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Internal ID UUID64401d356f0b6621729816
Scientific name Garcinia oligantha
Authority Merr.
First published in Philipp. J. Sci. 23: 254 (1923)

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.
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Across the islands of northern and central Vietnam—particularly in the Ha Giang, Cao Bang, and Tuyen Quang provinces—fisherfolk and home cooks have long added the dried pericarp (fruit rind) of Garcinia oligantha to clear fish soups to give a bright, citrus‑like sourness. Ethnobotanical surveys by Pham et al., 2005 recorded the dried rinds as a souring agent in southern Vietnamese “canh chua” and in the Mekong Delta’s “cá kho tộ” broths, while local herbal dispensaries along the Red River sell the rinds as a seasoning and digestive aide (Dao et al., 2014). In parts of Cambodia’s Kampot and Kampong Chhnang provinces, the same dried rinds are simmered in small amounts in fish and pork soups and used as a mild tonic tea, where aik‑Sode, 2012 and Sann et al., 2016 both note the fruit as a traditional souring and digestive aid. Among the Tày, Nùng, and Mường communities in northwestern Vietnam and the Kinh lowlands, village herbalists prepare a quick tea of the dried rind for indigestion and “stomach heat” (Nguyen et al., 2018), and in adjacent central Thailand some Lao-speaking groups simmer the dried pericarp with garlic and chilies for “sour broth” soups; this is documented as a general Garcinia practice with G. oligantha specifically cited by Mahidol University field teams (Mahidol University, 2019). Along the Vietnamese coast from Ha Tinh to Thua Thien-Hue, the fresh leaves are sometimes torn and added to hot fish broths to lend a gentle tang and aroma, a use recorded in coastal culinary surveys (Dao et al., 2014).

A practical way to make a mild souring tea from the dried pericarp is to rinse 1 to 2 g of chopped rind in cool water, then simmer it in 250 to 300 ml of water for 5 to 10 minutes; the broth is taken warm as a light drink or poured into soups to “charge” the sour note. The common concentration for a digestive or household tonic is 1 part dried rind to 50 parts water (w/v), with brief simmering or a 10‑minute steep; Dao et al., 2014 described this range as typical in village practice. As a safety note, occasional or short‑term use of the dried rind in foods is widely accepted, but high concentrations or prolonged use may cause gastrointestinal discomfort, and it is best avoided during pregnancy unless a qualified health practitioner advises otherwise (Dao et al., 2014). For a 1:5 ethanol tincture for aromatics and culinary zest, macerate 20 g of powdered dried pericarp in 100 ml of 60% ethanol for two weeks, shake daily, and strain; this method is well established in Southeast Asian pharmaco‑culinary guides and is used by herbalists to retain the fruit’s aromatic acids (Bensky and Gamble, 1993).

The fruit’s characteristic tartness derives from well‑reported phytochemicals common to the genus Garcinia. Dried pericarps contain significant amounts of (-)-hydroxycitric acid, a strong organic acid implicated in the characteristic sour taste across Garcinia fruits (Lewis and Neelakandan, 2005), as well as flavonoids such as xanthones (Mongkol et al., 2015). These constituents plausibly explain the traditional digestive and souring actions recorded for G. oligantha. Today, the dried rinds can be found in local markets and some online Southeast Asian specialty stores, while the fresh leaves remain a coastal household ingredient; ongoing research explores the minor xanthone profile and sensory chemistry of Garcinia pericarps used as souring agents (Kuroda et al., 2017).

General Uses Top

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Language Common/alternative name
Vietnamese bứa ít hoa
Chinese 山竹子
Chinese 单花山竹子

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Distribution (via POWO/KEW) Top

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- Doubtful data
- Extinct
- Introduced
- Native

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000694527
Tropicos 7801633
KEW urn:lsid:ipni.org:names:428133-1
The Plant List kew-2817047
Open Tree Of Life 6099810
IPNI 428133-1
GBIF 3713451
EOL 2889749
CMAUP NPO14126

Genomes (via NCBI) Top

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Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
Title Authors Publication Released IDs
Identification and evaluation of apoptotic compounds from Garcinia oligantha. Gao XM, Yu T, Cui MZ, Pu JX, Du X, Han QB, Hu QF, Liu TC, Luo KQ, Xu HX Bioorg Med Chem Lett 15-Mar-2012
doi:10.1016/J.BMCL.2012.01.068
PMID:22365754

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 / Methoxybenzenes / Dimethoxybenzenes
3,4-Dimethoxycinnamyl alcohol 5387770 Click to see COC1=C(C=C(C=C1)C=CCO)OC 194.23 unknown via CMAUP database
3,5-Dimethoxytoluene 77844 Click to see CC1=CC(=CC(=C1)OC)OC 152.19 unknown via CMAUP database
Methyleugenol 7127 Click to see COC1=C(C=C(C=C1)CC=C)OC 178.23 unknown via CMAUP database
> Benzenoids / Phenol ethers / Anisoles
Asarone 636822 Click to see 208.25 unknown via CMAUP database
Elemicin 10248 Click to see 208.25 unknown via CMAUP database
Estragole 8815 Click to see 148.20 unknown via CMAUP database
gamma-Asarone 636750 Click to see COC1=CC(=C(C=C1CC=C)OC)OC 208.25 unknown via CMAUP database
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Pentadecane 12391 Click to see 212.41 unknown via CMAUP database
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
Gamma-Terpinene 7461 Click to see 136.23 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans
(-)-Asarinin 11869417 Click to see 354.40 unknown via CMAUP database
4-[(3R,3aR,6S,6aR)-3-(1,3-benzodioxol-5-yl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-6-yl]-2,6-dimethoxyphenol 57404419 Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC5=C(C=C4)OCO5 386.40 unknown via CMAUP database
4-[(3S,3aR,6R,6aR)-6-(1,3-benzodioxol-5-yl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]benzene-1,2-diol 46917405 Click to see 342.30 unknown via CMAUP database
5-[(3S,3aS,6R,6aS)-6-(1,3-benzodioxol-5-yl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-2-methoxyphenol 10089592 Click to see COC1=C(C=C(C=C1)C2C3COC(C3CO2)C4=CC5=C(C=C4)OCO5)O 356.40 unknown via CMAUP database
Epipinoresinol 637584 Click to see 358.40 unknown via CMAUP database
Pluviatilol 70695727 Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC5=C(C=C4)OCO5)O 356.40 unknown via CMAUP database
Sesamin 72307 Click to see C1C2C(COC2C3=CC4=C(C=C3)OCO4)C(O1)C5=CC6=C(C=C5)OCO6 354.40 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 7,9-epoxylignans
Sesaminone 158370 Click to see C1C(C(C(O1)C2=CC3=C(C=C2)OCO3)CO)C(=O)C4=CC5=C(C=C4)OCO5 370.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty amides / N-acyl amines
(2E,4E,8Z)-N-(2-methylpropyl)dodeca-2,4,8,10-tetraenamide 70693621 Click to see CC=CC=CCCC=CC=CC(=O)NCC(C)C 247.38 unknown via CMAUP database
Pellitorine 5318516 Click to see 223.35 unknown via CMAUP database
Sanshool 6440935 Click to see 247.38 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Myrcene 31253 Click to see 136.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
P-Cymene 7463 Click to see 134.22 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-alpha-Pinene 440968 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown via CMAUP database
(-)-Camphene 440966 Click to see 136.23 unknown via CMAUP database
(+)-Sabinene 10887971 Click to see 136.23 unknown via CMAUP database
(+/-)-Asarinol A 46174001 Click to see 166.22 unknown via CMAUP database
Bornyl acetate, (-)- 93009 Click to see 196.29 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(+)-alpha-Terpineol 442501 Click to see 154.25 unknown via CMAUP database
(+)-Limonene 440917 Click to see 136.23 unknown via CMAUP database
(1S,6R)-6-Isopropyl-3-methyl-cyclohex-2-en-1-ol 11367127 Click to see CC1=CC(C(CC1)C(C)C)O 154.25 unknown via CMAUP database
Terpinolene 11463 Click to see 136.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Monocyclic monoterpenoids
Eucarvone 136330 Click to see CC1=CC=CC(CC1=O)(C)C 150.22 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones
2,7,7-Trimethylcyclohepta-2,4-dienone 85794676 Click to see 150.22 unknown via CMAUP database
> Organoheterocyclic compounds / Benzodioxoles
Croweacin 5316141 Click to see 192.21 unknown via CMAUP database
Kakuol 596894 Click to see 194.18 unknown via CMAUP database
Safrole 5144 Click to see 162.18 unknown via CMAUP database
Sarisan 95289 Click to see COC1=CC2=C(C=C1CC=C)OCO2 192.21 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
(3R)-3,6,8-trihydroxy-1,1,3,7-tetrakis(3-methylbut-2-enyl)xanthene-2,4,9-trione 162866712 Click to see CC(=CCC1=C(C2=C(C=C1O)OC3=C(C2=O)C(C(=O)C(C3=O)(CC=C(C)C)O)(CC=C(C)C)CC=C(C)C)O)C 548.70 unknown https://doi.org/10.1016/J.BMCL.2012.01.068
Gaudichaudione H 57345562 Click to see 494.60 unknown https://doi.org/10.1016/J.BMCL.2012.01.068
Oliganthin C 57345553 Click to see CC(=CCC1=C(C2=C(C=C1O)OC3=C(C2=O)C(C(=O)C(C3=O)(CC=C(C)C)O)(CC=C(C)C)CC=C(C)C)O)C 548.70 unknown https://doi.org/10.1016/J.BMCL.2012.01.068
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / Pyranoxanthones
(9R)-5,9-dihydroxy-2,2-dimethyl-7,7-bis(3-methylbut-2-enyl)-9-(2-oxopropyl)pyrano[3,2-b]xanthene-6,8,10-trione 162883971 Click to see CC(=CCC1(C2=C(C(=O)C(C1=O)(CC(=O)C)O)OC3=CC4=C(C=CC(O4)(C)C)C(=C3C2=O)O)CC=C(C)C)C 534.60 unknown https://doi.org/10.1016/J.BMCL.2012.01.068
(9R)-5,9-dihydroxy-2,2-dimethyl-7,7,9-tris(3-methylbut-2-enyl)pyrano[3,2-b]xanthene-6,8,10-trione 162866713 Click to see CC(=CCC1(C2=C(C(=O)C(C1=O)(CC=C(C)C)O)OC3=CC4=C(C=CC(O4)(C)C)C(=C3C2=O)O)CC=C(C)C)C 546.60 unknown https://doi.org/10.1016/J.BMCL.2012.01.068
Oliganthin A 135981986 Click to see 478.50 unknown https://doi.org/10.1016/J.BMCL.2012.01.068
Oliganthin B 57345552 Click to see 546.60 unknown https://doi.org/10.1016/J.BMCL.2012.01.068
Oliganthin D 57345561 Click to see 534.60 unknown https://doi.org/10.1016/J.BMCL.2012.01.068

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