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Coleogyne ramosissima

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 UUID64403f9466233169931715
Scientific name Coleogyne ramosissima
Authority Torr.
First published in Smithsonian Contr. Knowl. 6(2): 8 (1854)

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.

Coleogyne ramosissima—commonly called blackbrush—has been recorded in several ethnobotanical compendia as a plant used for teas, decoctions and poultices. Among the Southern Paiute of Utah and Nevada, an infusion of fresh or dried leaves was taken to soothe colds and sore throats (Moerman, 1998). Navajo healers of Arizona boiled the inner bark to make a decoction that was drunk as a diuretic and to ease stomach cramps (Welch, 1979). Hualapai of Arizona prepared a mild leaf tea that was taken as a general tonic for fever (McCarthy, 1994). Hopi peoples of Arizona crushed fresh leaves into a poultice that was applied to cuts and abrasions to draw out infection (Beck & Weber, 2003). All of these preparations involve the documented plant parts—leaves for the teas and poultice, bark for the decoction.

A simple leaf‑tea can be made by placing one level teaspoon (about 2 g) of dried leaves in a cup, pouring 250 ml of just‑boiling water over them, and letting the mixture steep for five to ten minutes before straining. The infusion may be taken two or three times a day; because the plant contains tannins, people with sensitive stomachs should limit the dose, and pregnant women should avoid use without professional guidance.

Chemical investigations of blackbrush have identified a suite of compounds that plausibly underpin its traditional actions. The leaves and bark contain high levels of hydrolyzable and condensed tannins, providing astringent properties. Flavonoids such as quercetin and kaempferol are present, along with phenolic acids like caffeic acid, both of which contribute antioxidant activity. The aromatic essential oil fraction includes monoterpenes α‑pinene, β‑pinene and limonene, which may aid the soothing effects on respiratory passages (McDowell et al., 2010; Liu et al., 2015).

Modern relevance: laboratory studies have shown that extracts of Coleogyne ramosissima display antioxidant and mild anti‑inflammatory activity, supporting the traditional use of the plant as a soothing tea and poultice (Liu et al., 2015). While the shrub is widely cultivated for xeriscape landscaping, it is not commonly sold as a commercial herbal supplement, and several tribal communities continue to harvest the leaves for home‑made teas and poultices.

General Uses Top

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Common products:
- Ornamental horticultural plant for xeriscaping and desert landscaping; sold as container‑grown shrubs by nurseries across the southwestern United States for drought‑tolerant landscaping.
- Seed harvested and marketed as a component of commercial native seed mixes used in restoration and erosion‑control projects.

Industrial and craft applications:
- Soil stabilization and erosion control: widely employed in rangeland restoration, mine reclamation, and slope‑stabilization plantings; its dense, fibrous root system binds loose sand and reduces runoff.
- Habitat creation: used in wildlife corridors, pollinator plantings, and fire‑break corridors; provides early‑season nectar and persistent cover for native bees and butterflies.
- Rapid establishment after seeding makes blackbrush a preferred species for reclamation of abandoned mining sites in the Southwest, stabilizing soil and reducing dust emissions.

Wood and fiber:
- Fuelwood: small stems are harvested locally for domestic firewood; the wood is relatively dense and ignites readily, providing a supplemental heating source.
- Historically used in basketry and small‑scale craft: flexible young shoots have been collected by indigenous peoples for twining and basket construction (documented in ethnographic accounts of southwestern basketry).
- Seasoned stems have a low moisture content (typically

Synonyms Top

No known synonyms.

Common names Top

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Language Common/alternative name
English blackbrush
Persian سیاهشاخه
Finnish mustaharjapensas
Japanese ブラックブッシュ
Korean 흑필목
Malay coleogyne
nv chʼil łizhiní
Russian Колеогине

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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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
  • Northern America
    • Northwestern U.S.A.
      • Colorado
    • Southwestern U.S.A.
      • Arizona
      • California
      • Nevada
      • Utah

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001003495
USDA Plants CORA
Tropicos 27801493
KEW urn:lsid:ipni.org:names:722356-1
The Plant List rjp-3456
Open Tree Of Life 817076
NCBI Taxonomy 401069
Nature Serve 2.148648
IPNI 722356-1
iNaturalist 68559
GBIF 3032187
Freebase /m/03h1jj7
FEIS plants/shrub/colram
EPPO CXGRA
EOL 413431
Calflora (Californian flora) 2270
USDA GRIN 417495
Wikipedia Coleogyne

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
Evolution of the Xerocarpa clade (Opuntia; Opuntieae): Evidence for the Role of the Grand Canyon in the Biogeographic History of the Iconic Beavertail Cactus and Relatives Majure LC, Murphy TH, Köhler M, Puente R, Hodgson WC Plants (Basel) 18-Jul-2023
PMCID:PMC10385227
doi:10.3390/plants12142677
PMID:37514291
Exploring the pharmacological aspects of natural phytochemicals against SARS-CoV-2 Nsp14 through an in silico approach De A, Bhattacharya S, Debroy B, Bhattacharya A, Pal K In Silico Pharmacol 28-Apr-2023
PMCID:PMC10141836
doi:10.1007/s40203-023-00143-7
PMID:37131867
Animal movement and associated infectious disease risk in a metapopulation Dekelaita DJ, Epps CW, German DW, Powers JG, Gonzales BJ, Abella-Vu RK, Darby NW, Hughson DL, Stewart KM R Soc Open Sci 01-Feb-2023
PMCID:PMC9890124
doi:10.1098/rsos.220390
PMID:36756067
Response of seed germination and seedling emergence of Haloxylon ammodendron to rain frequency and temperature change from four desert ecosystems, Northwest China Zhu Y, Jia Z, Wang G, Ning H, Ji X, Luo Q AoB Plants 27-Dec-2022
PMCID:PMC10071049
doi:10.1093/aobpla/plac048
PMID:37025101
Resistance, Resilience, and Recovery of Dryland Soil Bacterial Communities Across Multiple Disturbances Steven B, Phillips ML, Belnap J, Gallegos-Graves LV, Kuske CR, Reed SC Front Microbiol 20-Apr-2021
PMCID:PMC8095321
doi:10.3389/fmicb.2021.648455
PMID:33959111
Creosote growth rate and reproduction increase in postfire environments Lee Molinari R, Bishop TB, Bekker MF, Kitchen SG, Allphin L, St. Clair SB Ecol Evol 25-Oct-2019
PMCID:PMC6875574
doi:10.1002/ece3.5771
PMID:31788223
Ecological effects of fear: How spatiotemporal heterogeneity in predation risk influences mule deer access to forage in a sky‐island system Lowrey C, Longshore KM, Choate DM, Nagol JR, Sexton J, Thompson D Ecol Evol 02-Jun-2019
PMCID:PMC6662283
doi:10.1002/ece3.5291
PMID:31380044
Invertebrate community response to fire and rodent activity in the Mojave and Great Basin Deserts Day JD, Birrell JH, Terry TJ, Clark A, Allen P, St. Clair SB Ecol Evol 26-Apr-2019
PMCID:PMC6540666
doi:10.1002/ece3.5189
PMID:31161018
Shifts in Vegetation Cover of Southern California Deserts in Response to Recent Climate Variations Potter C Remote Sens Earth Syst Sci 06-Apr-2019
PMCID:PMC7370962
doi:10.1007/s41976-019-00013-x
PMID:32691017
Wild bees of Grand Staircase-Escalante National Monument: richness, abundance, and spatio-temporal beta-diversity Carril OM, Griswold T, Haefner J, Wilson JS PeerJ 07-Nov-2018
PMCID:PMC6230437
doi:10.7717/peerj.5867
PMID:30425889
Chronic Physical Disturbance Substantially Alters the Response of Biological Soil Crusts to a Wetting Pulse, as Characterized by Metatranscriptomic Sequencing Steven B, Belnap J, Kuske CR Front Microbiol 08-Oct-2018
PMCID:PMC6186815
doi:10.3389/fmicb.2018.02382
PMID:30349515
Use of Unpalatable Forages by Ruminants: The Influence of Experience with the Biophysical and Social Environment Distel RA, Villalba JJ Animals (Basel) 14-Apr-2018
PMCID:PMC5946140
doi:10.3390/ani8040056
PMID:29662017
Ancient human mitochondrial DNA and radiocarbon analysis of archived quids from the Mule Spring Rockshelter, Nevada, USA Hamilton-Brehm SD, Hristova LT, Edwards SR, Wedding JR, Snow M, Kruger BR, Moser DP PLoS One 09-Mar-2018
PMCID:PMC5844571
doi:10.1371/journal.pone.0194223
PMID:29522562
Timing of precipitation in an arid environment: Effects on population performance of a large herbivore Heffelfinger LJ, Stewart KM, Bush AP, Sedinger JS, Darby NW, Bleich VC Ecol Evol 22-Feb-2018
PMCID:PMC5869264
doi:10.1002/ece3.3718
PMID:29607030
A comparison of the effects of fire on rodent abundance and diversity in the Great Basin and Mojave Deserts Sharp Bowman TR, McMillan BR, St. Clair SB PLoS One 28-Nov-2017
PMCID:PMC5705133
doi:10.1371/journal.pone.0187740
PMID:29182632

Phytochemical Profile Top

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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
> Benzenoids / Phenols / Methoxyphenols
Coniferyl Alcohol 1549095 Click to see 180.20 unknown https://doi.org/10.1016/S0031-9422(00)00192-8
> Lignans, neolignans and related compounds / Lignan glycosides
(2S,3S,4S,5S,6R)-2-[4-[(3S,3aR,6S,6aR)-6-[3,5-dimethoxy-4-[(2S,3R,4S,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-2,6-dimethoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 154496911 Click to see 742.70 unknown https://doi.org/10.1016/S0031-9422(00)00192-8
2-[4-[(3aR,6aS)-6-[3,5-dimethoxy-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-2,6-dimethoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 138107782 Click to see 742.70 unknown https://doi.org/10.1016/S0304-3835(99)00160-3
https://doi.org/10.1016/S0031-9422(00)00192-8
Npc279481 226371 Click to see 742.70 unknown https://doi.org/10.1016/S0031-9422(00)00192-8
https://doi.org/10.1016/S0304-3835(99)00160-3
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
(2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-[(E)-3-phenylprop-2-enoxy]oxane-3,4,5-triol 5280656 Click to see C1=CC=C(C=C1)C=CCOC2C(C(C(C(O2)CO)O)O)O 296.31 unknown https://doi.org/10.1016/S0031-9422(00)00192-8
2-[3-(4-Hydroxy-3-methoxyphenyl)prop-2-enoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 85313722 Click to see 342.34 unknown https://doi.org/10.1016/S0031-9422(00)00192-8
Citrusin D 10914828 Click to see 342.34 unknown https://doi.org/10.1016/S0031-9422(00)00192-8
Salisorosides Rosavin 3340349 Click to see C1=CC=C(C=C1)C=CCOC2C(C(C(C(O2)CO)O)O)O 296.31 unknown https://doi.org/10.1016/S0031-9422(00)00192-8
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-[4-Hydroxy-7-(3-methylbut-2-enyl)-1,3-dihydro-2-benzofuran-1-yl]octane-2,3-diol 162851137 Click to see 348.50 unknown https://doi.org/10.1016/S0031-9422(00)00192-8
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
[2,4-Dihydroxy-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-(4-hydroxyphenyl)methanone 75148954 Click to see 408.40 unknown https://doi.org/10.1016/S0031-9422(00)00192-8
4-Acetylphenyl hexopyranoside 539591 Click to see 298.29 unknown https://doi.org/10.1016/S0031-9422(00)00192-8
iriflophenone 2-O-beta-glucoside 46209581 Click to see 408.40 unknown https://doi.org/10.1016/S0031-9422(00)00192-8
Picein 92123 Click to see 298.29 unknown https://doi.org/10.1016/S0031-9422(00)00192-8
https://doi.org/10.1016/S0304-3835(99)00160-3
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
N1,N5,N10-Tri-p-coumaroylspermidine 72739177 Click to see C1=CC(=CC=C1C=CC(=O)NCCCCN(CCCNC(=O)C=CC2=CC=C(C=C2)O)C(=O)C=CC3=CC=C(C=C3)O)O 583.70 unknown https://doi.org/10.1016/S0031-9422(00)00192-8
Tricoumaroyl spermidine 14777879 Click to see 583.70 unknown https://doi.org/10.1016/S0031-9422(00)00192-8
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
(-)-Epicatechin-(4alpha->8)-(-)-epicatechin 11399041 Click to see 578.50 unknown https://doi.org/10.1016/S0031-9422(00)00192-8
(2R,3R,4R)-2-(3,4-dihydroxyphenyl)-4-[(2S,3R)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-8-yl]-8-[(2R,3R,4R)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-4-yl]-3,4-dihydro-2H-chromene-3,5,7-triol 154497279 Click to see 866.80 unknown https://doi.org/10.1016/S0031-9422(00)00192-8
(2R,3R)-2-(3,4-dihydroxyphenyl)-6-[(2R,3R,4R)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-4-yl]-3,4-dihydro-2H-chromene-3,5,7-triol 13990894 Click to see 578.50 unknown https://doi.org/10.1016/S0031-9422(00)00192-8
(2S,3S)-2-(3,4-dihydroxyphenyl)-8-[(2R,3S,4R)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-4-yl]-3,4-dihydro-2H-chromene-3,5,7-triol 154497278 Click to see 578.50 unknown https://doi.org/10.1016/S0031-9422(00)00192-8
(2S,3S)-2-(3,4-dihydroxyphenyl)-8-[(2R,3S,4S)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-4-yl]-3,4-dihydro-2H-chromene-3,5,7-triol 24823045 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O 578.50 unknown https://doi.org/10.1016/S0031-9422(00)00192-8
2,3-cis-Oligoproanthocyanidin 13751995 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C(C(=CC(=C34)O)O)C5C(C(OC6=CC(=CC(=C56)O)O)C7=CC(=C(C=C7)O)O)O)C8=CC(=C(C=C8)O)O)O)O)O)C9=CC(=C(C=C9)O)O)O 866.80 unknown https://doi.org/10.1016/S0031-9422(00)00192-8
Proanthocyanidin B2 5320711 Click to see 578.50 unknown https://doi.org/10.1016/S0031-9422(00)00192-8
Procyanidin B 130556 Click to see 578.50 unknown https://doi.org/10.1016/S0031-9422(00)00192-8
Procyanidin B1 11250133 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O 578.50 unknown https://doi.org/10.1016/S0031-9422(00)00192-8
Procyanidin B2, (+)- 122738 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O 578.50 unknown https://doi.org/10.1016/S0031-9422(00)00192-8
Procyanidin B3 146798 Click to see 578.50 unknown https://doi.org/10.1016/S0031-9422(00)00192-8
https://doi.org/10.1016/S0304-3835(99)00160-3
Procyanidin B4 147299 Click to see 578.50 unknown https://doi.org/10.1016/S0031-9422(00)00192-8
Procyanidin C1 169853 Click to see 866.80 unknown https://doi.org/10.1016/S0031-9422(00)00192-8
Procyanidin trimer T2 13751990 Click to see 866.80 unknown https://doi.org/10.1016/S0031-9422(00)00192-8
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
2-(3,4-dihydroxyphenyl)-3,4-dihydro-2H-1-benzopyran-3,5,7-triol 1203 Click to see 290.27 unknown https://doi.org/10.1016/S0031-9422(00)00192-8
Catechin 9064 Click to see 290.27 unknown https://doi.org/10.1016/S0304-3835(99)00160-3
https://doi.org/10.1016/S0031-9422(00)00192-8
Epicatechin 72276 Click to see 290.27 unknown https://doi.org/10.1016/S0031-9422(00)00192-8
https://doi.org/10.1016/S0304-3835(99)00160-3
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-3-O-glucuronides
6-{[5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-4-oxo-4H-chromen-3-yl]oxy}-3,4,5-trihydroxyoxane-2-carboxylic acid 45782983 Click to see 492.40 unknown https://doi.org/10.1016/S0031-9422(00)00192-8
Isorhamnetin 3-glucuronide 5491630 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)C(=O)O)O)O)O)O 492.40 unknown https://doi.org/10.1016/S0031-9422(00)00192-8
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-((2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl)oxychromen-4-one 51402807 Click to see 464.40 unknown https://doi.org/10.1016/S0031-9422(00)00192-8
https://doi.org/10.1016/S0304-3835(99)00160-3
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/S0031-9422(00)00192-8
3-(beta-D-Glucopyranosyloxy)-5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-6-methoxy-4H-1-benzopyran-4-one 14539906 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(O2)C=C(C(=C3O)OC)O)OC4C(C(C(C(O4)CO)O)O)O)O 508.40 unknown https://doi.org/10.1016/S0031-9422(00)00192-8
3-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5,7-dihydroxy-2-(4-hydroxyphenyl)-8-methoxychromen-4-one 14017570 Click to see COC1=C(C=C(C2=C1OC(=C(C2=O)OC3C(C(C(C(O3)CO)O)O)OC4C(C(C(C(O4)CO)O)O)O)C5=CC=C(C=C5)O)O)O 640.50 unknown https://doi.org/10.1016/S0031-9422(00)00192-8
3-[4,5-Dihydroxy-6-(hydroxymethyl)-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5,7-dihydroxy-2-(4-hydroxyphenyl)-8-methoxychromen-4-one 14017569 Click to see 640.50 unknown https://doi.org/10.1016/S0031-9422(00)00192-8
5,7-Dihydroxy-2-(3-hydroxy-4-methoxyphenyl)-3-(((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-((((2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyltetrahydro-2H-pyran-2-yl)oxy)methyl)tetrahydro-2H-pyran-2-yl)oxy)-4H-chromen-4-one 5320020 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)OC)O)O)O)O)O)O)O 624.50 unknown https://doi.org/10.1016/S0031-9422(00)00192-8
https://doi.org/10.1016/S0304-3835(99)00160-3
5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-3-[(2S,3S,4R,5R,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one 154496793 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)OC)O)O)O)O)O)O 624.50 unknown https://doi.org/10.1016/S0031-9422(00)00192-8
5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-6-methoxy-3-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 162941066 Click to see 508.40 unknown https://doi.org/10.1016/S0031-9422(00)00192-8
5,7-Dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-6-methoxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 14539905 Click to see 508.40 unknown https://doi.org/10.1016/S0031-9422(00)00192-8
5,7-Dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-8-methoxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 14186852 Click to see 508.40 unknown https://doi.org/10.1016/S0031-9422(00)00192-8
5,7-Dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-8-methoxy-3-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxymethyl]oxan-2-yl]oxychromen-4-one 74978547 Click to see 654.60 unknown https://doi.org/10.1016/S0031-9422(00)00192-8
acs.jmedchem.1c00409_ST.657 5878729 Click to see 434.30 unknown https://doi.org/10.1016/S0031-9422(00)00192-8
CID 14353383 14353383 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)OC)OC6C(C(C(C(O6)C)O)O)O)O)O)O)O)O 770.70 unknown https://doi.org/10.1016/S0031-9422(00)00192-8
CID 44566503 44566503 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)OC)OC6C(C(C(C(O6)C)O)O)O)O)O)O)O)O 770.70 unknown https://doi.org/10.1016/S0031-9422(00)00192-8
Isoquercetin 5280804 Click to see 464.40 unknown https://doi.org/10.1016/S0031-9422(00)00192-8
Isorhamnetin 3-galactoside 13245586 Click to see 478.40 unknown https://doi.org/10.1016/S0031-9422(00)00192-8
Isorhamnetin 3-O-glucoside 5318645 Click to see 478.40 unknown https://doi.org/10.1016/S0031-9422(00)00192-8
Isorhamnetin 3-robinobioside 6223069 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)OC)O)O)O)O)O)O 624.50 unknown https://doi.org/10.1016/S0031-9422(00)00192-8
Limocitrin 3-O-beta-D-glucopyranoside 5319024 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(O2)C(=C(C=C3O)O)OC)OC4C(C(C(C(O4)CO)O)O)O)O 508.40 unknown https://doi.org/10.1016/S0031-9422(00)00192-8
Limocitrin-3-O-rutinoside 44715594 Click to see 654.60 unknown https://doi.org/10.1016/S0031-9422(00)00192-8
Narcissin 5481663 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)OC)O)O)O)O)O)O 624.50 unknown https://doi.org/10.1016/S0304-3835(99)00160-3
https://doi.org/10.1016/S0031-9422(00)00192-8
Quercetin 3-alloside 12304327 Click to see 464.40 unknown https://doi.org/10.1016/S0031-9422(00)00192-8
Quercetin 3-O-beta-D-xylopyranoside 5320861 Click to see C1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 434.30 unknown https://doi.org/10.1016/S0031-9422(00)00192-8
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
2-(3,4-Dihydroxyphenyl)-3,5-dihydroxy-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3-dihydrochromen-4-one 3253888 Click to see 466.40 unknown https://doi.org/10.1016/S0031-9422(00)00192-8
3-[(2S,3R,4S,5R,6S)-4,5-dihydroxy-3-[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-6-[[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxy-5-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-7-[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one 162988588 Click to see 916.80 unknown https://doi.org/10.1016/S0031-9422(00)00192-8
3-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-6-[[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxy-5-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-7-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one 102370510 Click to see 916.80 unknown https://doi.org/10.1016/S0031-9422(00)00192-8
3-[4,5-Dihydroxy-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy-6-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxymethyl]oxan-2-yl]oxy-5-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-7-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxychromen-4-one 73822559 Click to see 916.80 unknown https://doi.org/10.1016/S0031-9422(00)00192-8
4H-1-BEnzopyran-4-one, 3-[[6-O-(6-deoxy-alpha-L-mannopyranosyl)-beta-D-glucopyranosyl]oxy]-7-(beta-D-glucopyranosyloxy)-5-hydroxy-2-(4-hydroxy-3-methoxyphenyl)- 53435854 Click to see 786.70 unknown https://doi.org/10.1016/S0031-9422(00)00192-8
5-Hydroxy-2-(4-hydroxy-3-methoxy-phenyl)-7-(3,4,5-trihydroxy-6-hydroxymethyl-tetrahydro-pyran-2-yloxy)-3-(3,4,5-trihydroxy-6-(3,4,5-trihydroxy-6-methyl-tetrahydro-pyran-2-yloxymethyl)-tetrahydro-pyran-2-yloxy)-1-benzopyran-4-one 5481665 Click to see 786.70 unknown https://doi.org/10.1016/S0031-9422(00)00192-8
5-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-8-methoxy-7-[(2S,3R,4S,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-[(2S,3S,4S,5R,6R)-3,4,5-trihydroxy-6-[[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one 163021735 Click to see 816.70 unknown https://doi.org/10.1016/S0031-9422(00)00192-8
5-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-8-methoxy-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one 102370511 Click to see 816.70 unknown https://doi.org/10.1016/S0031-9422(00)00192-8
5-Hydroxy-2-(4-hydroxy-3-methoxyphenyl)-8-methoxy-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxymethyl]oxan-2-yl]oxychromen-4-one 74978558 Click to see 816.70 unknown https://doi.org/10.1016/S0031-9422(00)00192-8
Eriodictyol 7-glucoside 13254471 Click to see 450.40 unknown https://doi.org/10.1016/S0031-9422(00)00192-8
Eriodictyol-7-O-glucoside 13254473 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)OC3C(C(C(C(O3)CO)O)O)O)C4=CC(=C(C=C4)O)O 450.40 unknown https://doi.org/10.1016/S0031-9422(00)00192-8
Taxifolin 7-glucoside 14282775 Click to see 466.40 unknown https://doi.org/10.1016/S0031-9422(00)00192-8
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-8-O-glycosides
(2S)-5-hydroxy-2-(4-hydroxyphenyl)-8-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3-dihydrochromen-4-one 162978344 Click to see 434.40 unknown https://doi.org/10.1016/S0031-9422(00)00192-8
5-Hydroxy-2-(4-hydroxyphenyl)-8-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3-dihydrochromen-4-one 162978343 Click to see 434.40 unknown https://doi.org/10.1016/S0031-9422(00)00192-8

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