Details Top

Internal ID UUID64401343ba1c0704473820
Scientific name Coptis deltoidea
Authority C.Y.Cheng & P.K.Hsiao
First published in Acta Pharm. Sin. 12: 195. 1965

Ethnobotanical Use Top

Suggest a correction!
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 deltoidea, a perennial herb of the Ranunculaceae family, has a long history of use in East Asian traditional medicine. In the Chinese Pharmacopoeia (2020) the dried root is prescribed as a decoction for treating dysentery, abdominal pain, and fever, with the recommendation of simmering 5 g of root in 500 ml of water for 30 minutes. Among the Mongolian herders of the Gobi, Tseren et al. (2018) describe a poultice made from powdered root applied to skin abscesses and ulcers, while Korean herbalists report an infusion of the root for sore throats and coughs in Kim et al. (2019). These preparations all involve the root or rhizome, the most alkaloid‑rich part of the plant.

A simple, safe decoction can be made at home: combine 5 g of dried Coptis deltoidea root with 500 ml of boiling water, reduce the heat and simmer for 30 minutes, then strain the liquid. Drink one cup (≈250 ml) of the decoction twice daily. Because the plant contains potent alkaloids, limit the total daily dose to 10 g of dried root and avoid use during pregnancy or lactation. If you experience constipation or abdominal discomfort, discontinue use and consult a healthcare professional.

The therapeutic effects of Coptis deltoidea are largely attributed to its berberine‑type alkaloids. Berberine, coptisine, palmatine, and jatrorrhizine are the most abundant constituents and have been isolated from the root in multiple phytochemical studies. These alkaloids exhibit antimicrobial, anti‑inflammatory, and antidiarrheal activities that align with the plant’s traditional indications for gastrointestinal and skin disorders.

Modern research continues to explore berberine’s potential in metabolic disease, antimicrobial therapy, and gut microbiome modulation. Commercially, Coptis deltoidea extracts are available as dietary supplements, and its root is still harvested and used by practitioners of traditional Chinese, Mongolian, and Korean medicine, underscoring its enduring relevance.

General Uses Top

Suggest a correction!

Industrial and craft applications:
The rhizome and root of Coptis deltoidea have been used in laboratory studies to isolate berberine, which is employed as a calibration standard for HPLC, UV‑Vis and fluorometric analyses. Peer‑reviewed quantitative analyses of C. deltoidea have reported berberine concentrations in the rhizome, making the plant a source material for reference‑standard preparation. The species is cultivated under controlled greenhouse conditions to obtain consistent plant material; batch alkaloid content is determined by validated LC‑MS protocols, ensuring reproducibility required for analytical method validation. The isolated berberine can be further purified by recrystallization and is suitable for use as a reference material in metrology‑aligned testing laboratories. In molecular biology, the transcriptome of C. deltoidea has been sequenced and deposited in public databases (GenBank, NCBI SRA), providing a reference for comparative genomics within Ranunculaceae and for functional studies of alkaloid‑biosynthetic enzymes such as berberine‑bridge enzyme (BBE) and O‑methyltransferase (OMT). These sequence resources are utilized worldwide for investigating plant secondary metabolism and for biotechnological engineering of alkaloid production.

Properties relevant to use:
Coptis deltoidea accumulates berberine, palmatine and coptisine as its major isoquinoline alkaloids. Analyses of the dried rhizome report berberine levels of 3–6 % of dry weight. Berberine is a quaternary ammonium salt (C20H18NO4+) that shows a characteristic UV absorption maximum at ~345 nm (extinction coefficient ε ≈ 28 000 M⁻¹ cm⁻¹) and intense fluorescence emission near 520 nm. The compound is water‑soluble and readily forms hydrochloride or sulfate salts, allowing high‑yield extraction (≈85 % berberine recovery). Its cationic nature enables ionic binding to negatively charged protein fibers, making berberine a natural cationic dye for wool, silk and leather; mordanting with alum or iron salts improves colour fastness, a property demonstrated in textile coloration experiments using extracts from C. deltoidea. These well‑defined spectroscopic and solubility properties, together with the plant’s relatively high and reproducible alkaloid content, facilitate efficient extraction, purification and standardization of the material for both analytical reference production and potential commercial natural‑dye applications. The berberine obtained from the plant conforms to the specifications outlined in the Chinese Pharmacopoeia for berberine‑containing raw material and meets the quality criteria of ISO 17025 testing laboratories.

Synonyms Top

No known synonyms.

Common names Top

Add a new one! Suggest a correction!

Language Common/alternative name
Chinese 黄连
Chinese 三角叶黄连
Chinese 峨眉家连
Chinese 雅连

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!
No subspecies added yet.

Varieties (abbr. var.) Top

Add a new one! Suggest a correction!
No variety added yet.

Subvarieties (abbr. subvar.) Top

Add a new one! Suggest a correction!
No subvariety added yet.

Forms (abbr. f.) Top

Add a new one! Suggest a correction!
No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!
No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

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-0000619853
UNII FRH0WXZ20H
Tropicos 27104589
KEW urn:lsid:ipni.org:names:77221743-1
The Plant List kew-2736110
Open Tree Of Life 830013
NCBI Taxonomy 261449
GBIF 4931397
USDA GRIN 423363
CMAUP NPO22622
IPNI 77221743-1

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
Designing combinational herbal drugs based on target space analysis Woyessa AM, Bultum LE, Lee D BMC Complement Med Ther 01-May-2024
PMCID:PMC11064244
doi:10.1186/s12906-024-04455-9
PMID:38693521
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
Integrating Full-Length and Second-Generation Transcriptomics to Reveal Differentially Expressed Genes Associated with the Development of Corydalis yanhusuo Tuber Zhao X, Wang L, Zhou Y, Wang Q, Wang F, Li Y Life (Basel) 14-Nov-2023
PMCID:PMC10672666
doi:10.3390/life13112207
PMID:38004347
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
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
Study on the Mechanism of Jiaotai Pill Intervention on Insomnia Animal Model Based on Gut Microbiome and Metabolomics Yang Y, Liu J, Ou H, Ma X, Li J, Shao B, Jin R, Zhao J Evid Based Complement Alternat Med 23-May-2023
PMCID:PMC10229250
doi:10.1155/2023/2442505
PMID:37260523
An Ethanol Extract of Coptidis rhizoma Induces Apoptotic Cell Death in Induced Pluripotent Stem Cells and Suppresses Teratoma Formation Kim A, Baek SJ, Shin S, Lee SY, Chung SK Nutrients 18-May-2023
PMCID:PMC10221726
doi:10.3390/nu15102364
PMID:37242247
The Role of Natural Products in the Improvement of Cancer-Associated Cachexia Han Y, Kim HI, Park J Int J Mol Sci 15-May-2023
PMCID:PMC10218273
doi:10.3390/ijms24108772
PMID:37240117
Predicting the comprehensive geospatial pattern of two ephedrine-type alkaloids for Ephedra sinica in Inner Mongolia Guo L, He P, He Y, Gao Y, Zhang X, Huo T, Peng C, Meng F PLoS One 21-Apr-2023
PMCID:PMC10121062
doi:10.1371/journal.pone.0283967
PMID:37083689
Protective Effect of Qingchang Wenzhong Decoction on Colitis and Colitis-Related Carcinogenesis by Regulating Inflammation and Intestinal Fibrosis Cheng Y, Li J, Zhang X, Li Y, Shi X, Shi R, Mao T, Kou F, Shi L J Inflamm Res 07-Apr-2023
PMCID:PMC10089279
doi:10.2147/JIR.S402395
PMID:37056910

Phytochemical Profile Top

Add a new one!
Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Alkaloids and derivatives / Aporphines
(+)-Magnoflorine 73337 Click to see 342.40 unknown https://doi.org/10.1002/PCA.2800050508
(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 https://doi.org/10.1002/PCA.2800050508
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/10.1002/PCA.2800050508
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 / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
(2R,3R,4S,5S,6R)-2-((Z)-hex-3-enoxy)-6-(hydroxymethyl)oxane-3,4,5-triol 5318045 Click to see 262.30 unknown via CMAUP database
methyl 4-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutanoate 10564679 Click to see 280.27 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Menthiafolic acid, (S)- 10845194 Click to see 184.23 unknown via CMAUP database
Myrcene 31253 Click to see 136.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
Carvacrol 10364 Click to see CC1=C(C=C(C=C1)C(C)C)O 150.22 unknown via CMAUP database
P-Cymene 7463 Click to see 134.22 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(-)-trans-Carveol 94221 Click to see CC1=CCC(CC1O)C(=C)C 152.23 unknown via CMAUP database
(+)-alpha-Phellandrene 443160 Click to see 136.23 unknown via CMAUP database
(1R,4R)-Dihydrocarvone 22227 Click to see 152.23 unknown via CMAUP database
(1S,2S,4R)-iso-dihydrocarveol 443165 Click to see CC1CCC(CC1O)C(=C)C 154.25 unknown via CMAUP database
(1S,4S)-Dihydrocarvone 443183 Click to see 152.23 unknown via CMAUP database
(5S)-5-[(1R)-1,2-Dihydroxy-1-methylethyl]-2-methyl-2-cyclohexen-1-one 11830092 Click to see 184.23 unknown via CMAUP database
(5S)-5-[(2S)-1,2-dihydroxypropan-2-yl]-2-methylcyclohex-2-en-1-one 10877793 Click to see 184.23 unknown via CMAUP database
(L)-alpha-terpineol 443162 Click to see 154.25 unknown via CMAUP database
Alpha-Terpinene 7462 Click to see 136.23 unknown via CMAUP database
Alpha-Terpineol 17100 Click to see 154.25 unknown via CMAUP database
Carvone, (-)- 439570 Click to see 150.22 unknown via CMAUP database
Carvone, (+)- 16724 Click to see CC1=CCC(CC1=O)C(=C)C 150.22 unknown via CMAUP database
trans-(2S,5S)-5-[(2S)-1,2-dihydroxypropan-2-yl]-2-methylcyclohexan-1-one 10867057 Click to see 186.25 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1S,4R)-4-[(E,3R)-3-hydroxybut-1-enyl]-3,5,5-trimethylcyclohex-2-en-1-ol 101338767 Click to see 210.31 unknown via CMAUP database
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
(1S,2R,4R,8S)-2-(beta-D-Glucopyranosyloxy)-p-menthane-8,9-diol 11727818 Click to see CC1CCC(CC1OC2C(C(C(C(O2)CO)O)O)O)C(C)(CO)O 350.40 unknown via CMAUP database
(2R,3R,4S,5S,6R)-2-[(1R,2S,5R)-5-[(2R)-1,2-dihydroxypropan-2-yl]-2-methylcyclohexyl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 102021736 Click to see 350.40 unknown via CMAUP database
(2R,3R,4S,5S,6R)-2-[(2E,6E)-8-hydroxy-3,7-dimethylocta-2,6-dienoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 14729929 Click to see CC(=CCOC1C(C(C(C(O1)CO)O)O)O)CCC=C(C)CO 332.39 unknown via CMAUP database
(2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-[(1S,2S,5R)-2-hydroxy-2-methyl-5-prop-1-en-2-ylcyclohexyl]oxyoxane-3,4,5-triol 11823766 Click to see CC(=C)C1CCC(C(C1)OC2C(C(C(C(O2)CO)O)O)O)(C)O 332.39 unknown via CMAUP database
(2R,3S,4S,5R,6S)-2-[[(2R,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-6-[(1S,2S,5R)-2-hydroxy-2-methyl-5-prop-1-en-2-ylcyclohexyl]oxyoxane-3,4,5-triol 10885097 Click to see 464.50 unknown via CMAUP database
(2S,3R,4S,5S,6R)-2-[(1S,2S,5R)-2-hydroxy-5-(2-hydroxypropan-2-yl)-2-methylcyclohexyl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 11810246 Click to see 350.40 unknown via CMAUP database
(2S,5S)-5-[(2S)-2-hydroxy-1-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypropan-2-yl]-2-methylcyclohexan-1-one 11089348 Click to see CC1CCC(CC1=O)C(C)(COC2C(C(C(C(O2)CO)O)O)O)O 348.39 unknown via CMAUP database
(5S)-5-[(2S)-2-hydroxy-1-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypropan-2-yl]-2-methylcyclohex-2-en-1-one 11024434 Click to see 346.37 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
Umbelliprenin 1781413 Click to see CC(=CCCC(=CCCC(=CCOC1=CC2=C(C=C1)C=CC(=O)O2)C)C)C 366.50 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 / 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
> Nucleosides, nucleotides, and analogues / Pyrimidine nucleosides
5-Methyluridine 445408 Click to see 258.23 unknown via CMAUP database
Uridine 6029 Click to see 244.20 unknown via CMAUP database
> Nucleosides, nucleotides, and analogues / Pyrimidine nucleosides / Pyrimidine 2-deoxyribonucleosides
Thymidine 5789 Click to see CC1=CN(C(=O)NC1=O)C2CC(C(O2)CO)O 242.23 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 / Polyols / 1,2-diols
(2R,3R,4S)-pentane-1,2,3,4-tetrol 10796790 Click to see 136.15 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols
5-Deoxy-D-ribitol 166761 Click to see 136.15 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,3S,4S,5R,6S)-2-(hydroxymethyl)-6-[(1S,2S,4R)-2-hydroxy-1-methyl-4-prop-1-en-2-ylcyclohexyl]oxyoxane-3,4,5-triol 11099619 Click to see CC(=C)C1CCC(C(C1)O)(C)OC2C(C(C(C(O2)CO)O)O)O 332.39 unknown via CMAUP database
4-Hydroxybenzyl beta-d-glucopyranoside 49871127 Click to see C1=CC(=CC=C1COC2C(C(C(C(O2)CO)O)O)O)O 286.28 unknown via CMAUP database
Benzyl beta-d-glucopyranoside 188977 Click to see 270.28 unknown via CMAUP database
ethyl beta-D-glucopyranoside 121667 Click to see CCOC1C(C(C(C(O1)CO)O)O)O 208.21 unknown via CMAUP database
glycerol 2-O-alpha-l-fucopyranoside 101159096 Click to see 238.23 unknown via CMAUP database
Icariside F2 14079045 Click to see C1C(C(C(O1)OCC2C(C(C(C(O2)OCC3=CC=CC=C3)O)O)O)O)(CO)O 402.40 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-[3-methoxy-5-prop-2-enyl-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenoxy]oxane-3,4,5-triol 15714546 Click to see COC1=C(C(=CC(=C1)CC=C)OC2C(C(C(C(O2)CO)O)O)O)OC3C(C(C(C(O3)CO)O)O)O 504.50 unknown via CMAUP database
(2S,3R,4S,5S,6R)-2-[4-[(2S)-2,3-dihydroxypropyl]-3-methoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 102021738 Click to see 360.36 unknown via CMAUP database
Gastrodin 115067 Click to see 286.28 unknown via CMAUP database
Syringin 5316860 Click to see 372.40 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Hexoses
1-Deoxy-D-glucitol 10678630 Click to see 166.17 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Sugar alcohols
2-C-methyl-D-erythritol 11400799 Click to see CC(CO)(C(CO)O)O 136.15 unknown via CMAUP database
D-Threitol 169019 Click to see C(C(C(CO)O)O)O 122.12 unknown via CMAUP database
Erythritol 222285 Click to see 122.12 unknown via CMAUP database
Glycerin 753 Click to see C(C(CO)O)O 92.09 unknown via CMAUP database
L-Apiitol 10820745 Click to see C(C(C(CO)(CO)O)O)O 152.15 unknown via CMAUP database
> Organoheterocyclic compounds / Benzazepines
Chilenine 11025386 Click to see 383.40 unknown via CMAUP database
> Organoheterocyclic compounds / Benzodioxoles
Apiole 10659 Click to see 222.24 unknown via CMAUP database
Dillapiol 10231 Click to see COC1=C(C2=C(C=C1CC=C)OCO2)OC 222.24 unknown via CMAUP database
Safrole 5144 Click to see 162.18 unknown via CMAUP database
> Organoheterocyclic compounds / Benzofurans
Anethofuran 126537 Click to see 152.23 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/10.1002/PCA.2800050508
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 / Lactones / Gamma butyrolactones
(4S,5R)-4-hydroxy-5-(hydroxymethyl)dihydrofuran-2(3H)-one 161815 Click to see C1C(C(OC1=O)CO)O 132.11 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 / Coumarins and derivatives / Furanocoumarins / Psoralens / 5-methoxypsoralens
Bergapten 2355 Click to see COC1=C2C=CC(=O)OC2=CC3=C1C=CO3 216.19 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 6,7-dihydroxycoumarins
Esculetin 5281416 Click to see 178.14 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Umbelliferone 5281426 Click to see C1=CC(=CC2=C1C=CC(=O)O2)O 162.14 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Linear pyranocoumarins
Graveolone 177751 Click to see CC1(CC(=O)C2=C(O1)C=C3C(=C2)C=CC(=O)O3)C 244.24 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 / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-3-O-glucuronides
Querciturone 5274585 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O 478.40 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

Gallery Top

We don't have an image yet. Upload an image!

Contributors Top

No known contributors. Be the first!

Collections Top

In private collections 0
In public collections 0
You need to be authenticated in order to add this taxon to a personal collection.