Scientific name	Authority	First published in
Thalictrum japonicum	Thunb.	Trans. Linn. Soc. 2: 337 (1794)
Coptis japonica f. viridiflora	Honda ex Kadota	Fl. Japan 2a: 325 (2006)
Coptis anemonifolia	Siebold & Zucc.	Abh. Math.-Phys. Cl. Königl. Bayer. Akad. Wiss. 4(2): 180 (1845)
Coptis anemonifolia var. dissecta	Yatabe	Nippon Shokubutsumeii ed. 3: 46 1900
Coptis brachypetala	Siebold & Zucc.	Abh. Math.-Phys. Cl. Königl. Bayer. Akad. Wiss. 4(2): 180 (1845)
Coptis brachypetala var. major	Miq.	Prolus. Fl. Jap. 196 1867
Coptis japonica var. anemonifolia	(Siebold & Zucc.) H.Ohba	J. Jap. Bot. 75: 369 (2000)
Coptis japonica var. dissecta	(Yatabe) Nakai ex Satake	J. Jap. Bot. 24: 74 1949
Coptis japonica var. major	(Miq.) Satake	J. Jap. Bot. 24: 74 1949
Coptis occidentalis var. japonica	Huth	Bull. Herb. Boissier 5: 1086 1897
Coptis orientalis	Maxim.	Bull. Acad. Imp. Sci. Saint-Pétersbourg , sér. 3, 12: 60 (1868)

Common names Top

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Filter by language:

Language	Common/alternative name
English	japanese goldthread
Arabic	كوبتس اليابان
Japanese	オウレン
Japanese	黄連
Chinese	日本黃連

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 click to expand
- Eastern Asia
  - Japan
  - Korea

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000619855
UNII	8BO3NHJ535
Tropicos	100315791
KEW	urn:lsid:ipni.org:names:710316-1
The Plant List	kew-2736112
Open Tree Of Life	387829
NCBI Taxonomy	3442
IPNI	710316-1
iNaturalist	789253
GBIF	7277312
EPPO	CPXJA
EOL	5530437
USDA GRIN	403064
Wikipedia	Coptis_japonica
CMAUP	NPO13757

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

Transcriptomic Insights and Cytochrome P450 Gene Analysis in Kadsura coccinea for Lignan Biosynthesis

Fu H, Guo C, Peng J, Shao F, Sheng S, Wang S

Genes (Basel)

21-Feb-2024

PMCID:	PMC10969973
doi:	10.3390/genes15030270
PMID:	38540329

The CYP80A and CYP80G Are Involved in the Biosynthesis of Benzylisoquinoline Alkaloids in the Sacred Lotus (Nelumbo nucifera)

Hao C, Yu Y, Liu Y, Liu A, Chen S

Int J Mol Sci

05-Jan-2024

PMCID:	PMC10815925
doi:	10.3390/ijms25020702
PMID:	38255776

Modular assembly of an artificially concise biocatalytic cascade for the manufacture of phenethylisoquinoline alkaloids

Gao Y, Li F, Luo Z, Deng Z, Zhang Y, Yuan Z, Liu C, Rao Y

Nat Commun

02-Jan-2024

PMCID:	PMC10761944
doi:	10.1038/s41467-023-44420-7
PMID:	38167860

Xylose and shikimate transporters facilitates microbial consortium as a chassis for benzylisoquinoline alkaloid production

Gao M, Zhao Y, Yao Z, Su Q, Van Beek P, Shao Z

Nat Commun

28-Nov-2023

PMCID:	PMC10684500
doi:	10.1038/s41467-023-43049-w
PMID:	38016984

An Enzymatic Strategy for the Selective Methylation of High-Value-Added Tetrahydroprotoberberine Alkaloids

Zhao W, Liu M, Liu K, Liu H, Liu X, Liu J

Int J Mol Sci

16-Oct-2023

PMCID:	PMC10607743
doi:	10.3390/ijms242015214
PMID:	37894895

The leaf idioblastome of the medicinal plant Catharanthus roseus is associated with stress resistance and alkaloid metabolism

Guedes JG, Ribeiro R, Carqueijeiro I, Guimarães AL, Bispo C, Archer J, Azevedo H, Fonseca NA, Sottomayor M

J Exp Bot

07-Oct-2023

PMCID:	PMC10735432
doi:	10.1093/jxb/erad374
PMID:	37804484

Role of ABC Proteins in Secondary Metabolism and Immune (=Defensive) Response in Seaweeds

Salgado LT, Oliveira LS, Echevarria-Lima J, Reis VM, Sudatti DB, Thompson FL, Pereira RC

Cells

12-Sep-2023

PMCID:	PMC10526433
doi:	10.3390/cells12182259
PMID:	37759481

Cheong-sang-bang-pung-san alleviated hepatic lipid accumulation by regulating lipid metabolism in vitro and in vivo

Kang YM, Kim KY, Kim TI, Kim YJ, Kim HH, Kim K

Front Pharmacol

06-Sep-2023

PMCID:	PMC10511874
doi:	10.3389/fphar.2023.1223534
PMID:	37745047

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

Comparative Transcriptome Profiling Reveals Two WRKY Transcription Factors Positively Regulating Polysaccharide Biosynthesis in Polygonatum cyrtonema

Jiang W, Chen J, Duan X, Li Y, Tao Z

Int J Mol Sci

18-Aug-2023

PMCID:	PMC10454705
doi:	10.3390/ijms241612943
PMID:	37629123

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

Production of secondary metabolites using tissue culture-based biotechnological applications

Ozyigit II, Dogan I, Hocaoglu-Ozyigit A, Yalcin B, Erdogan A, Yalcin IE, Cabi E, Kaya Y

Front Plant Sci

29-Jun-2023

PMCID:	PMC10339834
doi:	10.3389/fpls.2023.1132555
PMID:	37457343

Multilayered regulation of secondary metabolism in medicinal plants

Zhao Y, Liu G, Yang F, Liang Y, Gao Q, Xiang C, Li X, Yang R, Zhang G, Jiang H, Yu L, Yang S

Mol Hortic

06-Jun-2023

PMCID:	PMC10514987
doi:	10.1186/s43897-023-00059-y
PMID:	37789448

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

Anti-inflammatory and anti-allergic effects of Cheonwangbosim-dan water extract: An in vitro and in vivo study

Jeon WY, Jin SE, Sohn E, Jo K, Ha H, Shin HK, Lee MY

Heliyon

11-May-2023

PMCID:	PMC10199208
doi:	10.1016/j.heliyon.2023.e16172
PMID:	37215857

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
(6As)-11-hydroxy-1,2,10-trimethoxy-6,6-dimethyl-5,6,6a,7-tetrahydro-4h-dibenzo[de,g]quinolinium	161487	Click to see C[N+]1(CCC2=CC(=C(C3=C2C1CC4=C3C(=C(C=C4)OC)O)OC)OC)C	356.40	unknown	via CMAUP database
Magnoflorine	73337	Click to see C[N+]1(CCC2=CC(=C(C3=C2C1CC4=C3C(=C(C=C4)OC)O)O)OC)C	342.40	unknown	https://doi.org/10.1021/JF9909297
Norisocorydine	12313549	Click to see COC1=C(C2=C(CC3C4=C2C(=C(C=C4CCN3)OC)OC)C=C1)O	327.40	unknown	via CMAUP database
> Alkaloids and derivatives / Benzophenanthridine alkaloids / Dihydrobenzophenanthridine alkaloids
Dihydrochelerythrine	485077	Click to see CN1CC2=C(C=CC(=C2OC)OC)C3=C1C4=CC5=C(C=C4C=C3)OCO5	349.40	unknown	via CMAUP database
> Alkaloids and derivatives / Benzophenanthridine alkaloids / Quaternary benzophenanthridine alkaloids
Sanguinarium	5154	Click to see C[N+]1=C2C(=C3C=CC4=C(C3=C1)OCO4)C=CC5=CC6=C(C=C52)OCO6	332.30	unknown	https://doi.org/10.1021/NP50050A055
> Alkaloids and derivatives / Phthalide isoquinolines
(+)-Hydrastine	656743	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
(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
Hydrastine	197835	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
(13aR)-3,10-dimethoxy-6,8,13,13a-tetrahydro-5H-isoquinolino[2,1-b]isoquinoline-2,9-diol	1152279	Click to see COC1=C(C2=C(CC3C4=CC(=C(C=C4CCN3C2)OC)O)C=C1)O	327.40	unknown	https://doi.org/10.1016/S0031-9422(00)95151-3
(14S)-16,17-dimethoxy-5,7-dioxa-13-azapentacyclo[11.8.0.02,10.04,8.015,20]henicosa-1(21),2,4(8),9,15(20),16,18-heptaen-14-ol	162905761	Click to see COC1=C(C2=C(C=C1)C=C3C4=CC5=C(C=C4CCN3C2O)OCO5)OC	353.40	unknown	https://doi.org/10.1248/YAKUSHI1881.1926.530_299
(S)-Scoulerine	439654	Click to see COC1=C(C2=C(CC3C4=CC(=C(C=C4CCN3C2)OC)O)C=C1)O	327.40	unknown	https://doi.org/10.1074/JBC.M002439200
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 COC1=CC=C2C=C3C4=CC5=C(C=C4CCN3C=C2C1=O)OCO5.Cl	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
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 COC1=CC2=C3C=C4C=CC5=C(C4=C[NH+]3CCC2=CC1=O)OCO5	322.30	unknown	via CMAUP database
16-Methoxy-5,7-dioxa-13-azoniapentacyclo[11.8.0.02,10.04,8.015,20]henicosa-1(13),2,4(8),9,14,16,18,20-octaen-17-olate	10426199	Click to see COC1=C(C=CC2=CC3=[N+](CCC4=CC5=C(C=C43)OCO5)C=C21)[O-]	321.30	unknown	https://doi.org/10.1021/NP50031A038
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 COC1=CC=C2C=C3C4=CC5=C(C=C4CC[NH+]3C=C2C1=O)OCO5	322.30	unknown	via CMAUP database
2,3,10-Trimethoxy-5,6-dihydroisoquinolino[2,1-b]isoquinolin-7-ium-9-ol;chloride	10547385	Click to see COC1=C(C2=C[N+]3=C(C=C2C=C1)C4=CC(=C(C=C4CC3)OC)OC)O.[Cl-]	373.80	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 COC1=CC=C2C=C3C4=CC(=C(C=C4CC[NH+]3C=C2C1=O)OC)OC	338.40	unknown	via CMAUP database
2,9,10-Trimethoxy-5,6-dihydroisoquinolino[2,1-b]isoquinolin-7-ium-3-ol;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
9,10-Dimethoxy-2,3-(methylenedioxy)-13,13a-didehydro-8-berbinol	24974	Click to see COC1=C(C2=C(C=C1)C=C3C4=CC5=C(C=C4CCN3C2O)OCO5)OC	353.40	unknown	https://doi.org/10.1248/YAKUSHI1881.1926.530_299
Benzo(g)-1,3-benzodioxolo(5,6-a)quinolizinium, 5,6-dihydro-9,10-dimethoxy-13-methyl-	148262	Click to see CC1=C2C=CC(=C(C2=C[N+]3=C1C4=CC5=C(C=C4CC3)OCO5)OC)OC	350.40	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/10.1021/NP50031A038
Berberine	2353	Click to see COC1=C(C2=C[N+]3=C(C=C2C=C1)C4=CC5=C(C=C4CC3)OCO5)OC	336.40	unknown	https://doi.org/10.1021/JF020674O https://doi.org/10.1016/S0031-9422(00)95151-3 https://doi.org/10.1271/BBB1961.52.1835 https://doi.org/10.1248/YAKUSHI1947.102.1_56 https://doi.org/10.1021/NP100645D https://doi.org/10.1021/JF980991O https://doi.org/10.1021/JF9909297 https://doi.org/10.1252/JCEJ.30.1098 https://doi.org/10.1074/JBC.M002439200 https://doi.org/10.1016/S0031-9422(00)84193-X https://doi.org/10.1016/S0031-9422(00)80807-9 https://doi.org/10.1007/BF02974076 https://doi.org/10.1055/S-2006-961541 https://doi.org/10.1016/S0031-9422(00)80318-0 https://doi.org/10.1016/S0176-1617(88)80077-4 https://doi.org/10.1055/S-2006-957791 https://doi.org/10.1016/S0031-9422(00)89789-7 https://doi.org/10.1007/BF00272964 https://doi.org/10.1055/S-2006-961910 https://doi.org/10.1016/J.PHYMED.2003.07.005 https://doi.org/10.1248/YAKUSHI1947.110.4_268
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
Bis(1,3)benzodioxolo(5,6-a:4',5'-g)quinolizinium, 6,7-dihydro-13-methyl-	147329	Click to see CC1=C2C=CC3=C(C2=C[N+]4=C1C5=CC6=C(C=C5CC4)OCO6)OCO3	334.30	unknown	via CMAUP database
Columbamine	72310	Click to see COC1=C(C2=C[N+]3=C(C=C2C=C1)C4=CC(=C(C=C4CC3)OC)O)OC	338.40	unknown	https://doi.org/10.1002/PCA.2800050508
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/S0031-9422(00)80318-0 https://doi.org/10.1016/J.PHYMED.2003.07.005 https://doi.org/10.1248/BPB.24.1277 https://doi.org/10.1248/YAKUSHI1947.110.4_268 https://doi.org/10.1021/JF980991O https://doi.org/10.1021/NP100645D https://doi.org/10.1021/JF9909297
Coptisine chloride	72321	Click to see C1C[N+]2=C(C=C3C=CC4=C(C3=C2)OCO4)C5=CC6=C(C=C51)OCO6.[Cl-]	355.80	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 CC1=C2C=CC3=C(C2=C[N+]4=C1C5=CC(=C(C=C5CC4)OC)O)OCO3	336.40	unknown	via CMAUP database
Demethyl eneberberine	101404949	Click to see COC1=C(C2=C[NH+]3CCC4=CC(=O)C(=CC4=C3C=C2C=C1)O)OC	324.30	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 COC1=C(C=C2C(=C1)CC[N+]3=C2C=C4C=CC5=C(C4=C3)OCO5)OC	336.40	unknown	https://doi.org/10.1021/NP50031A038
Jatrorrhizine	72323	Click to see COC1=C(C2=C[N+]3=C(C=C2C=C1)C4=CC(=C(C=C4CC3)O)OC)OC	338.40	unknown	via CMAUP database
Jatrorrhizine hydrochloride	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
Palmatine	19009	Click to see COC1=C(C2=C[N+]3=C(C=C2C=C1)C4=CC(=C(C=C4CC3)OC)OC)OC	352.40	unknown	https://doi.org/10.1016/S0031-9422(00)80318-0 https://doi.org/10.1007/BF02974076 https://doi.org/10.1016/J.PHYMED.2003.07.005 https://doi.org/10.1002/PCA.2800050508 https://doi.org/10.1016/S0031-9422(00)95151-3 https://doi.org/10.1248/YAKUSHI1947.110.4_268 https://doi.org/10.1055/S-2006-957791 https://doi.org/10.1021/JF980991O https://doi.org/10.1021/NP100645D
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
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
Scoulerine	22955	Click to see COC1=C(C2=C(CC3C4=CC(=C(C=C4CCN3C2)OC)O)C=C1)O	327.40	unknown	https://doi.org/10.1016/S0031-9422(00)95151-3
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 COC1=C(C=C2C(=C1)CC[N+]3=C2C=C4C=CC5=C(C4=C3)OCO5)O	322.30	unknown	via CMAUP database
Thalifendine	3084288	Click to see COC1=C(C=CC2=CC3=[N+](CCC4=CC5=C(C=C43)OCO5)C=C21)O	322.30	unknown	https://doi.org/10.1021/NP50031A038
Thalifendine chloride	5321913	Click to see COC1=C(C=CC2=CC3=[N+](CCC4=CC5=C(C=C43)OCO5)C=C21)O.[Cl-]	357.80	unknown	via CMAUP database
Worenine	20055073	Click to see CC1=C2C3=CC4=C(C=C3CC[N+]2=CC5=CC6=C(C=C15)OCO6)OCO4	334.30	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 / Benzyl alcohols
2-Aminobenzyl alcohol	21439	Click to see C1=CC=C(C(=C1)CO)N	123.15	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzylethers
2-(Methoxymethyl)aniline	12334306	Click to see COCC1=CC=CC=C1N	137.18	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 / Benzene and substituted derivatives / Diphenylethers
1-(1,2-Dihydroxyethyl)-3-[4-[2-hydroxy-4-(3-hydroxypropyl)-6-methoxyphenoxy]-3,5-dimethoxyphenyl]-4-(hydroxymethyl)-7,9-dimethoxy-2-oxaspiro[4.5]deca-6,9-dien-8-one	85220212	Click to see COC1=CC(=CC(=C1OC2=C(C=C(C=C2OC)C3C(C4(C=C(C(=O)C(=C4)OC)OC)C(O3)C(CO)O)CO)OC)O)CCCO	632.70	unknown	https://doi.org/10.1021/NP9700127
> Benzenoids / Benzene and substituted derivatives / Phenylmethylamines / Phenylbenzamines
2-[[2-(Methoxymethyl)anilino]methyl]aniline	66385053	Click to see COCC1=CC=CC=C1NCC2=CC=CC=C2N	242.32	unknown	via CMAUP database
Benzenemethanol, 2-[[(2-aminophenyl)methyl]amino]-	10977238	Click to see C1=CC=C(C(=C1)CNC2=CC=CC=C2CO)N	228.29	unknown	via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
4-(1-Hydroxyethyl)-2-methoxyphenol	17203	Click to see CC(C1=CC(=C(C=C1)O)OC)O	168.19	unknown	via CMAUP database
Eugenol	3314	Click to see COC1=C(C=CC(=C1)CC=C)O	164.20	unknown	via CMAUP database
> Hydrocarbons / Unsaturated hydrocarbons / Unsaturated aliphatic hydrocarbons
1-Tetradecene	14260	Click to see CCCCCCCCCCCCC=C	196.37	unknown	via CMAUP database
> Lignans, neolignans and related compounds / Aryltetralin lignans / 9,9p-dihydroxyaryltetralin lignans
Isolariciresinol, (+)-	160521	Click to see COC1=C(C=C2C(C(C(CC2=C1)CO)CO)C3=CC(=C(C=C3)O)OC)O	360.40	unknown	https://doi.org/10.1007/BF03216746 https://doi.org/10.1248/CPB.43.578
> Lignans, neolignans and related compounds / Coumarinolignans
3-(4-Hydroxy-3-methoxyphenyl)-2-(hydroxymethyl)-5-methoxy-2,3-dihydropyrano[3,2-h][1,4]benzodioxin-9-one	100151	Click to see COC1=C(C=CC(=C1)C2C(OC3=C4C(=CC(=C3O2)OC)C=CC(=O)O4)CO)O	386.40	unknown	https://doi.org/10.1016/S0031-9422(00)81760-4
Aquillochin	14282064	Click to see COC1=CC(=CC(=C1O)OC)C2C(OC3=C4C(=CC(=C3O2)OC)C=CC(=O)O4)CO	416.40	unknown	https://doi.org/10.1016/S0031-9422(00)81760-4
CID 335652	335652	Click to see COC1=C(C=CC(=C1)C2C(OC3=C4C(=CC(=C3O2)OC)C=CC(=O)O4)CO)O	386.40	unknown	https://doi.org/10.1016/S0031-9422(00)81760-4
Cleomiscosin A	442510	Click to see COC1=C(C=CC(=C1)C2C(OC3=C4C(=CC(=C3O2)OC)C=CC(=O)O4)CO)O	386.40	unknown	https://doi.org/10.1016/S0031-9422(00)81760-4
Cleomiscosin C	11464176	Click to see COC1=CC(=CC(=C1O)OC)C2C(OC3=C4C(=CC(=C3O2)OC)C=CC(=O)O4)CO	416.40	unknown	https://doi.org/10.1016/S0031-9422(00)81760-4
> Lignans, neolignans and related compounds / Furanoid lignans
(-)-Pinoresinol	12309636	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-[(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 COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)OC	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
4-[6-(4-Hydroxy-3-methoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-2-methoxyphenol	234817	Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)OC)O	358.40	unknown	via CMAUP database
CID 17750970	17750970	Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)OC)O	358.40	unknown	via CMAUP database
Epipinoresinol	637584	Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)OC)O	358.40	unknown	via CMAUP database
Medioresinol	181681	Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)OC	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	https://doi.org/10.1007/BF03216746 https://doi.org/10.1248/CPB.43.578
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 7,9-epoxylignans
(-)-Lariciresinol	23815394	Click to see COC1=C(C=CC(=C1)CC2COC(C2CO)C3=CC(=C(C=C3)O)OC)O	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 COC1=C(C=CC(=C1)CC2COC(C2CO)C3=CC(=C(C=C3)O)OC)O	360.40	unknown	via CMAUP database
> Lignans, neolignans and related compounds / Lignan glycosides
[(2S,3R,4R,5R,6R)-2-[[9-(1,3-benzodioxol-5-yl)-6,7-dimethoxy-1-oxo-3H-benzo[f][2]benzofuran-4-yl]oxy]-3-hydroxy-6-methyl-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-4-yl] acetate	71497048	Click to see CC1C(C(C(C(O1)OC2=C3COC(=O)C3=C(C4=CC(=C(C=C42)OC)OC)C5=CC6=C(C=C5)OCO6)O)OC(=O)C)OC7C(C(C(C(O7)CO)O)O)O	730.70	unknown	via CMAUP database
[(2S,3R,4S,5S,6R)-2-[[9-(1,3-benzodioxol-5-yl)-6,7-dimethoxy-1-oxo-3H-benzo[f][2]benzofuran-4-yl]oxy]-4-hydroxy-6-methyl-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-3-yl] acetate	71607539	Click to see CC1C(C(C(C(O1)OC2=C3COC(=O)C3=C(C4=CC(=C(C=C42)OC)OC)C5=CC6=C(C=C5)OCO6)OC(=O)C)O)OC7C(C(C(C(O7)CO)O)O)O	730.70	unknown	via CMAUP database
Lariciresinol 4'-O-glucoside	11972395	Click to see COC1=C(C=CC(=C1)CC2COC(C2CO)C3=CC(=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)OC)O	522.50	unknown	https://doi.org/10.1248/CPB.43.578
Patentiflorin A	11785812	Click to see CC1C(C(C(C(O1)OC2=C3COC(=O)C3=C(C4=CC(=C(C=C42)OC)OC)C5=CC6=C(C=C5)OCO6)O)O)O	526.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters / Fatty acid methyl esters
Methyl palmitate	8181	Click to see CCCCCCCCCCCCCCCC(=O)OC	270.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Myrcene	31253	Click to see CC(=CCCC(=C)C=C)C	136.23	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
p-CYMENE	7463	Click to see CC1=CC=C(C=C1)C(C)C	134.22	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(-)-alpha-Terpineol	443162	Click to see CC1=CCC(CC1)C(C)(C)O	154.25	unknown	via CMAUP database
Alpha-Terpineol	17100	Click to see CC1=CCC(CC1)C(C)(C)O	154.25	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
(1aS,4aS,7R,7aS,7bS)-1,1,7-Trimethyl-4-methylenedecahydro-1H-cyclopropa[e]azulen-7-ol	6432706	Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C	220.35	unknown	via CMAUP database
1,1,7-Trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol	522266	Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C	220.35	unknown	via CMAUP database
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
Ent-Spathulenol	13854255	Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C	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
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
7-Isopropenyl-4a-methyl-1-methylenedecahydronaphthalene	519361	Click to see CC(=C)C1CCC2(CCCC(=C)C2C1)C	204.35	unknown	via CMAUP database
beta-Selinene	442393	Click to see CC(=C)C1CCC2(CCCC(=C)C2C1)C	204.35	unknown	via CMAUP database
Naphthalene, 1,2,3,4,4a,5,6,8a-octahydro-4a,8-dimethyl-2-(1-methylethenyl)-, [2R-(2alpha,4aalpha,8abeta)]-	6432455	Click to see CC1=CCCC2(C1CC(CC2)C(=C)C)C	204.35	unknown	via CMAUP database
> Lipids and lipid-like molecules / Saccharolipids
[(2S,3S,4R,5S,6S)-3,4,5-trihydroxy-6-[(E)-3-[(2S,3R)-2-(4-hydroxy-3-methoxyphenyl)-3-(hydroxymethyl)-7-methoxy-2,3-dihydro-1-benzofuran-5-yl]prop-2-enoxy]oxan-2-yl]methyl 4-hydroxy-2-methylidenebutanoate	162942263	Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C=C3)O)OC)C=CCOC4C(C(C(C(O4)COC(=O)C(=C)CCO)O)O)O	618.60	unknown	https://doi.org/10.1021/NP9902791
[(2S,3S,4R,5S,6S)-3,4,5-trihydroxy-6-[(E)-3-[(2S,3S)-3-(hydroxymethyl)-7-methoxy-2-(3,4,5-trimethoxyphenyl)-2,3-dihydro-1-benzofuran-5-yl]prop-2-enoxy]oxan-2-yl]methyl 4-hydroxy-2-methylidenebutanoate	163041078	Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C(=C3)OC)OC)OC)C=CCOC4C(C(C(C(O4)COC(=O)C(=C)CCO)O)O)O	662.70	unknown	https://doi.org/10.1021/NP9902791
[(2S,3S,4S,5S,6S)-6-[(E)-3-[(2S,3S)-3-(acetyloxymethyl)-7-methoxy-2-(3,4,5-trimethoxyphenyl)-2,3-dihydro-1-benzofuran-5-yl]prop-2-enoxy]-3,4,5-trihydroxyoxan-2-yl]methyl 4-hydroxy-2-methylidenebutanoate	163003376	Click to see CC(=O)OCC1C(OC2=C1C=C(C=C2OC)C=CCOC3C(C(C(C(O3)COC(=O)C(=C)CCO)O)O)O)C4=CC(=C(C(=C4)OC)OC)OC	704.70	unknown	https://doi.org/10.1021/NP9902791
Woorenoside III	10462037	Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C(=C3)OC)OC)OC)C=CCOC4C(C(C(C(O4)COC(=O)C(=C)CCO)O)O)O	662.70	unknown	https://doi.org/10.1021/NP9902791 https://doi.org/10.1248/CPB.43.578
Woorenoside IV	10101270	Click to see CC(=O)OCC1C(OC2=C1C=C(C=C2OC)C=CCOC3C(C(C(C(O3)COC(=O)C(=C)CCO)O)O)O)C4=CC(=C(C(=C4)OC)OC)OC	704.70	unknown	https://doi.org/10.1021/NP9902791 https://doi.org/10.1248/CPB.43.578
Woorenoside V	10031791	Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C=C3)O)OC)C=CCOC4C(C(C(C(O4)COC(=O)C(=C)CCO)O)O)O	618.60	unknown	https://doi.org/10.1021/NP9902791 https://doi.org/10.1248/CPB.43.578 https://doi.org/10.1007/BF03216746
> 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	6432744	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	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
Beta-Sitosterol	222284	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Tyrosine and derivatives
Tyrosine	6057	Click to see C1=CC(=CC=C1CC(C(=O)O)N)O	181.19	unknown	https://doi.org/10.1016/S0031-9422(00)89789-7
> Organic nitrogen compounds / Organonitrogen compounds / Quaternary ammonium salts / Cholines
Choline	305	Click to see C[N+](C)(C)CCO	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 COC1=C(C=CC(=C1)C=CC(=O)OC2CC(CC(C2O)O)(C(=O)O)O)O	368.30	unknown	via CMAUP database
4-O-Feruloyl quinic acid	101024370	Click to see COC1=C(C=CC(=C1)C=CC(=O)OC2C(CC(CC2O)(C(=O)O)O)O)O	368.30	unknown	via CMAUP database
4-O-feruloyl-D-quinic acid	10177048	Click to see COC1=C(C=CC(=C1)C=CC(=O)OC2C(CC(CC2O)(C(=O)O)O)O)O	368.30	unknown	https://doi.org/10.1248/CPB.33.527
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 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
Feruloyl quinic acid (isomer of 886, 888)	6171347	Click to see COC1=C(C=CC(=C1)C=CC(=O)OC2C(CC(CC2O)(C(=O)O)O)O)O	368.30	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
> 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
> Organoheterocyclic compounds / Benzazepines
Chilenine	11025386	Click to see COC1=C(C2=C(C=C1)C3(C(=O)C4=CC5=C(C=C4CCN3C2=O)OCO5)O)OC	383.40	unknown	via CMAUP database
> Organoheterocyclic compounds / Benzodioxoles
16,17-Dimethoxy-5,7-dioxa-13-azapentacyclo[11.8.0.02,10.04,8.015,20]henicosa-1(21),2,4(8),9,11,15(20),16,18-octaene	162999195	Click to see COC1=C(C2=C(C=C1)C=C3C4=CC5=C(C=C4C=CN3C2)OCO5)OC	335.40	unknown	https://doi.org/10.1016/S0031-9422(00)84193-X
> 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
Coclaurine	160487	Click to see COC1=C(C=C2C(NCCC2=C1)CC3=CC=C(C=C3)O)O	285.34	unknown	https://doi.org/10.1074/JBC.M106405200
Machiline	281691	Click to see COC1=C(C=C2C(NCCC2=C1)CC3=CC=C(C=C3)O)O	285.34	unknown	https://doi.org/10.1074/JBC.M106405200
N-Methylcoclaurine	2752274	Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC=C(C=C3)O)O)OC	299.40	unknown	https://doi.org/10.1074/JBC.M106405200
Reticuline	439653	Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC(=C(C=C3)OC)O)O)OC	329.40	unknown	https://doi.org/10.1074/JBC.M002439200
> Organoheterocyclic compounds / Isoquinolines and derivatives / Isoquinolones and derivatives
16-Methoxy-5,7-dioxa-1-azapentacyclo[11.8.0.03,11.04,8.014,19]henicosa-2,4(8),9,11,13,15,18-heptaen-17-one	11723579	Click to see COC1=CC2=C3C=C4C=CC5=C(C4=CN3CCC2=CC1=O)OCO5	321.30	unknown	https://doi.org/10.1021/NP50031A038
2,9,10-Trimethoxy-5,6-dihydroisoquinolino[2,1-b]isoquinolin-3-one	10065647	Click to see COC1=C(C2=CN3CCC4=CC(=O)C(=CC4=C3C=C2C=C1)OC)OC	337.40	unknown	https://doi.org/10.1248/YAKUSHI1947.110.4_268 https://doi.org/10.1021/JF9909297
6,7-dimethoxy-3,4-dihydro-2H-isoquinolin-1-one	610097	Click to see COC1=C(C=C2C(=C1)CCNC2=O)OC	207.23	unknown	via CMAUP database
8-Oxocoptisine	5245667	Click to see C1CN2C(=CC3=C(C2=O)C4=C(C=C3)OCO4)C5=CC6=C(C=C51)OCO6	335.30	unknown	https://doi.org/10.1007/BF02974076 https://doi.org/10.1248/BPB.24.1277
Noroxyhydrastinine	89047	Click to see C1CNC(=O)C2=CC3=C(C=C21)OCO3	191.18	unknown	via CMAUP database
Oxyberberine	11066	Click to see COC1=C(C2=C(C=C1)C=C3C4=CC5=C(C=C4CCN3C2=O)OCO5)OC	351.40	unknown	https://doi.org/10.1007/BF02974076 https://doi.org/10.1021/NP50031A038
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
Lycoranine B	44130138	Click to see CC1=CC2=CC(=CC3=C2N1C(=O)C4=CC5=C(C=C43)OCO5)OC	307.30	unknown	via CMAUP database
Norsanguinarine	97679	Click to see C1OC2=C(O1)C3=CN=C4C(=C3C=C2)C=CC5=CC6=C(C=C54)OCO6	317.30	unknown	https://doi.org/10.1021/NP50050A055
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(-)-(7R,8S,7'E)-3,4,5,5'-tetramethoxy-4',7-epoxy-8,3'-neolign-7'-ene-9,9'-diol	10024043	Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C(=C3)OC)OC)OC)C=CCO	402.40	unknown	via CMAUP database
(2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-[(E)-3-[(2S,3R)-3-(hydroxymethyl)-7-methoxy-2-(3,4,5-trimethoxyphenyl)-2,3-dihydro-1-benzofuran-5-yl]prop-2-enoxy]oxane-3,4,5-triol	163036964	Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C(=C3)OC)OC)OC)C=CCOC4C(C(C(C(O4)CO)O)O)O	564.60	unknown	https://doi.org/10.1021/NP9902791
[(2R,3S)-7-methoxy-5-[(E)-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyprop-1-enyl]-2-(3,4,5-trimethoxyphenyl)-2,3-dihydro-1-benzofuran-3-yl]methyl acetate	10326334	Click to see CC(=O)OCC1C(OC2=C1C=C(C=C2OC)C=CCOC3C(C(C(C(O3)CO)O)O)O)C4=CC(=C(C(=C4)OC)OC)OC	606.60	unknown	https://doi.org/10.1021/NP9902791
[7-Methoxy-5-[3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyprop-1-enyl]-2-(3,4,5-trimethoxyphenyl)-2,3-dihydro-1-benzofuran-3-yl]methyl acetate	85111190	Click to see CC(=O)OCC1C(OC2=C1C=C(C=C2OC)C=CCOC3C(C(C(C(O3)CO)O)O)O)C4=CC(=C(C(=C4)OC)OC)OC	606.60	unknown	https://doi.org/10.1021/NP9902791 https://doi.org/10.1248/CPB.43.578 https://doi.org/10.1007/BF03216746
Woorenogenin	145709607	Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C(=C3)OC)OC)OC)C=CCO	402.40	unknown	https://doi.org/10.1248/CPB.43.578
Woorenoside I	10347890	Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C(=C3)OC)OC)OC)C=CCOC4C(C(C(C(O4)CO)O)O)O	564.60	unknown	https://doi.org/10.1021/NP9902791 https://doi.org/10.1248/CPB.43.578 https://doi.org/10.1007/BF03216746
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
2-Propenoic acid, 3-(3,4-dihydroxyphenyl)-, octadecyl ester, (E)-; trans-Caffeic acid stearyl ester	71374400	Click to see CCCCCCCCCCCCCCCCCCOC(=O)C=CC1=CC(=C(C=C1)O)O	432.60	unknown	via CMAUP database
Ethyl ferulate	736681	Click to see CCOC(=O)C=CC1=CC(=C(C=C1)O)OC	222.24	unknown	https://doi.org/10.1248/CPB.43.578
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
Ferulic acid	445858	Click to see COC1=C(C=CC(=C1)C=CC(=O)O)O	194.18	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Rhamnetin	5281691	Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)O)C3=CC(=C(C=C3)O)O)O	316.26	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Quercitrin	5280459	Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O	448.40	unknown	https://doi.org/10.1021/JF020674O
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 5-O-methylated flavonoids
5-O-Methylnaringenin	182315	Click to see COC1=CC(=CC2=C1C(=O)CC(O2)C3=CC=C(C=C3)O)O	286.28	unknown	https://doi.org/10.1016/S0031-9422(00)81760-4
Naringenin 5-methyl ether	188424	Click to see COC1=CC(=CC2=C1C(=O)CC(O2)C3=CC=C(C=C3)O)O	286.28	unknown	https://doi.org/10.1016/S0031-9422(00)81760-4
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
Wogonin	5281703	Click to see COC1=C(C=C(C2=C1OC(=CC2=O)C3=CC=CC=C3)O)O	284.26	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxy-dihydrochalcones
4,2',4'-Trihydroxy-6'-methoxydihydrochalcone	42607705	Click to see COC1=CC(=CC(=C1C(=O)CCC2=CC=C(C=C2)O)O)O	288.29	unknown	https://doi.org/10.1016/S0031-9422(00)81760-4

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Coptis japonica

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