Calophyllum polyanthum

Details Top

Internal ID UUID64400eef3d977868512805
Scientific name Calophyllum polyanthum
Authority Wall. ex Planch. & Triana
First published in Mém. Soc. Phys. Genève 12(2): 423. 1849

Ethnobotanical Use Top

Write a new one!
No ethnobotanical data added yet. Help us by writing one.

General Uses Top

Suggest a correction!

Common products:
Calophyllum polyanthum yields a non‑drying seed kernel oil (sometimes termed taman or ball‑nut oil) used industrially as a varnish and paint oil, and in soap making. The tree also provides construction and general‑purpose timber marketed locally as “surpun” or “taman.”

Industrial and craft applications:
Kernel oil is employed in varnishes, enamels, and protective coatings; it functions as a drying aid or blending component. The oil’s saponifiable fraction supports soap manufacturing, and the seed cake has potential as an industrial oil cake. Heartwood and mature timber are worked into beams, planking, furniture, and general carpentry where weather exposure is limited.

Food and beverages (non‑medicinal):
There is no verified culinary or beverage use; edible use is not supported by reliable references.

Colorants and tanning:
Tannins and gums in the bark/resin may be used for general tanning, but these applications are not clearly documented for this species in the literature surveyed.

Wood and fiber:
The wood is used for building components, furniture, and carpentry. It is typically sawn into planks and occasionally supplied as sleepers; sapwood is susceptible to dry‑wood borers.

Fragrance and cosmetics:
The kernel oil’s saponifiable nature is suitable for soap making; cosmetic use is otherwise not clearly reported.

Properties relevant to use:
The seed kernel oil is non‑drying to semi‑drying with a readily saponifiable fraction, supporting varnish/soap applications. The heartwood is hard, often of reddish coloration, while sapwood is paler and prone to insect attack.

Standards and regulation:
Timber supplies are typically classified and graded under national rules such as Indian Standard (IS) specifications for general construction wood; plant name and provenance are documented in accepted taxonomic databases such as Kew’s Plants of the World Online.

Sustainability and sourcing:
Local exploitation of larger trees reduces availability of high‑quality timber. While the species is widely distributed, matured heartwood suitable for construction is limited; harvesting pressure may impact resource sustainability in certain regions.

Synonyms Top

Scientific name Authority First published in
Calophyllum elatum Bedd. Rep. Conservator Forests 1863-1864: 31 (1864)
Calophyllum smilesianum Craib Bull. Misc. Inform. Kew 1924: 85 (1924)
Calophyllum smilesianum var. luteum Craib Bull. Misc. Inform. Kew 1924: 86 1924
Calophyllum williamsianum Craib Bull. Misc. Inform. Kew 1924: 86 (1924)

Common names Top

Add a new one! Suggest a correction!

Language Common/alternative name
Bengali কামদেব (উদ্ভিদ)
Bengali কামদেব
Kannada ಕೂವೆ ಮರ
Malayalam പുന്നപ്പൈൻ
Chinese 滇南红厚壳
Chinese 云南胡桐
Chinese 滇南紅厚殻

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!
No subspecies added yet.

Varieties (abbr. var.) Top

Add a new one! Suggest a correction!
No variety added yet.

Subvarieties (abbr. subvar.) Top

Add a new one! Suggest a correction!
No subvariety added yet.

Forms (abbr. f.) Top

Add a new one! Suggest a correction!
No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!
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
      • India
    • Indo-China
      • Cambodia
      • Laos
      • Myanmar
      • Thailand
      • Vietnam

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000581286
KEW urn:lsid:ipni.org:names:427265-1
The Plant List kew-2693442
Open Tree Of Life 3915311
NCBI Taxonomy 1679397
IPNI 427265-1
iNaturalist 569103
GBIF 5556276
USDA GRIN 411480
Wikipedia Calophyllum_polyanthum

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
Do carbon stocks and floristic diversity of tropical homegardens vary along an elevational gradient and based on holding size in central Kerala, India? Kumar BM Agrofor Syst 07-Apr-2023
PMCID:PMC10081327
doi:10.1007/s10457-023-00821-7
PMID:37193256
Siwalik plant megafossil diversity in the Eastern Himalayas: A review Khan MA, Mahato S, Spicer RA, Spicer TE, Ali A, Hazra T, Bera S Plant Divers 17-Dec-2022
PMCID:PMC10311196
doi:10.1016/j.pld.2022.12.003
PMID:37397603
Assessing the effectiveness of community managed forests for plant diversity conservation in Meghalaya, Northeast India Mir AH, Sarma K, Upadhaya K Plant Divers 15-Dec-2021
PMCID:PMC9209898
doi:10.1016/j.pld.2021.11.010
PMID:35769587
Naturally Occurring Calanolides: Occurrence, Biosynthesis, and Pharmacological Properties Including Therapeutic Potential Nahar L, Talukdar AD, Nath D, Nath S, Mehan A, Ismail FM, Sarker SD Molecules 28-Oct-2020
PMCID:PMC7663239
doi:10.3390/molecules25214983
PMID:33126458
The Arbuscular Mycorrhizal Fungus Funneliformis mosseae Alters Bacterial Communities in Subtropical Forest Soils during Litter Decomposition Gui H, Purahong W, Hyde KD, Xu J, Mortimer PE Front Microbiol 20-Jun-2017
PMCID:PMC5476864
doi:10.3389/fmicb.2017.01120
PMID:28676797
Arbuscular mycorrhiza enhance the rate of litter decomposition while inhibiting soil microbial community development Gui H, Hyde K, Xu J, Mortimer P Sci Rep 08-Feb-2017
PMCID:PMC5296878
doi:10.1038/srep42184
PMID:28176855
Photosynthesis and Photosynthetic Electron Flow in the Alpine Evergreen Species Quercus guyavifolia in Winter Huang W, Hu H, Zhang SB Front Plant Sci 20-Oct-2016
PMCID:PMC5071824
doi:10.3389/fpls.2016.01511
PMID:27812359
Molecular Mechanisms of Phosphorus Metabolism and Transport during Leaf Senescence Stigter KA, Plaxton WC Plants (Basel) 16-Dec-2015
PMCID:PMC4844268
doi:10.3390/plants4040773
PMID:27135351
Isolation, Bioactivity, and Production of ortho-Hydroxydaidzein and ortho-Hydroxygenistein Chang TS Int J Mol Sci 03-Apr-2014
PMCID:PMC4013590
doi:10.3390/ijms15045699
PMID:24705463
Medicinal plants from swidden fallows and sacred forest of the Karen and the Lawa in Thailand Junsongduang A, Balslev H, Inta A, Jampeetong A, Wangpakapattanawong P J Ethnobiol Ethnomed 24-Jun-2013
PMCID:PMC3702467
doi:10.1186/1746-4269-9-44
PMID:23800255
Chromanone Derivatives from the Pericarps of <i>Calophyllum polyanthum</i> Huan Wang, Qian‐Yun Sun, Fu‐Mei Yang, Chun‐Lin Long, Yue‐Hu Wang, Gui‐Hua Tang, Fu‐Wei Zhao, Hong‐Mei Niu, Qiao‐Qin Huang, Jin‐Jin Xu, Yusuke Wataya, Li‐Juan Ma Wiley 11-Nov-2010
doi:10.1002/HLCA.201000066
Monocyclic Phenolic Acids; Hydroxy- and Polyhydroxybenzoic Acids: Occurrence and Recent Bioactivity Studies Khadem S, Marles RJ Molecules 08-Nov-2010
PMCID:PMC6259451
doi:10.3390/molecules15117985
PMID:21060304
Two new 4-arylcoumarins from the seeds of Calophyllum polyanthum. Zhong H, Ruan JL, Yao QQ J Asian Nat Prod Res 01-Jul-2010
doi:10.1080/10286020.2010.484806
PMID:20628934
Two pyranocoumarins from the seeds of Calophyllum polyanthum. Ma CH, Chen B, Qi HY, Li BG, Zhang GL J Nat Prod 01-Sep-2004
doi:10.1021/NP0499158
PMID:15387670

Phytochemical Profile Top

Add a new one!
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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
Protocatechuic Acid 72 Click to see 154.12 unknown https://doi.org/10.1080/10286020.2010.484806
https://doi.org/10.1021/NP0499158
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
3,5-Dihydroxy-4-methoxybenzoic acid 78016 Click to see COC1=C(C=C(C=C1O)C(=O)O)O 184.15 unknown https://doi.org/10.1021/NP0499158
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Gallic acids
Gallic Acid 370 Click to see 170.12 unknown https://doi.org/10.1021/NP0499158
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
3,5-Dimethoxybenzoic Acid 14332 Click to see COC1=CC(=CC(=C1)C(=O)O)OC 182.17 unknown https://doi.org/10.1021/NP0499158
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / P-methoxybenzoic acids and derivatives
4-Methoxysalicylic Acid 75231 Click to see 168.15 unknown https://doi.org/10.1021/NP0499158
Isovanillic Acid 12575 Click to see 168.15 unknown https://doi.org/10.1080/10286020.2010.484806
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Ursolic Acid 64945 Click to see 456.70 unknown https://doi.org/10.1021/NP0499158
Urs-12-en-28-oic acid, 3-hydroxy-, (3beta)- 220774 Click to see 456.70 unknown https://doi.org/10.1021/NP0499158
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 Click to see 414.70 unknown https://doi.org/10.1021/NP0499158
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1021/NP0499158
beta-Sitosterol 3-O-beta-D-galactopyranoside 296119 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1021/NP0499158
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1021/NP0499158
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans
(3R)-3-[(2S,3R)-5-hydroxy-7-methoxy-2,3-dimethyl-8-(3-methylbut-2-enyl)-3,4-dihydro-2H-chromen-6-yl]hexanoic acid 163002112 Click to see 390.50 unknown https://doi.org/10.1002/HLCA.201000066
3-[5-hydroxy-7-methoxy-2,3-dimethyl-8-(3-methylbut-2-enyl)-3,4-dihydro-2H-chromen-6-yl]hexanoic acid 163002111 Click to see 390.50 unknown https://doi.org/10.1002/HLCA.201000066
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Chromones
(3R)-3-[(2R,3S)-5-hydroxy-7-methoxy-2,3-dimethyl-8-(3-methylbut-2-enyl)-4-oxo-2,3-dihydrochromen-6-yl]hexanoic acid 163188275 Click to see 404.50 unknown https://doi.org/10.1002/HLCA.201000066
3-[5-Hydroxy-7-methoxy-2,3-dimethyl-8-(3-methylbut-2-enyl)-4-oxo-2,3-dihydrochromen-6-yl]hexanoic acid 75576402 Click to see 404.50 unknown https://doi.org/10.1002/HLCA.201000066
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Pyranochromenes
(3R)-3-[(2R,3R)-5-hydroxy-2,3,8,8-tetramethyl-4-oxo-2,3-dihydropyrano[2,3-h]chromen-6-yl]octanoic acid 162889244 Click to see CCCCCC(CC(=O)O)C1=C2C(=C3C(=C1O)C(=O)C(C(O3)C)C)C=CC(O2)(C)C 416.50 unknown https://doi.org/10.1002/HLCA.201000066
(3R)-3-[(2R,3S)-5-hydroxy-2,3,8,8-tetramethyl-4-oxo-2,3-dihydropyrano[2,3-h]chromen-6-yl]octanoic acid 162889243 Click to see CCCCCC(CC(=O)O)C1=C2C(=C3C(=C1O)C(=O)C(C(O3)C)C)C=CC(O2)(C)C 416.50 unknown https://doi.org/10.1002/HLCA.201000066
(3R)-3-[(7R,8R)-5-hydroxy-2,2,7,8-tetramethyl-6-oxo-7,8-dihydropyrano[3,2-g]chromen-10-yl]-3-phenylpropanoic acid 162850349 Click to see 422.50 unknown https://doi.org/10.1002/HLCA.201000066
(3R)-3-[(7R,8S)-5-hydroxy-2,2,7,8-tetramethyl-6-oxo-7,8-dihydropyrano[3,2-g]chromen-10-yl]hexanoic acid 23250748 Click to see 388.50 unknown https://doi.org/10.1002/HLCA.201000066
(3R)-3-[(7R,8S)-5-hydroxy-2,2,7,8-tetramethyl-6-oxo-7,8-dihydropyrano[3,2-g]chromen-10-yl]octanoic acid 163030896 Click to see 416.50 unknown https://doi.org/10.1002/HLCA.201000066
(3S)-3-[(2S,3R)-5-hydroxy-2,3,8,8-tetramethyl-4-oxo-2,3-dihydropyrano[2,3-h]chromen-10-yl]hexanoic acid 162881125 Click to see CCCC(CC(=O)O)C1=CC(OC2=C1C3=C(C(=C2)O)C(=O)C(C(O3)C)C)(C)C 388.50 unknown https://doi.org/10.1002/HLCA.201000066
(3S)-3-[(7S,8S)-5-hydroxy-2,2,7,8-tetramethyl-6-oxo-7,8-dihydropyrano[3,2-g]chromen-10-yl]hexanoic acid 51414569 Click to see 388.50 unknown https://doi.org/10.1002/HLCA.201000066
3-(5-Hydroxy-2,2,7,8-tetramethyl-6-oxo-7,8-dihydropyrano[3,2-g]chromen-10-yl)-3-phenylpropanoic acid 12302861 Click to see 422.50 unknown https://doi.org/10.1002/HLCA.201000066
3-(5-Hydroxy-2,3,8,8-tetramethyl-4-oxo-2,3-dihydropyrano[2,3-h]chromen-10-yl)hexanoic acid 162881124 Click to see 388.50 unknown https://doi.org/10.1002/HLCA.201000066
3-(5-Hydroxy-2,3,8,8-tetramethyl-4-oxo-2,3-dihydropyrano[2,3-h]chromen-6-yl)octanoic acid 75576401 Click to see CCCCCC(CC(=O)O)C1=C2C(=C3C(=C1O)C(=O)C(C(O3)C)C)C=CC(O2)(C)C 416.50 unknown https://doi.org/10.1002/HLCA.201000066
CID 12300170 12300170 Click to see CCCCCC(CC(=O)O)C1=C2C(=C(C3=C1OC(C(C3=O)C)C)O)C=CC(O2)(C)C 416.50 unknown https://doi.org/10.1002/HLCA.201000066
Isoapetalic acid 341189 Click to see 388.50 unknown https://doi.org/10.1002/HLCA.201000066
methyl (3S)-3-[(7S,8S)-5-hydroxy-2,2,7,8-tetramethyl-6-oxo-7,8-dihydropyrano[3,2-g]chromen-10-yl]hexanoate 162921532 Click to see CCCC(CC(=O)OC)C1=C2C(=C(C3=C1OC(C(C3=O)C)C)O)C=CC(O2)(C)C 402.50 unknown https://doi.org/10.1002/HLCA.201000066
Methyl 3-(5-hydroxy-2,2,7,8-tetramethyl-6-oxo-7,8-dihydropyrano[3,2-g]chromen-10-yl)hexanoate 73802883 Click to see 402.50 unknown https://doi.org/10.1002/HLCA.201000066
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
Orobol 5281801 Click to see C1=CC(=C(C=C1C2=COC3=CC(=CC(=C3C2=O)O)O)O)O 286.24 unknown https://doi.org/10.1021/NP0499158
> Phenylpropanoids and polyketides / Neoflavonoids / Neoflavones
6,7-Dihydroxy-4-(4-methoxyphenyl)-2H-chromen-2-one 162920871 Click to see 284.26 unknown https://doi.org/10.1080/10286020.2010.484806
7-Hydroxy-4-(4-hydroxyphenyl)-6,8-dimethoxychromen-2-one 46856032 Click to see 314.29 unknown https://doi.org/10.1080/10286020.2010.484806
7-Hydroxy-4-(4-methoxyphenyl)chromen-2-one 5350173 Click to see 268.26 unknown https://doi.org/10.1080/10286020.2010.484806
7-Hydroxy-6,8-dimethoxy-4-(4-methoxyphenyl)chromen-2-one 46856033 Click to see 328.30 unknown https://doi.org/10.1080/10286020.2010.484806
> Phenylpropanoids and polyketides / Neoflavonoids / Prenylated neoflavonoids
(2R,3R,10R)-5-hydroxy-2,3-dimethyl-6-(3-methylbut-2-enyl)-10-phenyl-2,3,9,10-tetrahydropyrano[2,3-h]chromene-4,8-dione 162978900 Click to see CC1C(OC2=C(C1=O)C(=C(C3=C2C(CC(=O)O3)C4=CC=CC=C4)CC=C(C)C)O)C 406.50 unknown https://doi.org/10.1021/NP0499158
(2R,3S,10R)-5-hydroxy-2,3-dimethyl-6-(3-methylbut-2-enyl)-10-phenyl-2,3,9,10-tetrahydropyrano[2,3-h]chromene-4,8-dione 162978901 Click to see 406.50 unknown https://doi.org/10.1021/NP0499158
5-Hydroxy-2,3-dimethyl-6-(3-methylbut-2-enyl)-10-phenyl-2,3,9,10-tetrahydropyrano[2,3-h]chromene-4,8-dione 72747944 Click to see CC1C(OC2=C(C1=O)C(=C(C3=C2C(CC(=O)O3)C4=CC=CC=C4)CC=C(C)C)O)C 406.50 unknown https://doi.org/10.1021/NP0499158

Gallery Top

We don't have an image yet. Upload an image!

Contributors Top

No known contributors. Be the first!

Collections Top

In private collections 0
In public collections 0
You need to be authenticated in order to add this taxon to a personal collection.