Garcinia oligantha
Details Top
| 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.
- Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.
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).
Common names Top
Add a new one! Suggest a correction!| Language | Common/alternative name |
|---|---|
| Vietnamese | bứa ít hoa |
| Chinese | 山竹子 |
| Chinese | 单花山竹子 |
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
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Asia-temperate click to expand
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China
- China Southeast
- Hainan
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China
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Asia-tropical click to expand
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Indo-China
- Vietnam
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Indo-China
Links to other databases Top
Suggest others/fix!| 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
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)!
| 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 |
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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 |
Collections Top
| In private collections | 0 |
| In public collections | 0 |