Common products:
Live plants of Thalictrum simplex are sold by specialty nurseries as ornamental perennials for garden and landscape planting. The species is listed in commercial catalogs under the common name “simple meadow‑rue” and is promoted for its airy foliage and early‑summer bloom. Cut stems bearing the delicate, plume‑like inflorescences are harvested for use in fresh‑flower arrangements, where their fine texture provides contrast to larger blooms. Seeds of the species are offered by horticultural seed exchanges and are a common component of wild‑flower seed mixes for naturalistic plantings.

Properties relevant to use:
Thalictrum simplex is a herbaceous perennial that typically reaches 0.5–1.2 m in height. It develops a fibrous, clumping root system and produces finely divided, glaucous leaves that remain attractive throughout the growing season. The plant forms airy panicles of numerous small, pink‑purple to white flowers that appear in early to mid‑summer, giving a light, see‑through quality prized in garden design. It tolerates partial shade and prefers moist, well‑drained soils; it is cold‑hardy to USDA zones 4–8. Propagation is straightforward from seed or division; seeds exhibit high viability and germinate without special pretreatment.

Standards and regulation:
The trade in seeds and live plants follows national seed certification and plant health regulations. Seed lots are typically required to meet national purity and germination standards and may be audited under international seed‑testing guidelines. Import and export of Thalictrum simplex plants are subject to phytosanitary certification by the relevant National Plant Protection Organization (NPPO) and compliance with the International Plant Protection Convention (IPPC).

Sustainability and sourcing:
The species is native to temperate regions of North America and Eurasia and is not classified as invasive. Commercial material is derived from cultivated nursery stock; wild harvesting is generally avoided. Seed production is reliable and permits sustainable propagation with minimal impact on natural populations. Cultivation of Thalictrum simplex supports pollinator‑friendly gardens and can be integrated into low‑maintenance, naturalistic landscape schemes.

Synonyms Top

Scientific name	Authority	First published in
Thalictrum laetum	Jord.	Ann. Soc. Linn. Lyon , n.s., 7: 412 (1861)
Thalictrum lacerostipellatum	K.Koch & C.D.Bouché	Index Seminum (B, Berolinensis) 1854(App.): 13 (1855)
Thalictrum laserpitiifolium	Willd.	Enum. Pl. Hort. Berol. , Suppl.: 40 (1814)
Thalictrum nitidulum	Jord.	Observ. Pl. Nouv. 5: 17 (1847)
Thalictrum exaltatum	C.A.Mey.	Fl. Altaic. 2: 352 (1830)
Thalictrum dubium	Schumach.	Enum. Pl. Saell. 1: 167 (1801)
Thalictrum subfalcatum	Rouy & Foucaud	Fl. France 1: 26 (1893)
Thalictrum strictum	Ledeb.	Fl. Ross. 1: 10 (1841)
Thalictrum subspicatum	Jord.	Ann. Soc. Linn. Lyon , n.s., 7: 414 (1861)
Thalictrum regelianum	Brügger	Jahresber. Naturf. Ges. Graubündens , n.s., 23-24: 75 (1880)
Thalictrum rhodanense	Jord.	Ann. Soc. Linn. Lyon , n.s., 7: 413 (1861)
Thalictrum procerulum	Jord.	Ann. Soc. Linn. Lyon , n.s., 7: 413 (1861)
Thalictrum axilliflorum	Schur	Enum. Pl. Transsilv. : 10 (1866)
Thalictrum bauhini	Crantz	Stirp. Austr. Fasc. 2: 70 (1763)
Thalictrum confertiflorum	C.A.Mey. ex Trautv.	Trudy Imp. S.-Peterburgsk. Bot. Sada 8: 29 (1883)
Thalictrum columnare	Sennen	Bol. Soc. Aragonesa Ci. Nat. 11: 180 (1912)
Thalictrum catalaunicum	Pau	Not. Bot. Fl. Españ. 4: 111 (1891)
Thalictrum ussuriense	Luferov	Byull. Moskovsk. Obshch. Isp. Prir., Otd. Biol. 94(5): 105 (1989)
Thalictrum affine	Ledeb.	Fl. Ross. 1: 10 (1841)
Thalictrum mazandaranicum	Pakravan & Assadi	Feddes Repert. 123: 69 (2012)
Thalictrum flavum subsp. simplex	(L.) O.Bolòs & Vigo	Fl. Països Catalans 1: 243 (1984)
Thalictrum simplex var. glandulosum	W.T.Wang	Fl. Reipubl. Popularis Sin. 26: 620 (1979)
Thalictrum simplex var. bauhini	(Crantz) Osvač.	Fl. Slovenska 3: 243 (1982)

Common names Top

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Filter by language:

Language	Common/alternative name
Belarusian	Пылюшнік просты
Czech	žluťucha jednoduchá
German	einfache wiesenraute
Estonian	liht-ängelhein
Finnish	hoikkaängelmä
Finnish	etelänhoikkaängelmä
Upper Sorbian	jednory žiwotnik
Japanese	シベリアノカラマツ
mn	Энгийн буржгар
Norwegian Bokmål	rankfrøstjerne
Dutch	onvertakte ruit
Polish	rutewka pojedyncza
Russian	Василистник простой
Russian	Василистник прямой
Russian	Василисник прямой
Russian	Василисник простой
Slovenian	enostavni talin
Swedish	backruta
Swedish	vanlig backruta
Chinese	水黄连
Chinese	箭头唐松草

Subspecies (abbr. subsp./ssp.) Top

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Name	Authority	First published in
Thalictrum simplex subsp. altaicum	(Schischk.) Hand	Revis. Europa Thalictrum subsect. Thalictrum (Ranunculac.) : 221 (2001)
Thalictrum simplex subsp. amurense	(Maxim.) Hand	Revis. Europa Thalictrum subsect. Thalictrum (Ranunculac.) : 222 (2001)
Thalictrum simplex subsp. boreale	(F.Nyl.) Á.Löve & D.Löve	Bot. Not. 114: 52 1961
Thalictrum simplex subsp. galioides	(DC.) Korsh.	Izv. Imp. Tomsk. Univ. 5(2): 113 (1893)
Thalictrum simplex subsp. gallicum	(Rouy & Foucaud) Tutin	Feddes Repert. Spec. Nov. Regni Veg. 69: 55. 1964 (1964)
Thalictrum simplex subsp. rhodopaeum	(Rech.f.) Panov ex S.Kožuharov & Petrova	Ann. Bot. Fenn. 25: 390 (1988)
Thalictrum simplex subsp. tenuifolium	(Hartm.) Sterner	Acta Phytogeogr. Suec. 9: 102. 1938

Varieties (abbr. var.) Top

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Name	Authority	First published in
Thalictrum simplex var. affine	(Ledeb.) Regel	Bull. Soc. Imp. Naturalistes Moscou 34: 44 1861

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

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Asia-temperate click to expand
- Caucasus
  - North Caucasus
  - Transcaucasus
- China
  - China North-central
  - China South-central
  - Inner Mongolia
  - Manchuria
  - Qinghai
  - Xinjiang
- Eastern Asia
  - Japan
  - Korea
- Middle Asia
  - Kazakhstan
  - Kirgizstan
  - Uzbekistan
- Mongolia
  - Mongolia
- Russian Far East
  - Amur
  - Khabarovsk
  - Magadan
  - Primorye
- Siberia
  - Altay
  - Buryatiya
  - Chita
  - Irkutsk
  - Krasnoyarsk
  - Tuva
  - West Siberia
  - Yakutskiya
- Western Asia
  - Iran
  - 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
  - Czechoslovakia
  - Germany
  - Hungary
  - Poland
  - Switzerland
- Northern Europe
  - Denmark
  - Finland
  - Norway
  - Sweden
- Southeastern Europe
  - Bulgaria
  - Greece
  - Italy
  - Romania
  - Yugoslavia
- Southwestern Europe
  - France

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000454093
Tropicos	27100527
INPN	126213
Flora of Italy	1209
KEW	urn:lsid:ipni.org:names:304708-2
The Plant List	kew-2512711
Missouri Botanical Garden	286148
Open Tree Of Life	243507
Observations.org	144892
NCBI Taxonomy	495765
NBN Atlas	NBNSYS0200003296
IPNI	304708-2
iNaturalist	362449
iNaturalist	362445
iNaturalist	362447
GBIF	7276649
EPPO	THCSI
EOL	2874010
Elurikkus	7905
USDA GRIN	36455
Wikipedia	Thalictrum_simplex
CMAUP	NPO21451
Plantarium	38108

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

Organization, Phylogenetic Marker Exploitation, and Gene Evolution in the Plastome of Thalictrum (Ranunculaceae)

Xiang KL, Mao W, Peng HW, Erst AS, Yang YX, He WC, Wu ZQ

Front Plant Sci

20-May-2022

PMCID:	PMC9166237
doi:	10.3389/fpls.2022.897843
PMID:	35668810

Inhibition of the main protease of SARS-CoV-2 (Mpro) by repurposing/designing drug-like substances and utilizing nature’s toolbox of bioactive compounds

Antonopoulou I, Sapountzaki E, Rova U, Christakopoulos P

Comput Struct Biotechnol J

14-Mar-2022

PMCID:	PMC8920478
doi:	10.1016/j.csbj.2022.03.009
PMID:	35308802

Potential Antiviral Action of Alkaloids

Abookleesh FL, Al-Anzi BS, Ullah A

Molecules

28-Jan-2022

PMCID:	PMC8839337
doi:	10.3390/molecules27030903
PMID:	35164173

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

Asymbiotic seed germination and in vitro seedling development of Orchis militaris, an endangered orchid in Siberia

Nabieva AY

J Genet Eng Biotechnol

19-Aug-2021

PMCID:	PMC8377116
doi:	10.1186/s43141-021-00223-1
PMID:	34410556

Carbohydrate storage in herbs: the forgotten functional dimension of the plant economic spectrum

Lubbe FC, Klimeš A, Doležal J, Jandová V, Mudrák O, Janeček Š, Bartušková A, Klimešová J

Ann Bot

17-Feb-2021

PMCID:	PMC8103809
doi:	10.1093/aob/mcab014
PMID:	33595601

Current Updates on Naturally Occurring Compounds Recognizing SARS-CoV-2 Druggable Targets

Romeo I, Mesiti F, Lupia A, Alcaro S

Molecules

26-Jan-2021

PMCID:	PMC7865633
doi:	10.3390/molecules26030632
PMID:	33530467

In silico analysis of selected alkaloids against main protease (Mpro) of SARS-CoV-2

Garg S, Roy A

Chem Biol Interact

09-Nov-2020

PMCID:	PMC7649659
doi:	10.1016/j.cbi.2020.109309
PMID:	33181114

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

Opportunities to integrate herders’ indicators into formal rangeland monitoring: an example from Mongolia

Jamsranjav C, Fernández‐Giménez ME, Reid RS, Adya B

Ecol Appl

17-May-2019

PMCID:	PMC6851969
doi:	10.1002/eap.1899
PMID:	31020715

The list of species registered in taiga meadow community during succession under enhanced radioactive background

Gruzdev B, Maystrenko T, Belykh E, Rybak A

Data Brief

05-May-2018

PMCID:	PMC5993173
doi:	10.1016/j.dib.2018.04.121
PMID:	29892628

Impact of selected drugs and their binary mixtures on the germination of Sorghum bicolor (sorgo) seeds

Wieczerzak M, Kudłak B, Namieśnik J

Environ Sci Pollut Res Int

29-Apr-2018

PMCID:	PMC6061511
doi:	10.1007/s11356-018-2049-4
PMID:	29705907

Discovery of thalicthuberine as a novel antimitotic agent from nature that disrupts microtubule dynamics and induces apoptosis in prostate cancer cells

Levrier C, Rockstroh A, Gabrielli B, Kavallaris M, Lehman M, Davis RA, Sadowski MC, Nelson CC

Cell Cycle

27-Jul-2017

PMCID:	PMC5976206
doi:	10.1080/15384101.2017.1356512
PMID:	28749250

Habitat requirements of endangered species in a former coppice of high conservation value

Roleček J, Vild O, Sladký J, Řepka R

02-Mar-2017

PMCID:	PMC6166777
doi:	10.1007/s12224-016-9276-6
PMID:	30283231

Responses of Plant Community Composition and Biomass Production to Warming and Nitrogen Deposition in a Temperate Meadow Ecosystem

Zhang T, Guo R, Gao S, Guo J, Sun W

PLoS One

13-Apr-2015

PMCID:	PMC4395313
doi:	10.1371/journal.pone.0123160
PMID:	25874975

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
Trigonelline	5570	Click to see	137.14	unknown	via CMAUP database
> Alkaloids and derivatives / 6,6a-secoaporphines
2-(1,2-dimethoxy-5,6-dihydronaphtho[2,1-f][1,3]benzodioxol-4-yl)-N,N-dimethylethanamine	5321909	Click to see	355.40	unknown	https://doi.org/10.1055/S-2006-959545
2-(1,2-dimethoxynaphtho[2,1-f][1,3]benzodioxol-4-yl)-N-methylethanamine	15286473	Click to see	339.40	unknown	https://doi.org/10.1016/0031-9422(95)00959-0 https://doi.org/10.1055/S-2006-959545
2-(1,2-dimethoxynaphtho[2,1-f][1,3]benzodioxol-4-yl)-N,N-dimethylethanamine oxide	163192322	Click to see	369.40	unknown	https://doi.org/10.1055/S-2006-959545
N-[2-(1,2-dimethoxynaphtho[2,1-f][1,3]benzodioxol-4-yl)ethyl]-N-methylhydroxylamine	15286475	Click to see CN(CCC1=CC(=C(C2=C1C=CC3=CC4=C(C=C32)OCO4)OC)OC)O	355.40	unknown	https://doi.org/10.1016/0031-9422(95)00959-0
N,N-dimethyl-2-(1,2,3-trimethoxynaphtho[2,1-f][1,3]benzodioxol-4-yl)ethanamine	183328	Click to see	383.40	unknown	https://doi.org/10.1016/0031-9422(95)00959-0
Thalicthuberine	11245138	Click to see CN(C)CCC1=CC(=C(C2=C1C=CC3=CC4=C(C=C32)OCO4)OC)OC	353.40	unknown	https://doi.org/10.1055/S-2006-959545
> Alkaloids and derivatives / Aporphines
(+)-Magnoflorine	73337	Click to see	342.40	unknown	https://doi.org/10.1007/BF00568555
(12R)-7,15,16,17-tetramethoxy-11-methyl-3,5-dioxa-11-azapentacyclo[10.7.1.02,6.08,20.014,19]icosa-1,6,8(20),14,16,18-hexaene	163069202	Click to see	399.40	unknown	https://doi.org/10.1016/0031-9422(94)00933-K
(12R)-7,16,17-trimethoxy-11-methyl-3,5-dioxa-11-azapentacyclo[10.7.1.02,6.08,20.014,19]icosa-1,6,8(20),14,16,18-hexaene	1600002	Click to see	369.40	unknown	https://doi.org/10.1016/0031-9422(95)00959-0
(12S)-7,15,16,17-tetramethoxy-11-methyl-11-oxido-3,5-dioxa-11-azoniapentacyclo[10.7.1.02,6.08,20.014,19]icosa-1,6,8(20),14,16,18-hexaene	15226560	Click to see	415.40	unknown	https://doi.org/10.1016/0031-9422(94)00933-K
(6aR)-1,2,3,9,10-pentamethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinoline	163083176	Click to see	385.50	unknown	https://doi.org/10.1016/0031-9422(95)00959-0
(6aR)-2,3,9,10-tetramethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinolin-1-ol	102284337	Click to see	371.40	unknown	https://doi.org/10.1016/0031-9422(95)00959-0
(6aR)-2,3,9,10-tetramethoxy-6-methyl-6-oxido-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinolin-6-ium-1-ol	163188419	Click to see	387.40	unknown	https://doi.org/10.1016/0031-9422(95)00959-0
(6aS)-1,2,3,9,10-pentamethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinoline	15726908	Click to see	385.50	unknown	https://doi.org/10.1016/0031-9422(95)00959-0 https://doi.org/10.1007/BF00568555
(6As)-2,9,10-trimethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinolin-1-ol	6992288	Click to see	341.40	unknown	https://doi.org/10.1016/0031-9422(95)00959-0 https://doi.org/10.1007/BF00568555
(6S,6aR)-2,3,9,10-tetramethoxy-6-methyl-6-oxido-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinolin-6-ium-1-ol	163193512	Click to see	387.40	unknown	https://doi.org/10.1016/0031-9422(95)00959-0
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://doi.org/10.1016/0031-9422(95)00959-0
7,15,16,17-Tetramethoxy-11-methyl-3,5-dioxa-11-azapentacyclo[10.7.1.02,6.08,20.014,19]icosa-1,6,8(20),14,16,18-hexaene	23258108	Click to see CN1CCC2=C3C1CC4=C(C(=C(C=C4C3=C5C(=C2OC)OCO5)OC)OC)OC	399.40	unknown	https://doi.org/10.1016/0031-9422(94)00933-K
Leucoxylonine	15226561	Click to see	399.40	unknown	https://doi.org/10.1016/0031-9422(94)00933-K
Ocotein	3083793	Click to see CN1CCC2=C3C1CC4=CC(=C(C=C4C3=C5C(=C2OC)OCO5)OC)OC	369.40	unknown	https://doi.org/10.1016/0031-9422(95)00959-0
Ocoteine	52499	Click to see	369.40	unknown	https://doi.org/10.1016/0031-9422(95)00959-0
Preocoteine	176968	Click to see CN1CCC2=C3C1CC4=CC(=C(C=C4C3=C(C(=C2OC)OC)O)OC)OC	371.40	unknown	https://doi.org/10.1016/0031-9422(95)00959-0
Purpureine	98473	Click to see	385.50	unknown	https://doi.org/10.1016/0031-9422(95)00959-0
Thalicminine	167534	Click to see	365.30	unknown	via CMAUP database
Thaliporphine	100020	Click to see	341.40	unknown	https://doi.org/10.1007/BF00568555
> Alkaloids and derivatives / Pavine alkaloids
(-)-Argemonine	442168	Click to see	355.40	unknown	https://doi.org/10.1055/S-2006-959665
(1R,12R)-15,16-dimethoxy-20-methyl-6,8-dioxa-20-azapentacyclo[10.7.1.02,10.05,9.013,18]icosa-2,4,9,13,15,17-hexaen-4-ol	163105392	Click to see CN1C2CC3=CC(=C(C=C3C1CC4=C5C(=C(C=C24)O)OCO5)OC)OC	355.40	unknown	https://doi.org/10.1055/S-2006-959665
(1S)-4,5,12,13-tetramethoxy-17-methyl-17-azatetracyclo[7.7.1.02,7.010,15]heptadeca-2,4,6,10,12,14-hexaene	44558920	Click to see	355.40	unknown	https://doi.org/10.1016/0040-4039(64)83163-4
4,15,16-Trimethoxy-20-methyl-6,8-dioxa-20-azapentacyclo[10.7.1.02,10.05,9.013,18]icosa-2,4,9,13,15,17-hexaene	85305513	Click to see	369.40	unknown	https://doi.org/10.1002/(SICI)1099-1573(199608)10:5<414::AID-PTR876>3.0.CO;2-5 https://doi.org/10.1021/NP50083A021
> Alkaloids and derivatives / Protoberberine alkaloids and derivatives
16,17-Dimethoxy-6-tritio-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-octaene	10246509	Click to see	338.40	unknown	via CMAUP database
Berberine	2353	Click to see	336.40	unknown	https://doi.org/10.1007/BF00568555
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	via CMAUP database
Jatrorrhizine	72323	Click to see	338.40	unknown	via CMAUP database
Jatrorrhizine iodide	5459338	Click to see COC1=C(C2=C[N+]3=C(C=C2C=C1)C4=CC(=C(C=C4CC3)O)OC)OC.[I-]	465.30	unknown	via CMAUP database
Palmatine	19009	Click to see	352.40	unknown	via CMAUP database
> Alkaloids and derivatives / Protopine alkaloids
7-Hydroxy-8-methoxy-11-methyl-17,19-dioxa-11-azatetracyclo[12.7.0.0(4,9).0(16,20)]henicosa-1(21),4(9),5,7,14,16(20)-hexaen-2-one	5321910	Click to see	355.40	unknown	https://doi.org/10.1007/BF00568555
Allocryptopine	98570	Click to see	369.40	unknown	https://doi.org/10.1007/BF00568555 https://doi.org/10.1007/BF00574647
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/10.1055/S-2006-959665
Pseudoprotopine	185559	Click to see CN1CCC2=CC3=C(C=C2C(=O)CC4=CC5=C(C=C4C1)OCO5)OCO3	353.40	unknown	via CMAUP database
> Lignans, neolignans and related compounds
(-)-Repandine	10031631	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)OC)OC	608.70	unknown	via CMAUP database
(1S,14S)-9,20,21,25-tetramethoxy-15,30-dimethyl-7,23-dioxa-15,30-diazaheptacyclo[22.6.2.23,6.18,12.114,18.027,31.022,33]hexatriaconta-3(36),4,6(35),8,10,12(34),18(33),19,21,24,26,31-dodecaen-19-ol	10627884	Click to see	638.70	unknown	via CMAUP database
1-Isotetrandrine	5351212	Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=C(O3)C(=C(C=C7CCN6C)OC)OC)OC)OC	622.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
5-Octadecenoic acid	53435893	Click to see	282.50	unknown	https://doi.org/10.1007/BF00568733
Palmitic Acid	985	Click to see	256.42	unknown	https://doi.org/10.1007/BF00630450
Stearic Acid	5281	Click to see	284.50	unknown	https://doi.org/10.1007/BF00630450
trans-5-Octadecenoic acid	5282753	Click to see	282.50	unknown	https://doi.org/10.1007/BF00568733
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides
campesterol-3-O-beta-d-glucoside	12895788	Click to see	562.80	unknown	https://doi.org/10.1007/BF00630450
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
beta-Sitosterol 3-O-beta-D-galactopyranoside	296119	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C	576.80	unknown	https://doi.org/10.1007/BF00630450
Sitogluside	5742590	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C	576.80	unknown	https://doi.org/10.1007/BF00630450
Stigmasterol Glucoside	6602508	Click to see	574.80	unknown	https://doi.org/10.1007/BF00630450
> 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
CID 6971145	6971145	Click to see	189.13	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Ethers / Diarylethers
21,22,26-Trimethoxy-16,31-dimethyl-8,24-dioxa-16,31-diazaheptacyclo[23.6.2.13,7.19,13.115,19.028,32.023,34]hexatriaconta-3(36),4,6,9,11,13(35),19,21,23(34),25,27,32-dodecaen-10-ol	45356938	Click to see	608.70	unknown	via CMAUP database
> Organoheterocyclic compounds / Benzodioxoles
11,12-Dimethoxy-6,8,9,15-tetrahydro[1,3]benzodioxolo[4,5-c]benzo[g]azecin-14(7H)-one	371229	Click to see COC1=C(C=C2C(=C1)CCNCC3=C(CC2=O)C=CC4=C3OCO4)OC	355.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
5-Hydroxy-2-(4-methoxyphenyl)-7-(3,4,5-trihydroxy-6-((3,4,5-trihydroxy-6-methyloxan-2-yl)oxymethyl)oxan-2-yl)oxychromen-4-one	5480901	Click to see	592.50	unknown	https://doi.org/10.1007/BF00630450
Linarin	5317025	Click to see	592.50	unknown	https://doi.org/10.1007/BF00630450
> Phenylpropanoids and polyketides / Tannins
5,6,6',7,12-Pentamethoxy-2-methyl-1',2'-didehydroberbaman	494542	Click to see CN1CCC2=C3C1CC4=CC(=C(C=C4)OC)OC5=CC=C(CC6=NCCC7=CC(=C(C=C76)OC3=C(C(=C2OC)OC)OC)OC)C=C5	636.70	unknown	via CMAUP database
Hernandezine	72343	Click to see	652.80	unknown	https://doi.org/10.1007/BF00568555
Hernandezine (7CI, 8CI)	362567	Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=C(CCN6C)C(=C(C(=C7O3)OC)OC)OC)OC)OC	652.80	unknown	via CMAUP database
Thalsimine	362568	Click to see CN1CCC2=C3C1CC4=CC(=C(C=C4)OC)OC5=CC=C(CC6=NCCC7=CC(=C(C=C76)OC3=C(C(=C2OC)OC)OC)OC)C=C5	636.70	unknown	https://doi.org/10.1007/BF00568555

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Thalictrum simplex

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