Details Top

Internal ID UUID64401343a9040937006056
Scientific name Coptis chinensis
Authority Franch.
First published in J. Bot. (Morot) 11: 231 (1897)

Ethnobotanical Use Top

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Important notice
  • 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.

Coptis chinensis, known in Traditional Chinese Medicine as *Huang Lian* (gold‑thread), has a long history of use as an infusion and decoction. In the Han Chinese pharmacopeia, the dried root is boiled with water to produce a bitter tea that is taken for “heat” and “toxicity” in the stomach, treating diarrhea, dysentery, and abdominal pain (Chinese Pharmacopoeia, 2020). Among the Korean *Han Kang* practitioners, the same root is simmered for 30 minutes to make a decoction used to relieve stomach upset, fever, and sore throat (Korean Pharmacopoeia, 2018). In Japanese Kampo medicine, *Huang Lian* is combined with other herbs in a decoction to treat inflammatory bowel disease and to clear heat from the intestines (Kampo Handbook, 2019). All three traditions rely on the root, sometimes cut into small pieces, as the primary material for the infusion.

A simple, safe preparation is a 5‑gram decoction. Place 5 g of dried Coptis root in 200 mL of boiling water, reduce the heat, and simmer for 30 minutes. Strain the liquid, cool to a drinkable temperature, and sip one cup (≈200 mL) in the morning. Do not exceed 3 cups per day, and avoid use during pregnancy or lactation, as high doses can cause gastrointestinal upset and may affect fetal development. If you have liver or kidney disease, consult a healthcare professional before use.

The therapeutic effects of Coptis root are largely attributed to its alkaloid profile. Berberine, the most abundant constituent, has been shown to inhibit bacterial growth, reduce inflammation, and modulate glucose metabolism. Other alkaloids such as palmatine, jatrorrhizine, and coptisine also contribute to its antimicrobial and anti‑inflammatory properties. These compounds provide a biochemical basis for the traditional use of the root as a bitter, heat‑clearing decoction.

Modern research continues to validate the traditional claims. Recent clinical trials have examined berberine‑rich extracts for their efficacy in treating type 2 diabetes and dyslipidemia, and the root is now available as a standardized supplement in many health‑food stores. The enduring use of Coptis chinensis in East Asian medicine underscores its relevance as both a cultural heritage and a source of bioactive compounds for contemporary therapeutics.

General Uses Top

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Common products:
Commercial production centers on the isoquinoline alkaloid berberine, isolated as a high-purity, water-soluble extract from cultivated rhizomes of Coptis chinensis. Products include standardized berberine extracts for dye and specialty chemical use, and historical plant material traded as an ingredient in Chinese dye workshops.

Industrial and craft applications:
Berberine extracted from Coptis is employed as a bright yellow colorants for natural dye systems, particularly for protein fibers (silk, wool). Historical and modern references document its use for dyeing silk textiles and giving a yellow hue to yellow paper and other craft substrates. The colorant is applied via exhausted dye baths or post-mordanting routines analogous to those for other yellow plant dyes. For research, Coptis chinensis serves as a model organism for isoquinoline alkaloid biosynthesis; a high-quality genome assembly is available to support pathway and evolutionary studies.

Food and beverages (non-medicinal):
Coptis-derived berberine is used as a food-grade yellow colorant, specifically the hydrochloride salt (E100), in certain markets for confectionery and beverage coloring. Preparation involves extraction and acid-salt formation of the base; it is employed only as an approved color additive, with no application as a flavoring. Use scope varies by jurisdiction.

Colorants and tanning:
Berberine from Coptis chinensis provides an intense yellow dye for protein fibers. It is typically applied in aqueous solution under mildly acidic conditions; substantive binding to protein fibers allows direct dyeing without mordants in some processes. Its fluorescence under UV is noted in historical and modern textile dyeing descriptions; as a yellow dye, it is generally used on wool and silk rather than cotton. For tanning, Coptis is not a recognized tannin source.

Wood and fiber:
No documented uses of Coptis chinensis wood or bast fiber are recorded. Textiles dyed with Coptis-derived berberine include silk garments and craft textiles where the fiber is wool or silk dyed yellow.

Fragrance and cosmetics:
Although berberine is a colorant and trace component in some natural-dye formulations, there are no verified sources indicating its use as a fragrance or cosmetic additive, nor that Coptis chinensis contributes a fragrance profile in commercial products.

Properties relevant to use:
Berberine’s intense yellow coloration in aqueous and acidic media, with absorption in the yellow–green region, enables its use as a natural dye and food color. Solubility as the hydrochloride salt facilitates incorporation in aqueous dye baths and certain food applications. In research contexts, Coptis chinensis provides a valuable alkaloid-rich genotype for genetics and pathway studies; documented alkaloid accumulation under controlled cultivation conditions underpins dye/chemical extraction uses.

Standards and regulation:
Food colorant use of berberine hydrochloride is regulated as E100 (turmeric-derived colorants), with market-specific approvals; some jurisdictions do not permit berberine as a food color. Textile dye use is subject to standard fiber-specific fastness testing protocols rather than substance-specific standards; wastewater discharge of dye effluents is regulated locally.

Sustainability and sourcing:
Coptis chinensis is cultivated in China for alkaloid production; large-scale supply is met by agronomy, with wild harvesting discouraged. Sustainability considerations include crop yield stability and field cultivation practices; environmental controls for dye processing and waste management apply to downstream industrial use. Conservation status is documented in national Red List resources, further supporting cultivated sourcing.

Synonyms Top

Scientific name Authority First published in
Coptis chinensis var. angustiloba W.Y.Kong Bull. Bot. Res., Harbin 8(4): 109 (1988)
Coptis teeta var. chinensis (Franch.) Finet & Gagnep. Bull. Soc. Bot. France 51: 402 1904

Common names Top

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Language Common/alternative name
Arabic قبطيس صيني
cdo uòng-lièng
Korean 황련
lzh 黃連
Thai อึ่งน้อย
Vietnamese hoàng liên trung quốc
Chinese 鸡瓜莲
Chinese 黄连
Chinese 川莲
Chinese 黃連
Chinese 川连
Chinese 味连
Chinese 味莲
Chinese 黄莲 味莲、川莲、鸡瓜莲
Chinese 鸡爪连
Chinese 粪鬼伞

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

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
    • China
      • China North-central
      • China South-central
      • China Southeast

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000619848
UNII 67444F3ESD
Tropicos 27101250
KEW urn:lsid:ipni.org:names:710313-1
The Plant List kew-2736105
Open Tree Of Life 305766
NCBI Taxonomy 261450
IPNI 710313-1
iNaturalist 497721
GBIF 7277323
Freebase /m/027y7cx
EOL 2873644
USDA GRIN 402553
Wikipedia Coptis_chinensis
CMAUP NPO5649

Genomes (via NCBI) Top

Below is displayed the reference genome only!
If you wish to browse all genomes for this plant click here.
Accession Assembly
Name Level Submitter Released Coverage Size
GCA_015680905.1 ASM1568090v1 Chromosome Hubei University of Chinese Medicine 2020-12-01 73 892.31 Mb

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
Potential Effects of Traditional Chinese Medicine in Anti-Aging and Aging-Related Diseases: Current Evidence and Perspectives Ding X, Ma X, Meng P, Yue J, Li L, Xu L Clin Interv Aging 01-May-2024
PMCID:PMC11070163
doi:10.2147/CIA.S447514
PMID:38706635
Lipid metabolism disorder in diabetic kidney disease Han YZ, Du BX, Zhu XY, Wang YZ, Zheng HJ, Liu WJ Front Endocrinol (Lausanne) 29-Apr-2024
PMCID:PMC11089115
doi:10.3389/fendo.2024.1336402
PMID:38742197
The mechanisms of natural products for eye disorders by targeting mitochondrial dysfunction Sun GF, Qu XH, Jiang LP, Chen ZP, Wang T, Han XJ Front Pharmacol 25-Apr-2024
PMCID:PMC11079200
doi:10.3389/fphar.2024.1270073
PMID:38725662
Pathophysiology and management of testicular ischemia/reperfusion injury: Lessons from animal models Akhigbe RE, Odetayo AF, Akhigbe TM, Hamed MA, Ashonibare PJ Heliyon 21-Apr-2024
PMCID:PMC11058307
doi:10.1016/j.heliyon.2024.e27760
PMID:38694115
The Supplementation of Berberine in High-Carbohydrate Diets Improves Glucose Metabolism of Tilapia (Oreochromis niloticus) via Transcriptome, Bile Acid Synthesis Gene Expression and Intestinal Flora Liu H, Wei M, Tan B, Dong X, Xie S Animals (Basel) 20-Apr-2024
PMCID:PMC11047455
doi:10.3390/ani14081239
PMID:38672387
Active metabolites combination therapies: towards the next paradigm for more efficient and more scientific Chinese medicine Gao Q, Wu H, Chen M, Gu X, Wu Q, Xie T, Sui X Front Pharmacol 18-Apr-2024
PMCID:PMC11063311
doi:10.3389/fphar.2024.1392196
PMID:38698817
The gut-liver axis in fatty liver disease: role played by natural products Ming Z, Ruishi X, Linyi X, Yonggang Y, Haoming L, Xintian L Front Pharmacol 15-Apr-2024
PMCID:PMC11056694
doi:10.3389/fphar.2024.1365294
PMID:38686320
Obacunone, a Promising Phytochemical Triterpenoid: Research Progress on Its Pharmacological Activity and Mechanism Zhou Y, Gu J, Li J, Zhang H, Wang M, Li Y, Wang T, Wang J, Shi R Molecules 15-Apr-2024
PMCID:PMC11054759
doi:10.3390/molecules29081791
PMID:38675611
Multifaceted Materials for Enhanced Osteogenesis and Antimicrobial Properties on Bioplastic Polyetheretherketone Surfaces: A Review Bai Z, Zhao Y, Cui C, Yan J, Qin D, Tong J, Peng H, Liu Y, Sun L, Wu X, Li B, Li X ACS Omega 12-Apr-2024
PMCID:PMC11044237
doi:10.1021/acsomega.4c00923
PMID:38680314
Examining the Pathogenesis of MAFLD and the Medicinal Properties of Natural Products from a Metabolic Perspective Fu Y, Wang Z, Qin H Metabolites 12-Apr-2024
PMCID:PMC11052500
doi:10.3390/metabo14040218
PMID:38668346
Huanglian Jiedu decoction alleviates neurobehavioral damage in mice with chronic alcohol exposure through the RAS-RAF-MEK-ERK pathway Chen Y, Jiang L, Li M, Shen Y, Liu S, Yang D Heliyon 12-Apr-2024
PMCID:PMC11033144
doi:10.1016/j.heliyon.2024.e29556
PMID:38644875
Advances in the chemical constituents, pharmacological activity, and clinical application of Smilacis Glabrae Rhizoma: A review and predictive analysis of quality markers (Q-markers) Guo M, Zeng J, Wang Z, Shen Y Heliyon 12-Apr-2024
PMCID:PMC11031832
doi:10.1016/j.heliyon.2024.e29557
Huang Lian Jie Du Decoction enhances the anti-tumor efficacy of immune checkpoint inhibitors by activating TLR7/8 signalling in melanoma Liu S, Zhang Y, Zhu X, He S, Liu X, Lv X, Zuo F, Wu J BMC Complement Med Ther 11-Apr-2024
PMCID:PMC11007990
doi:10.1186/s12906-024-04444-y
PMID:38605368
Potential application mechanism of traditional Chinese medicine in treating immune checkpoint inhibitor-induced colitis Wang J, Guo Z, Shen M, Xie Q, Xiang H Front Immunol 10-Apr-2024
PMCID:PMC11039877
doi:10.3389/fimmu.2024.1366489
PMID:38660314
Traditional Chinese Medicine in Regulating Tumor Microenvironment Wang Z, Li M, Bi L, Hu X, Wang Y Onco Targets Ther 10-Apr-2024
PMCID:PMC11016250
doi:10.2147/OTT.S444214
PMID:38617090

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name PubChem ID Canonical SMILES MW Found in Proof
> Alkaloids and derivatives / Aporphines
(+)-Magnoflorine 73337 Click to see 342.40 unknown https://doi.org/10.1016/0021-9673(92)85319-O
(6As)-11-hydroxy-1,2,10-trimethoxy-6,6-dimethyl-5,6,6a,7-tetrahydro-4h-dibenzo[de,g]quinolinium 161487 Click to see 356.40 unknown via CMAUP database
Magnoflorine iodide, (+)-(RG) 131664584 Click to see 469.30 unknown via CMAUP database
Norisocorydine 12313549 Click to see 327.40 unknown via CMAUP database
> Alkaloids and derivatives / Benzophenanthridine alkaloids / Dihydrobenzophenanthridine alkaloids
Dihydrochelerythrine 485077 Click to see 349.40 unknown via CMAUP database
> Alkaloids and derivatives / Phthalide isoquinolines
(-)-Hydrastine 197835 Click to see 383.40 unknown via CMAUP database
(+)-Hydrastine 656743 Click to see 383.40 unknown via CMAUP database
(3S)-6,7-dimethoxy-3-(6-methyl-7,8-dihydro-5H-[1,3]dioxolo[4,5-g]isoquinolin-5-yl)-3H-2-benzofuran-1-one 371942 Click to see CN1CCC2=CC3=C(C=C2C1C4C5=C(C(=C(C=C5)OC)OC)C(=O)O4)OCO3 383.40 unknown via CMAUP database
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 via CMAUP database
> Alkaloids and derivatives / Protoberberine alkaloids and derivatives
10-Methoxy-5,6-dihydro-2H,9H-[1,3]dioxolo[4,5-g]isoquinolino[3,2-a]isoquinolin-9-one--hydrogen chloride (1/1) 85469308 Click to see 357.80 unknown via CMAUP database
13-Hydroxyberberine 24827073 Click to see COC1=C(C2=C[N+]3=C(C4=CC5=C(C=C4CC3)OCO5)C(=C2C=C1)O)OC.[Cl-] 387.80 unknown via CMAUP database
13-Methylberberine 148262 Click to see 350.40 unknown via CMAUP database
16-Methoxy-5,7-dioxa-1-azoniapentacyclo[11.8.0.03,11.04,8.014,19]henicosa-2,4(8),9,11,13,15,18-heptaen-17-one 101650328 Click to see 322.30 unknown via CMAUP database
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
17-Methoxy-5,7-dioxa-13-azoniapentacyclo[11.8.0.02,10.04,8.015,20]henicosa-1(21),2,4(8),9,14,17,19-heptaen-16-one 101280927 Click to see 322.30 unknown via CMAUP database
2-hydroxy-9,10-dimethoxy-6,7-dihydro-5H-isoquinolino[2,1-b]isoquinolin-7-ium-3-one 101404949 Click to see 324.30 unknown via CMAUP database
2,3,10-trimethoxy-6,7-dihydro-5H-isoquinolino[2,1-b]isoquinolin-7-ium-9-one 101280139 Click to see 338.40 unknown via CMAUP database
Berberastine 442180 Click to see COC1=C(C2=C[N+]3=C(C=C2C=C1)C4=CC5=C(C=C4C(C3)O)OCO5)OC 352.40 unknown https://doi.org/10.1002/PCA.2800050508
https://doi.org/10.1016/0021-9673(92)85319-O
Berberine 2353 Click to see 336.40 unknown https://doi.org/10.3892/IJMM_00000267
https://doi.org/10.1016/S0021-9673(96)00591-2
https://doi.org/10.1016/S0021-9673(98)00776-6
https://doi.org/10.1055/S-2001-10874
https://doi.org/10.1142/S0192415X05003557
https://doi.org/10.1016/S0021-9673(97)00972-2
https://doi.org/10.1002/PCA.2800050508
https://doi.org/10.1080/01483919008049572
https://doi.org/10.1111/J.1440-1681.2004.03951.X
https://doi.org/10.1016/0021-9673(92)85319-O
Berberine Chloride 12456 Click to see COC1=C(C2=C[N+]3=C(C=C2C=C1)C4=CC5=C(C=C4CC3)OCO5)OC.[Cl-] 371.80 unknown via CMAUP database
Columbamine 72310 Click to see 338.40 unknown https://doi.org/10.1016/S0021-9673(96)00591-2
https://doi.org/10.1016/0021-9673(92)85319-O
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/10.1016/S0021-9673(98)00776-6
https://doi.org/10.1111/J.1440-1681.2004.03951.X
https://doi.org/10.1016/0021-9673(92)85319-O
https://doi.org/10.1016/S0021-9673(96)00591-2
Coptisine hydrochloride 72321 Click to see 355.80 unknown via CMAUP database
Corysamine 147329 Click to see 334.30 unknown via CMAUP database
D-Tetrahydropalmatine 969488 Click to see COC1=C(C2=C(CC3C4=CC(=C(C=C4CCN3C2)OC)OC)C=C1)OC 355.40 unknown via CMAUP database
Dehydroapocavidine 9974201 Click to see 336.40 unknown via CMAUP database
DL-Tetrahydropalmatine 5417 Click to see COC1=C(C2=C(CC3C4=CC(=C(C=C4CCN3C2)OC)OC)C=C1)OC 355.40 unknown via CMAUP database
Epiberberine 160876 Click to see 336.40 unknown https://doi.org/10.1016/0021-9673(92)85319-O
https://doi.org/10.1016/S0021-9673(96)00591-2
https://doi.org/10.1016/S0021-9673(98)00776-6
Jatrorrhizine 72323 Click to see 338.40 unknown via CMAUP database
Jatrorrhizine Chloride 371256 Click to see COC1=C(C2=C[N+]3=C(C=C2C=C1)C4=CC(=C(C=C4CC3)O)OC)OC.[Cl-] 373.80 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/S0021-9673(98)00776-6
https://doi.org/10.1055/S-2001-10874
https://doi.org/10.1016/0021-9673(92)85319-O
https://doi.org/10.1016/S0021-9673(96)00591-2
Palmatine chloride 73442 Click to see COC1=C(C2=C[N+]3=C(C=C2C=C1)C4=CC(=C(C=C4CC3)OC)OC)OC.[Cl-] 387.90 unknown via CMAUP database
Palmatrubine 10547385 Click to see 373.80 unknown via CMAUP database
Pseudopalmatine 644002 Click to see COC1=C(C=C2C(=C1)CC[N+]3=CC4=CC(=C(C=C4C=C23)OC)OC)OC 352.40 unknown via CMAUP database
Stecepharine 15432813 Click to see C[N+]12CCC3=CC(=C(C(=C3C1CC4=C(C2)C(=C(C=C4)OC)O)O)OC)OC 372.40 unknown via CMAUP database
Tetrahydropalmatine 72301 Click to see COC1=C(C2=C(CC3C4=CC(=C(C=C4CCN3C2)OC)OC)C=C1)OC 355.40 unknown via CMAUP database
Tetrahydroscoulerine 45490416 Click to see 322.30 unknown via CMAUP database
Thalifendine 3084288 Click to see 322.30 unknown via CMAUP database
Thalifendine chloride 5321913 Click to see 357.80 unknown via CMAUP database
Worenine ion 20055073 Click to see 334.30 unknown via CMAUP database
> Benzenoids / Anthracenes
Palmidin A 5320384 Click to see 510.50 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Vanillic Acid 8468 Click to see COC1=C(C=CC(=C1)C(=O)O)O 168.15 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Cumenes
o-Cymene 10703 Click to see CC1=CC=CC=C1C(C)C 134.22 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
> Benzenoids / Phenols / Methoxyphenols
4-Hydroxy-3-methoxy-alpha-methylbenzyl Alcohol 17203 Click to see 168.19 unknown via CMAUP database
Eugenol 3314 Click to see 164.20 unknown via CMAUP database
> Hydrocarbons / Unsaturated hydrocarbons / Unsaturated aliphatic hydrocarbons
1-Tetradecene 14260 Click to see 196.37 unknown via CMAUP database
> Lignans, neolignans and related compounds
(1R,14R)-20,25-dimethoxy-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-dodecaene-9,21-diol 10257912 Click to see 594.70 unknown via CMAUP database
> Lignans, neolignans and related compounds / Aryltetralin lignans / 9,9p-dihydroxyaryltetralin lignans
(+)-Isolariciresinol 160521 Click to see 360.40 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans
(-)-Pinoresinol 12309636 Click to see 358.40 unknown via CMAUP database
(+-)-Pinoresinol 234817 Click to see 358.40 unknown via CMAUP database
4-[(3aR,6S,6aR)-6-(4-hydroxy-3-methoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-2-methoxyphenol 17750970 Click to see 358.40 unknown via CMAUP database
4-[(3R,3aR,6R,6aR)-6-(4-hydroxy-3-methoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-2-methoxyphenol 12309637 Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)OC)O 358.40 unknown via CMAUP database
4-[(3S,3aR,6aR)-3-(4-hydroxy-3-methoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-6-yl]-2,6-dimethoxyphenol 332425 Click to see 388.40 unknown via CMAUP database
4-[3-(4-Hydroxy-3-methoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-6-yl]-2,6-dimethoxyphenol 4546425 Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)OC 388.40 unknown via CMAUP database
Epipinoresinol 637584 Click to see 358.40 unknown via CMAUP database
Medioresinol, (+)- 181681 Click to see 388.40 unknown via CMAUP database
Pinoresinol 73399 Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)OC)O 358.40 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 7,9-epoxylignans
(-)-Lariciresinol 23815394 Click to see 360.40 unknown via CMAUP database
Lariciresinol 332427 Click to see COC1=C(C=CC(=C1)CC2COC(C2CO)C3=CC(=C(C=C3)O)OC)O 360.40 unknown via CMAUP database
Tetrahydro-2-(4-hydroxy-3-methoxyphenyl)-4-((4-hydroxy-3-methoxyphenyl)methyl)-3-furanmethanol 134203 Click to see 360.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters / Fatty acid methyl esters
Methyl Palmitate 8181 Click to see 270.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Myrcene 31253 Click to see 136.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
P-Cymene 7463 Click to see 134.22 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(L)-alpha-terpineol 443162 Click to see 154.25 unknown via CMAUP database
Alpha-Terpineol 17100 Click to see 154.25 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
beta-Cadinene 10657 Click to see 204.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
1H-Cycloprop[e]azulen-7-ol, decahydro-1,1,7-trimethyl-4-methylene-, [1ar-(1aalpha,4aalpha,7beta,7abeta,7balpha)]- 6432640 Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C 220.35 unknown via CMAUP database
beta-Spathulenol 522266 Click to see 220.35 unknown via CMAUP database
Npc143639 6432706 Click to see 220.35 unknown via CMAUP database
Spathulenol 92231 Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C 220.35 unknown via CMAUP database
Spathulenol, (-)- 13854255 Click to see 220.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
7-Isopropenyl-4a-methyl-1-methylenedecahydronaphthalene 519361 Click to see 204.35 unknown via CMAUP database
Beta-Selinene 442393 Click to see 204.35 unknown via CMAUP database
Npc246543 6432455 Click to see 204.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
[(1S,4aR,7S,7aS)-7-hydroxy-7-methyl-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-5-yl] (Z)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 6325178 Click to see CC1(CC(C2C1C(OC=C2)OC3C(C(C(C(O3)CO)O)O)O)OC(=O)C=CC4=CC(=C(C=C4)O)OC)O 524.50 unknown via CMAUP database
> 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 / Triterpenoids / Limonoids
Limonin 179651 Click to see 470.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Bile acids, alcohols and derivatives / Hydroxy bile acids, alcohols and derivatives / Trihydroxy bile acids, alcohols and derivatives
2,3-dimethyl-6-[(5S,10S,13R)-3,7,12-trihydroxy-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl]heptanoic acid 5322050 Click to see 464.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones
(1R,2R,7R,10R,13R,14R,16S,19R,20S)-19-(furan-2-yl)-9,9,13,20-tetramethyl-4,8,15-trioxahexacyclo[11.9.0.02,7.02,10.014,16.014,20]docosane-5,12,17-trione 45482319 Click to see 468.50 unknown via CMAUP database
(2E)-3-[(3aS,5aR,6R,7R,9aR,9bR,10aS)-3-(Furan-3-yl)-7-(2-hydroxypropan-2-yl)-3a,6,9a-trimethyl-1,9-dioxododecahydronaphtho[2,1-c]oxireno[d]pyran-6-yl]prop-2-enoic acid 54611038 Click to see 472.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones / Cardenolides and derivatives / Cardenolide glycosides and derivatives
Corchorozide A 56840797 Click to see CC1C(C(CC(O1)OC2CCC3(C4CCC5(C(CCC5(C4CCC3(C2)O)O)C6=CC(=O)OC6)C)C=O)O)O 534.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 Click to see 414.70 unknown via CMAUP database
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
Npc29 6432744 Click to see 414.70 unknown via CMAUP database
> Organic nitrogen compounds / Organonitrogen compounds / Quaternary ammonium salts / Cholines
Choline 305 Click to see 104.17 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
3-O-Feruloylquinic acid 9799386 Click to see 368.30 unknown via CMAUP database
4-O-Feruloylquinic acid 10177048 Click to see 368.30 unknown via CMAUP database
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 via CMAUP database
cis-Chlorogenic acid 1794425 Click to see 354.31 unknown via CMAUP database
Methyl 5-O-feruloylquinate 102004731 Click to see COC1=C(C=CC(=C1)C=CC(=O)OC2CC(CC(C2O)O)(C(=O)OC)O)O 382.40 unknown via CMAUP database
Npc196548 6171347 Click to see 368.30 unknown via CMAUP database
trans-(3S,5S)-1,3,5-trihydroxy-4-[(E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxycyclohexane-1-carboxylic acid 101024370 Click to see 368.30 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
Myrcenol 10975 Click to see CC(C)(CCCC(=C)C=C)O 154.25 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(2R,3R,4R,5S,6R)-2-[2-(3,4-dihydroxyphenyl)ethoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 6915839 Click to see 316.30 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
Gentisic Acid 5-O-Beta-Dglucopyranoside 10914066 Click to see 316.26 unknown via CMAUP database
> Organoheterocyclic compounds / Benzazepines
Chilenine 11025386 Click to see 383.40 unknown via CMAUP database
> Organoheterocyclic compounds / Isoquinolines and derivatives / Benzylisoquinolines
1-Benzylisoquinoline 23345 Click to see C1=CC=C(C=C1)CC2=NC=CC3=CC=CC=C32 219.28 unknown via CMAUP database
> 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/10.1055/S-2001-10874
https://doi.org/10.1016/0021-9673(92)85319-O
https://doi.org/10.1016/S0021-9673(96)00591-2
8-Oxocoptisine 5245667 Click to see 335.30 unknown via CMAUP database
Corydaldine 610097 Click to see 207.23 unknown via CMAUP database
Noroxyhydrastinine 89047 Click to see 191.18 unknown via CMAUP database
Oxyberberine 11066 Click to see 351.40 unknown via CMAUP database
Oxyberberrubine 5384082 Click to see COC1=C(C2=C(C=C1)C=C3C4=CC5=C(C=C4CCN3C2=O)OCO5)O 337.30 unknown via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Benzoquinolines / Phenanthridines and derivatives
17-Methoxy-13-methyl-5,7-dioxa-12-azapentacyclo[10.6.1.02,10.04,8.015,19]nonadeca-1(19),2,4(8),9,13,15,17-heptaen-11-one 44130138 Click to see CC1=CC2=CC(=CC3=C2N1C(=O)C4=CC5=C(C=C43)OCO5)OC 307.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
Caffeic acid n-octadecyl ester 71374400 Click to see 432.60 unknown via CMAUP database
Ferulate 54691413 Click to see 193.18 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
Ferulic Acid 445858 Click to see 194.18 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Coumarin glycosides
5-Methylcoumarin-4-cellobioside 196631 Click to see 500.40 unknown via CMAUP database
5-Methylcoumarin-4-gentiobioside 3080987 Click to see 500.40 unknown via CMAUP database
Gerberinside 196468 Click to see 338.31 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 / Coumarins and derivatives / Hydroxycoumarins
3,8-Dihydroxy-4-methoxy-2-oxochromene-5-carboxylic acid 3083044 Click to see COC1=C(C(=O)OC2=C(C=CC(=C21)C(=O)O)O)O 252.18 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 4-hydroxycoumarins
4-Hydroxy-5-methylcoumarin 54688203 Click to see 176.17 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Rhamnetin 5281691 Click to see 316.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Tricin 5281702 Click to see COC1=CC(=CC(=C1O)OC)C2=CC(=O)C3=C(C=C(C=C3O2)O)O 330.29 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
Wogonin 5281703 Click to see 284.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Hydroxyisoflavonoids
5,8-Dihydroxy-7-(4-hydroxy-5-methylcoumarin-3-yl)coumarin 54714258 Click to see 352.30 unknown via CMAUP database

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