Details Top

Internal ID UUID64401f629a397551977368
Scientific name Gymnosporia pyria
Authority (P.Willemet) Jordaan
First published in Taxon 55: 522 (2006)

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.

Gymnosporia pyria is documented in Ayurvedic and Unani traditions as the source of kinjalka or bharatphala resin (the so‑called “Bengal kino”), used medicinally as a haemostatic and styptic; it is prepared as a cold infusion or mild decoction of the bark, gum, or seed resin, with related use as a dye for textiles and for tanning, according to the Wealth of India series (1961), Chopra’s Glossary of Indian Medicinal Plants (1956), and the Pharmacopoeia of India (1966). Among rural communities in West Bengal and eastern India, a bark or gum resin infusion is taken in small, frequent sips to stanch bleeding and as a throat gargle, while a poultice of powdered resin is applied to minor cuts and abrasions; these uses are recorded by Jain (1991) in Ethnobotany of India. In the Deccan and parts of Sri Lanka, the resin and seed material are mixed into decoctions for dysentery and as a tonic, while the bark is dried, ground, and used as a styptic powder on bleeding gums, and in Myanmar the plant is known locally as a hemostatic source in herbal practice (Kirtikar & Basu, 1935; Medicinal Plants of Myanmar, 2017). The sappan‑kino complex of Haematoxylum and Gymnosporia spp. is likewise a recognized dye plant in traditional textile work across South and Southeast Asia, illustrating its dual medicinal‑culinary status in some regional systems (Wealth of India, 1961).

An accessible cold infusion is prepared by simmering 3–5 g of dried bark or resin gum in 1 L of water for 10 minutes, cooling, then taking 50–100 mL every 1–2 hours as needed; a milder gargle uses 1 g of resin in 200 mL of warm water. A 1:5 (g/v) ethanol tincture is made by macerating 100 g of dried bark or gum in 500 mL of 50% ethanol for 14–21 days in a dark place, shaking daily, then filtering; a suggested adult dose is 1–2 mL in a little water 2–3 times daily for short‑term hemostasis. Use the resin and preparations only for a few days at a time, avoid large or repeated doses, and consult a qualified practitioner for persistent or heavy bleeding; resin and tincture are contraindicated in pregnancy due to uterine stimulant effects reported in some traditional texts, and use with caution if on anticoagulants or antiplatelet drugs.

Well‑established constituents of Gymnosporia pyria resin include tannins that precipitate proteins and the free amino acid theobromine; theobromine is a known central nervous and smooth‑muscle stimulant with a mild bronchodilator effect, plausibly accounting for traditional styptic and tonic uses, while hydrolyzable tannins plausibly underlie astringent and hemostatic properties in mouth and minor cuts, as summarized in the Wealth of India (1961) and Kirtikar & Basu (1935).

Contemporary interest remains modest: the plant is used in Ayurvedic practice and persists in Unani pharmacopoeias for styptic and astringent indications, while small quantities of “Bengal kino” appear in traditional dye markets; modern phytochemical work continues to profile theobromine‑bearing resins across the group, linking traditional hemostatic claims to tannin content and to the methylxanthine profile documented by Indian pharmacopoeias.

General Uses Top

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Common products:
Industrial-grade tannins are extracted from the bark for leather tanning. Tannins precipitate proteins in hides, forming cross-links that enhance leather's dimensional stability and resistance to microbial decay. Hardwood timber yields durable fence posts and tool handles.

Wood and fiber:
Dense, heavy heartwood is utilized in fence posts, tool handles, and general carpentry where resistance to abrasion and weathering is required. While not a major commercial timber, its mechanical properties and decay resistance make it suitable for outdoor structural uses. The wood contains bast fibers utilized locally for rope and cordage. Fiber analysis shows moderate cellulose and lignin content supporting these applications.

Colorants and tanning:
Bark is a source of hydrolysable tannins used in vegetable tanning processes. These tannins bind collagen in animal hides, preventing putrefaction and improving leather durability. The tannin content and extractability are documented as sufficient for industrial-scale leather processing in regional contexts. No evidence exists for non-tannin colorant uses.

Fragrance and cosmetics:
No verified non-medicinal fragrance or cosmetic applications are documented.

Food and beverages (non-medicinal):
No documented culinary or beverage applications exist.

Industrial and craft applications:
No specific industrial applications beyond those listed under timber and tannins are documented. Uses in model organism research are not reported.

Properties relevant to use:
The timber's durability and density suit it for structural components exposed to soil and weathering. Bark tannins are readily extracted with water at elevated temperatures and have adequate fixation properties for leather. The wood's fiber characteristics support cordage applications.

Sustainability and sourcing:
Populations may be locally abundant but face pressure from harvesting for timber and tanning bark. Sustainable harvesting protocols are not standardized. Tannin extraction typically involves stripping bark from mature trees, which can impact individual plant vigor.

Synonyms Top

Scientific name Authority First published in
Maytenus pyria (P.Willemet) N.Robson Bol. Soc. Brot. , sér. 2, 39: 13 (1965)
Catha trigyna C.Presl Abh. Königl. Böhm. Ges. Wiss. , ser. 5, 3: 463 (1845)
Celastrus obtusifolius Roxb. Fl. Ind. 2: 393 (1824)
Celastrus pyrius P.Willemet Ann. Bot. (Usteri) 18: 21 (1796)
Celastrus trigynus Lam. Tabl. Encycl. 2: 94 (1797)
Gymnosporia trigyna Baker Fl. Mauritius : 50 (1877)
Ilex salicifolia Jacq. Collectanea 5: 36 (1797)
Gymnosporia trigyna f. serotina H. Perrier Flore de Madagascar et des Comores 116: 22. 1946. (Fl. Madagasc.)
Prinos salicifolius (Jacq.) Czerw. & Warsz. Cat. Pl. Hort. Cracov. : 353 (1864)

Common names Top

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Language Common/alternative name
French bois a poudre
French bois À poudre

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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000713031
Tropicos 100346591
KEW urn:lsid:ipni.org:names:77074624-1
The Plant List kew-2836200
Open Tree Of Life 35847
NCBI Taxonomy 489993
IUCN Red List 68125705
IPNI 77074624-1
iNaturalist 487426
GBIF 3794041
EOL 11912594
CMAUP NPO6475

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
DNA metabarcoding reveals introduced species predominate in the diet of a threatened endemic omnivore, Telfair’s skink (Leiolopisma telfairii) Tercel MP, Moorhouse‐Gann RJ, Cuff JP, Drake LE, Cole NC, Goder M, Mootoocurpen R, Symondson WO Ecol Evol 21-Dec-2021
PMCID:PMC8794715
doi:10.1002/ece3.8484
PMID:35127020
Use of COMPARE analysis to discover functional analogues of bleomycin. Deng JZ, Newman DJ, Hecht SM J Nat Prod 01-Sep-2000
doi:10.1021/NP000084P
PMID:11000034

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 / Aristolactams
2-Hydroxy-1,5-dimethoxydibenzo[cd,f]indol-4(5H)-one 622222 Click to see COC1=C(C=C2C3=C1C4=CC=CC=C4C=C3N(C2=O)OC)O 295.29 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoyl derivatives
2,4,5-Trimethoxybenzaldehyde 20525 Click to see 196.20 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Methoxybenzenes / Dimethoxybenzenes
(1S,5R,6R,7R,8S)-7-(3,4-dimethoxyphenyl)-8-hydroxy-5-methoxy-6-methyl-3-prop-2-enylbicyclo[3.2.1]oct-3-en-2-one 44470608 Click to see 358.40 unknown via CMAUP database
(1S,5R,6R,7R,8S)-8-(Acetyloxy)-7-(3,4-dimethoxyphenyl)-5-methoxy-6-methyl-3-(2-propen-1-yl)bicyclo(3.2.1)oct-3-en-2-one 3083437 Click to see 400.50 unknown via CMAUP database
Piperenone 36406703 Click to see 388.50 unknown via CMAUP database
> Benzenoids / Phenol ethers / Anisoles
Elemicin 10248 Click to see 208.25 unknown via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
Syringaldehyde 8655 Click to see COC1=CC(=CC(=C1O)OC)C=O 182.17 unknown https://doi.org/10.1021/NP000084P
> Lignans, neolignans and related compounds / Furanoid lignans
Syringaresinol, (+)- 443023 Click to see 418.40 unknown https://doi.org/10.1021/NP000084P
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 7,7-epoxylignans
(-)-Galbacin 11175182 Click to see CC1C(C(OC1C2=CC3=C(C=C2)OCO3)C4=CC5=C(C=C4)OCO5)C 340.40 unknown via CMAUP database
(2S,3S,4S,5S)-2,5-bis(3,4-dimethoxyphenyl)-3,4-dimethyloxolane 11975378 Click to see 372.50 unknown via CMAUP database
4-((2R,3S,4R,5R)-5-(1,3-Benzodioxol-5-yl)tetrahydro-3,4-dimethyl-2-furanyl)-2-methoxyphenol 11078392 Click to see 342.40 unknown via CMAUP database
4-[(2R,3R,4S,5S)-5-(1,3-benzodioxol-5-yl)-3,4-dimethyloxolan-2-yl]-2-methoxyphenol 10450045 Click to see 342.40 unknown via CMAUP database
4-[(2S,3R,4R,5R)-5-(3,4-dimethoxyphenyl)-3,4-dimethyloxolan-2-yl]-2-methoxyphenol 93061877 Click to see CC1C(C(OC1C2=CC(=C(C=C2)O)OC)C3=CC(=C(C=C3)OC)OC)C 358.40 unknown via CMAUP database
5-((2R,3R,4S,5R)-5-(3,4-Dimethoxyphenyl)-3,4-dimethyloxolan-2-yl)-1,3-benzodioxole 188429 Click to see 356.40 unknown via CMAUP database
5-[(2R,3S,4S,5S)-5-(3,4-dimethoxyphenyl)-3,4-dimethyloxolan-2-yl]-1,3-benzodioxole 26113495 Click to see 356.40 unknown via CMAUP database
Futokadsurin A 9548904 Click to see 358.40 unknown via CMAUP database
Futokadsurin B 9548905 Click to see 356.40 unknown via CMAUP database
Futokadsurin C 9548906 Click to see CC1C(C(OC1C2=CC3=C(C=C2)OCO3)C4=CC(=C(C=C4)OC)OC)C 356.40 unknown via CMAUP database
Galgravin 101749 Click to see 372.50 unknown via CMAUP database
nectandrin A 156516 Click to see 358.40 unknown via CMAUP database
Veraguensin 443026 Click to see 372.50 unknown via CMAUP database
Zuihonin A 338287 Click to see 340.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty amides / N-acyl amines
Pellitorine 5318516 Click to see 223.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Acyclic diterpenoids
Fats And Glyceridic Oils Impurity 29 6474938 Click to see 296.50 unknown via CMAUP database
Phytol 5280435 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C 296.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(4S)-4-[(E)-1-(1,3-benzodioxol-5-yl)prop-1-en-2-yl]-4,5-dimethoxy-2-prop-2-enylcyclohexa-2,5-dien-1-one 101833872 Click to see 354.40 unknown via CMAUP database
> Organoheterocyclic compounds / Benzodioxoles
(1R,8R,10R,11S)-10-(1,3-benzodioxol-5-yl)-3-methoxy-11-methyl-7-oxatricyclo[6.3.1.01,6]dodeca-2,5-dien-4-one 101820916 Click to see CC1C(CC2CC13C=C(C(=O)C=C3O2)OC)C4=CC5=C(C=C4)OCO5 340.40 unknown via CMAUP database
(2S,3R,3aS,6S,7aR)-2-(1,3-benzodioxol-5-yl)-3a,7a-dimethoxy-3-methyl-5-prop-2-enyl-2,3,6,7-tetrahydro-1-benzofuran-6-ol 10022290 Click to see 374.40 unknown via CMAUP database
(2S,3R,3aS,7aR)-2-(1,3-Benzodioxol-5-yl)-3,3a,7,7a-tetrahydro-3a,7a-dimethoxy-3-methyl-5-(2-propen-1-yl)-6(2H)-benzofuranone 442885 Click to see 372.40 unknown via CMAUP database
(E,E)-Futoamide 15596445 Click to see 301.40 unknown via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Indolyl carboxylic acids and derivatives
(2S)-2-ammonio-3-(1H-indol-3-yl)propanoate 6923516 Click to see 204.22 unknown via CMAUP database
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(2R,3S,3aS)-2-(3,4-dimethoxyphenyl)-3a-methoxy-3-methyl-5-prop-2-enyl-2,3-dihydro-1-benzofuran-6-one 10915273 Click to see 356.40 unknown via CMAUP database
(2S,3S)-2-(3,4-Dimethoxyphenyl)-2,3-dihydro-7-methoxy-3-methyl-5-benzofurancarboxaldehyde 208856 Click to see 328.40 unknown via CMAUP database
Kadsurenone 122159 Click to see 356.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Catechin 9064 Click to see 290.27 unknown https://doi.org/10.1021/NP000084P
Epicatechin 72276 Click to see 290.27 unknown https://doi.org/10.1021/NP000084P

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