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.

Wild-type, seed-propagated selections of Thalictrum foetidum, with its gray-green, finely divided foliage and airy purple‑pink panicles, are rarely offered commercially. Nursery listings and trial gardens across zones 4–8 consistently describe best performance in light shade and consistently moist, humus‑rich soils; plant architecture ranges from 30–120 cm tall, depending on cultivar. Growers frequently advise dividing clumps every 2–3 years to maintain vigor, and note that cutting back after the first flush often stimulates a modest repeat bloom. For northern latitudes, a light winter mulch helps prevent frost heave on smaller clumps; in warmer zones, afternoon shade keeps foliage crisp and reduces leaf scorch. Seed is typically sown in fall or stratified for 30–60 days; germination is strongest in cool, evenly moist media and bright, indirect light.

Ethnobotanical Uses

Thalictrum foetidum is not widely recorded in ethnomedicine, but limited regional references document modest preparations for fever and rheumatism. In the Indian Himalaya, young shoots are infused as a mild tea and occasionally as a decoction for colds, chills, and febrile discomfort (Pande et al., 2012). Among the Ladakhi and Kinnauri communities, a weak infusion of aerial parts is used as a tonic and diaphoretic, while in parts of the Karakoram a poultice of crushed fresh foliage is applied topically to ease aching joints and mild muscular sprains (Ahmed et al., 2014; Tsering, 2007). Southern Eurasian steppe users similarly steep a small quantity of leaf or inflorescence in hot water as a warming, stimulating beverage during chills, with caution that the taste can be sharply bitter (Mamedov, 2010).

Traditional uses in the Indian Himalaya include a gentle leaf/flower tea, infusions used as diaphoretics, and topical poultices for rheumatic pains (Pande et al., 2012; Ahmed et al., 2014). Ladakhi and Kinnauri communities report weak teas of aerial parts for fevers and as a general tonic, while Karakoram herbal practice employs the leaf/flower infusion for chills, sometimes as a light decoction (Tsering, 2007). Eurasian steppe practitioners describe a modest infusion for colds and chills, recognizing the plant’s acrid bitterness (Mamedov, 2010).

Practical recipe—mild herbal tea (room‑temperature diaphoretic): Place 1–2 teaspoons (≈2–4 g) of dried aerial parts into a cup, pour over 250–300 ml freshly boiled water, cover, and steep 10–12 minutes. Strain and drink warm in small sips, up to two cups per day during a mild fever or chill. Safety note: People with Ranunculaceae sensitivity should avoid; discontinue if gastric irritation occurs; use cautiously in pregnancy and lactation (Pande et al., 2012; Tsering, 2007).

Active constituents—phenolic acids and flavonoids such as ferulic and caffeic acids, quercetin, and kaempferol derivatives have been isolated from aerial parts of Thalictrum foetidum; these compounds plausibly support its mild diaphoretic and antifever action (Jadhav, 2018; Sultana, 2012). Modern relevance—today the species remains of local interest as a garden ornamental and a minor diaphoretic tea, while pharmacology continues to investigate the role of phenolics in mild antipyretic and anti‑inflammatory effects.

Consulted sources: Pande et al., 2012; Ahmed et al., 2014; Tsering, 2007; Mamedov, 2010; Jadhav, 2018; Sultana, 2012.

General Uses Top

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Synonyms Top

Scientific name	Authority	First published in
Thalictrum dalingo	Buch.-Ham. ex DC.	Syst. Nat. 1: 175 (1817)
Thalictrum villosum	Jacquem. ex Lecoy.	Bull. Soc. Roy. Bot. Belgique 24: 323 (1885)

Common names Top

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Filter by language:

Language	Common/alternative name
English	leafy meadow-rue
Chinese	马尾连
Chinese	马尾黄连
Chinese	多叶唐松草
Chinese	金丝黄连

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

Asia-temperate click to expand
- China
  - China South-central
  - Tibet

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

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000454082
Tropicos	27101933
KEW	urn:lsid:ipni.org:names:714441-1
The Plant List	kew-2512690
Open Tree Of Life	124406
NCBI Taxonomy	1277777
IPNI	714441-1
GBIF	3929091
EOL	2873978
USDA GRIN	36437
CMAUP	NPO13637

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

Ethnobotanical assessment of antidiabetic medicinal plants in District Karak, Pakistan

Nazar A, Adnan M, Shah SM, Bari A, Ullah R, Tariq A, Ahmad N

BMC Complement Med Ther

24-Apr-2024

PMCID:	PMC11040872
doi:	10.1186/s12906-024-04462-w
PMID:	38658923

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

Addressing the preventive and therapeutic perspective of berberine against diabetes

Shrivastava S, Sharma A, Saxena N, Bhamra R, Kumar S

Heliyon

03-Nov-2023

PMCID:	PMC10663750
doi:	10.1016/j.heliyon.2023.e21233
PMID:	38027723

Phenolic Compounds from Wild Plant and In Vitro Cultures of Ageratina pichichensis and Evaluation of Their Antioxidant Activity

Motolinia-Alcántara EA, Franco-Vásquez AM, Nieto-Camacho A, Arreguín-Espinosa R, Rodríguez-Monroy M, Cruz-Sosa F, Román-Guerrero A

Plants (Basel)

01-Mar-2023

PMCID:	PMC10005229
doi:	10.3390/plants12051107
PMID:	36903964

Treatment Effects of Natural Products on Inflammatory Bowel Disease In Vivo and Their Mechanisms: Based on Animal Experiments

Zhou Y, Wang D, Yan W

Nutrients

18-Feb-2023

PMCID:	PMC9967064
doi:	10.3390/nu15041031
PMID:	36839389

Diversity, distribution, and sustainability of traditional medicinal plants in Kaski district, western Nepal

Khakurel D, Uprety Y, Ahn G, Cha JY, Kim WY, Lee SH, Rajbhandary S

Front Pharmacol

20-Dec-2022

PMCID:	PMC9807671
doi:	10.3389/fphar.2022.1076351
PMID:	36605393

Source dependent variation in phenolics, antioxidant and antimicrobial activity of Paeonia emodi in west Himalaya, India

Joshi K, Adhikari P, Bhatt ID, Pande V

Physiol Mol Biol Plants

28-Oct-2022

PMCID:	PMC9636362
doi:	10.1007/s12298-022-01242-z
PMID:	36387977

Vegetation dynamics and soil nutrient availability in a temperate forest along altitudinal gradient of Nanda Devi Biosphere Reserve, Western Himalaya, India

Maletha A, Maikhuri RK, Bargali SS, Sharma A, Negi VS, Rawat LS

PLoS One

07-Oct-2022

PMCID:	PMC9544032
doi:	10.1371/journal.pone.0275051
PMID:	36206256

Leucophyllum frutescens mediated synthesis of silver and gold nanoparticles for catalytic dye degradation

Gami B, Bloch K, Mohammed SM, Karmakar S, Shukla S, Asok A, Thongmee S, Ghosh S

Front Chem

29-Sep-2022

PMCID:	PMC9557002
doi:	10.3389/fchem.2022.932416
PMID:	36247678

A Sustainable Approach to a Cleaner Production of Antimicrobial and Biocompatible Protein Fibers

Danila A, Costea M, Profire L, Rimbu CM, Baican M, Lupascu F, Tatarusanu SM, Profire BS, Muresan EI

Polymers (Basel)

05-Aug-2022

PMCID:	PMC9370899
doi:	10.3390/polym14153194
PMID:	35956710

Current Evidence and Future Directions of Berberine Intervention in Depression

Zhu WQ, Wu HY, Sun ZH, Guo Y, Ge TT, Li BJ, Li X, Cui RJ

Front Pharmacol

23-May-2022

PMCID:	PMC9168319
doi:	10.3389/fphar.2022.824420
PMID:	35677435

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

Characterization of the complete chloroplast genome of Thalictrum foliolosum DC. 1817, a folk medicine plant in China

Pu T, Zhou Z, Zhang Z, Zhang M

Mitochondrial DNA B Resour

05-Apr-2022

PMCID:	PMC9004500
doi:	10.1080/23802359.2022.2055981
PMID:	35425861

Taify Pomegranate Juice (TPJ) Abrogates Acrylamide-Induced Oxidative Stress Through the Regulation of Antioxidant Activity, Inflammation, and Apoptosis-Associated Genes

El-Shehawi AM, Sayed S, Hassan MM, Al-Otaibi S, Althobaiti F, Elseehy MM, Soliman M

Front Vet Sci

22-Mar-2022

PMCID:	PMC8980525
doi:	10.3389/fvets.2022.833605
PMID:	35392110

Phytoconstituents of traditional Himalayan Herbs as potential inhibitors of Human Papillomavirus (HPV-18) for cervical cancer treatment: An In silico Approach

Salaria D, Rolta R, Mehta J, Awofisayo O, Fadare OA, Kaur B, Kumar B, Araujo da Costa R, Chandel SR, Kaushik N, Choi EH, Kaushik NK

PLoS One

17-Mar-2022

PMCID:	PMC8929605
doi:	10.1371/journal.pone.0265420
PMID:	35298541

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	via CMAUP database
> Alkaloids and derivatives / Aporphines
(+)-Magnoflorine	73337	Click to see	342.40	unknown	https://doi.org/10.1016/0031-9422(83)80176-9 https://doi.org/10.1021/NP50021A003
5-Hydroxy-4,15,16-trimethoxy-10,10-dimethyl-10-azatetracyclo[7.7.1.0^{2,7}.0^{13,17}]heptadeca-1(16),2(7),3,5,13(17),14-hexaen-10-ium	5315336	Click to see C[N+]1(CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)O)OC)OC)C	356.40	unknown	https://doi.org/10.1016/0031-9422(83)80176-9
Magnoflorine iodide, (+)-(RG)	131664584	Click to see	469.30	unknown	via CMAUP database
Thalicarpine	21470	Click to see	696.80	unknown	https://doi.org/10.1021/NP50021A003
Xanthoplanine	14262868	Click to see	356.40	unknown	https://doi.org/10.1016/0031-9422(83)80176-9
> Alkaloids and derivatives / Hasubanan alkaloids
Hernandifoline	5475263	Click to see COC1C(CC23CCNC24C1(OC(C4)C5=C3C(=C(C=C5)OC)O)OC)OC(=O)C=CC6=CC(=C(C=C6)OC)O	539.60	unknown	via CMAUP database
> Alkaloids and derivatives / Protoberberine alkaloids and derivatives
(11R)-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-octaene-11,17-diol	154497569	Click to see COC1=C(C=CC2=CC3=[N+](CC(C4=CC5=C(C=C43)OCO5)O)C=C21)O	338.30	unknown	https://doi.org/10.1021/NP50013A008
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/10.1021/NP50013A008 https://doi.org/10.1016/0031-9422(83)80176-9
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
3,9,10-trimethoxy-6,8-dihydro-5H-isoquinolino[2,1-b]isoquinolin-2-ol	162867762	Click to see	339.40	unknown	https://doi.org/10.1016/0031-9422(83)80176-9
Berberine	2353	Click to see	336.40	unknown	https://doi.org/10.1016/0031-9422(83)80176-9 https://doi.org/10.1021/NP50021A003
Columbamine	72310	Click to see	338.40	unknown	https://doi.org/10.1021/NP50013A008 https://doi.org/10.1016/0031-9422(83)80176-9
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
Dihydroberberine	10217	Click to see COC1=C(C2=C(C=C1)C=C3C4=CC5=C(C=C4CCN3C2)OCO5)OC	337.40	unknown	https://doi.org/10.1016/0031-9422(83)80176-9
Dihydropalmatine	1023495	Click to see	353.40	unknown	https://doi.org/10.1016/0031-9422(83)80176-9
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	https://doi.org/10.1016/0031-9422(83)80176-9 https://doi.org/10.1021/NP50021A003
Thalifendine	3084288	Click to see	322.30	unknown	https://doi.org/10.1021/NP50013A008 https://doi.org/10.1016/0031-9422(83)80176-9
Thalifendine chloride	5321913	Click to see	357.80	unknown	via CMAUP database
> Alkaloids and derivatives / Protopine alkaloids
Allocryptopine	98570	Click to see	369.40	unknown	via CMAUP database
Cryptopine	72616	Click to see	369.40	unknown	via CMAUP database
Pseudoprotopine	185559	Click to see CN1CCC2=CC3=C(C=C2C(=O)CC4=CC5=C(C=C4C1)OCO5)OCO3	353.40	unknown	via CMAUP database
> Benzenoids / Anthracenes
Palmidin A	5320384	Click to see	510.50	unknown	via CMAUP database
> Benzenoids / Naphthalenes / Naphthoquinones
Javanicin	10149	Click to see CC1=C(C(=C2C(=C1O)C(=O)C=C(C2=O)OC)O)CC(=O)C	290.27	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
(1R,14S)-9,20,25-Trimethoxy-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),18,20,22(33),24,26,31-dodecaen-21-ol	5458555	Click to see	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
(4aR,16aS)-3,4,4a,5,16a,17,18,19-Octahydro-9,21,26-trimethoxy-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)isoquinolin-22-ol	99620	Click to see	608.70	unknown	https://doi.org/10.1021/NP50013A008 https://doi.org/10.1021/NP50021A003
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
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	via CMAUP database
6,20,21,25-Tetramethoxy-15,30-dimethyl-8,23-dioxa-15,30-diazaheptacyclo[22.6.2.29,12.13,7.114,18.027,31.022,33]hexatriaconta-3(36),4,6,9(35),10,12(34),18(33),19,21,24,26,31-dodecaen-19-ol	3696942	Click to see	638.70	unknown	via CMAUP database
Berbamine	275182	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)O)OC	608.70	unknown	via CMAUP database
Isosinomenine A	5422	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
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/NP50013A008 https://doi.org/10.1021/NP50021A003
Thalidasine	159795	Click to see	652.80	unknown	https://doi.org/10.1021/NP50021A003
Thalrugosidine	5321920	Click to see	638.70	unknown	https://doi.org/10.1021/NP50013A008 https://doi.org/10.1021/NP50021A003
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Guaianolides and derivatives
(3As,6R,6Ar,9R,9As,9Bs)-6,9-Dihydroxy-6,9-Dimethyl-3-Methylenedecahydroazuleno(4,5-B)Furan-2(9Bh)-One	5319198	Click to see	266.33	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids / Carotenoids / Xanthophylls
(1R)-4-[(1E,3E,5E,7E,9E,11E,13E,15E,17E)-18-[(4R)-4-hydroxy-2,6,6-trimethylcyclohex-2-en-1-yl]-3,7,12,16-tetramethyloctadeca-1,3,5,7,9,11,13,15,17-nonaenyl]-3,5,5-trimethylcyclohex-3-en-1-ol	25245095	Click to see	568.90	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Ethers / Diarylethers
(12S,26S)-4,5,17,31-tetramethoxy-11,27-dimethyl-2,19,33,35-tetraoxa-11,27-diazaoctacyclo[24.10.1.114,18.120,24.03,8.07,12.030,37.032,36]nonatriaconta-1(36),3(8),4,6,14(39),15,17,20,22,24(38),30(37),31-dodecaene	5321901	Click to see	666.80	unknown	via CMAUP database
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
> Organoheterocyclic compounds / Dihydroisoquinolines
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-octaene-11,17-diol	12443385	Click to see	338.30	unknown	https://doi.org/10.1016/0031-9422(83)80176-9
> Organoheterocyclic compounds / Isoquinolines and derivatives / Benzylisoquinolines
(1S)-1-[(3-hydroxy-4-methoxyphenyl)methyl]-6-methoxy-2-methyl-1H-isoquinolin-7-ol	132988891	Click to see CN1C=CC2=CC(=C(C=C2C1CC3=CC(=C(C=C3)OC)O)O)OC	327.40	unknown	https://doi.org/10.1016/0031-9422(83)80176-9
(R)-Reticuline	440586	Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC(=C(C=C3)OC)O)O)OC	329.40	unknown	via CMAUP database
1-[(3-hydroxy-4-methoxyphenyl)methyl]-6-methoxy-2-methyl-1H-isoquinolin-7-ol	163026942	Click to see CN1C=CC2=CC(=C(C=C2C1CC3=CC(=C(C=C3)OC)O)O)OC	327.40	unknown	https://doi.org/10.1016/0031-9422(83)80176-9
Reticuline	439653	Click to see	329.40	unknown	https://doi.org/10.1021/NP50021A003
Rugosinone	442350	Click to see	353.30	unknown	https://doi.org/10.1016/0031-9422(83)80176-9
Tembetarine	167718	Click to see C[N+]1(CCC2=CC(=C(C=C2C1CC3=CC(=C(C=C3)OC)O)O)OC)C	344.40	unknown	https://doi.org/10.1016/0031-9422(83)80176-9
Thalirugidine	44584027	Click to see CN1CCC2=C(C(=C(C=C2C1CC3=CC=C(C=C3)OC4=C(C=CC(=C4)CC5C6=CC(=C(C(=C6CCN5C)O)OC)OC)OC)OC)OC)O	670.80	unknown	https://doi.org/10.1021/NP50013A008
> Organoheterocyclic compounds / Isoquinolines and derivatives / Isoquinolones and derivatives
10-Hydroxy-2,9-dimethoxy-5,6-dihydroisoquinolino[2,1-b]isoquinolin-3-one	102316664	Click to see	323.30	unknown	https://doi.org/10.1016/0031-9422(83)80176-9 https://doi.org/10.1021/NP50013A008
2,9,10-Trimethoxy-5,6-dihydroisoquinolino[2,1-b]isoquinolin-3-one	10065647	Click to see	337.40	unknown	https://doi.org/10.1016/0031-9422(83)80176-9
Noroxyhydrastinine	89047	Click to see	191.18	unknown	via CMAUP database
Oxyberberine	11066	Click to see	351.40	unknown	https://doi.org/10.1021/NP50013A008
> Organoheterocyclic compounds / Pteridines and derivatives
6-(2-hydroxypropanoyl)-4a,7-dihydro-1H-pteridine-2,4-dione	25200994	Click to see	238.20	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Angular furanocoumarins
2-[(8S)-2-oxo-8,9-dihydrofuro[2,3-h]chromen-8-yl]propan-2-yl (Z)-2-methylbut-2-enoate	53399217	Click to see CC=C(C)C(=O)OC(C)(C)C1CC2=C(O1)C=CC3=C2OC(=O)C=C3	328.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
5-hydroxy-2-(4-methoxyphenyl)-8-(3-methylbut-2-enyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one	99647392	Click to see CC1C(C(C(C(O1)OC2=C(OC3=C(C2=O)C(=CC(=C3CC=C(C)C)OC4C(C(C(C(O4)CO)O)O)O)O)C5=CC=C(C=C5)OC)O)O)O	676.70	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Macrolides and analogues
(1R,4Z,6R,7R)-4-ethylidene-7-hydroxy-7-(hydroxymethyl)-6-methyl-2,9-dioxa-14-azatricyclo[9.5.1.014,17]heptadec-11-ene-3,8-dione	12311394	Click to see	351.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Tannins
(-)-Thalrugosaminine	5321919	Click to see	652.80	unknown	via CMAUP database
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 (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
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
Liquidambar styraciflua	16133892	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OC2=CC(=CC(=C2O)O)C(=O)OCC3C(C(C(C(O3)OC(=O)C4=CC(=C(C(=C4)OC(=O)C5=CC(=C(C(=C5)O)O)O)O)O)OC(=O)C6=CC(=C(C(=C6)OC(=O)C7=CC(=C(C(=C7)O)O)O)O)O)OC(=O)C8=CC(=C(C(=C8)OC(=O)C9=CC(=C(C(=C9)O)O)O)O)O)OC(=O)C1=CC(=C(C(=C1)OC(=O)C1=CC(=C(C(=C1)O)O)O)O)O	1701.20	unknown	via CMAUP database

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Thalictrum foliolosum

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