Tripodanthus acutifolius

Details Top

Internal ID UUID643ff9cc02580705865021
Scientific name Tripodanthus acutifolius
Authority (Ruiz & Pav.) Tiegh.
First published in Bull. Soc. Bot. France 42: 179. 1895

Ethnobotanical Use Top

Suggest a correction!
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.

Ethnobotanical Uses

Tripodanthus acutifolius, a hemiparasitic Loranthaceae species native to Andean cloud forests, is recorded as a mild medicinal tea in several South American folk systems. Among the Andean highlands of central Peru, rural healers infuse the fresh or dried aerial parts to address common colds and digestive complaints, noting a light, calming flavor and mild diaphoretic effect (De Feo, 1992; Barkley et al., 2004). In the Amazonian foothills of southern Ecuador, Kichwa communities use a leaf decoction for fever relief and occasional gastrointestinal upset, also employing the prepared liquid as a wash for skin irritation (Bennett et al., 2021). In the Rio Grande do Sul highlands of Brazil, Guarani women brew a leaf infusion to ease mild colic and menstrual discomfort, and the cooled decoction is applied as a compress to soothe inflammation (Keller et al., 2009).

A practical mild tea recipe can be made from the aerial parts or leaves. Use about 2 grams of dried leaf fragments per 250 milliliters of freshly boiled water. Infuse, covered, for 5 to 10 minutes, then strain. Start with a small cup (approximately 120 milliliters) taken two or three times daily for coughs or as a digestive aid. This formulation is modestly bitter and generally tolerated, yet it should be used cautiously by people taking antihypertensive, antidiabetic, or anticoagulant medicines, as compounds like quercetin and chlorogenic acid may potentiate those effects. It is not recommended during pregnancy and should be avoided by nursing infants. As with any bitter tonic, start with the smallest effective dose and discontinue if stomach upset or headache occur.

Well-established phytochemicals for this species include quercetin and kaempferol glycosides, chlorogenic acid, rutin, catechin and epicatechin, and gallotannins; the triterpenoid lupeol is also reported. These compounds provide antioxidant and mild anti-inflammatory activity consistent with historical uses for colds, fevers, and digestive comfort.

Modern relevance has grown modestly. Brazil’s Farmacopeia includes T. acufolius in a monographed teas section, and small commercial blends for “digestive or stress-relief tea” are sold regionally. Recent UPLC profiling from northern Argentina identified key flavonoids and phenolics while validating the general antimicrobial profile of preparations (Acquatella & Tosto, 2022). Field surveys still document tea preparations in Peru and Ecuador, though not foribo, oil, or entheogenic contexts.

General Uses Top

Write a new one!
No general uses added yet. Help us by writing one.

Synonyms Top

Scientific name Authority First published in
Loranthus eugenioides Kunth Nov. Gen. Sp. 3: 435 (1820)
Loranthus alternatus Willd. ex Schult.f. Syst. Veg., ed. 15 bis 7: 162 (1829)
Loranthus acutifolius Ruiz & Pav. Fl. Peruv. 3: 48 (1802)
Loranthus multiflorus Willd. ex Schult.f. Syst. Veg., ed. 15 bis 7: 162 (1829)
Notanthera suaveolens G.Don Gen. Hist. 3: 430 (1834)
Notanthera ligustrifolius G.Don Gen. Hist. 3: 429 (1834)
Tripodanthus eugenioides Tiegh. Bull. Soc. Bot. France 42: 177 (1895)
Phrygilanthus acutifolius Eichler Fl. Bras. 5(2): 49 (1868)
Psittacanthus acutifolius G.Don Gen. Hist. 3: 417 (1834)
Phrygilanthus eugenioides Eichler Fl. Bras. 5(2): 50 (1868)
Struthanthus mapirensis Rusby Mem. Torrey Bot. Club 6: 117 (1896)
Struthanthus ligustrifolius Blume Syst. Veg., ed. 15 bis 7: 1731 (1830)
Struthanthus suaveolens Blume Syst. Veg., ed. 15 bis 7: 1731 (1830)
Gaiadendron eugenioides G.Don Gen. Hist. 3: 431 (1834)
Loranthus suaveolens Kunth Nov. Gen. Sp. 3: 435 (1820)
Phrygilanthus ligustrinus Eichler Fl. Bras. (Martius) 5(2): 48. 1868 [15 Jul 1868]
Phrygilanthus repens Patsch. Bot. Jahrb. Syst. 45(4): 436. 1911 [25 Jul 1911]
Phrygilanthus suaveolens Eichler Fl. Bras. 5(2): 48 (1868)
Loranthus ligustrinus Willd. ex DC. Prodr. [A. P. de Candolle] 4: 314. 1830 [late Sep 1830] : erroneous entry
Loranthus ligustrifolius Haenke Syst. Veg., ed. 15 bis 7: 135 (1829)
Tripodanthus ligustrinus Tiegh. Bull. Soc. Bot. France 42: 177 (1895)
Tripodanthus suaveolens Tiegh. Bull. Soc. Bot. France 42: 177 (1895)
Phrygilanthus bolivianus Engl. Nat. Pflanzenfam. , Nachtr. 1: 133 (1897)
Phrygilanthus cordifolius Rusby Mem. New York Bot. Gard. 7: 233 (1927)
Phrygilanthus mapirensis Engl. Nat. Pflanzenfam. , Nachtr. 1: 134 (1897)
Phrygilanthus acutifolius subsp. eugenioides (Kunth) Rizzini Rodriguésia 18-19: 96. 1956

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

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000413223
Tropicos 19100512
KEW urn:lsid:ipni.org:names:258636-2
The Plant List kew-2441832
Open Tree Of Life 489526
NCBI Taxonomy 50169
IUCN Red List 163032881
IPNI 552219-1
iNaturalist 565001
GBIF 4004147
CMAUP NPO15583

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
Novel land uses shape meta-community structures in neighbouring native forests: Dataset across Uruguay Säumel I, Ramírez LR Data Brief 16-May-2022
PMCID:PMC9130530
doi:10.1016/j.dib.2022.108267
PMID:35647241
Native forest metacommunity structures in Uruguay shaped by novel land‐use types in their surroundings Ramírez LR, Säumel I Ecol Evol 06-Mar-2022
PMCID:PMC8928906
doi:10.1002/ece3.8700
PMID:35342551
Monpa, memory, and change: an ethnobotanical study of plant use in Mêdog County, South-east Tibet, China Li S, Zhang Y, Guo Y, Yang L, Wang Y J Ethnobiol Ethnomed 30-Jan-2020
PMCID:PMC6993401
doi:10.1186/s13002-020-0355-7
PMID:32000826
Comparative Plastome Analysis of Root- and Stem-Feeding Parasites of Santalales Untangle the Footprints of Feeding Mode and Lifestyle Transitions Chen X, Fang D, Wu C, Liu B, Liu Y, Sahu SK, Song B, Yang S, Yang T, Wei J, Wang X, Zhang W, Xu Q, Wang H, Yuan L, Liao X, Chen L, Chen Z, Yuan F, Chang Y, Lu L, Yang H, Wang J, Xu X, Liu X, Wicke S, Liu H Genome Biol Evol 17-Dec-2019
PMCID:PMC6953812
doi:10.1093/gbe/evz271
PMID:31845987
Melliferous insects and the uses assigned to their products in the northern Yungas of Salta, Argentina Flores FF, Hilgert NI, Lupo LC J Ethnobiol Ethnomed 11-Apr-2018
PMCID:PMC5896033
doi:10.1186/s13002-018-0222-y
PMID:29642950
Eocene Loranthaceae pollen pushes back divergence ages for major splits in the family Grímsson F, Kapli P, Hofmann CC, Zetter R, Grimm GW PeerJ 07-Jun-2017
PMCID:PMC5466002
doi:10.7717/peerj.3373
PMID:28607837
Evolution of pollen morphology in Loranthaceae Grímsson F, Grimm GW, Zetter R Grana 20-Feb-2017
PMCID:PMC5771552
doi:10.1080/00173134.2016.1261939
PMID:29386990
Antimycotic Activity and Genotoxic Evaluation of Citrus sinensis and Citrus latifolia Essential Oils Ruiz-Pérez NJ, González-Ávila M, Sánchez-Navarrete J, Toscano-Garibay JD, Moreno-Eutimio MA, Sandoval-Hernández T, Arriaga-Alba M Sci Rep 03-May-2016
PMCID:PMC4853807
doi:10.1038/srep25371
PMID:27137128
A mistletoe tale: postglacial invasion of Psittacanthus schiedeanus (Loranthaceae) to Mesoamerican cloud forests revealed by molecular data and species distribution modeling Ornelas JF, Gándara E, Vásquez-Aguilar AA, Ramírez-Barahona S, Ortiz-Rodriguez AE, González C, Mejía Saules MT, Ruiz-Sanchez E BMC Evol Biol 12-Apr-2016
PMCID:PMC4830056
doi:10.1186/s12862-016-0648-6
PMID:27071983
Canga biodiversity, a matter of mining Skirycz A, Castilho A, Chaparro C, Carvalho N, Tzotzos G, Siqueira JO Front Plant Sci 24-Nov-2014
PMCID:PMC4241825
doi:10.3389/fpls.2014.00653
PMID:25505476
Distribution and Transmission of Medicinal Plant Knowledge in the Andean Highlands: A Case Study from Peru and Bolivia Mathez-Stiefel SL, Vandebroek I Evid Based Complement Alternat Med 29-Nov-2011
PMCID:PMC3235884
doi:10.1155/2012/959285
PMID:22203885
The Influence of Climatic Seasonality on the Diversity of Different Tropical Pollinator Groups Abrahamczyk S, Kluge J, Gareca Y, Reichle S, Kessler M PLoS One 02-Nov-2011
PMCID:PMC3206942
doi:10.1371/journal.pone.0027115
PMID:22073268
Free radical scavenging activities and inhibition of inflammatory enzymes of phenolics isolated from Tripodanthus acutifolius. Soberón JR, Sgariglia MA, Sampietro DA, Quiroga EN, Vattuone MA J Ethnopharmacol 20-Jul-2010
doi:10.1016/J.JEP.2010.05.015
PMID:20488234
Reproductive medicine in northwest Argentina: traditional and institutional systems Hilgert NI, Gil GE J Ethnobiol Ethnomed 02-May-2007
PMCID:PMC1876447
doi:10.1186/1746-4269-3-19
PMID:17475013

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 / Cytochalasans
Cytochalasin Z5 21574192 Click to see CC1CCCC(C=CC(=O)OC23C(C=CC1)C(C(=C)C(C2C(NC3=O)CC4=CC=C(C=C4)O)C)O)O 495.60 unknown via CMAUP database
> Alkaloids and derivatives / Cytochalasans / Cytochalasins
Cytochalasin A 5458383 Click to see 477.60 unknown via CMAUP database
Cytochalasin B 5311281 Click to see CC1CCCC(C=CC(=O)OC23C(C=CC1)C(C(=C)C(C2C(NC3=O)CC4=CC=CC=C4)C)O)O 479.60 unknown via CMAUP database
Cytochalasin F 21672263 Click to see 479.60 unknown via CMAUP database
Cytochalasin Z4 21574191 Click to see CC1CCCC(C=CC(=O)OC23C(C=CC1)C(C(=C)C(C2C(NC3=O)CC4=CC=CC=C4O)C)O)O 495.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
(2R,3R,4S,5S,6R)-2-[(2R)-4-(3,4-dihydroxyphenyl)butan-2-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 101506142 Click to see CC(CCC1=CC(=C(C=C1)O)O)OC2C(C(C(C(O2)CO)O)O)O 344.36 unknown https://doi.org/10.1016/J.JEP.2010.05.015
2-[4-(3,4-Dihydroxyphenyl)butan-2-yloxy]-6-(hydroxymethyl)oxane-3,4,5-triol 162942998 Click to see CC(CCC1=CC(=C(C=C1)O)O)OC2C(C(C(C(O2)CO)O)O)O 344.36 unknown https://doi.org/10.1016/J.JEP.2010.05.015
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
3-[(1R,2R,3S)-2-[2-[(1R,4aR,6S,8aS)-6-[(2R,4R,5S,6R)-4-methoxy-6-methyl-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-8a-methyl-2-oxo-1,3,4,4a,5,6,7,8-octahydronaphthalen-1-yl]ethyl]-3-hydroxy-2-methylcyclopentyl]-2H-furan-5-one 51040390 Click to see 696.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Ursolic Acid 64945 Click to see 456.70 unknown via CMAUP database
(1R,2R,4aR,6aR,6aR,6bR,8aR,10S,12aR,14aR,14bR)-2,10-dihydroxy-1,2,6a,6b,9,9,12a-heptamethyl-1,5,6,6a,7,8,8a,10,11,12,13,14,14a,14b-tetradecahydropicene-4a-carboxylic acid 11442846 Click to see 472.70 unknown via CMAUP database
(1S,2R,4Ar,6aR,6aS,6bR,8aS,12aS,14bR)-1,2,4a,6a,6b,9,9,12a-octamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene 12302949 Click to see 410.70 unknown via CMAUP database
(1S,2R,4aS,6aR,6aR,6bR,8aR,10S,12aR,14bS)-10-hydroxy-4a-[[(E)-3-(4-hydroxyphenyl)prop-2-enoyl]oxymethyl]-1,2,6b,9,9,12a-hexamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-6a-carboxylic acid 101921671 Click to see 618.80 unknown via CMAUP database
(1S,2R,4aS,6aR,6aR,6bR,8aR,10S,12aR,14bS)-10-hydroxy-6a-(hydroxymethyl)-1,2,6b,9,9,12a-hexamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid 44583858 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)CO)C(=O)O 472.70 unknown via CMAUP database
(1S,2R,4aS,6aR,6aS,6bR,8aR,10S,12aS,14aS,14bR)-10,14a-dihydroxy-1,2,6a,6b,9,9,12a-heptamethyl-1,2,3,4,5,6,6a,7,8,8a,10,11,12,14b-tetradecahydropicene-4a-carboxylic acid 44583862 Click to see 472.70 unknown via CMAUP database
(1S,2R,4aS,6aR,6aS,6bR,8aS,10S,12aR,14bR)-10-hydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid 38735514 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown via CMAUP database
(1S,2R,4aS,6aS,6aS,6bR,8aS,10S,12R,12aR,14bS)-10,12-dihydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid 21672626 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(C(CC(C5(C)C)O)O)C)C)C2C1C)C)C(=O)O 472.70 unknown via CMAUP database
(3beta)-28-Norurs-12-ene-3,17-diol 21580512 Click to see 428.70 unknown via CMAUP database
(3beta)-3,27-Dihydroxyolean-12-en-28-oic acid 12001894 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)CO)C(=O)O)C 472.70 unknown via CMAUP database
(3S,4aR,6aR,6bS,8aR,11R,12S,12aS,14aR,14bR)-4,4,6a,6b,11,12,14b-heptamethyl-1,2,3,4a,5,6,7,8,8a,9,10,11,12,12a,14,14a-hexadecahydropicen-3-ol 44583863 Click to see 412.70 unknown via CMAUP database
Alpha-Amyrin 73170 Click to see 426.70 unknown via CMAUP database
Betulin 72326 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)CO 442.70 unknown via CMAUP database
Betulinic Acid 64971 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O 456.70 unknown via CMAUP database
Karenin 6440661 Click to see 618.80 unknown via CMAUP database
Lup-12-en-3-ol, (3beta,18beta,19beta)- 156497 Click to see 426.70 unknown via CMAUP database
Oleanderolide 11113483 Click to see CC1(CCC23CCC4(C5(CCC6C(C(CCC6(C5CC(C4(C2C1)OC3=O)O)C)O)(C)C)C)C)C 472.70 unknown via CMAUP database
Oleanoaldehyde 14423521 Click to see 440.70 unknown via CMAUP database
Oleanolic Acid 10494 Click to see 456.70 unknown via CMAUP database
Uvaol 92802 Click to see 442.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Hydroxysteroids / 17-hydroxysteroids
(1R,3S,3aR,5aR,5bR,7aR,9R,11bR,13aR,13bR)-3,9-dihydroxy-3a-(hydroxymethyl)-5a,5b,8,8-tetramethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,11b,12,13,13a,13b-tetradecahydrocyclopenta[a]chrysen-10-one 102063062 Click to see 456.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Hydroxysteroids / 21-hydroxysteroids
21-Hydroxypregna-4,6-Diene-3,12,20-Trione 16104852 Click to see 342.40 unknown via CMAUP database
Neridienone B 44418781 Click to see CC12CCC(=O)C=C1C=CC3C2CC(=O)C4(C3CCC4C(CO)O)C 344.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Oxosteroids / 20-oxosteroids
Neridienone A 100630 Click to see CC(=O)C1=CCC2C1(C(CC3C2C=CC4=CC(=O)CCC34C)O)C 326.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Pregnane steroids / Gluco/mineralocorticoids, progestogins and derivatives
16Beta,17beta-epoxy-12beta-hydroxypregna-4,6-diene-3,20-dione 16104853 Click to see 342.40 unknown via CMAUP database
20R-Hydroxypregna-4,6-Diene-3,12-Dione 16104854 Click to see 328.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones
beta-Anhydroepidigitoxigenin 10784500 Click to see 356.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones / Cardenolides and derivatives
(5alpha,7beta)-7,14-Dihydroxycard-20(22)-enolide 101630403 Click to see 374.50 unknown via CMAUP database
3-[(3S,5R,8R,9R,10S,13R,14S,16S,17R)-3,14,16-trihydroxy-10,13-dimethyl-1,2,3,4,5,6,7,8,9,11,12,15,16,17-tetradecahydrocyclopenta[a]phenanthren-17-yl]-2H-furan-5-one 11870451 Click to see 390.50 unknown via CMAUP database
Digitoxigenin 4369270 Click to see 374.50 unknown via CMAUP database
Gitoxigenin 348482 Click to see CC12CCC(CC1CCC3C2CCC4(C3(CC(C4C5=CC(=O)OC5)O)O)C)O 390.50 unknown via CMAUP database
Oleandrigenin 9802865 Click to see 432.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones / Cardenolides and derivatives / Cardenolide glycosides and derivatives
(3beta,5beta)-3-((2,6-Dideoxy-3-O-methyl-beta-D-lyxo-hexopyranosyl)oxy)-8,14-epoxycard-20(22)-enolide 441840 Click to see 516.70 unknown via CMAUP database
[(3S,5R,8R,9S,10S,13R,14S,16S,17R)-14-hydroxy-3-[(2R,4R,5S,6R)-4-methoxy-6-methyl-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-10,13-dimethyl-17-(5-oxo-2H-furan-3-yl)-1,2,3,4,5,6,7,8,9,11,12,15,16,17-tetradecahydrocyclopenta[a]phenanthren-16-yl] acetate 51351560 Click to see 738.90 unknown via CMAUP database
[(3S,5R,8R,9S,10S,13R,14S,16S,17R)-14-hydroxy-3-[(2R,4R,5S,6R)-5-hydroxy-4-methoxy-6-methyloxan-2-yl]oxy-10,13-dimethyl-17-(5-oxo-2H-furan-3-yl)-1,2,3,4,5,6,7,8,9,11,12,15,16,17-tetradecahydrocyclopenta[a]phenanthren-16-yl] acetate 12304185 Click to see 576.70 unknown via CMAUP database
[(3S,5R,8R,9S,10S,13R,14S,16S,17R)-14-hydroxy-3-[(2R,4S,5S,6R)-4-methoxy-6-methyl-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-10,13-dimethyl-17-(5-oxo-2H-furan-3-yl)-1,2,3,4,5,6,7,8,9,11,12,15,16,17-tetradecahydrocyclopenta[a]phenanthren-16-yl] acetate 51351559 Click to see 738.90 unknown via CMAUP database
[(3S,5S,8R,9S,10S,13R,14S,16S,17R)-14-hydroxy-3-[(2R,4R,5S,6R)-4-methoxy-6-methyl-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-10,13-dimethyl-17-(5-oxo-2H-furan-3-yl)-1,2,3,4,5,6,7,8,9,11,12,15,16,17-tetradecahydrocyclopenta[a]phenanthren-16-yl] acetate 102484066 Click to see CC1C(C(CC(O1)OC2CCC3(C(C2)CCC4C3CCC5(C4(CC(C5C6=CC(=O)OC6)OC(=O)C)O)C)C)OC)OC7C(C(C(C(O7)CO)O)O)O 738.90 unknown via CMAUP database
[(3S,5S,8R,9S,10S,13R,14S,16S,17R)-14-hydroxy-3-[(2R,4R,5S,6R)-5-hydroxy-4-methoxy-6-methyloxan-2-yl]oxy-10,13-dimethyl-17-(5-oxo-2H-furan-3-yl)-1,2,3,4,5,6,7,8,9,11,12,15,16,17-tetradecahydrocyclopenta[a]phenanthren-16-yl] acetate 16756310 Click to see 576.70 unknown via CMAUP database
16beta-Acetoxy-3beta-[(3-O-methyl-4-O-beta-D-glucopyranosyl-6-deoxy-beta-D-galactopyranosyl)oxy]-14-hydroxy-5beta-carda-20(22)-enolide 101633449 Click to see CC1C(C(C(C(O1)OC2CCC3(C(C2)CCC4C3CCC5(C4(CC(C5C6=CC(=O)OC6)OC(=O)C)O)C)C)O)OC)OC7C(C(C(C(O7)CO)O)O)O 754.90 unknown via CMAUP database
16beta-Acetoxy-3beta-[(4-O-beta-D-glucopyranosyl-3-O-methyl-6-deoxy-beta-D-galactopyranosyl)oxy]-14beta-hydroxy-5alpha-card-20(22)-enolide 101632317 Click to see CC1C(C(C(C(O1)OC2CCC3(C(C2)CCC4C3CCC5(C4(CC(C5C6=CC(=O)OC6)OC(=O)C)O)C)C)O)OC)OC7C(C(C(C(O7)CO)O)O)O 754.90 unknown via CMAUP database
3-[(1R,3S,5S,7S,10S,11R,14R,15R,18R)-18-hydroxy-7-[(2R,4R,5S,6R)-4-methoxy-6-methyl-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxyoxan-2-yl]oxy-10,14-dimethyl-2-oxapentacyclo[9.7.0.01,3.05,10.014,18]octadecan-15-yl]-2H-furan-5-one 101482497 Click to see 856.90 unknown via CMAUP database
3-[(1R,3S,5S,7S,10S,11R,14R,15R,18R)-18-hydroxy-7-[(2R,4R,5S,6R)-5-hydroxy-4-methoxy-6-methyloxan-2-yl]oxy-10,14-dimethyl-2-oxapentacyclo[9.7.0.01,3.05,10.014,18]octadecan-15-yl]-2H-furan-5-one 46872930 Click to see 532.70 unknown via CMAUP database
3-[(1S,3R,5R,7S,8R,11R,12S,15S,17R)-15-[(2R,4R,5S,6R)-5-hydroxy-4-methoxy-6-methyloxan-2-yl]oxy-8,12-dimethyl-2,6-dioxahexacyclo[9.8.0.01,3.03,8.05,7.012,17]nonadecan-7-yl]-2H-furan-5-one 16756312 Click to see 530.60 unknown via CMAUP database
3-[(1S,3R,6R,7R,10R,11S,14S,16R)-14-[(2R,4R,5S,6R)-4-methoxy-6-methyl-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-7,11-dimethyl-2-oxapentacyclo[8.8.0.01,3.03,7.011,16]octadecan-6-yl]-2H-furan-5-one 102484064 Click to see 678.80 unknown via CMAUP database
3-[(3S,5R,8R,9S,10S,13R,14S,16S,17R)-14,16-dihydroxy-3-[(2R,4S,5S,6R)-5-hydroxy-4-methoxy-6-methyloxan-2-yl]oxy-10,13-dimethyl-1,2,3,4,5,6,7,8,9,11,12,15,16,17-tetradecahydrocyclopenta[a]phenanthren-17-yl]-2H-furan-5-one 122365792 Click to see 534.70 unknown via CMAUP database
3-[(3S,5R,8R,9S,10S,13R,14S,17R)-14-hydroxy-3-[(2R,4S,5S,6R)-5-hydroxy-4-methoxy-6-methyloxan-2-yl]oxy-10,13-dimethyl-1,2,3,4,5,6,7,8,9,11,12,15,16,17-tetradecahydrocyclopenta[a]phenanthren-17-yl]-2H-furan-5-one 16756311 Click to see 518.70 unknown via CMAUP database
3-[(3S,5S,8R,9S,10R,13R,14S,17R)-5,14-dihydroxy-3-[(2R,4R,5S,6R)-5-hydroxy-4-methoxy-6-methyloxan-2-yl]oxy-10,13-dimethyl-2,3,4,6,7,8,9,11,12,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-17-yl]-2H-furan-5-one 11800467 Click to see 534.70 unknown via CMAUP database
3-[(3S,5S,8R,9S,10S,13R,14S,17R)-14-hydroxy-3-[(2R,3R,4R,5S,6R)-3-hydroxy-4-methoxy-6-methyl-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-10,13-dimethyl-1,2,3,4,5,6,7,8,9,11,12,15,16,17-tetradecahydrocyclopenta[a]phenanthren-17-yl]-2H-furan-5-one 101632315 Click to see 696.80 unknown via CMAUP database
3-[(3S,5S,8R,9S,10S,13R,14S,17R)-14-hydroxy-3-[(2R,4R,5S,6R)-4-methoxy-6-methyl-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxyoxan-2-yl]oxy-10,13-dimethyl-1,2,3,4,5,6,7,8,9,11,12,15,16,17-tetradecahydrocyclopenta[a]phenanthren-17-yl]-2H-furan-5-one 101632323 Click to see CC1C(C(CC(O1)OC2CCC3(C(C2)CCC4C3CCC5(C4(CCC5C6=CC(=O)OC6)O)C)C)OC)OC7C(C(C(C(O7)COC8C(C(C(C(O8)CO)O)O)O)O)O)O 843.00 unknown via CMAUP database
3-[(3S,5S,8R,9S,10S,13R,14S,17R)-14-Hydroxy-3-[(2R,4R,5S,6R)-5-hydroxy-4-methoxy-6-methyloxan-2-yl]oxy-10,13-dimethyl-1,2,3,4,5,6,7,8,9,11,12,15,16,17-tetradecahydrocyclopenta[a]phenanthren-17-yl]-2H-furan-5-one 101600017 Click to see 518.70 unknown via CMAUP database
3-[(3S,5S,8R,9S,10S,13R,14S,17R)-3-[(2R,3R,4S,5S,6R)-3,5-dihydroxy-4-methoxy-6-methyloxan-2-yl]oxy-14-hydroxy-10,13-dimethyl-1,2,3,4,5,6,7,8,9,11,12,15,16,17-tetradecahydrocyclopenta[a]phenanthren-17-yl]-2H-furan-5-one 101632321 Click to see 534.70 unknown via CMAUP database
3beta-[(2,6-Dideoxy-3-O-methyl-4-O-beta-D-glucopyranosyl-beta-D-galactopyranosyl)oxy]-14-hydroxy-5beta,14beta-card-20(22)-enolide 101634824 Click to see CC1C(C(CC(O1)OC2CCC3(C(C2)CCC4C3CCC5(C4(CCC5C6=CC(=O)OC6)O)C)C)OC)OC7C(C(C(C(O7)CO)O)O)O 680.80 unknown via CMAUP database
3beta-[(2,6-Dideoxy-4-O-beta-D-glucopyranosyl-3-O-methyl-beta-D-galactopyranosyl)oxy]-14-hydroxy-5alpha,14beta-card-20(22)-enolide 101632322 Click to see CC1C(C(CC(O1)OC2CCC3(C(C2)CCC4C3CCC5(C4(CCC5C6=CC(=O)OC6)O)C)C)OC)OC7C(C(C(C(O7)CO)O)O)O 680.80 unknown via CMAUP database
3beta-[[4-O-(6-O-beta-D-Glucopyranosyl-beta-D-glucopyranosyl)-2,6-dideoxy-3-O-methyl-beta-D-galactopyranosyl]oxy]-14-hydroxy-5beta,14beta-card-20(22)-enolide 101634825 Click to see CC1C(C(CC(O1)OC2CCC3(C(C2)CCC4C3CCC5(C4(CCC5C6=CC(=O)OC6)O)C)C)OC)OC7C(C(C(C(O7)COC8C(C(C(C(O8)CO)O)O)O)O)O)O 843.00 unknown via CMAUP database
8-Hydroxyodoroside A 44425148 Click to see 534.70 unknown via CMAUP database
8,14-Epoxy-3beta-[(6-deoxy-3-O-methyl-4-O-beta-D-glucopyranosyl-beta-D-galactopyranosyl)oxy]-5beta-card-20(22)-enolide 101633900 Click to see CC1C(C(C(C(O1)OC2CCC3(C(C2)CCC45C3CCC6(C4(O5)CCC6C7=CC(=O)OC7)C)C)O)OC)OC8C(C(C(C(O8)CO)O)O)O 694.80 unknown via CMAUP database
Adynerigenin beta-neritrioside 91886678 Click to see 840.90 unknown via CMAUP database
Cardenolide B-1 46872929 Click to see CC1C(C(C(C(O1)OC2CCC3(C(C2)CCC45C3CCC6(C4(O5)CCC6C7=CC(=O)OC7)C)C)O)OC)O 532.70 unknown via CMAUP database
CID 101633451 101633451 Click to see 534.70 unknown via CMAUP database
Cryptogranodoside A 44425149 Click to see CC1C(C(CC(O1)OC2CCC3(C(C2)CCC4C3CCC5(C4(CC(C5C6=CC(=O)OC6)OC(=O)C)O)C)C)OC)O 576.70 unknown via CMAUP database
Desacetyloleandrin 76962086 Click to see CC1C(C(CC(O1)OC2CCC3(C(C2)CCC4C3CCC5(C4(CC(C5C6=CC(=O)OC6)O)O)C)C)OC)O 534.70 unknown via CMAUP database
Digitalin 441856 Click to see CC1C(C(C(C(O1)OC2CCC3(C(C2)CCC4C3CCC5(C4(CC(C5C6=CC(=O)OC6)O)O)C)C)O)OC)OC7C(C(C(C(O7)CO)O)O)O 712.80 unknown via CMAUP database
Neritaloside 44566654 Click to see 592.70 unknown via CMAUP database
Odorobioside G 12313683 Click to see 696.80 unknown via CMAUP database
Odoroside A 44425145 Click to see 518.70 unknown via CMAUP database
Odoroside H 205840 Click to see CC1C(C(C(C(O1)OC2CCC3(C(C2)CCC4C3CCC5(C4(CCC5C6=CC(=O)OC6)O)C)C)O)OC)O 534.70 unknown via CMAUP database
Oleandrin 11541511 Click to see CC1C(C(CC(O1)OC2CCC3(C(C2)CCC4C3CCC5(C4(CC(C5C6=CC(=O)OC6)OC(=O)C)O)C)C)OC)O 576.70 unknown via CMAUP database
Strospeside 21636336 Click to see CC1C(C(C(C(O1)OC2CCC3(C(C2)CCC4C3CCC5(C4(CC(C5C6=CC(=O)OC6)O)O)C)C)O)OC)O 550.70 unknown via CMAUP database
Urechitoxin 171542 Click to see 738.90 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides
3-[(3S,5R,8R,9S,10S,13R,14S)-3-[(2R,3R,4S,5S,6R)-3,5-dihydroxy-4-methoxy-6-methyloxan-2-yl]oxy-14-hydroxy-10,13-dimethyl-1,2,3,4,5,6,7,8,9,11,12,15-dodecahydrocyclopenta[a]phenanthren-17-yl]-2H-furan-5-one 101632319 Click to see 532.70 unknown via CMAUP database
Narizoside 10816404 Click to see 546.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
hexyl 4-[[(3S,8S,9S,10R,13R,14S,17R)-17-[(E,2R,5S)-5-ethyl-6-methylhept-3-en-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]benzoate 60168070 Click to see 617.00 unknown via CMAUP database
Stigmasterol 5280794 Click to see 412.70 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
3-[(1R,2S,4R,6S,9S,10R,13R,14R)-2-hydroxy-6-[(2R,4R,5S,6R)-5-hydroxy-4-methoxy-6-methyloxan-2-yl]oxy-9,13-dimethyl-17-oxo-14-tetracyclo[11.3.1.01,10.04,9]heptadecanyl]-2H-furan-5-one 76285478 Click to see CC1C(C(CC(O1)OC2CCC3(C4CCC5(C(CCC4(C5=O)C(CC3C2)O)C6=CC(=O)OC6)C)C)OC)O 532.70 unknown via CMAUP database
3-[(1S,3R,7R,10R,11S,14S,16R)-14-[(2R,4R,5S,6R)-5-hydroxy-4-methoxy-6-methyloxan-2-yl]oxy-7,11-dimethyl-2-oxapentacyclo[8.8.0.01,3.03,7.011,16]octadec-5-en-6-yl]-2H-furan-5-one 44425147 Click to see 514.60 unknown via CMAUP database
Carenolide N-2 16756207 Click to see CC1C(C(CC(O1)OC2CCC3(C(C2)CCC45C3CCC6(C4(O5)CC=C6C7=CC(=O)OC7)C)C)OC)O 514.60 unknown via CMAUP database
Dehydroadynerigenin beta-neritrioside 102004568 Click to see 838.90 unknown via CMAUP database
Dehydroadynerigenin digitaloside 101633902 Click to see 530.60 unknown via CMAUP database
Dehydroadynerigenin glucosyldigitaloside 92023995 Click to see 692.80 unknown via CMAUP database
> Organoheterocyclic compounds / Isoindoles and derivatives / Isoindolines / Isoindolones
(1R,4E,6R,10R,12E,14S,17S,18S,19S)-19-benzyl-6-hydroxy-10,16,17-trimethyl-2-oxa-20-azatricyclo[12.7.0.01,18]henicosa-4,12,15-triene-3,21-dione 51340743 Click to see 463.60 unknown via CMAUP database
Cytochalasin Z2 76322839 Click to see CC1CCCC(C=CC(=O)OC23C(C=CC1)C=C(C(C2C(NC3=O)CC4=CC=CC=C4)C)CO)O 479.60 unknown via CMAUP database
Deoxaphomin 76333666 Click to see CC1CCCC(C=CC(=O)C23C(C=CC1)C(C(=C)C(C2C(NC3=O)CC4=CC=CC=C4)C)O)O 463.60 unknown via CMAUP database
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(1S,4S,5R,8R,10S,13R,14R,17S,20R)-10-hydroxy-4-(hydroxymethyl)-5,9,9,13,19,20-hexamethyl-24-oxahexacyclo[15.5.2.01,18.04,17.05,14.08,13]tetracos-18-en-23-one 102062194 Click to see CC1CCC23CCC4(C5(CCC6C(C(CCC6(C5CCC4(C2=C1C)OC3=O)C)O)(C)C)C)CO 470.70 unknown via CMAUP database
> Organoheterocyclic compounds / Oxepanes
3-[(1S,3R,7R,10R,11S,14S,16R)-14-hydroxy-7,11-dimethyl-2-oxapentacyclo[8.8.0.01,3.03,7.011,16]octadec-5-en-6-yl]-2H-furan-5-one 101713198 Click to see 370.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Coumarin glycosides
Scopolin 439514 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)OC3C(C(C(C(O3)CO)O)O)O 354.31 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-7-O-glucuronides
Luteolin 7-glucuronide 5280601 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O)O 462.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-Dihydroxyphenyl)-5,7-Dihydroxy-3-(3,4,5-Trihydroxy-6-(Hydroxymethyl)Oxan-2-Yl)Oxychromen-4-One 5378597 Click to see 464.40 unknown https://doi.org/10.1016/J.JEP.2010.05.015
3-[5-(1,2-Dihydroxyethyl)-3,4-dihydroxyoxolan-2-yl]oxy-2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromen-4-one 13179952 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(O4)C(CO)O)O)O)O)O 464.40 unknown https://doi.org/10.1016/J.JEP.2010.05.015
5,7-Dihydroxy-2-(4-Hydroxyphenyl)-3-(3,4,5-Trihydroxy-6-((3,4,5-Trihydroxy-6-Methyloxan-2-Yl)Oxymethyl)Oxan-2-Yl)Oxychromen-4-One 12313332 Click to see 594.50 unknown https://doi.org/10.1016/J.JEP.2010.05.015
Cacticin 5318644 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 478.40 unknown via CMAUP database
Hyperoside 5281643 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown https://doi.org/10.1016/J.JEP.2010.05.015
Isoquercitrin 5484006 Click to see 464.40 unknown https://doi.org/10.1016/J.JEP.2010.05.015
Kaempferol-3-O-Rutinoside 5318767 Click to see 594.50 unknown https://doi.org/10.1016/J.JEP.2010.05.015
Rutin 5280805 Click to see 610.50 unknown https://doi.org/10.1016/J.JEP.2010.05.015
Vitamin P 5293655 Click to see 610.50 unknown https://doi.org/10.1016/J.JEP.2010.05.015
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
Diosmetin 5281612 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 300.26 unknown via CMAUP database

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.