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Desfontainia spinosa

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 UUID64401667005b9730146222
Scientific name Desfontainia spinosa
Authority Ruiz & Pav.
First published in Fl. Peruv. 2: 47 (1799)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Linkia spinosa Poir. Encycl. [J. Lamarck & al.] Suppl. 3. 449. 1814 [3 Sep 1814]

Common names Top

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Language Common/alternative name
English taique
Spanish taique
Korean 타이케
Dutch desfontaineaceae
Russian Дефонтения
Chinese 枸骨叶
Chinese 枸骨黄
Chinese 离水花属
Chinese 拉美冬青科
Chinese 虎刺叶科
Chinese 離水花科
Chinese 离水花科

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-0000642027
USDA Plants DESP4
Tropicos 19000612
KEW urn:lsid:ipni.org:names:546059-1
The Plant List kew-2761883
PFAF Desfontainia spinosa
Open Tree Of Life 107904
NCBI Taxonomy 34247
NBN Atlas NHMSYS0020823744
IUCN Red List 135733204
IPNI 546059-1
iNaturalist 578318
GBIF 6388688
Freebase /m/0gyf8l
EPPO DSFSP
USDA GRIN 13601

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
Behavioural responses by a bumble bee to competition with a niche‐constructing congener Rosenberger NM, Aizen MA, Dickson RG, Harder LD J Anim Ecol 23-Dec-2021
PMCID:PMC9305565
doi:10.1111/1365-2656.13646
PMID:34862619
A Phytosociological Study on Andean Rainforests of Peru, and a Comparison with the Surrounding Countries Galán-de-Mera A, Campos-de-la-Cruz J, Linares-Perea E, Montoya-Quino J, Torres-Marquina I, Vicente-Orellana JA Plants (Basel) 26-Nov-2020
PMCID:PMC7761437
doi:10.3390/plants9121654
PMID:33256180
Between semelparity and iteroparity: Empirical evidence for a continuum of modes of parity Hughes PW Ecol Evol 07-Sep-2017
PMCID:PMC5648687
doi:10.1002/ece3.3341
PMID:29075446
Species interactions in an Andean bird–flowering plant network: phenology is more important than abundance or morphology Gonzalez O, Loiselle BA PeerJ 13-Dec-2016
PMCID:PMC5157195
doi:10.7717/peerj.2789
PMID:27994982
The ethnobotany of psychoactive plant use: a phylogenetic perspective Alrashedy NA, Molina J PeerJ 05-Oct-2016
PMCID:PMC5068365
doi:10.7717/peerj.2546
PMID:27761334
Nectar Concentration and Composition of 26 Species from the Temperate Forest of South America CHALCOFF VR, AIZEN MA, GALETTO L Ann Bot 01-Mar-2006
PMCID:PMC2803636
doi:10.1093/aob/mcj043
PMID:16373370
Iridoids from Desfostainia Spinosa Peter J. Houghton, Lian Lu Ming Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)82565-0
Spinosides A and B. Two cytotoxic cucurbitacin glycosides from Desfontainia spinosa Kalakota S. Reddy, Ashok J. Amonkar, Thomas G. McCloud, Ching-Jer Chang, John M. Cassady Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(88)83016-4
Iridoids, iridoid-triterpenoid congeners and lignans from Desfontainia spinosa Peter J. Houghton, Lu Ming Lian Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)81172-3
Triterpenoids from Desfontainia spinosa Peter J. Houghton, Lu Ming Lian Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)81179-6

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 / Aporphines
Liriodenine 10144 Click to see C1OC2=C(O1)C3=C4C(=C2)C=CN=C4C(=O)C5=CC=CC=C53 275.26 unknown https://doi.org/10.1016/S0031-9422(00)81172-3
> Lignans, neolignans and related compounds / Furanoid lignans
Syringaresinol, (+)- 443023 Click to see 418.40 unknown https://doi.org/10.1016/S0031-9422(00)81172-3
> Lignans, neolignans and related compounds / Lignan glycosides
(+)-syringaresinol beta-D-glucoside 443024 Click to see 580.60 unknown https://doi.org/10.1016/S0031-9422(00)81172-3
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Iridoids and derivatives
Loganetin 10466307 Click to see 228.24 unknown https://doi.org/10.1016/S0031-9422(00)82565-0
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
Secologanin 161276 Click to see 388.40 unknown https://doi.org/10.1016/S0031-9422(00)81172-3
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
(-)-Loganin 87691 Click to see 390.40 unknown https://doi.org/10.1016/S0031-9422(00)82565-0
Loganic Acid 89640 Click to see 376.36 unknown https://doi.org/10.1016/S0031-9422(00)82565-0
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
(1R,2R,4aS,6aR,6aS,6bR,8aR,9S,10R,11R,12aR,14bS)-9-[[2-[(2S,3R,4S)-3-ethenyl-5-methoxycarbonyl-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydro-2H-pyran-4-yl]acetyl]oxymethyl]-1,10,11-trihydroxy-1,2,6a,6b,9,12a-hexamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 101318310 Click to see 891.00 unknown https://doi.org/10.1016/S0031-9422(00)81172-3
methyl (2S,3R,4S)-4-[2-[[(2R,3R,4S,4aR,6aR,6bS,8aS,11R,12R,12aS,14aR,14bR)-2,3,12-trihydroxy-4,6a,6b,11,12,14b-hexamethyl-8a-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycarbonyl-1,2,3,4a,5,6,7,8,9,10,11,12a,14,14a-tetradecahydropicen-4-yl]methoxy]-2-oxoethyl]-3-ethenyl-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydro-2H-pyran-5-carboxylate 101318311 Click to see 1053.20 unknown https://doi.org/10.1016/S0031-9422(00)81172-3
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Ursolic Acid 64945 Click to see 456.70 unknown https://doi.org/10.1016/S0031-9422(00)81179-6
19Alpha-Hydroxyasiatic Acid 490367 Click to see 504.70 unknown https://doi.org/10.1016/S0031-9422(00)81179-6
24-Hydroxytormentic acid 14055737 Click to see 504.70 unknown https://doi.org/10.1016/S0031-9422(00)81179-6
Acetylursolic acid 15917992 Click to see 498.70 unknown https://doi.org/10.1016/S0031-9422(00)81179-6
Pomolic Acid 382831 Click to see 472.70 unknown https://doi.org/10.1016/S0031-9422(00)81179-6
Ursolic acid acetate 6475119 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC(=O)C)C)C)C2C1C)C)C(=O)O 498.70 unknown https://doi.org/10.1016/S0031-9422(00)81179-6
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins / Cucurbitacin glycosides
Spinoside A 5281325 Click to see 716.90 unknown https://doi.org/10.1016/0031-9422(88)83016-4
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(-)-Sweroside 161036 Click to see 358.34 unknown https://doi.org/10.1016/S0031-9422(00)81172-3
(3S,4R,4aS)-4-ethenyl-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4,4a,5,6-tetrahydro-3H-pyrano[3,4-c]pyran-8-one 354447 Click to see 358.34 unknown https://doi.org/10.1016/S0031-9422(00)81172-3

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