Details Top

Internal ID UUID643fe2994c869757251153
Scientific name Manilkara kauki
Authority Dubard
First published in Ann. Mus. Colon. Marseille , sér. 3, 3: 9 (1915)

Ethnobotanical Use Top

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General Uses Top

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Common products:
- Raw gutta-percha obtained as a coagulum from the latex of Manilkara kauki; processed into blocks, slabs, sheets, or powders. Refined grades are compounded with fillers and plasticizers for use as a thermoplastic base for molding, sheathing, and coating.

Industrial and craft applications:
- Coarse sheathing for early telegraph and telephone conductors (historic). Core materials for early golf balls (historically). General-purpose thermoplastic for carving, moldings, and durable, water-resistant craft items. Excellent electrical insulator; resistant to water and many acids; softens under heat and hardens upon cooling.

Food and beverages (non-medicinal):
- No documented food or beverage uses.

Colorants and tanning:
- The sapote family is noted as a source of natural brown dyes for protein fibers (historical craft use). Tanning capacity not documented for this taxon.

Wood and fiber:
- Wood noted as hard and dense; specific commercial timber applications and fiber uses not documented.

Fragrance and cosmetics:
- Fragrance or cosmetic uses not documented.

Properties relevant to use:
- The gum is a gutta-percha type consisting mainly of trans‑1,4‑polyisoprene with resinous constituents, yielding a rigid, water-resistant, electrically insulating, and thermoplastic material. Insoluble in water; softens on heating.

Standards and regulation:
- Historic regulation of gutta‑percha product grades and trade based on ISO/ASTM standards for natural rubber/gutta‑percha materials.

Sustainability and sourcing:
- Wild harvesting and regional tapping practices have led to local scarcity; replacement by synthetic polymers for many applications is now common. Standardized sustainable tapping methods are not documented for this species.

Synonyms Top

Scientific name Authority First published in
Imbricaria malabarica Poir. Encycl. 4: 434 (1798)
Kaukenia kauki Kuntze Revis. Gen. Pl. 2: 406 (1891)
Mimusops bojeri A.DC. Prodr. 8: 205 (1844)
Mimusops browniana Benth. Fl. Austral. 4: 285 (1868)
Mimusops elengi Bojer Hortus Maurit. : 198 (1837)
Mimusops hookeri A.DC. Prodr. 8: 204 (1844)
Mimusops kauki L. Sp. Pl. : 349 (1753)
Mimusops manilkara G.Don Gen. Hist. 4: 35 (1837)
Achras mammosa Sieber ex A.DC. Prodr. 8: 204 (1844)
Achras octodecemfida Stokes. Bot. Mat. Med. 2: 294 (1812)
Mimusops kauki var. browniana A.DC. Prodr. 8: 203 (1844)

Common names Top

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Language Common/alternative name
ban sabo kecik
Indonesian sawo kecik
Japanese サオ
Japanese マライサオ
Japanese サワノキ
jv sawo kecik
Malay sawo kecil
Chinese 凹叶人心果

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

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-tropical
    • Indian Subcontinent
      • India
      • Sri Lanka
    • Indo-China
      • Cambodia
      • Myanmar
      • Thailand
      • Vietnam
    • Malesia
      • Borneo
      • Jawa
      • Lesser Sunda Islands
      • Malaya
      • Maluku
      • Philippines
      • Sulawesi
      • Sumatera
    • Papuasia
      • New Guinea

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000235898
UNII Q7DE8405JO
USDA Plants MAKA3
Tropicos 28700873
KEW urn:lsid:ipni.org:names:787653-1
The Plant List kew-120182
Open Tree Of Life 603204
NCBI Taxonomy 233707
IPNI 787653-1
iNaturalist 348725
GBIF 2885150
Freebase /m/04f1c57
EOL 1154592
USDA GRIN 102657
Wikipedia Manilkara_kauki

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
Plant Extracts as Skin Care and Therapeutic Agents Michalak M Int J Mol Sci 22-Oct-2023
PMCID:PMC10607442
doi:10.3390/ijms242015444
PMID:37895122
Searching for Natural Plants with Antimelanogenesis and Antityrosinase Properties for Cosmeceutical or Nutricosmetics Applications: A Systematic Review Tung XY, Yip JQ, Gew LT ACS Omega 06-Sep-2023
PMCID:PMC10515176
doi:10.1021/acsomega.3c02994
PMID:37744793
Integrating traditional ecological knowledge into habitat restoration: implications for meeting forest restoration challenges Haq SM, Pieroni A, Bussmann RW, Abd-ElGawad AM, El-Ansary HO J Ethnobiol Ethnomed 10-Aug-2023
PMCID:PMC10413632
doi:10.1186/s13002-023-00606-3
PMID:37559120
Commodity risk assessment of Acer palmatum plants grafted on Acer davidii from China Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Faccoli M, Iacopetti G, Mikulová A, Mosbach‐Schulz O, Stergulc F, Gonthier P EFSA J 12-May-2022
PMCID:PMC9096882
doi:10.2903/j.efsa.2022.7298
PMID:35592020
Simultaneous micronization and purification of bioactive fraction by supercritical antisolvent technology Hiendrawan S, Veriansyah B, Widjojokusumo E, Tjandrawinata RR J Adv Pharm Technol Res 01-Apr-2017
PMCID:PMC5416655
doi:10.4103/japtr.JAPTR_164_16
PMID:28516056
Secondary Metabolites from Leaves of Manilkara subsericea (Mart.) Dubard de Almeida FB, Fernandes CP, Romao W, Vanini G, Costa HB, França HS, Santos MG, Carvalho JC, Falcão DQ, Rocha L Pharmacogn Mag 01-Oct-2015
PMCID:PMC4787084
doi:10.4103/0973-1296.172957
PMID:27013790
Triterpene Esters and Biological Activities from Edible Fruits of Manilkara subsericea (Mart.) Dubard, Sapotaceae Fernandes CP, Corrêa AL, Lobo JF, Caramel OP, de Almeida FB, Castro ES, Souza KF, Burth P, Amorim LM, Santos MG, Ferreira JL, Falcão DQ, Carvalho JC, Rocha L Biomed Res Int 20-Dec-2012
PMCID:PMC3591231
doi:10.1155/2013/280810
PMID:23509702
Mimusops manilkara, constituents of fruit and seed G. Misra, C.R. Mitra Elsevier BV 12-Feb-2003
doi:10.1016/S0031-9422(00)85821-5
Triterpenoids of mimusops manilkara trunk bark G. Misra, S.K. Nigam, C.R. Mitra Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)85365-0

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids / Scalarane sesterterpenoids
(3I(2),13I+/-)-3-Methoxy-13-methyl-27-norolean-14-ene 12305297 Click to see 440.70 unknown https://doi.org/10.1016/S0031-9422(00)85365-0
4,4,6a,8a,11,11,12b,14b-Octamethyl-1,2,3,4,4a,5,6,6a,8,8a,9,10,11,12,12a,12b,13,14,14a,14b-icosahydropicen-3-ol 344467 Click to see 426.70 unknown https://doi.org/10.1016/S0031-9422(00)85365-0
D-Friedoolean-14-en-3-one 500344 Click to see 424.70 unknown https://doi.org/10.1016/S0031-9422(00)85365-0
Sawamilletin 609451 Click to see CC1(CCC2(CC=C3C4(CCC5C(C(CCC5(C4CCC3(C2C1)C)C)OC)(C)C)C)C)C 440.70 unknown https://doi.org/10.1016/S0031-9422(00)85365-0
Taraxerol 92097 Click to see 426.70 unknown https://doi.org/10.1016/S0031-9422(00)85365-0
Taraxerone 92785 Click to see 424.70 unknown https://doi.org/10.1016/S0031-9422(00)85365-0
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,3aR,5aR,5bR,7aR,9R,11aR,11bS,13aS,13bR)-3a,5a,5b,8,8,11a-hexamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-ol 162996338 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(00)85365-0
(3S,4aR,6aR,6bS,8aR,11S,12S,12aR,14aR,14bR)-4,4,6a,6b,8a,11,12,14b-octamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picen-3-ol 12358384 Click to see 426.70 unknown https://doi.org/10.1016/S0031-9422(00)85365-0
(4,4,6a,6b,8a,11,11,14b-Octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl) acetate 345510 Click to see 468.80 unknown https://doi.org/10.1016/S0031-9422(00)85365-0
(4,4,6a,6b,8a,11,12,14b-octamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picen-3-yl) octanoate 74369062 Click to see 552.90 unknown https://doi.org/10.1016/S0031-9422(00)85821-5
[(3R,4aR,6aR,6bS,8aR,11R,12S,12aR,14aR,14bR)-4,4,6a,6b,8a,11,12,14b-octamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picen-3-yl] octanoate 162926181 Click to see CCCCCCCC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4C(C(CC5)C)C)C)C)C)C 552.90 unknown https://doi.org/10.1016/S0031-9422(00)85821-5
alpha-Amyrenol 225688 Click to see 426.70 unknown https://doi.org/10.1016/S0031-9422(00)85365-0
alpha-Amyrin acetate 92842 Click to see 468.80 unknown https://doi.org/10.1016/S0031-9422(00)85365-0
beta-Amyrenol 225689 Click to see 426.70 unknown https://doi.org/10.1016/S0031-9422(00)85365-0
Beta-Amyrin 73145 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(00)85365-0
Beta-Amyrin Acetate 92156 Click to see 468.80 unknown https://doi.org/10.1016/S0031-9422(00)85365-0
Lup-20(29)-en-3-ol, (3beta)- 521518 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(00)85365-0
Npc25529 293754 Click to see 468.80 unknown https://doi.org/10.1016/S0031-9422(00)85365-0
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3R,5S,9S,10R,13S,14R,17S)-17-[(E,2S,5S)-5-ethyl-6-methylhept-3-en-2-yl]-10,13-dimethyl-2,3,4,5,6,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 162958784 Click to see 412.70 unknown https://doi.org/10.1016/S0031-9422(00)85821-5
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
2-(3,4-Dihydroxyphenyl)-3,6,7-trihydroxy-2,3-dihydro-4H-chromen-4-one 235240 Click to see C1=CC(=C(C=C1C2C(C(=O)C3=CC(=C(C=C3O2)O)O)O)O)O 304.25 unknown https://doi.org/10.1016/S0031-9422(00)85821-5
2-(3,6,7-Trihydroxy-chroman-4-one 54603556 Click to see C1=CC(=C(C=C1C2C(C(=O)C3=CC(=C(C=C3O2)O)O)O)O)O 304.25 unknown https://doi.org/10.1016/S0031-9422(00)85821-5
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Quercetin 5280343 Click to see 302.23 unknown https://doi.org/10.1016/S0031-9422(00)85821-5

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