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Uncaria attenuata

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID643ff004715d9551157727
Scientific name Uncaria attenuata
Authority Korth.
First published in Verh. Nat. Gesch. Ned. Bezitt., Bot. : 170 (1842)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Nauclea attenuata Walp. Repert. Bot. Syst. 2: 513 (1843)
Uncaria bulusanensis Elmer Leafl. Philipp. Bot. 9: 3271 (1934)
Uncaria athemiata Treub Ann. Jard. Bot. Buitenzorg 3: 52 (1883)
Uruparia attenuata Kuntze Revis. Gen. Pl. 1: 301 (1891)

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
      • Andaman Islands
      • Thailand
    • Malesia
      • Borneo
      • Jawa
      • Malaya
      • Philippines
      • Sulawesi
      • Sumatera

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000329196
Tropicos 100271318
KEW urn:lsid:ipni.org:names:768211-1
The Plant List kew-209754
Open Tree Of Life 3881133
NCBI Taxonomy 1840405
IPNI 768211-1
iNaturalist 426299
GBIF 5338153
EOL 1107373

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
Natural Corynanthe-Type Cholinesterase Inhibitors from Malaysian Uncaria attenuata Korth.: Isolation, Characterization, In Vitro and In Silico Studies Chear NJ, Ching-Ga TA, Khaw KY, León F, Tan WN, Yusof SR, McCurdy CR, Murugaiyah V, Ramanathan S Metabolites 07-Mar-2023
PMCID:PMC10059728
doi:10.3390/metabo13030390
PMID:36984830
Natural Products for the Prevention and Control of the COVID-19 Pandemic: Sustainable Bioresources Singla RK, He X, Chopra H, Tsagkaris C, Shen L, Kamal MA, Shen B Front Pharmacol 01-Dec-2021
PMCID:PMC8671886
doi:10.3389/fphar.2021.758159
PMID:34925017
Secondary Metabolites from Rubiaceae Species Martins D, Nunez CV Molecules 22-Jul-2015
PMCID:PMC6331836
doi:10.3390/molecules200713422
PMID:26205062
Structure and synthesis of two new types of oxindole alkaloids found from Uncaria salaccensis. Dhavadee PONGLUX, Sumphan WONGSERIPIPATANA, Norio AIMI, Masashi NISHIMURA, Midori ISHIKAWA, Hiroyuki SADA, Joju HAGINIWA, Shin-ichiro SAKAI Pharmaceutical Society of Japan 08-Dec-2011
doi:10.1248/CPB.38.573
Alkaloids of Uncaria P. Tantivatana, D. Ponglux, S. Wongseripipatana, J. Phillipson Georg Thieme Verlag KG 07-Nov-2008
doi:10.1055/S-2008-1074973
Determinação por RMN das configurações relativas e conformações de alcalóides oxindólicos isolados de Uncaria guianensis Carlos Alberto Carbonezi, Lidilhone Hamerski, Otavio Aparecido Flausino Jr., Maysa Furlan, Vanderlan da Silva Bolzani, Maria Claudia Marx Young FapUNIFESP (SciELO) 26-Apr-2005
doi:10.1590/S0100-40422004000600007
Alkaloids of Uncaria attenuata from Thailand Dhavadee Ponglux, Tanomjit Supavita, Robert Verpoorte, David Phillipson Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(80)83025-1
Alkaloids of Uncaria attenuata, U. orientalis and U. Canescens J. David Phillipson, Sarah R. Hemingway Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(75)85310-6

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 / Corynanthean-type alkaloids
methyl (E)-2-[(2R,3R,12bR)-3-ethenyl-1,2,3,4,6,7,12,12b-octahydroindolo[2,3-a]quinolizin-2-yl]-3-methoxyprop-2-enoate 163191295 Click to see COC=C(C1CC2C3=C(CCN2CC1C=C)C4=CC=CC=C4N3)C(=O)OC 366.50 unknown https://doi.org/10.1016/0031-9422(75)85310-6
Methyl 2-(3-ethenyl-1,2,3,4,6,7,12,12b-octahydroindolo[2,3-a]quinolizin-2-yl)-3-methoxyprop-2-enoate 3281521 Click to see COC=C(C1CC2C3=C(CCN2CC1C=C)C4=CC=CC=C4N3)C(=O)OC 366.50 unknown https://doi.org/10.1016/0031-9422(75)85310-6
> Alkaloids and derivatives / Yohimbine alkaloids
19-Epiajmalicine 179460 Click to see 352.40 unknown https://doi.org/10.1590/S0100-40422004000600007
3-Isoajmalicine 11416867 Click to see CC1C2CN3CCC4=C(C3CC2C(=CO1)C(=O)OC)NC5=CC=CC=C45 352.40 unknown https://doi.org/10.1055/S-2008-1074973
Hbpnzwwaqvkypj-rvxzydepsa- 21636096 Click to see CC1C2CN3CCC4=C(C3C(C2C(=CO1)C(=O)OC)O)NC5=CC=CC=C45 368.40 unknown https://doi.org/10.1016/0031-9422(80)83025-1
Lamuran 251561 Click to see CC1C2CN3CCC4=C(C3CC2C(=CO1)C(=O)OC)NC5=CC=CC=C45 352.40 unknown https://doi.org/10.1016/0031-9422(80)83025-1
methyl (1S,15S,16R,20S,21R)-21-hydroxy-16-methyl-17-oxa-3,13-diazapentacyclo[11.8.0.02,10.04,9.015,20]henicosa-2(10),4,6,8,18-pentaene-19-carboxylate 21586699 Click to see 368.40 unknown https://doi.org/10.1016/0031-9422(80)83025-1
Methyl-14-hydroxy-19-methyl-16,17-didehydro-18-oxayohimban-16 carboxylate 73806793 Click to see 368.40 unknown https://doi.org/10.1016/0031-9422(80)83025-1
Rauniticine 72338 Click to see 352.40 unknown https://doi.org/10.1016/0031-9422(80)83025-1
Tetrahydroalstonine 72340 Click to see CC1C2CN3CCC4=C(C3CC2C(=CO1)C(=O)OC)NC5=CC=CC=C45 352.40 unknown https://doi.org/10.1016/0031-9422(80)83025-1
> Organic acids and derivatives / Peptidomimetics / Depsipeptides / Cyclic depsipeptides
cyclo[N(Me)Ile-ObAla(2R-Me,3S-pentyl)-Val-N(Me)Phe-OVal-Pro] 162925012 Click to see 741.00 unknown https://doi.org/10.1248/CPB.38.573
> Organoheterocyclic compounds / Indoles and derivatives / Indolines
Ytwqdqxqxnahqj-rdjzcztqsa- 14565317 Click to see 300.35 unknown https://doi.org/10.1248/CPB.38.573
> Organoheterocyclic compounds / Indolizidines
Corynoxine 10475115 Click to see 384.50 unknown https://doi.org/10.1248/CPB.38.573
Isorhynchophylline 3037048 Click to see CCC1CN2CCC3(C2CC1C(=COC)C(=O)OC)C4=CC=CC=C4NC3=O 384.50 unknown https://doi.org/10.1248/CPB.38.573
methyl (E)-2-[(2R,6'S,7'R,8'aR)-6'-ethyl-3-oxospiro[1H-indole-2,1'-3,5,6,7,8,8a-hexahydro-2H-indolizine]-7'-yl]-3-methoxyprop-2-enoate 163188592 Click to see 384.50 unknown https://doi.org/10.1016/0031-9422(75)85310-6
methyl (E)-2-[(6'S,7'S)-6'-ethyl-2-oxospiro[1H-indole-3,1'-3,5,6,7,8,8a-hexahydro-2H-indolizine]-7'-yl]-3-methoxyprop-2-enoate 5316104 Click to see 384.50 unknown https://doi.org/10.1248/CPB.38.573
methyl 2-(6'-ethyl-3-oxospiro[1H-indole-2,1'-3,5,6,7,8,8a-hexahydro-2H-indolizine]-7'-yl)-3-methoxyprop-2-enoate 162930445 Click to see CCC1CN2CCC3(C2CC1C(=COC)C(=O)OC)C(=O)C4=CC=CC=C4N3 384.50 unknown https://doi.org/10.1016/0031-9422(75)85310-6
Mitraphylline 94160 Click to see 368.40 unknown https://doi.org/10.1590/S0100-40422004000600007
Uncarine B 12304286 Click to see CC1C2CN3CCC4(C3CC2C(=CO1)C(=O)OC)C5=CC=CC=C5NC4=O 368.40 unknown https://doi.org/10.1055/S-2008-1074973

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