Coptis teeta
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
Suggest a correction!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
Add a new one! Suggest a correction!| 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
Add a new one! Suggest a correction!| Name | Authority | First published in |
|---|---|---|
| Coptis teeta subsp. lohitensis | Pandit & Babu | Bot. J. Linn. Soc. 111: 377 (1993) |
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
Suggest others/fix!| 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.
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.
If you wish to see all the related articles click here.
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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