Chrysothamnus viscidiflorus - Unknown
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Internal ID UUID643fcc72476b3994756704
Scientific name Chrysothamnus viscidiflorus
Authority Nutt.
First published in Trans. Amer. Philos. Soc. , ser. 2, 7: 324 (1840)

Description Top

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Synonyms Top

Scientific name Authority First published in
Chrysothamnus viscidiflorus var. typicus (H.M.Hall & Clem.) Cronquist
Chrysothamnus viscidiflorus var. viscidiflorus (Hook.) Nutt.

Common names Top

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Language Common/alternative name
English yellow rabbitbrush
English green rabbitbrush
English sticky-leaf rabbitbrush
English green rubber rabbit-brush
English douglas rabbitbrush
English douglas' rabbitbrush
nv chʼil dilyésiitsoh

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Chrysothamnus viscidiflorus subsp. axillaris (D.D.Keck) L.C.Anderson Great Basin Naturalist 40(2): 118. 1980
Chrysothamnus viscidiflorus subsp. lanceolatus H.M.Hall & Clem. Phylogen. Meth. 181, pl. 26 (1923)
Chrysothamnus viscidiflorus subsp. planifolius L.C.Anderson Madroño 17: 223 (1964)
Chrysothamnus viscidiflorus subsp. puberulus H.M.Hall & Clem. Phylogen. Meth. 182, pl. 26 (1923)
Chrysothamnus viscidiflorus subsp. viscidiflorus (Hook.) Nutt.

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
    • North-central U.S.A.
      • Nebraska
      • South Dakota
    • Northwestern U.S.A.
      • Colorado
      • Idaho
      • Montana
      • Oregon
      • Washington
      • Wyoming
    • South-central U.S.A.
      • New Mexico
    • Southwestern U.S.A.
      • Arizona
      • California
      • Nevada
      • Utah
    • Western Canada
      • British Columbia

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000062835
Canadensys 2984
USDA Plants CHVI8
Tropicos 2702285
KEW urn:lsid:ipni.org:names:194300-1
The Plant List gcc-1983
Open Tree Of Life 1008411
NCBI Taxonomy 72914
Nature Serve 2.145776
IPNI 194300-1
iNaturalist 76329
GBIF 3148638
Freebase /m/05p0fmv
FEIS plants/shrub/chrvis
EPPO CYTVI
EOL 467632
Calflora (Californian flora) 2099
USDA GRIN 104150
Wikipedia Chrysothamnus_viscidiflorus

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
The impact of selected xanthophylls on oil hydrolysis by pancreatic lipase: in silico and in vitro studies Dąbrowski G, Czaplicki S, Szustak M, Korkus E, Gendaszewska-Darmach E, Konopka I Sci Rep 01-Feb-2024
PMCID:PMC10834431
doi:10.1038/s41598-024-53312-9
PMID:38302772
Plant macrofossil data for 48-0 ka in the USGS North American Packrat Midden Database, version 5.0 Strickland LE, Thompson RS, Shafer SL, Bartlein PJ, Pelltier RT, Anderson KH, Schumann RR, McFadden AK Sci Data 12-Jan-2024
PMCID:PMC10786896
doi:10.1038/s41597-023-02616-y
PMID:38216580
Protein Supplementation and Grazing Behavior for Cows on Differing Late-Season Rangeland Grazing Systems Sprinkle JE, Sagers JK, Hall JB, Ellison MJ, Yelich JV, Brennan JR, Taylor JB, Lamb JB Animals (Basel) 11-Nov-2021
PMCID:PMC8614474
doi:10.3390/ani11113219
PMID:34827951
A Dual Role of Vanadium in Environmental Systems—Beneficial and Detrimental Effects on Terrestrial Plants and Humans Hanus-Fajerska E, Wiszniewska A, Kamińska I Plants (Basel) 31-May-2021
PMCID:PMC8227766
doi:10.3390/plants10061110
PMID:34072768
A Systematic Review on Comparative Analysis, Toxicology, and Pharmacology of Medicinal Plants Against Haemonchus contortus Ali R, Rooman M, Mussarat S, Norin S, Ali S, Adnan M, Khan SN Front Pharmacol 10-May-2021
PMCID:PMC8141741
doi:10.3389/fphar.2021.644027
PMID:34040520
Grazing behavior and production for cattle on differing late-season rangeland grazing systems with or without protein supplementation Sprinkle JE, Sagers JK, Hall JB, Ellison MJ, Yelich JV, Brennan JR, Taylor JB, Lamb JB Transl Anim Sci 16-Dec-2019
PMCID:PMC6999180
doi:10.1093/tas/txz100
PMID:32704954
Grazing behavior and production characteristics among cows differing in residual feed intake while grazing late season Idaho rangeland Sprinkle JE, Taylor JB, Clark PE, Hall JB, Strong NK, Roberts-Lew MC J Anim Sci 10-Dec-2019
PMCID:PMC6986444
doi:10.1093/jas/skz371
PMID:31820799
Nitrogen addition pulse has minimal effect in big sagebrush (Artemisia tridentata) communities on the Pinedale Anticline, Wyoming (USA) Beltz CW, Mobley ML, Burke IC PLoS One 31-May-2019
PMCID:PMC6544214
doi:10.1371/journal.pone.0206563
PMID:31150398
Isolation of a Novel Flavanonol and an Alkylresorcinol with Highly Potent Anti-Trypanosomal Activity from Libyan Propolis Siheri W, Ebiloma GU, Igoli JO, Gray AI, Biddau M, Akrachalanont P, Alenezi S, Alwashih MA, Edrada-Ebel R, Muller S, Lawrence CE, Fearnley J, Watson DG, De Koning HP Molecules 15-Mar-2019
PMCID:PMC6471328
doi:10.3390/molecules24061041
PMID:30884752
Hemiparasitic plants increase alpine plant richness and evenness but reduce arbuscular mycorrhizal fungal colonization in dominant plant species McKibben M, Henning JA PeerJ 07-Nov-2018
PMCID:PMC6228546
doi:10.7717/peerj.5682
PMID:30425882
Short‐term, low‐level nitrogen deposition dampens a trophic cascade between bears and plants Grinath JB Ecol Evol 25-Oct-2018
PMCID:PMC6262928
doi:10.1002/ece3.4593
PMID:30519438
Phytochemical Study of the Ecuadorian Species Lepechinia mutica (Benth.) Epling and High Antifungal Activity of Carnosol against Pyricularia oryzae Ramírez J, Gilardoni G, Ramón E, Tosi S, Picco AM, Bicchi C, Vidari G Pharmaceuticals (Basel) 19-Apr-2018
PMCID:PMC6027405
doi:10.3390/ph11020033
PMID:29671794
Seasonal temperature acclimatization in a semi-fossorial mammal and the role of burrows as thermal refuges Milling CR, Rachlow JL, Chappell MA, Camp MJ, Johnson TR, Shipley LA, Paul DR, Forbey JS PeerJ 16-Mar-2018
PMCID:PMC5858582
doi:10.7717/peerj.4511
PMID:29576977
AN INVERTEBRATE ECOSYSTEM ENGINEER UNDER THE UMBRELLA OF SAGE-GROUSE CONSERVATION Carlisle JD, Stewart DR, Chalfoun AD West N Am Nat 16-Jan-2017
PMCID:PMC10552609
doi:10.3398/064.077.0406
PMID:37799165
Extracting Plant Phenology Metrics in a Great Basin Watershed: Methods and Considerations for Quantifying Phenophases in a Cold Desert Snyder KA, Wehan BL, Filippa G, Huntington JL, Stringham TK, Snyder DK Sensors (Basel) 18-Nov-2016
PMCID:PMC5134607
doi:10.3390/s16111948
PMID:27869752

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 / Acetophenones
(R)-Bitalin A 12414277 Click to see CC(=O)C1=CC2=C(C=C1)OC(C2)C(=C)CO 218.25 unknown https://doi.org/10.1016/S0031-9422(00)84171-0
1-[(2S)-5-hydroxy-2-(3-hydroxyprop-1-en-2-yl)-2,3-dihydro-1-benzofuran-6-yl]ethanone 60099133 Click to see CC(=O)C1=C(C=C2CC(OC2=C1)C(=C)CO)O 234.25 unknown https://doi.org/10.1016/S0031-9422(00)84171-0
1-[5-Hydroxy-2-(3-hydroxyprop-1-en-2-yl)-2,3-dihydro-1-benzofuran-6-yl]ethanone 15601733 Click to see CC(=O)C1=C(C=C2CC(OC2=C1)C(=C)CO)O 234.25 unknown https://doi.org/10.1016/S0031-9422(00)84171-0
2-[(2S)-5-Acetyl-2,3-dihydrobenzofuran-2-yl]allyl alcohol 10262829 Click to see CC(=O)C1=CC2=C(C=C1)OC(C2)C(=C)CO 218.25 unknown https://doi.org/10.1016/S0031-9422(00)84171-0
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acid esters / o-Hydroxybenzoic acid esters
5-{2-Fluoro-5-[3-(3-hydroxy-2-methoxycarbonyl-phenoxy)-propenyl]-phenyl}-isoxazole-3-carboxylic acid 447994 Click to see COC(=O)C1=C(C=CC=C1OCC=CC2=CC(=C(C=C2)F)C3=CC(=NO3)C(=O)O)O 413.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.03.021
> Benzenoids / Phenol ethers / Anisoles
Elemicin 10248 Click to see COC1=CC(=CC(=C1OC)OC)CC=C 208.25 unknown https://doi.org/10.1016/0031-9422(80)83015-9
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
6-(Hydroxymethyl)hept-6-ene-2,5-dione 16085190 Click to see CC(=O)CCC(=O)C(=C)CO 156.18 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.03.021
7-Hydroxy-6-methyl-5-heptene-2-one 10964618 Click to see CC(=O)CCC=C(C)CO 142.20 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.03.021
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(1S,4aS,5R,8aS)-5-[(E)-5-acetyloxy-3-methylpent-3-enyl]-1,4a-dimethyl-6-methylidene-3,4,5,7,8,8a-hexahydro-2H-naphthalene-1-carboxylic acid 102239743 Click to see CC(=CCOC(=O)C)CCC1C(=C)CCC2C1(CCCC2(C)C(=O)O)C 362.50 unknown https://doi.org/10.1016/0031-9422(80)83015-9
(1S,4aS,5R,8aS)-5-[(E)-5-hydroxy-3-methylpent-3-enyl]-1,4a-dimethyl-6-methylidene-3,4,5,7,8,8a-hexahydro-2H-naphthalene-1-carboxylic acid 14287145 Click to see CC(=CCO)CCC1C(=C)CCC2C1(CCCC2(C)C(=O)O)C 320.50 unknown https://doi.org/10.1016/0031-9422(80)83015-9
5-(5-hydroxy-3-methylpent-3-enyl)-1,4a-dimethyl-6-methylidene-3,4,5,7,8,8a-hexahydro-2H-naphthalene-1-carboxylic acid 73678322 Click to see CC(=CCO)CCC1C(=C)CCC2C1(CCCC2(C)C(=O)O)C 320.50 unknown https://doi.org/10.1016/0031-9422(80)83015-9
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(R)-3-Methyl-6-((R)-6-methylhept-5-en-2-yl)cyclohex-2-enone 11321983 Click to see CC1=CC(=O)C(CC1)C(C)CCC=C(C)C 220.35 unknown https://doi.org/10.1016/0031-9422(80)83015-9
2-Cyclohexen-1-one, 6-(1,5-dimethyl-4-hexenyl)-3-methyl- 10857025 Click to see CC1=CC(=O)C(CC1)C(C)CCC=C(C)C 220.35 unknown https://doi.org/10.1016/0031-9422(80)83015-9
alpha-Curcumene 92139 Click to see CC1=CC=C(C=C1)C(C)CCC=C(C)C 202.33 unknown https://doi.org/10.1016/0031-9422(80)83015-9
Ar-Curcumene 3083834 Click to see CC1=CC=C(C=C1)C(C)CCC=C(C)C 202.33 unknown https://doi.org/10.1016/0031-9422(80)83015-9
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
(1R,4S,8aR)-4,8a-dimethyl-6-propan-2-yl-1,2,3,4a,7,8-hexahydronaphthalene-1,4,5-triol 162816962 Click to see CC(C)C1=C(C2C(CC1)(C(CCC2(C)O)O)C)O 254.36 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.03.021
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
(1R,4S,6R,7R,8S)-4,11-dimethyl-8-propan-2-yl-5,12-dioxatricyclo[9.1.0.04,6]dodecan-7-ol 162956571 Click to see CC(C)C1CCC2(C(O2)CCC3(C(C1O)O3)C)C 254.36 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.03.021
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
Pumilaside A 10526066 Click to see CC(C)C1CCC2(C(CCC(C2C1OC3C(C(C(C(O3)CO)O)O)O)(C)O)O)C 418.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.03.021
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(4R,4aR,6aS,6aS,6bR,7S,8aR,11R,12aR,14aS,14bR)-7-hydroxy-11-(hydroxymethyl)-4,4a,6a,6b,8a,11,14a-heptamethyl-2,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-tetradecahydro-1H-picen-3-one 162865915 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(C(CC5(C4CC(CC5)(C)CO)C)O)C)C)C)C 458.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.03.021
[5-Acetyloxy-10-hydroxy-4a-(hydroxymethyl)-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicen-4-yl] 2-methylbut-2-enoate 73810256 Click to see CC=C(C)C(=O)OC1CC(CC2C1(C(CC3(C2=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C)OC(=O)C)CO)(C)C 598.90 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.03.021
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
[(1R,2R,3R,4R,7S,8Z,12S,13S,14S,16S)-14-acetyloxy-16-formyl-2,3-dihydroxy-4,9,13,16-tetramethyl-5-oxo-6-oxatricyclo[11.3.0.03,7]hexadec-8-en-12-yl] acetate 162860141 Click to see CC1C(=O)OC2C1(C(C3C(CC(C3(C(CCC(=C2)C)OC(=O)C)C)OC(=O)C)(C)C=O)O)O 466.50 unknown https://doi.org/10.1016/0031-9422(80)83015-9
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
4'-Hydroxyacetophenone 7469 Click to see CC(=O)C1=CC=C(C=C1)O 136.15 unknown https://doi.org/10.1016/0031-9422(80)83015-9
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / 2,2-dimethyl-1-benzopyrans
[2-(2,2-dimethyl-4-oxo-3H-chromen-6-yl)-2-oxoethyl] acetate 163005695 Click to see CC(=O)OCC(=O)C1=CC2=C(C=C1)OC(CC2=O)(C)C 276.28 unknown https://doi.org/10.1016/S0031-9422(00)84171-0
2,2-Dimethyl-4-oxochroman-6-carboxylic acid 11746130 Click to see CC1(CC(=O)C2=C(O1)C=CC(=C2)C(=O)O)C 220.22 unknown https://doi.org/10.1016/S0031-9422(00)84171-0
6-(2-hydroxyacetyl)-2,2-dimethyl-3H-chromen-4-one 163042609 Click to see CC1(CC(=O)C2=C(O1)C=CC(=C2)C(=O)CO)C 234.25 unknown https://doi.org/10.1016/S0031-9422(00)84171-0
> Phenylpropanoids and polyketides / Coumarins and derivatives / Coumarin glycosides
Scopolin tetraacetate 14414542 Click to see CC(=O)OCC1C(C(C(C(O1)OC2=C(C=C3C=CC(=O)OC3=C2)OC)OC(=O)C)OC(=O)C)OC(=O)C 522.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.03.021
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(+/-)-Eriodictyol 11095 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)O)O 288.25 unknown https://doi.org/10.1016/S0031-9422(99)00110-7
(2R)-5,7-dihydroxy-2-(4-hydroxyphenyl)-2,3-dihydro-4H-chromen-4-one 667495 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O 272.25 unknown https://doi.org/10.1016/S0031-9422(99)00110-7
5,7-Dihydroxy-2-(4-hydroxyphenyl)chroman-4-one 932 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O 272.25 unknown https://doi.org/10.1016/S0031-9422(99)00110-7
Eriodictyol 440735 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)O)O 288.25 unknown https://doi.org/10.1016/S0031-9422(99)00110-7
Naringenin 439246 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O 272.25 unknown https://doi.org/10.1016/S0031-9422(99)00110-7
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
[(2S,3R)-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-oxo-2,3-dihydrochromen-3-yl] acetate 162987253 Click to see CC(=O)OC1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)O)O 346.30 unknown https://doi.org/10.1016/S0031-9422(99)00110-7
[2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-4-oxo-2,3-dihydrochromen-3-yl] acetate 3536734 Click to see CC(=O)OC1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)O)O 346.30 unknown https://doi.org/10.1016/S0031-9422(99)00110-7
Taxifolin 3-O-acetate 442540 Click to see CC(=O)OC1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)O)O 346.30 unknown https://doi.org/10.1016/S0031-9422(99)00110-7
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown https://doi.org/10.1016/S0031-9422(99)00110-7
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Isorhamnetin 5281654 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 316.26 unknown https://doi.org/10.1016/S0031-9422(99)00110-7
Quercetin 5280343 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 302.23 unknown https://doi.org/10.1016/S0031-9422(99)00110-7
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one 26339717 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 448.40 unknown https://doi.org/10.1016/S0031-9422(99)00110-7
Quercetin 3-O-rhamnoside 5353915 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 448.40 unknown https://doi.org/10.1016/S0031-9422(99)00110-7
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
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 CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)OC5C(C(C(C(O5)C)O)O)O)C6=CC(=C(C=C6)O)OC)OC7C(C(C(C(O7)C)O)O)O)O)O)O)O)O 916.80 unknown https://doi.org/10.1016/S0031-9422(99)00110-7
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
(2R)-5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-2,3-dihydrochromen-4-one 12310452 Click to see COC1=C(C=CC(=C1)C2CC(=O)C3=C(C=C(C=C3O2)O)O)O 302.28 unknown https://doi.org/10.1016/S0031-9422(99)00110-7
[(2R,3R)-5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-4-oxo-2,3-dihydrochromen-3-yl] acetate 163008624 Click to see CC(=O)OC1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)O)OC 360.30 unknown https://doi.org/10.1016/S0031-9422(99)00110-7
[5,7-Dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-4-oxo-2,3-dihydrochromen-3-yl] acetate 163008623 Click to see CC(=O)OC1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)O)OC 360.30 unknown https://doi.org/10.1016/S0031-9422(99)00110-7
3-Methoxyluteolin 5280681 Click to see COC1=C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)O)O 316.26 unknown https://doi.org/10.1016/S0031-9422(99)00110-7
Homoeriodictyol 73635 Click to see COC1=C(C=CC(=C1)C2CC(=O)C3=C(C=C(C=C3O2)O)O)O 302.28 unknown https://doi.org/10.1016/S0031-9422(99)00110-7
Homoeriodictyol (+/-)- 3512637 Click to see COC1=C(C=CC(=C1)C2CC(=O)C3=C(C=C(C=C3O2)O)O)O 302.28 unknown https://doi.org/10.1016/S0031-9422(99)00110-7
Quercetin 3,3'-dimethyl ether 5316900 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC)O 330.29 unknown https://doi.org/10.1016/S0031-9422(99)00110-7
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
5,7-dihydroxy-2-(3-hydroxy-4-methoxyphenyl)-3,4-dihydro-2H-1-benzopyran-4-one 3593 Click to see COC1=C(C=C(C=C1)C2CC(=O)C3=C(C=C(C=C3O2)O)O)O 302.28 unknown https://doi.org/10.1016/S0031-9422(99)00110-7
5,7-Dihydroxy-2-(3-hydroxy-4-methoxyphenyl)chroman-4-one 676152 Click to see COC1=C(C=C(C=C1)C2CC(=O)C3=C(C=C(C=C3O2)O)O)O 302.28 unknown https://doi.org/10.1016/S0031-9422(99)00110-7
Quercetin 3,3',4'-trimethyl ether 5383438 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC)OC 344.30 unknown https://doi.org/10.1016/S0031-9422(99)00110-7
Quercetin 3,4'-dimethyl ether 5380905 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC)O 330.29 unknown https://doi.org/10.1016/S0031-9422(99)00110-7
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
[(2S,3S)-2-(3,4-dihydroxyphenyl)-5-hydroxy-7-methoxy-4-oxo-2,3-dihydrochromen-3-yl] acetate 162860029 Click to see CC(=O)OC1C(OC2=CC(=CC(=C2C1=O)O)OC)C3=CC(=C(C=C3)O)O 360.30 unknown https://doi.org/10.1016/S0031-9422(99)00110-7
[2-(3,4-Dihydroxyphenyl)-5-hydroxy-7-methoxy-4-oxo-2,3-dihydrochromen-3-yl] acetate 14861266 Click to see CC(=O)OC1C(OC2=CC(=CC(=C2C1=O)O)OC)C3=CC(=C(C=C3)O)O 360.30 unknown https://doi.org/10.1016/S0031-9422(99)00110-7
3-O-acetylpadmatin 10406203 Click to see CC(=O)OC1C(OC2=CC(=CC(=C2C1=O)O)OC)C3=CC(=C(C=C3)O)O 360.30 unknown https://doi.org/10.1016/S0031-9422(99)00110-7
3,7-Di-O-methylquercetin 5280417 Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)OC)C3=CC(=C(C=C3)O)O)O 330.29 unknown https://doi.org/10.1016/S0031-9422(99)00110-7
Pachypodol 5281677 Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)OC)C3=CC(=C(C=C3)O)OC)O 344.30 unknown https://doi.org/10.1016/S0031-9422(99)00110-7

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