Hypericum revolutum - Unknown
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Internal ID UUID6440216b8f5d3368719105
Scientific name Hypericum revolutum
Authority Vahl
First published in Symb. Bot. 1: 66 (1790)

Description Top

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Synonyms Top

Scientific name Authority First published in
Hypericum kalmianum Vahl Symb. Bot. 1: 66 (1790)
Hypericum kalmii Forssk. Fl. Aegypt.-Arab. : cxviii (1775)

Common names Top

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Language Common/alternative name
Afrikaans kerriebos
Japanese ヒペリクム・レウォルツム
Japanese ヒュペリクム・レヴォルトゥム

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Hypericum revolutum subsp. keniense (Schweinf.) N.Robson Fl. Trop. E. Africa , Guttif.: 28 (1978)
Hypericum revolutum subsp. revolutum

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
  • Africa
    • East Tropical Africa
      • Kenya
      • Tanzania
      • Uganda
    • Northeast Tropical Africa
      • Eritrea
      • Ethiopia
      • Sudan
    • South Tropical Africa
      • Malawi
      • Mozambique
      • Zambia
      • Zimbabwe
    • Southern Africa
      • Cape Provinces
      • Kwazulu-Natal
      • Northern Provinces
      • Swaziland
    • West Tropical Africa
      • Nigeria
    • West-central Tropical Africa
      • Burundi
      • Cameroon
      • Congo
      • Gulf Of Guinea Islands
      • Rwanda
      • Zaïre

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000728231
Tropicos 7800907
KEW urn:lsid:ipni.org:names:433800-1
The Plant List kew-2858847
Open Tree Of Life 577792
NCBI Taxonomy 451067
IUCN Red List 146455427
IPNI 433800-1
iNaturalist 467987
GBIF 7330049
Freebase /m/0nd2qqz
EOL 5707756
USDA GRIN 410231
Wikipedia Hypericum_revolutum
CMAUP NPO26095

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
Traditional lore on the healing effects of therapeutic plants used by the local communities around Simien Mountains National Park, northwestern Ethiopia Seraw E, Melkamu Y, Masresha G J Ethnobiol Ethnomed 17-Apr-2024
PMCID:PMC11025143
doi:10.1186/s13002-024-00678-9
PMID:38632559
Modeling habitat suitability for the lesser‐known populations of endangered mountain nyala (Tragelaphus buxtoni) in the Arsi and Ahmar Mountains, Ethiopia Worku EA, Evangelista PH, Atickem A, Bekele A, Bro‐Jørgensen J, Stenseth NC Ecol Evol 15-Apr-2024
PMCID:PMC11017409
doi:10.1002/ece3.11235
PMID:38623519
Shifting mammal communities and declining species richness along an elevational gradient on Mount Kenya Snider MH, Helgen KM, Young HS, Agwanda B, Schuttler S, Titcomb GC, Branch D, Dommain R, Kays R Ecol Evol 09-Apr-2024
PMCID:PMC11004549
doi:10.1002/ece3.11151
PMID:38601855
High species richness in the lichen genus Peltigera (Ascomycota, Lecanoromycetes): 34 species in the dolichorhizoid and scabrosoid clades of section Polydactylon, including 24 new to science Magain N, Miadlikowska J, Goffinet B, Goward T, Pardo-De la Hoz CJ, Jüriado I, Simon A, Mercado-Díaz JA, Barlow T, Moncada B, Lücking R, Spielmann A, Canez L, Wang LS, Nelson P, Wheeler T, Lutzoni F, Sérusiaux E Persoonia 08-Aug-2023
PMCID:PMC11041898
doi:10.3767/persoonia.2023.51.01
PMID:38665978
Woody species diversity and regeneration status of Sub-Alpine forest of Mount Adama exclosure site, Northwestern highlands of Ethiopia Mengistu DA, Bekele DA, Gela AG, Meshesha DT, Getahun MM Heliyon 20-May-2023
PMCID:PMC10220367
doi:10.1016/j.heliyon.2023.e16473
PMID:37251442
Species Diversity, Structure, and Regeneration Status of Woody Plants in Saleda Yohans Church Forest, South Wollo, Ethiopia Mekonnen AB, Mohammed AS, Demissew A Scientifica (Cairo) 17-Apr-2023
PMCID:PMC10125748
doi:10.1155/2023/3853463
PMID:37101718
Important Medicinal and Food Taxa (Orders and Families) in Kenya, Based on Three Quantitative Approaches Mutie FM, Mbuni YM, Rono PC, Mkala EM, Nzei JM, Phumthum M, Hu GW, Wang QF Plants (Basel) 02-Mar-2023
PMCID:PMC10005506
doi:10.3390/plants12051145
PMID:36904005
Antibacterial, Antioxidant Potency, and Chemical Composition of Essential Oils from Dried Powdered Leaves and Flowers of Hypericum revolutum subsp. keniense (Schweinf.) Sengera GO, Kenanda EO, Onyancha JM Evid Based Complement Alternat Med 03-Jan-2023
PMCID:PMC9831702
doi:10.1155/2023/4125885
PMID:36636606
Ethnobotanical study of endemic and non-endemic medicinal plants used by indigenous people in environs of Gullele botanical garden Addis Ababa, central Ethiopia: A major focus on Asteraceae family Woldeamanuel MM, Geda MK, Mohapatra S, Bastia TK, Rath P, Panda AK Front Pharmacol 23-Nov-2022
PMCID:PMC9727095
doi:10.3389/fphar.2022.1020097
PMID:36506590
Density and characteristics of tree cavities inside and outside Volcanoes National Park, Rwanda Niringiyimana A, Nzarora A, Twahirwa JC, van der Hoek Y Ecol Evol 27-Oct-2022
PMCID:PMC9608801
doi:10.1002/ece3.9461
PMID:36311396
Human-wildlife conflict and community perceptions towards wildlife conservation in and around Wof-Washa Natural State Forest, Ethiopia Yazezew D BMC Zool 27-Sep-2022
PMCID:PMC10127036
doi:10.1186/s40850-022-00154-5
PMID:37170343
Woody species diversity and carbon stock of church forests along age gradient in Dangila district, Awi-zone, Ethiopia Sewagegn GB, Abate DF, Yohannis Gebremariam Girma Heliyon 05-Sep-2022
PMCID:PMC9463591
doi:10.1016/j.heliyon.2022.e10491
PMID:36097492
Antioxidant Activity and Anti-Nutritional Factors of Selected Wild Edible Plants Collected from Northeastern Ethiopia Adamu E, Asfaw Z, Demissew S, Baye K Foods 01-Aug-2022
PMCID:PMC9368519
doi:10.3390/foods11152291
PMID:35954058
Antidepressant Effects of South African Plants: An Appraisal of Ethnobotanical Surveys, Ethnopharmacological and Phytochemical Studies Bonokwane MB, Lekhooa M, Struwig M, Aremu AO Front Pharmacol 29-Jun-2022
PMCID:PMC9277359
doi:10.3389/fphar.2022.895286
PMID:35846999
Woody Species Composition, Plant Communities, and Environmental Determinants in Gennemar Dry Afromontane Forest, Southern Ethiopia Ahmed S, Lemessa D, Seyum A Scientifica (Cairo) 22-Jun-2022
PMCID:PMC9242778
doi:10.1155/2022/7970435
PMID:35784587

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
> Lignans, neolignans and related compounds
(2R)-3-hydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)-2-[4-(3-hydroxypropyl)-2-methoxyphenoxy]propan-1-one 15690603 Click to see COC1=CC(=CC(=C1O)OC)C(=O)C(CO)OC2=C(C=C(C=C2)CCCO)OC 406.40 unknown via CMAUP database
(2S)-3-hydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)-2-[4-(3-hydroxypropyl)-2-methoxyphenoxy]propan-1-one 92466671 Click to see COC1=CC(=CC(=C1O)OC)C(=O)C(CO)OC2=C(C=C(C=C2)CCCO)OC 406.40 unknown via CMAUP database
erythro-Guaiacylglycerol |A-dihydroconiferyl ether 13893597 Click to see COC1=C(C=CC(=C1)CCCO)OC(CO)C(C2=CC(=C(C=C2)O)OC)O 378.40 unknown via CMAUP database
> Lignans, neolignans and related compounds / Aryltetralin lignans / 9,9p-dihydroxyaryltetralin lignans
Isoolivil 5316262 Click to see COC1=C(C=C2C(C(C(CC2=C1)(CO)O)CO)C3=CC(=C(C=C3)O)OC)O 376.40 unknown via CMAUP database
> Lignans, neolignans and related compounds / Flavonolignans
(inverted exclamation markA)-Hydnocarpin 11213425 Click to see COC1=C(C=CC(=C1)C2C(OC3=C(O2)C=CC(=C3)C4=CC(=O)C5=C(C=C(C=C5O4)O)O)CO)O 464.40 unknown via CMAUP database
5,7-dihydroxy-2-[(2R,3R)-2-(4-hydroxy-3,5-dimethoxyphenyl)-3-(hydroxymethyl)-2,3-dihydro-1,4-benzodioxin-6-yl]chromen-4-one 10791345 Click to see COC1=CC(=CC(=C1O)OC)C2C(OC3=C(O2)C=CC(=C3)C4=CC(=O)C5=C(C=C(C=C5O4)O)O)CO 494.40 unknown via CMAUP database
5'-Methoxyhydnocarpin 5281879 Click to see COC1=CC(=CC2=C1OC(C(O2)C3=CC(=C(C=C3)O)OC)CO)C4=CC(=O)C5=C(C=C(C=C5O4)O)O 494.40 unknown via CMAUP database
Hydnocarpin D 11431204 Click to see COC1=C(C=CC(=C1)C2C(OC3=C(O2)C=C(C=C3)C4=CC(=O)C5=C(C=C(C=C5O4)O)O)CO)O 464.40 unknown via CMAUP database
Palstatin 5323578 Click to see COC1=CC(=CC(=C1O)OC)C2C(OC3=C(O2)C=C(C=C3OC)C4=CC(=O)C5=C(C=C(C=C5O4)O)O)CO 524.50 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 7,7-epoxylignans
4-[(2R,3S,4S,5R)-5-(4-hydroxy-3,5-dimethoxyphenyl)-3,4-bis(hydroxymethyl)oxolan-2-yl]-2,6-dimethoxyphenol 25136967 Click to see COC1=CC(=CC(=C1O)OC)C2C(C(C(O2)C3=CC(=C(C(=C3)OC)O)OC)CO)CO 436.50 unknown via CMAUP database
Huazhongilexin 15690604 Click to see COC1=CC(=CC(=C1O)OC)C2C(C(C(O2)C3=CC(=C(C(=C3)OC)O)OC)CO)CO 436.50 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 7,9-epoxylignans
(-)-Olivil 5273570 Click to see COC1=C(C=CC(=C1)CC2(COC(C2CO)C3=CC(=C(C=C3)O)OC)O)O 376.40 unknown via CMAUP database
> Lignans, neolignans and related compounds / Lignan glycosides
(2R,3R,4R,5R,6S)-2-[3-[4-[(1R,2S)-1,3-dihydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)propan-2-yl]oxy-3-methoxyphenyl]propoxy]-6-methyloxane-3,4,5-triol 15690602 Click to see CC1C(C(C(C(O1)OCCCC2=CC(=C(C=C2)OC(CO)C(C3=CC(=C(C(=C3)OC)O)OC)O)OC)O)O)O 554.60 unknown via CMAUP database
(2R,3R,4R,5R,6S)-2-[3-[4-[(1S,2R)-1,3-dihydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)propan-2-yl]oxy-3-methoxyphenyl]propoxy]-6-methyloxane-3,4,5-triol 101606109 Click to see CC1C(C(C(C(O1)OCCCC2=CC(=C(C=C2)OC(CO)C(C3=CC(=C(C(=C3)OC)O)OC)O)OC)O)O)O 554.60 unknown via CMAUP database
(2S,3R,4S,5S,6R)-2-[4-[(3S,3aR,6S,6aR)-3-(4-hydroxy-3-methoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-6-yl]-2-methoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 486614 Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)OC5C(C(C(C(O5)CO)O)O)O)OC)O 520.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
(2R,3R,4S,5S,6R)-2-[(Z)-hex-3-enoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 5318045 Click to see CCC=CCCOC1C(C(C(C(O1)CO)O)O)O 262.30 unknown via CMAUP database
(2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-[(E)-3-(2,3,4-trimethoxyphenyl)prop-2-enoxy]oxane-3,4,5-triol 11972373 Click to see COC1=C(C(=C(C=C1)C=CCOC2C(C(C(C(O2)CO)O)O)O)OC)OC 386.40 unknown via CMAUP database
(4S)-3,5,5-trimethyl-4-[(3R)-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]cyclohex-2-en-1-one 38346955 Click to see CC1=CC(=O)CC(C1CCC(C)OC2C(C(C(C(O2)CO)O)O)O)(C)C 372.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Hexacosanol 68171 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCO 382.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Linoleic Acid 5280450 Click to see CCCCCC=CCC=CCCCCCCCC(=O)O 280.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(1S,5S,7S,8R)-4-hydroxy-8-methyl-1-[(2R)-2-methylbutanoyl]-5,7-bis(3-methylbut-2-enyl)-8-(4-methylpent-3-enyl)bicyclo[3.3.1]non-3-ene-2,9-dione 162995000 Click to see CCC(C)C(=O)C12C(=O)C=C(C(C1=O)(CC(C2(C)CCC=C(C)C)CC=C(C)C)CC=C(C)C)O 482.70 unknown https://doi.org/10.1002/HLCA.19890720307
(1S,5S,7S,8R)-4-hydroxy-8-methyl-5,7-bis(3-methylbut-2-enyl)-8-(4-methylpent-3-enyl)-1-(2-methylpropanoyl)bicyclo[3.3.1]non-3-ene-2,9-dione 162909437 Click to see CC(C)C(=O)C12C(=O)C=C(C(C1=O)(CC(C2(C)CCC=C(C)C)CC=C(C)C)CC=C(C)C)O 468.70 unknown https://doi.org/10.1002/HLCA.19890720307
(7S,8R)-4-hydroxy-8-methyl-5,7-bis(3-methylbut-2-enyl)-8-(4-methylpent-3-enyl)-1-(2-methylpropanoyl)bicyclo[3.3.1]non-3-ene-2,9-dione 9956290 Click to see CC(C)C(=O)C12C(=O)C=C(C(C1=O)(CC(C2(C)CCC=C(C)C)CC=C(C)C)CC=C(C)C)O 468.70 unknown https://doi.org/10.1002/HLCA.19890720307
4-Hydroxy-8-methyl-1-(2-methylbutanoyl)-5,7-bis(3-methylbut-2-enyl)-8-(4-methylpent-3-enyl)bicyclo[3.3.1]non-3-ene-2,9-dione 14336347 Click to see CCC(C)C(=O)C12C(=O)C=C(C(C1=O)(CC(C2(C)CCC=C(C)C)CC=C(C)C)CC=C(C)C)O 482.70 unknown https://doi.org/10.1002/HLCA.19890720307
4-Hydroxy-8-methyl-5,7-bis(3-methylbut-2-enyl)-8-(4-methylpent-3-enyl)-1-(2-methylpropanoyl)bicyclo[3.3.1]non-3-ene-2,9-dione 360843 Click to see CC(C)C(=O)C12C(=O)C=C(C(C1=O)(CC(C2(C)CCC=C(C)C)CC=C(C)C)CC=C(C)C)O 468.70 unknown https://doi.org/10.1002/HLCA.19890720307
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
4-[(4R)-2,6,6-trimethyl-4-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycyclohexen-1-yl]butan-2-one 101606458 Click to see CC1=C(C(CC(C1)OC2C(C(C(C(O2)CO)O)O)O)(C)C)CCC(=O)C 372.50 unknown via CMAUP database
CID 11968607 11968607 Click to see CC1=C(C(C(CC1)OC2C(C(C(C(O2)CO)O)O)O)(C)C)CCC(=O)C 372.50 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
(1S,3R,4R,5R)-3-[3-(3,4-dihydroxyphenyl)prop-2-enoyloxy]-1,4,5-trihydroxy-cyclohexanecarboxylic acid 9476 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(E)-4-[(1S,4S,6R)-2,2,6-trimethyl-4-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-7-oxabicyclo[4.1.0]heptan-1-yl]but-3-en-2-one 10385469 Click to see CC(=O)C=CC12C(CC(CC1(O2)C)OC3C(C(C(C(O3)CO)O)O)O)(C)C 386.40 unknown via CMAUP database
Phenylethyl beta-D-glucopyranoside 11289099 Click to see C1=CC=C(C=C1)CCOC2C(C(C(C(O2)CO)O)O)O 284.30 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-[(3,5,6,7-tetramethoxy-9,10-dihydrophenanthren-2-yl)oxy]oxane-3,4,5-triol 15690608 Click to see COC1=C(C(=C2C(=C1)CCC3=CC(=C(C=C32)OC)OC4C(C(C(C(O4)CO)O)O)O)OC)OC 478.50 unknown via CMAUP database
> Organoheterocyclic compounds / Benzofurans / Dibenzofurans
1,4,7-Trimethoxydibenzofuran-3-ol 42611453 Click to see COC1=CC2=C(C=C1)C3=C(C=C(C(=C3O2)OC)O)OC 274.27 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.12.016
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / 2,2-dimethyl-1-benzopyrans
(2R)-1-(5,7-dihydroxy-2,2,6-trimethylchromen-8-yl)-2-methylbutan-1-one 162861800 Click to see CCC(C)C(=O)C1=C(C(=C(C2=C1OC(C=C2)(C)C)O)C)O 290.40 unknown https://doi.org/10.1002/HLCA.19870700705
(2R)-2-methyl-1-[(1R,2R,11S)-7,9,15-trihydroxy-3,3,8,14,19,19-hexamethyl-16-[(2R)-2-methylbutanoyl]-4,12,18-trioxapentacyclo[11.7.1.02,11.05,10.017,21]henicosa-5(10),6,8,13(21),14,16-hexaen-6-yl]butan-1-one 162975790 Click to see CCC(C)C(=O)C1=C(C(=C(C2=C1OC(C3C2OC4=C5C3CC(OC5=C(C(=C4C)O)C(=O)C(C)CC)(C)C)(C)C)O)C)O 580.70 unknown https://doi.org/10.1002/HLCA.19870700705
1-(5,7-Dihydroxy-2,2,6-trimethyl-2 h-1-benzopyran-8-yl)-2-methyl-1-propanone 360842 Click to see CC1=C(C2=C(C(=C1O)C(=O)C(C)C)OC(C=C2)(C)C)O 276.33 unknown https://doi.org/10.1002/HLCA.19870700705
1-(5,7-Dihydroxy-2,2,6-trimethylchromen-8-yl)-2-methylbutan-1-one 360841 Click to see CCC(C)C(=O)C1=C(C(=C(C2=C1OC(C=C2)(C)C)O)C)O 290.40 unknown https://doi.org/10.1002/HLCA.19870700705
2-methyl-1-[(1R,2R,11S)-7,9,15-trihydroxy-3,3,8,14,19,19-hexamethyl-16-(2-methylpropanoyl)-4,12,18-trioxapentacyclo[11.7.1.02,11.05,10.017,21]henicosa-5(10),6,8,13(21),14,16-hexaen-6-yl]propan-1-one 21595247 Click to see CC1=C(C2=C(C(=C1O)C(=O)C(C)C)OC(C3C2OC4=C5C3CC(OC5=C(C(=C4C)O)C(=O)C(C)C)(C)C)(C)C)O 552.70 unknown https://doi.org/10.1002/HLCA.19870700705
2-Methyl-1-[7,9,15-trihydroxy-3,3,8,14,19,19-hexamethyl-16-(2-methylbutanoyl)-4,12,18-trioxapentacyclo[11.7.1.02,11.05,10.017,21]henicosa-5(10),6,8,13(21),14,16-hexaen-6-yl]butan-1-one 13912601 Click to see CCC(C)C(=O)C1=C(C(=C(C2=C1OC(C3C2OC4=C5C3CC(OC5=C(C(=C4C)O)C(=O)C(C)CC)(C)C)(C)C)O)C)O 580.70 unknown https://doi.org/10.1002/HLCA.19870700705
2-Methyl-1-[7,9,15-trihydroxy-3,3,8,14,19,19-hexamethyl-16-(2-methylpropanoyl)-4,12,18-trioxapentacyclo[11.7.1.02,11.05,10.017,21]henicosa-5(10),6,8,13(21),14,16-hexaen-6-yl]propan-1-one 13912600 Click to see CC1=C(C2=C(C(=C1O)C(=O)C(C)C)OC(C3C2OC4=C5C3CC(OC5=C(C(=C4C)O)C(=O)C(C)C)(C)C)(C)C)O 552.70 unknown https://doi.org/10.1002/HLCA.19870700705
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-[4-[(2R,3S)-3-(hydroxymethyl)-5-(3-hydroxypropyl)-7-methoxy-2,3-dihydro-1-benzofuran-2-yl]-2-methoxyphenoxy]oxane-3,4,5-triol 10625848 Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)OC)CCCO 522.50 unknown via CMAUP database
Dihydrodehydrodiconiferyl alcohol 384679 Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C=C3)O)OC)CCCO 360.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
4-Hydroxycinnamic acid 322 Click to see C1=CC(=CC=C1C=CC(=O)O)O 164.16 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives
6-Demethoxycapillarisin 5316511 Click to see C1=CC(=CC=C1O)OC2=CC(=O)C3=C(C=C(C=C3O2)O)O 286.24 unknown via CMAUP database
Demethoxy-7-O-methylcapillarisin 71391689 Click to see COC1=CC(=C2C(=C1)OC(=CC2=O)OC3=CC=C(C=C3)O)O 300.26 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
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
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
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
[(2S,3R,4R,5R,6S)-6-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-4-hydroxy-5-[(E)-3-(4-hydroxyphenyl)prop-2-enoyl]oxy-2-methyloxan-3-yl] (Z)-3-(4-hydroxyphenyl)prop-2-enoate 49822437 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)OC(=O)C=CC5=CC=C(C=C5)O)O)OC(=O)C=CC6=CC=C(C=C6)O 724.70 unknown via CMAUP database
[(2S,3R,4R,5R,6S)-6-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-4-hydroxy-5-[(Z)-3-(4-hydroxyphenyl)prop-2-enoyl]oxy-2-methyloxan-3-yl] (E)-3-(4-hydroxyphenyl)prop-2-enoate 11700461 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)OC(=O)C=CC5=CC=C(C=C5)O)O)OC(=O)C=CC6=CC=C(C=C6)O 724.70 unknown via CMAUP database
2'',4''-Di-O-(E-p-Coumaroyl)afzelin 11765457 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)OC(=O)C=CC5=CC=C(C=C5)O)O)OC(=O)C=CC6=CC=C(C=C6)O 724.70 unknown via CMAUP database
3-[(2S,3R,4R,5R,6S)-4,5-dihydroxy-6-methyl-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-5,7-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one 10721917 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)C)O)O)O)O)O 578.50 unknown via CMAUP database
3-[3-O-(4-Hydroxy-cis-cinnamoyl)-4-O-(4-hydroxy-trans-cinnamoyl)-alpha-L-rhamnopyranosyloxy]-5,7,4'-trihydroxyflavone 45783016 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)O)OC(=O)C=CC5=CC=C(C=C5)O)OC(=O)C=CC6=CC=C(C=C6)O 724.70 unknown via CMAUP database
3'',4''-Di-O-p-coumaroylafzelin 51136469 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)O)OC(=O)C=CC5=CC=C(C=C5)O)OC(=O)C=CC6=CC=C(C=C6)O 724.70 unknown via CMAUP database
Afzelin 5316673 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 432.40 unknown via CMAUP database
Baohuoside I 5488822 Click to see CC1C(C(C(C(O1)OC2=C(OC3=C(C(=CC(=C3C2=O)O)O)CC=C(C)C)C4=CC=C(C=C4)OC)O)O)O 514.50 unknown via CMAUP database
Baohuoside II 5481982 Click to see CC1C(C(C(C(O1)OC2=C(OC3=C(C(=CC(=C3C2=O)O)O)CC=C(C)C)C4=CC=C(C=C4)O)O)O)O 500.50 unknown via CMAUP database
Hyperoside 5281643 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown via CMAUP database
Quercetin-3-O-[alpha-L-rhamnopyranosyl-(1->2)-alpha-L-rhamnopyranoside] 10698716 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)O)C)O)O)O)O)O 594.50 unknown via CMAUP database
Quercitrin 5280459 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 via CMAUP database
Trifolin 5282149 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
3-[(2S,3R,4R,5R,6S)-4,5-dihydroxy-6-methyl-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-2-(3-hydroxy-4-methoxyphenyl)-8-(3-methylbut-2-enyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 101437361 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=C(C3=O)C(=CC(=C4CC=C(C)C)OC5C(C(C(C(O5)CO)O)O)O)O)C6=CC(=C(C=C6)OC)O)C)O)O)O)O)O 838.80 unknown via CMAUP database
5-hydroxy-2-(3-hydroxy-4-methoxyphenyl)-8-(3-methylbut-2-enyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one 101437362 Click to see CC1C(C(C(C(O1)OC2=C(OC3=C(C2=O)C(=CC(=C3CC=C(C)C)OC4C(C(C(C(O4)CO)O)O)O)O)C5=CC(=C(C=C5)OC)O)O)O)O 692.70 unknown via CMAUP database
Baohuoside V 25087702 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=C(C3=O)C(=CC(=C4CC=C(C)C)OC5C(C(C(C(O5)CO)O)O)O)O)C6=CC=C(C=C6)O)C)O)O)O)O)O 808.80 unknown via CMAUP database
Epimedin A 13916051 Click to see CC1C(C(C(C(O1)OC2=C(OC3=C(C2=O)C(=CC(=C3CC=C(C)C)OC4C(C(C(C(O4)CO)O)O)O)O)C5=CC=C(C=C5)OC)OC6C(C(C(C(O6)CO)O)O)O)O)O 838.80 unknown via CMAUP database
Epimedin A1 92043273 Click to see CC1C(C(C(C(O1)OC2=C(OC3=C(C2=O)C(=CC(=C3CC=C(C)C)OC4C(C(C(C(O4)CO)O)O)O)O)C5=CC=C(C=C5)OC)O)OC6C(C(C(C(O6)CO)O)O)O)O 838.80 unknown via CMAUP database
Epimedin B 5748393 Click to see CC1C(C(C(C(O1)OC2=C(OC3=C(C2=O)C(=CC(=C3CC=C(C)C)OC4C(C(C(C(O4)CO)O)O)O)O)C5=CC=C(C=C5)OC)OC6C(C(C(CO6)O)O)O)O)O 808.80 unknown via CMAUP database
Epimedin C 5748394 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=C(C3=O)C(=CC(=C4CC=C(C)C)OC5C(C(C(C(O5)CO)O)O)O)O)C6=CC=C(C=C6)OC)C)O)O)O)O)O 822.80 unknown via CMAUP database
Epimedokoreanoside I 87759921 Click to see CC1C(C(C(C(O1)OC2=C(OC3=C(C2=O)C(=CC(=C3CC=C(C)C)OC4C(C(C(C(O4)CO)O)O)O)O)C5=CC=C(C=C5)OC)O)OC6C(C(C(C(O6)COC(=O)C)O)O)O)OC(=O)C 922.90 unknown via CMAUP database
Epimedoside A 5317093 Click to see CC1C(C(C(C(O1)OC2=C(OC3=C(C2=O)C(=CC(=C3CC=C(C)C)OC4C(C(C(C(O4)CO)O)O)O)O)C5=CC=C(C=C5)O)O)O)O 662.60 unknown via CMAUP database
Icariin 5318997 Click to see CC1C(C(C(C(O1)OC2=C(OC3=C(C2=O)C(=CC(=C3CC=C(C)C)OC4C(C(C(C(O4)CO)O)O)O)O)C5=CC=C(C=C5)OC)O)O)O 676.70 unknown via CMAUP database
Icariside I 5745470 Click to see CC(=CCC1=C(C=C(C2=C1OC(=C(C2=O)O)C3=CC=C(C=C3)OC)O)OC4C(C(C(C(O4)CO)O)O)O)C 530.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
3'-O-Methyltricetin 11267045 Click to see COC1=CC(=CC(=C1O)O)C2=CC(=O)C3=C(C=C(C=C3O2)O)O 316.26 unknown via CMAUP database
Tricin 5281702 Click to see COC1=CC(=CC(=C1O)OC)C2=CC(=O)C3=C(C=C(C=C3O2)O)O 330.29 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
2-(1,3-Benzodioxol-5-yl)-5-hydroxy-6,7-dimethoxychromen-4-one 5321057 Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC4=C(C=C3)OCO4)O)OC 342.30 unknown via CMAUP database

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