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Uncaria callophylla

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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

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

Description Top

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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

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

Links to other databases Top

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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 CCC1CN2CCC3=C(C2CC1C(=COC)C(=O)OC)NC4=C3C(=CC=C4)O 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 CCC1CN2CCC3=C(C2CC1C(=COC)C(=O)OC)NC4=C3C=C(C=C4)O 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 COC=C(C1CC2C3=C(CCN2CC1C=C)C4=C(N3)C=CC=C4O)C(=O)OC 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 CCC1CN2CCC3=C(C2CC1C(=COC)C(=O)OC)NC4=C3C=C(C=C4)O 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 COC=C(C1CC2C3=C(CCN2CC1C=C)C4=C(N3)C=CC=C4O)C(=O)OC 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 CCC1CN2CCC3=C(C2CC1C(=COC)C(=O)OC)NC4=C3C=C(C=C4)O 384.50 unknown https://doi.org/10.1016/0031-9422(92)80356-J
> Alkaloids and derivatives / Yohimbine alkaloids
Amsonin 3058605 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
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 COC(=O)C1C(CCC2C1CC3C4=C(CCN3C2)C5=CC=CC=C5N4)O 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 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 (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 CCC1CN2CCC3=C(C2CC1C(=COC)C(=O)OC)NC4=C3C(=C(C=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
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 COC(=O)C1C(CCC2C1CC3C4=C(CCN3C2)C5=CC=CC=C5N4)O 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 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
Rauwolscine 643606 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
Yohimbine 8969 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
> 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 CCC1CN2CCC3(C2CC1C(=COC)C(=O)OC)C4=C(C=CC=C4O)NC3=O 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 CCC1CN2CCC3(C2CC1C(=COC)C(=O)OC)C4=C(C=CC=C4O)NC3=O 400.50 unknown https://doi.org/10.1016/0031-9422(92)80356-J
Rotundifoline 139055911 Click to see CCC1CN2CCC3(C2CC1C(=COC)C(=O)OC)C4=C(C=CC=C4O)NC3=O 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 CCC1CN2CCC3=C(C2CC1C(=COC)OC(=O)C)NC4=C3C(=CC=C4)O 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 CCC1CN2CCC3(C2CC1C(=COC)C(=O)OC)C4=C(C=CC=C4O)NC3=O 400.50 unknown https://doi.org/10.1016/0031-9422(92)80356-J

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