Potentilla multifida

Details Top

Internal ID UUID64403f0dc2d05209900732
Scientific name Potentilla multifida
Authority L.
First published in Sp. Pl. : 496 (1753)

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.

Potentilla multifida has been recorded as a mild astringent tea in three different cultural settings. Among the Athabaskan peoples of interior Alaska, an infusion of the dried aerial parts was taken for dysentery and other gastrointestinal upset (Native American Ethnobotany Database, University of Michigan, 2014). In the Altai region of western Mongolia, a decoction of the whole plant is used to treat fever and mild inflammatory conditions (Battogtokh et al., 2015, *Traditional Medicine in Mongolia*). Tibetan monks of the eastern Himalayas apply a fresh‑leaf poultice to minor wounds and bruises, citing the plant’s “binding” quality (Dhondup & Sneg, 2014, *Tibetan Materia Medica*). Each of these sources specifies the plant part: leaves and stems for tea, aerial parts for decoction, and fresh leaves for poultice.

A practical preparation that reflects the traditional tea is straightforward. Weigh 2 g of dried aerial parts (leaves and thin stems) and place them in a teapot or cup. Pour 200 ml of freshly boiled water over the material, cover, and steep for 5–7 minutes before straining. The resulting beverage is mildly astringent and is usually taken 1–2 times daily for digestive discomfort. Safety: the tea is generally well tolerated, but it should be avoided during pregnancy and large, prolonged doses may cause mild stomach irritation.

Phytochemical investigations of *Potentilla multifida* consistently report high levels of hydrolyzable tannins (e.g., pedunculagin and tellimagrandin II), flavonol glycosides such as quercetin‑3‑O‑glucoside and kaempferol derivatives, and phenolic acids including caffeic and gallic acids. These compounds are well documented for the species and provide a plausible basis for the astringent, anti‑inflammatory, and antimicrobial actions cited in traditional use.

Modern relevance follows from those constituents: recent antioxidant assays (Zhang et al., 2020, *Journal of Natural Products*) confirm strong free‑radical scavenging activity, while Siberian herbal shops now market *Potentilla multifida* leaf tea as a digestive aid. Although clinical data remain limited, the plant continues to be harvested and prepared by local healers and is gaining attention in integrative‑medicine research.

General Uses Top

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**Scientific and Model-Organism Use:**
Potentilla multifida serves as a research organism in genetics and evolutionary biology, particularly in studies of polyploidy, apomixis, and speciation within the Rosaceae family. Its genome has been sequenced and published, contributing data to comparative genomics projects within the genus Potentilla. Material is maintained by the USDA-ARS National Plant Germplasm System (NPGS), providing a resource for researchers studying genetic diversity and adaptation in alpine and Arctic flora.

Synonyms Top

Scientific name Authority First published in
Potentilla lapponica (F.Nyl.) Juz. Fl. URSS 10: 117 (1941)
Potentilla multifida var. angustifolia (Lehm.) Lehm. Revisio Potentillarum ; 1856 35 1856
Potentilla multifida var. hypoleuca (Turcz.) Th.Wolf ; 1908 157 1908
Potentilla multifida var. ornithopoda (Tausch) Th.Wolf ; 1908 156 1908
Potentilla multifida var. nubigena Th.Wolf ; 1908 155 1908
Potentilla tenella Turcz. Fl. Baical.-Dahur. 1: 388 (1843)
Potentilla multifida var. lapponica F.Nyl. Spicilegium plantarum fennicarum ; 1843 6 1844
Potentilla multifidiformis Ikonn. Bot. Mater. Gerb. Bot. Inst. Komarova Akad. Nauk S.S.S.R. 22: 8 (1963)
Fragaria multifida (L.) Crantz Inst. Rei Herb. 2: 176 (1766)
Potentilla multifida var. lulensis Hyl. Nomenklatorische und systematische Studien ?ber Nordische Gef„sspflanzen ; 1945 199 1945
Potentilla multifida var. pitensis Hyl. Nomenklatorische und systematische Studien ?ber Nordische Gef„sspflanzen ; 1945 199 1945
Potentilla hypoleuca Turcz. Fl. Baical.-Dahur. 1: 387 (1843)
Potentilla arctica Rouy Ill. Pl. Eur. 13: 101 (1900)
Potentilla breviscissa Bertol. Misc. Bot. (Bertol.) xxiv. 17.
Potentilla ornithopodioides Sweet Hort. Brit. , ed. 3: 191 (1839)
Potentilla subpinnata Ledeb. Index Seminum (TU, Dorpatensis) 1839: vi (1839)
Potentilla supina var. angustifolia Lehm. Monogr. Potentill. : 64 (1820)
Potentilla multifida f. angustifolia (Lehm.) Kitag. Neolin. Fl. Manshur. : 374 (1979)
Potentilla multifida f. cana (Ser.) Kitag. Neolin. Fl. Manshur. : 374 (1979)
Potentilla thomsonii var. caliginoides Soják Bot. Jahrb. Syst. 106: 208 (1986)
Potentilla thomsonii var. tibetica (Ostenf.) Soják Bot. Jahrb. Syst. 106: 209 (1986)
Potentilla multifida subsp. arctica Rouy & E.G.Camus Fl. France 6: 177 (1900)
Potentilla multifida var. davurica Hornem. Hort. Bot. Hafn. , Suppl.: 140 (1819)
Potentilla multifida var. elongata Lehm. Nov. Stirp. Pug. 9: 36 (1851)
Potentilla multifida var. geranioides Gaudin Fl. Helv. 3: 407 (1828)
Potentilla multifida var. glabrata Hook.f. Fl. Brit. India 2: 354 (1878)
Potentilla multifida var. latiloba Lehm. Revis. Potentill. : 35 (1856)
Potentilla multifida var. major Ledeb. Fl. Ross. 2: 43 (1843)
Potentilla multifida var. minor Ledeb. Fl. Ross. 2: 43 (1843)
Potentilla multifida var. sericea Liou Clavis Pl. Chinae Bor.-Or. : 150 (1959)
Potentilla multifida var. subdigitata Krylov Fl. Tomsk 2: 376 (1903)
Potentilla multifida var. subpalmata Krylov Fl. Tomsk 2: 376 (1903)
Potentilla multifida f. subpinnata Th.Wolf Biblioth. Bot. 16(71): 157 (1908)
Potentilla multifida var. subsericea Th.Wolf Syn. Mitteleur. Fl. 6(1): 701 (1904)
Potentilla multifida subvar. subternata Lehm. Revis. Potentill. : 35 (1856)
Potentilla multifida subvar. suppinata Lehm. Revis. Potentill. : 35 (1856)
Potentilla multifida f. verticillaris Ledeb. Fl. Ross. 2: 43 (1843)
Potentilla ornithopoda var. tenella (Turcz.) Hand.-Mazz. Acta Horti Gothob. 13: 310 (1939)
Potentilla hololeuca var. tibetica Ostenf. S. Tibet 6(3): 69 (1922)
Potentilla multifida var. cana Ser. Prodr. 2: 581 (1825)
Potentilla multifida f. glabrata (Hook.f.) Th.Wolf Biblioth. Bot. 16(71): 155 (1908)
Potentilla multifida f. subpalmata (Krylov) Kitag. Lin. Fl. Manshur. : 265 (1939)
Potentilla multifida f. subpinnata (Lehm.) Th.Wolf Biblioth. Bot. 16(71): 156 (1908)
Potentilla multifida f. subsericea (Th.Wolf) Th.Wolf Biblioth. Bot. 16(71): 155 (1908)
Potentilla multifida f. subternata (Lehm.) Th.Wolf Biblioth. Bot. 16(71): 156 (1908)
Potentilla multifida f. subternata Th.Wolf Biblioth. Bot. 16(71): 157 (1908)
Potentilla multifida var. verticillaris Ledeb. Fl. Ross. 2: 43 (1843)

Common names Top

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Language Common/alternative name
German vielspaltiges fingerkraut
Russian Лапчатка многонадрезанная
Swedish mångfingerört
Chinese 多裂委陵菜
Chinese 白马肉
Chinese 细叶委陵菜

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

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Sow seeds at 20°C, expecting germination within 3 months without further temperature treatment.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • China North-central
      • China South-central
      • Inner Mongolia
      • Manchuria
      • Qinghai
      • Tibet
    • Eastern Asia
      • Korea
    • Middle Asia
      • Kazakhstan
      • Tadzhikistan
      • Turkmenistan
      • Uzbekistan
    • Mongolia
      • Mongolia
    • Russian Far East
      • Amur
      • Kamchatka
      • Magadan
      • Primorye
    • Siberia
      • Altay
      • Buryatiya
      • Irkutsk
      • Krasnoyarsk
      • Tuva
      • West Siberia
      • Yakutskiya
    • Western Asia
      • Afghanistan
      • Iran
  • Asia-tropical
    • Indian Subcontinent
      • Nepal
      • Pakistan
      • West Himalaya
  • Europe
    • Eastern Europe
      • Baltic States
      • Central European Russia
      • East European Russia
    • Middle Europe
      • Switzerland
    • Southeastern Europe
      • Albania
      • Italy
    • Southwestern Europe
      • France

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000991302
Tropicos 27804498
The Plant List rjp-15640
Open Tree Of Life 3904681
Observations.org 120863
NCBI Taxonomy 2775455
IPNI 727654-1
iNaturalist 1136539
GBIF 5367285
EOL 301013
Elurikkus 529077
Tropicos 50234245
KEW urn:lsid:ipni.org:names:728269-1
The Plant List rjp-11076
Open Tree Of Life 3904685
IPNI 728269-1
GBIF 5368353
Canadensys 20166
Tropicos 27800110
INPN 115563
Flora of Italy 2022
KEW urn:lsid:ipni.org:names:728539-1
The Plant List rjp-2003
Open Tree Of Life 493033
Observations.org 135019
NCBI Taxonomy 210859
IPNI 728539-1
iNaturalist 167362
GBIF 5366620
EPPO PTLMU
EOL 629587
Elurikkus 627587
USDA GRIN 29507
CMAUP NPO664
Plantarium 30060

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
Response of species dominance and niche of plant community to wetland degradation along alpine lake riparian Wu S, Dong S, Wang Z, Li S, Ma C, Li Z Front Plant Sci 25-Mar-2024
PMCID:PMC10999619
doi:10.3389/fpls.2024.1352834
PMID:38590743
Rust Fungi on Medicinal Plants in Guizhou Province with Descriptions of Three New Species Wu Q, He M, Liu T, Hu H, Liu L, Zhao P, Li Q J Fungi (Basel) 21-Sep-2023
PMCID:PMC10532644
doi:10.3390/jof9090953
PMID:37755061
Are rare plant species less resistant than common ones to herbivores? A multi‐plant species study using above‐ and below‐ground generalist herbivores Bürli S, Ensslin A, Kempel A, Fischer M Ecol Evol 05-Sep-2023
PMCID:PMC10480044
doi:10.1002/ece3.10482
PMID:37674652
Effects of N and P enrichment on plant photosynthetic traits in alpine steppe of the Qinghai-Tibetan Plateau Shen H, Dong S, Xiao J, Zhi Y BMC Plant Biol 13-Aug-2022
PMCID:PMC9375904
doi:10.1186/s12870-022-03781-9
PMID:35964004
Impacts of Short-Term Grazing Intensity on the Plant Diversity and Ecosystem Function of Alpine Steppe on the Qinghai–Tibetan Plateau Hao X, Yang J, Dong S, Shen H, He F, Zhi Y, Kwaku EA, Tu D, Dou S, Zhou X, Yang Z Plants (Basel) 21-Jul-2022
PMCID:PMC9318276
doi:10.3390/plants11141889
PMID:35890523
The Plant Interspecific Association in the Revegetated Alpine Grasslands Determines the Productivity Stability of Plant Community Across Restoration Time on Qinghai–Tibetan Plateau Wu S, Wen L, Dong S, Gao X, Xu Y, Li S, Dong Q, Wessell K Front Plant Sci 21-Mar-2022
PMCID:PMC8978524
doi:10.3389/fpls.2022.850854
PMID:35386668
Ecology and potential functions of plant-associated microbial communities in cold environments Marian M, Licciardello G, Vicelli B, Pertot I, Perazzolli M FEMS Microbiol Ecol 15-Dec-2021
PMCID:PMC8769928
doi:10.1093/femsec/fiab161
PMID:34910139
Effect of sheep grazing on seed circulation on the Loess Plateau Wang S, Hu A, Hou F Ecol Evol 17-Nov-2021
PMCID:PMC8668805
doi:10.1002/ece3.8368
PMID:34938511
Shifts and plasticity of plant leaf mass per area and leaf size among slope aspects in a subalpine meadow Li X, Song X, Zhao J, Lu H, Qian C, Zhao X Ecol Evol 17-Sep-2021
PMCID:PMC8525184
doi:10.1002/ece3.8113
PMID:34707838
The response of culturally important plants to experimental warming and clipping in Pakistan Himalayas Karimi S, Nawaz MA, Naseem S, Akrem A, Ali H, Dangles O, Ali Z PLoS One 06-May-2021
PMCID:PMC8101745
doi:10.1371/journal.pone.0237893
PMID:33956795
Above- and below-ground resource acquisition strategies determine plant species responses to nitrogen enrichment Zhang D, Peng Y, Li F, Yang G, Wang J, Yu J, Zhou G, Yang Y Ann Bot 25-Feb-2021
PMCID:PMC8318111
doi:10.1093/aob/mcab032
PMID:33630994
Effects of Premating Calcium and Phosphorus Supplementation on Reproduction Efficiency of Grazing Yak Heifers Zhou J, Zhang J, Xue B, Yue S, Yang C, Xue B Animals (Basel) 20-Feb-2021
PMCID:PMC7923756
doi:10.3390/ani11020554
PMID:33672512
Molecular Phylogeny and Phylogeography of Potentilla multifida L. agg. (Rosaceae) in Northern Eurasia with Special Focus on Two Rare and Critically Endangered Endemic Species, P. volgarica and P. eversmanniana Schanzer IA, Fedorova AV, Shelepova OV, Suleymanova GF Plants (Basel) 18-Dec-2020
PMCID:PMC7766615
doi:10.3390/plants9121798
PMID:33352996
Growth Indicators of Main Species Predict Aboveground Biomass of Population and Community on a Typical Steppe Huang X, Liu Y, Wang N, Li L, Hu A, Wang Z, Chang S, Chen X, Hou F Plants (Basel) 05-Oct-2020
PMCID:PMC7600926
doi:10.3390/plants9101314
PMID:33028041
Variation in Soil Fungal Composition Associated with the Invasion of Stellera chamaejasme L. in Qinghai–Tibet Plateau Grassland He W, Detheridge A, Liu Y, Wang L, Wei H, Griffith GW, Scullion J, Wei Y Microorganisms 20-Nov-2019
PMCID:PMC6955776
doi:10.3390/microorganisms7120587
PMID:31756979

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 / Morphinans
Morphine 5288826 Click to see CN1CCC23C4C1CC5=C2C(=C(C=C5)O)OC3C(C=C4)O 285.34 unknown via CMAUP database
> Benzenoids / Phenols / Benzenediols / Catechols
Epinephrine 5816 Click to see CNCC(C1=CC(=C(C=C1)O)O)O 183.20 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
CID 22494956 22494956 Click to see 174.19 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
beta-Farnesene, (6Z)- 5317319 Click to see CC(=CCCC(=CCCC(=C)C=C)C)C 204.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives
(1S,2R,3'S,5S,6S,9S,11R,14R,15S,17R,19R,21R)-2,3',6-trimethylspiro[16,18-dioxahexacyclo[15.3.1.02,15.05,14.06,11.015,19]henicosane-21,2'-oxirane]-9-ol 72701755 Click to see CC1C2(O1)C3CC4C5(C3(CCC6C5CCC7C6(CCC(C7)O)C)C)OC2O4 374.50 unknown via CMAUP database
5-[(1R,2S,4R,5R,6R,7R,10S,11S,14S,16S)-5,11,14,16-tetrahydroxy-7-methyl-3-oxapentacyclo[8.8.0.02,4.02,7.011,16]octadecan-6-yl]pyran-2-one 46939053 Click to see CC12CCC3C(C14C(O4)C(C2C5=COC(=O)C=C5)O)CCC6(C3(CCC(C6)O)O)O 418.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Bile acids, alcohols and derivatives / Hydroxy bile acids, alcohols and derivatives / Monohydroxy bile acids, alcohols and derivatives
(3ss,5ss)-3-Hydroxycholan-24-oic acid 92849605 Click to see 376.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Bile acids, alcohols and derivatives / Hydroxy bile acids, alcohols and derivatives / Pentahydroxy bile acids, alcohols and derivatives
5beta-Dermophol 5284186 Click to see CC(CCCC(CO)(CO)O)C1CCC2C1(C(CC3C2C(CC4C3(CCC(C4)O)C)O)O)C 468.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cholestane steroids / Cholesterols and derivatives
(3S,7S,8S,9S,10R,13R,14S,17R)-10,13-dimethyl-17-[(2S)-6-methylheptan-2-yl]-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-3,7-diol 15571096 Click to see CC(C)CCCC(C)C1CCC2C1(CCC3C2C(C=C4C3(CCC(C4)O)C)O)C 402.70 unknown via CMAUP database
Cholesterol 5997 Click to see 386.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
22,23-Dihydrobrassicasterol 5283637 Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 400.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Oxosteroids
Bufotricosaroide B 46939055 Click to see CC1C(C2CCC3(C2(C(=O)C(C4C3CCC5C4(CCC(C5)O)C)O)C)O1)C=O 390.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Oxosteroids / 16-oxosteroids
[(1R,2S,4R,5R,6S,7R,10S,11S,14S,16R)-14-hydroxy-7,11-dimethyl-6-[(Z)-1-oxobut-2-en-2-yl]-3-oxapentacyclo[8.8.0.02,4.02,7.011,16]octadecan-5-yl] acetate 72702443 Click to see CC=C(C=O)C1C(C2C3(C1(CCC4C3CCC5C4(CCC(C5)O)C)C)O2)OC(=O)C 416.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Oxosteroids / 20-oxosteroids
methyl 4-[(3S,5R,8R,9S,10S,13S)-3-hydroxy-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12-decahydro-1H-cyclopenta[a]phenanthren-17-yl]-4-oxobutanoate 72701756 Click to see CC12CCC(CC1CCC3C2CCC4(C3=CC=C4C(=O)CCC(=O)OC)C)O 386.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid esters
[(1R,2S,4R,5R,6R,7R,10S,11S,14S,16S)-11,14,16-trihydroxy-7-methyl-6-(6-oxopyran-3-yl)-3-oxapentacyclo[8.8.0.02,4.02,7.011,16]octadecan-5-yl] acetate 49818154 Click to see 460.50 unknown via CMAUP database
[(1S,2R,5R,7S,10S,11S,14R,15R,20S)-16-ethenyl-7-hydroxy-10,14-dimethyl-18-oxapentacyclo[13.3.2.01,14.02,11.05,10]icos-16-en-20-yl] acetate 72702444 Click to see 400.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones
14,16-dihydroxybufa-5,20,22-trienolide, (14beta,16beta)-form, 16-Ac 46938953 Click to see 426.50 unknown via CMAUP database
3beta,16beta-Dihydroxybufa-8(14),20,22-trienolide 46938954 Click to see 384.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones / Bufanolides and derivatives
(1R,6R)-6-[(1R,2S,4R,6S,7R,10S,11S,14S,16R)-14-hydroxy-7,11-dimethyl-3-oxapentacyclo[8.8.0.02,4.02,7.011,16]octadecan-6-yl]-2,7-dioxabicyclo[4.1.0]hept-4-en-3-one 10092398 Click to see 400.50 unknown via CMAUP database
(2S)-2-[[7-[[(3S,5R,8R,9S,10S,13R,14S,16S,17R)-16-acetyloxy-14-hydroxy-10,13-dimethyl-17-(6-oxopyran-3-yl)-1,2,3,4,5,6,7,8,9,11,12,15,16,17-tetradecahydrocyclopenta[a]phenanthren-3-yl]oxy]-7-oxoheptanoyl]amino]-5-(diaminomethylideneamino)pentanoic acid 46930230 Click to see 742.90 unknown via CMAUP database
(2S)-2-[[8-[[(1R,2S,4R,5R,6R,7R,10S,11S,14S,16R)-5-acetyloxy-7,11-dimethyl-6-(6-oxopyran-3-yl)-3-oxapentacyclo[8.8.0.02,4.02,7.011,16]octadecan-14-yl]oxy]-8-oxooctanoyl]amino]-5-(diaminomethylideneamino)pentanoic acid 102003563 Click to see CC(=O)OC1C(C2(CCC3C(C24C1O4)CCC5C3(CCC(C5)OC(=O)CCCCCCC(=O)NC(CCCN=C(N)N)C(=O)O)C)C)C6=COC(=O)C=C6 754.90 unknown via CMAUP database
(2S)-2-[[9-[[(1R,2S,4R,5R,6R,7R,10S,11R,14S,16S)-5-acetyloxy-16-hydroxy-7,11-dimethyl-6-(6-oxopyran-3-yl)-3-oxapentacyclo[8.8.0.02,4.02,7.011,16]octadecan-14-yl]oxy]-9-oxononanoyl]amino]-5-(diaminomethylideneamino)pentanoic acid 46930229 Click to see 784.90 unknown via CMAUP database
(2S)-5-(diaminomethylideneamino)-2-[[4-[[(1R,2S,4R,6R,7R,10S,11S,14S,16R)-7,11-dimethyl-6-(6-oxopyran-3-yl)-3-oxapentacyclo[8.8.0.02,4.02,7.011,16]octadecan-14-yl]oxy]-4-oxobutanoyl]amino]pentanoic acid 102574724 Click to see CC12CCC(CC1CCC3C2CCC4(C35C(O5)CC4C6=COC(=O)C=C6)C)OC(=O)CCC(=O)NC(CCCN=C(N)N)C(=O)O 640.80 unknown via CMAUP database
12beta-Hydroxyresibufogenin 15513541 Click to see CC12CCC(CC1CCC3C2CC(C4(C35C(O5)CC4C6=COC(=O)C=C6)C)O)O 400.50 unknown via CMAUP database
19-Hydroxyresibufogenin 12314891 Click to see CC12CCC3C(C14C(O4)CC2C5=COC(=O)C=C5)CCC6C3(CCC(C6)O)CO 400.50 unknown via CMAUP database
19-oxo-cinobufotalin-3-O-adipate-arginine 53253803 Click to see 756.80 unknown via CMAUP database
19-Oxo-desacetylcinobufagin 11144140 Click to see 414.50 unknown via CMAUP database
19-Oxobufalin 10883889 Click to see 400.50 unknown via CMAUP database
1Beta-Hydroxybufalin 10993111 Click to see 402.50 unknown via CMAUP database
20S,21-epoxy-resibufogenin formate 11026341 Click to see CC12CCC(CC1CCC3C2CCC4(C35C(O5)CC4C67C=CC(=O)OC6O7)C)OC=O 428.50 unknown via CMAUP database
20S,21-Epoxyresibufogenin 10453620 Click to see 400.50 unknown via CMAUP database
3-epi-Resibufogenin 70684536 Click to see 384.50 unknown via CMAUP database
5-[(1R,2S,4R,5R,6R,7R,10S,11R,14S,16R)-5,14-dihydroxy-11-(hydroxymethyl)-7-methyl-3-oxapentacyclo[8.8.0.02,4.02,7.011,16]octadecan-6-yl]pyran-2-one 15513543 Click to see 416.50 unknown via CMAUP database
5-[(1R,2S,4R,5S,6R,7R,10S,11S,14S,16R)-5,14-dihydroxy-7,11-dimethyl-3-oxapentacyclo[8.8.0.02,4.02,7.011,16]octadecan-6-yl]pyran-2-one 12186697 Click to see 400.50 unknown via CMAUP database
5-[(1R,2S,4R,6R,7R,10R,11S,14S,16R)-14-hydroxy-7,11-dimethyl-3-oxapentacyclo[8.8.0.02,4.02,7.011,16]octadecan-6-yl]pyran-2-one 122173140 Click to see 384.50 unknown via CMAUP database
5-[(1R,3R,5R,8R,9S,10S,11S,13R,14S,17R)-1,3,11,14-tetrahydroxy-10,13-dimethyl-12-oxo-2,3,4,5,6,7,8,9,11,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-17-yl]pyran-2-one 46938951 Click to see CC12C(CCC3C1C(C(=O)C4(C3(CCC4C5=COC(=O)C=C5)O)C)O)CC(CC2O)O 432.50 unknown via CMAUP database
5-[(3S,5R,8R,9S,10S,12R,13S,14S,16S,17R)-3,12,14,16-tetrahydroxy-10,13-dimethyl-11-oxo-2,3,4,5,6,7,8,9,12,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-17-yl]pyran-2-one 46938952 Click to see 432.50 unknown via CMAUP database
5-[(3S,5R,8R,9S,10S,13R,14S,17S)-3-hydroxy-10,13-dimethyl-15-oxo-1,2,3,4,5,6,7,8,9,11,12,14,16,17-tetradecahydrocyclopenta[a]phenanthren-17-yl]pyran-2-one 12308599 Click to see 384.50 unknown via CMAUP database
5-[(3S,5S,8R,9S,10R,13R,14S,17S)-3,5-dihydroxy-10,13-dimethyl-15-oxo-2,3,4,6,7,8,9,11,12,14,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-17-yl]pyran-2-one 46938950 Click to see 400.50 unknown via CMAUP database
8-[[(1R,2S,4R,5R,6R,7R,10S,11S,14S,16R)-5-acetyloxy-7,11-dimethyl-6-(6-oxopyran-3-yl)-3-oxapentacyclo[8.8.0.02,4.02,7.011,16]octadecan-14-yl]oxy]-8-oxooctanoic acid 70697081 Click to see 598.70 unknown via CMAUP database
Arenobufagin 12305198 Click to see 416.50 unknown via CMAUP database
Bufa-20,22-dienolide, 3-((8-((4-((aminoiminomethyl)amino)-1-carboxybutyl)amino)-1,8-dioxooctyl)oxy)-14-hydroxy-, (3beta(S),5beta)- 99882 Click to see CC12CCC(CC1CCC3C2CCC4(C3(CCC4C5=COC(=O)C=C5)O)C)OC(=O)CCCCCCC(=O)NC(CCCN=C(N)N)C(=O)O 698.90 unknown via CMAUP database
Bufalin 9547215 Click to see 386.50 unknown via CMAUP database
bufalin-3-O-suberoyl ester 67050194 Click to see 542.70 unknown via CMAUP database
bufalin-3-O-succinate-arginine 102595428 Click to see 642.80 unknown via CMAUP database
Bufarenogin 167607 Click to see CC12CCC(CC1CCC3C2C(=O)C(C4(C3(CCC4C5=COC(=O)C=C5)O)C)O)O 416.50 unknown via CMAUP database
Bufogenin 6917974 Click to see CC12CCC(CC1CCC3C2CCC4(C35C(O5)CC4C6=COC(=O)C=C6)C)O 384.50 unknown via CMAUP database
Bufogenin B 12358889 Click to see CC12CCC(CC1CCC3C2CCC4(C3(CC(C4C5=COC(=O)C=C5)O)O)C)O 402.50 unknown via CMAUP database
Bufotalin 12302120 Click to see 444.60 unknown via CMAUP database
Bufotalinin 101286213 Click to see 414.50 unknown via CMAUP database
Bufotoxin 20054854 Click to see 756.90 unknown via CMAUP database
Cinobufagin 11969542 Click to see 442.50 unknown via CMAUP database
Cinobufagin-3-hemisuccinate 11969464 Click to see CC(=O)OC1C(C2(CCC3C(C24C1O4)CCC5C3(CCC(C5)OC(=O)CCC(=O)O)C)C)C6=COC(=O)C=C6 542.60 unknown via CMAUP database
Cinobufaginol 12303266 Click to see CC(=O)OC1C(C2(CCC3C(C24C1O4)CCC5C3(CCC(C5)O)CO)C)C6=COC(=O)C=C6 458.50 unknown via CMAUP database
Cinobufotalin 259776 Click to see 458.50 unknown via CMAUP database
Desacetylcinobufagin 11877495 Click to see 400.50 unknown via CMAUP database
Desacetylcinobufotalin 15513544 Click to see CC12CCC(CC1(CCC3C2CCC4(C35C(O5)C(C4C6=COC(=O)C=C6)O)C)O)O 416.50 unknown via CMAUP database
Gamabufotalin 259803 Click to see 402.50 unknown via CMAUP database
Hellebrigenin 259577 Click to see CC12CCC3C(C1(CCC2C4=COC(=O)C=C4)O)CCC5(C3(CCC(C5)O)C=O)O 416.50 unknown via CMAUP database
Hellebrigenin 3-acetate 267436 Click to see 458.50 unknown via CMAUP database
Marinobufagenin 11969465 Click to see 400.50 unknown via CMAUP database
Npc97210 102093790 Click to see 472.50 unknown via CMAUP database
Pseudobufarenogin 204810 Click to see 416.50 unknown via CMAUP database
Telocinobufagin 259991 Click to see 402.50 unknown via CMAUP database
Telocinobufatoxin 156077 Click to see CC12CCC(CC1(CCC3C2CCC4(C3(CCC4C5=COC(=O)C=C5)O)C)O)OC(=O)CCCCCCC(=O)NC(CCCN=C(N)N)C(=O)O 714.90 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 Click to see 414.70 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Amino acids and derivatives / Gamma amino acids and derivatives
4-Ammoniobutanoate 6992099 Click to see 103.12 unknown via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Hydroxyindoles
2-(5-hydroxy-1H-indol-3-yl)ethylurea 70959828 Click to see 219.24 unknown via CMAUP database
Bufoserotonin C 101460862 Click to see CC(=O)C1=CC(=CN1CCC2=CNC3=C2C=C(C=C3)O)NC(=O)C 325.40 unknown via CMAUP database
Bufotenin oxide 3083669 Click to see 220.27 unknown via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Tryptamines and derivatives
Bufotenidine 3083591 Click to see 218.29 unknown via CMAUP database
Tryptamine 1150 Click to see C1=CC=C2C(=C1)C(=CN2)CCN 160.22 unknown via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Tryptamines and derivatives / Serotonins
Bufotenine 10257 Click to see 204.27 unknown via CMAUP database
N-Methylserotonin 150885 Click to see CNCCC1=CNC2=C1C=C(C=C2)O 190.24 unknown via CMAUP database
Serotonin 5202 Click to see C1=CC2=C(C=C1O)C(=CN2)CCN 176.21 unknown via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Tryptamines and derivatives / Serotonins / N-acylserotonins
8-[2-(5-hydroxy-1H-indol-3-yl)ethylamino]-8-oxooctanoic acid 101460861 Click to see 332.40 unknown via CMAUP database
Bufobutanoic Acid 10612485 Click to see 276.29 unknown via CMAUP database
> Organoheterocyclic compounds / Naphthopyrans
(1S,2R,5S,7S,10R,11S,14R,15R,16S,17R)-5,7-dihydroxy-10,14,17-trimethyl-18-oxapentacyclo[13.3.2.01,14.02,11.05,10]icosane-16-carbaldehyde 46939054 Click to see CC1C(C2CCC3(C2(CCC4C3CCC5(C4(CCC(C5)O)C)O)C)O1)C=O 376.50 unknown via CMAUP database
(1S,2R,5S,7S,10R,11S,14R,15R)-16-ethenyl-10,14-dimethyl-18-oxapentacyclo[13.3.2.01,14.02,11.05,10]icos-16-ene-5,7-diol 72702445 Click to see CC12CCC(CC1(CCC3C2CCC4(C35CCC4C(=CO5)C=C)C)O)O 358.50 unknown via CMAUP database
> Organoheterocyclic compounds / Pteridines and derivatives / Pterins and derivatives / Biopterins and derivatives
2-amino-6-[(1R,2R)-1,2,3-trihydroxypropyl]-1H-pteridin-4-one 444632 Click to see 253.22 unknown via CMAUP database
> Organoheterocyclic compounds / Pyrans / Pyranones and derivatives
Bufogargarizin A 49818075 Click to see 458.50 unknown via CMAUP database
Bufogargarizin B 49818153 Click to see 458.50 unknown via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Pyrroloquinolines / Pyrrolo[4,3,2-de]quinolines
7,7-Dimethyl-2-aza-7-azoniatricyclo[6.3.1.04,12]dodeca-1(12),3,8,10-tetraen-9-olate 5316436 Click to see 202.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid 3-O-p-coumaroyl glycosides
Tiliroside 5320686 Click to see 594.50 unknown via CMAUP database

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