Verbascum phlomoides - Unknown
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Details Top

Internal ID UUID643ffa7bf0451926437730
Scientific name Verbascum phlomoides
Authority L.
First published in Sp. Pl. : 1194 (1753)

Description Top

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Synonyms Top

Scientific name Authority First published in
Verbascum slavonicum Kit. Pl. Banat. Rar. : 26 (1828)
Verbascum saxatile Salisb. Prodr. Stirp. Chap. Allerton : 104 (1796)
Verbascum rugulosum Willd. Enum. Pl. : 224 (1809)
Verbascum semidecurrens Kit. ex Nyman Consp. Fl. Eur. : 526 (1881)
Verbascum viminale Guss. Pl. Rar. : 101 (1826)
Verbascum pumilum Stoj. & Stef. Oesterr. Bot. Z. 72: 89. 1923
Verbascum rolletianum hort. ex Roem. & Schult. Syst. Veg., ed. 15 bis 4: 333 (1819)
Verbascum australe Schrad. Monogr. Verbasci 1: 28 (1813)
Verbascum argyrostachyon Ten. Relaz. Viagg. Abruzzo : 52 (1832)
Verbascum bulgaricum Velen. Fl. Bulg. : 408 (1891)
Verbascum calvescens Schur Enum. Pl. Transsilv. : 481 (1866)
Verbascum belasitzae Stoj. & Stef. Fl. Bulg. : 987 (1925)
Verbascum italicum Moric. Fl. Venet. 1: 116 (1820)
Verbascum macranthum Hoffmanns. & Link Fl. Portug. 1: 215 (1811)
Verbascum nemorosum Schrad. Monogr. Verbasci 1: 32 (1813)
Verbascum condensatum Schrad. Monogr. Verbasci 1: 31 (1813)
Verbascum grandiflorum Mill. Gard. Dict. ed. 8 : n.º 5 (1768)
Thapsus phlomoides Opiz Seznam : 96 (1852)
Flomosia condensata Raf. Fl. Tellur. 4: 89 (1838)
Flomosia nemarosa Raf. Fl. Tellur. 4: 89 (1838)
Flomosia phlomoides Raf. Fl. Tellur. 4: 89 (1838)
Verbascum phlomoides var. glabrescens Zalewski Kosmos (Lvov) 5/6: 14 (1896)

Common names Top

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Language Common/alternative name
English orange mullein
English pale yellow mullein
English clasping-leaf mullein
English woolly mullein
English wooly mullein
Spanish gordolobo bastardo
Spanish gordolobo anaranjado
Azerbaijani bozaqgülünəbənzər sığırquyruğu
Belarusian Дзіванна касматая
Bulgarian лечебен лопен
Czech divizna sápovitá
Welsh pannog oren
German windblumen-königskerze
German gewöhnlich-königskerze
Finnish rohtotulikukka
French molène faux phlomis
French molene faux phlomis
French molène faux-phlomis
Upper Sorbian wołmjana dźiwizna
Hungarian szöszös ökörfarkkóró
Norwegian Bokmål hjertekongslys
Dutch keizerskaars
Dutch oranje toorts
Polish dziewanna kutnerowata
Romanian lumnărică
Russian коровяк лекарственный
Russian коровяк мохнатый
Slovak divozel sápovitý
Slovenian navadni lučnik
Serbian Дивизма
Swedish läkekungsljus
Ukrainian дивина звичайна

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
  • Asia-temperate
    • Caucasus
      • North Caucasus
      • Transcaucasus
    • Middle Asia
      • Kazakhstan
    • Siberia
      • Altay
    • Western Asia
      • East Aegean Islands
      • Turkey
  • Europe
    • Eastern Europe
      • Belarus
      • Central European Russia
      • Krym
      • South European Russia
      • Ukraine
    • Middle Europe
      • Austria
      • Belgium
      • Czechoslovakia
      • Germany
      • Hungary
      • Poland
      • Switzerland
    • Northern Europe
      • Great Britain
    • Southeastern Europe
      • Albania
      • Bulgaria
      • Greece
      • Italy
      • Romania
      • Sicilia
      • Turkey-in-Europe
      • Yugoslavia
    • Southwestern Europe
      • Corse
      • France
      • Portugal
      • Sardegna
      • Spain
  • Northern America
    • Eastern Canada
      • Ontario
      • Prince Edward Island
      • Québec
    • North-central U.S.A.
      • Illinois
      • Iowa
      • Minnesota
      • Missouri
      • Wisconsin
    • Northeastern U.S.A.
      • Connecticut
      • Indiana
      • Maine
      • Massachusetts
      • Michigan
      • New Jersey
      • New York
      • Ohio
      • Pennsylvania
      • Rhode Island
      • Vermont
      • West Virginia
    • Northwestern U.S.A.
      • Colorado
      • Oregon
      • Washington
    • Southeastern U.S.A.
      • Arkansas
      • Delaware
      • District Of Columbia
      • Georgia
      • Kentucky
      • Maryland
      • North Carolina
      • South Carolina
      • Tennessee
      • Virginia
    • Western Canada
      • Alberta
      • British Columbia
      • Manitoba
      • Saskatchewan

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000419193
UNII O6F787X697
Canadensys 9328
USDA Plants VEPH
Tropicos 29200219
INPN 128627
Flora of Italy 4749
KEW urn:lsid:ipni.org:names:770045-1
The Plant List kew-2453401
Open Tree Of Life 934439
Observations.org 7611
NCBI Taxonomy 90365
NBN Atlas NBNSYS0000004048
Nature Serve 2.130489
IPNI 770045-1
iNaturalist 170140
GBIF 3171948
WisFlora 5337
EPPO VESPH
EOL 578533
Elurikkus 8131
USDA GRIN 102312
Wikipedia Verbascum_phlomoides

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
A systematic methodology to assess the identity of plants in historical texts: A case study based on the Byzantine pharmacy text John the Physician's Therapeutics Lardos A, Patmore K, Allkin R, Lazarou R, Nesbitt M, Scott AC, Zipser B J Ethnopharmacol 25-Mar-2024
PMCID:PMC7615571
doi:10.1016/j.jep.2023.117622
PMID:38128894
Proportion of Over-The-Counter Medicines Containing a Plant Component and Those with Synthetic Substances Administered among Children in a Bulgarian Population Hadzhieva B, Petkova-Dimitrova V Pharmaceuticals (Basel) 31-Jan-2024
PMCID:PMC10892009
doi:10.3390/ph17020192
PMID:38399407
Ethnobotanical and ethnomedicinal research into medicinal plants in the Mt Stara Planina region (south-eastern Serbia, Western Balkans) Jarić S, Kostić O, Miletić Z, Marković M, Sekulić D, Mitrović M, Pavlović P J Ethnobiol Ethnomed 10-Jan-2024
PMCID:PMC10782642
doi:10.1186/s13002-024-00647-2
PMID:38200599
Natural Products for the Prevention and Treatment of Common Cold and Viral Respiratory Infections Mammari N, Albert Q, Devocelle M, Kenda M, Kočevar Glavač N, Sollner Dolenc M, Mercolini L, Tóth J, Milan N, Czigle S, Varbanov M Pharmaceuticals (Basel) 28-Apr-2023
PMCID:PMC10220542
doi:10.3390/ph16050662
PMID:37242445
Leucosceptosides A and B: Two Phenyl-Ethanoid Glycosides with Important Occurrence and Biological Activities Frezza C, De Vita D, Toniolo C, Sciubba F, Tomassini L, Venditti A, Bianco A, Serafini M, Foddai S Biomolecules 02-Dec-2022
PMCID:PMC9775335
doi:10.3390/biom12121807
PMID:36551235
Inhibition of the main protease of SARS-CoV-2 (Mpro) by repurposing/designing drug-like substances and utilizing nature’s toolbox of bioactive compounds Antonopoulou I, Sapountzaki E, Rova U, Christakopoulos P Comput Struct Biotechnol J 14-Mar-2022
PMCID:PMC8920478
doi:10.1016/j.csbj.2022.03.009
PMID:35308802
Influence of Habitat Types on Diversity and Species Composition of Urban Flora—A Case Study in Serbia Glišić M, Jakovljević K, Lakušić D, Šinžar-Sekulić J, Vukojičić S, Tabašević M, Jovanović S Plants (Basel) 25-Nov-2021
PMCID:PMC8704744
doi:10.3390/plants10122572
PMID:34961043
Verbascoside Protects Gingival Cells against High Glucose-Induced Oxidative Stress via PKC/HMGB1/RAGE/NFκB Pathway Hsieh PF, Yu CC, Chu PM, Hsieh PL Antioxidants (Basel) 12-Sep-2021
PMCID:PMC8464661
doi:10.3390/antiox10091445
PMID:34573077
Acteoside Counteracts Interleukin-1β-Induced Catabolic Processes through the Modulation of Mitogen-Activated Protein Kinases and the NFκB Cellular Signaling Pathway Lim H, Kim DK, Kim TH, Kang KR, Seo JY, Cho SS, Yun Y, Choi YY, Leem J, Kim HW, Jo GU, Oh CJ, Oh DS, Chun HS, Kim JS Oxid Med Cell Longev 24-Mar-2021
PMCID:PMC8016581
doi:10.1155/2021/8684725
PMID:33833854
Potential Ecological and Human Health Risks of Heavy Metals in Soils in Selected Copper Mining Areas—A Case Study: The Bor Area Filimon MN, Caraba IV, Popescu R, Dumitrescu G, Verdes D, Petculescu Ciochina L, Sinitean A Int J Environ Res Public Health 05-Feb-2021
PMCID:PMC7914753
doi:10.3390/ijerph18041516
PMID:33562751
In silico Screening of Natural Compounds as Potential Inhibitors of SARS-CoV-2 Main Protease and Spike RBD: Targets for COVID-19 Teli DM, Shah MB, Chhabria MT Front Mol Biosci 19-Jan-2021
PMCID:PMC7852456
doi:10.3389/fmolb.2020.599079
PMID:33542917
Extracts of Thai Perilla frutescens nutlets attenuate tumour necrosis factor-α-activated generation of microparticles, ICAM-1 and IL-6 in human endothelial cells Paradee N, Utama-ang N, Uthaipibull C, Porter JB, Garbowski MW, Srichairatanakool S Biosci Rep 29-May-2020
PMCID:PMC7260356
doi:10.1042/BSR20192110
PMID:32426811
Phytoremediation Potential, Photosynthetic and Antioxidant Response to Arsenic-Induced Stress of Dactylis glomerata L. Sown on Fly Ash Deposits Gajić G, Djurdjević L, Kostić O, Jarić S, Stevanović B, Mitrović M, Pavlović P Plants (Basel) 22-May-2020
PMCID:PMC7284476
doi:10.3390/plants9050657
PMID:32456107
Natural Sources and Bioactivities of 2,4-Di-Tert-Butylphenol and Its Analogs Zhao F, Wang P, Lucardi RD, Su Z, Li S Toxins (Basel) 06-Jan-2020
PMCID:PMC7020479
doi:10.3390/toxins12010035
PMID:31935944
Safety and efficacy of a tincture derived from Verbascum thapsus L. when used as a sensory additive in feed for all animal species Bampidis V, Azimonti G, Bastos MD, Christensen H, Kouba M, Kos Durjava M, López‐Alonso M, López Puente S, Marcon F, Mayo B, Pechová A, Petkova M, Ramos F, Sanz Y, Villa RE, Woutersen R, Brantom P, Chesson A, Westendorf J, Gregoretti L, Manini P, Dusemund B EFSA J 06-Dec-2019
PMCID:PMC7008842
doi:10.2903/j.efsa.2019.5910
PMID:32626200

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
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
(1S,4aS,5S,7S,7aR)-1,4a,5,6,7,7a-Hexahydro-4a,5,7-trihydroxy-7-methylcyclopenta[c]pyran-1-yl beta-D-glucopyranoside 145706031 Click to see CC1(CC(C2(C1C(OC=C2)OC3C(C(C(C(O3)CO)O)O)O)O)O)O 364.34 unknown https://doi.org/10.1016/0031-9422(72)85053-2
(2S,3R,4S,5S,6R)-2-[[(1S,4aR,5S,7aS)-7-(hydroxymethyl)-5-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxy-1,4a,5,7a-tetrahydrocyclopenta[c]pyran-1-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 163080111 Click to see C1C(C(C(C(O1)OC2C=C(C3C2C=COC3OC4C(C(C(C(O4)CO)O)O)O)CO)O)O)O 478.40 unknown https://doi.org/10.1007/S10600-009-9420-0
[(3R,4R,5R,6S)-6-[[(1S,4aR,5S,7aS)-7-(hydroxymethyl)-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,7a-tetrahydrocyclopenta[c]pyran-5-yl]oxy]-4,5-dihydroxyoxan-3-yl] (Z)-3-(4-hydroxyphenyl)prop-2-enoate 163193402 Click to see C1C(C(C(C(O1)OC2C=C(C3C2C=COC3OC4C(C(C(C(O4)CO)O)O)O)CO)O)O)OC(=O)C=CC5=CC=C(C=C5)O 624.60 unknown https://doi.org/10.1016/S0031-9422(96)00446-3
[4,5-Dihydroxy-6-[[7-(hydroxymethyl)-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,7a-tetrahydrocyclopenta[c]pyran-5-yl]oxy]oxan-3-yl] 3-(4-hydroxyphenyl)prop-2-enoate 162955899 Click to see C1C(C(C(C(O1)OC2C=C(C3C2C=COC3OC4C(C(C(C(O4)CO)O)O)O)CO)O)O)OC(=O)C=CC5=CC=C(C=C5)O 624.60 unknown https://doi.org/10.1016/S0031-9422(96)00446-3
2-[[5-Hydroxy-7-(hydroxymethyl)-1,4a,5,7a-tetrahydrocyclopenta[c]pyran-1-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 348157 Click to see C1=COC(C2C1C(C=C2CO)O)OC3C(C(C(C(O3)CO)O)O)O 346.33 unknown https://doi.org/10.1007/S10600-009-9420-0
Aucubin 91458 Click to see C1=COC(C2C1C(C=C2CO)O)OC3C(C(C(C(O3)CO)O)O)O 346.33 unknown https://doi.org/10.1007/S10600-009-9420-0
Phlomoidoside 102445639 Click to see C1C(C(C(C(O1)OC2C=C(C3C2C=COC3OC4C(C(C(C(O4)CO)O)O)O)CO)O)O)OC(=O)C=CC5=CC=C(C=C5)O 624.60 unknown https://doi.org/10.1016/S0031-9422(96)00446-3
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
(2R,3R,4R,5R,6S)-2-[(2R,3S,4R,5R,6S)-4,5-dihydroxy-6-[(2R,3R,4S,5S,6R)-5-hydroxy-2-[[(1S,4S,5R,8R,9R,10S,13S,14R,17S,18R)-9-(hydroxymethyl)-4,5,9,13,20,20-hexamethyl-24-oxahexacyclo[15.5.2.01,18.04,17.05,14.08,13]tetracos-15-en-10-yl]oxy]-6-methyl-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-4-yl]oxy-2-(hydroxymethyl)oxan-3-yl]oxy-6-methyloxane-3,4,5-triol 162984269 Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OC3C(C(OC(C3OC4C(C(C(C(O4)CO)O)O)O)OC5CCC6(C(C5(C)CO)CCC7(C6C=CC89C7(CCC1(C8CC(CC1)(C)C)CO9)C)C)C)C)O)CO)O)O)O 1073.30 unknown https://doi.org/10.1016/S0031-9422(96)00446-3
(2R,3R,4R,5R,6S)-2-[(2R,3S,4R,5R,6S)-6-[(2R,3R,4S,5R,6R)-6-[[(3S,4R,4aR,6aS,6aR,6bS,8aS,12aR,14aR,14bR)-6a-hydroxy-4,8a-bis(hydroxymethyl)-4,6a,6b,11,11,14b-hexamethyl-2,3,4a,5,6,7,8,9,10,12,12a,14a-dodecahydro-1H-picen-3-yl]oxy]-4-hydroxy-2-methyl-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-3-yl]oxy-4,5-dihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy-6-methyloxane-3,4,5-triol 162875660 Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OC3C(OC(C(C3O)OC4C(C(C(C(O4)CO)O)O)O)OC5CCC6(C(C5(C)CO)CCC7(C6C=CC8(C7(CCC9(C8CC(CC9)(C)C)CO)C)O)C)C)C)CO)O)O)O 1091.30 unknown https://doi.org/10.1002/CBER.19801130510
2-[4,5-Dihydroxy-6-[5-hydroxy-2-[[9-(hydroxymethyl)-4,5,9,13,20,20-hexamethyl-24-oxahexacyclo[15.5.2.01,18.04,17.05,14.08,13]tetracos-15-en-10-yl]oxy]-6-methyl-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-4-yl]oxy-2-(hydroxymethyl)oxan-3-yl]oxy-6-methyloxane-3,4,5-triol 73157220 Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OC3C(C(OC(C3OC4C(C(C(C(O4)CO)O)O)O)OC5CCC6(C(C5(C)CO)CCC7(C6C=CC89C7(CCC1(C8CC(CC1)(C)C)CO9)C)C)C)C)O)CO)O)O)O 1073.30 unknown https://doi.org/10.1016/S0031-9422(96)00446-3
2-[5-Hydroxy-2-[[9-(hydroxymethyl)-4,5,9,13,20,20-hexamethyl-24-oxahexacyclo[15.5.2.01,18.04,17.05,14.08,13]tetracos-15-en-10-yl]oxy]-6-methyl-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-4-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 162936539 Click to see CC1C(C(C(C(O1)OC2CCC3(C(C2(C)CO)CCC4(C3C=CC56C4(CCC7(C5CC(CC7)(C)C)CO6)C)C)C)OC8C(C(C(C(O8)CO)O)O)O)OC9C(C(C(C(O9)CO)O)O)O)O 927.10 unknown https://doi.org/10.1016/S0031-9422(96)00446-3
2-[6-[6-[[6a-hydroxy-4,8a-bis(hydroxymethyl)-4,6a,6b,11,11,14b-hexamethyl-2,3,4a,5,6,7,8,9,10,12,12a,14a-dodecahydro-1H-picen-3-yl]oxy]-4-hydroxy-2-methyl-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-3-yl]oxy-4,5-dihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy-6-methyloxane-3,4,5-triol 162875659 Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OC3C(OC(C(C3O)OC4C(C(C(C(O4)CO)O)O)O)OC5CCC6(C(C5(C)CO)CCC7(C6C=CC8(C7(CCC9(C8CC(CC9)(C)C)CO)C)O)C)C)C)CO)O)O)O 1091.30 unknown https://doi.org/10.1002/CBER.19801130510
Desrhamnosylverbascosaponin 102445401 Click to see CC1C(C(C(C(O1)OC2CCC3(C(C2(C)CO)CCC4(C3C=CC56C4(CCC7(C5CC(CC7)(C)C)CO6)C)C)C)OC8C(C(C(C(O8)CO)O)O)O)OC9C(C(C(C(O9)CO)O)O)O)O 927.10 unknown https://doi.org/10.1016/S0031-9422(96)00446-3
Verbascosaponin 188264 Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OC3C(C(OC(C3OC4C(C(C(C(O4)CO)O)O)O)OC5CCC6(C(C5(C)CO)CCC7(C6C=CC89C7(CCC1(C8CC(CC1)(C)C)CO9)C)C)C)C)O)CO)O)O)O 1073.30 unknown https://doi.org/10.1016/S0031-9422(96)00446-3
https://doi.org/10.1002/JLAC.199319930167
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
2-[[5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 3917786 Click to see C1=COC(C2C1C(C3C2(O3)CO)O)OC4C(C(C(C(O4)CO)O)O)O 362.33 unknown https://doi.org/10.1007/S10600-009-9420-0
Catalpol 91520 Click to see C1=COC(C2C1C(C3C2(O3)CO)O)OC4C(C(C(C(O4)CO)O)O)O 362.33 unknown https://doi.org/10.1007/S10600-009-9420-0
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
Forsythoside B 23928102 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)COC4C(C(CO4)(CO)O)O)OCCC5=CC(=C(C=C5)O)O)O)O)O)O 756.70 unknown https://doi.org/10.1016/S0031-9422(96)00446-3
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
[(2R,3S,4S,5R,6R)-6-[(2R)-2-(3,4-dihydroxyphenyl)-2-hydroxyethoxy]-4-hydroxy-2-(hydroxymethyl)-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl] (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate 163185483 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OCC(C3=CC(=C(C=C3)O)O)O)CO)OC(=O)C=CC4=CC(=C(C=C4)O)O)O)O)O)O 640.60 unknown https://doi.org/10.1007/S10600-012-0125-4
[6-[2-(3,4-Dihydroxyphenyl)-2-hydroxyethoxy]-4-hydroxy-2-(hydroxymethyl)-5-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-3-yl] 3-(3,4-dihydroxyphenyl)prop-2-enoate 4484593 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OCC(C3=CC(=C(C=C3)O)O)O)CO)OC(=O)C=CC4=CC(=C(C=C4)O)O)O)O)O)O 640.60 unknown https://doi.org/10.1007/S10600-012-0125-4
2-(3,4-Dihydroxyphenyl)ethyl 3-O-(6-Deoxy-alpha-L-mannopyranosyl)-4-O-[(2E)-3-(3,4-dihydroxyphenyl)-2-propenoyl]-beta-D-glucopyranoside 132274946 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)CO)OCCC4=CC(=C(C=C4)O)O)O)O)O)O 624.60 unknown https://doi.org/10.1016/S0031-9422(96)00446-3
Verbascoside 5281800 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)CO)OCCC4=CC(=C(C=C4)O)O)O)O)O)O 624.60 unknown https://doi.org/10.1016/S0031-9422(96)00446-3
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acid esters / Coumaric acid esters
[4,5-Dihydroxy-2-[[2-(hydroxymethyl)-10-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-5-yl]oxy]-6-methyloxan-3-yl] 3-(4-hydroxyphenyl)prop-2-enoate 85446975 Click to see CC1C(C(C(C(O1)OC2C3C=COC(C3C4(C2O4)CO)OC5C(C(C(C(O5)CO)O)O)O)OC(=O)C=CC6=CC=C(C=C6)O)O)O 654.60 unknown https://doi.org/10.1007/S10600-009-9420-0
Saccatoside 15736668 Click to see CC1C(C(C(C(O1)OC2C3C=COC(C3C4(C2O4)CO)OC5C(C(C(C(O5)CO)O)O)O)OC(=O)C=CC6=CC=C(C=C6)O)O)O 654.60 unknown https://doi.org/10.1007/S10600-009-9420-0
Specioside 11948661 Click to see C1=COC(C2C1C(C3C2(O3)CO)OC(=O)C=CC4=CC=C(C=C4)O)OC5C(C(C(C(O5)CO)O)O)O 508.50 unknown https://doi.org/10.1016/S0031-9422(96)00446-3
> 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 https://doi.org/10.1007/S10600-012-0125-4
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/10.1007/S10600-012-0125-4
> 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 https://doi.org/10.1007/S10600-012-0125-4
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/10.1007/S10600-012-0125-4
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Rutin 5280805 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)O 610.50 unknown https://doi.org/10.1007/S10600-012-0125-4
Vitamin P 5293655 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)O 610.50 unknown https://doi.org/10.1007/S10600-012-0125-4
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
4H-1-Benzopyran-4-one, 7-[[6-O-(6-deoxy-alpha-L-mannopyranosyl)-beta-D-glucopyranosyl]oxy]-2,3-dihydro-5-hydroxy-2-(3-hydroxy-4-methoxyphenyl)-, (S)- 3594 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/10.1055/S-0028-1101600
7-(alpha-D-Glucopyranosyloxy)-5-hydroxy-2-(4-hydroxyphenyl)-4H-1-benzopyran-4-one 12304095 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O 432.40 unknown https://doi.org/10.1007/S10600-012-0125-4
Apigenin 7-O-glucoside 5385553 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O 432.40 unknown https://doi.org/10.1007/S10600-012-0125-4
Hesperidin 10621 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/10.1055/S-0028-1101600
Luteolin 7-galactoside 5291488 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown https://doi.org/10.1007/S10600-012-0125-4
Luteolin 7-O-glucoside 5280637 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown https://doi.org/10.1007/S10600-012-0125-4
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavonoid O-glycosides
3-[7-[(2R,3R,4S,5S,6S)-3,4-dihydroxy-6-(hydroxymethyl)-5-methyloxan-2-yl]oxy-3-(4-methoxyphenyl)-4-oxochromen-2-yl]oxy-3-oxopropanoic acid 162879552 Click to see CC1C(OC(C(C1O)O)OC2=CC3=C(C=C2)C(=O)C(=C(O3)OC(=O)CC(=O)O)C4=CC=C(C=C4)OC)CO 530.50 unknown https://doi.org/10.1007/S10600-009-9420-0

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