Common products:
- Ornamental perennial herb grown in temperate gardens for its delicate, finely divided foliage and airy inflorescences; sold by commercial nurseries and online retailers as a garden plant (e.g., commercial plant catalogues list Thalictrum cultratum among hardy perennials suitable for partially shaded borders).
- Cut foliage from cultivated plants is harvested for use in floral arrangements, where its feathery leaves provide texture and volume as a filler material.

Properties relevant to use:
- Morphologically, the species forms dense clumps of erect stems up to about 70 cm tall, bearing deeply lobed leaflets that give a fine, fern‑like appearance; these traits are prized by designers seeking airy garden textures and by florists looking for lightweight, decorative foliage.
- Chemically, the plant accumulates benzylisoquinoline alkaloids and flavonoid glycosides; these compounds have been examined in comparative phytochemical surveys, providing data for taxonomic studies but not for commercial extraction.
- The species has been incorporated into DNA‑based phylogenetic investigations of Ranunculaceae; nuclear ribosomal (ITS) and chloroplast (matK) sequences from Thalictrum cultratum are deposited in public sequence repositories (e.g., GenBank), facilitating comparative systematics and evolutionary research.

Standards and regulation:
- The international trade of live Thalictrum cultratum plants is governed by phytosanitary requirements set by the International Plant Protection Convention (IPPC) and enforced through national plant health authorities; exporters must obtain phytosanitary certificates to certify freedom from regulated pests.
- In many jurisdictions, the horticultural trade of ornamental perennials follows national labeling standards (e.g., EU Plant Variety Rights or U.S. Plant Variety Protection) and may be subject to regional restrictions on invasive species; no specific regulatory listing has been identified for T. cultratum.

Sustainability and sourcing:
- Commercial production is primarily through vegetative division of mature clumps and by seed propagation, enabling large‑scale nursery output without reliance on wild collection.
- Because the species is propagated in cultivation, its horticultural use exerts minimal pressure on natural populations; the plant is not listed on CITES appendices and is considered a low‑impact ornamental with a sustainable supply chain.

Synonyms Top

Scientific name	Authority	First published in
Thalictrum deciternatum	B.Boivin	J. Arnold Arbor. 26: 112 (1945)
Thalictrum yui	B.Boivin	J. Arnold Arbor. 26: 115 (1945)

Common names Top

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Filter by language:

Language	Common/alternative name
English	knife-like meadow rue
Chinese	马尾连
Chinese	马尾黄连
Chinese	西藏水黄连
Chinese	高原唐松草
Chinese	草黄连

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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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 click to expand
- China
  - China North-central
  - China South-central
  - Tibet

Asia-tropical click to expand
- Indian Subcontinent
  - East Himalaya
  - Nepal
  - Pakistan
  - West Himalaya
- Indo-China
  - Myanmar

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0001129326
Tropicos	27100518
KEW	urn:lsid:ipni.org:names:714354-1
The Plant List	tro-27100518
Open Tree Of Life	583170
Observations.org	506040
NCBI Taxonomy	341022
IPNI	714354-1
GBIF	3929860
EOL	2873967
Elurikkus	441752
USDA GRIN	36427
CMAUP	NPO24447

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

Genome size data for eight endemic plant species from the Nanda Devi Biosphere Reserve (Western Himalaya)

Arora J, Lakhanpaul S, Manish K, Pandit MK

Data Brief

18-Apr-2024

PMCID:	PMC11068558
doi:	10.1016/j.dib.2024.110450
PMID:	38708313

Molecular Docking Study of Several Seconder Metabolites from Medicinal Plants as Potential Inhibitors of COVID-19 Main Protease

BİLGİNER S, GÖZCÜ S, GÜVENALP Z

Turk J Pharm Sci

31-Aug-2022

PMCID:	PMC9438759
doi:	10.4274/tjps.galenos.2021.83548
PMID:	36047576

Screening an In-House Isoquinoline Alkaloids Library for New Blockers of Voltage-Gated Na+ Channels Using Voltage Sensor Fluorescent Probes: Hits and Biases

Coquerel Q, Legendre C, Frangieh J, Waard SD, Montnach J, Cmarko L, Khoury J, Hassane CS, Bréard D, Siegler B, Fajloun Z, De Pomyers H, Mabrouk K, Weiss N, Henrion D, Richomme P, Mattei C, Waard MD, Le Ray AM, Legros C

Molecules

28-Jun-2022

PMCID:	PMC9268414
doi:	10.3390/molecules27134133
PMID:	35807390

Jatrorrhizine: A Review of Sources, Pharmacology, Pharmacokinetics and Toxicity

Zhong F, Chen Y, Chen J, Liao H, Li Y, Ma Y

Front Pharmacol

13-Jan-2022

PMCID:	PMC8793695
doi:	10.3389/fphar.2021.783127
PMID:	35095493

Distribution of Therapeutic Efficacy of Ranunculales Plants Used by Ethnic Minorities on the Phylogenetic Tree of Chinese Species

Hao DC, Zhang Y, He CN, Xiao PG

Evid Based Complement Alternat Med

12-Jan-2022

PMCID:	PMC8769838
doi:	10.1155/2022/9027727
PMID:	35069772

8-, 9-, and 11-Aryloxy Dimeric Aporphines and Their Pharmacological Activities

Ali G, Cuny GD

Molecules

27-Jul-2021

PMCID:	PMC8347945
doi:	10.3390/molecules26154521
PMID:	34361671

Unraveling Plant Natural Chemical Diversity for Drug Discovery Purposes

Lautié E, Russo O, Ducrot P, Boutin JA

Front Pharmacol

07-Apr-2020

PMCID:	PMC7154113
doi:	10.3389/fphar.2020.00397
PMID:	32317969

Chloroplast primers for clade‐wide phylogenetic studies of Thalictrum

Morales‐Briones DF, Arias T, Di Stilio VS, Tank DC

Appl Plant Sci

16-Oct-2019

PMCID:	PMC6814179
doi:	10.1002/aps3.11294
PMID:	31667022

Natural Products and Acute Myeloid Leukemia: A Review Highlighting Mechanisms of Action

Hwang D, Kim M, Park H, Jeong MI, Jung W, Kim B

Nutrients

03-May-2019

PMCID:	PMC6567155
doi:	10.3390/nu11051010
PMID:	31058874

Meiotic abnormalities affect genetic constitution and pollen viability in dicots from Indian cold deserts

Kaur D, Singhal VK

BMC Plant Biol

07-Jan-2019

PMCID:	PMC6323802
doi:	10.1186/s12870-018-1596-7
PMID:	30616590

Floristic Diversity and Distribution Pattern of Plant Communities along Altitudinal Gradient in Sangla Valley, Northwest Himalaya

Sharma P, Rana JC, Devi U, Randhawa SS, Kumar R

ScientificWorldJournal

14-Oct-2014

PMCID:	PMC4212538
doi:	10.1155/2014/264878
PMID:	25383363

Antiviral Activity of Some Plants Used in Nepalese Traditional Medicine

Rajbhandari M, Mentel R, Jha PK, Chaudhary RP, Bhattarai S, Gewali MB, Karmacharya N, Hipper M, Lindequist U

Evid Based Complement Alternat Med

25-Oct-2007

PMCID:	PMC2781767
doi:	10.1093/ecam/nem156
PMID:	18955262

Nine Bisbenzylisoquinoline Alkaloids from Thalictrum cultratum

Wasala H. M. W. Herath, S. Fazal Hussain, Alan J. Freyer, Hélène Guinaudeau, Maurice Shamma

American Chemical Society (ACS)

17-Mar-2005

doi:	10.1021/NP50052A024

Bisbenzylisoquinoline Alkaloids from Thalictrum cultratum. The Structures of Thalrugosinone and Thalpindione

S. Fazal Hussain, Hélène Guinaudeau, Alan J. Freyer, Maurice Shamma

American Chemical Society (ACS)

17-Mar-2005

doi:	10.1021/NP50042A014

Seven New Aporphine-Benzylisoquinoline Alkaloids from Thalictrum cultratum

S. Fazal Hussain, Alan J. Freyer, Hélène Guinaudeau, Maurice Shamma, M. Tariq Siddiqui

American Chemical Society (ACS)

11-Mar-2005

doi:	10.1021/NP50045A019

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 / Aporphines
(+)-Magnoflorine	73337	Click to see	342.40	unknown	https://doi.org/10.1016/S0031-9422(00)84580-X
(6aS)-8-[4-[[(1S)-7-hydroxy-6-methoxy-2-methyl-3,4-dihydro-1H-isoquinolin-1-yl]methyl]phenoxy]-1,2,3,10-tetramethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinolin-9-ol	10484580	Click to see	668.80	unknown	https://doi.org/10.1021/NP50045A019
1-[[4,5-dimethoxy-2-[(1,2,3,10-tetramethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinolin-9-yl)oxy]phenyl]methyl]-6,7-dimethoxy-2-methyl-3,4-dihydro-1H-isoquinolin-5-ol	3420841	Click to see	742.90	unknown	https://doi.org/10.1021/NP50045A019
6-methoxy-2-methyl-1-[[4-[(1,2,9,10-tetramethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinolin-8-yl)oxy]phenyl]methyl]-3,4-dihydro-1H-isoquinolin-7-ol	13892252	Click to see	652.80	unknown	https://doi.org/10.1021/NP50045A019
6-methoxy-2-methyl-1-[[4-[(14,15,16-trimethoxy-10-methyl-10-azatetracyclo[7.7.1.02,7.013,17]heptadeca-1,3,5,7,9(17),13,15-heptaen-6-yl)oxy]phenyl]methyl]-3,4-dihydro-1H-isoquinolin-7-ol	101216513	Click to see	620.70	unknown	https://doi.org/10.1021/NP50045A019
7-methoxy-2-methyl-1-[[4-[(1,2,3,9,10-pentamethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinolin-8-yl)oxy]phenyl]methyl]-3,4-dihydro-1H-isoquinolin-6-ol	13892256	Click to see	682.80	unknown	https://doi.org/10.1021/NP50045A019
8-[4-[(6,7-dimethoxy-2-methyl-3,4-dihydro-1H-isoquinolin-1-yl)methyl]phenoxy]-1,2,9,10-tetramethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinoline	13892251	Click to see	666.80	unknown	https://doi.org/10.1021/NP50045A019
Adiantifoline	167937	Click to see	726.90	unknown	https://doi.org/10.1021/NP50045A019
Thalmelatidine	56842063	Click to see	740.80	unknown	https://doi.org/10.1021/NP50045A019
> Alkaloids and derivatives / Protoberberine alkaloids and derivatives
16-Methoxy-5,7-dioxa-13-azoniapentacyclo[11.8.0.02,10.04,8.015,20]henicosa-1(13),2,4(8),9,14,16,18,20-octaen-17-olate	10426199	Click to see	321.30	unknown	https://doi.org/10.1016/S0031-9422(00)84580-X
Berberine	2353	Click to see	336.40	unknown	https://doi.org/10.1016/S0031-9422(00)84580-X
Columbamine	72310	Click to see	338.40	unknown	https://doi.org/10.1016/S0031-9422(00)84580-X
Palmatine	19009	Click to see	352.40	unknown	https://doi.org/10.1016/S0031-9422(00)84580-X
Thalifendine	3084288	Click to see	322.30	unknown	https://doi.org/10.1016/S0031-9422(00)84580-X
> Lignans, neolignans and related compounds
(-)-5-Hydroxythalmine	184486	Click to see CN1CCC2=C3C(=C(C=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=CC(=C(C(=C7CCN6C)O)OC)O3)OC)OC)O	624.70	unknown	https://doi.org/10.1021/NP50045A018
(-)-Thalmiculimine	184489	Click to see	622.70	unknown	https://doi.org/10.1021/NP50045A018
(-)-Thalmiculine	184621	Click to see	638.70	unknown	https://doi.org/10.1021/NP50045A018
(21S)-10,15,26-trimethoxy-20-methyl-12,28-dioxa-4,20-diazaheptacyclo[27.2.2.17,11.113,17.123,27.03,8.021,35]hexatriaconta-1(31),3,7(36),8,10,13(35),14,16,23(34),24,26,29,32-tridecaen-14-ol	101428567	Click to see	592.70	unknown	https://doi.org/10.1021/NP50045A018
(3S,21S)-10,15,26-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-14-ol	102148178	Click to see	608.70	unknown	https://doi.org/10.1021/NP50045A018 https://doi.org/10.1021/NP50052A024
(4aR,16aS)-3,4,4a,5,16a,17,18,19-Octahydro-9,21,22,26-tetramethoxy-4,17-dimethyl-2H-1,24:12,15-dietheno-6,10-metheno-16H-pyrido(2',3':17,18)(1,10)dioxacycloeicosino(2,3,4-ij)isoquinoline	100231	Click to see	622.70	unknown	https://doi.org/10.1021/NP50052A024
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-21-carbaldehyde	13892231	Click to see CN1CCC2=C3C(=C(C=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=C(O3)C(=C(C=C7CCN6C=O)OC)OC)OC)OC)OC	666.80	unknown	https://doi.org/10.1021/NP50042A014
1H-8,9,13-(1,3)Butadien(1)yl(4)ylidene-4,6:15,18-dietheno-20,24-metheno-10H-pyrido(2,3-t)(1,13,6)dioxaazacyclotricosin-32-ol, 2,3,11,12,13,14,25,25a-octahydro-21,31,33-trimethoxy-1,12-dimethyl-, (13S,25aS)-	442366	Click to see	608.70	unknown	https://doi.org/10.1021/NP50042A014
2-Northalmine	180979	Click to see	594.70	unknown	https://doi.org/10.1021/NP50042A014
5-Hydroxythalidasine	184487	Click to see	668.80	unknown	https://doi.org/10.1021/NP50052A024 https://doi.org/10.1021/NP50045A018
Aromoline	362574	Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=CC(=C(C=C7CCN6C)OC)O3)O)O)OC	594.70	unknown	https://doi.org/10.1021/NP50052A024
Oxyacanthine	442333	Click to see	608.70	unknown	https://doi.org/10.1021/NP50052A024
Talysopine	179390	Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC(=C(C=C4)OC)OC5=CC=C(CC6C7=C(CCN6C)C(=C(C(=C7O3)OC)OC)O)C=C5)OC	638.70	unknown	https://doi.org/10.1021/NP50052A024 https://doi.org/10.1021/NP50045A018
Thalictine	181168	Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC(=C(C=C4)O)OC5=CC=C(CC6C7=CC(=C(C(=C7CCN6C)O3)OC)OC)C=C5)OC	608.70	unknown	https://doi.org/10.1021/NP50045A018
Thalidasine	159795	Click to see	652.80	unknown	https://doi.org/10.1021/NP50052A024 https://doi.org/10.1021/NP50042A014
Thalmiculatimine	184485	Click to see	592.70	unknown	https://doi.org/10.1021/NP50045A018
Thalmidine	100230	Click to see CN1CCC2=CC3=C(C=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=C(O3)C(=C(C=C7CCN6C)OC)OC)OC)OC	622.70	unknown	https://doi.org/10.1021/NP50045A018
Thalrugosidine	5321920	Click to see	638.70	unknown	https://doi.org/10.1021/NP50045A018
> Organoheterocyclic compounds / Isoquinolines and derivatives / Benzylisoquinolines
(1S)-1-[[4-[5-[[(1S)-7-hydroxy-6-methoxy-2-methyl-3,4-dihydro-1H-isoquinolin-1-yl]methyl]-2-methoxyphenoxy]phenyl]methyl]-6,7-dimethoxy-2-methyl-3,4-dihydro-1H-isoquinolin-5-ol	44584030	Click to see	640.80	unknown	https://doi.org/10.1021/NP50052A024
> Organoheterocyclic compounds / Isoquinolines and derivatives / Isoquinolones and derivatives
2,9,10-Trimethoxy-5,6-dihydroisoquinolino[2,1-b]isoquinolin-3-one	10065647	Click to see	337.40	unknown	https://doi.org/10.1016/S0031-9422(00)84580-X
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
3,5,3',4'-Tetrahydroxy-6,7,8-trimethoxyflavone	44260067	Click to see	376.30	unknown	via CMAUP database
3,5,7-Trihydroxy-2-(4-hydroxy-3-methoxyphenyl)-6,8-dimethoxy-4H-1-benzopyran-4-one	12311234	Click to see	376.30	unknown	via CMAUP database
3,5,7,3',4'-Pentahydroxy-6,8-dimethoxyflavone	14483219	Click to see	362.30	unknown	via CMAUP database
Kaempferol	5280863	Click to see	286.24	unknown	via CMAUP database
Quercetin	5280343	Click to see	302.23	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides
2-(3,4-dihydroxyphenyl)-5-hydroxy-7-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one	13871824	Click to see	432.40	unknown	via CMAUP database
5,7-dihydroxy-2-(4-hydroxyphenyl)-6-[(2R,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one	57511421	Click to see	432.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
Orientin	5281675	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(C(O4)CO)O)O)O)O)O	448.40	unknown	via CMAUP database
Vitexin	5280441	Click to see	432.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Cacticin	5318644	Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O	478.40	unknown	via CMAUP database
Hyperoside	5281643	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	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
2-(3,4-Dihydroxyphenyl)-5,7,8-trihydroxy-3-methoxy-4H-chromen-4-one	5386958	Click to see	332.26	unknown	via CMAUP database
3-Methoxyluteolin	5280681	Click to see COC1=C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)O)O	316.26	unknown	via CMAUP database
5,7,8,4'-Tetrahydroxy-3-methoxyflavone	5319442	Click to see COC1=C(OC2=C(C1=O)C(=CC(=C2O)O)O)C3=CC=C(C=C3)O	316.26	unknown	via CMAUP database
Gossypetin 3,3'-dimethyl ether	21676153	Click to see	346.30	unknown	via CMAUP database
Quercetagetin 3-methyl ether	5320475	Click to see COC1=C(OC2=C(C1=O)C(=C(C(=C2)O)O)O)C3=CC(=C(C=C3)O)O	332.26	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
5,7,2'-Trihydroxy-3,6,4',5'-tetramethoxyflavone	44259895	Click to see	390.30	unknown	via CMAUP database
5,7,3'-Trihydroxy-3,6,4',5'-tetramethoxyflavone	44258045	Click to see	390.30	unknown	via CMAUP database
5,7,3',4'-Tetrahydroxy-3,6,5'-trimethoxyflavone	44258041	Click to see	376.30	unknown	via CMAUP database
5,7,3',4',5'-Pentahydroxy-3,6-dimethoxyflavone	44259884	Click to see	362.30	unknown	via CMAUP database
5,7,8,3',4'-Pentahydroxy-3,6-dimethoxyflavone	21676156	Click to see COC1=C(C(=C2C(=C1O)C(=O)C(=C(O2)C3=CC(=C(C=C3)O)O)OC)O)O	362.30	unknown	via CMAUP database
5,7,8,4'-Tetrahydroxy-3,6-dimethoxyflavone	44260054	Click to see	346.30	unknown	via CMAUP database
6-Hydroxykaempferol 3,6-dimethyl ether	5352032	Click to see	330.29	unknown	via CMAUP database
Axillarin	5281603	Click to see	346.30	unknown	via CMAUP database
Jaceidin	5464461	Click to see	360.30	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Benthamitin	44259900	Click to see	432.40	unknown	via CMAUP database
Casticin	5315263	Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C(=C(C=C3O2)OC)OC)O)OC)O	374.30	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
3',4',5,7-Tetrahydroxy-3,8-dimethoxyflavone	5748553	Click to see COC1=C(C=C(C2=C1OC(=C(C2=O)OC)C3=CC(=C(C=C3)O)O)O)O	346.30	unknown	via CMAUP database
5-Hydroxy-3,6,7,8,3',4',5'-heptamethoxyflavone	44260077	Click to see	448.40	unknown	via CMAUP database
5,2'-Dihydroxy-3,6,7,8,4',5'-hexamethoxyflavone	44260086	Click to see	434.40	unknown	via CMAUP database
5,3'-Dihydroxy-3,6,7,8,4'-pentamethoxyflavone	369954	Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)OC)OC)O)OC)O	404.40	unknown	via CMAUP database
5,3',4'-Trihydroxy-3,6,7,8-tetramethoxyflavone	54799	Click to see COC1=C(C(=C2C(=C1O)C(=O)C(=C(O2)C3=CC(=C(C=C3)O)O)OC)OC)OC	390.30	unknown	via CMAUP database
5,3',5'-Trihydroxy-3,6,7,8,4'-pentamethoxyflavone	44260074	Click to see COC1=C(C=C(C=C1O)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)OC)OC)O)OC)O	420.40	unknown	via CMAUP database
5,4'-Dihydroxy-3,6,7,8,3'-pentamethoxyflavone	100625	Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)OC)OC)O)OC)O	404.40	unknown	via CMAUP database
5,6,3',5'-Tetrahydroxy-3,7,8,4'-tetramethoxyflavone	44260073	Click to see COC1=C(C=C(C=C1O)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)OC)O)O)OC)O	406.30	unknown	via CMAUP database
5,7-Dihydroxy-2-(4-hydroxy-3-methoxy-phenyl)-3,6,8-trimethoxy-chromen-4-one	5386959	Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)O)OC)O)OC)O	390.30	unknown	via CMAUP database
5,7-Dihydroxy-3,6,8,3',4',5'-hexamethoxyflavone	5386963	Click to see	434.40	unknown	via CMAUP database
5,7,2'-Trihydroxy-3,6,8,4',5'-pentamethoxyflavone	5487077	Click to see COC1=C(C=C(C(=C1)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)O)OC)O)OC)O)OC	420.40	unknown	via CMAUP database
5,7,2',4'-Tetrahydroxy-3,6,8,5'-tetramethoxyflavone	21676158	Click to see	406.30	unknown	via CMAUP database
5,7,2',4'-Tetrahydroxy-3,8,5'-trimethoxyflavone	44260043	Click to see COC1=C(C=C(C(=C1)C2=C(C(=O)C3=C(O2)C(=C(C=C3O)O)OC)OC)O)O	376.30	unknown	via CMAUP database
5,7,2',4'-Tetrahydroxy-8,5'-dimethoxyflavone	44258626	Click to see COC1=C(C=C(C(=C1)C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)OC)O)O	346.30	unknown	via CMAUP database
5,7,2',5'-Tetrahydroxy-3,6,8,4'-tetramethoxyflavone	44260085	Click to see COC1=C(C=C(C(=C1)O)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)O)OC)O)OC)O	406.30	unknown	via CMAUP database
5,7,3'-Trihydroxy-3,6,8,4'-Tetramethoxyflavone	21599528	Click to see	390.30	unknown	via CMAUP database
5,7,3'-Trihydroxy-3,6,8,4',5'-pentamethoxyflavone	5352085	Click to see COC1=CC(=CC(=C1OC)O)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)O)OC)O)OC	420.40	unknown	via CMAUP database
5,7,3',4'-Tetrahydroxy-3,6,8-trimethoxyflavone	5386962	Click to see	376.30	unknown	via CMAUP database
5,7,3',4'-Tetrahydroxy-3,6,8,5'-tetramethoxyflavone	44260072	Click to see	406.30	unknown	via CMAUP database
5,7,3',4',5'-Pentahydroxy-3,6,8-trimethoxyflavone	11383767	Click to see	392.30	unknown	via CMAUP database
5,7,3',5'-Tetrahydroxy-3,6,8,4'-tetramethoxyflavone	44260071	Click to see COC1=C(C=C(C=C1O)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)O)OC)O)OC)O	406.30	unknown	via CMAUP database
5,7,4'-Trihydroxy-3,6,8,3',5'-pentamethoxyflavone	21676159	Click to see	420.40	unknown	via CMAUP database
5,7,4'-Trihydroxy-3,8-dimethoxyflavone	13983738	Click to see	330.29	unknown	via CMAUP database
Agecorynin D	14162688	Click to see COC1=C(C=C(C(=C1)C2=CC(=O)C3=C(C(=C(C(=C3O2)OC)OC)OC)O)O)O	390.30	unknown	via CMAUP database
Calycopterin	10429470	Click to see	374.30	unknown	via CMAUP database
Conyzatin	13916282	Click to see	404.40	unknown	via CMAUP database
Digicitrin	10071564	Click to see COC1=CC(=CC(=C1OC)O)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)OC)OC)O)OC	434.40	unknown	via CMAUP database
Gossypetin 3,8,3'-trimethyl ether	5386961	Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(O2)C(=C(C=C3O)O)OC)OC)O	360.30	unknown	via CMAUP database
Hibiscetin 3,8,4'-trimethyl ether	44260037	Click to see	376.30	unknown	via CMAUP database
Sarothrin	5386960	Click to see	360.30	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Tannins
(-)-Thalrugosaminine	5321919	Click to see	652.80	unknown	https://doi.org/10.1021/NP50052A024 https://doi.org/10.1021/NP50045A018

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Thalictrum cultratum

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