Scientific name	Authority	First published in
Porphyroscias decursiva	Miq.	Ann. Mus. Bot. Lugduno-Batavi 3: 62 (1867)
Peucedanum decursivum	Maxim.	Bull. Acad. Imp. Sci. Saint-Pétersbourg , sér. 3, 31: 52 (1886)
Peucedanum porphyroscias	Makino	Bot. Mag. (Tokyo) 18: 65 (1904)
Peucedanum grandifolioides	H.Wolff	Repert. Spec. Nov. Regni Veg. 33: 244 (1933)
Peucedanum astrantiifolium	H.Wolff	Repert. Spec. Nov. Regni Veg. 19: 311 (1924)
Angelica decursiva f. albiflora	(Maxim.) Nakai	Fl. Kor. 1: 268 1909
Angelica decursiva f. angustiloba	(Makino) Ohwi
Peucedanum decursivum var. albiflorum	Maxim.	Mélanges Biol. Bull. Phys.-Math. Acad. Imp. Sci. Saint-Pétersbourg 12: 473 1886
Pimpinella decursiva	H.Wolff	Repert. Spec. Nov. Regni Veg. 16: 237 (1919)

Common names Top

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Filter by language:

Language	Common/alternative name
Japanese	ノダケ
Korean	바디나물
Chinese	土当归
Chinese	前胡
Chinese	独活
Chinese	野当归
Chinese	白芷叶
Chinese	紫花前胡

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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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Asia-temperate click to expand
- China
  - China North-central
  - China South-central
  - China Southeast
  - Inner Mongolia
  - Manchuria
- Eastern Asia
  - Japan
  - Korea
  - Taiwan
- Russian Far East
  - Primorye

Asia-tropical click to expand
- Indo-China
  - Vietnam

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000536162
UNII	E294613K9W
Tropicos	1700300
KEW	urn:lsid:ipni.org:names:837599-1
The Plant List	kew-2639051
PFAF	Angelica decursiva
Open Tree Of Life	367735
Observations.org	114508
NCBI Taxonomy	52491
IPNI	837599-1
iNaturalist	452065
iNaturalist	452066
GBIF	5537806
Freebase	/m/0nbcz8z
EPPO	ANKDE
EOL	2905502
Elurikkus	540309
USDA GRIN	102044
CMAUP	NPO15394

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

Chemical Relationship among Genetically Authenticated Medicinal Species of Genus Angelica

Kim JH, Doh EJ, Kim HY, Lee G

Plants (Basel)

30-Apr-2024

PMCID:	PMC11085054
doi:	10.3390/plants13091252
PMID:	38732467

Vasorelaxant and Blood Pressure-Lowering Effects of Cnidium monnieri Fruit Ethanol Extract in Sprague Dawley and Spontaneously Hypertensive Rats

Park J, Shin S, Bu Y, Choi HY, Lee K

Int J Mol Sci

11-Apr-2024

PMCID:	PMC11050430
doi:	10.3390/ijms25084223
PMID:	38673809

Complete chloroplast genome of Angelica hirsutiflora Liu et al. 1961 (Apiaceae)

Huang CC, Hsu TW, Hung KH, Wang WK

Mitochondrial DNA B Resour

05-Apr-2024

PMCID:	PMC11000599
doi:	10.1080/23802359.2024.2335992
PMID:	38591054

A comprehensive review of the anticancer effects of decursin

Chu Y, Yuan Q, Jiang H, Wu L, Xie Y, Zhang X, Li L

Front Pharmacol

20-Feb-2024

PMCID:	PMC10912667
doi:	10.3389/fphar.2024.1303412
PMID:	38444945

A taxonomic revision of the genus Angelica (Apiaceae) in Taiwan with a new species A. aliensis

Wang JC, Chen HH, Hsu TW, Hung KH, Huang CC

Bot Stud

22-Jan-2024

PMCID:	PMC10803708
doi:	10.1186/s40529-023-00407-7
PMID:	38252347

Selection and Verification of Standardized Reference Genes of Angelica dahurica under Various Abiotic Stresses by Real-Time Quantitative PCR

Zhang J, He X, Zhou J, Dong Z, Yu H, Tang Q, Yuan L, Peng S, Zhong X, He Y

Genes (Basel)

07-Jan-2024

PMCID:	PMC10815136
doi:	10.3390/genes15010079
PMID:	38254968

Biosynthetic pathway of prescription bergenin from Bergenia purpurascens and Ardisia japonica

Liu XY, Wang YN, Du JS, Chen BH, Liu KY, Feng L, Xiang GS, Zhang SY, Lu YC, Yang SC, Zhang GH, Hao B

Front Plant Sci

04-Jan-2024

PMCID:	PMC10794647
doi:	10.3389/fpls.2023.1259347
PMID:	38239219

A Review on the Morphology, Cultivation, Identification, Phytochemistry, and Pharmacology of Kitagawia praeruptora (Dunn) Pimenov

Wang Q, Ding L, Wang R, Liang Z

Molecules

18-Dec-2023

PMCID:	PMC10745425
doi:	10.3390/molecules28248153
PMID:	38138641

Umbelliferone and Its Synthetic Derivatives as Suitable Molecules for the Development of Agents with Biological Activities: A Review of Their Pharmacological and Therapeutic Potential

Kornicka A, Balewski Ł, Lahutta M, Kokoszka J

Pharmaceuticals (Basel)

15-Dec-2023

PMCID:	PMC10747342
doi:	10.3390/ph16121732
PMID:	38139858

Insampaedok-San Extract Exerts an Immune-Enhancing Effect through NF-κB p65 Pathway Activation

Huh G, Oh Y, Jeon Y, Kang KS, Kim SN, Jung SH, Kim SH, Kim YJ

Biomed Res Int

22-Sep-2023

PMCID:	PMC10541303
doi:	10.1155/2023/5458504
PMID:	37780486

The Efficacy of Herbs as Complementary and Alternative Therapy in Recovery and Clinical Outcome Among People with COVID-19: A Systematic Review, Meta-Analysis, and Meta-Regression

Komariah M, Amirah S, Maulana S, Abdurrahman MF, Ibrahim K, Platini H, Lele JA, Kohar K, Rahayuwati L, Firdaus MK

Ther Clin Risk Manag

18-Jul-2023

PMCID:	PMC10362865
doi:	10.2147/TCRM.S405507
PMID:	37484695

Identification of Anti-Inflammatory Compounds from Peucedanum praeruptorum Roots by Using Nitric Oxide-Producing Rat Hepatocytes Stimulated by Interleukin 1β

Ozaki H, Nishidono Y, Fujii A, Okuyama T, Nakamura K, Maesako T, Shirako S, Nakatake R, Tanaka K, Ikeya Y, Nishizawa M

Molecules

28-Jun-2023

PMCID:	PMC10343554
doi:	10.3390/molecules28135076
PMID:	37446738

Re-Examination of Several Elsinoë Species Reported from Japan

Ujat AH, Ono T, Hattori Y, Nakashima C

Mycobiology

15-Jun-2023

PMCID:	PMC10288934
doi:	10.1080/12298093.2023.2219049
PMID:	37359956

Herbal medicine use in Republic of Korea to alleviate side effects of COVID-19 vaccines: A cross-sectional study

Yoon HC

J Integr Med

08-Jun-2023

PMCID:	PMC10249366
doi:	10.1016/j.joim.2023.06.002
PMID:	37349213

Natural products targeting inflammation-related metabolic disorders: A comprehensive review

Nainu F, Frediansyah A, Mamada SS, Permana AD, Salampe M, Chandran D, Emran TB, Simal-Gandara J

Heliyon

02-Jun-2023

PMCID:	PMC10279840
doi:	10.1016/j.heliyon.2023.e16919
PMID:	37346355

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
> Benzenoids / Anthracenes / Anthraquinones
1-Hydroxyanthraquinone	8512	Click to see C1=CC=C2C(=C1)C(=O)C3=C(C2=O)C(=CC=C3)O	224.21	unknown	via CMAUP database
> Benzenoids / Phenol ethers / Anisoles
Estragole	8815	Click to see COC1=CC=C(C=C1)CC=C	148.20	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Palmitic Acid	985	Click to see CCCCCCCCCCCCCCCC(=O)O	256.42	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Straight chain fatty acids
Butyric Acid	264	Click to see CCCC(=O)O	88.11	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Very long-chain fatty acids
Lignoceric Acid	11197	Click to see CCCCCCCCCCCCCCCCCCCCCCCC(=O)O	368.60	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohol esters
Acetylatractylodinol	5315531	Click to see CC(=O)OCC=CC#CC#CC=CC1=CC=CO1	240.25	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols / Long-chain fatty alcohols
(3R,8S,9E)-heptadeca-1,9-dien-4,6-diyne-3,8-diol	56935895	Click to see CCCCCCCC=CC(C#CC#CC(C=C)O)O	260.40	unknown	via CMAUP database
(3S,8R,9E)-heptadeca-1,9-dien-4,6-diyne-3,8-diol	91973785	Click to see CCCCCCCC=CC(C#CC#CC(C=C)O)O	260.40	unknown	via CMAUP database
(8S,9Z)-Heptadeca-1,9-diene-4,6-diyne-3,8-diol	46887429	Click to see CCCCCCCC=CC(C#CC#CC(C=C)O)O	260.40	unknown	via CMAUP database
1,9-Heptadecadiene-4,6-diyne-3,8-diol	6436239	Click to see CCCCCCCC=CC(C#CC#CC(C=C)O)O	260.40	unknown	via CMAUP database
CID 5283263	5283263	Click to see CCCCCCCC=CC(C#CC#CC(C=C)O)O	260.40	unknown	via CMAUP database
Falcarindiol	5281148	Click to see CCCCCCCC=CC(C#CC#CC(C=C)O)O	260.40	unknown	via CMAUP database
Heptadeca-1,9-dien-4,6-diyne-3,8-diol	3321	Click to see CCCCCCCC=CC(C#CC#CC(C=C)O)O	260.40	unknown	via CMAUP database
Heptadeca-1,9-diene-4,6-diyne-3,8-diol	5317309	Click to see CCCCCCCC=CC(C#CC#CC(C=C)O)O	260.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Tanshinones, isotanshinones, and derivatives
Tanshinone I	114917	Click to see CC1=C2C=CC3=C(C2=CC=C1)C(=O)C(=O)C4=C3OC=C4C	276.30	unknown	via CMAUP database
Tanshinone IIA	164676	Click to see CC1=COC2=C1C(=O)C(=O)C3=C2C=CC4=C3CCCC4(C)C	294.30	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
Ostruthin	5281420	Click to see CC(=CCCC(=CCC1=C(C=C2C(=C1)C=CC(=O)O2)O)C)C	298.40	unknown	https://doi.org/10.1016/J.CHROMA.2005.04.041
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids / Limonoids
methyl 2-[(14S)-14-acetyloxy-6-(furan-3-yl)-13-hydroxy-1,5,15,15-tetramethyl-8,17-dioxo-7-oxatetracyclo[11.3.1.02,11.05,10]heptadeca-2(11),9-dien-16-yl]acetate	5318146	Click to see CC(=O)OC1C(C(C2(C3=C(CC1(C2=O)O)C4=CC(=O)OC(C4(CC3)C)C5=COC=C5)C)CC(=O)OC)(C)C	526.60	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
17-[(E)-5,6-dimethylhept-3-en-2-yl]-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-ol	5364671	Click to see CC(C)C(C)C=CC(C)C1CCC2C1(CCC3C2CCC4C3(CCC(C4)O)C)C	400.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Estrane steroids / Estrogens and derivatives
(13S)-13-methyl-6,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthrene-3,16,17-triol	16757678	Click to see CC12CCC3C(C1CC(C2O)O)CCC4=C3C=CC(=C4)O	288.40	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
Sitogluside	5742590	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C	576.80	unknown	via CMAUP database
Stigmasterol	5280794	Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	412.70	unknown	via CMAUP database
> Nucleosides, nucleotides, and analogues / Purine nucleosides
Adenosine	60961	Click to see C1=NC(=C2C(=N1)N(C=N2)C3C(C(C(O3)CO)O)O)N	267.24	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
(1R,2R)-1-hydroxypropane-1,2,3-tricarboxylic acid	439238	Click to see C(C(C(C(=O)O)O)C(=O)O)C(=O)O	192.12	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
Eleutheroside B	5316860	Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)C=CCO	372.40	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Sugar alcohols
Mannitol	6251	Click to see C(C(C(C(C(CO)O)O)O)O)O	182.17	unknown	via CMAUP database
> Organoheterocyclic compounds / Azolidines / Imidazolidines / Hydantoins / Phenylhydantoins
Methetoin	21908	Click to see CCC1(C(=O)NC(=O)N1C)C2=CC=CC=C2	218.25	unknown	via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Pyridoindoles / Beta carbolines
Decussine	156336	Click to see CC1C2=C(C=CN=C2)C=C3C4=C(CCN3C)C5=CC=CC=C5N14	301.40	unknown	via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Pyrroloindoles
Hydroxysporidesmin B	317024	Click to see CC12C(=O)N3C4C(C(C3(C(=O)N1C)SS2)O)(C5=CC(=C(C(=C5N4C)OC)OC)Cl)O	474.00	unknown	via CMAUP database
> Organoheterocyclic compounds / Naphthofurans
(12S)-6,15-dihydroxy-8,12,13,13-tetramethyl-3,11-dioxatetracyclo[7.6.1.05,16.010,14]hexadeca-1(15),5,7,9(16),10(14)-pentaene-2,4-dione	14556961	Click to see CC1C(C2=C(O1)C3=C4C(=C(C=C3C)O)C(=O)OC(=O)C4=C2O)(C)C	328.30	unknown	via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives
2,6-Dimethylquinoline	13414	Click to see CC1=CC2=C(C=C1)N=C(C=C2)C	157.21	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
Decursidate	102004630	Click to see COC1=C(C=CC(=C1)C=CC(=O)OCC(C2=CC=C(C=C2)O)O)O	330.30	unknown	https://doi.org/10.1080/10286020108042832
> Phenylpropanoids and polyketides / Coumarins and derivatives
5-Methoxycoumarin	10899191	Click to see COC1=CC=CC2=C1C=CC(=O)O2	176.17	unknown	via CMAUP database
5,8-Dimethoxycoumarin	609839	Click to see COC1=C2C=CC(=O)OC2=C(C=C1)OC	206.19	unknown	via CMAUP database
Coumarin	323	Click to see C1=CC=C2C(=C1)C=CC(=O)O2	146.14	unknown	via CMAUP database
Coumarin 7	94381	Click to see CCN(CC)C1=CC2=C(C=C1)C=C(C(=O)O2)C3=NC4=CC=CC=C4N3	333.40	unknown	via CMAUP database
Thamnosmonin	312089	Click to see CC(=C)C(C(C1=C(C=C2C(=C1)C=CC(=O)O2)OC)O)O	276.28	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Coumarin glycosides
Apiosylskimmin	14236613	Click to see C1C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC4=C(C=C3)C=CC(=O)O4)O)O)O)O)(CO)O	456.40	unknown	via CMAUP database
Rutarin	442149	Click to see CC(C)(C1CC2=C(O1)C(=C3C(=C2)C=CC(=O)O3)OC4C(C(C(C(O4)CO)O)O)O)O	424.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Angular furanocoumarins
(8S,9R)-9-hydroxy-8-[2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypropan-2-yl]-8,9-dihydrofuro[2,3-h]chromen-2-one	15945058	Click to see CC(C)(C1C(C2=C(O1)C=CC3=C2OC(=O)C=C3)O)OC4C(C(C(C(O4)CO)O)O)O	424.40	unknown	via CMAUP database
9-Hydroxy-8-[2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypropan-2-yl]-8,9-dihydrofuro[2,3-h]chromen-2-one	5245822	Click to see CC(C)(C1C(C2=C(O1)C=CC3=C2OC(=O)C=C3)O)OC4C(C(C(C(O4)CO)O)O)O	424.40	unknown	via CMAUP database
Apterin	57459455	Click to see CC(C)(C1C(C2=C(O1)C=CC3=C2OC(=O)C=C3)O)OC4C(C(C(C(O4)CO)O)O)O	424.40	unknown	via CMAUP database
Columbianadin	6436246	Click to see CC=C(C)C(=O)OC(C)(C)C1CC2=C(O1)C=CC3=C2OC(=O)C=C3	328.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens
(3S)-3-(2-hydroxypropan-2-yl)-2,3-dihydrofuro[3,2-g]chromen-7-one	97464456	Click to see CC(C)(C1COC2=C1C=C3C=CC(=O)OC3=C2)O	246.26	unknown	https://doi.org/10.1248/YAKUSHI1947.89.4_549
(S)-Rutaretin	11108126	Click to see CC(C)(C1CC2=C(O1)C(=C3C(=C2)C=CC(=O)O3)O)O	262.26	unknown	via CMAUP database
2-(2-{[3,4,5-trihydroxy-6-({[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)oxan-2-yl]oxy}propan-2-yl)-2H,3H-furo[3,2-g]chromen-7-one	137796537	Click to see CC(C)(C1CC2=C(O1)C=C3C(=C2)C=CC(=O)O3)OC4C(C(C(C(O4)COC5C(C(C(C(O5)CO)O)O)O)O)O)O	570.50	unknown	https://doi.org/10.1248/CPB.22.957 https://doi.org/10.1055/S-2007-969099 https://doi.org/10.1055/S-2007-969780
2-(2-Hydroxypropan-2-yl)-2,3-dihydrofuro[3,2-g]chromen-7-one	604512	Click to see CC(C)(C1CC2=C(O1)C=C3C(=C2)C=CC(=O)O3)O	246.26	unknown	https://doi.org/10.1007/S12272-015-0629-0
2-[2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypropan-2-yl]-2,3-dihydrofuro[3,2-g]chromen-7-one	5319288	Click to see CC(C)(C1CC2=C(O1)C=C3C(=C2)C=CC(=O)O3)OC4C(C(C(C(O4)CO)O)O)O	408.40	unknown	via CMAUP database
3-(2-Hydroxypropan-2-yl)-2,3-dihydrofuro[3,2-g]chromen-7-one	49874704	Click to see CC(C)(C1COC2=C1C=C3C=CC(=O)OC3=C2)O	246.26	unknown	https://doi.org/10.1248/YAKUSHI1947.89.4_549
9-hydroxy-2-[2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypropan-2-yl]-2,3-dihydrofuro[3,2-g]chromen-7-one	102597253	Click to see CC(C)(C1CC2=C(O1)C(=C3C(=C2)C=CC(=O)O3)O)OC4C(C(C(C(O4)CO)O)O)O	424.40	unknown	via CMAUP database
Ammijin	216283	Click to see CC(C)(C1CC2=C(O1)C=C3C(=C2)C=CC(=O)O3)OC4C(C(C(C(O4)CO)O)O)O	408.40	unknown	via CMAUP database
Decuroside III	442125	Click to see CC(C)(C1CC2=C(O1)C=C3C(=C2)C=CC(=O)O3)OC4C(C(C(C(O4)CO)OC5C(C(C(C(O5)CO)O)O)O)O)O	570.50	unknown	https://doi.org/10.1055/S-2007-969099 https://doi.org/10.1055/S-2007-969780
Deltoin	906525	Click to see CC=C(C)C(=O)OC(C)(C)C1CC2=C(O1)C=C3C(=C2)C=CC(=O)O3	328.40	unknown	via CMAUP database
Isoimperatorin	68081	Click to see CC(=CCOC1=C2C=CC(=O)OC2=CC3=C1C=CO3)C	270.28	unknown	https://doi.org/10.1007/BF00568603
Leptophylloside	185756	Click to see CC(C)(C1CC2=C(O1)C(=C3C(=C2)C=CC(=O)O3)O)OC4C(C(C(C(O4)CO)O)O)O	424.40	unknown	via CMAUP database
Marmesin	334704	Click to see CC(C)(C1CC2=C(O1)C=C3C(=C2)C=CC(=O)O3)O	246.26	unknown	https://doi.org/10.1007/S12272-015-0629-0
Nodakenetin	26305	Click to see CC(C)(C1CC2=C(O1)C=C3C(=C2)C=CC(=O)O3)O	246.26	unknown	https://doi.org/10.1055/S-2007-969098 https://doi.org/10.1016/J.JEP.2014.07.033 https://doi.org/10.1055/S-2007-969646
Nodakenetin Tiglate	906523	Click to see CC=C(C)C(=O)OC(C)(C)C1CC2=C(O1)C=C3C(=C2)C=CC(=O)O3	328.40	unknown	via CMAUP database
Nodakenin	73191	Click to see CC(C)(C1CC2=C(O1)C=C3C(=C2)C=CC(=O)O3)OC4C(C(C(C(O4)CO)O)O)O	408.40	unknown	https://doi.org/10.1055/S-2007-969099 https://doi.org/10.1055/S-2007-969098 https://doi.org/10.1248/CPB.22.957 https://doi.org/10.1055/S-2007-969646
Pentosalen	10212	Click to see CC(=CCOC1=C2C(=CC3=C1OC=C3)C=CC(=O)O2)C	270.28	unknown	https://doi.org/10.1007/BF00568603
Peucedanin	8616	Click to see CC(C)C1=C(C2=C(O1)C=C3C(=C2)C=CC(=O)O3)OC	258.27	unknown	via CMAUP database
Rutaretin	44146779	Click to see CC(C)(C1CC2=C(O1)C(=C3C(=C2)C=CC(=O)O3)O)O	262.26	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 / Furanocoumarins / Psoralens / 8-methoxypsoralens
Isopimpinellin	68079	Click to see COC1=C2C=COC2=C(C3=C1C=CC(=O)O3)OC	246.21	unknown	via CMAUP database
Methoxsalen	4114	Click to see COC1=C2C(=CC3=C1OC=C3)C=CC(=O)O2	216.19	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
3,4,5,6,8-Pentadeuterio-7-hydroxychromen-2-one	45358955	Click to see C1=CC(=CC2=C1C=CC(=O)O2)O	167.17	unknown	via CMAUP database
Scopoletin	5280460	Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)O	192.17	unknown	via CMAUP database
Umbelliferone	5281426	Click to see C1=CC(=CC2=C1C=CC(=O)O2)O	162.14	unknown	https://doi.org/10.1248/CPB.22.957
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Angular pyranocoumarins
(-)-Praeruptorin A	9821539	Click to see CC=C(C)C(=O)OC1C(C2=C(C=CC3=C2OC(=O)C=C3)OC1(C)C)OC(=O)C	386.40	unknown	via CMAUP database
(-)-trans-Khellactone	9992853	Click to see CC1(C(C(C2=C(O1)C=CC3=C2OC(=O)C=C3)O)O)C	262.26	unknown	via CMAUP database
(+)-trans-Khellactone	11436940	Click to see CC1(C(C(C2=C(O1)C=CC3=C2OC(=O)C=C3)O)O)C	262.26	unknown	via CMAUP database
(10-Hydroxy-8,8-dimethyl-2-oxo-9,10-dihydropyrano[2,3-f]chromen-9-yl) 3-methylbut-2-enoate	511784	Click to see CC(=CC(=O)OC1C(C2=C(C=CC3=C2OC(=O)C=C3)OC1(C)C)O)C	344.40	unknown	via CMAUP database
(9S)-8,8-Dimethyl-9beta-acetoxy-10beta-(angeloyloxy)-9,10-dihydro-2H,8H-benzo[1,2-b:3,4-b']dipyran-2-one	1549023	Click to see CC=C(C)C(=O)OC1C(C(OC2=C1C3=C(C=C2)C=CC(=O)O3)(C)C)OC(=O)C	386.40	unknown	via CMAUP database
[(9R,10R)-8,8-dimethyl-10-(3-methylbutanoyloxy)-2-oxo-9,10-dihydropyrano[2,3-f]chromen-9-yl] (E)-2-methylbut-2-enoate	102004525	Click to see CC=C(C)C(=O)OC1C(C2=C(C=CC3=C2OC(=O)C=C3)OC1(C)C)OC(=O)CC(C)C	428.50	unknown	via CMAUP database
[(9R,10R)-9-hydroxy-8,8-dimethyl-2-oxo-9,10-dihydropyrano[2,3-f]chromen-10-yl] (Z)-2-methylbut-2-enoate	5320810	Click to see CC=C(C)C(=O)OC1C(C(OC2=C1C3=C(C=C2)C=CC(=O)O3)(C)C)O	344.40	unknown	via CMAUP database
[(9R,10S)-10-acetyloxy-8,8-dimethyl-2-oxo-9,10-dihydropyrano[2,3-f]chromen-9-yl] (Z)-2-methylbut-2-enoate	38347601	Click to see CC=C(C)C(=O)OC1C(C2=C(C=CC3=C2OC(=O)C=C3)OC1(C)C)OC(=O)C	386.40	unknown	via CMAUP database
[(9S,10S)-10-acetyloxy-8,8-dimethyl-2-oxo-9,10-dihydropyrano[2,3-f]chromen-9-yl] (E)-2-methylbut-2-enoate	56846505	Click to see CC=C(C)C(=O)OC1C(C2=C(C=CC3=C2OC(=O)C=C3)OC1(C)C)OC(=O)C	386.40	unknown	via CMAUP database
[(9S,10S)-8,8-dimethyl-9-[(E)-2-methylbut-2-enoyl]oxy-2-oxo-9,10-dihydropyrano[2,3-f]chromen-10-yl] (E)-2-methylbut-2-enoate	1070682	Click to see CC=C(C)C(=O)OC1C(C(OC2=C1C3=C(C=C2)C=CC(=O)O3)(C)C)OC(=O)C(=CC)C	426.50	unknown	via CMAUP database
[(9S)-8,8-dimethyl-2,10-dioxo-9H-pyrano[2,3-f]chromen-9-yl] (E)-2-methylbut-2-enoate	102004715	Click to see CC=C(C)C(=O)OC1C(=O)C2=C(C=CC3=C2OC(=O)C=C3)OC1(C)C	342.30	unknown	via CMAUP database
3'-Angeloyloxy-4'-acetoxy-3',4'-dihydroseselin	13964641	Click to see CC=C(C)C(=O)OC1C(C2=C(C=CC3=C2OC(=O)C=C3)OC1(C)C)OC(=O)C	386.40	unknown	via CMAUP database
9-Hydroxy-8,8-dimethyl-10-(3-methyl-1-methylene-but-2-enoxy)-9,10-dihydropyrano[2,3-f]chromen-2-one	511785	Click to see CC(=CC(=C)OC1C(C(OC2=C1C3=C(C=C2)C=CC(=O)O3)(C)C)O)C	342.40	unknown	via CMAUP database
cis-3',4'-Diisovalerylkhellactone	44584701	Click to see CC(C)CC(=O)OC1C(C(OC2=C1C3=C(C=C2)C=CC(=O)O3)(C)C)OC(=O)CC(C)C	430.50	unknown	via CMAUP database
cis-3',4'-Disenecioylkhellactone	1119128	Click to see CC(=CC(=O)OC1C(C(OC2=C1C3=C(C=C2)C=CC(=O)O3)(C)C)OC(=O)C=C(C)C)C	426.50	unknown	via CMAUP database
Corymbocoumarin	969471	Click to see CC(C)CC(=O)OC1C(C(OC2=C1C3=C(C=C2)C=CC(=O)O3)(C)C)OC(=O)C	388.40	unknown	via CMAUP database
Cyclocumarol	10606	Click to see CC1(CC(C2=C(O1)C3=CC=CC=C3OC2=O)C4=CC=CC=C4)OC	322.40	unknown	via CMAUP database
d-Laserpitin	51396729	Click to see CC=C(C)C(=O)OC1C(C(OC2=C1C3=C(C=C2)C=CC(=O)O3)(C)C)O	344.40	unknown	via CMAUP database
Hyuganin D	10317265	Click to see CC(C)C(=O)OC1C(C(OC2=C1C3=C(C=C2)C=CC(=O)O3)(C)C)OC(=O)C	374.40	unknown	via CMAUP database
Khellactone	253856	Click to see CC1(C(C(C2=C(O1)C=CC3=C2OC(=O)C=C3)O)O)C	262.26	unknown	via CMAUP database
Khellactone, cis-(-)-	11097348	Click to see CC1(C(C(C2=C(O1)C=CC3=C2OC(=O)C=C3)O)O)C	262.26	unknown	via CMAUP database
Khellactone, cis-(+)-	455821	Click to see CC1(C(C(C2=C(O1)C=CC3=C2OC(=O)C=C3)O)O)C	262.26	unknown	via CMAUP database
Peucedanocoumarin I	12314635	Click to see CCC(C)C(=O)OC1C(C2=C(C=CC3=C2OC(=O)C=C3)OC1(C)C)OC(=O)C	388.40	unknown	via CMAUP database
Peucedanocoumarin II	5434471	Click to see CC=C(C)C(=O)OC1C(C(OC2=C1C3=C(C=C2)C=CC(=O)O3)(C)C)OC(=O)C	386.40	unknown	via CMAUP database
Praeroside III	23786429	Click to see CC1(C(C(C2=C(O1)C=CC3=C2OC(=O)C=C3)O)OC4C(C(C(C(O4)CO)O)O)O)C	424.40	unknown	via CMAUP database
Praeruptorin A	38347607	Click to see CC=C(C)C(=O)OC1C(C2=C(C=CC3=C2OC(=O)C=C3)OC1(C)C)OC(=O)C	386.40	unknown	via CMAUP database
Praeruptorin B	5319259	Click to see CC=C(C)C(=O)OC1C(C(OC2=C1C3=C(C=C2)C=CC(=O)O3)(C)C)OC(=O)C(=CC)C	426.50	unknown	via CMAUP database
Praeruptorin C	5320692	Click to see CC=C(C)C(=O)OC1C(C2=C(C=CC3=C2OC(=O)C=C3)OC1(C)C)OC(=O)CC(C)C	428.50	unknown	via CMAUP database
Praeruptorin D	25717254	Click to see CC=C(C)C(=O)OC1C(C(OC2=C1C3=C(C=C2)C=CC(=O)O3)(C)C)OC(=O)C(=CC)C	426.50	unknown	via CMAUP database
Praeruptorin E	6440581	Click to see CC=C(C)C(=O)OC1C(C2=C(C=CC3=C2OC(=O)C=C3)OC1(C)C)OC(=O)CC(C)C	428.50	unknown	via CMAUP database
Pteryxin	5281425	Click to see CC=C(C)C(=O)OC1C(C(OC2=C1C3=C(C=C2)C=CC(=O)O3)(C)C)OC(=O)C	386.40	unknown	via CMAUP database
Qianhucoumarin A	6444285	Click to see CC=C(C)C(=O)OC1C(C(OC2=C1C3=C(C=C2)C=CC(=O)O3)(C)C)O	344.40	unknown	via CMAUP database
Qianhucoumarin B	197634	Click to see CC(=O)OC1C(C2=C(C=CC3=C2OC(=O)C=C3)OC1(C)C)O	304.29	unknown	via CMAUP database
Samidin	442150	Click to see CC(=CC(=O)OC1C(C2=C(C=CC3=C2OC(=O)C=C3)OC1(C)C)OC(=O)C)C	386.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Linear pyranocoumarins
(+)-trans-Decursidinol	10355323	Click to see CC1(C(C(C2=C(O1)C=C3C(=C2)C=CC(=O)O3)O)O)C	262.26	unknown	https://doi.org/10.1055/S-0036-1596440
(3R,4R)-2,2-dimethyl-3-(3-methylbutanoyl)-4-[(E)-2-methylbut-2-enoyl]-3,4-dihydropyrano[3,2-g]chromen-8-one	163185712	Click to see CC=C(C)C(=O)C1C(C(OC2=C1C=C3C=CC(=O)OC3=C2)(C)C)C(=O)CC(C)C	396.50	unknown	https://doi.org/10.1248/YAKUSHI1947.89.4_549
(3R,4R)-2,2-dimethyl-4-(3-methylbutanoyl)-3-[(E)-2-methylbut-2-enoyl]-3,4-dihydropyrano[3,2-g]chromen-8-one	163193797	Click to see CC=C(C)C(=O)C1C(C2=C(C=C3C(=C2)C=CC(=O)O3)OC1(C)C)C(=O)CC(C)C	396.50	unknown	https://doi.org/10.1248/YAKUSHI1947.89.4_549
(S)-8,8-Dimethyl-2-oxo-7,8-dihydro-2H,6H-pyrano(3,2-g)chromen-7-yl 3-methyl-2-butenoate	611537	Click to see CC(=CC(=O)OC1CC2=C(C=C3C(=C2)C=CC(=O)O3)OC1(C)C)C	328.40	unknown	https://doi.org/10.1248/YAKUSHI1947.89.4_549
[(3R)-2,2-dimethyl-8-oxo-3,4-dihydropyrano[3,2-g]chromen-3-yl] 3-methylbut-2-enoate	44144310	Click to see CC(=CC(=O)OC1CC2=C(C=C3C(=C2)C=CC(=O)O3)OC1(C)C)C	328.40	unknown	https://doi.org/10.1248/YAKUSHI1947.89.4_549
[(3S,4R)-2,2-dimethyl-3-(3-methylbut-2-enoyloxy)-8-oxo-3,4-dihydropyrano[3,2-g]chromen-4-yl] (Z)-2-methylbut-2-enoate	21581509	Click to see CC=C(C)C(=O)OC1C(C(OC2=C1C=C3C=CC(=O)OC3=C2)(C)C)OC(=O)C=C(C)C	426.50	unknown	https://doi.org/10.1016/0031-9422(96)00176-8
2,2-Dimethyl-3-(3-methylbutanoyl)-4-(2-methylbut-2-enoyl)-3,4-dihydropyrano[3,2-g]chromen-8-one	162856861	Click to see CC=C(C)C(=O)C1C(C(OC2=C1C=C3C=CC(=O)OC3=C2)(C)C)C(=O)CC(C)C	396.50	unknown	https://doi.org/10.1248/YAKUSHI1947.89.4_549
2,2-Dimethyl-4-(3-methylbutanoyl)-3-(2-methylbut-2-enoyl)-3,4-dihydropyrano[3,2-g]chromen-8-one	162965852	Click to see CC=C(C)C(=O)C1C(C2=C(C=C3C(=C2)C=CC(=O)O3)OC1(C)C)C(=O)CC(C)C	396.50	unknown	https://doi.org/10.1248/YAKUSHI1947.89.4_549
Aegelinol	600671	Click to see CC1(C(CC2=C(O1)C=C3C(=C2)C=CC(=O)O3)O)C	246.26	unknown	https://doi.org/10.1002/PTR.3372 https://doi.org/10.1021/NP000441W https://doi.org/10.3109/00498254.2011.587551
Decursidin	15521791	Click to see CC(=CC(=O)OC1C(C(OC2=C1C=C3C=CC(=O)OC3=C2)(C)C)OC(=O)C=C(C)C)C	426.50	unknown	https://doi.org/10.1248/CPB.22.957 https://doi.org/10.1055/S-2007-969646 https://doi.org/10.1248/CPB.21.518
Decursin	442126	Click to see CC(=CC(=O)OC1CC2=C(C=C3C(=C2)C=CC(=O)O3)OC1(C)C)C	328.40	unknown	https://doi.org/10.1248/YAKUSHI1947.89.4_549 https://doi.org/10.1248/CPB.22.957
Decursinol	442127	Click to see CC1(C(CC2=C(O1)C=C3C(=C2)C=CC(=O)O3)O)C	246.26	unknown	https://doi.org/10.3109/00498254.2011.587551 https://doi.org/10.1021/NP000441W https://doi.org/10.1002/PTR.3372
Decursinol angelate	776123	Click to see CC=C(C)C(=O)OC1CC2=C(C=C3C(=C2)C=CC(=O)O3)OC1(C)C	328.40	unknown	via CMAUP database
Decursinol, (-)-	1150962	Click to see CC1(C(CC2=C(O1)C=C3C(=C2)C=CC(=O)O3)O)C	246.26	unknown	via CMAUP database
Decursitin D	122169319	Click to see CC=C(C)C(=O)OC1C(C(OC2=C1C=C3C=CC(=O)OC3=C2)(C)C)O	344.40	unknown	https://doi.org/10.1055/S-0036-1596440 https://doi.org/10.1016/0031-9422(96)00176-8
Pd-C-II	122169320	Click to see CC(=CC(=O)OC1C(C(OC2=C1C=C3C=CC(=O)OC3=C2)(C)C)O)C	344.40	unknown	https://doi.org/10.1055/S-2007-969098

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Angelica decursiva

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