Details Top

Internal ID UUID64401344894b4920358794
Scientific name Coptis teeta
Authority Wall.
First published in Trans. Med. Phys. Soc. Calcutta 8: 87 (1836).

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.

Among the Sherpa of eastern Sikkim, India, dried rhizomes of Coptis teeta are boiled in water to make a bitter decoction that is taken for fever and diarrhoea (Singh & Chauhan, 2009). The Lepcha community of West Bengal/Darjeeling prepares an infusion of fresh rhizomes, drinking the warm liquid as a tonic that stimulates digestion and relieves dyspepsia (Koirala et al., 2018). In the Tibetan monastic practice of Bhutan, powdered root is macerated in about 45 % ethanol to produce a 1 : 5 w/v tincture that is administered in small drops for liver‑related complaints (Mishra et al., 2021). Nepalese healers also crush fresh rhizomes into a moist poultice and apply it topically to treat skin infections, citing the plant’s antimicrobial reputation (Singh & Chauhan, 2009). All of these applications rely on the rhizome, the part that contains the plant’s characteristic bitter alkaloids.

A simple, safe preparation of a mild tea (decoction) can be made from the dried, sliced rhizome. Measure about 2 g (roughly one level teaspoon) of dried Coptis teeta rhizome and place it in a pot with 200 ml of water. Bring the water to a boil, then reduce to a gentle simmer and keep it cooking for 10 minutes. Turn off the heat and allow the mixture to steep for an additional 5 minutes before straining the liquid. The resulting warm beverage can be sipped slowly. Do not exceed two cups per day. Because the herb contains berberine, which can stimulate uterine contractility, it is not recommended for pregnant or lactating women. People taking anticoagulants, antidiabetic medication, or drugs that affect liver enzymes should consult a healthcare professional before regular use.

Coptis teeta is chemically characterized by a suite of isoquinoline alkaloids: berberine, palmatine, coptisine, jatrorrhizine and columbamine have all been reported from the rhizome (Miller & Nakagawa, 2017; Duke, 2003). These compounds are well known for their antimicrobial, anti‑inflammatory and gastrointestinal‑calming actions, offering a plausible chemical basis for the plant’s traditional use against fever, dysentery and liver complaints.

Modern scientific work continues to validate the traditional indications; recent in‑vitro studies have demonstrated that the berberine‑rich extracts of Coptis teeta inhibit a range of gastrointestinal pathogens (Miller & Nakagawa, 2017). Dried rhizome material is now sold by several specialty herbal suppliers and a few commercial tincture preparations, while healers in the Eastern Himalaya still rely on the time‑honoured decoction and poultice for fever and digestive distress.

General Uses Top

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Scientific/model-organism use:
- The complete chloroplast genome of Coptis teeta (≈158 kb) has been sequenced and deposited in NCBI GenBank. The sequence is accessible through the NCBI Organelle Genome Resource and has been used in phylogenetic reconstructions of the genus and family (Liu et al., 2019).
- C. teeta is included in the DNA‑barcoding reference library compiled by the Consortium for the Barcode of Life (CBOL) Plant Working Group (2012), providing a reference for the standard plant barcodes rbcL and matK within Ranunculaceae.
- Roots of C. teeta supply berberine and coptisine, which are employed as certified reference standards in high‑performance liquid chromatography (HPLC) and LC‑MS for quantification of these alkaloids (Zhang et al., 2018). Standards are prepared by extraction from fresh root tissue and purification to ≥98 % purity, meeting the International Pharmacopoeia specifications for berberine chloride.

Properties relevant to use:
- Berberine exhibits a λmax at 345 nm with an extinction coefficient ≈20 000 L mol⁻¹ cm⁻¹, allowing sensitive UV detection. Coptisine shows fluorescence under 365 nm excitation, facilitating fluorescence detection. Dried root tissue contains up to 2 % (w/w) berberine and ~0.5 % coptisine, supporting efficient extraction for analytical standards.

Standards and regulation:
- The IUCN Red List (2022) classifies C. teeta as Vulnerable (VU) because of its limited geographic distribution and observed population decline.
- Laboratories that produce analytical reference materials from C. teeta must comply with ISO/IEC 17025:2017, which requires documented traceability and uncertainty assessment. The International Pharmacopoeia monograph for berberine chloride specifies a minimum purity of ≥98 %; berberine isolated from C. teeta meets this requirement.
- Scientific collection in the species’ native range (India, Bhutan, China, Nepal) requires national permits (e.g., India’s Wildlife Protection Act) and adherence to the Convention on Biological Diversity’s sustainable‑use guidelines.

Sustainability and sourcing:
- Sustainable harvesting recommendations include removing ≤10 % of mature individuals per population and avoiding collection during the flowering period. Seed germination after 4 weeks of cold stratification yields >70 % success, and rhizome division produces clonal plants within 6–8 weeks (Sharma et al., 2020).
- Ex situ conservation includes seed storage in the Millennium Seed Bank (Kew Gardens) under standard conditions (–20 °C, 5 % relative humidity) and living collections in Eastern Himalayan botanical gardens. These resources provide material for research while reducing pressure on wild populations.

Synonyms Top

Scientific name Authority First published in
Coptis teetoides C.Y.Cheng Acta Pharm. Sin. 12: 196 1965
Helleborus teeta Baill. Traité Bot. Méd. Phan. 1: 470 (1883)

Common names Top

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Language Common/alternative name
Arabic كوبتس تيتا
Burmese ခန်းတောက်ပင်နှင့် ခန်းတောက်မြစ်
Chinese 黄连
Chinese 云南黄连
Chinese 云南黄连*(云连、印度黄连、家黄连、云黄连)
Chinese 鸡脚黄连
Chinese 云连
Chinese 云黄连
Chinese 印度黄连
Chinese 家黄连

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Coptis teeta subsp. lohitensis Pandit & Babu Bot. J. Linn. Soc. 111: 377 (1993)

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

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000619879
UNII 89EY10LXBN
Tropicos 27104596
KEW urn:lsid:ipni.org:names:710326-1
The Plant List kew-2736135
Open Tree Of Life 830015
NCBI Taxonomy 261448
IUCN Red List 50126583
IPNI 710327-1
iNaturalist 497722
GBIF 7277297
Freebase /m/0405lfy
EOL 2873649
USDA GRIN 410462
Wikipedia Coptis_teeta
CMAUP NPO23519
CMAUP NPO29008

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_052059685.1 Cteeta_hap1_1.0 Chromosome Kunming Institution of Botany, Chinese Academy of Sciences 2025-08-15 32 841.41 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
Genome-wide identification and expression analysis of the C2H2-zinc finger transcription factor gene family and screening of candidate genes involved in floral development in Coptis teeta Wall. (Ranunculaceae) Duan SF, Zhao Y, Yu JC, Xiang GS, Xiao L, Cui R, Hu QQ, Baldwin TC, Lu YC, Liang YL Front Genet 22-Jan-2024
PMCID:PMC10839097
doi:10.3389/fgene.2024.1349673
PMID:38317660
Study on medicinal food plants in the Gaoligongshan Biosphere Reserve, the richest biocultural diversity center in China Cheng Z, Lin S, Wu Z, Lin C, Zhang Q, Xu C, Li J, Long C J Ethnobiol Ethnomed 15-Jan-2024
PMCID:PMC10790445
doi:10.1186/s13002-023-00638-9
PMID:38225656
Targeting key RNA methylation enzymes to improve the outcome of colorectal cancer chemotherapy (Review) Shao C, Han Y, Huang Y, Zhang Z, Gong T, Zhang Y, Tian X, Fang M, Han X, Li M Int J Oncol 19-Dec-2023
PMCID:PMC10783943
doi:10.3892/ijo.2023.5605
PMID:38131226
Transcriptome and Metabolome Analysis of Isoquinoline Alkaloid Biosynthesis of Coptis chinensis in Different Years Min X, Zhu T, Hu X, Hou C, He J, Liu X Genes (Basel) 18-Dec-2023
PMCID:PMC10742649
doi:10.3390/genes14122232
PMID:38137054
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
Comparative study on main compounds and hypoglycemic effects of dispensing granules of Coptidis Rhizoma and Scutellaria–Coptis herb couple with traditional decoction Yu H, Tang H, Hu G, Chen Z, Guo M, Jiang B, Zhang E, Hu C Chin Med 31-Oct-2023
PMCID:PMC10617169
doi:10.1186/s13020-023-00848-z
PMID:37907988
Protective Application of Chinese Herbal Compounds and Formulae in Intestinal Inflammation in Humans and Animals Yang Y, Xiao G, Cheng P, Zeng J, Liu Y Molecules 26-Sep-2023
PMCID:PMC10574200
doi:10.3390/molecules28196811
PMID:37836654
Modern drug discovery using ethnobotany: A large-scale cross-cultural analysis of traditional medicine reveals common therapeutic uses Domingo-Fernández D, Gadiya Y, Mubeen S, Bollerman TJ, Healy MD, Chanana S, Sadovsky RG, Healey D, Colluru V iScience 25-Aug-2023
PMCID:PMC10494464
doi:10.1016/j.isci.2023.107729
PMID:37701812
Effect of heat-clearing and dampness-eliminating Chinese medicine for high-risk cervical cancer papillomavirus infection: a systematic review and meta-analysis of randomized controlled trials Huang S, Qi Y, Chen S, He B, Chen X, Xu J Front Med (Lausanne) 24-Aug-2023
PMCID:PMC10484520
doi:10.3389/fmed.2023.1022030
PMID:37692777
Therapeutic potential of Coptis chinensis for arthritis with underlying mechanisms Li M, Tian F, Guo J, Li X, Ma L, Jiang M, Zhao J Front Pharmacol 11-Aug-2023
PMCID:PMC10450980
doi:10.3389/fphar.2023.1243820
PMID:37637408
Biologically Active Compounds from Probiotic Microorganisms and Plant Extracts Used as Biopreservatives Teneva D, Denev P Microorganisms 27-Jul-2023
PMCID:PMC10458850
doi:10.3390/microorganisms11081896
PMID:37630457
Recent trends of machine learning applied to multi-source data of medicinal plants Zhang Y, Wang Y J Pharm Anal 25-Jul-2023
PMCID:PMC10785154
doi:10.1016/j.jpha.2023.07.012
PMID:38223450
Coptisine Inhibits Influenza Virus Replication by Upregulating p21 He MF, Liang JH, Shen YN, Zhang CW, Yang KY, Liu LC, Xie Q, Hu C, Song X, Wang Y Molecules 14-Jul-2023
PMCID:PMC10386263
doi:10.3390/molecules28145398
PMID:37513270
From Xiaoke to diabetes mellitus: a review of the research progress in traditional Chinese medicine for diabetes mellitus treatment Meng X, Liu X, Tan J, Sheng Q, Zhang D, Li B, Zhang J, Zhang F, Chen H, Cui T, Li M, Zhang S Chin Med 22-Jun-2023
PMCID:PMC10288731
doi:10.1186/s13020-023-00783-z
PMID:37349778
Phytochemicals as Antimicrobials: Prospecting Himalayan Medicinal Plants as Source of Alternate Medicine to Combat Antimicrobial Resistance Ashraf MV, Pant S, Khan MA, Shah AA, Siddiqui S, Jeridi M, Alhamdi HW, Ahmad S Pharmaceuticals (Basel) 15-Jun-2023
PMCID:PMC10302623
doi:10.3390/ph16060881
PMID:37375828

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 via CMAUP database
(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 via CMAUP database
Berberine 2353 Click to see 336.40 unknown via CMAUP database
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 via CMAUP database
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
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 via CMAUP database
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 via CMAUP database
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 / 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
d-beta-Phellandrene 442484 Click to see 136.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
beta-Cadinene 10657 Click to see CC1=CCC2C(C1)C(CC=C2C)C(C)C 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 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 / 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 / Sugar alcohols
Mannitol 6251 Click to see 182.17 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
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 C1CNC(=O)C2=CC3=C(C=C21)OCO3 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
> 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 / Flavonoids / Flavones / Flavonols
Rhamnetin 5281691 Click to see 316.26 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

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