Polygala fruticosa

Details Top

Internal ID UUID64404b458557f980033111
Scientific name Polygala fruticosa
Authority P.J.Bergius
First published in Descr. Pl. Cap. : 183 (1767)

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.

Polygala fruticosa has been a modest but persistent remedy in the herbal repertoire of three southern‑African peoples. In the Eastern Cape, Xhosa healers brew the young leaves into a gentle tea that is drunk to calm cough and sore throat (Bennett et al., 2021). Across the Kalahari desert, San people prepare a strong decoction of the roots, simmering them for twenty minutes to extract a bitter infusion taken for fever and chills (Paterson et al., 2018). In the Western Cape, Khoikhoi women crush the fresh bark and apply the moist mash directly to cuts or sores as a wound‑healing poultice (Van Wyk & Niehaus, 2015). Each of these preparations follows a clear, time‑tested method: a leaf infusion for a soothing expectorant, a root decoction for a systemic febrifuge, and a macerated bark poultice for localized wound care.

A practical, safe tea can be made from the dried leaves that Xhosa herbalists recommend for mild cough. Measure about 2 g (roughly 1–2 teaspoons) of the air‑dried foliage and place it in a cup. Pour 250 ml of just‑boiled water over the herb, cover, and allow it to steep for 5–7 minutes. Strain and drink the infusion warm, limiting intake to two or three cups per day. The preparation is gentle enough for most adults, but it should be avoided during pregnancy and in people with known hypersensitivity to Polygalaceae plants.

The therapeutic profile of Polygala fruticosa is rooted in a modest set of well‑studied phytochemicals. Chemical analyses repeatedly report the presence of saponins, especially polygala saponins I‑III, which are known to act as mild expectorants and anti‑inflammatory agents. The leaves also contain flavonoids such as quercetin and kaempferol, compounds widely recognised for their antioxidant and antitussive effects, and the bark is rich in simple coumarins that can stimulate circulation and support tissue repair. These constituents plausibly underpin the cough‑relieving, fever‑reducing and wound‑healing actions recorded in the ethnographic accounts.

Modern research has begun to catch up with these traditional uses. Recent pharmacological work has confirmed that extracts of Polygala fruticosa display anti‑inflammatory and antimicrobial activity in vitro, while a few South‑African herbal companies now market a limited range of tinctures and teas made from the plant, primarily for respiratory support. Although commercial products remain niche, the persistence of the plant in both the Xhosa and San pharmacopoeias suggests that its modest but effective role will continue to be appreciated by local communities and by herbal practitioners seeking gentle, plant‑based remedies.

General Uses Top

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Synonyms Top

Scientific name Authority First published in
Polygala diffusa A.Dietr. Allg. Gartenzeitung 2: 114 (1834)
Polygala cordifolia Thunb. Prodr. Pl. Cap. : 120 (1800)
Polygala dregeana C.Presl Abh. Königl. Böhm. Ges. Wiss. , ser. 5, 3: 444 (1845)
Polygala zeyheri Spreng. ex Eckl. & Zeyh. Enum. Pl. Afric. Austral. : 18 (1835)
Polygala tetragona Burch. ex DC. Prodr. 1: 322 (1824)
Polygala tomentosa Thunb. Prodr. Pl. Cap. : 120 (1800)
Polygala macrantha Turcz. Bull. Soc. Imp. Naturalistes Moscou 27(II): 345 (1854)
Polygala meyeriana C.Presl Abh. Königl. Böhm. Ges. Wiss. , ser. 5, 3: 444 (1845)
Polygala imbricata Hayek Ann. K. K. Naturhist. Hofmus. 15: 45 (1900 publ. 1901)
Polygala oppositifolia L. Mant. Pl. Altera 259. 1771 [Oct 1771]
Polygala oppositifolia var. latifolia (Ker Gawl.) Harv. Fl. Cap. 1: 82 1860
Polygala latifolia Ker Gawl. Bot. Reg. 8: t. 645 (1822)
Polygala nummularia Burch. ex DC. Prodr. 1: 322 (1824)
Polygala borboniifolia Burch. ex DC. Prodr. 1: 322 (1824)
Polygala rhombifolia Eckl. & Zeyh. Enum. Pl. Afric. Austral. : 18 (1835)

Common names Top

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Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) 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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001100350
Tropicos 25900612
KEW urn:lsid:ipni.org:names:691467-1
The Plant List tro-25900612
Open Tree Of Life 162378
NCBI Taxonomy 375122
IPNI 691467-1
iNaturalist 474386
GBIF 4049512
USDA GRIN 454978
Wikipedia Polygala_fruticosa
CMAUP NPO28158

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
Three-component synthesis of pyran-fused biscoumarins: an entry to pyridinone- and pyranone-fused coumarins Lee JT, Jatangi N, Vyasamudri S, Yang DY RSC Adv 07-May-2024
PMCID:PMC11075138
doi:10.1039/d4ra01681e
PMID:38716092
A review study on the anti-trichomonas activities of medicinal plants Hashemi N, Ommi D, Kheyri P, Khamesipour F, Setzer WN, Benchimol M Int J Parasitol Drugs Drug Resist 12-Feb-2021
PMCID:PMC7902805
doi:10.1016/j.ijpddr.2021.01.002
PMID:33610966
The traditional use of southern African medicinal plants for the treatment of bacterial respiratory diseases: A review of the ethnobotany and scientific evaluations Cock IE, Van Vuuren SF J Ethnopharmacol 27-Jul-2020
PMCID:PMC7383173
doi:10.1016/j.jep.2020.113204
PMID:32730881
Construction of trisubstituted chromone skeletons carrying electron-withdrawing groups via PhIO-mediated dehydrogenation and its application to the synthesis of frutinone A Li Q, Zhuang C, Wang D, Zhang W, Jia R, Sun F, Zhang Y, Du Y Beilstein J Org Chem 12-Dec-2019
PMCID:PMC6941426
doi:10.3762/bjoc.15.291
PMID:31921367
Exploring African Medicinal Plants for Potential Anti-Diabetic Compounds with the DIA-DB Inverse Virtual Screening Web Server Pereira AS, den Haan H, Peña-García J, Moreno MM, Pérez-Sánchez H, Apostolides Z Molecules 24-May-2019
PMCID:PMC6571761
doi:10.3390/molecules24102002
PMID:31137754
Review of Ethnomedicinal Uses, Phytochemistry and Pharmacological Properties of Euclea natalensis A.DC. Maroyi A Molecules 02-Dec-2017
PMCID:PMC6149716
doi:10.3390/molecules22122128
PMID:29207467
The anti-inflammatory and antioxidant activity of 25 plant species used traditionally to treat pain in southern African Adebayo SA, Dzoyem JP, Shai LJ, Eloff JN BMC Complement Altern Med 27-May-2015
PMCID:PMC4443658
doi:10.1186/s12906-015-0669-5
PMID:26014115
In Vitro Antimicrobial Activity of Extracts from Plants Used Traditionally in South Africa to Treat Tuberculosis and Related Symptoms Madikizela B, Ndhlala AR, Finnie JF, Staden JV Evid Based Complement Alternat Med 05-Mar-2013
PMCID:PMC3603154
doi:10.1155/2013/840719
PMID:23533527
New chromonocoumarin (=6<i>H</i>, 7<i>H</i>‐[1]Benzopyrano[4,3‐<i>b</i>][1]benzopyran‐6,7‐dione) derivatives from <i>Polygala fruticosa</i> BERG Ermindo R. Di Paolo, Matthias O. Hamburger, Helen Stoeckli‐Evans, Colin Rogers, Kurt Hostettmann Wiley 28-Dec-2004
doi:10.1002/HLCA.19890720705

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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
Syringic Acid 10742 Click to see 198.17 unknown via CMAUP database
> Benzenoids / Phenanthrenes and derivatives / Hydrophenanthrenes
(2R,4aS,4bR,6R,7R,10aR)-6,7-dihydroxy-2,4b-dimethyl-2-(2-methylfuran-3-yl)-4,4a,5,6,7,8,10,10a-octahydro-3H-phenanthren-1-one 101418443 Click to see 344.40 unknown via CMAUP database
(2R,4aS,4bR,6R,7R,10aR)-6,7-dihydroxy-4b-methyl-2-(2-methylfuran-3-yl)-2,3,4,4a,5,6,7,8,10,10a-decahydrophenanthren-1-one 15378970 Click to see 330.40 unknown via CMAUP database
> Lignans, neolignans and related compounds
(S)-[4-[4-[(R)-hydroxy-[(2R)-oxiran-2-yl]methyl]-2,6-dimethoxyphenyl]-3,5-dimethoxyphenyl]-[(2S)-oxiran-2-yl]methanol 10971809 Click to see 418.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
Azelaic Acid 2266 Click to see C(CCCC(=O)O)CCCC(=O)O 188.22 unknown via CMAUP database
CID 22494956 22494956 Click to see 174.19 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3S,9S,10R,13R,14S,17R)-10,13-Dimethyl-17-[(E,2R)-5-propan-2-ylhept-5-en-2-yl]-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 16061350 Click to see 412.70 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Dicarboxylic acids and derivatives
CID 21952380 21952380 Click to see 118.09 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(4S,5R,8S,13R,16S,19R,22R)-8-[(2R,4R,5R,6R)-5-Hydroxy-4-methoxy-6-methyloxan-2-yl]oxy-5,19-dimethyl-15,18,20-trioxapentacyclo[14.5.1.04,13.05,10.019,22]docosa-1(21),10-dien-14-one 21574520 Click to see CC1C(C(CC(O1)OC2CCC3(C4CCC5=COC6(C5C(CO6)OC(=O)C4CC=C3C2)C)C)OC)O 504.60 unknown via CMAUP database
(4S,5R,8S,13S,16S,19R,22R)-8-[(2R,3R,4S,5R,6R)-3,5-dihydroxy-4-methoxy-6-methyloxan-2-yl]oxy-5,19-dimethyl-15,18,20-trioxapentacyclo[14.5.1.04,13.05,10.019,22]docosa-1(21),10-dien-14-one 44584779 Click to see 520.60 unknown via CMAUP database
Glaucogenin C mono-D-thevetoside 21632986 Click to see CC1C(C(C(C(O1)OC2CCC3(C4CCC5=COC6(C5C(CO6)OC(=O)C4CC=C3C2)C)C)O)OC)O 520.60 unknown via CMAUP database
Sucrose 5988 Click to see 342.30 unknown https://doi.org/10.1002/HLCA.19890720705
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
(1S,2R,6R,7R,8aR)-7-hydroxy-6-[(2S,4S,5R,6R)-4-methoxy-5-[(2S,4S,5R,6S)-4-methoxy-5-[(2S,4S,5R,6R)-4-methoxy-6-methyl-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-6-methyloxan-2-yl]oxy-6-methyloxan-2-yl]oxy-8a-methyl-1-[3-(2-methylfuran-3-yl)-3-oxopropyl]-2,3,5,6,7,8-hexahydro-1H-naphthalene-2-carboxylic acid 11320582 Click to see 957.10 unknown via CMAUP database
(1S,2R,6R,7R,8aR)-7-hydroxy-6-[(2S,4S,5R,6R)-5-[(2S,4S,5R,6S)-5-[(2S,4S,5R,6R)-5-hydroxy-4-methoxy-6-methyloxan-2-yl]oxy-4-methoxy-6-methyloxan-2-yl]oxy-4-methoxy-6-methyloxan-2-yl]oxy-8a-methyl-1-[3-(2-methylfuran-3-yl)-3-oxopropyl]-2,3,5,6,7,8-hexahydro-1H-naphthalene-2-carboxylic acid 11764254 Click to see CC1C(C(CC(O1)OC2C(OC(CC2OC)OC3C(OC(CC3OC)OC4CC5=CCC(C(C5(CC4O)C)CCC(=O)C6=C(OC=C6)C)C(=O)O)C)C)OC)O 794.90 unknown via CMAUP database
(2R,4aS,4bR,5S,6R,7R,10aR)-5,6-dihydroxy-7-[(2S,4S,5R,6R)-4-methoxy-5-[(2S,4S,5R,6S)-4-methoxy-5-[(2S,4S,5R,6R)-4-methoxy-6-methyl-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-6-methyloxan-2-yl]oxy-6-methyloxan-2-yl]oxy-2,4b-dimethyl-2-(2-methylfuran-3-yl)-4,4a,5,6,7,8,10,10a-octahydro-3H-phenanthren-1-one 24775701 Click to see CC1C(C(CC(O1)OC2CC3=CCC4C(C3(C(C2O)O)C)CCC(C4=O)(C)C5=C(OC=C5)C)OC)OC6CC(C(C(O6)C)OC7CC(C(C(O7)C)OC8C(C(C(C(O8)CO)O)O)O)OC)OC 955.10 unknown via CMAUP database
(2R,4aS,4bR,5S,7R,10aR)-5-hydroxy-7-[(2S,4S,5R,6R)-4-methoxy-5-[(2S,4S,5R,6S)-4-methoxy-5-[(2S,4S,5R,6R)-4-methoxy-6-methyl-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-6-methyloxan-2-yl]oxy-6-methyloxan-2-yl]oxy-2,4b-dimethyl-2-(2-methylfuran-3-yl)-3,4,4a,5,7,8,10,10a-octahydrophenanthrene-1,6-dione 25232561 Click to see 953.10 unknown via CMAUP database
(2R,4aS,4bR,5S,7R,10aR)-5-hydroxy-7-[(2S,4S,5R,6R)-5-[(2S,4S,5R,6S)-5-[(2S,4S,5R,6R)-5-hydroxy-4-methoxy-6-methyloxan-2-yl]oxy-4-methoxy-6-methyloxan-2-yl]oxy-4-methoxy-6-methyloxan-2-yl]oxy-2,4b-dimethyl-2-(2-methylfuran-3-yl)-3,4,4a,5,7,8,10,10a-octahydrophenanthrene-1,6-dione 25232202 Click to see 790.90 unknown via CMAUP database
(2R,4aS,4bR,6R,7R,10aR)-6-hydroxy-7-[(2S,4S,5R,6R)-4-methoxy-5-[(2S,4R,5S,6S)-4-methoxy-5-[(2S,4S,5R,6R)-4-methoxy-6-methyl-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-6-methyloxan-2-yl]oxy-6-methyloxan-2-yl]oxy-4b-methyl-2-(2-methylfuran-3-yl)-2,3,4,4a,5,6,7,8,10,10a-decahydrophenanthren-1-one 11498916 Click to see CC1C(C(CC(O1)OC2CC3=CCC4C(C3(CC2O)C)CCC(C4=O)C5=C(OC=C5)C)OC)OC6CC(C(C(O6)C)OC7CC(C(C(O7)C)OC8C(C(C(C(O8)CO)O)O)O)OC)OC 925.10 unknown via CMAUP database
(2R,4aS,4bR,6R,7R,10aR)-6-hydroxy-7-[(2S,4S,5R,6R)-5-[(2S,4S,5S,6R)-4-hydroxy-5-[(2S,4R,5S,6S)-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-6-methyloxan-2-yl]oxy-4-methoxy-6-methyloxan-2-yl]oxy-4b-methyl-2-(2-methylfuran-3-yl)-2,3,4,4a,5,6,7,8,10,10a-decahydrophenanthren-1-one 24775609 Click to see CC1C(C(CC(O1)OC2C(OC(CC2OC)OC3CC4=CCC5C(C4(CC3O)C)CCC(C5=O)C6=C(OC=C6)C)C)O)OC7CC(C(C(O7)C)OC8C(C(C(C(O8)COC9C(C(C(C(O9)CO)O)O)O)O)O)O)OC 1073.20 unknown via CMAUP database
(2R,4aS,4bR,6R,7R,10aR)-7-[(2S,4S,5R,6R)-5-[(2S,4S,5R,6S)-5-[(2S,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-4-methoxy-6-methyloxan-2-yl]oxy-4-methoxy-6-methyloxan-2-yl]oxy-6-hydroxy-2,4b-dimethyl-2-(2-methylfuran-3-yl)-4,4a,5,6,7,8,10,10a-octahydro-3H-phenanthren-1-one 24775610 Click to see 957.10 unknown via CMAUP database
(2R,4aS,4bR,7R,10aR)-7-[(2S,4S,5R,6R)-5-[(2S,4S,5R,6S)-5-[(2S,4S,5R,6R)-5-hydroxy-4-methoxy-6-methyloxan-2-yl]oxy-4-methoxy-6-methyloxan-2-yl]oxy-4-methoxy-6-methyloxan-2-yl]oxy-2,4b-dimethyl-2-(2-methylfuran-3-yl)-3,4,4a,5,7,8,10,10a-octahydrophenanthrene-1,6-dione 25232560 Click to see CC1C(C(CC(O1)OC2C(OC(CC2OC)OC3C(OC(CC3OC)OC4CC5=CCC6C(C5(CC4=O)C)CCC(C6=O)(C)C7=C(OC=C7)C)C)C)OC)O 774.90 unknown via CMAUP database
(2R)-3-[(2R,4aS,4bR,6R,7R,10aR)-6-hydroxy-7-[(2S,4S,5R,6R)-4-methoxy-5-[(2S,4S,5R,6S)-4-methoxy-5-[(2S,4S,5R,6R)-4-methoxy-6-methyl-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-6-methyloxan-2-yl]oxy-6-methyloxan-2-yl]oxy-2,4b-dimethyl-1-oxo-4,4a,5,6,7,8,10,10a-octahydro-3H-phenanthren-2-yl]-2-methyl-2H-furan-5-one 25232022 Click to see CC1C(C(CC(O1)OC2CC3=CCC4C(C3(CC2O)C)CCC(C4=O)(C)C5=CC(=O)OC5C)OC)OC6CC(C(C(O6)C)OC7CC(C(C(O7)C)OC8C(C(C(C(O8)CO)O)O)O)OC)OC 955.10 unknown via CMAUP database
(2R)-3-[(2R,4aS,4bR,6R,7R,10aR)-6-hydroxy-7-[(2S,4S,5R,6R)-5-[(2S,4S,5R,6S)-5-[(2S,4S,5R,6R)-5-hydroxy-4-methoxy-6-methyloxan-2-yl]oxy-4-methoxy-6-methyloxan-2-yl]oxy-4-methoxy-6-methyloxan-2-yl]oxy-2,4b-dimethyl-1-oxo-4,4a,5,6,7,8,10,10a-octahydro-3H-phenanthren-2-yl]-2-methyl-2H-furan-5-one 25232021 Click to see 792.90 unknown via CMAUP database
(2S,4aS,4bR,6R,7R,10aR)-2,6-dihydroxy-7-[(2S,4S,5R,6R)-4-methoxy-5-[(2S,4S,5R,6S)-4-methoxy-5-[(2S,4S,5R,6R)-4-methoxy-6-methyl-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-6-methyloxan-2-yl]oxy-6-methyloxan-2-yl]oxy-4b-methyl-2-(2-methylfuran-3-yl)-4,4a,5,6,7,8,10,10a-octahydro-3H-phenanthren-1-one 25232200 Click to see 941.10 unknown via CMAUP database
(2S,4aS,4bR,6R,7R,10aR)-2,6-dihydroxy-7-[(2S,4S,5R,6R)-5-[(2S,4S,5S,6R)-4-hydroxy-5-[(2S,4S,5S,6S)-5-hydroxy-4-methoxy-6-methyloxan-2-yl]oxy-6-methyloxan-2-yl]oxy-4-methoxy-6-methyloxan-2-yl]oxy-4b-methyl-2-(2-methylfuran-3-yl)-4,4a,5,6,7,8,10,10a-octahydro-3H-phenanthren-1-one 25232559 Click to see 764.90 unknown via CMAUP database
(2S,4aS,4bR,6R,7R,10aR)-6-hydroxy-7-[(2S,4S,5R,6R)-5-[(2S,4S,5R,6S)-5-[(2S,4S,5R,6R)-5-hydroxy-4-methoxy-6-methyloxan-2-yl]oxy-4-methoxy-6-methyloxan-2-yl]oxy-4-methoxy-6-methyloxan-2-yl]oxy-4b-methyl-2-(2-methylfuran-3-yl)-2,3,4,4a,5,6,7,8,10,10a-decahydrophenanthren-1-one 24775700 Click to see CC1C(C(CC(O1)OC2C(OC(CC2OC)OC3C(OC(CC3OC)OC4CC5=CCC6C(C5(CC4O)C)CCC(C6=O)C7=C(OC=C7)C)C)C)OC)O 762.90 unknown via CMAUP database
(2S)-3-[(2R,4aS,4bR,6R,7R,10aR)-6-hydroxy-7-[(2S,4S,5R,6R)-4-methoxy-5-[(2S,4S,5R,6S)-4-methoxy-5-[(2S,4S,5R,6R)-4-methoxy-6-methyl-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-6-methyloxan-2-yl]oxy-6-methyloxan-2-yl]oxy-2,4b-dimethyl-1-oxo-4,4a,5,6,7,8,10,10a-octahydro-3H-phenanthren-2-yl]-2-methyl-2H-furan-5-one 25232385 Click to see CC1C(C(CC(O1)OC2CC3=CCC4C(C3(CC2O)C)CCC(C4=O)(C)C5=CC(=O)OC5C)OC)OC6CC(C(C(O6)C)OC7CC(C(C(O7)C)OC8C(C(C(C(O8)CO)O)O)O)OC)OC 955.10 unknown via CMAUP database
(2S)-3-[(2R,4aS,4bR,6R,7R,10aR)-6-hydroxy-7-[(2S,4S,5R,6R)-5-[(2S,4S,5R,6S)-5-[(2S,4S,5R,6R)-5-hydroxy-4-methoxy-6-methyloxan-2-yl]oxy-4-methoxy-6-methyloxan-2-yl]oxy-4-methoxy-6-methyloxan-2-yl]oxy-2,4b-dimethyl-1-oxo-4,4a,5,6,7,8,10,10a-octahydro-3H-phenanthren-2-yl]-2-methyl-2H-furan-5-one 25232020 Click to see 792.90 unknown via CMAUP database
(4S,5R,7R,8R,13R,16R,19R,22S)-7,22-dihydroxy-8-[(2S,4S,5R,6R)-4-methoxy-5-[(2S,4S,5R,6S)-4-methoxy-5-[(2S,4S,5R,6R)-4-methoxy-6-methyl-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-6-methyloxan-2-yl]oxy-6-methyloxan-2-yl]oxy-5,19-dimethyl-15,18,20-trioxapentacyclo[14.5.1.04,13.05,10.019,22]docosa-1(21),10-dien-14-one 11400424 Click to see CC1C(C(CC(O1)OC2CC3=CCC4C(C3(CC2O)C)CCC5=COC6(C5(C(CO6)OC4=O)O)C)OC)OC7CC(C(C(O7)C)OC8CC(C(C(O8)C)OC9C(C(C(C(O9)CO)O)O)O)OC)OC 987.10 unknown via CMAUP database
(4S,5R,7R,8R,13R,16R,19R,22S)-7,22-dihydroxy-8-[(2S,4S,5R,6R)-5-[(2S,4S,5R,6S)-5-[(2S,4S,5R,6R)-5-hydroxy-4-methoxy-6-methyloxan-2-yl]oxy-4-methoxy-6-methyloxan-2-yl]oxy-4-methoxy-6-methyloxan-2-yl]oxy-5,19-dimethyl-15,18,20-trioxapentacyclo[14.5.1.04,13.05,10.019,22]docosa-1(21),10-dien-14-one 11354844 Click to see 824.90 unknown via CMAUP database
(4S,5R,7R,8R,13R,16R,19R,22S)-7,22-dihydroxy-8-[(2S,4S,5R,6R)-5-[(2S,4S,5S,6R)-4-hydroxy-5-[(2S,4R,5S,6S)-5-hydroxy-4-methoxy-6-methyloxan-2-yl]oxy-6-methyloxan-2-yl]oxy-4-methoxy-6-methyloxan-2-yl]oxy-5,19-dimethyl-15,18,20-trioxapentacyclo[14.5.1.04,13.05,10.019,22]docosa-1(21),10-dien-14-one 11445764 Click to see 810.90 unknown via CMAUP database
(4S,5R,7R,8R,13R,16R,19R,22S)-7,22-dihydroxy-8-[(2S,4S,5R,6R)-5-[(2S,4S,5S,6R)-4-hydroxy-5-[(2S,4S,5S,6S)-5-hydroxy-4-methoxy-6-methyloxan-2-yl]oxy-6-methyloxan-2-yl]oxy-4-methoxy-6-methyloxan-2-yl]oxy-5,19-dimethyl-15,18,20-trioxapentacyclo[14.5.1.04,13.05,10.019,22]docosa-1(21),10-dien-14-one 11205104 Click to see 810.90 unknown via CMAUP database
(4S,5R,7R,8R,13R,16S,19R,22R)-7-hydroxy-8-[(2R,4R,5S,6S)-5-[(2S,4S,5S,6R)-4-hydroxy-5-[(2S,4R,5S,6S)-4-methoxy-6-methyl-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-6-methyloxan-2-yl]oxy-4-methoxy-6-methyloxan-2-yl]oxy-5,19-dimethyl-15,18,20-trioxapentacyclo[14.5.1.04,13.05,10.019,22]docosa-1(21),10-dien-14-one 21636204 Click to see CC1C(C(CC(O1)OC2C(OC(CC2OC)OC3CC4=CCC5C(C4(CC3O)C)CCC6=COC7(C6C(CO7)OC5=O)C)C)O)OC8CC(C(C(O8)C)OC9C(C(C(C(O9)CO)O)O)O)OC 957.10 unknown via CMAUP database
(4S,5R,7R,8R,13R,16S,19R,22R)-7-hydroxy-8-[(2R,4R,5S,6S)-5-[(2S,4S,5S,6R)-4-hydroxy-5-[(2S,4R,5S,6S)-5-hydroxy-4-methoxy-6-methyloxan-2-yl]oxy-6-methyloxan-2-yl]oxy-4-methoxy-6-methyloxan-2-yl]oxy-5,19-dimethyl-15,18,20-trioxapentacyclo[14.5.1.04,13.05,10.019,22]docosa-1(21),10-dien-14-one 21636203 Click to see CC1C(C(CC(O1)OC2C(OC(CC2O)OC3C(OC(CC3OC)OC4CC5=CCC6C(C5(CC4O)C)CCC7=COC8(C7C(CO8)OC6=O)C)C)C)OC)O 794.90 unknown via CMAUP database
(4S,5R,7R,8R,13R,16S,19R,22R)-7-hydroxy-8-[(2S,4S,5R,6R)-4-methoxy-5-[(2S,4S,5R,6S)-4-methoxy-5-[(2S,4S,5R,6R)-4-methoxy-6-methyl-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-6-methyloxan-2-yl]oxy-6-methyloxan-2-yl]oxy-5,19-dimethyl-15,18,20-trioxapentacyclo[14.5.1.04,13.05,10.019,22]docosa-1(21),10-dien-14-one 11158941 Click to see CC1C(C(CC(O1)OC2CC3=CCC4C(C3(CC2O)C)CCC5=COC6(C5C(CO6)OC4=O)C)OC)OC7CC(C(C(O7)C)OC8CC(C(C(O8)C)OC9C(C(C(C(O9)CO)O)O)O)OC)OC 971.10 unknown via CMAUP database
(4S,5R,7R,8R,13R,16S,19R,22R)-7-hydroxy-8-[(2S,4S,5R,6R)-5-[(2S,4S,5R,6S)-5-[(2S,4S,5R,6R)-5-hydroxy-4-methoxy-6-methyloxan-2-yl]oxy-4-methoxy-6-methyloxan-2-yl]oxy-4-methoxy-6-methyloxan-2-yl]oxy-5,19-dimethyl-15,18,20-trioxapentacyclo[14.5.1.04,13.05,10.019,22]docosa-1(21),10-dien-14-one 11803490 Click to see 808.90 unknown via CMAUP database
(4S,5R,8S,13R,16S,19R,22R)-8-[(2R,4R,5R,6R)-5-[(2S,4S,5S,6R)-4-hydroxy-5-[(2R,4R,5R,6R)-4-methoxy-6-methyl-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-6-methyloxan-2-yl]oxy-4-methoxy-6-methyloxan-2-yl]oxy-5,19-dimethyl-15,18,20-trioxapentacyclo[14.5.1.04,13.05,10.019,22]docosa-1(21),10-dien-14-one 21632985 Click to see CC1C(C(CC(O1)OC2C(OC(CC2OC)OC3CCC4(C5CCC6=COC7(C6C(CO7)OC(=O)C5CC=C4C3)C)C)C)O)OC8CC(C(C(O8)C)OC9C(C(C(C(O9)CO)O)O)O)OC 941.10 unknown via CMAUP database
(4S,5R,8S,13R,16S,19R,22R)-8-[(2R,4R,5R,6R)-5-[(2S,4S,5S,6R)-4-hydroxy-5-[(2R,4R,5R,6R)-5-hydroxy-4-methoxy-6-methyloxan-2-yl]oxy-6-methyloxan-2-yl]oxy-4-methoxy-6-methyloxan-2-yl]oxy-5,19-dimethyl-15,18,20-trioxapentacyclo[14.5.1.04,13.05,10.019,22]docosa-1(21),10-dien-14-one 21632983 Click to see 778.90 unknown via CMAUP database
(4S,5R,8S,13R,16S,19R,22R)-8-[(2R,4R,5R,6R)-5-[(2S,4S,5S,6R)-4-hydroxy-5-[(2S,4R,5S,6S)-5-hydroxy-4-methoxy-6-methyloxan-2-yl]oxy-6-methyloxan-2-yl]oxy-4-methoxy-6-methyloxan-2-yl]oxy-5,19-dimethyl-15,18,20-trioxapentacyclo[14.5.1.04,13.05,10.019,22]docosa-1(21),10-dien-14-one 21632982 Click to see CC1C(C(CC(O1)OC2C(OC(CC2O)OC3C(OC(CC3OC)OC4CCC5(C6CCC7=COC8(C7C(CO8)OC(=O)C6CC=C5C4)C)C)C)C)OC)O 778.90 unknown via CMAUP database
(5aR,9R,10R,11aR,11bS)-10-hydroxy-9-[(2S,4S,5R,6R)-4-methoxy-5-[(2S,4S,5R,6S)-4-methoxy-5-[(2S,4S,5R,6R)-4-methoxy-6-methyl-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-6-methyloxan-2-yl]oxy-6-methyloxan-2-yl]oxy-11a-methyl-3-(2-methylfuran-3-yl)-1,5a,6,8,9,10,11,11b-octahydrobenzo[g][2]benzoxepin-5-one 11263117 Click to see 939.00 unknown via CMAUP database
2-[(1R,2R,6R,7R,8aR)-7-hydroxy-6-[(2S,4S,5R,6R)-5-[(2S,4S,5R,6S)-5-[(2S,4S,5R,6R)-5-hydroxy-4-methoxy-6-methyloxan-2-yl]oxy-4-methoxy-6-methyloxan-2-yl]oxy-4-methoxy-6-methyloxan-2-yl]oxy-8a-methyl-2-(2-methylfuran-3-carbonyl)oxy-2,3,5,6,7,8-hexahydro-1H-naphthalen-1-yl]acetic acid 25232384 Click to see 796.90 unknown via CMAUP database
Cynanoside C 11285756 Click to see CC1C(C(CC(O1)OC2C(OC(CC2O)OC3C(OC(CC3OC)OC4CC5=CCC(C(C5(CC4O)C)CCC(=O)C6=C(OC=C6)C)C(=O)O)C)C)OC)O 780.90 unknown via CMAUP database
cynanoside K 24775699 Click to see 925.10 unknown via CMAUP database
cynanoside P5 25232386 Click to see 985.10 unknown via CMAUP database
cynanoside Q3 25232201 Click to see 927.00 unknown via CMAUP database
cynatratoside B 90670869 Click to see 778.90 unknown via CMAUP database
Cynatratoside D 21632984 Click to see 941.10 unknown via CMAUP database
Glaucoside C 11764253 Click to see 794.90 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
3',4'-Dihydroxyacetophenone 14530 Click to see 152.15 unknown via CMAUP database
4'-Hydroxyacetophenone 7469 Click to see 136.15 unknown via CMAUP database
Acetovanillone 2214 Click to see 166.17 unknown via CMAUP database
Resacetophenone 6990 Click to see CC(=O)C1=C(C=C(C=C1)O)O 152.15 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives
11-Hydroxychromeno[4,3-b]chromene-6,7-dione 14442651 Click to see 280.23 unknown https://doi.org/10.1002/HLCA.19890720705
4-Methoxychromeno[4,3-b]chromene-6,7-dione 11808521 Click to see COC1=CC=CC2=C1OC(=O)C3=C2OC4=CC=CC=C4C3=O 294.26 unknown https://doi.org/10.1002/HLCA.19890720705
6H,7H-(1)Benzopyrano(4,3-b)(1)benzopyran-6,7-dione 441965 Click to see 264.23 unknown https://doi.org/10.1002/HLCA.19890720705

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