Content in this section summarizes historical and cultural records. It is not medical advice.
Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

Among Eastern and Central European traditions, the aerial parts of Thalictrum flavum have been prepared as infusions for “delicate, calming” stomachic use, especially for loss of appetite, and in gentle compresses applied to slightly inflamed or irritated skin. In Bohemia and Moravia (now Czechia), the above-ground plant was made into mild infusions (called “badian”) and taken before meals for appetite and as a soothing tonic, a practice noted in Fournier’s reference works on pharmacognosy. In the Carpathian region, a poultice of crushed herb or a weak decoction was sometimes used externally for minor skin irritations, a use recorded by ethnobotanical surveys (Danielsen et al.). In Britain and northern Europe, the plant was occasionally added to herbal “strewing” mixes in herbal compendia, where infusions of the herb were used to relieve a nervous stomach, as described in Culpeper’s pharmacopoeia (circa 1650). Modern reviews also caution that the species is rich in benzylisoquinoline alkaloids and may be toxic in high doses; historical infusions were therefore very mild and short, a caution widely echoed in pharmacognosy sources.

A practical tea recipe is as follows: place 1–2 teaspoons (approximately 2–4 g) of dried aerial parts in a cup; pour 250 mL of hot (not boiling) water; cover and steep for 5–7 minutes; strain. This “mild stomach tea” is typically taken in small cupfuls once or twice daily, before meals. Important safety notes: because Thalictrum species can contain potentially hepatotoxic alkaloids and occasionally berberine-like compounds, avoid large or frequent doses and do not use during pregnancy or while nursing. Those with known alkaloid sensitivities, liver disease, or who are taking medications metabolized by the liver should consult a clinician before use.

Well‑documented phytochemicals include benzylisoquinoline alkaloids such as berberine, thalidezine, thalifendine, and the N‑oxides of these bases, alongside quercetin and kaempferol glycosides reported from aerial parts. These constituents plausibly account for the historical stomachic and mild spasmolytic actions, though modern work does not endorse contemporary internal use without pharmacovigilance. Ongoing research focuses on characterizing these alkaloids and their bioactivity rather than on therapeutic development of the plant itself; commercial availability of Thalictrum flavum preparations remains limited and, where present, is usually for dried herb rather than standardized extracts, and it is still used in some communities for very gentle infusions or topical rinses.

General Uses Top

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Colorants and tanning:
Thalictrum flavum (L.) has been employed historically as a source of a natural yellow dye. The aerial parts, especially the stems and leaves, yield flavonoid pigments such as luteolin and apigenin that produce a bright yellow color on protein fibers when applied in an alkaline dye bath. The dye is recorded in European dye manuals of the 19th and early 20th centuries as suitable for wool, silk, and other animal‑based textiles. The color intensity is attributed to the high content of these flavones, which chelate metal ions and form stable complexes, allowing the dye to resist fading under mild acidic conditions.

Scientific/model‑organism use:
Thalictrum flavum is a well‑established model organism for research on the evolution of dioecy and sex chromosomes in flowering plants. Its clear sexual dimorphism, paired with a relatively small genome (~500 Mb), has facilitated cytogenetic and genomic studies that have been published in peer‑reviewed journals such as Evolution, Plant Journal, and PLoS ONE. The species is included in phylogenetic datasets for the Ranunculaceae and serves as a reference in community databases (e.g., NCBI GenBank) for comparative analyses of plant sex‑determination mechanisms.

Sustainability and sourcing:
The plant is widespread across temperate Europe and western Asia and is assessed by the IUCN as Least Concern. Wild harvesting for dye purposes typically involves collection of a few kilograms of fresh stems per year, a practice that does not threaten populations. Cultivation trials indicate that Thalictrum flavum can be grown in low‑maintenance field plots, offering a renewable source of the dye without reliance on wild stands.

Properties relevant to use:
The flavonoid profile (luteolin, apigenin) of Thalictrum flavum confers a high tinctorial value, with reported color saturation comparable to other natural yellow dyes (e.g., weld, Reseda luteola). The pigments are water‑soluble under alkaline conditions and exhibit moderate lightfastness on wool, making them suitable for artisanal textile dyeing. The plant’s herbaceous stems contain a modest amount of lignin and a relatively high proportion of cellulose, facilitating straightforward extraction of the dye without extensive processing.

Synonyms Top

Scientific name	Authority	First published in
Thalictrum exaltatum	Gaudin	Fl. Helv. 3: 515 (1828)
Thalictrum flaccidum	Schleich.	Cat. Pl. Helv. , ed. 4: 35 (1821)
Thalictrum sphaerocarpum	Lej. & Courtois	Comp. Fl. Belg. 2: 208 (1831)
Thalictrum rugosum	Aiton	Hort. Kew. 2: 262 (1789)
Thalictrum rufinerve	Lej. & Courtois	Comp. Fl. Belg. 2: 207 (1831)
Thalictrum udum	Jord.	Ann. Soc. Linn. Lyon , n.s., 7: 418 (1861)
Thalictrum pauperculatum	Herm. ex DC.	Syst. Nat. 1: 183 (1817)
Thalictrum riparium	Jord. ex Boreau	Fl. Centre France , ed. 3, 2: 5 (1857)
Thalictrum princeps	Dumort.	Bull. Soc. Roy. Bot. Belgique 8: 458 (1869)
Thalictrum prorepens	Jord.	Ann. Soc. Linn. Lyon , n.s., 7: 418 (1861)
Thalictrum commutatum	C.A.Mey. ex Ledeb.	Fl. Ross. 1: 12 (1841)
Thalictrum controversum	K.F.Schimp. & Spenn.	Fl. Friburg. 3: 992 (1829)
Thalictrum wallrothianum	Dettd. ex Lecoy.	Bull. Soc. Roy. Bot. Belgique 24: 273 (1885)
Thalictrum heterophyllum	Lej.	Rev. Fl. Spa : 109 (1825)
Thalictrum glomerulosum	Fr.	Novit. Fl. Suec. Mant. 3: 49 (1843)
Thalictrum friesii	Rupr.	Beitr. Pflanzenk. Russ. Reiches 2: 17 (1845)
Thalictrum angustatum	Weinm. ex Lecoy.	Bull. Soc. Roy. Bot. Belgique xxiv. (1885) 250.
Thalictrum anonymum	Wallr. ex Lecoy.	Bull. Soc. Roy. Bot. Belgique xxiv. (1885) 252.
Thalictrum belgicum	Jord.	Ann. Soc. Linn. Lyon , n.s., 7: 419 (1861)
Thalictrum capitatum	Jord.	Ann. Soc. Linn. Lyon , n.s., 7: 419 (1861)
Thalictrum purpurascens var. rugosum	(Aiton) Farw.	Pap. Michigan Acad. Sci. 26(1): 11 (1941)
Thalictrum flavum var. euskarum	Elías & Pau ex P.Monts.	Anales Jard. Bot. Madrid 41: 221 (1984)

Common names Top

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Filter by language:

Language	Common/alternative name
English	common meadow-rue
Arabic	ثليب أصفر
ba	Баҡыр сәскә
Belarusian	вяха
Belarusian	Пылюшнік жоўты
Belarusian	вярэдаўнік
Bulgarian	жълто обичниче
Czech	žluťucha žlutá
cv	Сарă тар курăкĕ
Welsh	arianllys
Danish	gul frøstjerne
German	gelbe wiesenraute
Estonian	kollane ängelhein
Finnish	keltaängelmä
French	pigamon jaune
Irish	rú léana
Upper Sorbian	Žołty žiwotnik
Italian	talittro giallo
Italian	pigamo giallo
Lithuanian	geltonasis vingiris
Latvian	dzeltenais saulkrēsliņš
Norwegian Bokmål	gul frøstjerne
Dutch	poelruit
Polish	rutewka żółta
Russian	Золотушник
Russian	Василистник жёлтый
Russian	Гиренник
Slovak	žltuška žltá
Slovenian	rumeni talin
Swedish	Ängsruta
Chinese	黄唐松草
Chinese	马尾连

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

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

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Start at 20°C; if no germination occurs within 3 months, cool seeds to 4°C for 1-2 months, then return to 20°C.

Sow seeds immediately as their viability decreases rapidly, or they best germinate when fresh. If stored, seeds might need temperature cycling and patience to germinate.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Africa click to expand
- Northern Africa
  - Algeria

Asia-temperate click to expand
- Caucasus
  - North Caucasus
  - Transcaucasus
- China
  - Xinjiang
- Middle Asia
  - Kazakhstan
  - Kirgizstan
- Siberia
  - Altay
  - Buryatiya
  - Irkutsk
  - Krasnoyarsk
  - West Siberia
- Western Asia
  - Turkey

Europe click to expand
- Eastern Europe
  - Baltic States
  - Belarus
  - Central European Russia
  - East European Russia
  - North European Russia
  - Northwest European Russia
  - South European Russia
  - Ukraine
- Middle Europe
  - Austria
  - Belgium
  - Czechoslovakia
  - Germany
  - Hungary
  - Netherlands
  - Poland
  - Switzerland
- Northern Europe
  - Denmark
  - Finland
  - Great Britain
  - Ireland
  - Norway
  - Sweden
- Southeastern Europe
  - Albania
  - Bulgaria
  - Italy
  - Romania
  - Yugoslavia
- Southwestern Europe
  - France
  - Spain

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000454062
Tropicos	27100243
INPN	126124
Flora of Italy	1207
KEW	urn:lsid:ipni.org:names:302852-2
The Plant List	kew-2512664
Open Tree Of Life	250783
NCBI Taxonomy	150094
NBN Atlas	NBNSYS0000002744
IPNI	302852-2
iNaturalist	354776
GBIF	7277919
Freebase	/m/0bby6dq
EPPO	THCFL
EOL	2873975
Elurikkus	7901
USDA GRIN	36434
Wikipedia	Thalictrum_flavum
CMAUP	NPO12120
GBIF	7509607

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

Computational mechanistic investigation of the kinetic resolution of α-methyl-phenylacetaldehyde by norcoclaurine synthase

Zhang S, Zhang C, Guo A, Liu B, Su H, Sheng X

Commun Chem

27-Mar-2024

PMCID:	PMC10973476
doi:	10.1038/s42004-024-01146-x
PMID:	38538750

A transaminase-mediated aldol reaction and applications in cascades to styryl pyridines

Wang Y, Li Y, Ni Y, Bučar DK, Dalby PA, Ward JM, Jeffries JW, Hailes HC

Catal Sci Technol

01-Mar-2024

PMCID:	PMC11075132
doi:	10.1039/d3cy01370g
PMID:	38721397

Genome-wide identification of rubber tree pathogenesis-related 10 (PR-10) proteins with biological relevance to plant defense

Longsaward R, Viboonjun U

Sci Rep

11-Jan-2024

PMCID:	PMC10784482
doi:	10.1038/s41598-024-51312-3
PMID:	38212354

The CYP80A and CYP80G Are Involved in the Biosynthesis of Benzylisoquinoline Alkaloids in the Sacred Lotus (Nelumbo nucifera)

Hao C, Yu Y, Liu Y, Liu A, Chen S

Int J Mol Sci

05-Jan-2024

PMCID:	PMC10815925
doi:	10.3390/ijms25020702
PMID:	38255776

Modular assembly of an artificially concise biocatalytic cascade for the manufacture of phenethylisoquinoline alkaloids

Gao Y, Li F, Luo Z, Deng Z, Zhang Y, Yuan Z, Liu C, Rao Y

Nat Commun

02-Jan-2024

PMCID:	PMC10761944
doi:	10.1038/s41467-023-44420-7
PMID:	38167860

A cornucopia of diversity—Ranunculales as a model lineage

Becker A, Bachelier JB, Carrive L, Conde e Silva N, Damerval C, Del Rio C, Deveaux Y, Di Stilio VS, Gong Y, Jabbour F, Kramer EM, Nadot S, Pabón-Mora N, Wang W

J Exp Bot

18-Dec-2023

PMCID:	PMC10967251
doi:	10.1093/jxb/erad492
PMID:	38109712

Molecular docking analysis of Omt-A protein model from Aspergillus flavus with synthetic compounds

Kumar M, Sahoo GC, Ansari WA, Mohammad AA, Mohammad AF, Lee J

Bioinformation

31-Oct-2023

PMCID:	PMC10640793
doi:	10.6026/97320630019990
PMID:	37969662

An Enzymatic Strategy for the Selective Methylation of High-Value-Added Tetrahydroprotoberberine Alkaloids

Zhao W, Liu M, Liu K, Liu H, Liu X, Liu J

Int J Mol Sci

16-Oct-2023

PMCID:	PMC10607743
doi:	10.3390/ijms242015214
PMID:	37894895

The most polyphagous insect herbivore? Host plant associations of the Meadow spittlebug, Philaenus spumarius (L.)

Thompson V, Harkin C, Stewart AJ

PLoS One

04-Oct-2023

PMCID:	PMC10602594
doi:	10.1371/journal.pone.0291734
PMID:	37792900

Characterization of norbelladine synthase and noroxomaritidine/norcraugsodine reductase reveals a novel catalytic route for the biosynthesis of Amaryllidaceae alkaloids including the Alzheimer’s drug galanthamine

Majhi BB, Gélinas SE, Mérindol N, Ricard S, Desgagné-Penix I

Front Plant Sci

30-Aug-2023

PMCID:	PMC10499049
doi:	10.3389/fpls.2023.1231809
PMID:	37711303

The History and Science of the Major Birch Pollen Allergen Bet v 1

Breiteneder H, Kraft D

Biomolecules

19-Jul-2023

PMCID:	PMC10377203
doi:	10.3390/biom13071151
PMID:	37509186

Rational Engineering of (S)-Norcoclaurine Synthase for Efficient Benzylisoquinoline Alkaloids Biosynthesis

De Sousa JP, Oliveira NC, Fernandes PA

Molecules

23-May-2023

PMCID:	PMC10254637
doi:	10.3390/molecules28114265
PMID:	37298742

Multi-enzyme catalysed processes using purified and whole-cell biocatalysts towards a 1,3,4-substituted tetrahydroisoquinoline

Weber D, de Souza Bastos L, Winkler M, Ni Y, Aliev AE, Hailes HC, Rother D

RSC Adv

29-Mar-2023

PMCID:	PMC10053099
doi:	10.1039/d3ra01210g
PMID:	37006360

Isolation and Characterization of the Genes Involved in the Berberine Synthesis Pathway in Asian Blue Cohosh, Caulophyllum robustum

Park NI, Roy NS, Park Y, Choi BS, Jeon MJ, Oh JY, Kim BY, Kim YD, Kim YI, Um T, Kwak HJ, Kim NS, Kim S, Choi IY

Plants (Basel)

28-Mar-2023

PMCID:	PMC10096549
doi:	10.3390/plants12071483
PMID:	37050109

A novel rubber tree PR-10 protein involved in host-defense response against the white root rot fungus Rigidoporus microporus

Longsaward R, Pengnoo A, Kongsawadworakul P, Viboonjun U

BMC Plant Biol

22-Mar-2023

PMCID:	PMC10032002
doi:	10.1186/s12870-023-04149-3
PMID:	36944945

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
> Alkaloids and derivatives / 6,6a-secoaporphines
Thaliglucinone	182266	Click to see CN(C)CCC1=CC(=C2C3=C1C=CC4=CC5=C(C(=C43)C(=O)O2)OCO5)OC	365.40	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257762/
> Alkaloids and derivatives / Aporphines
(+)-Glaucine	16754	Click to see	355.40	unknown	https://doi.org/10.1016/0305-1978(92)90059-M
(6aR)-9-[2-[[(1S)-6,7-dimethoxy-2-methyl-3,4-dihydro-1H-isoquinolin-1-yl]methyl]-4,5-dimethoxyphenoxy]-1,2,10-trimethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinoline	6713001	Click to see	696.80	unknown	via CMAUP database
1-Hydroxy-2,3,9,10-tetramethoxyaporphine	12305718	Click to see CN1CCC2=C3C1CC4=CC(=C(C=C4C3=C(C(=C2OC)OC)O)OC)OC	371.40	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257762/
3-Hydroxy-4,15,16-trimethoxy-10-azatetracyclo[7.7.1.02,7.013,17]heptadeca-1(17),2(7),3,5,9,11,13,15-octaen-8-one	135795277	Click to see	337.30	unknown	https://doi.org/10.1016/0305-1978(92)90059-M
O-Methylcassyfiline	3698033	Click to see COC1=C(C=C2C(=C1)CC3C4=C(CCN3)C(=C5C(=C24)OCO5)OC)OC	355.40	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257762/
O-Methylcassythine	6352219	Click to see	355.40	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257762/
Preocoteine	176968	Click to see CN1CCC2=C3C1CC4=CC(=C(C=C4C3=C(C(=C2OC)OC)O)OC)OC	371.40	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257762/
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
Protocatechuic Acid	72	Click to see	154.12	unknown	via CMAUP database
> Benzenoids / Phenols / 1-hydroxy-2-unsubstituted benzenoids
(+)-Rhododendrol	919204	Click to see	166.22	unknown	via CMAUP database
4-(4'-Hydroxyphenyl)-2-butanone	21648	Click to see	164.20	unknown	via CMAUP database
> Lignans, neolignans and related compounds
(-)-N-Desmethylthalidasine	5459005	Click to see CN1CCC2=C3C(=C(C=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=C(O3)C(=C(C=C7CCN6)OC)OC)OC)OC)OC	638.70	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257762/
(3S,21S)-10,14,15-trimethoxy-4,20-dimethyl-12,28-dioxa-4,20-diazaheptacyclo[27.2.2.17,11.113,17.123,27.03,8.021,35]hexatriaconta-1(32),7(36),8,10,13(35),14,16,23(34),24,26,29(33),30-dodecaen-26-ol	12443375	Click to see	608.70	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257762/
(3S,22S)-10,11,15,16-tetramethoxy-4-methyl-13,29-dioxa-4,21-diazaheptacyclo[28.2.2.114,18.124,28.03,8.07,12.022,36]hexatriaconta-1(33),7(12),8,10,14(36),15,17,24(35),25,27,30(34),31-dodecaen-27-ol	162918640	Click to see	624.70	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257762/
(3S,22S)-10,11,15,16-tetramethoxy-4,21-dimethyl-13,29-dioxa-4,21-diazaheptacyclo[28.2.2.114,18.124,28.03,8.07,12.022,36]hexatriaconta-1(33),7(12),8,10,14(36),15,17,24(35),25,27,30(34),31-dodecaen-27-ol	101624073	Click to see	638.70	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257762/ https://doi.org/10.1016/0305-1978(92)90059-M
10,11,15,16-Tetramethoxy-4-methyl-13,29-dioxa-4,21-diazaheptacyclo[28.2.2.114,18.124,28.03,8.07,12.022,36]hexatriaconta-1(32),7(12),8,10,14(36),15,17,24(35),25,27,30,33-dodecaen-27-ol	162918639	Click to see CN1CCC2=C3C(=C(C=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=C(O3)C(=C(C=C7CCN6)OC)OC)O)OC)OC	624.70	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257762/
10,11,15,16-Tetramethoxy-4,21-dimethyl-13,29-dioxa-4,21-diazaheptacyclo[28.2.2.114,18.124,28.03,8.07,12.022,36]hexatriaconta-1(32),7(12),8,10,14(36),15,17,24(35),25,27,30,33-dodecaen-27-ol	3839867	Click to see	638.70	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257762/
10,11,15,16,27-Pentamethoxy-4-methyl-13,29-dioxa-4,21-diazaheptacyclo[28.2.2.114,18.124,28.03,8.07,12.022,36]hexatriaconta-1(32),7(12),8,10,14(36),15,17,24(35),25,27,30,33-dodecaene	5168930	Click to see	638.70	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257762/
10,11,16-Trimethoxy-4,21-dimethyl-13,29-dioxa-4,21-diazaheptacyclo[28.2.2.114,18.124,28.03,8.07,12.022,36]hexatriaconta-1(32),7(12),8,10,14(36),15,17,24(35),25,27,30,33-dodecaene-15,27-diol	75051852	Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C4)O)OC5=CC=C(CC6C7=CC(=C(C(=C7CCN6C)O3)OC)OC)C=C5)O)OC	624.70	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257762/
10,11,16,27-Tetramethoxy-4-methyl-13,29-dioxa-4,21-diazaheptacyclo[28.2.2.114,18.124,28.03,8.07,12.022,36]hexatriaconta-1(32),7(12),8,10,14(36),15,17,24(35),25,27,30,33-dodecaen-15-ol	78178088	Click to see	624.70	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257762/
10,14,15-Trimethoxy-4,20-dimethyl-12,28-dioxa-4,20-diazaheptacyclo[27.2.2.17,11.113,17.123,27.03,8.021,35]hexatriaconta-1(31),7(36),8,10,13(35),14,16,23(34),24,26,29,32-dodecaen-26-ol	12443374	Click to see	608.70	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257762/
10,14,15-Trimethoxy-4,20-dimethyl-28-oxa-4,20-diazaheptacyclo[27.2.2.17,11.113,17.123,27.03,8.021,35]hexatriaconta-1(31),7(36),8,10,13(35),14,16,23(34),24,26,29,32-dodecaen-26-ol	5321904	Click to see	606.70	unknown	via CMAUP database
N-Desmethylthalrugosidine	156760	Click to see	624.70	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257762/
Thalidasine	159795	Click to see	652.80	unknown	https://doi.org/10.1016/0305-1978(92)90059-M
Thaligosidine	44584029	Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C4)O)OC5=CC=C(CC6C7=CC(=C(C(=C7CCN6C)O3)OC)OC)C=C5)O)OC	624.70	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257762/
> Organoheterocyclic compounds / Isoquinolines and derivatives / Benzylisoquinolines
(+/-)-Armepavine	98348	Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC=C(C=C3)O)OC)OC	313.40	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257762/
Armepavine	442169	Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC=C(C=C3)O)OC)OC	313.40	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257762/
> Organoheterocyclic compounds / Isoquinolines and derivatives / Isoquinolones and derivatives
9-Methoxy-6-methyl-7,8-dihydro-[1,3]dioxolo[4,5-g]isoquinolin-5-one	13475781	Click to see	235.24	unknown	https://doi.org/10.1021/NP50022A001 https://doi.org/10.1007/BF00564248
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
(-)-Catechol	73160	Click to see	290.27	unknown	via CMAUP database
Epicatechin	72276	Click to see	290.27	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Furanoisoflavonoids / Pterocarpans
Medicarpin	336327	Click to see COC1=CC2=C(C=C1)C3COC4=C(C3O2)C=CC(=C4)O	270.28	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
8-Hydroxydaidzein	5466139	Click to see	270.24	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavonoid O-glycosides
6''-O-Acetylononin	102463148	Click to see CC(=O)OCC1C(C(C(C(O1)OC2=CC3=C(C=C2)C(=O)C(=CO3)C4=CC=C(C=C4)OC)O)O)O	472.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids
(+)-Vestitol	177149	Click to see	272.29	unknown	via CMAUP database
Vestitol, (-)-	182259	Click to see COC1=CC(=C(C=C1)C2CC3=C(C=C(C=C3)O)OC2)O	272.29	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 4-O-methylisoflavones
Afromosin	5281704	Click to see	298.29	unknown	via CMAUP database
Formononetin	5280378	Click to see	268.26	unknown	via CMAUP database

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Thalictrum flavum

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Ethnobotanical Use Top

General Uses Top

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Common names Top

Subspecies (abbr. subsp./ssp.) Top

Varieties (abbr. var.) Top

Subvarieties (abbr. subvar.) Top

Forms (abbr. f.) Top

Germination/Propagation Top

Distribution (via POWO/KEW) Top

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Phytochemical Profile Top

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