Scientific name	Authority	First published in
Fumaria angustifolia	Gilib.	Fl. Lit. Inch. ii. 113. 1782
Fumaria diffusa	Arn. ex Parl.	Giorn. Bot. Ital. 1(1): 127 (1844)
Fumaria gasparinii	Bab.	Trans. Bot. Soc. Edinburgh 1: 36 (1841)
Fumaria major	V.Ten.	Bull. Acc. Asp. Nat. i. (1842) 24.
Fumaria media	Loisel.	J. Bot. (Paris) 2: 357 (1809)
Fumaria muralis	Gren. & Godr.	Fl. France [Grenier] 1: 67. 1847 [1848 publ. Nov 1847]
Fumaria officinalis var. elegans	Pugsley	J. Bot. 50(Suppl. 1): 52 1912
Fumaria officinarum	Neck.	Delic. Gallo-Belg. 2: 298 (1768)
Fumaria petteri	V.Ten.	Bull. Acc. Asp. Nat. i. (1842) 25.
Fumaria pulchella	Salisb.	Prodr. Stirp. Chap. Allerton : 377 (1796)

Common names Top

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Filter by language:

Language	Common/alternative name
English	drug fumitory
English	common fumitory
Spanish	señorina real
Spanish	palomilla
Spanish	cuello de paloma
Spanish	camisita de la virgen
Spanish	camisitas de jesus
Spanish	camisitas de jesús
Spanish	fumaria oficinal
Spanish	fumaria viciosoi
Spanish	fumaria wirtgenii
Spanish	gitanillas
Spanish	hierba de conejo
Spanish	palomilla comun
Spanish	palomilla común
Spanish	palomilla oficinal
Spanish	panalitos del nino jesus
Spanish	panalitos del nino jesús
Spanish	piececitos
Spanish	sangre de toro
Spanish	senorina real
Afrikaans	duiwekerwel
Arabic	بقلة الملك
Azerbaijani	dərman şahtərəsi
Azerbaijani	aptek şahtərəsi
ba	Тиле кишер
Belarusian	Дымніца лекавая
Bulgarian	лечебен росопас
Catalan	fumdeterra
Catalan	fumària oficinal
Catalan	fumàries oficinals
Czech	zemědým lékařský
Welsh	mwg-y-ddaear cyffredin
Danish	læge-jordrøg
German	gemeiner erdrauch
German	gewöhnliche erdrauch
German	gewöhnlicher erdrauch
German	echter erdrauch
Esperanto	fumario
Esperanto	oficina fumario
Estonian	harilik punand
Persian	شاهتره
Persian	شاه تره
Persian	شاتره
Persian	شاطره
Finnish	peltoemäkki
Finnish	fumeria officinalis
French	fumeterre officinale
Irish	camán searraigh díge
gd	lus deathach-thalmhainn
Galician	herba dona
Manx	booa ghone
Croatian	ljekovita dimnjača
Upper Sorbian	lěkarski kokrik
Hungarian	orvosi füstike
Armenian	Տերուկ դեղագործական
Icelandic	reykjurt
Italian	fumaria officinale
Japanese	カラクサケマン
Japanese	唐草毛鬘
Georgian	შავთარა
Kabyle	tiqqad n yesɣi
Kazakh	Дәрілік Шытыра
Kazakh	Шытыра
Cornish	mog dor
Lithuanian	vaistinė žvirbliarūtė
Macedonian	Обична чадливка
Macedonian	Димарка
Norwegian Bokmål	jordrøyk
Dutch	gewone duivekervel
Dutch	gewone duivenkervel
Norwegian Nynorsk	jordrøyk
os	Фæздæггæрдæг
Polish	dymnica pospolita
Polish	dymnica lekarska
Russian	Дикая рута
Russian	Дымянка аптечная
Russian	Дымянка лекарственная
Samogitian	zoikė rūtā
Slovak	zemedym lekársky
Serbian	Димњача
Swedish	jordrök
Turkish	Şahtare
Turkish	Şahtere otu
Ukrainian	Рутка лікарська
Chinese	烟堇
Chinese	药用烟堇
Chinese	欧烟堇
Chinese	球果紫菫

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!

Name	Authority	First published in
Fumaria officinalis subsp. cilicica	(Hausskn.) Lidén	Opera Bot. 88: 83 (1986)
Fumaria officinalis subsp. wirtgenii	(W.D.J.Koch) Arcang.	Comp. Fl. Ital. : 27 (1882)

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!

No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000693355
UNII	DM87NN227Z
Florida Plant Atlas	1793
Flora of Alabama	2242
Canadensys	7104
USDA Plants	FUOF
Tropicos	24000018
INPN	99108
Flora of Italy	1304
KEW	urn:lsid:ipni.org:names:30017594-2
The Plant List	kew-2815499
Open Tree Of Life	76888
Observations.org	6800
NCBI Taxonomy	200993
NBN Atlas	NBNSYS0000002793
Nature Serve	2.140202
IPNI	673050-1
iNaturalist	53785
GBIF	5334217
Freebase	/m/0dn25m
WisFlora	3653
EPPO	FUMOF
EOL	590512
Elurikkus	4811
Calflora (Californian flora)	3647
USDA GRIN	70905
Wikipedia	Fumaria_officinalis

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 Theranostics: Controlled, Targeted Delivery and Imaging of Herbal Molecules

Setia A, Vallamkonda B, Challa RR, Mehata AK, Badgujar P, Muthu MS

Nanotheranostics

25-Mar-2024

PMCID:	PMC10988210
doi:	10.7150/ntno.94987
PMID:	38577318

From Plant to Chemistry: Sources of Antinociceptive Non-Opioid Active Principles for Medicinal Chemistry and Drug Design

Turnaturi R, Piana S, Spoto S, Costanzo G, Reina L, Pasquinucci L, Parenti C

Molecules

09-Feb-2024

PMCID:	PMC10892999
doi:	10.3390/molecules29040815
PMID:	38398566

Australian Cool-Season Pulse Seed-Borne Virus Research: 1. Alfalfa and Cucumber Mosaic Viruses and Less Important Viruses

Jones RA, Congdon BS

Viruses

18-Jan-2024

PMCID:	PMC10819373
doi:	10.3390/v16010144
PMID:	38257844

Effectiveness and Selectivity of Pre- and Post-Emergence Herbicides for Weed Control in Grain Legumes

Kousta A, Katsis C, Tsekoura A, Chachalis D

Plants (Basel)

11-Jan-2024

PMCID:	PMC10818810
doi:	10.3390/plants13020211
PMID:	38256764

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

Anti-leishmanial effects of Eryngium planum and Ecbilliun elaterum methanolic extract against Leishmania major

Ghaderian E, Esboei BR, Mousavi P, Pourhajibagher M, Homayouni MM, Zeinali M

AMB Express

03-Jan-2024

PMCID:	PMC10764691
doi:	10.1186/s13568-023-01656-2
PMID:	38170375

Corrigendum to “Fumaria officinalis-loaded chitosan nanoparticles dispersed in an alginate hydrogel promote diabetic wounds healing by upregulating VEGF, TGF-β, and b-FGF genes: A preclinical investigation”

Yang X, Mo W, Shi Y, Fang X, Xu Y, He X, Xu Y

Heliyon

23-Nov-2023

PMCID:	PMC10851214
doi:	10.1016/j.heliyon.2023.e22626
PMID:	38332881

From Plant to Chemistry: Sources of Active Opioid Antinociceptive Principles for Medicinal Chemistry and Drug Design

Turnaturi R, Piana S, Spoto S, Costanzo G, Reina L, Pasquinucci L, Parenti C

Molecules

14-Oct-2023

PMCID:	PMC10609244
doi:	10.3390/molecules28207089
PMID:	37894567

Comparative analysis of the complete chloroplast genome of Papaveraceae to identify rearrangements within the Corydalis chloroplast genome

Kim SC, Ha YH, Park BK, Jang JE, Kang ES, Kim YS, Kimspe TH, Kim HJ

PLoS One

21-Sep-2023

PMCID:	PMC10513226
doi:	10.1371/journal.pone.0289625
PMID:	37733832

Asian herbal medicine for atopic dermatitis: a systematic review

Limantara NV, Sadono R, Widhiati S, Danarti R

Dermatol Reports

25-Aug-2023

PMCID:	PMC10993657
doi:	10.4081/dr.2023.9727
PMID:	38585491

Drug-Repurposing Strategy for Dimethyl Fumarate

Giunta S, D’Amico AG, Maugeri G, Bucolo C, Romano GL, Rossi S, Eandi CM, Pricoco E, D’Agata V

Pharmaceuticals (Basel)

07-Jul-2023

PMCID:	PMC10386358
doi:	10.3390/ph16070974
PMID:	37513886

Natural antioxidants that act against Alzheimer’s disease through modulation of the NRF2 pathway: a focus on their molecular mechanisms of action

Sidiropoulou GA, Metaxas A, Kourti M

Front Endocrinol (Lausanne)

03-Jul-2023

PMCID:	PMC10351420
doi:	10.3389/fendo.2023.1217730
PMID:	37465125

Fumaria officinalis-loaded chitosan nanoparticles dispersed in an alginate hydrogel promote diabetic wounds healing by upregulating VEGF, TGF-β, and b-FGF genes: A preclinical investigation

Yang X, Mo W, Shi Y, Fang X, Xu Y, He X, Xu Y

Heliyon

29-Jun-2023

PMCID:	PMC10372204
doi:	10.1016/j.heliyon.2023.e17704
PMID:	37519642

The effect of oral use of concentrated pomegranate juice by mothers on hyperbilirubinemia in neonates under phototherapy: A randomized clinical trial

Rezapour M, Zahedpasha Y, Kamalinejad M, Memariani Z, Alijanpour M, Ahmadpour-Kacho M, Mozaffarpur SA, Shirafkan H

J Res Med Sci

12-Jun-2023

PMCID:	PMC10366972
doi:	10.4103/jrms.jrms_313_22
PMID:	37496646

Dimethyl Fumarate and Intestine: From Main Suspect to Potential Ally against Gut Disorders

Manai F, Zanoletti L, Arfini D, Micco SG, Gjyzeli A, Comincini S, Amadio M

Int J Mol Sci

08-Jun-2023

PMCID:	PMC10298566
doi:	10.3390/ijms24129912
PMID:	37373057

Phytochemical Profile Top

Add a new one!

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
> Alkaloids and derivatives / Aporphines
Corytuberine	160500	Click to see CN1CCC2=CC(=C(C3=C2C1CC4=C3C(=C(C=C4)OC)O)O)OC	327.40	unknown	https://doi.org/10.1002/(SICI)1099-1565(199901/02)10:1<6::AID-PCA431>3.0.CO;2-0
Corytuberine, pentahydrate	347379	Click to see CN1CCC2=CC(=C(C3=C2C1CC4=C3C(=C(C=C4)OC)O)O)OC	327.40	unknown	https://doi.org/10.1002/(SICI)1099-1565(199901/02)10:1<6::AID-PCA431>3.0.CO;2-0
> Alkaloids and derivatives / Phthalide isoquinolines
(-)-alpha-Hydrastine	442247	Click to see CN1CCC2=CC3=C(C=C2C1C4C5=C(C(=C(C=C5)OC)OC)C(=O)O4)OCO3	383.40	unknown	https://doi.org/10.1002/MRC.1417
(-)-Corlumine	157478	Click to see CN1CCC2=CC(=C(C=C2C1C3C4=C(C5=C(C=C4)OCO5)C(=O)O3)OC)OC	383.40	unknown	https://doi.org/10.1002/MRC.1417
(+)-Adlumine	442155	Click to see CN1CCC2=CC(=C(C=C2C1C3C4=C(C5=C(C=C4)OCO5)C(=O)O3)OC)OC	383.40	unknown	https://doi.org/10.1002/MRC.1417
6,7-Dimethoxy-3-(6-methyl-5,6,7,8-tetrahydro[1,3]dioxolo[4,5-g]isoquinolin-5-yl)-2-benzofuran-1(3H)-one	1309	Click to see CN1CCC2=CC3=C(C=C2C1C4C5=C(C(=C(C=C5)OC)OC)C(=O)O4)OCO3	383.40	unknown	https://doi.org/10.1002/MRC.1417
Corlumine	72615	Click to see CN1CCC2=CC(=C(C=C2C1C3C4=C(C5=C(C=C4)OCO5)C(=O)O3)OC)OC	383.40	unknown	https://doi.org/10.1002/MRC.1417
> Alkaloids and derivatives / Protoberberine alkaloids and derivatives
(13aR)-3,10-dimethoxy-6,8,13,13a-tetrahydro-5H-isoquinolino[2,1-b]isoquinoline-2,9-diol	1152279	Click to see COC1=C(C2=C(CC3C4=CC(=C(C=C4CCN3C2)OC)O)C=C1)O	327.40	unknown	https://doi.org/10.1139/V69-178
(S)-N-Methylcanadine	439844	Click to see C[N+]12CCC3=CC4=C(C=C3C1CC5=C(C2)C(=C(C=C5)OC)OC)OCO4	354.40	unknown	https://doi.org/10.1016/S0040-4039(00)85276-4
16,17-Dimethoxy-1-methyl-5,7-dioxa-1-azoniapentacyclo[11.8.0.03,11.04,8.014,19]henicosa-3(11),4(8),9,14,16,18-hexaene	101723814	Click to see C[N+]12CCC3=CC(=C(C=C3C1CC4=C(C2)C5=C(C=C4)OCO5)OC)OC	354.40	unknown	https://doi.org/10.1016/S0031-9422(00)86978-2
Coptisine	72322	Click to see C1C[N+]2=C(C=C3C=CC4=C(C3=C2)OCO4)C5=CC6=C(C=C51)OCO6	320.30	unknown	https://doi.org/10.1002/(SICI)1099-1565(199901/02)10:1<6::AID-PCA431>3.0.CO;2-0
L-sinactine	8016594	Click to see COC1=C(C=C2C3CC4=C(CN3CCC2=C1)C5=C(C=C4)OCO5)OC	339.40	unknown	https://doi.org/10.1002/MRC.1417 https://doi.org/10.1016/S0031-9422(00)86978-2
N-Methylsinactine	163184404	Click to see C[N+]12CCC3=CC(=C(C=C3C1CC4=C(C2)C5=C(C=C4)OCO5)OC)OC	354.40	unknown	https://doi.org/10.1016/S0031-9422(00)86978-2
Scoulerine	22955	Click to see COC1=C(C2=C(CC3C4=CC(=C(C=C4CCN3C2)OC)O)C=C1)O	327.40	unknown	https://doi.org/10.1139/V69-178
Sinactine	5321317	Click to see COC1=C(C=C2C3CC4=C(CN3CCC2=C1)C5=C(C=C4)OCO5)OC	339.40	unknown	https://doi.org/10.1016/S0031-9422(00)86978-2 https://doi.org/10.1002/MRC.1417
> Alkaloids and derivatives / Protopine alkaloids
Cryptopine	72616	Click to see CN1CCC2=CC(=C(C=C2C(=O)CC3=C(C1)C4=C(C=C3)OCO4)OC)OC	369.40	unknown	https://doi.org/10.1002/MRC.1417 https://doi.org/10.1016/S0031-9422(00)86978-2
Protopine	4970	Click to see CN1CCC2=CC3=C(C=C2C(=O)CC4=C(C1)C5=C(C=C4)OCO5)OCO3	353.40	unknown	https://doi.org/10.1002/MRC.1417 https://doi.org/10.1016/S0031-9422(00)86978-2
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
3-Hydroxybenzoic acid	7420	Click to see C1=CC(=CC(=C1)O)C(=O)O	138.12	unknown	https://doi.org/10.1002/(SICI)1099-1565(199901/02)10:1<6::AID-PCA431>3.0.CO;2-0
> Benzenoids / Indanes / Indanones
(7R)-6'-methylspiro[6H-cyclopenta[g][1,3]benzodioxole-7,5'-7,8-dihydro-[1,3]dioxolo[4,5-g]isoquinoline]-8-one	10247361	Click to see CN1CCC2=CC3=C(C=C2C14CC5=C(C4=O)C6=C(C=C5)OCO6)OCO3	351.40	unknown	https://doi.org/10.1139/V69-178 https://doi.org/10.1016/S0031-9422(00)86978-2 https://doi.org/10.1139/V68-476
6'-methylspiro[6H-cyclopenta[g][1,3]benzodioxole-7,5'-7,8-dihydro-[1,3]dioxolo[4,5-g]isoquinoline]-8-one	629545	Click to see CN1CCC2=CC3=C(C=C2C14CC5=C(C4=O)C6=C(C=C5)OCO6)OCO3	351.40	unknown	https://doi.org/10.1139/V69-178 https://doi.org/10.1016/S0031-9422(00)86978-2 https://doi.org/10.1139/V68-476
Fumariline	159888	Click to see CN1CCC2=CC3=C(C=C2C14CC5=C(C4=O)C6=C(C=C5)OCO6)OCO3	351.40	unknown	https://doi.org/10.1016/S0031-9422(00)86978-2 https://doi.org/10.1002/(SICI)1099-1565(199901/02)10:1<6::AID-PCA431>3.0.CO;2-0 https://doi.org/10.1139/V68-476 https://doi.org/10.1139/V69-178
Parfumine	185623	Click to see CN1CCC2=CC(=C(C=C2C13CC4=C(C3=O)C5=C(C=C4)OCO5)O)OC	353.40	unknown	https://doi.org/10.1002/(SICI)1099-1565(199901/02)10:1<6::AID-PCA431>3.0.CO;2-0 https://doi.org/10.1002/MRC.1417
Spiro[7H-indeno[4,5-d]-1,3-dioxole-7,1'(2'H)-isoquinolin]-8(6H)-one, 3',4'-dihydro-7'-hydroxy-6'-methoxy-2'-methyl-	376403	Click to see CN1CCC2=CC(=C(C=C2C13CC4=C(C3=O)C5=C(C=C4)OCO5)O)OC	353.40	unknown	https://doi.org/10.1002/MRC.1417
> Benzenoids / Indenes and isoindenes / Indenoazepines
Bulgaramine	178829	Click to see CN1CCC2=CC(=C(C=C2C3=C1C4=C(C3)C=CC5=C4OCO5)OC)OC	351.40	unknown	https://doi.org/10.1021/NP50036A030
> Organic acids and derivatives / Carboxylic acids and derivatives / Dicarboxylic acids and derivatives
Fumaric Acid	444972	Click to see C(=CC(=O)O)C(=O)O	116.07	unknown	https://doi.org/10.1002/(SICI)1099-1565(199901/02)10:1<6::AID-PCA431>3.0.CO;2-0
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
Chlorogenic Acid	1794427	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	https://doi.org/10.1016/S0031-9422(00)86978-2
> Organoheterocyclic compounds / Benzazepines
(1R,12S)-12,15-dihydroxy-16-methoxy-21-methyl-6,8-dioxa-21-azapentacyclo[10.9.0.02,10.05,9.013,18]henicosa-2(10),3,5(9),13,15,17-hexaen-11-one	162930739	Click to see CN1CCC2=CC(=C(C=C2C3(C1C4=C(C3=O)C5=C(C=C4)OCO5)O)O)OC	369.40	unknown	https://doi.org/10.1139/CJR38B-054 https://doi.org/10.1016/S0031-9422(00)86978-2
Manske alkaloid F 38	632772	Click to see CN1CCC2=CC(=C(C=C2C3(C1C4=C(C3=O)C5=C(C=C4)OCO5)O)O)OC	369.40	unknown	https://doi.org/10.1016/S0031-9422(00)86978-2 https://doi.org/10.1139/V71-503 https://doi.org/10.1139/CJR38B-054
> Organoheterocyclic compounds / Isoquinolines and derivatives
Corydamine	5316094	Click to see CNCCC1=CC2=C(C=C1C3=NC=C4C(=C3)C=CC5=C4OCO5)OCO2	350.40	unknown	https://doi.org/10.1002/MRC.1417
> Organoheterocyclic compounds / Tetrahydroisoquinolines
(1R,8'R)-6,7-dimethoxy-2-methylspiro[3,4-dihydroisoquinoline-1,7'-6,8-dihydrocyclopenta[g][1,3]benzodioxole]-8'-ol	12309931	Click to see CN1CCC2=CC(=C(C=C2C13CC4=C(C3O)C5=C(C=C4)OCO5)OC)OC	369.40	unknown	https://doi.org/10.1139/V69-178 https://doi.org/10.1139/V68-476
(1R,8'S)-6,7-dimethoxy-2-methyl-spiro[3,4-dihydroisoquinoline-1,7'-6,8-dihydrocyclopenta[g][1,3]benzodioxole]-8'-ol	442236	Click to see CN1CCC2=CC(=C(C=C2C13CC4=C(C3O)C5=C(C=C4)OCO5)OC)OC	369.40	unknown	https://doi.org/10.1139/V68-476 https://doi.org/10.1002/(SICI)1099-1565(199901/02)10:1<6::AID-PCA431>3.0.CO;2-0
(1S,8'R)-6-methoxy-2-methyl-2-oxidospiro[3,4-dihydroisoquinolin-2-ium-1,7'-6,8-dihydrocyclopenta[g][1,3]benzodioxole]-7,8'-diol	101630424	Click to see C[N+]1(CCC2=CC(=C(C=C2C13CC4=C(C3O)C5=C(C=C4)OCO5)O)OC)[O-]	371.40	unknown	https://doi.org/10.1016/S0031-9422(00)86978-2
(1S,8'R)-6-methoxy-2-methylspiro[3,4-dihydroisoquinoline-1,7'-6,8-dihydrocyclopenta[g][1,3]benzodioxole]-7,8'-diol	21627986	Click to see CN1CCC2=CC(=C(C=C2C13CC4=C(C3O)C5=C(C=C4)OCO5)O)OC	355.40	unknown	https://doi.org/10.1002/(SICI)1099-1565(199901/02)10:1<6::AID-PCA431>3.0.CO;2-0 https://doi.org/10.1016/S0031-9422(00)97426-0 https://doi.org/10.1139/V68-476 https://doi.org/10.1139/V69-178
(7R,8R)-6'-methylspiro[6,8-dihydrocyclopenta[g][1,3]benzodioxole-7,5'-7,8-dihydro-[1,3]dioxolo[4,5-g]isoquinoline]-8-ol	162919483	Click to see CN1CCC2=CC3=C(C=C2C14CC5=C(C4O)C6=C(C=C5)OCO6)OCO3	353.40	unknown	https://doi.org/10.1016/S0031-9422(00)86978-2
[(1S,8'R)-6,7-dimethoxy-2-methylspiro[3,4-dihydroisoquinoline-1,7'-6,8-dihydrocyclopenta[g][1,3]benzodioxole]-8'-yl] acetate	102181853	Click to see CC(=O)OC1C2=C(CC13C4=CC(=C(C=C4CCN3C)OC)OC)C=CC5=C2OCO5	411.40	unknown	https://doi.org/10.1002/MRC.1417
[(1S,8'R)-7-hydroxy-6-methoxy-2-methylspiro[3,4-dihydroisoquinoline-1,7'-6,8-dihydrocyclopenta[g][1,3]benzodioxole]-8'-yl] acetate	101316764	Click to see CC(=O)OC1C2=C(CC13C4=CC(=C(C=C4CCN3C)OC)O)C=CC5=C2OCO5	397.40	unknown	https://doi.org/10.1002/MRC.1417 https://doi.org/10.1139/V71-022
Dihydroparfumidine	179411	Click to see CN1CCC2=CC(=C(C=C2C13CC4=C(C3O)C5=C(C=C4)OCO5)OC)OC	369.40	unknown	https://doi.org/10.1016/S0031-9422(00)86978-2
Fumaricine	609998	Click to see CN1CCC2=CC(=C(C=C2C13CC4=C(C3O)C5=C(C=C4)OCO5)OC)OC	369.40	unknown	https://doi.org/10.1139/V69-178 https://doi.org/10.1139/V68-476
Fumariline, dihydro-	605542	Click to see CN1CCC2=CC3=C(C=C2C14CC5=C(C4O)C6=C(C=C5)OCO6)OCO3	353.40	unknown	https://doi.org/10.1016/S0031-9422(00)86978-2
Fumaritine	12309932	Click to see CN1CCC2=CC(=C(C=C2C13CC4=C(C3O)C5=C(C=C4)OCO5)O)OC	355.40	unknown	https://doi.org/10.1139/V69-178
Fumarophycin	631930	Click to see CC(=O)OC1C2=C(CC13C4=CC(=C(C=C4CCN3C)OC)O)C=CC5=C2OCO5	397.40	unknown	https://doi.org/10.1002/MRC.1417
O-Methylfumarophycine	182268	Click to see CC(=O)OC1C2=C(CC13C4=CC(=C(C=C4CCN3C)OC)OC)C=CC5=C2OCO5	411.40	unknown	https://doi.org/10.1002/MRC.1417
Spiro[7H-indeno[4,5-d]-1,3-dioxole-7,1'(2'H)-isoquinoline]-7',8-diol, 3',4',6,8-tetrahydro-6'-methoxy-2'-methyl-, (7S-trans)-	366269	Click to see CN1CCC2=CC(=C(C=C2C13CC4=C(C3O)C5=C(C=C4)OCO5)O)OC	355.40	unknown	https://doi.org/10.1139/V69-178
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
Caffeic Acid	689043	Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O	180.16	unknown	https://doi.org/10.1016/S0031-9422(00)86978-2
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	51402807	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	https://doi.org/10.1016/S0031-9422(00)86978-2
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/10.1016/S0031-9422(00)86978-2

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Fumaria officinalis

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