Verbascum densiflorum - Unknown
Part: Unknown
Author: Public Domain - WikiMedia

Verbascum densiflorum - Unknown
Part: Unknown
Author: Public Domain - WikiMedia

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Details Top

Internal ID UUID643ffac0d4817832552281
Scientific name Verbascum densiflorum
Authority Bertol.
First published in Rar. Lig. [Ital.] Pl. 3: 52 (1810)

Description Top

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No description added yet. Help us by writing one.

Synonyms Top

Scientific name Authority First published in
Verbascum velenovskyi Horak Oesterr. Bot. Z. 50: 208 (1900)
Verbascum thapsiforme Schrad. Monogr. Verbasci 1: 21 (1813)
Verbascum messanense Tineo Fl. Sicul. Syn. 2: 887 (1845)
Verbascum bicolle Schrank Baier. Fl. 1: 465 (1789)
Verbascum macrantherum Halácsy Oesterr. Bot. Z. 42: 373 (1892)
Verbascum cuspidatum Schrad. Monogr. Verbasci 1: 23 (1813)

Common names Top

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Language Common/alternative name
English mullein
English denseflower mullein
English denseflowered mullein
English dense-flowered mullein
Spanish acebustre
ab Амшәҳа
Azerbaijani uca sığırquyruğu
Belarusian Дзіванна скіпетрападобная
Bulgarian гъстоцветен лопен
Catalan denseflower mullein
Catalan faux bouillon blanc
Czech divizna velkokvětá
Welsh pannog ddwysflodeuog
German dichtblütige königskerze
German großblütige königskerze
German faux bouillon blanc
Finnish akantulikukka
French molène à fleurs denses
French molène faux bouillon-blanc
French molène faux bouillon blanc
French molene a fleurs denses
French faux bouillon-blanc
French faux bouillon blanc
Upper Sorbian wulka dźiwizna
Hungarian dúsvirágú ökörfarkkóró
Lithuanian didžiažiedė tūbė
Lithuanian faux bouillon blanc
Macedonian Мопен
Dutch stalkaars
os Арсызагалæг
Polish dziewanna wielkokwiatowa
Romanian lumânărică
Russian Коровяк высокий
Russian Коровяк скипетровидный
Russian Коровяк густоцветковый
Slovak divozel veľkokvetý
Swedish Ölandskungsljus
Swedish faux bouillon blanc
Ukrainian Дивина густоквіткова
Ukrainian Дивина скіпетровидна
Ukrainian дивина густоквіткова
Ukrainian дивина скіпетровидна
Ukrainian дивина великоцвіта
Chinese 毒鱼草

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

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Sow seeds at 20°C, expecting germination within 3 months without further temperature treatment.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Europe
    • Eastern Europe
      • Baltic States
      • Belarus
      • Central European Russia
      • East European Russia
      • Krym
      • South European Russia
      • Ukraine
    • Middle Europe
      • Austria
      • Belgium
      • Czechoslovakia
      • Germany
      • Netherlands
      • Poland
      • Switzerland
    • Northern Europe
      • Denmark
      • Sweden
    • Southeastern Europe
      • Albania
      • Bulgaria
      • Greece
      • Italy
      • Romania
      • Sicilia
      • Turkey-in-Europe
      • Yugoslavia
    • Southwestern Europe
      • France
      • Spain
  • Northern America
    • North-central U.S.A.
      • Iowa
      • Missouri
      • Wisconsin
    • Northeastern U.S.A.
      • Massachusetts
      • Michigan

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000420566
UNII FH9G6709EL
USDA Plants VEDE4
Tropicos 29203784
INPN 128567
Flora of Italy 4750
KEW urn:lsid:ipni.org:names:811003-1
The Plant List kew-2454940
Open Tree Of Life 3883072
Observations.org 7608
NCBI Taxonomy 1534716
NBN Atlas NBNSYS0000004047
Nature Serve 2.132570
IPNI 811003-1
iNaturalist 62339
GBIF 3171939
Freebase /m/0bbwlcs
WisFlora 5335
EPPO VESDE
EOL 484420
USDA GRIN 41145
Wikipedia Verbascum_densiflorum
CMAUP NPO16142

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
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
Characterization of saponins from the leaves and stem bark of Jatropha curcas L. for surface-active properties Rai S, Kafle A, Devkota HP, Bhattarai A Heliyon 28-Apr-2023
PMCID:PMC10176063
doi:10.1016/j.heliyon.2023.e15807
PMID:37187903
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
Understanding old herbal secrets: The renaissance of traditional medicinal plants beyond the twenty classic species? Scherrer MM, Zerbe S, Petelka J, Säumel I Front Pharmacol 24-Mar-2023
PMCID:PMC10079881
doi:10.3389/fphar.2023.1141044
PMID:37033626
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
Operational definition of complementary, alternative, and integrative medicine derived from a systematic search Ng JY, Dhawan T, Dogadova E, Taghi-Zada Z, Vacca A, Wieland LS, Moher D BMC Complement Med Ther 12-Apr-2022
PMCID:PMC9006507
doi:10.1186/s12906-022-03556-7
PMID:35413882
Vegetation characteristics control local sediment and nutrient retention on but not underneath vegetation in floodplain meadows Kretz L, Bondar-Kunze E, Hein T, Richter R, Schulz-Zunkel C, Seele-Dilbat C, van der Plas F, Vieweg M, Wirth C PLoS One 02-Dec-2021
PMCID:PMC8638890
doi:10.1371/journal.pone.0252694
PMID:34855757
Medical Species Used in Russia for the Management of Diabetes and Related Disorders Shikov AN, Narkevich IA, Akamova AV, Nemyatykh OD, Flisyuk EV, Luzhanin VG, Povydysh MN, Mikhailova IV, Pozharitskaya ON Front Pharmacol 20-Jul-2021
PMCID:PMC8330883
doi:10.3389/fphar.2021.697411
PMID:34354589
In Silico Screening of Natural Products Isolated from Mexican Herbal Medicines against COVID-19 Rivero-Segura NA, Gomez-Verjan JC Biomolecules 04-Feb-2021
PMCID:PMC7913859
doi:10.3390/biom11020216
PMID:33557097
The In Vivo Antinociceptive and Antiinflammatory Effects of Verbascum exuberans Hub.-Mor. EYİİŞ E, KAYGISIZ B, KILIÇ FS, AYHANCI A Turk J Pharm Sci 23-Dec-2020
PMCID:PMC7786066
doi:10.4274/tjps.galenos.2019.77992
PMID:33389947
Contribution to the Orophilous Cushion-Like Vegetation of Central-Southern and Insular Greece Musarella CM, Brullo S, del Galdo GG Plants (Basel) 30-Nov-2020
PMCID:PMC7760968
doi:10.3390/plants9121678
PMID:33266088
Traditional Use of Medicinal Plants in South-Eastern Serbia (Pčinja District): Ethnopharmacological Investigation on the Current Status and Comparison With Half a Century Old Data Živković J, Ilić M, Šavikin K, Zdunić G, Ilić A, Stojković D Front Pharmacol 08-Jul-2020
PMCID:PMC7360817
doi:10.3389/fphar.2020.01020
PMID:32733251
The phoma-like dilemma Hou LW, Groenewald JZ, Pfenning LH, Yarden O, Crous PW, Cai L Stud Mycol 21-May-2020
PMCID:PMC7452269
doi:10.1016/j.simyco.2020.05.001
PMID:32904212
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
The composition of the aphid fauna (Insecta, Hemiptera) of the Royal Botanic Gardens, Kew Wieczorek K, Fulcher TK, Chłond D Sci Rep 10-Jul-2019
PMCID:PMC6620339
doi:10.1038/s41598-019-46441-z
PMID:31292495

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 / Anthracenes
(10S)-10-[(9R)-4,5-dihydroxy-2-methyl-10-oxo-9H-anthracen-9-yl]-1,3,8-trihydroxy-6-methyl-10H-anthracen-9-one 44567184 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2C4C5=C(C(=CC(=C5)C)O)C(=O)C6=C4C=C(C=C6O)O)C=CC=C3O 494.50 unknown via CMAUP database
> Benzenoids / Anthracenes / Anthracenecarboxylic acids and derivatives / Anthracenecarboxylic acids
4-hydroxy-9,10-dioxo-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(oxalooxymethyl)oxan-2-yl]oxyanthracene-2-carboxylic acid 11972451 Click to see C1=CC2=C(C(=C1)OC3C(C(C(C(O3)COC(=O)C(=O)O)O)O)O)C(=O)C4=C(C2=O)C=C(C=C4O)C(=O)O 518.40 unknown via CMAUP database
Rhein 10168 Click to see C1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=C(C=C3O)C(=O)O 284.22 unknown via CMAUP database
Rhein-8-glucoside 5320961 Click to see C1=CC2=C(C(=C1)OC3C(C(C(C(O3)CO)O)O)O)C(=O)C4=C(C2=O)C=C(C=C4O)C(=O)O 446.40 unknown via CMAUP database
Sennidin A 92826 Click to see C1=CC2=C(C(=C1)O)C(=O)C3=C(C2C4C5=C(C(=CC=C5)O)C(=O)C6=C4C=C(C=C6O)C(=O)O)C=C(C=C3O)C(=O)O 538.50 unknown via CMAUP database
Sennoside A 73111 Click to see C1=CC2=C(C(=C1)OC3C(C(C(C(O3)CO)O)O)O)C(=O)C4=C(C2C5C6=C(C(=CC=C6)OC7C(C(C(C(O7)CO)O)O)O)C(=O)C8=C5C=C(C=C8O)C(=O)O)C=C(C=C4O)C(=O)O 862.70 unknown via CMAUP database
Sennoside C 46173829 Click to see C1=CC2=C(C(=C1)OC3C(C(C(C(O3)CO)O)O)O)C(=O)C4=C(C2C5C6=C(C(=CC=C6)OC7C(C(C(C(O7)CO)O)O)O)C(=O)C8=C5C=C(C=C8O)C(=O)O)C=C(C=C4O)CO 848.80 unknown via CMAUP database
> Benzenoids / Anthracenes / Anthraquinones
8-[(6-O-beta-D-Glucopyranosyl-beta-D-glucopyranosyl)oxy]-1-hydroxy-3-methoxy-6-methylanthraquinone 5320543 Click to see CC1=CC2=C(C(=C1)OC3C(C(C(C(O3)COC4C(C(C(C(O4)CO)O)O)O)O)O)O)C(=O)C5=C(C2=O)C=C(C=C5O)OC 608.50 unknown via CMAUP database
Aloe emodin 10207 Click to see C1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=C(C=C3O)CO 270.24 unknown via CMAUP database
Aloe-emodin-glucoside 147295 Click to see C1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=C(C=C3O)COC4C(C(C(C(O4)CO)O)O)O 432.40 unknown via CMAUP database
Chrysophanein 6324923 Click to see CC1=CC2=C(C(=C1)OC3C(C(C(C(O3)CO)O)O)O)C(=O)C4=C(C2=O)C=CC=C4O 416.40 unknown via CMAUP database
Chrysophanic acid 10208 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=CC=C3O 254.24 unknown via CMAUP database
Physcione 10639 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=C(C=C3O)OC 284.26 unknown via CMAUP database
Pulmatin 442731 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=CC=C3OC4C(C(C(C(O4)CO)O)O)O 416.40 unknown via CMAUP database
Rheochrysin 168938 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=C(C=C3OC4C(C(C(C(O4)CO)O)O)O)OC 446.40 unknown via CMAUP database
> Benzenoids / Anthracenes / Anthraquinones / Hydroxyanthraquinones
Emodin 3220 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=C(C=C3O)O 270.24 unknown via CMAUP database
Emodin 1-O-beta-D-glucoside 5319333 Click to see CC1=CC2=C(C(=C1)OC3C(C(C(C(O3)CO)O)O)O)C(=O)C4=C(C2=O)C=C(C=C4O)O 432.40 unknown via CMAUP database
Emodin-8-glucoside 99649 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=C(C=C3OC4C(C(C(C(O4)CO)O)O)O)O 432.40 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Gallic acids
Gallic Acid 370 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)O 170.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Galloyl esters
[(2S)-2,3-dihydroxypropyl] 3,4,5-trihydroxybenzoate 51543740 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC(CO)O 244.20 unknown via CMAUP database
6-O-galloyl-beta-D-glucose 5317463 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(C(O2)O)O)O)O 332.26 unknown via CMAUP database
Methyl gallate 7428 Click to see COC(=O)C1=CC(=C(C(=C1)O)O)O 184.15 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
6-Epiharpagide 4678529 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/10.1007/S10600-009-9420-0
Harpagide 93045 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/10.1007/S10600-009-9420-0
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
(2S,3R,4S,5S,6R)-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-(hydroxymethyl)oxane-3,4,5-triol 10441198 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)OC1C(C(C(C(O1)CO)O)O)O)O)O)O 1089.30 unknown https://doi.org/10.1248/CPB.45.2029
2-[4,5-Dihydroxy-6-[5-hydroxy-2-[[2-hydroxy-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-(hydroxymethyl)oxane-3,4,5-triol 74152951 Click to see CC1C(C(C(C(O1)OC2CCC3(C(C2(C)CO)CCC4(C3C=CC56C4(CC(C7(C5CC(CC7)(C)C)CO6)O)C)C)C)OC8C(C(C(C(O8)CO)O)O)O)OC9C(C(C(C(O9)CO)OC1C(C(C(C(O1)CO)O)O)O)O)O)O 1105.30 unknown https://doi.org/10.1248/CPB.45.2029
2-[4,5-Dihydroxy-6-[5-hydroxy-2-[[2-hydroxy-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 76153036 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(CC(C1(C8CC(CC1)(C)C)CO9)O)C)C)C)C)O)CO)O)O)O 1089.30 unknown https://doi.org/10.1248/CPB.45.2029
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-(hydroxymethyl)oxane-3,4,5-triol 85144331 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)OC1C(C(C(C(O1)CO)O)O)O)O)O)O 1089.30 unknown https://doi.org/10.1248/CPB.45.2029
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/10.1248/CPB.45.2029
2-[5-Hydroxy-2-[[2-hydroxy-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 78178010 Click to see CC1C(C(C(C(O1)OC2CCC3(C(C2(C)CO)CCC4(C3C=CC56C4(CC(C7(C5CC(CC7)(C)C)CO6)O)C)C)C)OC8C(C(C(C(O8)CO)O)O)O)OC9C(C(C(C(O9)CO)O)O)O)O 943.10 unknown https://doi.org/10.1248/CPB.45.2029
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/10.1248/CPB.45.2029
Buddlejasaponin I 54582846 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(CC(C1(C8CC(CC1)(C)C)CO9)O)C)C)C)C)O)CO)O)O)O 1089.30 unknown https://doi.org/10.1248/CPB.45.2029
Buddlejasaponin IV 153940 Click to see CC1C(C(C(C(O1)OC2CCC3(C(C2(C)CO)CCC4(C3C=CC56C4(CC(C7(C5CC(CC7)(C)C)CO6)O)C)C)C)OC8C(C(C(C(O8)CO)O)O)O)OC9C(C(C(C(O9)CO)O)O)O)O 943.10 unknown https://doi.org/10.1248/CPB.45.2029
Clinopodiside B 190817 Click to see CC1C(C(C(C(O1)OC2CCC3(C(C2(C)CO)CCC4(C3C=CC56C4(CC(C7(C5CC(CC7)(C)C)CO6)O)C)C)C)OC8C(C(C(C(O8)CO)O)O)O)OC9C(C(C(C(O9)CO)OC1C(C(C(C(O1)CO)O)O)O)O)O)O 1105.30 unknown https://doi.org/10.1248/CPB.45.2029
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/10.1248/CPB.45.2029
Songarosaponin D 101917118 Click to see CC1C(C(C(C(O1)OC2CCC3(C(C2(C)CO)CCC4(C3C=CC56C4(CC(C7(C5CC(CC7)(C)C)CO6)O)C)C)C)OC8C(C(C(C(O8)CO)O)O)O)OC9C(C(C(C(O9)CO)OC1C(C(C(C(O1)CO)O)O)O)O)O)O 1105.30 unknown https://doi.org/10.1248/CPB.45.2029
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids / L-alpha-amino acids
(2S)-5-amino-2-ammonio-5-oxopentanoate 6992086 Click to see C(CC(=O)N)C(C(=O)[O-])[NH3+] 146.14 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
1-[1-hydroxy-3-methyl-8-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxynaphthalen-2-yl]ethanone 5319972 Click to see CC1=CC2=C(C(=CC=C2)OC3C(C(C(C(O3)CO)O)O)O)C(=C1C(=O)C)O 378.40 unknown via CMAUP database
1-[1,6-dihydroxy-3-methyl-8-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxynaphthalen-2-yl]ethanone 100753 Click to see CC1=CC2=CC(=CC(=C2C(=C1C(=O)C)O)OC3C(C(C(C(O3)CO)O)O)O)O 394.40 unknown via CMAUP database
2-methyl-4-oxo-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromene-5-carboxylic acid 5315687 Click to see CC1=CC(=O)C2=C(C=C(C=C2O1)OC3C(C(C(C(O3)CO)O)O)O)C(=O)O 382.30 unknown via CMAUP database
4-[(6-O-Galloyl-beta-D-glucopyranosyl)oxy]-4-deoxygallic acid 11972354 Click to see C1=C(C=C(C(=C1O)OC2C(C(C(C(O2)COC(=O)C3=CC(=C(C(=C3)O)O)O)O)O)O)O)C(=O)O 484.40 unknown via CMAUP database
Ethanone, 1-[8-[[6-O-(carboxycarbonyl)-beta-D-glucopyranosyl]oxy]-1-hydroxy-6-methoxy-3-methyl-2-naphthalenyl]- 5321979 Click to see CC1=CC2=CC(=CC(=C2C(=C1C(=O)C)O)OC3C(C(C(C(O3)COC(=O)C(=O)O)O)O)O)OC 480.40 unknown via CMAUP database
Raspberryketone glucoside 5320521 Click to see CC(=O)CCC1=CC=C(C=C1)OC2C(C(C(C(O2)CO)O)O)O 326.34 unknown via CMAUP database
Torachrysone 8-O-Glucoside 11972479 Click to see CC1=CC2=CC(=CC(=C2C(=C1C(=O)C)O)OC3C(C(C(C(O3)CO)O)O)O)OC 408.40 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Hexoses
[(2R,3R,4S,5S,6R)-2,4,5-trihydroxy-6-(hydroxymethyl)oxan-3-yl] (E)-3-phenylprop-2-enoate 11972309 Click to see C1=CC=C(C=C1)C=CC(=O)OC2C(C(C(OC2O)CO)O)O 310.30 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Chromones
2-[(2S)-2-Hydroxypropyl]-5-methyl-7-hydroxy-4H-1-benzopyran-4-one 45272307 Click to see CC1=CC(=CC2=C1C(=O)C=C(O2)CC(C)O)O 234.25 unknown via CMAUP database
2H-1-Benzopyran-5-acetic acid, 3,4-dihydro-7-hydroxy-2-methyl-4-oxo-, (S)- 5319543 Click to see CC1CC(=O)C2=C(C=C(C=C2O1)O)CC(=O)O 236.22 unknown via CMAUP database
4H-1-Benzopyran-4-one, 5-acetyl-7-hydroxy-2-methyl- 5315891 Click to see CC1=CC(=O)C2=C(C=C(C=C2O1)O)C(=O)C 218.20 unknown via CMAUP database
7-Hydroxy-2-methyl-4-oxo-4H-1-benzopyran-5-acetic acid 14429402 Click to see CC1=CC(=O)C2=C(C=C(C=C2O1)O)CC(=O)O 234.20 unknown via CMAUP database
7-Hydroxy-2-methyl-4-oxo-4H-1-benzopyran-5-carboxylic acid 5315688 Click to see CC1=CC(=O)C2=C(C=C(C=C2O1)O)C(=O)O 220.18 unknown via CMAUP database
Cassiachromone 5319500 Click to see CC1=CC(=O)C2=C(C=C(C=C2O1)O)CC(=O)C 232.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acid esters
[4,5-Dihydroxy-6-[[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]-2-methyloxan-3-yl] 3-(4-methoxyphenyl)prop-2-enoate 74155541 Click to see CC1C(C(C(C(O1)OC2C3C=COC(C3C4(C2O4)CO)OC5C(C(C(C(O5)CO)O)O)O)O)O)OC(=O)C=CC6=CC=C(C=C6)OC 668.60 unknown https://doi.org/10.1007/S10600-009-9420-0
Verbascoside A 15736674 Click to see CC1C(C(C(C(O1)OC2C3C=COC(C3C4(C2O4)CO)OC5C(C(C(C(O5)CO)O)O)O)O)O)OC(=O)C=CC6=CC=C(C=C6)OC 668.60 unknown https://doi.org/10.1007/S10600-009-9420-0
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
3,3'-Digalloylprocyanidin B2 124016 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)OC(=O)C6=CC(=C(C(=C6)O)O)O)O)O)C7=CC(=C(C=C7)O)O)OC(=O)C8=CC(=C(C(=C8)O)O)O 882.70 unknown via CMAUP database
procyanidin B1 3-O-gallate 12795888 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)OC(=O)C6=CC(=C(C(=C6)O)O)O)O)O)C7=CC(=C(C=C7)O)O)O 730.60 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Catechin gallates
(-)-Epicatechin gallate 107905 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O 442.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
(+)-Catechin 5-O-beta-D-glucopyranoside 6324898 Click to see C1C(C(OC2=C1C(=CC(=C2)O)OC3C(C(C(C(O3)CO)O)O)O)C4=CC(=C(C=C4)O)O)O 452.40 unknown via CMAUP database
> 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 via CMAUP database
> Phenylpropanoids and polyketides / Stilbenes
Rhapontigenin 5320954 Click to see COC1=C(C=C(C=C1)C=CC2=CC(=CC(=C2)O)O)O 258.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Stilbenes / Stilbene glycosides
[(2R,3S,4S,5R,6S)-6-[4-[(E)-2-(3,5-dihydroxyphenyl)ethenyl]phenoxy]-3,4,5-trihydroxyoxan-2-yl]methyl 3,4,5-trihydroxybenzoate 5322088 Click to see C1=CC(=CC=C1C=CC2=CC(=CC(=C2)O)O)OC3C(C(C(C(O3)COC(=O)C4=CC(=C(C(=C4)O)O)O)O)O)O 542.50 unknown via CMAUP database
Resveratrol 4'-O-beta-D-(2''-O-galloyl)-glucopyranoside 10325054 Click to see C1=CC(=CC=C1C=CC2=CC(=CC(=C2)O)O)OC3C(C(C(C(O3)CO)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O 542.50 unknown via CMAUP database
Resveratroloside 5322089 Click to see C1=CC(=CC=C1C=CC2=CC(=CC(=C2)O)O)OC3C(C(C(C(O3)CO)O)O)O 390.40 unknown via CMAUP database
Rhapontin 637213 Click to see COC1=C(C=C(C=C1)C=CC2=CC(=CC(=C2)OC3C(C(C(C(O3)CO)O)O)O)O)O 420.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Tannins
1-O,6-O-Digalloyl-2-O-cinnamoyl-beta-D-glucopyranose 6325082 Click to see C1=CC=C(C=C1)C=CC(=O)OC2C(C(C(OC2OC(=O)C3=CC(=C(C(=C3)O)O)O)COC(=O)C4=CC(=C(C(=C4)O)O)O)O)O 614.50 unknown via CMAUP database
1,2,6-Trigalloylglucose 440308 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)O)O 636.50 unknown via CMAUP database
1,6-bis-O-galloyl-beta-D-glucose 440221 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)O)O)O 484.40 unknown via CMAUP database
2-Cinnamoyl-1-galloylglucose 5315898 Click to see C1=CC=C(C=C1)C=CC(=O)OC2C(C(C(OC2OC(=O)C3=CC(=C(C(=C3)O)O)O)CO)O)O 462.40 unknown via CMAUP database
beta-Glucogallin 124021 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OC2C(C(C(C(O2)CO)O)O)O 332.26 unknown via CMAUP database

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