
doi:10.1111/pbi.13863
PMID:35638340
Poorly Investigated Ecuadorian Medicinal Plants Armijos C, Ramírez J, Vidari G Plants (Basel) 16-Jun-2022
PMCID:PMC9229133
doi:10.3390/plants11121590
PMID:35736741
Morpho-agronomic evaluation of native maize races associated with Mexican tropical climate agroforestry systems Hernández-Salinas G, Toledano-Toledano F, Pérez-García M, Sánchez-Valera OV, Ramírez-Rivera ED, Serna-Lagunes R, Rocandio-Rodríguez M, Purroy-Vásquez R, Fernández-López CL, López-Morales F, Garduño-Espinosa J PLoS One 14-Jun-2022
PMCID:PMC9197038
doi:10.1371/journal.pone.0269896
PMID:35700205
No Reduction in Yield of Young Robusta Coffee When Grown under Shade Trees in Ecuadorian Amazonia Piato K, Subía C, Lefort F, Pico J, Calderón D, Norgrove L Life (Basel) 29-May-2022
PMCID:PMC9224700
doi:10.3390/life12060807
PMID:35743838
Standard Patch Test Results and Clinical Relevance: A Cross-Sectional Study of 10-year Retrospective Experience Bilgic A, Bozca BC, Subası GY, Dicle Ö, Uzun S, Yılmaz E, Alpsoy E, Akman-Karakas A Indian J Dermatol 01-May-2022
PMCID:PMC9644757
doi:10.4103/ijd.ijd_965_21
PMID:36386088

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 / Benzoic acid esters
Benzyl Benzoate 2345 Click to see C1=CC=C(C=C1)COC(=O)C2=CC=CC=C2 212.24 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
cis-Nerolidol 5320128 Click to see CC(=CCCC(=CCCC(C)(C=C)O)C)C 222.37 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(1aS,4aS,7aS,7bR)-1,1,7-trimethyl-4-methylidene-2,3,4a,5,6,7,7a,7b-octahydro-1aH-cyclopropa[e]azulene 91746456 Click to see CC1CCC2C1C3C(C3(C)C)CCC2=C 204.35 unknown https://doi.org/10.1002/HLCA.19870700711
Alloaromadendren 91746537 Click to see CC1CCC2C1C3C(C3(C)C)CCC2=C 204.35 unknown https://doi.org/10.1002/HLCA.19870700711
Viridiflorene 10910653 Click to see CC1CCC2=C(CCC3C(C12)C3(C)C)C 204.35 unknown https://doi.org/10.1002/HLCA.19870700711
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Eudesmanolides, secoeudesmanolides, and derivatives
Encelin 72540 Click to see CC12CC3C(CC1C(=C)C(=O)C=C2)C(=C)C(=O)O3 244.28 unknown via CMAUP database
Farinosin 442240 Click to see CC12CC3C(CC1C(=C)C(=O)C=C2)C(C(=O)O3)(C)O 262.30 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
5-Acetyl-2-methoxybenzaldehyde 288758 Click to see CC(=O)C1=CC(=C(C=C1)OC)C=O 178.18 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / 2,2-dimethyl-1-benzopyrans
6-Vinyl-7-methoxy-2,2-dimethylchromene 188454 Click to see CC1(C=CC2=CC(=C(C=C2O1)OC)C=C)C 216.27 unknown via CMAUP database
Encecalin 114703 Click to see CC(=O)C1=C(C=C2C(=C1)C=CC(O2)(C)C)OC 232.27 unknown via CMAUP database
Eupatoriochromene 100768 Click to see CC(=O)C1=C(C=C2C(=C1)C=CC(O2)(C)C)O 218.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
2-(2,4-Dihydroxyphenyl)-5,6-dimethoxybenzofuran 44260110 Click to see COC1=C(C=C2C(=C1)C=C(O2)C3=C(C=C(C=C3)O)O)OC 286.28 unknown https://doi.org/10.1016/S0031-9422(00)89391-7
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acid esters
Benzyl alcohol, cinnamate 15558051 Click to see C1=CC=C(C=C1)COC(=O)C=CC2=CC=CC=C2 238.28 unknown via CMAUP database
Benzyl cinnamate 5273469 Click to see C1=CC=C(C=C1)COC(=O)C=CC2=CC=CC=C2 238.28 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acids
Cinnamic acid 444539 Click to see C1=CC=C(C=C1)C=CC(=O)O 148.16 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamyl alcohols
1-Dideuterio-3-phenylprop-2-en-1-ol 10534709 Click to see C1=CC=C(C=C1)C=CCO 136.19 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Furanoisoflavonoids / Pterocarpans
Medicarpin 336327 Click to see COC1=CC2=C(C=C1)C3COC4=C(C3O2)C=CC(=C4)O 270.28 unknown https://doi.org/10.1016/S0031-9422(00)89391-7
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids
(3S)-Sativanone 46881075 Click to see COC1=CC=C(C=C1)C2COC3=C(C2=O)C=CC(=C3)O 270.28 unknown https://doi.org/10.1016/S0031-9422(00)89391-7
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 3-hydroxy,4-methoxyisoflavonoids
(3R)-7-hydroxy-3-(3-hydroxy-4-methoxyphenyl)-2,3-dihydrochromen-4-one 163193954 Click to see COC1=C(C=C(C=C1)C2COC3=C(C2=O)C=CC(=C3)O)O 286.28 unknown https://doi.org/10.1016/S0031-9422(00)89391-7
3'-Hydroxy-8-O-methylretusin 44257262 Click to see COC1=C(C=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3OC)O)O 314.29 unknown https://doi.org/10.1016/S0031-9422(00)89391-7
Calycosin 5280448 Click to see COC1=C(C=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)O)O 284.26 unknown https://doi.org/10.1016/S0031-9422(00)89391-7
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 4-O-methylisoflavones
Formononetin 5280378 Click to see COC1=CC=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)O 268.26 unknown https://doi.org/10.1016/S0031-9422(00)89391-7
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 7-O-methylated isoflavonoids / 7-O-methylisoflavones
7,3',4'-Trimethoxyisoflavone 628528 Click to see COC1=CC2=C(C=C1)C(=O)C(=CO2)C3=CC(=C(C=C3)OC)OC 312.30 unknown https://doi.org/10.1016/0031-9422(79)80020-5

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