Scopolia japonica is a flowering plant species in the nightshade family Solanaceae. It is found in the genus Scopolia, which is one of eight genera in the tribe Hyoscyameae. The roots of this plant contain coumarins umbelliferone and scopoletin, and the hairy roots technique has been used to produce the alkaloids scopolamine and hyoscyamine.

Synonyms Top

Scientific name	Authority	First published in
Scopolina japonica	(Maxim.) Kuntze	Revis. Gen. Pl. 2: 452. 1891.

Common names Top

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Language	Common/alternative name
Japanese	オニヒルグサヤ
Japanese	ロートエキス
Japanese	ロートコン
Japanese	ロート根
Japanese	莨菪
Japanese	莨菪根
Japanese	ハシリドコロ
Korean	미치광이풀
Chinese	东莨菪

Subspecies (abbr. subsp./ssp.) Top

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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

Area

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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-0001025516
UNII	04AC8ASX63
Tropicos	29607449
KEW	urn:lsid:ipni.org:names:818000-1
Open Tree Of Life	435703
NCBI Taxonomy	221162
IPNI	818000-1
iNaturalist	700353
GBIF	7299219
Freebase	/m/0c3vwkl
EPPO	SLJJA
USDA GRIN	318442
Wikipedia	Scopolia_japonica
CMAUP	NPO3890

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

A Sample-Centric and Knowledge-Driven Computational Framework for Natural Products Drug Discovery

Gaudry A, Pagni M, Mehl F, Moretti S, Quiros-Guerrero LM, Cappelletti L, Rutz A, Kaiser M, Marcourt L, Queiroz EF, Ioset JR, Grondin A, David B, Wolfender JL, Allard PM

ACS Cent Sci

20-Feb-2024

PMCID:	PMC10979503
doi:	10.1021/acscentsci.3c00800
PMID:	38559298

Hairy root culture: a potent method for improved secondary metabolite production of Solanaceous plants

Biswas D, Chakraborty A, Mukherjee S, Ghosh B

Front Plant Sci

04-Sep-2023

PMCID:	PMC10507345
doi:	10.3389/fpls.2023.1197555
PMID:	37731987

From Plants to Psycho-Neurology: Unravelling the Therapeutic Benefits of Bioactive Compounds in Brain Disorders

Grosso C, Santos M, Barroso MF

Antioxidants (Basel)

11-Aug-2023

PMCID:	PMC10451187
doi:	10.3390/antiox12081603
PMID:	37627598

Anti-Inflammatory Properties of Extract of the Hairy Root of Native Portulaca Oleracea L. and Its Effect on Some Inflammatory Genes Expression in Rat Microglial Cells

Babashpour S, Piri K, Sabouni F, Babashpour S

Iran J Biotechnol

01-Jul-2023

PMCID:	PMC10858354
doi:	10.30498/ijb.2023.323542.3249
PMID:	38344701

Natural Coumarin Derivatives Activating Nrf2 Signaling Pathway as Lead Compounds for the Design and Synthesis of Intestinal Anti-Inflammatory Drugs

Di Stasi LC

Pharmaceuticals (Basel)

30-Mar-2023

PMCID:	PMC10142712
doi:	10.3390/ph16040511
PMID:	37111267

Pepper Mild Mottle Virus: An Infectious Pathogen in Pepper Production and a Potential Indicator of Domestic Water Quality

Ochar K, Ko HC, Woo HJ, Hahn BS, Hur O

Viruses

19-Jan-2023

PMCID:	PMC9962380
doi:	10.3390/v15020282
PMID:	36851496

Easily Operable Quantification Method of 21 Plant-Derived Alkaloids in Human Serum by Automatic Sample Preparation and Liquid Chromatography–Tandem Mass Spectrometry

Taniguchi M, Takamura N, Watanabe T, Ishimaru R, Chinaka S, Miki A, Miyazaki H, Tsuchihashi H, Zaitsu K

Chromatographia

29-Oct-2022

PMCID:	PMC9617228
doi:	10.1007/s10337-022-04212-5
PMID:	36341308

Beauty of the beast: anticholinergic tropane alkaloids in therapeutics

Shim KH, Kang MJ, Sharma N, An SS

Nat Prod Bioprospect

16-Sep-2022

PMCID:	PMC9478010
doi:	10.1007/s13659-022-00357-w
PMID:	36109439

Spillover of a Tobamovirus from the Australian Indigenous Flora to Invasive Weeds

Xu W, Li H, Sivasithamparam K, Tran DT, Jones MG, Chen X, Wylie SJ

Viruses

29-Jul-2022

PMCID:	PMC9413628
doi:	10.3390/v14081676
PMID:	36016296

Development and application of DNA markers to detect adulteration with Scopolia japonica in the medicinal herb Atractylodes lancea

Oh SH, Kim YD, Jang CS

Food Sci Biotechnol

26-Nov-2021

PMCID:	PMC8733082
doi:	10.1007/s10068-021-01008-5
PMID:	35059233

Fungal Endophytes as Efficient Sources of Plant-Derived Bioactive Compounds and Their Prospective Applications in Natural Product Drug Discovery: Insights, Avenues, and Challenges

Singh A, Singh DK, Kharwar RN, White JF, Gond SK

Microorganisms

19-Jan-2021

PMCID:	PMC7833388
doi:	10.3390/microorganisms9010197
PMID:	33477910

New Frontiers on Human Safe Insecticides and Fungicides: An Opinion on Trehalase Inhibitors

Matassini C, Parmeggiani C, Cardona F

Molecules

01-Jul-2020

PMCID:	PMC7411730
doi:	10.3390/molecules25133013
PMID:	32630325

Natural Antispasmodics: Source, Stereochemical Configuration, and Biological Activity

Martínez-Pérez EF, Juárez ZN, Hernández LR, Bach H

Biomed Res Int

08-Oct-2018

PMCID:	PMC6196993
doi:	10.1155/2018/3819714
PMID:	30402474

Enhanced production of the pharmaceutically important polyphenolic compounds in Vitex agnus castus L. shoot cultures by precursor feeding strategy

Skrzypczak‐Pietraszek E, Piska K, Pietraszek J

Eng Life Sci

05-Feb-2018

PMCID:	PMC6999492
doi:	10.1002/elsc.201800003
PMID:	32624908

Worldwide Occurrence and Investigations of Contamination of Herbal Medicines by Tropane Alkaloids

Chan TY

Toxins (Basel)

15-Sep-2017

PMCID:	PMC5618217
doi:	10.3390/toxins9090284
PMID:	28914776

Phytochemical Profile Top

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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
4,15,16-Trimethoxy-10-azatetracyclo[7.7.1.0^{2,7}.0^{13,17}]heptadeca-1(16),2,4,6,13(17),14-hexaen-3-ol	5320211	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 / 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	via CMAUP database
> Alkaloids and derivatives / Tropane alkaloids
(+)-Hyoscyamine	637577	Click to see CN1C2CCC1CC(C2)OC(=O)C(CO)C3=CC=CC=C3	289.40	unknown	https://doi.org/10.1016/S0021-9673(99)00447-1
(1R,2S,3R,4R)-8-azabicyclo[3.2.1]octane-1,2,3,4-tetrol	45109805	Click to see C1CC2(C(C(C(C1N2)O)O)O)O	175.18	unknown	via CMAUP database
(8-methyl-8-azabicyclo[3.2.1]octan-3-yl) (2R)-3-hydroxy-2-phenylpropanoate	25817	Click to see CN1C2CCC1CC(C2)OC(=O)C(CO)C3=CC=CC=C3	289.40	unknown	https://doi.org/10.1016/S0021-9673(99)00447-1
(S)-((1R,3r,5S)-8-methyl-8-azabicyclo[3.2.1]octan-3-yl) 3-hydroxy-2-phenylpropanoate	6931560	Click to see CN1C2CCC1CC(C2)OC(=O)C(CO)C3=CC=CC=C3	289.40	unknown	https://doi.org/10.1271/BBB1961.50.2715 https://doi.org/10.1055/S-2006-961415
Atropine	174174	Click to see CN1C2CCC1CC(C2)OC(=O)C(CO)C3=CC=CC=C3	289.40	unknown	via CMAUP database
Calystegine B4	10559162	Click to see C1CC2(C(C(C(C1N2)O)O)O)O	175.18	unknown	https://doi.org/10.1016/0008-6215(96)00204-2
Hyoscyamine	154417	Click to see CN1C2CCC1CC(C2)OC(=O)C(CO)C3=CC=CC=C3	289.40	unknown	https://doi.org/10.1016/S0021-9673(99)00447-1
L-Hyoscyamine	64692	Click to see CN1C2CCC1CC(C2)OC(=O)C(CO)C3=CC=CC=C3	289.40	unknown	https://doi.org/10.1271/BBB1961.50.2715 https://doi.org/10.1016/S0021-9673(99)00447-1 https://doi.org/10.1055/S-2006-961415
L-Hyoscyamine	3661	Click to see CN1C2CCC1CC(C2)OC(=O)C(CO)C3=CC=CC=C3	289.40	unknown	https://doi.org/10.1016/S0031-9422(00)88438-1 https://doi.org/10.1002/ARDP.18882260502 https://doi.org/10.1248/YAKUSHI1881.1924.508_425
Levsin	5318386	Click to see CN1C2CCC1CC(C2)OC(=O)C(CO)C3=CC=CC=C3	289.40	unknown	via CMAUP database
Nortropanoline	3693124	Click to see C1CC2(C(C(C(C1N2)O)O)O)O	175.18	unknown	https://doi.org/10.1016/0008-6215(96)00204-2
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Methane	297	Click to see C	16.04	unknown	via CMAUP database
> Lipids and lipid-like molecules / Saccharolipids / Acyltrehaloses
CID 85149698	85149698	Click to see CCCCCCCCCCCCCCCCCC(=O)OC1C(C(C(OC1OC2C(C(C(C(O2)CO)O)O)O)COC(=O)C)O)O	650.80	unknown	https://doi.org/10.1016/S0031-9422(00)88438-1
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins
(2S,3R,4S,5S,6R)-2-[(2R,3R,4R,5R,6R)-6-[(1R,2S,3R,3'S,4R,5'R,6S,7S,8R,9S,12S,13R,16S)-3,3'-dihydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-16-yl]oxy-4,5-dihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol	101635854	Click to see CC1CC(C2(C(C3C(O2)C(C4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)CO)O)O)O)O)O)C)C)O)C)OC1)O	770.90	unknown	https://doi.org/10.1248/CPB.40.2981
(2S,3R,4S,5S,6R)-2-[(2S,3R,4S,5S,6R)-2-[(2R,3R,4R,5R,6R)-6-[(1R,2S,3R,3'S,4R,5'R,6S,7S,8R,9S,12S,13R,16S)-3,3'-dihydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-16-yl]oxy-4,5-dihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol	101635853	Click to see CC1CC(C2(C(C3C(O2)C(C4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)CO)O)O)OC9C(C(C(C(O9)CO)O)O)O)O)O)C)C)O)C)OC1)O	933.00	unknown	https://doi.org/10.1248/CPB.40.2981
2-[2-[4,5-Dihydroxy-2-(hydroxymethyl)-6-(5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-16-yl)oxyoxan-3-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol	73025438	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)CO)O)O)OC9C(C(C(C(O9)CO)O)O)O)O)O)C)C)C)OC1	901.00	unknown	https://doi.org/10.1248/CPB.40.2981
Funkioside D	21670027	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)CO)O)O)OC9C(C(C(C(O9)CO)O)O)O)O)O)C)C)C)OC1	901.00	unknown	https://doi.org/10.1248/CPB.40.2981
Scopoloside I	46174004	Click to see CC1CC(C2(C(C3C(O2)C(C4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)CO)O)O)OC9C(C(C(C(O9)CO)O)O)O)O)O)C)C)O)C)OC1)O	933.00	unknown	https://doi.org/10.1248/CPB.40.2981
Scopoloside II	46174005	Click to see CC1CC(C2(C(C3C(O2)C(C4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)CO)O)O)O)O)O)C)C)O)C)OC1)O	770.90	unknown	https://doi.org/10.1248/CPB.40.2981
> Organic acids and derivatives / Hydroxy acids and derivatives / Beta hydroxy acids and derivatives
(-)-Scopolamine	5184	Click to see CN1C2CC(CC1C3C2O3)OC(=O)C(CO)C4=CC=CC=C4	303.35	unknown	https://doi.org/10.1016/S0031-9422(00)88438-1 https://doi.org/10.1002/ARDP.18882260502 https://doi.org/10.1002/ARDP.18902280209
(+)-Scopolamine	673473	Click to see CN1C2CC(CC1C3C2O3)OC(=O)C(CO)C4=CC=CC=C4	303.35	unknown	via CMAUP database
[(1R,2S,4S,5S)-9-methyl-3-oxa-9-azatricyclo[3.3.1.02,4]nonan-7-yl] (2S)-3-hydroxy-2-phenylpropanoate	11968014	Click to see CN1C2CC(CC1C3C2O3)OC(=O)C(CO)C4=CC=CC=C4	303.35	unknown	via CMAUP database
[(2R,4S)-9-methyl-3-oxa-9-azatricyclo[3.3.1.02,4]nonan-7-yl] (2R)-3-hydroxy-2-phenylpropanoate	134767951	Click to see CN1C2CC(CC1C3C2O3)OC(=O)C(CO)C4=CC=CC=C4	303.35	unknown	https://doi.org/10.1271/BBB1961.50.2715 https://doi.org/10.1016/S0021-9673(99)00447-1 https://doi.org/10.1055/S-2006-961415
6-beta,7-beta-Epoxy-3-alpha-tropanyl S-(-)-tropate	6432494	Click to see CN1C2CC(CC1C3C2O3)OC(=O)C(CO)C4=CC=CC=C4	303.35	unknown	via CMAUP database
Atroscine	452977	Click to see CN1C2CC(CC1C3C2O3)OC(=O)C(CO)C4=CC=CC=C4	303.35	unknown	via CMAUP database
Hyoscine	3000322	Click to see CN1C2CC(CC1C3C2O3)OC(=O)C(CO)C4=CC=CC=C4	303.35	unknown	via CMAUP database
Isoptpo Hyoscine	5284456	Click to see CN1C2CC(CC1C3C2O3)OC(=O)C(CO)C4=CC=CC=C4	303.35	unknown	via CMAUP database
Scopalamine	6451257	Click to see CN1C2CC(CC1C3C2O3)OC(=O)C(CO)C4=CC=CC=C4	303.35	unknown	via CMAUP database
Sdccgsbi-0051046.P002	2723877	Click to see CN1C2CC(CC1C3C2O3)OC(=O)C(CO)C4=CC=CC=C4	303.35	unknown	via CMAUP database
Transderm-V	5809	Click to see CN1C2CC(CC1C3C2O3)OC(=O)C(CO)C4=CC=CC=C4	303.35	unknown	via CMAUP database
Tropic acid ester with scopine	153311	Click to see CN1C2CC(CC1C3C2O3)OC(=O)C(CO)C4=CC=CC=C4	303.35	unknown	https://doi.org/10.1055/S-2006-961415 https://doi.org/10.1016/S0021-9673(99)00447-1 https://doi.org/10.1016/S0031-9422(00)88438-1 https://doi.org/10.1271/BBB1961.50.2715 https://doi.org/10.1002/ARDP.18882260502 https://doi.org/10.1002/ARDP.18902280209
> Organic acids and derivatives / Peptidomimetics / Hybrid peptides
[NMe-Ser7]MC-RY	146684759	Click to see CC1C(NC(=O)C(NC(=O)C(C(NC(=O)C(NC(=O)C(NC(=O)C(N(C(=O)CCC(NC1=O)C(=O)O)C)CO)C)CCCN=C(N)N)C(=O)O)C)CC2=CC=C(C=C2)O)C=CC(=CC(C)C(CC3=CC=CC=C3)OC)C	1063.20	unknown	https://doi.org/10.1016/S0031-9422(00)88438-1
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
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
> Organic oxygen compounds / Organooxygen compounds / Ethers / Acetals / Ketals
Nigericin	34230	Click to see CC1CCC(OC1C(C)C(=O)O)CC2CC(C(C3(O2)C(CC(O3)(C)C4CCC(O4)(C)C5C(CC(O5)C6C(CC(C(O6)(CO)O)C)C)C)C)C)OC	725.00	unknown	https://doi.org/10.1002/ARDP.18882260502 https://doi.org/10.1002/ARDP.18902280904 https://doi.org/10.1248/YAKUSHI1881.1924.508_425
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Chromones
(6R)-17,18-dimethoxy-6-prop-1-en-2-yl-2,7,14,21-tetraoxapentacyclo[11.9.0.03,11.04,8.015,20]docosa-1(13),3(11),4(8),9,15,17,19-heptaen-12-one	10501591	Click to see CC(=C)C1CC2=C(O1)C=CC3=C2OC4=C(C3=O)OC5=CC(=C(C=C5OC4)OC)OC	408.40	unknown	via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Pyranochromenes
13-Homo-13-oxa-6a,12a-dehydrodeguelin	10092854	Click to see CC1(C=CC2=C(O1)C=CC3=C2OC4=C(C3=O)OC5=CC(=C(C=C5OC4)OC)OC)C	408.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Coumarin glycosides
6-methoxy-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydrochromen-2-one	11953803	Click to see COC1=C(C=C2C(=C1)CCC(=O)O2)OC3C(C(C(C(O3)CO)O)O)O	356.32	unknown	via CMAUP database
Fabiatrin	10994544	Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)OC3C(C(C(C(O3)COC4C(C(C(CO4)O)O)O)O)O)O	486.40	unknown	via CMAUP database
Scopolin	439514	Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)OC3C(C(C(C(O3)CO)O)O)O	354.31	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Scopoletin	5280460	Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)O	192.17	unknown	https://doi.org/10.1002/ARDP.18882260503
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 6-prenylated flavans / 6-prenylated flavanones
(2S)-6-(Gamma,Gamma-Dimethylallyl)-5-Hydroxy-3',4'-Dimethoxy-6'',6''-Dimethylpyran(2'',3'':7,8)Flavanone	44559036	Click to see CC(=CCC1=C(C2=C(C3=C1OC(C=C3)(C)C)OC(CC2=O)C4=CC(=C(C=C4)OC)OC)O)C	450.50	unknown	via CMAUP database
(2S)-6-(gamma,gamma-dimethylallyl)-5,3'-dihydroxy-4'-methoxy-6'',6''-dimethylpyran[2'',3'':7,8]flavanone	44559037	Click to see CC(=CCC1=C(C2=C(C3=C1OC(C=C3)(C)C)OC(CC2=O)C4=CC(=C(C=C4)OC)O)O)C	436.50	unknown	via CMAUP database
(2S)-6-(gamma,gamma-dimethylallyl)-5,4'-dihydroxy-3'-methoxy-6'',6''-dimethylpyran[2'',3'':7,8]flavanone	44559077	Click to see CC(=CCC1=C(C2=C(C3=C1OC(C=C3)(C)C)OC(CC2=O)C4=CC(=C(C=C4)O)OC)O)C	436.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Furanoisoflavonoids / Pterocarpans
Anhydropisatin	11822566	Click to see COC1=CC2=C(C=C1)C3=C(CO2)C4=CC5=C(C=C4O3)OCO5	296.27	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Rotenoids
Rotenonone	442819	Click to see CC(=C)C1CC2=C(O1)C=CC3=C2OC4=C(C3=O)C5=CC(=C(C=C5OC4=O)OC)OC	406.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Rotenoids / Rotenones
(1)Benzopyrano(3,4-b)furo(2,3-h)(1)benzopyran-6(12H)-one, 1,2-dihydro-8,9-dimethoxy-2-(1-methylethenyl)-, (R)-	99190	Click to see CC(=C)C1CC2=C(O1)C=CC3=C2OC4=C(C3=O)C5=CC(=C(C=C5OC4)OC)OC	392.40	unknown	via CMAUP database
(1R,13R)-6-acetyl-13-hydroxy-16,17-dimethoxy-2,7,20-trioxapentacyclo[11.8.0.03,11.04,8.014,19]henicosa-3(11),4(8),5,9,14,16,18-heptaen-12-one	10549503	Click to see CC(=O)C1=CC2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4(C3=O)O)OC)OC	410.40	unknown	via CMAUP database
(1R,14R)-14,17,18-trimethoxy-7,7-dimethyl-2,8,21-trioxapentacyclo[12.8.0.03,12.04,9.015,20]docosa-3(12),4(9),5,10,15,17,19-heptaen-13-one	100970022	Click to see CC1(C=CC2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4(C3=O)OC)OC)OC)C	424.40	unknown	via CMAUP database
(1R,14S)-14-hydroxy-17,18-dimethoxy-7,7-dimethyl-2,8,21-trioxapentacyclo[12.8.0.03,12.04,9.015,20]docosa-3(12),4(9),5,10,15,17,19-heptaen-13-one	11962145	Click to see CC1(C=CC2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4(C3=O)O)OC)OC)C	410.40	unknown	via CMAUP database
(1R,5R,6S,14R)-5,6,14-trihydroxy-17,18-dimethoxy-7,7-dimethyl-2,8,21-trioxapentacyclo[12.8.0.03,12.04,9.015,20]docosa-3(12),4(9),10,15,17,19-hexaen-13-one	11797541	Click to see CC1(C(C(C2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4(C3=O)O)OC)OC)O)O)C	444.40	unknown	via CMAUP database
(1R,5S,6R,14R)-5,6,14-trihydroxy-17,18-dimethoxy-7,7-dimethyl-2,8,21-trioxapentacyclo[12.8.0.03,12.04,9.015,20]docosa-3(12),4(9),10,15,17,19-hexaen-13-one	10049103	Click to see CC1(C(C(C2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4(C3=O)O)OC)OC)O)O)C	444.40	unknown	via CMAUP database
(1R,6R,13R)-13,16,17-trimethoxy-6-prop-1-en-2-yl-2,7,20-trioxapentacyclo[11.8.0.03,11.04,8.014,19]henicosa-3(11),4(8),9,14,16,18-hexaen-12-one	100970024	Click to see CC(=C)C1CC2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4(C3=O)OC)OC)OC	424.40	unknown	via CMAUP database
(1R)-1beta,2beta,7aalpha-Trihydroxy-9,10-dimethoxy-3,3-dimethyl-1,2,13,13aalpha-tetrahydro-3H-bis[1]benzopyrano[3,4-b:6',5'-e]pyran-7(7aH)-one	10694586	Click to see CC1(C(C(C2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4(C3=O)O)OC)OC)O)O)C	444.40	unknown	via CMAUP database
(1S)-1alpha,2alpha,7aalpha-Trihydroxy-9,10-dimethoxy-3,3-dimethyl-1,2,13,13aalpha-tetrahydro-3H-bis[1]benzopyrano[3,4-b:6',5'-e]pyran-7(7aH)-one	10789429	Click to see CC1(C(C(C2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4(C3=O)O)OC)OC)O)O)C	444.40	unknown	via CMAUP database
(2R)-1,2,12,12aalpha-Tetrahydro-6abeta-methoxy-2alpha-isopropenyl-8,9-dimethoxy-[1]benzopyrano[3,4-b]furo[2,3-h][1]benzopyran-6(6aH)-one	100970021	Click to see CC(=C)C1CC2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4(C3=O)OC)OC)OC	424.40	unknown	via CMAUP database
(6Ar,12aR)-9,12a-dihydroxy-2,3-dimethoxy-8-(3-methylbut-2-enyl)-6,6a-dihydrochromeno[3,4-b]chromen-12-one	51136534	Click to see CC(=CCC1=C(C=CC2=C1OC3COC4=CC(=C(C=C4C3(C2=O)O)OC)OC)O)C	412.40	unknown	via CMAUP database
(7aS)-13,13aalpha-Dihydro-7abeta-methoxy-9,10-dimethoxy-3,3-dimethyl-3H-bis[1]benzopyrano[3,4-b:6',5'-e]pyran-7(7aH)-one	100970023	Click to see CC1(C=CC2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4(C3=O)OC)OC)OC)C	424.40	unknown	via CMAUP database
11-Hydroxytephrosin	155725	Click to see CC1(C=CC2=C(O1)C=C(C3=C2OC4COC5=CC(=C(C=C5C4(C3=O)O)OC)OC)O)C	426.40	unknown	via CMAUP database
alpha-Toxicarol	442826	Click to see CC1(C=CC2=C(O1)C=C(C3=C2OC4COC5=CC(=C(C=C5C4C3=O)OC)OC)O)C	410.40	unknown	via CMAUP database
Deguelin	107935	Click to see CC1(C=CC2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4C3=O)OC)OC)C	394.40	unknown	via CMAUP database
Dehydrodeguelin	3083803	Click to see CC1(C=CC2=C(O1)C=CC3=C2OC4=C(C3=O)C5=CC(=C(C=C5OC4)OC)OC)C	392.40	unknown	via CMAUP database
Dehydrotoxicarol	5491616	Click to see CC1(C=CC2=C(O1)C=C(C3=C2OC4=C(C3=O)C5=CC(=C(C=C5OC4)OC)OC)O)C	408.40	unknown	via CMAUP database
rel-(7aR,13aR)-9,10-Dimethoxy-3,3-dimethyl-13,13a-dihydro-3H-pyrano[2,3-c:6,5-f']dichromen-7(7aH)-one	184223	Click to see CC1(C=CC2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4C3=O)OC)OC)C	394.40	unknown	via CMAUP database
Rotenolon II	99189	Click to see CC(=C)C1CC2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4(C3=O)O)OC)OC	410.40	unknown	via CMAUP database
Rotenolone	68184	Click to see CC(=C)C1CC2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4(C3=O)O)OC)OC	410.40	unknown	via CMAUP database
Rotenone	6758	Click to see CC(=C)C1CC2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4C3=O)OC)OC	394.40	unknown	via CMAUP database
Tephrosin	114909	Click to see CC1(C=CC2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4(C3=O)O)OC)OC)C	410.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
Isobavachromene	5889042	Click to see CC1(C=CC2=C(O1)C=CC(=C2O)C(=O)C=CC3=CC=C(C=C3)O)C	322.40	unknown	via CMAUP database
Pongachalcone II	10712965	Click to see CC1(C=CC2=C(O1)C=CC(=C2O)C(=O)C=CC3=CC(=C(C=C3)O)OC)C	352.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Stilbenes
2,2-dimethyl-7-[(E)-2-(3,4,5-trimethoxyphenyl)ethenyl]chromene	10689330	Click to see CC1(C=CC2=C(O1)C=C(C=C2)C=CC3=CC(=C(C(=C3)OC)OC)OC)C	352.40	unknown	via CMAUP database
4-[(E)-2-(5-methoxy-2,2-dimethylchromen-7-yl)ethenyl]phenol	10542828	Click to see CC1(C=CC2=C(O1)C=C(C=C2OC)C=CC3=CC=C(C=C3)O)C	308.40	unknown	via CMAUP database
5-Methoxy-2,2-dimethyl-7-[2-(4-hydroxy-3-methoxyphenyl)ethenyl]-2H-1-benzopyran	10520980	Click to see CC1(C=CC2=C(O1)C=C(C=C2OC)C=CC3=CC(=C(C=C3)O)OC)C	338.40	unknown	via CMAUP database

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Scopolia japonica

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