Xanthorhiza simplicissima - Unknown
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Details Top

Internal ID UUID64404d2867d0e126345571
Scientific name Xanthorhiza simplicissima
Authority Marshall
First published in Arbust. Amer. : 168 (1785)

Description Top

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Synonyms Top

Scientific name Authority First published in
Xanthorhiza apiifolia L'Hér. Stirp. Nov. 79 (t. 38). 1788
Xanthorhiza tinctoria Woodh. Med. Repos. 5: 160 (1802)

Common names Top

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Language Common/alternative name
English brook-feather
English shrub yellowroot
English shrubby yellow-root
English yellowroot
Arabic صفراء العروق كرفسية الورق
Czech Žlutokořen
Czech žlutokořen jednoduchý
German xanthoriza
German gelbwurz
Japanese ヒイラギナンテンモドキ
Dutch yellowroot
Chinese 黄根木
Chinese 黃根木

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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Germination/Propagation Top

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Sow at 4°C for 3 weeks, then increase to 20°C.
Sow seeds immediately as their viability decreases rapidly, or they best germinate when fresh. If stored, seeds might need temperature cycling and patience to germinate.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Northern America
    • Northeastern U.S.A.
      • Maine
      • Massachusetts
      • New Hampshire
      • New York
      • Ohio
      • West Virginia
    • South-central U.S.A.
      • Texas
    • Southeastern U.S.A.
      • Alabama
      • Florida
      • Georgia
      • Kentucky
      • Louisiana
      • Maryland
      • Mississippi
      • North Carolina
      • South Carolina
      • Tennessee
      • Virginia

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001129483
UNII 5HL7AB91T2
Florida Plant Atlas 3989
Flora of Alabama 3084
USDA Plants XASI
UConn 551
Tropicos 27100865
KEW urn:lsid:ipni.org:names:715221-1
The Plant List tro-27100865
Missouri Botanical Garden 286172
PFAF Xanthorhiza simplicissima
Open Tree Of Life 768466
NCBI Taxonomy 13762
Nature Serve 2.140919
IPNI 715221-1
iNaturalist 170344
GBIF 3033662
Freebase /m/0c9k2n
EPPO XARSI
EOL 595068
USDA GRIN 404013
CMAUP NPO1473

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
Clinically Effective Molecules of Natural Origin for Obesity Prevention or Treatment Hidalgo-Lozada GM, Villarruel-López A, Nuño K, García-García A, Sánchez-Nuño YA, Ramos-García CO Int J Mol Sci 25-Feb-2024
PMCID:PMC10931663
doi:10.3390/ijms25052671
PMID:38473918
Natural Phytochemicals as SIRT Activators—Focus on Potential Biochemical Mechanisms Wiciński M, Erdmann J, Nowacka A, Kuźmiński O, Michalak K, Janowski K, Ohla J, Biernaciak A, Szambelan M, Zabrzyński J Nutrients 14-Aug-2023
PMCID:PMC10459499
doi:10.3390/nu15163578
PMID:37630770
From Plants to Wound Dressing and Transdermal Delivery of Bioactive Compounds Isopencu GO, Covaliu-Mierlă CI, Deleanu IM Plants (Basel) 16-Jul-2023
PMCID:PMC10386126
doi:10.3390/plants12142661
PMID:37514275
Effects of TCM on polycystic ovary syndrome and its cellular endocrine mechanism Chen H, Deng C, Meng Z, Meng S Front Endocrinol (Lausanne) 16-May-2023
PMCID:PMC10228207
doi:10.3389/fendo.2023.956772
PMID:37260441
Botanical Ingredient Forensics: Detection of Attempts to Deceive Commonly Used Analytical Methods for Authenticating Herbal Dietary and Food Ingredients and Supplements Gafner S, Blumenthal M, Foster S, Cardellina JH II, Khan IA, Upton R J Nat Prod 30-Jan-2023
PMCID:PMC9972475
doi:10.1021/acs.jnatprod.2c00929
PMID:36716213
Berberine—A Promising Therapeutic Approach to Polycystic Ovary Syndrome in Infertile/Pregnant Women Ionescu OM, Frincu F, Mehedintu A, Plotogea M, Cirstoiu M, Petca A, Varlas V, Mehedintu C Life (Basel) 02-Jan-2023
PMCID:PMC9864590
doi:10.3390/life13010125
PMID:36676074
The Protective Effects of Nutraceutical Components in Methotrexate-Induced Toxicity Models—An Overview Marin GE, Neag MA, Burlacu CC, Buzoianu AD Microorganisms 18-Oct-2022
PMCID:PMC9608860
doi:10.3390/microorganisms10102053
PMID:36296329
The exploration of anti-Vibrio parahaemolyticus substances from Phellodendri Chinensis Cortex as a preservative for shrimp storage Zheng H, Liu Y, Cai J, Zhang M, Wen Y, Guo L Front Microbiol 13-Sep-2022
PMCID:PMC9514719
doi:10.3389/fmicb.2022.1004262
PMID:36177459
The vessel wall thickness–vessel diameter relationship across woody angiosperms Echeverría A, Petrone‐Mendoza E, Segovia‐Rivas A, Figueroa‐Abundiz VA, Olson ME Am J Bot 12-Jun-2022
PMCID:PMC9328290
doi:10.1002/ajb2.1854
PMID:35435252
Berberine: A Promising Treatment for Neurodegenerative Diseases Cheng Z, Kang C, Che S, Su J, Sun Q, Ge T, Guo Y, Lv J, Sun Z, Yang W, Li B, Li X, Cui R Front Pharmacol 20-May-2022
PMCID:PMC9164284
doi:10.3389/fphar.2022.845591
PMID:35668943
In Silico Design of Dual-Binding Site Anti-Cholinesterase Phytochemical Heterodimers as Treatment Options for Alzheimer’s Disease Amat-ur-Rasool H, Ahmed M, Hasnain S, Ahmed A, Carter WG Curr Issues Mol Biol 29-Dec-2021
PMCID:PMC8929005
doi:10.3390/cimb44010012
PMID:35723391
Complete biosynthesis of the bisbenzylisoquinoline alkaloids guattegaumerine and berbamunine in yeast Payne JT, Valentic TR, Smolke CD Proc Natl Acad Sci U S A 20-Dec-2021
PMCID:PMC8713753
doi:10.1073/pnas.2112520118
PMID:34903659
Inhibitory Role of Berberine, an Isoquinoline Alkaloid, on NLRP3 Inflammasome Activation for the Treatment of Inflammatory Diseases Sarbadhikary P, George BP, Abrahamse H Molecules 15-Oct-2021
PMCID:PMC8537060
doi:10.3390/molecules26206238
PMID:34684819
Berberine modulates hyper-inflammation in mouse macrophages stimulated with polyinosinic-polycytidylic acid via calcium-CHOP/STAT pathway Kim HJ, Kim YJ, Park W Sci Rep 28-May-2021
PMCID:PMC8163795
doi:10.1038/s41598-021-90752-z
PMID:34050236
Nephroprotective activity of natural products against chemical toxicants: The role of Nrf2/ARE signaling pathway Molaei E, Molaei A, Abedi F, Hayes AW, Karimi G Food Sci Nutr 01-May-2021
PMCID:PMC8194945
doi:10.1002/fsn3.2320
PMID:34136201

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name PubChem ID Canonical SMILES MW Found in Proof
> Alkaloids and derivatives / Protoberberine alkaloids and derivatives
Berberine 2353 Click to see COC1=C(C2=C[N+]3=C(C=C2C=C1)C4=CC5=C(C=C4CC3)OCO5)OC 336.40 unknown https://doi.org/10.1002/JPS.2600830327
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives
N-Formyl-4-hydroxybenzamide 71370414 Click to see C1=CC(=CC=C1C(=O)NC=O)O 165.15 unknown via CMAUP database
N-Formylbenzamide 151196 Click to see C1=CC=C(C=C1)C(=O)NC=O 149.15 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzamides
4-Hydroxybenzamide 65052 Click to see C1=CC(=CC=C1C(=O)N)O 137.14 unknown via CMAUP database
N-[(S)-2-Hydroxy-2-phenylethyl]benzamide 6542363 Click to see C1=CC=C(C=C1)C(CNC(=O)C2=CC=CC=C2)O 241.28 unknown via CMAUP database
> Lignans, neolignans and related compounds
Obamegine 441064 Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=C(O3)C(=C(C=C7CCN6C)OC)O)O)OC 594.70 unknown via CMAUP database
Repandine 10031631 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=CC(=C(C=C7CCN6C)OC)O3)O)OC)OC 608.70 unknown via CMAUP database
> Lignans, neolignans and related compounds / Cyclobutane lignans
(3beta,4alpha-Diphenylcyclobutane-1beta,2alpha-diyl)bis[(2,4-dihydroxyphenyl)methanone] 102228233 Click to see C1=CC=C(C=C1)C2C(C(C2C(=O)C3=C(C=C(C=C3)O)O)C(=O)C4=C(C=C(C=C4)O)O)C5=CC=CC=C5 480.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1S,9R,10R,16R)-14,16-dimethyl-6,14-diazatetracyclo[7.5.3.01,10.02,7]heptadec-2(7)-en-5-one 6916253 Click to see CC1CC2CC3=C(CCC(=O)N3)C4(C1)C2CCCN4C 274.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,2R,5S,6R,9R,10S,11S,14R,15R,19S,21R,22R)-10-(hydroxymethyl)-2,5,6,10,14,21-hexamethyl-23-oxahexacyclo[19.2.1.02,19.05,18.06,15.09,14]tetracos-17-ene-11,22-diol 44253988 Click to see CC12CCC(C(C1CCC3(C2CC=C4C3(CCC5(C4CC6(CC5OC6O)C)C)C)C)(C)CO)O 472.70 unknown via CMAUP database
(1R,2R,5S,6R,9R,10S,11S,14R,15R,19S,21R,22R)-10-(hydroxymethyl)-22-methoxy-2,5,6,10,14,21-hexamethyl-23-oxahexacyclo[19.2.1.02,19.05,18.06,15.09,14]tetracos-17-en-11-ol 44253989 Click to see CC12CCC(C(C1CCC3(C2CC=C4C3(CCC5(C4CC6(CC5OC6OC)C)C)C)C)(C)CO)O 486.70 unknown via CMAUP database
(1R,2S,4aS,6aR,6aS,6bS,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 162948465 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown https://doi.org/10.1016/S0031-9422(00)91326-8
(2R,4aS,6aR,6aS,6bR,8aR,9S,10S,12aR,14bR)-10-hydroxy-9-(hydroxymethyl)-2,4a,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-2-carboxylic acid 21594159 Click to see CC12CCC(CC1C3=CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)CO)O)C)(C)C(=O)O 472.70 unknown via CMAUP database
(3S,4S,4aR,6aR,6bS,8aR,9R,11R,12aS,14aR,14bR)-4,11-bis(hydroxymethyl)-4,6a,6b,8a,11,14b-hexamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene-3,9-diol 14335966 Click to see CC12CCC(C(C1CCC3(C2CC=C4C3(CCC5(C4CC(CC5O)(C)CO)C)C)C)(C)CO)O 474.70 unknown via CMAUP database
24-Hydroxy-beta-amyrin 14167253 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)O)C)C)C2C1)C)C)C 442.70 unknown via CMAUP database
3-Oxoazukisapogenol 44253990 Click to see CC12CCC(CC1C3=CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)CO)C)(C)C(=O)O 470.70 unknown via CMAUP database
3beta,22beta,24-Trihydroxyoleana-12-ene-30-oic acid gamma-lactone 102482971 Click to see CC12CCC(C(C1CCC3(C2CC=C4C3(CCC5(C4CC6(CC5OC6=O)C)C)C)C)(C)CO)O 470.70 unknown via CMAUP database
beta-Ursolic acid 220774 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown https://doi.org/10.1016/S0031-9422(00)91326-8
Melilotigenin B 91895471 Click to see CC1(CC2C3=CCC4C5(CCC(=O)C(C5CCC4(C3(CCC2(C(=O)C1)C)C)C)(C)CO)C)C 454.70 unknown via CMAUP database
Melilotigenin C 10551785 Click to see CC1(CC2C3=CCC4C5(CCC(=O)C(C5CCC4(C3(CCC2(C(C1)O)C)C)C)(C)CO)C)C 456.70 unknown via CMAUP database
Soyasapogenol B 115012 Click to see CC1(CC2C3=CCC4C5(CCC(C(C5CCC4(C3(CCC2(C(C1)O)C)C)C)(C)CO)O)C)C 458.70 unknown via CMAUP database
Soyasapogenol E 13632872 Click to see CC1(CC2C3=CCC4C5(CCC(C(C5CCC4(C3(CCC2(C(=O)C1)C)C)C)(C)CO)O)C)C 456.70 unknown via CMAUP database
> Organoheterocyclic compounds / Benzazepines
(1R)-18,19-dimethoxy-6,8-dioxa-14-azapentacyclo[12.8.0.03,11.05,9.017,22]docosa-3,5(9),10,17(22),18,20-hexaene-2,15-dione 163189171 Click to see COC1=C(C2=C(C=C1)C3C(=O)C4=CC5=C(C=C4CCN3C(=O)C2)OCO5)OC 381.40 unknown https://doi.org/10.1002/JPS.2600830327
Puntarenine 100216 Click to see COC1=C(C2=C(C=C1)C3C(=O)C4=CC5=C(C=C4CCN3C(=O)C2)OCO5)OC 381.40 unknown https://doi.org/10.1002/JPS.2600830327
> Organoheterocyclic compounds / Benzopyrans
Oxytropisoflavan B 46918734 Click to see COC1=C(C(=C(C=C1)C2CC3(CCC(=O)C=C3OC2)O)O)OC 320.30 unknown via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Benzoylindoles
Oxytrofalcatin A 46850030 Click to see C1=CC=C(C=C1)C(=O)N2C=C(C3=CC=CC=C32)O 237.25 unknown via CMAUP database
Oxytrofalcatin B 46850031 Click to see C1=CC=C2C(=C1)C(=CN2C(=O)C3=CC=C(C=C3)O)O 253.25 unknown via CMAUP database
Oxytrofalcatin C 46850032 Click to see COC1=CN(C2=CC=CC=C21)C(=O)C3=CC=C(C=C3)O 267.28 unknown via CMAUP database
Oxytrofalcatin D 46850205 Click to see COC1=CN(C2=C1C(=CC=C2)O)C(=O)C3=CC=C(C=C3)O 283.28 unknown via CMAUP database
Oxytrofalcatin E 46850206 Click to see CC(=CCC1=C(C=CC(=C1)C(=O)N2C=C(C3=CC=CC=C32)O)O)C 321.40 unknown via CMAUP database
Oxytrofalcatin F 46850207 Click to see C1=CC=C2C(=C1)C(=CN2C(=O)C3=CC(=CC=C3)O)O 253.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
3-(4-Hydroxy-3-methoxyphenyl)prop-2-enoic acid 709 Click to see COC1=C(C=CC(=C1)C=CC(=O)O)O 194.18 unknown https://doi.org/10.1016/S0031-9422(00)91326-8
Ferulic acid 445858 Click to see COC1=C(C=CC(=C1)C=CC(=O)O)O 194.18 unknown https://doi.org/10.1016/S0031-9422(00)91326-8
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(2S)-7-hydroxyflavanone 688857 Click to see C1C(OC2=C(C1=O)C=CC(=C2)O)C3=CC=CC=C3 240.25 unknown via CMAUP database
Liquiritigenin 114829 Click to see C1C(OC2=C(C1=O)C=CC(=C2)O)C3=CC=C(C=C3)O 256.25 unknown via CMAUP database
Pinocembrin 68071 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=CC=C3 256.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin 5280443 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 270.24 unknown via CMAUP database
Chrysin 5281607 Click to see C1=CC=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O 254.24 unknown via CMAUP database
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 via CMAUP database
> 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 via CMAUP database
Kaempferol 5280863 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown via CMAUP database
Myricetin 5281672 Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O 318.23 unknown via CMAUP database
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 via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
3-[(2S,3R,4S,5R,6R)-4,5-Dihydroxy-3-[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-6-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxy-5,7-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one 10919701 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)OC6C(C(C(C(O6)C)O)O)O)O)O)O)O)O 740.70 unknown via CMAUP database
3-[(2S,3R,4S,5R,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-2-(4-hydroxyphenyl)-7-methoxychromen-4-one 60200223 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)OC)C5=CC=C(C=C5)O)CO)O)O)O)O)O 608.50 unknown via CMAUP database
3-[6-O-(3-O-beta-D-Xylopyranosyl-alpha-L-rhamnopyranosyl)-beta-D-galactopyranosyloxy]-4',5,7-trihydroxyflavone 21668680 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)O)O)O)O)OC6C(C(C(CO6)O)O)O)O 726.60 unknown via CMAUP database
4',5,7-Trihydroxy-3-[2-O-alpha-L-rhamnopyranosyl-6-O-(3-O-beta-D-xylopyranosyl-alpha-L-rhamnopyranosyl)-beta-D-galactopyranosyloxy]flavone 10865825 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)COC6C(C(C(C(O6)C)O)OC7C(C(C(CO7)O)O)O)O)O)O)O)O)O 872.80 unknown via CMAUP database
Biorobin 15944778 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)O)O)O)O)O)O 594.50 unknown via CMAUP database
Oxytroflavoside A 60200065 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)OC)C5=CC=C(C=C5)O)COC(=O)CC(C)(CC(=O)O)O)O)O)O)O)O 752.70 unknown via CMAUP database
Oxytroflavoside B 60200066 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)OC)C5=CC=C(C=C5)O)CO)O)OC(=O)CC(C)(CC(=O)O)O)O)O)O 752.70 unknown via CMAUP database
Oxytroflavoside C 60200220 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)OC)C5=CC=C(C=C5)O)CO)OC(=O)CC(C)(CC(=O)O)O)O)O)O)O 752.70 unknown via CMAUP database
Oxytroflavoside D 60200221 Click to see CC(CC(=O)O)(CC(=O)OCC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)OC)C4=CC=C(C=C4)O)O)O)O)O 606.50 unknown via CMAUP database
Oxytroflavoside E 60200222 Click to see CC(CC(=O)O)(CC(=O)OCC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)OC)C4=CC=C(C=C4)OC5C(C(C(C(O5)CO)O)O)O)O)O)O)O 768.70 unknown via CMAUP database
Oxytroflavoside G 60200370 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)OC)C5=CC=C(C=C5)O)OC6C(C(C(C(O6)C)O)O)O)O)O)O)O)O 754.70 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
kaempferol 3-O-[alpha-L-rhamnopyranosyl(1->2)-beta-D-galactopyranosyl]-7-O-alpha-L-rhamnopyranoside 57397583 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)OC5C(C(C(C(O5)C)O)O)O)C6=CC=C(C=C6)O)CO)O)O)O)O)O 740.70 unknown via CMAUP database
Robinin 5281693 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)O)O)O)O)O)O 740.70 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
(2S)-7-Methoxyflavanone 688883 Click to see COC1=CC2=C(C=C1)C(=O)CC(O2)C3=CC=CC=C3 254.28 unknown via CMAUP database
5-Hydroxy-7-methoxy-2-phenylchroman-4-one 73201 Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=CC=C3)O 270.28 unknown via CMAUP database
Liquiritigenin 7-methylether 14157884 Click to see COC1=CC2=C(C=C1)C(=O)CC(O2)C3=CC=C(C=C3)O 270.28 unknown via CMAUP database
Oxyayanin A 5281676 Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)OC)C3=CC(=C(C=C3O)OC)O)O 360.30 unknown via CMAUP database
Sakuranetin 73571 Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=C(C=C3)O)O 286.28 unknown via CMAUP database
> Phenylpropanoids and polyketides / Homoisoflavonoids / Homoisoflavans / Homoisoflavanones
(3S)-7-hydroxy-3-[(4-hydroxyphenyl)methyl]-2,3-dihydrochromen-4-one 26088035 Click to see C1C(C(=O)C2=C(O1)C=C(C=C2)O)CC3=CC=C(C=C3)O 270.28 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Furanoisoflavonoids / Pterocarpans
(6aR)-9,10-Dimethoxy-6aalpha,11aalpha-dihydro-6H-benzofuro[3,2-c][1]benzopyran-3,8-diol 46918735 Click to see COC1=C(C=C2C3COC4=C(C3OC2=C1OC)C=CC(=C4)O)O 316.30 unknown via CMAUP database
(l)-Edunol 182148 Click to see CC(=CCC1=CC2=C(C=C1O)OCC3C2OC4=CC5=C(C=C34)OCO5)C 352.40 unknown via CMAUP database
Maackiain 91510 Click to see C1C2C(C3=C(O1)C=C(C=C3)O)OC4=CC5=C(C=C24)OCO5 284.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
Daidzein 5281708 Click to see C1=CC(=CC=C1C2=COC3=C(C2=O)C=CC(=C3)O)O 254.24 unknown via CMAUP database
Pseudobaptigenin 5281805 Click to see C1OC2=C(O1)C=C(C=C2)C3=COC4=C(C3=O)C=CC(=C4)O 282.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavanquinones
5-[(3R)-7-hydroxy-3,4-dihydro-2H-chromen-3-yl]-2,3-dimethoxycyclohexa-2,5-diene-1,4-dione 10403457 Click to see COC1=C(C(=O)C(=CC1=O)C2CC3=C(C=C(C=C3)O)OC2)OC 316.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavonoid O-glycosides
Daidzein-4'-glucoside 49862229 Click to see C1=CC(=CC=C1C2=COC3=C(C2=O)C=CC(=C3)O)OC4C(C(C(C(O4)CO)O)O)O 416.40 unknown via CMAUP database
Sophoricoside 5321398 Click to see C1=CC(=CC=C1C2=COC3=CC(=CC(=C3C2=O)O)O)OC4C(C(C(C(O4)CO)O)O)O 432.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 3-O-methylated isoflavonoids / 3-O-methylisoflavones
3'-Methoxydaidzein 5319422 Click to see COC1=C(C=CC(=C1)C2=COC3=C(C2=O)C=CC(=C3)O)O 284.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids
(R)-Isomucronulatol 10380176 Click to see COC1=C(C(=C(C=C1)C2CC3=C(C=C(C=C3)O)OC2)O)OC 302.32 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 3-hydroxy,4-methoxyisoflavonoids
(3R)-3-(2,3-Dihydroxy-4-methoxyphenyl)-3,4-dihydro-2H-1-benzopyran-7-ol 15939757 Click to see COC1=C(C(=C(C=C1)C2CC3=C(C=C(C=C3)O)OC2)O)O 288.29 unknown via CMAUP database
2H-1-Benzopyran-7-ol, 3,4-dihydro-3-(3-hydroxy-2,4-dimethoxyphenyl)-, (3R)- 13873811 Click to see COC1=C(C(=C(C=C1)C2CC3=C(C=C(C=C3)O)OC2)OC)O 302.32 unknown via CMAUP database
Calycosin 5280448 Click to see COC1=C(C=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)O)O 284.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 4-O-methylisoflavones
2'-Hydroxybiochanin A 5282075 Click to see COC1=CC(=C(C=C1)C2=COC3=CC(=CC(=C3C2=O)O)O)O 300.26 unknown via CMAUP database
Formononetin 5280378 Click to see COC1=CC=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)O 268.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 7-O-methylated isoflavonoids / 7-O-methylisoflavones
Isoformononetin 3764 Click to see COC1=CC2=C(C=C1)C(=O)C(=CO2)C3=CC=C(C=C3)O 268.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxy-dihydrochalcones
2',4'-Dihydroxydihydrochalcone 586491 Click to see C1=CC=C(C=C1)CCC(=O)C2=C(C=C(C=C2)O)O 242.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
1-(2-Hydroxy-4-methoxyphenyl)-3-phenylprop-2-en-1-one 265720 Click to see COC1=CC(=C(C=C1)C(=O)C=CC2=CC=CC=C2)O 254.28 unknown via CMAUP database
2-Propen-1-one, 1-(2-hydroxy-4-methoxyphenyl)-3-(4-hydroxyphenyl)- 592216 Click to see COC1=CC(=C(C=C1)C(=O)C=CC2=CC=C(C=C2)O)O 270.28 unknown via CMAUP database
2-Propen-1-one, 1-(2,4-dihydroxyphenyl)-3-phenyl- 344530 Click to see C1=CC=C(C=C1)C=CC(=O)C2=C(C=C(C=C2)O)O 240.25 unknown via CMAUP database
2',4'-Dihydroxychalcone 5376979 Click to see C1=CC=C(C=C1)C=CC(=O)C2=C(C=C(C=C2)O)O 240.25 unknown via CMAUP database
Chalcone, 2',4'-dihydroxy-4-methoxy- 166795 Click to see COC1=CC=C(C=C1)C=CC(=O)C2=C(C=C(C=C2)O)O 270.28 unknown via CMAUP database
GU17;ISL;Isoliquiritigen 425 Click to see C1=CC(=CC=C1C=CC(=O)C2=C(C=C(C=C2)O)O)O 256.25 unknown via CMAUP database
Trihydroxychalcone 638278 Click to see C1=CC(=CC=C1C=CC(=O)C2=C(C=C(C=C2)O)O)O 256.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 3-prenylated chalcones
1-[2,4-Dihydroxy-3-(3-methylbut-2-enyl)phenyl]-3-(4-hydroxyphenyl)prop-2-en-1-one 193568 Click to see CC(=CCC1=C(C=CC(=C1O)C(=O)C=CC2=CC=C(C=C2)O)O)C 324.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Cinnamylphenols
1-(4-Hydroxy-2-methoxyphenyl)-3-phenylprop-2-en-1-one 71442332 Click to see COC1=C(C=CC(=C1)O)C(=O)C=CC2=CC=CC=C2 254.28 unknown via CMAUP database

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