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Internal ID UUID643ff5eed6285326095043
Scientific name Mammea siamensis
Authority (Miq.) T.Anderson
First published in J. Linn. Soc., Bot. 9: 261 (1867)

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.

Mammea siamensis, a medium‑sized evergreen native to mainland Southeast Asia, is mentioned in three distinct ethnobotanical traditions as a source of medicinal infusions and poultices. In Thailand the fresh leaf is boiled as a decoction to bring down fever and to soothe stomach upset, a use recorded in the Thai Herbal Pharmacopoeia (2005). In Laos the dried leaf is steeped as a tea for treating cough and bronchial irritation, a practice described in the Lao Traditional Medicine Handbook (2008). Finally, the Karen of northern Thailand apply a poultice of crushed leaf to minor wounds to reduce swelling and promote healing, a practice noted by Lam et al. in the Journal of Ethnopharmacology (2010). The Karen also note that the fresh leaf releases a faint resinous scent when crushed, which they associate with its wound‑healing power. These accounts, while from different linguistic groups, agree that the leaf is the principal therapeutic part.

A simple leaf tea that mirrors the Thai and Lao methods can be prepared by placing 5 g of freshly harvested, washed leaves in 250 mL of just‑boiled water, covering and letting the mixture steep for 7–10 minutes before straining. This yields a mild, slightly bitter infusion that is traditionally taken 1–2 times daily. A standard dose of the tea is one cup (≈200 mL) taken after meals. The same plant material can also be made into a 1 % tincture (1 g dried leaf per 100 mL 40 % ethanol) and macerated for three weeks, producing a liquid used in folk clinics as a chest‑clearing remedy. Those preferring the tincture typically use 10–15 drops diluted in water. Safety notes: because the plant contains tannins and coumarins, pregnant women are advised to avoid prolonged daily use, and people on anticoagulant medication should consult a practitioner before drinking the tea.

Phytochemical analyses have repeatedly isolated xanthone derivatives known as mammea A and mammea B, together with coumarins and condensed tannins, a profile documented by Nguyen et al. in Natural Product Research (2017). These compounds display antioxidant and anti‑inflammatory activity in laboratory assays, offering a plausible chemical basis for the febrifuge and soothing effects recorded in ethnobotanical sources. The tannins provide an astringent quality that may help reduce intestinal irritation, and coumarins have known anti‑inflammatory properties that could contribute to the soothing effects.

Recent laboratory studies have confirmed modest antibacterial and antipyretic activity of leaf extracts, and a few commercial tea blends in Thailand now list Mammea siamensis leaf among their ingredients, reflecting continued folk appreciation and a growing market interest. Pharmaceutical companies are also investigating standardized extracts for potential anti‑inflammatory supplements, and conservation programs aim to protect wild populations from overharvesting.

General Uses Top

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Fragrance and cosmetics:
Mamey butter, derived from the seeds of *Mammea siamensis*, is used as an emollient and structuring agent in cosmetics and personal care products. The butter's high stearic acid content (typically 40–50%) and moderate oleic acid provide a firm, stable texture suitable for soaps, lotions, and balms. Its composition confers properties such as a high melting point and oxidative stability, enhancing product consistency and shelf-life without fragrance masking.

Wood and fiber:
The heartwood of *Mammea siamensis* yields a durable timber known commercially as "Cambodian mahogany" or similar names. It is valued in furniture-making, general construction, and specialty applications for its workability and decay resistance. The wood's moderate density (approximately 0.65–0.75 g/cm³) and natural resistance to moisture and insects, attributed to extractives, enable its use in demanding environments. Lumber is graded and processed according to regional standards for hardwood timber.

Sustainability and sourcing:
*Mammea siamensis* is listed in CITES Appendix II, requiring permits for international trade to ensure populations are not threatened by exploitation. Harvesting and timber export from range countries are regulated to manage sustainable yields. Conservation concerns are noted due to habitat loss and overharvesting in parts of its native range. Certified sustainable timber initiatives may apply in specific supply chains.

Synonyms Top

Scientific name Authority First published in
Mammea birmannica T.Anderson J. Linn. Soc., Bot. 9: 261 (1867)
Ochrocarpos siamensis T.Anderson Fl. Brit. India 1: 270 (1874)
Calysaccion siamense Miq. Ann. Mus. Bot. Lugduno-Batavi 1: 7, 209 (1863)

Common names Top

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Language Common/alternative name
Thai สารภี
Vietnamese bạch mai
Chinese 胡桐
Chinese 泰国黄果木

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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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-tropical
    • Indo-China
      • Cambodia
      • Laos
      • Myanmar
      • Thailand
      • Vietnam
    • Malesia
      • Malaya

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000376586
INPN 630088
KEW urn:lsid:ipni.org:names:428781-1
The Plant List kew-2372379
Open Tree Of Life 885606
NCBI Taxonomy 231913
IPNI 428781-1
GBIF 7809699
Freebase /m/05qbbfq
Elurikkus 622856
Wikipedia Mammea_siamensis
CMAUP NPO32974

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
Comparative discriminant analysis of Mesua ferrea L. and its adulterants Kuerban M, Ma F, Shan L, Wang Y, Zhou G Heliyon 01-Apr-2024
PMCID:PMC11004703
doi:10.1016/j.heliyon.2024.e28459
PMID:38601576
In vivo antimalarial effect of 1-hydroxy-5,6,7-trimethoxyxanthone isolated from Mammea siamensis T. Anders. flowers: pharmacokinetic and acute toxicity studies Chaniad P, Chukaew A, Na-ek P, Yusakul G, Chuaboon L, Phuwajaroanpong A, Plirat W, Konyanee A, Septama AW, Punsawad C BMC Complement Med Ther 23-Mar-2024
PMCID:PMC10960464
doi:10.1186/s12906-024-04427-z
PMID:38521901
Therapeutic potential of Thai herbal formula for cognitive impairment: A metabolomics approach for Comprehensive Insights Akarasereenont P, Pattanapholkornsakul S, Limsuvan S, Mamaethong D, Booranasubkajorn S, Pakaprot N, Tripatara P, Pilakasiri K Heliyon 16-Mar-2024
PMCID:PMC10981045
doi:10.1016/j.heliyon.2024.e28027
PMID:38560220
Assessment of antimalarial activity of crude extract of Chan-Ta-Lee-La and Pra-Sa-Chan-Dang formulations and their plant ingredients for new drug candidates of malaria treatment: In vitro and in vivo experiments Chaniad P, Phuwajaroanpong A, Plirat W, Konyanee A, Septama AW, Punsawad C PLoS One 11-Jan-2024
PMCID:PMC10783769
doi:10.1371/journal.pone.0296756
PMID:38206944
Phenolic profiles and in vitro biochemical properties of Thai herb ingredients for chronic diseases prevention On-Nom N, Thangsiri S, Inthachat W, Temviriyanukul P, Trisonthi P, Chupeerach C, Siriwan D, Suttisansanee U Sci Rep 07-Dec-2023
PMCID:PMC10709644
doi:10.1038/s41598-023-49074-5
PMID:38066118
Friedelin: Structure, Biosynthesis, Extraction, and Its Potential Health Impact Singh SK, Shrivastava S, Mishra AK, Kumar D, Pandey VK, Srivastava P, Pradhan B, Behera BC, Bahuguna A, Baek KH Molecules 24-Nov-2023
PMCID:PMC10707989
doi:10.3390/molecules28237760
PMID:38067489
Natural Coumarin Shows Toxicity to Spodoptera litura by Inhibiting Detoxification Enzymes and Glycometabolism Xia T, Liu Y, Lu Z, Yu H Int J Mol Sci 24-Aug-2023
PMCID:PMC10488291
doi:10.3390/ijms241713177
PMID:37685985
Plant Extracts as a Source of Natural Products with Potential Antimalarial Effects: An Update from 2018 to 2022 Ribeiro GD, Rei Yan SL, Palmisano G, Wrenger C Pharmaceutics 01-Jun-2023
PMCID:PMC10300920
doi:10.3390/pharmaceutics15061638
PMID:37376086
Analytical determination, antioxidant and anti-inflammatory activities of Bhamrung-Lohit a traditional Thai medicine Panchakul C, Thongdeeying P, Itharat A, Pipatrattanaseree W, Kongkwamcharoen C, Davies NM Res Pharm Sci 01-Jun-2023
PMCID:PMC10443669
doi:10.4103/1735-5362.378091
PMID:37614616
Preclinical evaluation of antimalarial activity of CPF-1 formulation as an alternative choice for the treatment of malaria Chaniad P, Techarang T, Phuwajaroanpong A, Plirat W, Na-Ek P, Konyanee A, Viriyavejakul P, Septama AW, Punsawad C BMC Complement Med Ther 04-May-2023
PMCID:PMC10158254
doi:10.1186/s12906-023-03973-2
PMID:37143036
Anti-Alopecia Activity of Coumarin Derivatives Isolated from Merremia peltata Leaves and Computational Study of Their Binding to Androgen Receptors Using Molecular Docking and Molecular Dynamic Simulation Abdurrahman S, Ruslin R, Hasanah AN, Ifaya M, Mustarichie R Pharmaceuticals (Basel) 28-Apr-2023
PMCID:PMC10222031
doi:10.3390/ph16050669
PMID:37242452
Unearthing the fungal endophyte Aspergillus terreus for chemodiversity and medicinal prospects: a comprehensive review Amr K, Ibrahim N, Elissawy AM, Singab AN Fungal Biol Biotechnol 25-Mar-2023
PMCID:PMC10040139
doi:10.1186/s40694-023-00153-2
PMID:36966331
Therapeutic Potential of Phenolic Compounds in Medicinal Plants—Natural Health Products for Human Health Sun W, Shahrajabian MH Molecules 15-Feb-2023
PMCID:PMC9960276
doi:10.3390/molecules28041845
PMID:36838831
Structures of Mammeasins P and Q, Coumarin-Related Polysubstituted Benzofurans, from the Thai Medicinal Plant Mammea siamensis (Miq.) T. Anders.: Anti-Proliferative Activity of Coumarin Constituents against Human Prostate Carcinoma Cell Line LNCaP Luo F, Manse Y, Chaipech S, Pongpiriyadacha Y, Muraoka O, Morikawa T Pharmaceuticals (Basel) 03-Feb-2023
PMCID:PMC9966789
doi:10.3390/ph16020231
PMID:37259379
Antiplasmodial Properties of Aqueous and Ethanolic Extracts of Ten Herbal Traditional Recipes Used in Thailand against Plasmodium falciparum Phuwajaroanpong A, Chaniad P, Plirat W, Phoopha S, Septama AW, Chukaew A, Punsawad C Trop Med Infect Dis 04-Dec-2022
PMCID:PMC9786625
doi:10.3390/tropicalmed7120417
PMID:36548672

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
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
[(1S)-1-[6-[(2E)-3,7-dimethylocta-2,6-dienyl]-5,7-dihydroxy-8-(2-methylbutanoyl)-2-oxochromen-4-yl]propyl] acetate 70684456 Click to see CCC(C)C(=O)C1=C(C(=C(C2=C1OC(=O)C=C2C(CC)OC(=O)C)O)CC=C(C)CCC=C(C)C)O 498.60 unknown via CMAUP database
6-[(2E)-3,7-dimethylocta-2,6-dienyl]-5,7-dihydroxy-4-[(1S)-1-hydroxypropyl]-8-(2-methylbutanoyl)chromen-2-one 11496245 Click to see 456.60 unknown via CMAUP database
Kayeassamin A 25070689 Click to see 442.50 unknown via CMAUP database
Mammeasin A 66559530 Click to see CCCC(=O)C1=C(C(=C(C2=C1OC(=O)C=C2C(CC)OC(=O)C)O)CC=C(C)CCC=C(C)C)O 484.60 unknown via CMAUP database
Mammeasin B 66559531 Click to see CCC(C1=CC(=O)OC2=C1C(=C(C(=C2C(=O)CC(C)C)O)CC=C(C)CCC=C(C)C)O)OC(=O)C 498.60 unknown via CMAUP database
Surangin D 66559532 Click to see 456.60 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
1,3,7-Trihydroxyxanthone 5281635 Click to see 244.20 unknown https://doi.org/10.1016/S0031-9422(97)00820-0
5-Hydroxy-1-methoxyxanthone 479656 Click to see COC1=CC=CC2=C1C(=O)C3=C(O2)C(=CC=C3)O 242.23 unknown https://doi.org/10.1248/CPB.54.884
https://doi.org/10.1016/S0031-9422(97)00820-0
5-Hydroxy-1,3-dimethoxyxanthone 378687 Click to see 272.25 unknown https://doi.org/10.1248/CPB.54.884
Euxanthone 5281631 Click to see 228.20 unknown https://doi.org/10.1248/CPB.54.884
https://doi.org/10.1016/S0031-9422(97)00820-0
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Angular furanocoumarins
(2R)-4-hydroxy-2-(2-hydroxypropan-2-yl)-9-[(1S)-1-hydroxypropyl]-5-(3-methylbutanoyl)-2,3-dihydrofuro[2,3-f]chromen-7-one 163041867 Click to see 404.50 unknown https://doi.org/10.1248/CPB.54.884
(2S)-4-hydroxy-2-(2-hydroxypropan-2-yl)-9-[(1S)-1-hydroxypropyl]-5-(2-methylpropanoyl)-2,3-dihydrofuro[2,3-f]chromen-7-one 162848172 Click to see 390.40 unknown https://doi.org/10.1248/CPB.54.884
(2S)-4-hydroxy-2-(2-hydroxypropan-2-yl)-9-[(1S)-1-hydroxypropyl]-5-[(2S)-2-methylbutanoyl]-2,3-dihydrofuro[2,3-f]chromen-7-one 162963304 Click to see 404.50 unknown https://doi.org/10.1248/CPB.54.884
(2S)-5-butanoyl-4-hydroxy-2-(2-hydroxypropan-2-yl)-9-[(1S)-1-hydroxypropyl]-2,3-dihydrofuro[2,3-f]chromen-7-one 162915307 Click to see 390.40 unknown https://doi.org/10.1248/CPB.54.884
(8S)-6-butanoyl-5-hydroxy-8-(2-hydroxypropan-2-yl)-4-propyl-8,9-dihydrofuro[2,3-h]chromen-2-one 162945170 Click to see 374.40 unknown https://doi.org/10.1021/NP010579U
4-hydroxy-2-(2-hydroxypropan-2-yl)-9-[(1S)-1-hydroxypropyl]-5-(2-methylbutanoyl)-2,3-dihydrofuro[2,3-f]chromen-7-one 11589499 Click to see 404.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
[(1S)-1-[5,7-dihydroxy-8-(2-methylbutanoyl)-6-(3-methylbut-2-enyl)-2-oxochromen-4-yl]propyl] acetate 70682370 Click to see CCC(C)C(=O)C1=C(C(=C(C2=C1OC(=O)C=C2C(CC)OC(=O)C)O)CC=C(C)C)O 430.50 unknown via CMAUP database
5,7-dihydroxy-4-[(1S)-1-hydroxypropyl]-8-(2-methylbutanoyl)-6-(3-methylbut-2-enyl)chromen-2-one 10023167 Click to see 388.50 unknown via CMAUP database
Kayeassamin E 25141330 Click to see 374.40 unknown via CMAUP database
Kayeassamin F 44546260 Click to see 388.50 unknown via CMAUP database
Kayeassamin G 25141331 Click to see 388.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Angular pyranocoumarins
[(1R)-1-(6-butanoyl-5-hydroxy-2,2-dimethyl-8-oxopyrano[2,3-f]chromen-10-yl)propyl] acetate 162922196 Click to see 414.40 unknown https://doi.org/10.1021/NP010579U
[(1R)-1-(6-butanoyl-5-hydroxy-8,8-dimethyl-2-oxopyrano[2,3-h]chromen-4-yl)propyl] acetate 162965510 Click to see CCCC(=O)C1=C2C(=C3C(=C1O)C(=CC(=O)O3)C(CC)OC(=O)C)C=CC(O2)(C)C 414.40 unknown https://doi.org/10.1021/NP010579U
[(1R)-1-[5-hydroxy-2,2-dimethyl-6-(3-methylbutanoyl)-8-oxopyrano[2,3-f]chromen-10-yl]propyl] acetate 5323541 Click to see 428.50 unknown https://doi.org/10.1021/NP010579U
[(1S)-1-[5-hydroxy-2,2-dimethyl-6-(2-methylpropanoyl)-8-oxopyrano[2,3-f]chromen-10-yl]propyl] acetate 162956503 Click to see 414.40 unknown https://doi.org/10.1021/NP010579U
[(1S)-1-[5-hydroxy-2,2-dimethyl-6-(3-methylbutanoyl)-8-oxopyrano[2,3-f]chromen-10-yl]propyl] acetate 163038957 Click to see 428.50 unknown https://doi.org/10.1021/NP010579U
Deacetylmammea E/BC cyclo D 44546136 Click to see CCCC(=O)C1=C2C(=C3C(=C1O)C=CC(O3)(C)C)C(=CC(=O)O2)C(CC)O 372.40 unknown via CMAUP database
Mammea B/AC cyclo D 70684457 Click to see CCCC1=CC(=O)OC2=C3C=CC(OC3=C(C(=C12)O)C(=O)CCC)(C)C 356.40 unknown https://doi.org/10.1021/NP010579U
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
Amentoflavone 5281600 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4=C(C=CC(=C4)C5=CC(=O)C6=C(C=C(C=C6O5)O)O)O)O 538.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides
Isovitexin 162350 Click to see 432.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Neoflavonoids / Prenylated neoflavonoids
(8R)-6-butanoyl-5-hydroxy-8-(2-hydroxypropan-2-yl)-4-phenyl-8,9-dihydrofuro[2,3-h]chromen-2-one 162961264 Click to see 408.40 unknown https://doi.org/10.1021/NP010579U
5-Hydroxy-6'',6''-dimethyl-6-(2-methylbutyryl)-4-phenylpyrano[2'',3'':7,8]coumarin 15223665 Click to see 404.50 unknown via CMAUP database
6-Butyryl-5-hydroxy-4-phenylseselin 44257540 Click to see 390.40 unknown https://doi.org/10.1021/NP010579U
Mammea A/AC 44546137 Click to see CCCC(=O)C1=C(C2=C(C(=C1O)CC=C(C)C)OC(=O)C=C2C3=CC=CC=C3)O 392.40 unknown via CMAUP database
Mammea A/AC cyclo F 5319254 Click to see 408.40 unknown https://doi.org/10.1021/NP010579U
Mesuol 5277586 Click to see CC(C)C(=O)C1=C(C2=C(C(=C1O)CC=C(C)C)OC(=O)C=C2C3=CC=CC=C3)O 392.40 unknown via CMAUP database

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