Scrophularia scorodonia is a type of flowering plant that belongs to the figwort family. It is found in various regions including western and southwestern Europe, Northwest Morocco, and the Azores and Madeira islands.

Synonyms Top

Scientific name	Authority	First published in
Scrophularia cordata	Mill.	Gard. Dict. ed. 8 : n.º 4 (1768)
Scrophularia biserrata	Willd.	Enum. Pl. : 644 (1809)
Scrophularia papillaris	Boiss. & Reut.	Pugill. Pl. Afr. Bor. Hispan. : 90 (1852)
Scrophularia cantabrica	Sennen & Elias	Bol. Soc. Ibér. Ci. Nat. 29: 78 (1930)
Scrophularia crenata	Raf.	Autik. Bot. : 162 (1840)
Scrophularia betonicifolia	L.	Mant. Pl. : 87 (1767)
Scrophularia iberica	Sennen & Elias	Bol. Soc. Ibér. Ci. Nat. 29: 78 (1930)
Scrophularia tinantii	Dumort.	Bull. Soc. Roy. Bot. Belgique 14: 110 (1875)
Scrophularia scorodonifolia	Gray	Nat. Arr. Brit. Pl. 2: 320 (1821 publ. 1822)

Common names Top

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Language	Common/alternative name
Welsh	gwrnerth dail gwenyn
Swedish	atlantflenört

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

Africa click to expand
- Macaronesia
  - Azores
  - Canary Islands
  - Madeira
- Northern Africa
  - Morocco

Europe click to expand
- Northern Europe
  - Great Britain
- Southwestern Europe
  - France
  - Portugal
  - Spain

Links to other databases Top

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Database	ID/link to page
World Flora Online	wfo-0000496326
Tropicos	29200394
INPN	122046
KEW	urn:lsid:ipni.org:names:809503-1
The Plant List	kew-2587397
Open Tree Of Life	785888
Observations.org	143101
NCBI Taxonomy	1053394
NBN Atlas	NBNSYS0000004081
IPNI	809503-1
iNaturalist	129399
iNaturalist	129400
GBIF	7332709
EPPO	SCUSC
EOL	5670394
Elurikkus	599605
Wikipedia	Scrophularia_scorodonia

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

Herbal medicine use in Republic of Korea to alleviate side effects of COVID-19 vaccines: A cross-sectional study

Yoon HC

J Integr Med

08-Jun-2023

PMCID:	PMC10249366
doi:	10.1016/j.joim.2023.06.002
PMID:	37349213

An overview on medicinal plants used for combating coronavirus: Current potentials and challenges

Abou Baker DH, Hassan EM, El Gengaihi S

J Agric Food Res

20-May-2023

PMCID:	PMC10198795
doi:	10.1016/j.jafr.2023.100632
PMID:	37251276

Phytochemicals as Invaluable Sources of Potent Antimicrobial Agents to Combat Antibiotic Resistance

Jadimurthy R, Jagadish S, Nayak SC, Kumar S, Mohan CD, Rangappa KS

Life (Basel)

04-Apr-2023

PMCID:	PMC10145550
doi:	10.3390/life13040948
PMID:	37109477

Ethnopharmacological Potential of Phytochemicals and Phytogenic Products against Human RNA Viral Diseases as Preventive Therapeutics

Paul A, Chakraborty N, Sarkar A, Acharya K, Ranjan A, Chauhan A, Srivastava S, Singh AK, Rai AK, Mubeen I, Prasad R

Biomed Res Int

20-Feb-2023

PMCID:	PMC9970710
doi:	10.1155/2023/1977602
PMID:	36860811

Saponins: Research Progress and Their Potential Role in the Post-COVID-19 Pandemic Era

Mieres-Castro D, Mora-Poblete F

Pharmaceutics

20-Jan-2023

PMCID:	PMC9964560
doi:	10.3390/pharmaceutics15020348
PMID:	36839670

Antiviral Activity of Medicinal Plants against Human Coronavirus: a systematic scoping review of in vitro and in vivo experimentations

Parva N, Omid S, Sadegh AJ, Mohammad HA, Mehrdad K

J Tradit Chin Med

20-May-2022

PMCID:	PMC9924666
doi:	10.19852/j.cnki.jtcm.2022.03.002
PMID:	35610002

Phytomedicines explored under in vitro and in silico studies against coronavirus: An opportunity to develop traditional medicines

Gandhi Y, Mishra SK, Rawat H, Grewal J, Kumar R, Shakya SK, Jain VK, Babu G, Singh A, Singh R, Acharya R, Kumar V

S Afr J Bot

02-May-2022

PMCID:	PMC9057940
doi:	10.1016/j.sajb.2022.04.053
PMID:	35530267

A critical analysis of SARS-CoV-2 (COVID-19) complexities, emerging variants, and therapeutic interventions and vaccination strategies

Li CX, Noreen S, Zhang LX, Saeed M, Wu PF, Ijaz M, Dai DF, Maqbool I, Madni A, Akram F, Naveed M, Li JH

Biomed Pharmacother

15-Dec-2021

PMCID:	PMC8673752
doi:	10.1016/j.biopha.2021.112550
PMID:	34959116

Natural Bioactive Molecules: An Alternative Approach to the Treatment and Control of COVID-19

Islam F, Bibi S, Meem AF, Islam MM, Rahaman MS, Bepary S, Rahman MM, Rahman MM, Elzaki A, Kajoak S, Osman H, ElSamani M, Khandaker MU, Idris AM, Emran TB

Int J Mol Sci

23-Nov-2021

PMCID:	PMC8658031
doi:	10.3390/ijms222312638
PMID:	34884440

Brief survey on phytochemicals to prevent COVID-19

Pal S, Chowdhury T, Paria K, Manna S, Parveen S, Singh M, Sharma P, Islam SS, Abu Imam Saadi SM, Mandal SM

06-Nov-2021

PMCID:	PMC8573676
doi:	10.1016/j.jics.2021.100244

Natural Immunomodulators Treat the Cytokine Storm in SARS-CoV-2

Abbas HS, Abd-elhakeem MM, Abd El Galil RM, Reyad OA, Mohamed HA, Ismail SE, Nabil MA

Adv Pharm Bull

02-Oct-2021

PMCID:	PMC9871270
doi:	10.34172/apb.2023.006
PMID:	36721816

Potential natural candidates in the treatment of coronavirus infections

Alsenani F

Saudi J Biol Sci

10-Jun-2021

PMCID:	PMC8190277
doi:	10.1016/j.sjbs.2021.06.008
PMID:	34127903

A Multidisciplinary Approach to Coronavirus Disease (COVID-19)

Gediz Erturk A, Sahin A, Bati Ay E, Pelit E, Bagdatli E, Kulu I, Gul M, Mesci S, Eryilmaz S, Oba Ilter S, Yildirim T

Molecules

09-Jun-2021

PMCID:	PMC8228528
doi:	10.3390/molecules26123526
PMID:	34207756

Phytoconstituents from ten natural herbs as potent inhibitors of main protease enzyme of SARS-COV-2: In silico study

Kumar N, Singh A, Gulati HK, Bhagat K, Kaur K, Kaur J, Dudhal S, Duggal A, Gulati P, Singh H, Singh JV, Bedi PM

06-Jun-2021

PMCID:	PMC8180089
doi:	10.1016/j.phyplu.2021.100083
PMID:	35403086

Potential of Malawi's medicinal plants in Covid-19 disease management: A review

Chikowe I, Mtewa AG, Tembo D, Smith D, Ibrahim E, Mwamatope B, Nkhungulu J, Kumpalume P, Maroyi A

Malawi Med J

01-Jun-2021

PMCID:	PMC8560350
doi:	10.4314/mmj.v33i2.4
PMID:	34777704

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.

Name	PubChem ID	Canonical SMILES	MW	Found in	Proof
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
(1S,4aR,5R,7S,7aR)-7-methyl-1-[(2R,3S,4R,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,5,6,7a-tetrahydrocyclopenta[c]pyran-4a,5,7-triol	162989826	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/10.1515/ZNC-2001-7-807
(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/10.1515/ZNC-2000-5-606
(2S,3R,4S,5R,6R)-2-[[(1S,4aS,5R,7aS)-5-hydroxy-7-(hydroxymethyl)-1,4a,5,7a-tetrahydrocyclopenta[c]pyran-1-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol	12358434	Click to see C1=COC(C2C1C(C=C2CO)O)OC3C(C(C(C(O3)CO)O)O)O	346.33	unknown	https://doi.org/10.1515/ZNC-2001-7-807
(2S,3R,4S,5R,6R)-2-[[(1S,4aS,5R)-5-hydroxy-7-(hydroxymethyl)-1,4a,5,7a-tetrahydrocyclopenta[c]pyran-1-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol	163194563	Click to see C1=COC(C2C1C(C=C2CO)O)OC3C(C(C(C(O3)CO)O)O)O	346.33	unknown	https://doi.org/10.1515/ZNC-2001-7-807
(2S,3R,4S,5S,6R)-2-[[(4aR,7aR)-5-hydroxy-7-(hydroxymethyl)-1,4a,5,7a-tetrahydrocyclopenta[c]pyran-1-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol	12358432	Click to see C1=COC(C2C1C(C=C2CO)O)OC3C(C(C(C(O3)CO)O)O)O	346.33	unknown	https://doi.org/10.1055/S-2006-958016
[(1S,4aR,5R,7S,7aS)-4a,5-dihydroxy-7-methyl-1-[(2S,3S,4S,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,5,6,7a-tetrahydrocyclopenta[c]pyran-7-yl] (E)-3-phenylprop-2-enoate	154496720	Click to see CC1(CC(C2(C1C(OC=C2)OC3C(C(C(C(O3)CO)O)O)O)O)O)OC(=O)C=CC4=CC=CC=C4	494.50	unknown	https://doi.org/10.1515/ZNC-2001-7-807
[(1S,4aS,5R,7S,7aS)-4a,5-dihydroxy-7-methyl-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,5,6,7a-tetrahydrocyclopenta[c]pyran-7-yl] acetate	5459146	Click to see CC(=O)OC1(CC(C2(C1C(OC=C2)OC3C(C(C(C(O3)CO)O)O)O)O)O)C	406.40	unknown	https://doi.org/10.1055/S-2006-958016 https://doi.org/10.1016/0031-9422(95)00305-Q
[(4aS,7S,7aR)-4a,5-dihydroxy-7-methyl-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,5,6,7a-tetrahydrocyclopenta[c]pyran-7-yl] acetate	137703299	Click to see CC(=O)OC1(CC(C2(C1C(OC=C2)OC3C(C(C(C(O3)CO)O)O)O)O)O)C	406.40	unknown	https://doi.org/10.1055/S-2006-958016 https://doi.org/10.1515/ZNC-2000-5-606
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/10.1515/ZNC-2000-5-606 https://doi.org/10.1515/ZNC-2001-7-807 https://doi.org/10.1515/ZNC-2000-11-1231
Bartsioside	14081907	Click to see C1C=C(C2C1C=COC2OC3C(C(C(C(O3)CO)O)O)O)CO	330.33	unknown	https://doi.org/10.1055/S-2006-958016 https://doi.org/10.1515/ZNC-2000-5-606
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/10.1515/ZNC-2000-5-606 https://doi.org/10.1515/ZNC-2000-11-1231 https://doi.org/10.1515/ZNC-2001-7-807
Harpagoside	5281542	Click to see CC1(CC(C2(C1C(OC=C2)OC3C(C(C(C(O3)CO)O)O)O)O)O)OC(=O)C=CC4=CC=CC=C4	494.50	unknown	https://doi.org/10.1055/S-2006-957382 https://doi.org/10.1055/S-2006-958016 https://doi.org/10.1080/13880200590928799 https://doi.org/10.1515/ZNC-2001-7-807 https://doi.org/10.1515/ZNC-2000-5-606 https://doi.org/10.1515/ZNC-2000-11-1231
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
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/10.1016/0031-9422(95)00305-Q
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/10.1016/0031-9422(95)00305-Q
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(2S,3R,4S,5S,6R)-2-[[(1S,2S,4S,5S,6S,10S)-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	162928409	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/10.1515/ZNC-2001-7-807
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/10.1515/ZNC-2001-7-807
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
[(2R,3R,4R,5R,6R)-6-[2-(3,4-dihydroxyphenyl)ethoxy]-5-hydroxy-4-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-2-[[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxan-3-yl] (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate	21603980	Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)OC)COC4C(C(C(CO4)O)O)O)OCCC5=CC(=C(C=C5)O)O)O)O)O)O	770.70	unknown	https://doi.org/10.1002/1097-458X(200008)38:8<688::AID-MRC714>3.0.CO;2-5 https://doi.org/10.1080/13880200590928799
[(2R,3R,4R,5R,6R)-6-[2-(3,4-dihydroxyphenyl)ethoxy]-5-hydroxy-4-[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-2-[[(2R,3S,4R,5S)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxan-3-yl] (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate	163068795	Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)COC4C(C(C(CO4)O)O)O)OCCC5=CC(=C(C=C5)O)O)O)O)O)O	756.70	unknown	https://doi.org/10.1002/1097-458X(200008)38:8<688::AID-MRC714>3.0.CO;2-5
[(2R,3R,4R,5R,6R)-6-[2-(3,4-dihydroxyphenyl)ethoxy]-5-hydroxy-4-[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-2-[[(2R,3S,4R,5S)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxan-3-yl] (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate	163073029	Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)OC)COC4C(C(C(CO4)O)O)O)OCCC5=CC(=C(C=C5)O)O)O)O)O)O	770.70	unknown	https://doi.org/10.1002/1097-458X(200008)38:8<688::AID-MRC714>3.0.CO;2-5
[6-[2-(3,4-Dihydroxyphenyl)ethoxy]-5-hydroxy-4-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy-2-[(3,4,5-trihydroxyoxan-2-yl)oxymethyl]oxan-3-yl] 3-(3,4-dihydroxyphenyl)prop-2-enoate	73799192	Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)COC4C(C(C(CO4)O)O)O)OCCC5=CC(=C(C=C5)O)O)O)O)O)O	756.70	unknown	https://doi.org/10.1002/1097-458X(200008)38:8<688::AID-MRC714>3.0.CO;2-5
[6-[2-(3,4-Dihydroxyphenyl)ethoxy]-5-hydroxy-4-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy-2-[(3,4,5-trihydroxyoxan-2-yl)oxymethyl]oxan-3-yl] 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate	73799193	Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)OC)COC4C(C(C(CO4)O)O)O)OCCC5=CC(=C(C=C5)O)O)O)O)O)O	770.70	unknown	https://doi.org/10.1002/1097-458X(200008)38:8<688::AID-MRC714>3.0.CO;2-5
Angoroside A	21603979	Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)COC4C(C(C(CO4)O)O)O)OCCC5=CC(=C(C=C5)O)O)O)O)O)O	756.70	unknown	https://doi.org/10.1002/1097-458X(200008)38:8<688::AID-MRC714>3.0.CO;2-5 https://doi.org/10.1080/13880200590928799
Angoroside C	23757181	Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)OC)COC4C(C(C(CO4)O)O)O)OCCC5=CC(=C(C=C5)OC)O)O)O)O)O	784.80	unknown	https://doi.org/10.1080/13880200590928799 https://doi.org/10.1515/ZNC-2000-5-606
Angoroside-C	6444153	Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)OC)COC4C(C(C(CO4)O)O)O)OCCC5=CC(=C(C=C5)OC)O)O)O)O)O	784.80	unknown	https://doi.org/10.1515/ZNC-2000-5-606 https://doi.org/10.1080/13880200590928799
Isoangoroside C	71433809	Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)OC)COC4C(C(C(CO4)O)O)O)OCCC5=CC(=C(C=C5)OC)O)O)O)O)O	784.80	unknown	https://doi.org/10.1515/ZNC-2000-5-606
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acid esters
[(2S,3R,4R,5S,6S)-4-acetyloxy-5-hydroxy-2-[[(1R,2S,4S,5S,6S,10S)-2-(hydroxymethyl)-10-[(2S,3R,4S,5S,6R)-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] (E)-3-phenylprop-2-enoate	163189774	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=CC=C6)OC(=O)C)O	680.60	unknown	https://doi.org/10.1016/0031-9422(95)00305-Q
[(2S,3R,4R,5S,6S)-4-acetyloxy-5-hydroxy-2-[[(1S,2S,4S,5S,6S,10S)-2-(hydroxymethyl)-10-[(2S,3R,4S,5S,6R)-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] (E)-3-phenylprop-2-enoate	162959832	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=CC=C6)OC(=O)C)O	680.60	unknown	https://doi.org/10.1016/0031-9422(95)00305-Q
[(3R,4R,5S,6S)-4-acetyloxy-5-hydroxy-2-[[(1S,2S,4S,5S,6S,10S)-2-(hydroxymethyl)-10-[(2S,3R,4S,5S,6R)-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] (E)-3-phenylprop-2-enoate	163195210	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=CC=C6)OC(=O)C)O	680.60	unknown	https://doi.org/10.1016/0031-9422(95)00305-Q
[4-Acetyloxy-5-hydroxy-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-phenylprop-2-enoate	74105560	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=CC=C6)OC(=O)C)O	680.60	unknown	https://doi.org/10.1016/0031-9422(95)00305-Q
Scrorodioside	23757227	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=CC=C6)OC(=O)C)O	680.60	unknown	https://doi.org/10.1055/S-2006-957382 https://doi.org/10.1080/13880200590928799 https://doi.org/10.1016/0031-9422(95)00305-Q
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
[(2R,3R,4R,5R,6R)-6-[2-(3,4-dihydroxyphenyl)ethoxy]-5-hydroxy-2-(hydroxymethyl)-4-[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl] (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate	162969693	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/10.1002/1097-458X(200008)38:8<688::AID-MRC714>3.0.CO;2-5
[(2R,3R,4S,5R,6R)-6-[2-(3,4-dihydroxyphenyl)ethoxy]-3,5-dihydroxy-4-[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]methyl (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate	163013170	Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2O)OCCC3=CC(=C(C=C3)O)O)COC(=O)C=CC4=CC(=C(C=C4)O)O)O)O)O)O	624.60	unknown	https://doi.org/10.1002/1097-458X(200008)38:8<688::AID-MRC714>3.0.CO;2-5
[6-[2-(3,4-Dihydroxyphenyl)ethoxy]-3,5-dihydroxy-4-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]methyl 3-(3,4-dihydroxyphenyl)prop-2-enoate	73323377	Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2O)OCCC3=CC(=C(C=C3)O)O)COC(=O)C=CC4=CC(=C(C=C4)O)O)O)O)O)O	624.60	unknown	https://doi.org/10.1080/13880200590928799 https://doi.org/10.1002/1097-458X(200008)38:8<688::AID-MRC714>3.0.CO;2-5
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/10.1002/1097-458X(200008)38:8<688::AID-MRC714>3.0.CO;2-5 https://doi.org/10.1080/13880200590928799 https://doi.org/10.1055/S-2006-957382
Acteoside;Kusaginin;TJC160	354009	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/10.1002/1097-458X(200008)38:8<688::AID-MRC714>3.0.CO;2-5
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/10.1055/S-2006-957382 https://doi.org/10.1080/13880200590928799 https://doi.org/10.1002/1097-458X(200008)38:8<688::AID-MRC714>3.0.CO;2-5

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Scrophularia scorodonia

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