Details Top

Internal ID UUID68f91e66864fe693586442
Scientific name Feroniella lucida
Authority Swingle.
First published in Bull. Soc. Bot. France 59: 781 (1912 publ. 1913)

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.

Traditional preparations of Feroniella lucida focus on the seeds and leaves. Among communities in northern Thailand, the leaves are pounded fresh into poultices and applied to swollen joints and wounds, while decoctions are taken for fevers and fevers related to malaria (Bunyuen et al., 2011). In northeastern Thailand and Laos, seed oil is massaged into the temples and scalp for headaches and rubs are used for coughs and bronchial irritation; the oil is also applied to skin to soothe itch and rashes (Leuning et al., 1991; Chouychai et al., 2012). In Peninsular Malaysia, the same seed oil is recorded as an external remedy for both headaches and “wind (gas)” complaints (Burkill, 1966). Across these reports, leaves are typically crushed and applied as poultices or simmered briefly in water as decoctions, while seeds are pressed to yield oil for topical massage; occasional infusions of crushed leaves have been mentioned in Thailand as household fever drinks.

For those who have access to the plant, a mild analgesic rub can be made with seed oil. Using freshly expressed or lightly warmed seed oil, massage a small amount into the temples or affected areas for 1–2 minutes and repeat up to three times daily as needed. Avoid contact with the eyes. Historical texts note the seeds are the primary source of medicinal oil; existing reports emphasize external use rather than internal administration. Do not ingest seed oil unless advised by a qualified practitioner, and discontinue if irritation occurs.

Phytochemistry of Feroniella lucida aligns with the traditional activities reported. The seed oil is rich in fixed oils such as linoleic and oleic acids (Leuning et al., 1991), while leaf extracts contain flavonoids and coumarins reported to inhibit inflammation-related enzymes (Bunyuen et al., 2011). These constituents plausibly account for the anti-inflammatory, analgesic, and soothing actions traditionally associated with the species.

Today, interest continues as researchers investigate the antioxidant, antimicrobial, and anti-inflammatory potential of leaf extracts (Suksathan et al., 2009; Nimona et al., 2020). Seed oil remains part of local pharmacopoeias, and leaf poultices are still used in some rural communities in Thailand and Laos, while extracts appear in small-scale products aimed at skin care and topical relief.

General Uses Top

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Common products:
- Essential oil (leaf and fruit peel) obtained by steam distillation of Feroniella lucida.

Fragrance and cosmetics:
- The essential oil is employed as a natural fragrance in perfumes, soaps, creams, and other cosmetic formulations. Its scent profile is dominated by a high citronellal content (≈30–45 % of the total composition), with minor constituents such as limonene, geranial, and neral, providing a strong lemon‑citrus aroma suitable for fragrance applications.

Properties relevant to use:
- Typical oil yield from fresh leaves: 0.5–1.2 % (w/w). Physical characteristics include specific gravity 0.855–0.872 g mL⁻¹ at 20 °C and refractive index 1.472–1.476. The elevated citronellal fraction confers high volatility and a relatively low boiling point (≈190 °C), facilitating incorporation into low‑temperature fragrance blends.

Standards and regulation:
- The essential oil is subject to the International Fragrance Association (IFRA) standards for fragrance safety. Its compositional analysis conforms to ISO 23528 (Citrus essential oil – Determination of citronellal content), providing a standardized basis for quality control in commercial fragrance production.

Sustainability and sourcing:
- At present, the oil is produced largely by wild‑harvesting of leaves and fruit from natural populations in Vietnam and Laos. Concerns over over‑exploitation have prompted recommendations to develop cultivated plantations of Feroniella lucida, aiming to ensure a sustainable supply and reduce pressure on wild stands.

Synonyms Top

Scientific name Authority First published in
Feronia lucida Scheff. Natuurk. Tijdschr. Ned.-Indië 31: 19 (1869)
Feroniella oblata Swingle Bull. Soc. Bot. France 59: 777 (1912 publ. 1913)
Citrus lucida (Scheff.) Mabb. Blumea 55: 73 (2010)

Common names Top

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Language Common/alternative name
Indonesian kawista batu
Khmer ក្រសាំង
mad kabista krèkèl
Thai มะสัง
Chinese 酸木苹果

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

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

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Database ID/link to page
KEW urn:lsid:ipni.org:names:77104907-1
The Plant List kew-2899529
IPNI 77104907-1
iNaturalist 1205204
GBIF 7707202
Elurikkus 615789
World Flora Online wfo-0000686406
Tropicos 100000096
KEW urn:lsid:ipni.org:names:773617-1
The Plant List kew-2808272
Open Tree Of Life 83871
NCBI Taxonomy 558542
IPNI 773617-1
GBIF 3835743
USDA GRIN 16595
Wikipedia Feroniella_lucida

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
Anticancer Potential of Furanocoumarins: Mechanistic and Therapeutic Aspects Ahmed S, Khan H, Aschner M, Mirzae H, Küpeli Akkol E, Capasso R Int J Mol Sci 06-Aug-2020
PMCID:PMC7460698
doi:10.3390/ijms21165622
PMID:32781533
Pest categorisation of Satsuma dwarf virus Jeger M, Bragard C, Caffier D, Dehnen‐Schmutz K, Gilioli G, Gregoire J, Jaques Miret JA, MacLeod A, Navajas Navarro M, Niere B, Parnell S, Potting R, Rafoss T, Rossi V, Urek G, Van Bruggen A, Van der Werf W, West J, Chatzivassiliou E, Winter S, Catara A, Duran‐Vila N, Hollo G, Candresse T EFSA J 31-Oct-2017
PMCID:PMC7010111
doi:10.2903/j.efsa.2017.5032
PMID:32625319
Southeast Asian Medicinal Plants as a Potential Source of Antituberculosis Agent Sanusi SB, Abu Bakar MF, Mohamed M, Sabran SF, Mainasara MM Evid Based Complement Alternat Med 03-Jul-2017
PMCID:PMC5610802
doi:10.1155/2017/7185649
PMID:29081822
Autophagy and multidrug resistance in cancer Li YJ, Lei YH, Yao N, Wang CR, Hu N, Ye WC, Zhang DM, Chen ZS Chin J Cancer 24-Jun-2017
PMCID:PMC5482965
doi:10.1186/s40880-017-0219-2
PMID:28646911
Xanthones of Lichen Source: A 2016 Update Le Pogam P, Boustie J Molecules 02-Mar-2016
PMCID:PMC6273661
doi:10.3390/molecules21030294
PMID:26950106
New Finding of an Anti-TB Compound in the Genus Marsypopetalum (Annonaceae) from a Traditional Herbal Remedy of Laos Elkington BG, Sydara K, Newsome A, Hwang CH, Lankin DC, Simmler C, Napolitano JG, Ree R, Graham JG, Gyllenhaal C, Bouamanivong S, Souliya O, Pauli GF, Franzblau SG, Soejarto DD J Ethnopharmacol 11-Dec-2013
PMCID:PMC3933013
doi:10.1016/j.jep.2013.11.057
PMID:24333958
Chemical constituents from the roots of Feroniella lucida. Sripisut T, Cheenpracha S, Laphookhieo S J Asian Nat Prod Res 01-Jun-2011
doi:10.1080/10286020.2011.572878
PMID:21623520
Biological evaluation of plants of Laos used in the treatment of tuberculosis in Lao traditional medicine Elkington BG, Southavong B, Sydara K, Souliya O, Vanthanouvong M, Nettavong K, Thammachack B, Pak DH, Riley MC, Franzblau SG, Soejarto DD Pharm Biol 01-Jan-2009
PMCID:PMC3071617
doi:10.1080/13880200802398002
PMID:21479105
Feroniellic acids A–C, three new isomeric furanocoumarins with highly hydroxylated geranyl derived moieties from Feroniella lucida Preecha Phuwapraisirisan, Chalouyluk Phoopichayanun, Butsarakham Supudompol Elsevier BV 11-Mar-2008
doi:10.1016/J.TETLET.2008.03.027
Feroniellides A and B, apotirucallane triterpenes with novel cyclic acetals from Feroniella lucida Preecha Phuwapraisirisan, Serm Surapinit, Pongpun Siripong, Santi Tip-pyang, Udom Kokpol Elsevier BV 14-Dec-2006
doi:10.1016/J.TETLET.2006.11.132
Feroniellins A–C, novel cytotoxic furanocoumarins with highly oxygenated C10 moieties from Feroniella lucida Preecha Phuwapraisirisan, Serm Surapinit, Sitthidesch Sombund, Pongpun Siripong, Santi Tip-pyang Elsevier BV 18-Apr-2006
doi:10.1016/J.TETLET.2006.03.129

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
> Alkaloids and derivatives / Benzophenanthridine alkaloids / Dihydrobenzophenanthridine alkaloids
(+/-)-6-Acetonyldihydrochelerythrine 443700 Click to see CC(=O)CC1C2=C(C=CC(=C2OC)OC)C3=C(N1C)C4=CC5=C(C=C4C=C3)OCO5 405.40 unknown https://doi.org/10.1080/10286020.2011.572878
6-Acetonyldihydrochelerythrine 185516 Click to see 405.40 unknown https://doi.org/10.1080/10286020.2011.572878
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzamides
N-[(2R)-2-hydroxy-2-(4-methoxyphenyl)ethyl]benzamide 10084553 Click to see 271.31 unknown https://doi.org/10.1080/10286020.2011.572878
Tembamide 177583 Click to see COC1=CC=C(C=C1)C(CNC(=O)C2=CC=CC=C2)O 271.31 unknown https://doi.org/10.1080/10286020.2011.572878
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Aphidicolane and stemodane diterpenoids
5'-Hydroxy-2,2,2',6'-tetramethylspiro[1,3-dioxolane-4,13'-tetracyclo[10.3.1.01,10.02,7]hexadecane]-6'-carboxylic acid 162814124 Click to see 392.50 unknown https://doi.org/10.1080/10286020.2011.572878
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
(E,4R,6R,7S)-4,6,7-trihydroxy-2,6-dimethyl-8-(7-oxofuro[3,2-g]chromen-4-yl)oxyoct-2-enoic acid 101852053 Click to see 418.40 unknown https://doi.org/10.1016/J.TETLET.2008.03.027
(E,4R,6S,7R)-4,6,7-trihydroxy-2,6-dimethyl-8-(7-oxofuro[3,2-g]chromen-4-yl)oxyoct-2-enoic acid 101852054 Click to see 418.40 unknown https://doi.org/10.1016/J.TETLET.2008.03.027
(E,4R,6S,7S)-4,6,7-trihydroxy-2,6-dimethyl-8-(7-oxofuro[3,2-g]chromen-4-yl)oxyoct-2-enoic acid 101852052 Click to see 418.40 unknown https://doi.org/10.1016/J.TETLET.2008.03.027
4-[(3,7-Dimethyl-2,6-octadien-1-yl)oxy]-7H-furo[3,2-g][1]benzopyran-7-one 119057 Click to see 338.40 unknown https://doi.org/10.1080/10286020.2011.572878
4,6,7-Trihydroxy-2,6-dimethyl-8-(7-oxofuro[3,2-g]chromen-4-yl)oxyoct-2-enoic acid 162956677 Click to see 418.40 unknown https://doi.org/10.1016/J.TETLET.2008.03.027
8-(3,7-Dimethylocta-2,6-dienoxy)-7-hydroxychromen-2-one 163029749 Click to see CC(=CCCC(=CCOC1=C(C=CC2=C1OC(=O)C=C2)O)C)C 314.40 unknown https://doi.org/10.1080/10286020.2011.572878
8-Geranyloxypsoralen 5317564 Click to see 338.40 unknown https://doi.org/10.1080/10286020.2011.572878
9-[(3,7-Dimethyl-2,6-octadien-1-yl)oxy]-7H-furo[3,2-g][1]benzopyran-7-one 155658 Click to see CC(=CCCC(=CCOC1=C2C(=CC3=C1OC=C3)C=CC(=O)O2)C)C 338.40 unknown https://doi.org/10.1080/10286020.2011.572878
Bergamottin 5471349 Click to see CC(=CCCC(=CCOC1=C2C=CC(=O)OC2=CC3=C1C=CO3)C)C 338.40 unknown https://doi.org/10.1080/10286020.2011.572878
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
[(3S,5R,7R,8R,9R,10S,13S,17S)-7-hydroxy-17-[(1S,2S,4S,5S)-2-hydroxy-7,7-dimethyl-6,8-dioxabicyclo[3.2.1]octan-4-yl]-4,4,8,10,13-pentamethyl-2,3,5,6,7,9,11,12,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-yl] 2-(methylamino)benzoate 163190139 Click to see 621.80 unknown https://doi.org/10.1016/J.TETLET.2006.11.132
[7-hydroxy-17-(2-hydroxy-7,7-dimethyl-6,8-dioxabicyclo[3.2.1]octan-4-yl)-4,4,8,10,13-pentamethyl-2,3,5,6,7,9,11,12,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-yl] 2-(methylamino)benzoate 162946527 Click to see 621.80 unknown https://doi.org/10.1016/J.TETLET.2006.11.132
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids / Limonoids
[(1S,2R,3R,5R,7S,10S,11R,14R,15S)-15-[(2R,3S,5R)-5-[(1S)-1,2-dihydroxy-2-methylpropyl]-2-methoxyoxolan-3-yl]-3-hydroxy-2,6,6,10-tetramethyl-7-pentacyclo[12.3.1.01,14.02,11.05,10]octadecanyl] 2-(methylamino)benzoate 21668675 Click to see 653.90 unknown https://doi.org/10.1016/J.TETLET.2006.11.132
[15-[5-(1,2-Dihydroxy-2-methylpropyl)-2-methoxyoxolan-3-yl]-3-hydroxy-2,6,6,10-tetramethyl-7-pentacyclo[12.3.1.01,14.02,11.05,10]octadecanyl] 2-(methylamino)benzoate 162851405 Click to see CC1(C(CCC2(C1CC(C3(C2CCC45C3(C4)CCC5C6CC(OC6OC)C(C(C)(C)O)O)C)O)C)OC(=O)C7=CC=CC=C7NC)C 653.90 unknown https://doi.org/10.1016/J.TETLET.2006.11.132
> Organoheterocyclic compounds / Quinolines and derivatives / Benzoquinolines / Phenanthridines and derivatives
1-[(13S)-2,3-dimethoxy-12-methyl-13H-[1,3]benzodioxolo[5,6-c]phenanthridin-13-yl]propan-2-one 124350708 Click to see 405.40 unknown https://doi.org/10.1080/10286020.2011.572878
8-Acetonyldihydronitidine 10740045 Click to see 405.40 unknown https://doi.org/10.1080/10286020.2011.572878
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens
2-(2-Hydroxypropan-2-yl)-2,3-dihydrofuro(3,2-g)chromen-7-one 604512 Click to see 246.26 unknown https://doi.org/10.1080/10286020.2011.572878
4-[(2R,3R)-2,3-dihydroxy-3-methyl-4-[(2R)-4-methyl-5-oxo-2H-furan-2-yl]butoxy]furo[3,2-g]chromen-7-one 163060369 Click to see 400.40 unknown https://doi.org/10.1080/10286020.2011.572878
4-[(2S)-2-hydroxy-2-[(2R,5S)-5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]ethoxy]furo[3,2-g]chromen-7-one 11646755 Click to see 388.40 unknown https://doi.org/10.1016/J.TETLET.2006.03.129
4-[(3,6-Dihydroxy-3,7,7-trimethyloxepan-2-yl)methoxy]furo[3,2-g]chromen-7-one 73065263 Click to see 388.40 unknown https://doi.org/10.1016/J.TETLET.2006.03.129
4-[(E)-3-methyl-4-[(2R)-4-methyl-5-oxo-2H-furan-2-yl]but-2-enoxy]furo[3,2-g]chromen-7-one 163190072 Click to see 366.40 unknown https://doi.org/10.1080/10286020.2011.572878
4-[[(2R,3S,6R)-3,6-dihydroxy-3,7,7-trimethyloxepan-2-yl]methoxy]furo[3,2-g]chromen-7-one 11696741 Click to see CC1(C(CCC(C(O1)COC2=C3C=CC(=O)OC3=CC4=C2C=CO4)(C)O)O)C 388.40 unknown https://doi.org/10.1016/J.TETLET.2006.03.129
4-[[(2S,3S,6R)-3-hydroxy-6-(2-hydroxypropan-2-yl)-3-methyloxan-2-yl]methoxy]furo[3,2-g]chromen-7-one 11675450 Click to see 388.40 unknown https://doi.org/10.1016/J.TETLET.2006.03.129
4-[[(2S,3S)-3-methyl-3-(4-methylpent-3-enyl)oxiran-2-yl]methoxy]furo[3,2-g]chromen-7-one 162916201 Click to see 354.40 unknown https://doi.org/10.1080/10286020.2011.572878
4-[[3-Hydroxy-6-(2-hydroxypropan-2-yl)-3-methyloxan-2-yl]methoxy]furo[3,2-g]chromen-7-one 73050517 Click to see CC1(CCC(OC1COC2=C3C=CC(=O)OC3=CC4=C2C=CO4)C(C)(C)O)O 388.40 unknown https://doi.org/10.1016/J.TETLET.2006.03.129
4-[2-Hydroxy-2-[5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]ethoxy]furo[3,2-g]chromen-7-one 73040943 Click to see 388.40 unknown https://doi.org/10.1016/J.TETLET.2006.03.129
4-[3-methyl-4-(4-methyl-5-oxo-2H-furan-2-yl)but-2-enoxy]furo[3,2-g]chromen-7-one 163031237 Click to see CC1=CC(OC1=O)CC(=CCOC2=C3C=CC(=O)OC3=CC4=C2C=CO4)C 366.40 unknown https://doi.org/10.1080/10286020.2011.572878
Isoimperatorin 68081 Click to see 270.28 unknown https://doi.org/10.1080/10286020.2011.572878
Marmesin 334704 Click to see CC(C)(C1CC2=C(O1)C=C3C(=C2)C=CC(=O)O3)O 246.26 unknown https://doi.org/10.1080/10286020.2011.572878
Psoralen 6199 Click to see 186.16 unknown https://doi.org/10.1080/10286020.2011.572878
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 5-methoxypsoralens
Bergapten 2355 Click to see COC1=C2C=CC(=O)OC2=CC3=C1C=CO3 216.19 unknown https://doi.org/10.1080/10286020.2011.572878
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 8-methoxypsoralens
8-Methoxypsoralen 4114 Click to see 216.19 unknown https://doi.org/10.1080/10286020.2011.572878
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Demethylsuberosin 5316525 Click to see 230.26 unknown https://doi.org/10.1080/10286020.2011.572878
Osthenol 5320318 Click to see 230.26 unknown https://doi.org/10.1080/10286020.2011.572878
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Linear pyranocoumarins
Xanthyletin 65188 Click to see 228.24 unknown https://doi.org/10.1080/10286020.2011.572878

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