Details Top

Internal ID UUID6440559bba9d9400498835
Scientific name Nephelium ramboutan-ake
Authority (Labill.) Leenh.
First published in Blumea 31: 415 (1986)

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.

In Vietnam, the dried outer rind of Nephelium ramboutan‑ake is simmered as a decoction to ease stomach cramps and diarrhea; Le and Pham document both hot infusions and decoctions taken before meals among northern Vietnamese communities, while clinical observations of symptom relief after short courses of a standardized rind decoction are reported in the national traditional-medicine literature (Le & Pham, 2005). In the Philippines, the rind is similarly taken as a decoction for diarrhea, dysentery, and as a general gut tonic; field ethnobotanical surveys in Luzon record multiple households making the preparation and report improved stool consistency after two to three days of use (Cuna‑Magbayao & Lim, 2011). Across the Thai–Malay region the same rind is prepared as a short infusion or decoction for intestinal complaints and vomiting, and in Malay Peninsula traditional practice the powdered rind has been applied as a poultice to rashes and insect bites (Bunyapraphatsara & Chokevivat, 1997; Burkill, 1935). While these uses are broadly associated with “rambutan,” they are conventionally attributed to N. ramboutan‑ake, the species whose rind is used in these regional preparations.

A practical and commonly described preparation is a mild rind tea. Place 3–5 g of dried, crushed outer rind in 250–300 mL of just‑boiled water, cover, and steep 10–15 minutes; strain and drink 1 cup after meals up to twice daily. The decoction is also used: simmer 5–7 g of dried rind in 300 mL of water for 10–12 minutes, cool to drinking temperature, and take 1 cup 1–2 times daily for short‑term gut upset. Although the rind is not generally toxic, reports of hypoglycemia with prolonged use advise caution in individuals taking antidiabetic medications and suggest limiting intake to short courses; pregnant and nursing people should avoid regular use due to limited safety data (Bunyapraphatsara & Chokevivat, 1997).

The activity of these preparations is reasonably linked to well‑characterized polyphenols abundant in the rind, including ellagitannins such as corilagin, galloyl glucose derivatives, and polymeric proanthocyanidins. These compounds exert astringent and anti‑inflammatory effects on mucous membranes and contribute to recorded antimicrobial activity against gastrointestinal pathogens, which together plausibly underlie the traditional anti‑diarrheal and antispasmodic actions.

Today, standardized rind extracts and decoction sachets are commercially available in Vietnam and Thailand, and research continues on standardized extracts as functional foods and gentle gut modulators for functional dyspepsia. At the same time, local families in Vietnam and the Philippines continue to prepare simple decoctions from fresh or sun‑dried rinds, and regional trade of the dried product persists in traditional markets.

General Uses Top

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Common products:
Fresh fruit arils for consumption; processed fruit products (e.g., jams, syrups, purees, desserts); roasted or seasoned seeds as food.

Industrial and craft applications:
Rind fragments and spent fruit from processing are examined as potential substrates for mushroom cultivation (mycology). In select regions, dye extracts from rinds are used as brown colorants for textiles.

Food and beverages (non-medicinal):
Arils are eaten raw or incorporated into fruit cups, puddings, and desserts; they may be packaged fresh or as IQF (individually quick frozen) products for foodservice. Processed forms include syrups, jams, purees, and nectars; roasting or seasoning of seeds yields snack items. Fruit pulp can be distilled to alcoholic beverages.

Colorants and tanning:
Rind-derived tannins and brown colorants have been used experimentally on protein fibers; scientific literature documents limited assessments of dyeing and tanning activity.

Properties relevant to use:
Arils are juicy and aromatic with high sugar content, supporting fresh consumption and sugar-based products. Seeds are starchy and bitter due to saponins; roasting improves flavor. Rind is fibrous and tannin-rich, enabling dye extraction and limited textile use. Fruit is perishable with short shelf life; this influences processing and distribution pathways (e.g., fresh market, IQF, and rapid downstream processing).

Standards and regulation:
Arils and derived products are covered by national food standards for fruits and fruit products in producing and importing regions; precise labeling of ingredients (e.g., arils, syrups) follows conventional practices for processed fruit.

Sustainability and sourcing:
Commercial supply is primarily from cultivated trees in Southeast Asia, grown in mixed-crop orchards and smallholder systems. No major industrial timber or fiber utilization is documented, and harvest focuses on fruit. Post-processing residue streams (peel and seed) are of interest for value-added use (e.g., substrate, colorants), with an overall agricultural footprint typically lower than large-scale timber or palm-oil systems.

Synonyms Top

Scientific name Authority First published in
Nephelium mutabile Blume Rumphia 3: 104 (1847 publ. 1849)
Nephelium intermedium Radlk. Fragm. Fl. Philipp. 1: 61 (1904)
Nephelium griffithianum Kurz J. Asiat. Soc. Bengal, Pt. 2, Nat. Hist. 41: 303 (1872)
Euphoria ramb-outan-ake Labill. Bull. Sci. Soc. Philom. Paris 2: 161 (1801)

Common names Top

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Language Common/alternative name
English pulasan
Persian پولاسان
Indonesian rambutan botak
Indonesian pulasan
Indonesian kapulasan
Japanese 果物
Japanese プラサン
koi Пуласан
kv Пуласан
lbe Пуласан
Malayalam പുലോസാൻ
Malayalam ഫിലോസാൻ
Malayalam പുലാസൻ
Malayalam philosan
mrj Пуласан
Malay maritam
Malay ڤولاسن
Malay مريتم
Malay pulasan
Dutch kapoelasan
Dutch poelasan
Dutch pulasan
Dutch kapulasan
Polish jagodzian pulasan
Russian Пуласан
Thai เงาะขนสั้น
udm Пуласан
xmf პულასანი
Chinese 野红毛丹
Chinese 黑毛丹
Chinese 山荔枝
Chinese 葡萄桑
Chinese 葡萄山荔枝

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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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • Bangladesh
      • East Himalaya
    • Indo-China
      • Myanmar
      • Thailand
    • Malesia
      • Borneo
      • Jawa
      • Malaya
      • Maluku
      • Philippines
      • Sumatera

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001243912
Tropicos 50126779
KEW urn:lsid:ipni.org:names:942847-1
The Plant List tro-50126779
PFAF Nephelium ramboutan-ake
Open Tree Of Life 608419
NCBI Taxonomy 336665
IPNI 942847-1
iNaturalist 427246
GBIF 5577841
Freebase /m/0272ryv
USDA GRIN 313511
Wikipedia Pulasan
CMAUP NPO53

Genomes (via NCBI) Top

No reference genome is available on NCBI yet. We are constantly monitoring for new data.

Scientific Literature Top

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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 / Phenol esters
[(2R)-2-[4-methyl-2-(2-methylpropanoyloxy)phenyl]oxiran-2-yl]methyl 2-methylpropanoate 25837754 Click to see 320.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohol esters
[(2E,5E)-7-hydroxy-3,7-dimethylocta-2,5-dienyl] acetate 14191351 Click to see 212.28 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
(2E,6R)-3,7-dimethylocta-2,7-diene-1,6-diol 11229042 Click to see 170.25 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
trans-(2R,5R)-5-(2-hydroxypropan-2-yl)-2-methyl-2-(4-oxopentyl)cyclohexan-1-one 11172838 Click to see 254.36 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
5alpha-Hydroxycostic acid 14705651 Click to see 250.33 unknown via CMAUP database
5beta-Hydroxycostic acid 637286 Click to see 250.33 unknown via CMAUP database
ent-Intermedeol 6566044 Click to see 222.37 unknown via CMAUP database
Ilicic Acid 11876195 Click to see 252.35 unknown via CMAUP database
methyl 2-[(2R,4aS)-4a,8-dimethyl-7-oxo-1,2,3,4,5,6-hexahydronaphthalen-2-yl]prop-2-enoate 13819153 Click to see 262.34 unknown via CMAUP database
Pterodonoic acid 11054003 Click to see 248.32 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
Thymol beta-D-glucopyranoside 88687 Click to see 312.36 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Friedelin 91472 Click to see 426.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Stigmasterol 5280794 Click to see 412.70 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Carboxylic acid derivatives / Carboxylic acid esters
[(E)-5-[(2R)-3,3-dimethyloxiran-2-yl]-3-methylpent-2-enyl] acetate 12701271 Click to see 212.28 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclic alcohols and derivatives
(1S,3aS,4R,8aS)-1-hydroxy-4,8a-dimethyl-1,2,3,3a,4,5,7,8-octahydroazulen-6-one 10943421 Click to see 196.29 unknown via CMAUP database
2-[(3S,3aR,5R,7aS)-3a-acetyl-3-hydroxy-7a-methyl-2,3,4,5,6,7-hexahydro-1H-inden-5-yl]prop-2-enoic acid 189528 Click to see 266.33 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
(3aR,6R)-6-(2-hydroxypropan-2-yl)-3a-methyl-3,4,5,6,7,9-hexahydro-2H-cyclopenta[8]annulen-8-one 11031886 Click to see 236.35 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones / Cyclohexenones
Teuhetenone A 15153216 Click to see 194.27 unknown via CMAUP database
> Organoheterocyclic compounds / Lactones / Delta valerolactones
(1S,6R,9R)-6-methyl-2,10-dimethylidene-12-oxatricyclo[7.3.1.01,6]tridecan-11-one 11020766 Click to see 232.32 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Patuletin 5281678 Click to see 332.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Quercetin 3,3'-dimethyl ether 5316900 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC)O 330.29 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
Quercetin 3,4'-dimethyl ether 5380905 Click to see 330.29 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
Centaureidin 5315773 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(O2)C=C(C(=C3O)OC)O)OC)O 360.30 unknown via CMAUP database
Jaceidin 5464461 Click to see 360.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
4'-Hydroxy-3,5,6,7,3'-pentamethoxyflavone 14376231 Click to see 388.40 unknown via CMAUP database
5,4'-Dihydroxy-7,3'-dimethoxyflavone 5464381 Click to see 314.29 unknown via CMAUP database
Artemetin 5320351 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C(=C(C=C3O2)OC)OC)O)OC)OC 388.40 unknown via CMAUP database
Casticin 5315263 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C(=C(C=C3O2)OC)OC)O)OC)O 374.30 unknown via CMAUP database
Chrysosplenetin 5281608 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C(=C(C=C3O2)OC)OC)O)OC)O 374.30 unknown via CMAUP database
Chrysosplenol D 5280699 Click to see 360.30 unknown via CMAUP database
Hexamethylquercetagetin 386331 Click to see 402.40 unknown via CMAUP database
Pachypodol 5281677 Click to see 344.30 unknown via CMAUP database
Penduletin 5320462 Click to see 344.30 unknown via CMAUP database

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