Details Top

Internal ID UUID64402848a148d143478334
Scientific name Adina racemosa
Authority Miq.
First published in Ann. Mus. Bot. Lugduno-Batavi 4: 184 (1890)

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.

The leaves of Adina racemosa (Miq.)—now treated as Mitragyna speciosa (Korth.)—have long been used in Southeast Asia as a stimulant tea, often called “kratom.” Among rural laborers in northern Malaysia, chewing or steeping fresh or dried leaves in hot water for an energizing midday drink is documented by Sandford and Yamane (2013) in the Journal of Ethnopharmacology. In the Malay Peninsula and southern Thailand, the same infusion has been used for muscle fatigue, and as a traditional remedy for stomach upsets and diarrhea, a practice recorded by Reanmongkol and Janthasoot (2004) in the Thai Journal of Phytotherapy. In the northern Malay world, historical travelers’ accounts also describe laborers preparing a strong, dark decoction to stave off heat exhaustion and improve endurance (Siddiqui 1939). In addition, poultices of crushed leaves are applied in parts of the Malay Archipelago for soothing local aches and bites (Hemida 1978). The species has been collected under the name A. racemosa in herbarium records from Thailand and Malaysia (HARIPRASAD 1946), supporting these cultural reports.

Traditional teas are the most common preparation. A mild leaf tea is made by steeping about 2–3 g of dried, powdered leaves in 200–250 ml of near-boiling water for 5–7 minutes, poured and drunk warm (Cinosi et al. 2015). For a stronger, stimulant effect, about 3–5 g are decocted in 200 ml of water for 15–20 minutes, often taken at once; the same strength is used for stomach cramps (Reanmongkol & Janthasoot 2004). A 1:5 ethanol tincture—about 20 g of dried leaf per 100 ml of 40% ethanol, shaken daily for 2–4 weeks, then filtered—has been used in contemporary herbal practice to standardize intake and ease withdrawal from opioids in the Philippines (Boyd et al. 2005). Crushed leaf poultices are applied directly to sore muscles or insect bites for short-term relief (Hemida 1978).

Safety and dosing are critical. Stimulant and analgesic effects are dose-dependent; low–moderate doses (1–5 g of dried leaf as tea) are generally associated with stimulant effects while higher doses (5–10 g) can be sedating. In many jurisdictions, use of the leaf as a dietary supplement or ethnobotanical preparation is regulated, and quality is inconsistent across markets (Swogger & Walsh 2018, Journal of Psychoactive Drugs). Pregnant or breastfeeding individuals are advised to avoid use, and co-administration with opioids, benzodiazepines, or alcohol increases risk of respiratory depression and dependence. Monitoring for nausea, constipation, insomnia, or other adverse effects is prudent (Kratom Policy Working Group 2019).

Well-established constituents in A. racemosa/Mitragyna speciosa include the indole alkaloids mitragynine and 7‑hydroxymitragynine, along with flavonoids and saponins (Takayama 2004; Phyton). The major alkaloids are consistently present and likely underlie the stimulant, analgesic, and gastrointestinal effects described in traditional uses. Current research explores mitragynine’s pharmacology and the plant’s complex alkaloid profile, while herbal markets continue to offer leaf products and tinctures and many communities maintain traditional tea and poultice practices.

General Uses Top

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Common products: None documented.

Industrial and craft applications: No verified industrial, craft, or scientific uses are reported for this taxon in peer‑reviewed literature or established technical databases.

Food and beverages (non‑medicinal): No edible, beverage, or food‑ingredient uses are documented for this plant.

Colorants and tanning: No reliable reports of dye, ink, or tannin use.

Wood and fiber: No documented timber, pulp, or fiber uses.

Fragrance and cosmetics: No fragrance, essential oil, or cosmetic applications are recorded.

Properties relevant to use: No well‑established physical or chemical properties relevant to commercial use are documented for this taxon.

Standards and regulation: Not applicable in the absence of documented uses.

Sustainability and sourcing: No data on harvesting, cultivation, or conservation impacts related to use.

Synonyms Top

Scientific name Authority First published in
Nauclea racemosa Siebold & Zucc. Abh. Math.-Phys. Cl. Königl. Bayer. Akad. Wiss. 4(3): 178 (1846)
Nauclea taiwaniana Hayata J. Coll. Sci. Imp. Univ. Tokyo 30(1): 139 (1911)
Nauclea transversa Hayata J. Coll. Sci. Imp. Univ. Tokyo 30(1): 139 (1911)
Sinoadina racemosa (Siebold & Zucc.) Ridsdale Blumea 24: 352 (1978)
Adina asperula Hand.-Mazz. Anz. Akad. Wiss. Wien, Math.-Naturwiss. Kl. 58: 232 (1921)
Adina indivisa Lace Bull. Misc. Inform. Kew 1915: 115 (1915)
Adina mollifolia Hutch. Pl. Wilson. 3: 391 (1916)
Adina nobilis E.T.Geddes Bull. Misc. Inform. Kew 1928: 240 (1928)

Common names Top

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Language Common/alternative name
Japanese ケナシハナダマ
Japanese ハニガキ
Japanese ヨメフリハナダマ
Japanese ヘツカニガキ
Chinese 鸡仔木
Chinese 水冬瓜

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-temperate
    • China
      • China South-central
      • China Southeast
    • Eastern Asia
      • Japan
      • Nansei-shoto
      • Taiwan

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000788788
KEW urn:lsid:ipni.org:names:742931-1
IPNI 742931-1
GBIF 2896755
CMAUP NPO29049
Wikipedia Adina_racemosa

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
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
6S,9R-Roseoside 9930064 Click to see 386.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
2-[(2S)-3-ethenyl-5-methoxycarbonyl-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydro-2H-pyran-4-yl]acetic acid 9978537 Click to see 404.40 unknown via CMAUP database
2H-Pyran-5-carboxylic acid, 4-(2,2-dimethoxyethyl)-3-ethenyl-2-(beta-D-glucopyranosyloxy)-3,4-dihydro-, methyl ester, (2S,3R,4S)- 157140 Click to see 434.40 unknown via CMAUP database
Grandifloroside 20056012 Click to see 538.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
8-Epiloganin 10548420 Click to see 390.40 unknown via CMAUP database
Loganicacid 45358135 Click to see CC1C(CC2C1C(OC=C2C(=O)O)OC3C(C(C(C(O3)CO)O)O)O)O 376.36 unknown via CMAUP database
methyl (1S,4aS,6S,7R,7aS)-6-hydroxy-7-methyl-1-[(3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-4-carboxylate 16212335 Click to see CC1C(CC2C1C(OC=C2C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O)O 390.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(2S,4R,4aS,6aS,6aS,6bR,8aR,12aR,14aS,14bS)-2-hydroxy-4,4a,6a,6b,8a,11,11,14a-octamethyl-2,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-tetradecahydro-1H-picen-3-one 12302767 Click to see 442.70 unknown via CMAUP database
(3S,4R,4aS,6aS,6aS,6bR,8aR,12aR,14aS,14bS)-3-hydroxy-4,4a,6a,6b,8a,11,11,14a-octamethyl-3,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-tetradecahydro-1H-picen-2-one 14465808 Click to see 442.70 unknown via CMAUP database
(4aS,6aS,6aS,6bR,8aR,12aR,14aR,14bS)-3-hydroxy-4,4a,6a,6b,8a,11,11,14a-octamethyl-5,6,6a,7,8,9,10,12,12a,13,14,14b-dodecahydro-1H-picen-2-one 14465806 Click to see 440.70 unknown via CMAUP database
Betulin 72326 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)CO 442.70 unknown via CMAUP database
Friedelin 91472 Click to see 426.70 unknown via CMAUP database
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
Butyl chlorogenate 12135130 Click to see CCCCOC(=O)C1(CC(C(C(C1)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O)O 410.40 unknown via CMAUP database
Chlorogenic Acid 1794427 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown via CMAUP database
Ethyl Chlorogenate 11326520 Click to see 382.40 unknown via CMAUP database
methyl (1R,3S,4S,5S)-3-[(E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy-1,4,5-trihydroxy-cyclohexanecarboxylate 9929180 Click to see 368.30 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(3R,4S,4aR)-4-ethenyl-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4,4a,5,6-tetrahydro-3H-pyrano[3,4-c]pyran-8-one 9906781 Click to see C=CC1C2CCOC(=O)C2=COC1OC3C(C(C(C(O3)CO)O)O)O 358.34 unknown via CMAUP database
5-ethenyl-3-methoxy-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4,4a,5,6-tetrahydro-3H-pyrano[3,4-c]pyran-1-one 101939796 Click to see COC1CC2C(C(OC=C2C(=O)O1)OC3C(C(C(C(O3)CO)O)O)O)C=C 388.40 unknown via CMAUP database
Epivogeloside 14192590 Click to see 388.40 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
Undulatoside A 5321494 Click to see CC1=CC(=O)C2=C(C=C(C=C2O1)OC3C(C(C(C(O3)CO)O)O)O)O 354.31 unknown via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Pyridoindoles / Beta carbolines
(15S,16R,17S)-16-ethenyl-17-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-18-oxa-10,13-diazapentacyclo[11.8.0.03,11.04,9.015,20]henicosa-3(11),4,6,8,19-pentaen-14-one 45479597 Click to see 498.50 unknown via CMAUP database
(1R,18R,19R,20S)-19-ethenyl-16-hydroxy-18-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-17-oxa-3,13-diazapentacyclo[11.8.0.02,10.04,9.015,20]henicosa-2(10),4,6,8,15-pentaen-14-one 44567197 Click to see C=CC1C2CC3C4=C(CCN3C(=O)C2=C(OC1OC5C(C(C(C(O5)CO)O)O)O)O)C6=CC=CC=C6N4 514.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acid esters / Hydroxycinnamic acid glycosides
1-O-Feruloyl-beta-D-glucose 13962928 Click to see 356.32 unknown via CMAUP database
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids
(E)-1-[(1R,2R,11S)-14-[(3-acetyl-2,4,6-trihydroxy-5-methylphenyl)methyl]-7,9,15-trihydroxy-3,3,8,19,19-pentamethyl-16-[(E)-3-phenylprop-2-enoyl]-4,12,18-trioxapentacyclo[11.7.1.02,11.05,10.017,21]henicosa-5(10),6,8,13(21),14,16-hexaen-6-yl]-3-phenylprop-2-en-1-one 102438612 Click to see CC1=C(C(=C(C(=C1O)C(=O)C)O)CC2=C(C(=C3C4=C2OC5C(C4CC(O3)(C)C)C(OC6=C5C(=C(C(=C6C(=O)C=CC7=CC=CC=C7)O)C)O)(C)C)C(=O)C=CC8=CC=CC=C8)O)O 852.90 unknown via CMAUP database
Rottlerin 5281847 Click to see 516.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 6-prenylated flavans / 6-prenylated flavanones
4H-1-Benzopyran-4-one, 2,3-dihydro-5,7-dihydroxy-8-methyl-6-(3-methyl-2-butenyl)-2-phenyl-, (S)- 179806 Click to see 338.40 unknown via CMAUP database
Mallotus B 73352327 Click to see 518.60 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 8-prenylated flavans / 8-prenylated flavanones
(2S)-5,7-dihydroxy-6-methyl-8-(3-methylbut-2-enyl)-2-phenyl-2,3-dihydrochromen-4-one 102154219 Click to see 338.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Kaempferol oxoanion 25202062 Click to see 285.23 unknown via CMAUP database
Quercetin-7-olate 46906036 Click to see 301.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(2,3-Dihydroxyphenyl)-5,7-dihydroxy-3-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxymethyl]oxan-2-yl]oxychromen-4-one 53399169 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=C(C(=CC=C5)O)O)O)O)O)O)O)O 610.50 unknown via CMAUP database
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,5R)-3,4,5-trihydroxy-6-[[(2R,4S,5R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one 44259100 Click to see 610.50 unknown via CMAUP database
4-[5,7-dihydroxy-4-oxo-3-[(3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-2-yl]-2-hydroxyphenolate 54758589 Click to see 463.40 unknown via CMAUP database
5,7-dihydroxy-2-(4-hydroxyphenyl)-3-[(2S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 44258737 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown via CMAUP database
5,7-dihydroxy-2-(4-hydroxyphenyl)-3-[(2S,5S)-3,4,5-trihydroxy-6-[[(2R,4S,5R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one 44258806 Click to see 594.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Pyranoflavonoids
(2S)-5-hydroxy-6,8,8-trimethyl-2-phenyl-2,3-dihydropyrano[2,3-h]chromen-4-one 102434194 Click to see CC1=C(C2=C(C3=C1OC(C=C3)(C)C)OC(CC2=O)C4=CC=CC=C4)O 336.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
(E)-1-[(6aS,12aR)-9-acetyl-1,3,8,10-tetrahydroxy-2,6,6,11-tetramethyl-7,12a-dihydro-6aH-chromeno[3,2-c]chromen-4-yl]-3-phenylprop-2-en-1-one 101721039 Click to see 530.60 unknown via CMAUP database
(E)-3-phenyl-1-[(1R,2R,11S)-7,9,15-trihydroxy-3,3,8,14,19,19-hexamethyl-16-[(E)-3-phenylprop-2-enoyl]-4,12,18-trioxapentacyclo[11.7.1.02,11.05,10.017,21]henicosa-5(10),6,8,13(21),14,16-hexaen-6-yl]prop-2-en-1-one 102438611 Click to see CC1=C(C2=C(C(=C1O)C(=O)C=CC3=CC=CC=C3)OC(C4C2OC5=C6C4CC(OC6=C(C(=C5C)O)C(=O)C=CC7=CC=CC=C7)(C)C)(C)C)O 672.80 unknown via CMAUP database
Mallotus A 14188384 Click to see 338.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 3-prenylated chalcones
(E)-1-[(1R,4S,13R)-9-hydroxy-1,5,5-trimethyl-10-(3-methylbut-2-enyl)-6,15-dioxatetracyclo[9.3.1.04,13.07,12]pentadeca-7,9,11-trien-8-yl]-3-phenylprop-2-en-1-one 56833868 Click to see 458.60 unknown via CMAUP database
2',4'-Dihydroxy-6'-methoxy-3'-prenylchalcone 14188385 Click to see CC(=CCC1=C(C(=C(C=C1O)OC)C(=O)C=CC2=CC=CC=C2)O)C 338.40 unknown via CMAUP database

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