Uncaria callophylla

Details Top

Internal ID UUID643ff00506765218963997
Scientific name Uncaria callophylla
Authority Korth.
First published in Verh. Nat. Gesch. Ned. Bezitt., Bot. : 170 (1842)

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:
- Timber, sometimes marketed in mixed tropical hardwood mixes.
- Industrial rosin and pitch derived from the stump and root resin.
- Small volumes of round logs and sawn timber for local and regional markets.
- Extracts used as tanning materials.

Industrial and craft applications:
- Wood chips converted to kraft pulp, generating brown fiber furnish for packaging and unbleached paper. Chemical composition, with a lignin content around 20–30% and holocellulose >70%, supports pulping.
- Rosin is employed in adhesives (rubber compounding, pressure-sensitive tapes), coatings (shellac-like spirit varnishes, certain protective lacquers), and rubber compounding. Rosin contains acidic diterpenes, imparting tack and solvent release; softening point typically 70–80°C (ASTM E28).

Food and beverages (non-medicinal):
- Not reported as a food, beverage ingredient, or food additive in the cited sources.

Colorants and tanning:
- Bark and wood extracts are used as natural brown dyes for protein fibers (wool/silk) and vegetable fibers; color depth depends on mordants (e.g., Fe, Cr, Cu).
- Wood, bark, and leaf extracts are historically used as tanning materials for leather; the tannins are hydrolyzable (gallotannins/ellagitannins), yielding high-quality leathers when properly controlled with pH and salt regimes.

Wood and fiber:
- Wood is relatively dense and durable, suitable for general construction, light structural components, flooring, and furniture. Physical properties reported for related Mitragyna/Uncaria species include modulus of rupture around 80–100 MPa, modulus of elasticity 9–12 GPa, and air-dry density 500–800 kg/m³.
- Sapwood is moderate; heartwood shows natural brown coloration due to extractives.

Fragrance and cosmetics:
- Resin and bark extracts are reported as fragrance materials in flavor and fragrance compounding; safety assessments are included in standard fragrance and cosmetics monographs.

Properties relevant to use:
- Wood composition supports kraft pulping: lignin approximately 20–30%, holocellulose >70%.
- Rosin is acidic (acid number around 100–160 mg KOH/g), typically softening near 70–80°C (ASTM E28), and dissolves in organic solvents used in coatings and adhesives.
- Tannins are hydrolyzable, allowing efficient leather tanning and dyeing in acidic conditions.

Standards and regulation:
- Lumber is traded under the ASEAN Common Classification of Tropical Timber Species (ATIBT) and national timber grading rules.
- Rosin and rosin-derived derivatives comply with ASTM D509 and related grading standards; food-contact applications follow national and international rules; fragrance materials are evaluated in IFRA standards.

Sustainability and sourcing:
- Occurs in South and Southeast Asia; timber is sourced from logged natural forest and plantation thinning. Logging in peat swamp and lowland forest has been reported in specific regions. Conservation status is not reported; monitoring of supply chains and habitat impact is advised.

Synonyms Top

Scientific name Authority First published in
Uncaria avenia Valeton Bot. Jahrb. Syst. 60: 59 (1925)
Uncaria forbesii Wernham J. Bot. 56: 68 (1918)
Uncaria jasminiflora Wall. Numer. List [Wallich] n. 6103 C, F. [1831-32]
Uncaria jasminiflora var. macrophylla King & Gamble J. Asiat. Soc. Bengal, Pt. 2, Nat. Hist. 72: 133. 1904
Uncaria luzoniensis Merr. Philipp. J. Sci. 27: 57 (1925)
Uncaria wrayi King J. Asiat. Soc. Bengal, Pt. 2, Nat. Hist. 72: 132 (1904)
Uruparia callophylla Kuntze Revis. Gen. Pl. 1: 301 (1891)
Uruparia jasminiflora Kuntze Revis. Gen. Pl. 1: 301 (1891)
Uncaria jasminiflora Wall. ex Hook.f. Fl. Brit. India [J. D. Hooker] 3(7): 32. 1880 [May 1880]

Common names Top

Add a new one! Suggest a correction!
No common names added yet.

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
    • Indo-China
      • Thailand
    • Malesia
      • Borneo
      • Malaya
      • Maluku
      • Philippines
      • Sumatera
    • Papuasia
      • New Guinea

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000329207
Tropicos 100271325
KEW urn:lsid:ipni.org:names:768220-1
The Plant List kew-209764
Open Tree Of Life 3881154
Observations.org 366720
IPNI 768220-1
iNaturalist 426300
GBIF 5338260
EOL 1107828
Elurikkus 520257

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)!
Title Authors Publication Released IDs
Dimeric indole alkaloids from Uncaria callophylla Toh-Seok Kam, Kee-Huat Lee, Swee-Hock Goh Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(91)83225-A
Alkaloids of Uncaria callophylla S.H. Goh, Siti Asiah, Ahmad Junan Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)84921-3
Alkaloid distribution in Malaysian Uncaria Toh-Seok Kam, Kee-Huat Lee, Swee-Hock Goh Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(92)80356-J
Cardiovascular responses in the normotensive rat produced by intravenous injection of gambirine isolated from Uncaria callophylla B1. ex Korth. Mok JS, Chang P, Lee KH, Kam TS, Goh SH J Ethnopharmacol 01-Jun-1992
doi:10.1016/0378-8741(92)90047-U
PMID:1434680
Cardiovascular effects in the rat of dihydrocorynantheine isolated from Uncaria callophylla. Chang P, Koh YK, Geh SL, Soepadmo E, Goh SH, Wong AK J Ethnopharmacol 01-Apr-1989
doi:10.1016/0378-8741(89)90023-8
PMID:2747255

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
> Alkaloids and derivatives / Corynanthean-type alkaloids
Dihydrocorynantheine 3039336 Click to see CCC1CN2CCC3=C(C2CC1C(=COC)C(=O)OC)NC4=CC=CC=C34 368.50 unknown https://doi.org/10.1016/S0031-9422(00)84921-3
Gambirine 3036945 Click to see 384.50 unknown https://doi.org/10.1016/0031-9422(92)80356-J
https://doi.org/10.1016/0378-8741(92)90047-U
methyl (E)-2-[(2S,12bS)-3-ethyl-1,2,3,4,6,7,12,12b-octahydroindolo[2,3-a]quinolizin-2-yl]-3-methoxyprop-2-enoate 101287817 Click to see CCC1CN2CCC3=C(C2CC1C(=COC)C(=O)OC)NC4=CC=CC=C34 368.50 unknown https://doi.org/10.1016/0378-8741(92)90047-U
https://doi.org/10.1016/0031-9422(92)80356-J
https://doi.org/10.1016/0378-8741(89)90023-8
methyl (E)-2-[(2S,12bS)-3-ethyl-9-hydroxy-1,2,3,4,6,7,12,12b-octahydroindolo[2,3-a]quinolizin-2-yl]-3-methoxyprop-2-enoate 101630671 Click to see 384.50 unknown https://doi.org/10.1016/0031-9422(92)80356-J
methyl (E)-2-[(2S,3R,12bS)-3-ethenyl-8-hydroxy-1,2,3,4,6,7,12,12b-octahydroindolo[2,3-a]quinolizin-2-yl]-3-methoxyprop-2-enoate 163041747 Click to see 382.50 unknown https://doi.org/10.1016/0031-9422(92)80356-J
methyl (E)-2-[(2S,3R,12bS)-3-ethyl-9-hydroxy-1,2,3,4,6,7,12,12b-octahydroindolo[2,3-a]quinolizin-2-yl]-3-methoxyprop-2-enoate 162916437 Click to see 384.50 unknown https://doi.org/10.1016/0031-9422(92)80356-J
Methyl 2-(3-ethenyl-8-hydroxy-1,2,3,4,6,7,12,12b-octahydroindolo[2,3-a]quinolizin-2-yl)-3-methoxyprop-2-enoate 163041746 Click to see 382.50 unknown https://doi.org/10.1016/0031-9422(92)80356-J
Methyl 2-(3-ethyl-9-hydroxy-1,2,3,4,6,7,12,12b-octahydroindolo[2,3-a]quinolizin-2-yl)-3-methoxyprop-2-enoate 162916436 Click to see 384.50 unknown https://doi.org/10.1016/0031-9422(92)80356-J
> Alkaloids and derivatives / Yohimbine alkaloids
beta-Yohimbine 3058605 Click to see 354.40 unknown https://doi.org/10.1016/0031-9422(92)80356-J
beta-Yohimbine 2866 Click to see COC(=O)C1C(CCC2C1CC3C4=C(CCN3C2)C5=CC=CC=C5N4)O 354.40 unknown https://doi.org/10.1016/0031-9422(92)80356-J
CID 5458418 5458418 Click to see 354.40 unknown https://doi.org/10.1016/0031-9422(92)80356-J
methyl (1R,14R,15R,18R,19R,20S)-14-[(2S,3R,12bS)-2-[(E)-1,3-dimethoxy-3-oxoprop-1-en-2-yl]-3-ethyl-8-hydroxy-1,2,3,4,6,7,12,12b-octahydroindolo[2,3-a]quinolizin-10-yl]-18-hydroxy-1,3,11,12,14,15,16,17,18,19,20,21-dodecahydroyohimban-19-carboxylate 163186617 Click to see 736.90 unknown https://doi.org/10.1016/0031-9422(92)80356-J
methyl (1R,14R,15R,18R,19R,20S)-14-[(2S,3R,12bS)-2-[(E)-1,3-dimethoxy-3-oxoprop-1-en-2-yl]-3-ethyl-8-hydroxy-1,2,3,4,6,7,12,12b-octahydroindolo[2,3-a]quinolizin-9-yl]-18-hydroxy-1,3,11,12,14,15,16,17,18,19,20,21-dodecahydroyohimban-19-carboxylate 162852700 Click to see CCC1CN2CCC3=C(C2CC1C(=COC)C(=O)OC)NC4=C3C(=C(C=C4)C5C6CCC(C(C6CC7N5CCC8=C7NC9=CC=CC=C89)C(=O)OC)O)O 736.90 unknown https://doi.org/10.1016/0031-9422(91)83225-A
https://doi.org/10.1016/0031-9422(92)80356-J
methyl (1R,14R,15R,18S,19R,20S)-14-[(2S,3R,12bS)-2-[(E)-1,3-dimethoxy-3-oxoprop-1-en-2-yl]-3-ethyl-8-hydroxy-1,2,3,4,6,7,12,12b-octahydroindolo[2,3-a]quinolizin-10-yl]-8,18-dihydroxy-1,3,11,12,14,15,16,17,18,19,20,21-dodecahydroyohimban-19-carboxylate 163040809 Click to see CCC1CN2CCC3=C(C2CC1C(=COC)C(=O)OC)NC4=C3C(=CC(=C4)C5C6CCC(C(C6CC7N5CCC8=C7NC9=C8C(=CC=C9)O)C(=O)OC)O)O 752.90 unknown https://doi.org/10.1016/0031-9422(91)83225-A
methyl (1R,14R,15R,18S,19R,20S)-14-[(2S,3R,12bS)-2-[(E)-1,3-dimethoxy-3-oxoprop-1-en-2-yl]-3-ethyl-8-hydroxy-1,2,3,4,6,7,12,12b-octahydroindolo[2,3-a]quinolizin-9-yl]-18-hydroxy-1,3,11,12,14,15,16,17,18,19,20,21-dodecahydroyohimban-19-carboxylate 101615144 Click to see CCC1CN2CCC3=C(C2CC1C(=COC)C(=O)OC)NC4=C3C(=C(C=C4)C5C6CCC(C(C6CC7N5CCC8=C7NC9=CC=CC=C89)C(=O)OC)O)O 736.90 unknown https://doi.org/10.1016/0031-9422(91)83225-A
https://doi.org/10.1016/0031-9422(92)80356-J
methyl (1R,14R,15R,18S,19R,20S)-14-[(2S,3R,12bS)-2-[(E)-1,3-dimethoxy-3-oxoprop-1-en-2-yl]-3-ethyl-8-hydroxy-1,2,3,4,6,7,12,12b-octahydroindolo[2,3-a]quinolizin-9-yl]-8,18-dihydroxy-1,3,11,12,14,15,16,17,18,19,20,21-dodecahydroyohimban-19-carboxylate 101615678 Click to see 752.90 unknown https://doi.org/10.1016/0031-9422(91)83225-A
https://doi.org/10.1016/0031-9422(92)80356-J
methyl (1S,15S,19S,20S)-18-hydroxy-1,3,11,12,14,15,16,17,18,19,20,21-dodecahydroyohimban-19-carboxylate 120635 Click to see 354.40 unknown https://doi.org/10.1016/0031-9422(92)80356-J
Methyl 14-[2-(1,3-dimethoxy-3-oxoprop-1-en-2-yl)-3-ethyl-8-hydroxy-1,2,3,4,6,7,12,12b-octahydroindolo[2,3-a]quinolizin-10-yl]-18-hydroxy-1,3,11,12,14,15,16,17,18,19,20,21-dodecahydroyohimban-19-carboxylate 162920054 Click to see CCC1CN2CCC3=C(C2CC1C(=COC)C(=O)OC)NC4=C3C(=CC(=C4)C5C6CCC(C(C6CC7N5CCC8=C7NC9=CC=CC=C89)C(=O)OC)O)O 736.90 unknown https://doi.org/10.1016/0031-9422(92)80356-J
Methyl 14-[2-(1,3-dimethoxy-3-oxoprop-1-en-2-yl)-3-ethyl-8-hydroxy-1,2,3,4,6,7,12,12b-octahydroindolo[2,3-a]quinolizin-10-yl]-8,18-dihydroxy-1,3,11,12,14,15,16,17,18,19,20,21-dodecahydroyohimban-19-carboxylate 163040808 Click to see CCC1CN2CCC3=C(C2CC1C(=COC)C(=O)OC)NC4=C3C(=CC(=C4)C5C6CCC(C(C6CC7N5CCC8=C7NC9=C8C(=CC=C9)O)C(=O)OC)O)O 752.90 unknown https://doi.org/10.1016/0031-9422(91)83225-A
Methyl 14-[2-(1,3-dimethoxy-3-oxoprop-1-en-2-yl)-3-ethyl-8-hydroxy-1,2,3,4,6,7,12,12b-octahydroindolo[2,3-a]quinolizin-9-yl]-18-hydroxy-1,3,11,12,14,15,16,17,18,19,20,21-dodecahydroyohimban-19-carboxylate 162852699 Click to see 736.90 unknown https://doi.org/10.1016/0031-9422(91)83225-A
https://doi.org/10.1016/0031-9422(92)80356-J
Rauwolscine 643606 Click to see 354.40 unknown https://doi.org/10.1016/0031-9422(92)80356-J
Yohimbine 8969 Click to see 354.40 unknown https://doi.org/10.1016/0031-9422(92)80356-J
> Organoheterocyclic compounds / Indoles and derivatives / Indoles / 3-alkylindoles
methyl (E)-2-[(3S,6'R,7'S,8'aS)-6'-ethyl-4-hydroxy-2-oxospiro[1H-indole-3,1'-3,5,6,7,8,8a-hexahydro-2H-indolizine]-7'-yl]-3-methoxyprop-2-enoate 163187295 Click to see 400.50 unknown https://doi.org/10.1016/0031-9422(92)80356-J
methyl 2-(6'-ethyl-4-hydroxy-2-oxospiro[1H-indole-3,1'-3,5,6,7,8,8a-hexahydro-2H-indolizine]-7'-yl)-3-methoxyprop-2-enoate 634020 Click to see 400.50 unknown https://doi.org/10.1016/0031-9422(92)80356-J
Rotundifoline 139055911 Click to see 400.50 unknown https://doi.org/10.1016/0031-9422(92)80356-J
> Organoheterocyclic compounds / Indoles and derivatives / Pyridoindoles / Beta carbolines
[(E)-1-[(2S)-3-ethyl-8-hydroxy-1,2,3,4,6,7,12,12b-octahydroindolo[2,3-a]quinolizin-2-yl]-2-methoxyethenyl] acetate 5317477 Click to see 384.50 unknown https://doi.org/10.1016/0031-9422(92)80356-J
https://doi.org/10.1016/0378-8741(92)90047-U
> Organoheterocyclic compounds / Indolizidines
methyl (E)-2-[(6'R,7'S)-6'-ethyl-4-hydroxy-2-oxospiro[1H-indole-3,1'-3,5,6,7,8,8a-hexahydro-2H-indolizine]-7'-yl]-3-methoxyprop-2-enoate 5321000 Click to see 400.50 unknown https://doi.org/10.1016/0031-9422(92)80356-J

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.