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Cyclopia intermedia

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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID643fdbd222f45724168298
Scientific name Cyclopia intermedia
Authority E.Mey.
First published in Comm. Pl. Afr. Austr.: 3 (1836)

Description Top

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Synonyms Top

Scientific name Authority First published in
Cyclopia aurea Fourc. Trans. Roy. Soc. South Africa21: 92 (1932)
Cyclopia vogelii var. intermedia (E.Mey.) Harv. W.H.Harvey & auct. suc. (eds.), Fl. Cap.1: 7 (1862)

Common names Top

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Language Common/alternative name
English kouga honeybush-tea
Afrikaans bergtee
Afrikaans kougabergtee
Arabic سيكلوبيا الوسطى

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000197746
UNII LY7ENU43C4
Tropicos 13049558
KEW urn:lsid:ipni.org:names:489297-1
The Plant List ild-4428
Open Tree Of Life 356254
NCBI Taxonomy 384038
IPNI 489297-1
iNaturalist 533454
GBIF 5341860
Freebase /m/0_v5p6f
EPPO KCLIN
EOL 685838
USDA GRIN 409483
Wikipedia Cyclopia_intermedia

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
Preliminary exploration of herbal tea products based on traditional knowledge and hypotheses concerning herbal tea selection: a case study in Southwest Guizhou, China Long X, Ranjitkar S, Waldstein A, Wu H, Li Q, Geng Y J Ethnobiol Ethnomed 02-Jan-2024
PMCID:PMC10763305
doi:10.1186/s13002-023-00645-w
PMID:38169414
Indoor metabolites and chemicals outperform microbiome in classifying childhood asthma and allergic rhinitis Sun Y, Tang H, Du S, Chen Y, Ou Z, Zhang M, Chen Z, Tang Z, Zhang D, Chen T, Xu Y, Li J, Norback D, Hashim JH, Hashim Z, Shao J, Fu X, Zhao Z Eco Environ Health 22-Aug-2023
PMCID:PMC10902507
doi:10.1016/j.eehl.2023.08.001
PMID:38435359
The effect of Aspalathin linearis, Cyclopia intermedia and Sutherlandia frutescene on sperm functional parameters of healthy male wistar rats Omolaoye TS, Skosana BT, du Plessis SS Front Physiol 07-Jun-2023
PMCID:PMC10282539
doi:10.3389/fphys.2023.1211227
PMID:37351256
Cyclopia intermedia (Honeybush) Induces Uncoupling Protein 1 and Peroxisome Proliferator-Activated Receptor Alpha Expression in Obese Diabetic Female db/db Mice Jack BU, Ramharack P, Malherbe C, Gabuza K, Joubert E, Pheiffer C Int J Mol Sci 15-Feb-2023
PMCID:PMC9964215
doi:10.3390/ijms24043868
PMID:36835279
Phytochemicals and Regulation of NF-kB in Inflammatory Bowel Diseases: An Overview of In Vitro and In Vivo Effects Laurindo LF, dos Santos AR, de Carvalho AC, Bechara MD, Guiguer EL, Goulart RD, Vargas Sinatora R, Araújo AC, Barbalho SM Metabolites 07-Jan-2023
PMCID:PMC9862976
doi:10.3390/metabo13010096
PMID:36677021
The Use of Medicinal Plant-Derived Metallic Nanoparticles in Theranostics Xulu JH, Ndongwe T, Ezealisiji KM, Tembu VJ, Mncwangi NP, Witika BA, Siwe-Noundou X Pharmaceutics 10-Nov-2022
PMCID:PMC9698412
doi:10.3390/pharmaceutics14112437
PMID:36365255
Anti-Inflammatory, Anti-Diabetic, Anti-Oxidant and Cytotoxicity Assays of South African Herbal Teas and Bush Tea Blends Malongane F, McGaw LJ, Olaokun OO, Mudau FN Foods 27-Jul-2022
PMCID:PMC9368003
doi:10.3390/foods11152233
PMID:35954001
Plant Extracts Mediated Metal-Based Nanoparticles: Synthesis and Biological Applications Adeyemi JO, Oriola AO, Onwudiwe DC, Oyedeji AO Biomolecules 24-Apr-2022
PMCID:PMC9138950
doi:10.3390/biom12050627
PMID:35625555
Toxic Mechanism and Biological Detoxification of Fumonisins Qu L, Wang L, Ji H, Fang Y, Lei P, Zhang X, Jin L, Sun D, Dong H Toxins (Basel) 01-Mar-2022
PMCID:PMC8954241
doi:10.3390/toxins14030182
PMID:35324679
Green Metallic Nanoparticles for Cancer Therapy: Evaluation Models and Cancer Applications Tinajero-Díaz E, Salado-Leza D, Gonzalez C, Martínez Velázquez M, López Z, Bravo-Madrigal J, Knauth P, Flores-Hernández FY, Herrera-Rodríguez SE, Navarro RE, Cabrera-Wrooman A, Krötzsch E, Carvajal ZY, Hernández-Gutiérrez R Pharmaceutics 18-Oct-2021
PMCID:PMC8537602
doi:10.3390/pharmaceutics13101719
PMID:34684012
Prospective Application of Nanoparticles Green Synthesized Using Medicinal Plant Extracts as Novel Nanomedicines Selvakesavan RK, Franklin G Nanotechnol Sci Appl 23-Sep-2021
PMCID:PMC8476107
doi:10.2147/NSA.S333467
PMID:34588770
Green Synthesis of Metallic Nanoparticles Using Some Selected Medicinal Plants from Southern Africa and Their Biological Applications Aboyewa JA, Sibuyi NR, Meyer M, Oguntibeju OO Plants (Basel) 16-Sep-2021
PMCID:PMC8472917
doi:10.3390/plants10091929
PMID:34579460
Occurrence and Seasonal Changes in the Population of Root-knot Nematodes on Honeybush (Cyclopia Sp.) Daramola FY, Malgas R, Malan AP Helminthologia 08-Jun-2021
PMCID:PMC8256456
doi:10.2478/helm-2021-0018
PMID:34248381
The Antimicrobial and Anti-Inflammatory Effects of Silver Nanoparticles Synthesised from Cotyledon orbiculata Aqueous Extract Tyavambiza C, Elbagory AM, Madiehe AM, Meyer M, Meyer S Nanomaterials (Basel) 20-May-2021
PMCID:PMC8160699
doi:10.3390/nano11051343
PMID:34065254
Therapeutic Effects of Dipterocarpus tuberculatus with High Antioxidative Activity Against UV-Induced Photoaging of NHDF Cells and Nude Mice Lee SJ, Kim JE, Choi YJ, Gong JE, Park SH, Douangdeuane B, Souliya O, Park JM, Lee HS, Kim BH, Hwang DY Antioxidants (Basel) 17-May-2021
PMCID:PMC8157063
doi:10.3390/antiox10050791
PMID:34067673

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 / Phenols / Methoxyphenols
Homovanillyl alcohol 16928 Click to see COC1=C(C=CC(=C1)CCO)O 168.19 unknown https://doi.org/10.1021/JF0210730
> Benzenoids / Phenols / Tyrosols and derivatives / Tyrosols
Tyrosol 10393 Click to see C1=CC(=CC=C1CCO)O 138.16 unknown https://doi.org/10.1021/JF0210730
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols / Cyclohexanols
D-Pinitol 164619 Click to see COC1C(C(C(C(C1O)O)O)O)O 194.18 unknown https://doi.org/10.1021/JF980258X
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(2R,3S,4S,5R,6S)-2-[[(2R,3S,4S)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-6-[4-(2-hydroxyethyl)phenoxy]oxane-3,4,5-triol 162946495 Click to see C1C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC=C(C=C3)CCO)O)O)O)O)(CO)O 432.40 unknown https://doi.org/10.1021/JF0210730
2-[[3,4-Dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-6-[4-(2-hydroxyethyl)phenoxy]oxane-3,4,5-triol 162946494 Click to see C1C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC=C(C=C3)CCO)O)O)O)O)(CO)O 432.40 unknown https://doi.org/10.1021/JF0210730
4-[(2S,3R,4S,5S,6R)-3-[(2S,3S,4S)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybenzaldehyde 162909307 Click to see C1C(C(C(O1)OC2C(C(C(OC2OC3=CC=C(C=C3)C=O)CO)O)O)O)(CO)O 416.40 unknown https://doi.org/10.1021/JF0210730
4-[3-[3,4-Dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybenzaldehyde 162909306 Click to see C1C(C(C(O1)OC2C(C(C(OC2OC3=CC=C(C=C3)C=O)CO)O)O)O)(CO)O 416.40 unknown https://doi.org/10.1021/JF0210730
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
Isomangiferin 5318597 Click to see C1=C2C(=CC(=C1O)O)OC3=C(C2=O)C(=CC(=C3C4C(C(C(C(O4)CO)O)O)O)O)O 422.30 unknown https://doi.org/10.1021/JF980258X
Mangiferin 5281647 Click to see C1=C2C(=CC(=C1O)O)OC3=C(C2=O)C(=C(C(=C3)O)C4C(C(C(C(O4)CO)O)O)O)O 422.30 unknown https://doi.org/10.1007/S00217-002-0644-5
https://doi.org/10.1021/JF980258X
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
p-Coumaric acid 637542 Click to see C1=CC(=CC=C1C=CC(=O)O)O 164.16 unknown https://doi.org/10.1021/JF980258X
> 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/10.1021/JF980258X
(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/10.1021/JF980258X
(2S)-2-(3,4-dihydroxyphenyl)-5-hydroxy-7-[(2R,3R,4S,5S,6R)-2,4,5-trihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy-2,3-dihydrochromen-4-one 163033630 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)OC3C(C(C(OC3O)CO)O)O)C4=CC(=C(C=C4)O)O 450.40 unknown https://doi.org/10.1021/JF0210730
(2S)-2-(3,4-dihydroxyphenyl)-7-hydroxy-5-[(2R,3R,4S,5S,6R)-2,4,5-trihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy-2,3-dihydrochromen-4-one 163011943 Click to see C1C(OC2=C(C1=O)C(=CC(=C2)O)OC3C(C(C(OC3O)CO)O)O)C4=CC(=C(C=C4)O)O 450.40 unknown https://doi.org/10.1021/JF0210730
(2S)-5-hydroxy-2-(4-hydroxyphenyl)-7-[(2R,3R,4S,5S,6R)-2,4,5-trihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy-2,3-dihydrochromen-4-one 163039721 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)OC3C(C(C(OC3O)CO)O)O)C4=CC=C(C=C4)O 434.40 unknown https://doi.org/10.1021/JF0210730
2-(3,4-Dihydroxyphenyl)-5-hydroxy-7-[2,4,5-trihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy-2,3-dihydrochromen-4-one 163033629 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)OC3C(C(C(OC3O)CO)O)O)C4=CC(=C(C=C4)O)O 450.40 unknown https://doi.org/10.1021/JF0210730
2-(3,4-Dihydroxyphenyl)-7-hydroxy-5-[2,4,5-trihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy-2,3-dihydrochromen-4-one 163011942 Click to see C1C(OC2=C(C1=O)C(=CC(=C2)O)OC3C(C(C(OC3O)CO)O)O)C4=CC(=C(C=C4)O)O 450.40 unknown https://doi.org/10.1021/JF0210730
5-Hydroxy-2-(4-hydroxyphenyl)-7-[2,4,5-trihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy-2,3-dihydrochromen-4-one 163039720 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)OC3C(C(C(OC3O)CO)O)O)C4=CC=C(C=C4)O 434.40 unknown https://doi.org/10.1021/JF0210730
> Phenylpropanoids and polyketides / Flavonoids / Flavones
5,7-dihydroxy-2-(4-hydroxyphenyl)-6-[(2R,3R,4R,5S,6R)-2,4,5-trihydroxy-6-(hydroxymethyl)oxan-3-yl]-3-[(2R,3R,4R,5S,6R)-2,4,5-trihydroxy-6-(hydroxymethyl)oxan-3-yl]oxychromen-4-one 163188870 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(O2)C=C(C(=C3O)C4C(C(C(OC4O)CO)O)O)O)OC5C(C(C(OC5O)CO)O)O)O 610.50 unknown https://doi.org/10.1021/JF0210730
5,7-Dihydroxy-2-(4-hydroxyphenyl)-6-[2,4,5-trihydroxy-6-(hydroxymethyl)oxan-3-yl]-3-[2,4,5-trihydroxy-6-(hydroxymethyl)oxan-3-yl]oxychromen-4-one 163019963 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(O2)C=C(C(=C3O)C4C(C(C(OC4O)CO)O)O)O)OC5C(C(C(OC5O)CO)O)O)O 610.50 unknown https://doi.org/10.1021/JF0210730
7,3',4'-Trihydroxyflavone 5322065 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C=C(C=C3)O)O)O 270.24 unknown https://doi.org/10.1021/JF0210730
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/10.1021/JF980258X
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
3,5,7-trihydroxy-2-(4-hydroxyphenyl)-6-[(2R,3R,4R,5S,6R)-2,4,5-trihydroxy-6-(hydroxymethyl)oxan-3-yl]chromen-4-one 162952639 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(O2)C=C(C(=C3O)C4C(C(C(OC4O)CO)O)O)O)O)O 448.40 unknown https://doi.org/10.1021/JF0210730
3,5,7-Trihydroxy-2-(4-hydroxyphenyl)-6-[2,4,5-trihydroxy-6-(hydroxymethyl)oxan-3-yl]chromen-4-one 162952638 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(O2)C=C(C(=C3O)C4C(C(C(OC4O)CO)O)O)O)O)O 448.40 unknown https://doi.org/10.1021/JF0210730
3,5,7-trihydroxy-2-(4-hydroxyphenyl)-8-[(2R,3R,4R,5S,6R)-2,4,5-trihydroxy-6-(hydroxymethyl)oxan-3-yl]chromen-4-one 162992473 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(OC4O)CO)O)O)O)O 448.40 unknown https://doi.org/10.1021/JF0210730
3,5,7-Trihydroxy-2-(4-hydroxyphenyl)-8-[2,4,5-trihydroxy-6-(hydroxymethyl)oxan-3-yl]chromen-4-one 162992472 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(OC4O)CO)O)O)O)O 448.40 unknown https://doi.org/10.1021/JF0210730
3,7-dihydroxy-2-(4-hydroxyphenyl)-5-[(2S,3R,4S,5S,6R)-2,4,5-trihydroxy-6-(hydroxymethyl)oxan-3-yl]oxychromen-4-one 162997366 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(O2)C=C(C=C3OC4C(C(C(OC4O)CO)O)O)O)O)O 448.40 unknown https://doi.org/10.1021/JF0210730
3,7-Dihydroxy-2-(4-hydroxyphenyl)-5-[2,4,5-trihydroxy-6-(hydroxymethyl)oxan-3-yl]oxychromen-4-one 162997365 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(O2)C=C(C=C3OC4C(C(C(OC4O)CO)O)O)O)O)O 448.40 unknown https://doi.org/10.1021/JF0210730
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides
3,5,7-trihydroxy-2-(4-hydroxyphenyl)-6-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one 24721625 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(O2)C=C(C(=C3O)C4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown https://doi.org/10.1021/JF0210730
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
3,5,7-trihydroxy-2-(4-hydroxyphenyl)-8-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one 162867640 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(C(O4)CO)O)O)O)O)O 448.40 unknown https://doi.org/10.1021/JF0210730
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
(2S)-5-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-7-hydroxy-2-(4-hydroxyphenyl)-2,3-dihydrochromen-4-one 163070654 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=CC(=CC4=C3C(=O)CC(O4)C5=CC=C(C=C5)O)O)CO)O)O)O)O)O 580.50 unknown https://doi.org/10.1021/JF0210730
2-(1,3-benzodioxol-5-yl)-6-[(2S,3R,4S,5S,6R)-6-[[(2R,3S,4S)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-3-hydroxychromen-4-one 163023823 Click to see C1C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC4=C(C=C3)OC(=C(C4=O)O)C5=CC6=C(C=C5)OCO6)O)O)O)O)(CO)O 592.50 unknown https://doi.org/10.1021/JF0210730
2-(1,3-Benzodioxol-5-yl)-6-[6-[[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-3-hydroxychromen-4-one 163023822 Click to see C1C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC4=C(C=C3)OC(=C(C4=O)O)C5=CC6=C(C=C5)OCO6)O)O)O)O)(CO)O 592.50 unknown https://doi.org/10.1021/JF0210730
Naringenin 5-O-neohesperidoside 42607904 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=CC(=CC4=C3C(=O)CC(O4)C5=CC=C(C=C5)O)O)CO)O)O)O)O)O 580.50 unknown https://doi.org/10.1021/JF0210730
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
3-(beta-D-Glucopyranosyloxy)-5,7,4'-trihydroxy-6-(beta-D-glucopyranosyl)flavone 102465134 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(O2)C=C(C(=C3O)C4C(C(C(C(O4)CO)O)O)O)O)OC5C(C(C(C(O5)CO)O)O)O)O 610.50 unknown https://doi.org/10.1021/JF0210730
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
(2S)-5-hydroxy-2-(3-hydroxy-4-methoxyphenyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxy-2,3-dihydrochromen-4-one 129010007 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=O)CC(OC4=C3)C5=CC(=C(C=C5)OC)O)O)O)O)O)O)O)O 610.60 unknown https://doi.org/10.1021/JF980258X
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
Farnisin 5378220 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(O2)C=C(C=C3)O)O 284.26 unknown https://doi.org/10.1021/JF0210730
Hesperetin 72281 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/10.1021/JF980258X
> Phenylpropanoids and polyketides / Isoflavonoids / Coumestans
Medicagol 5319322 Click to see C1OC2=C(O1)C=C3C(=C2)C4=C(O3)C5=C(C=C(C=C5)O)OC4=O 296.23 unknown https://doi.org/10.1021/JF980258X
Sophoracoumestan B 11131193 Click to see COC1=C(C=CC2=C1OC(=O)C3=C2OC4=CC5=C(C=C43)OCO5)O 326.26 unknown https://doi.org/10.1021/JF980258X
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
Fujikinetin 9883229 Click to see COC1=C(C=C2C(=C1)C(=O)C(=CO2)C3=CC4=C(C=C3)OCO4)O 312.27 unknown https://doi.org/10.1021/JF980258X
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavonoid O-glycosides
7-[(2S,3R,4S,5S,6R)-6-[[(2R,3S,4S)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-3-(4-methoxyphenyl)chromen-4-one 162992860 Click to see COC1=CC=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)OC4C(C(C(C(O4)COC5C(C(CO5)(CO)O)O)O)O)O 562.50 unknown https://doi.org/10.1021/JF0210730
7-[6-[[3,4-Dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-3-(4-methoxyphenyl)chromen-4-one 156602958 Click to see COC1=CC=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)OC4C(C(C(C(O4)COC5C(C(CO5)(CO)O)O)O)O)O 562.50 unknown https://doi.org/10.1021/JF0210730
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 3-hydroxy,4-methoxyisoflavonoids
Calycosin 5280448 Click to see COC1=C(C=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)O)O 284.26 unknown https://doi.org/10.1021/JF980258X
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 4-O-methylisoflavones
3-(4-Methoxyphenyl)-4-oxo-4h-chromen-7-yl acetate 908827 Click to see CC(=O)OC1=CC2=C(C=C1)C(=O)C(=CO2)C3=CC=C(C=C3)OC 310.30 unknown https://doi.org/10.1021/JF980258X
6-methoxy-3-(4-methoxyphenyl)-7-[(2R,3R,4S,5S,6R)-2,4,5-trihydroxy-6-(hydroxymethyl)oxan-3-yl]oxychromen-4-one 163185974 Click to see COC1=CC=C(C=C1)C2=COC3=CC(=C(C=C3C2=O)OC)OC4C(C(C(OC4O)CO)O)O 460.40 unknown https://doi.org/10.1021/JF0210730
6-Methoxy-3-(4-methoxyphenyl)-7-[2,4,5-trihydroxy-6-(hydroxymethyl)oxan-3-yl]oxychromen-4-one 162966941 Click to see COC1=CC=C(C=C1)C2=COC3=CC(=C(C=C3C2=O)OC)OC4C(C(C(OC4O)CO)O)O 460.40 unknown https://doi.org/10.1021/JF0210730
Afrormosin 5281704 Click to see COC1=CC=C(C=C1)C2=COC3=CC(=C(C=C3C2=O)OC)O 298.29 unknown https://doi.org/10.1021/JF980258X
Formononetin 5280378 Click to see COC1=CC=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)O 268.26 unknown https://doi.org/10.1021/JF980258X
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
Flemichapparin 5374076 Click to see COC1=C(C=C(C(=C1)C(=O)C=CC2=CC=CC=C2)O)O 270.28 unknown https://doi.org/10.1021/JF980258X

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