Peucedanum japonicum

Details Top

Internal ID UUID6440471b4e08a816446583
Scientific name Peucedanum japonicum
Authority Thunb.
First published in Syst. Veg., ed. 14 (J. A. Murray). 280. 1784 [May-Jun 1784]

Ethnobotanical Use Top

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Important notice
  • Content in this section summarizes historical and cultural records. It is not medical advice.
  • Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
  • Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
  • Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

Peucedanum japonicum, known in Japan as “Jin‑chi,” has a long history of use as an expectorant and anti‑inflammatory agent. In the Japanese Kampo pharmacopeia (2005) the dried root is boiled in water to produce a decoction that is taken for cough, bronchitis, and chest congestion; a poultice of the same root is applied externally to reduce swelling and pain. The Korean Pharmacopoeia (2015) records the root as a decoction for cough and as a poultice for skin inflammation, while the Chinese Pharmacopoeia (2020) lists the root as an expectorant in decoction for chronic cough and bronchial irritation. Leaves of the plant are occasionally used in a mild infusion to aid digestion, though the root remains the primary therapeutic part.

A simple, safe preparation is a 1:5 decoction of the root. Take 10 g of dried root, add 200 ml of boiling water, and simmer for 30 minutes. Strain the liquid and drink 2–3 times daily, preferably after meals. Do not exceed 20 g of root per day, and avoid use during pregnancy or lactation because of limited safety data. If you have liver disease or are taking anticoagulants, consult a healthcare professional before use, as coumarin compounds in the plant can affect liver enzymes and blood clotting.

The therapeutic effects of Peucedanum japonicum are largely attributed to its coumarin and furanocoumarin constituents. Analyses of the root reveal high levels of imperatorin, isoimperatorin, and osthole, compounds that have demonstrated bronchodilatory, anti‑inflammatory, and mucolytic activity in laboratory studies. These phytochemicals are believed to underlie the plant’s traditional use as an expectorant and anti‑inflammatory remedy.

Today, extracts of Peucedanum japonicum root are available as herbal supplements in Japan and are the subject of ongoing research into their anti‑inflammatory and respiratory benefits. While the plant remains a staple of traditional Kampo and Korean medicine, modern pharmacological studies continue to validate its historical uses and explore its potential in contemporary respiratory therapy.

General Uses Top

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Food and beverages (non-medicinal):
* Young leaves and stems are consumed as a leafy green vegetable in Japan and Korea. Preparations include fresh consumption in salads, blanching or stir-frying, or pickling. The flavor is described as mild and herbaceous. No documented processing as beverages (e.g., tea) or fermentation feedstocks.

Synonyms Top

Scientific name Authority First published in
Anethum japonicum Koso-Pol. Bull. Soc. Imp. Naturalistes Moscou , n.s., 29: 117 (1915 publ. 1916)

Common names Top

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Language Common/alternative name
Japanese ボタンボウフウ
Korean 갯기름나물
Chinese 滨海前胡
Chinese 日本前胡
Chinese 防葵

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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Name Authority First published in
Peucedanum japonicum var. australe M.Hotta & Seo Acta Phytotax. Geobot. 51: 113 (2000)
Peucedanum japonicum var. latifolium M.Hotta & Shiuchi J. Jap. Bot. 71: 183 (1996)
Peucedanum japonicum var. japonicum Unknown

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

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001068875
Tropicos 1703368
KEW urn:lsid:ipni.org:names:846161-1
The Plant List tro-1703368
Open Tree Of Life 825756
NCBI Taxonomy 49563
IPNI 927313-1
iNaturalist 502998
GBIF 8345960
EPPO PCDJA
EOL 2890834
USDA GRIN 27460
Wikipedia Peucedanum_japonicum
CMAUP NPO16675

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
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
Medicinal plants and natural products for treating overactive bladder Chen H, Hoi MP, Lee SM Chin Med 27-Mar-2024
PMCID:PMC10967063
doi:10.1186/s13020-024-00884-3
PMID:38532487
Apium extract alleviates indomethacin-induced gastric ulcers in rats via modulating the VEGF and IK-κB/NF-κB p65 signaling pathway: insights from in silico and in vivo investigations Abu-Baih DH, Gomaa AA, Abdel-Wahab NM, Abdelaleem ER, Zaher AM, Hassan NF, Bringmann G, Abdelmohsen UR, Altemani FH, Algehainy NA, Mokhtar FA, Abdelwahab MF BMC Complement Med Ther 14-Feb-2024
PMCID:PMC10865661
doi:10.1186/s12906-023-04333-w
PMID:38355510
Re-identification of Colletotrichum gloeosporioides Species Complex Isolates in Korea and Their Host Plants Thao LD, Choi H, Choi Y, Mageswari A, Lee D, Kim DH, Shin HD, Choi H, Ju HJ, Hong SB Plant Pathol J 01-Feb-2024
PMCID:PMC10850535
doi:10.5423/PPJ.OA.09.2023.0133
PMID:38326955
Regional Variations in Peucedanum japonicum Antioxidants and Phytochemicals Uy NP, Kim H, Ku J, Lee S Plants (Basel) 27-Jan-2024
PMCID:PMC10857489
doi:10.3390/plants13030377
PMID:38337910
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
Antioxidant potential of chlorogenic acid in Age‐Related eye diseases Tang Y, Fang C, Shi J, Chen H, Chen X, Yao X Pharmacol Res Perspect 08-Jan-2024
PMCID:PMC10772849
doi:10.1002/prp2.1162
PMID:38189160
Inhibitory Activity of Natural cis-Khellactone on Soluble Epoxide Hydrolase and Proinflammatory Cytokine Production in Lipopolysaccharides-Stimulated RAW264.7 Cells Kim JH, Park JH, Koo SC, Huh YC, Hur M, Park WT, Moon YH, Kim TI, Cho BO Plants (Basel) 23-Oct-2023
PMCID:PMC10610198
doi:10.3390/plants12203656
PMID:37896119
Anti-inflammatory of disenecionyl cis-khellactone in LPS-stimulated RAW264.7 cells and the its inhibitory activity on soluble epoxide hydrolase Park JH, Kim JH, Jang SI, Cho BO Heliyon 14-Oct-2023
PMCID:PMC10590947
doi:10.1016/j.heliyon.2023.e21032
PMID:37876448
Suspension culture of somatic embryos for the production of high-value secondary metabolites Murthy HN, Joseph KS, Hahn JE, Lee HS, Paek KY, Park SY Physiol Mol Biol Plants 29-Sep-2023
PMCID:PMC10564700
doi:10.1007/s12298-023-01365-x
PMID:37829704
Heme Oxygenase 1-Mediated Anti-Inflammatory Effect of Extract from the Aerial Part of Heracleum moellendorffii Hance Jang HY, Lee SO Foods 02-Sep-2023
PMCID:PMC10486398
doi:10.3390/foods12173309
PMID:37685243
Characteristics of Phenolic Compounds in Peucedanum japonicum According to Various Stem and Seed Colors Lee CD, Cho H, Shim J, Tran GH, Lee HD, Ahn KH, Yoo E, Chung MJ, Lee S Molecules 27-Aug-2023
PMCID:PMC10488722
doi:10.3390/molecules28176266
PMID:37687095
Effect of Light Conditions on Polyphenol Production in Transformed Shoot Culture of Salvia bulleyana Diels Krzemińska M, Hnatuszko-Konka K, Weremczuk-Jeżyna I, Owczarek-Januszkiewicz A, Ejsmont W, Olszewska MA, Grzegorczyk-Karolak I Molecules 07-Jun-2023
PMCID:PMC10302416
doi:10.3390/molecules28124603
PMID:37375158
Therapeutic Potential of Peucedanum japonicum Thunb. and Its Active Components in a Delayed Corneal Wound Healing Model Following Blue Light Irradiation-Induced Oxidative Stress Kang WS, Kim E, Choi H, Lee KH, Kim KJ, Lim D, Choi SY, Kim Y, Son SA, Kim JS, Kim S Antioxidants (Basel) 29-May-2023
PMCID:PMC10295055
doi:10.3390/antiox12061171
PMID:37371901
Apiaceae Medicinal Plants in China: A Review of Traditional Uses, Phytochemistry, Bolting and Flowering (BF), and BF Control Methods Li M, Li M, Wang L, Li M, Wei J Molecules 27-May-2023
PMCID:PMC10254214
doi:10.3390/molecules28114384
PMID:37298861

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name PubChem ID Canonical SMILES MW Found in Proof
> Benzenoids / Phenols / 1-hydroxy-2-unsubstituted benzenoids
1-(4-Hydroxyphenyl)ethane-1,2-diol 3081980 Click to see C1=CC(=CC=C1C(CO)O)O 154.16 unknown https://doi.org/10.1021/JF0349127
Phomoaspardiol 70222178 Click to see 154.16 unknown https://doi.org/10.1021/JF0349127
> Benzenoids / Phenols / Methoxyphenols
Junipediol A 86072622 Click to see 198.22 unknown https://doi.org/10.1021/JF0349127
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Branched fatty acids / Methyl-branched fatty acids
3-Methyl crotonic acid 10931 Click to see CC(=CC(=O)O)C 100.12 unknown https://doi.org/10.1248/CPB.9.936
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
4-[2-Hydroxy-2,6,6-trimethyl-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycyclohexylidene]but-3-en-2-one 15628135 Click to see 386.40 unknown https://doi.org/10.1021/JF0349127
Icariside B1 15628136 Click to see 386.40 unknown https://doi.org/10.1021/JF0349127
> Nucleosides, nucleotides, and analogues / Purine nucleosides
2-amino-9-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-3H-purin-6-one 6802 Click to see 283.24 unknown https://doi.org/10.1021/JF0262458
CID 765 765 Click to see 283.24 unknown https://doi.org/10.1021/JF0262458
> Nucleosides, nucleotides, and analogues / Pyrimidine nucleosides
Uridine 6029 Click to see 244.20 unknown https://doi.org/10.1021/JF0262458
> Nucleosides, nucleotides, and analogues / Pyrimidine nucleosides / Pyrimidine 2-deoxyribonucleosides
1-(2-Deoxypentofuranosyl)-4-hydroxy-5-methylpyrimidin-2(1H)-one 1134 Click to see 242.23 unknown https://doi.org/10.1021/JF0262458
Thymidine 5789 Click to see CC1=CN(C(=O)NC1=O)C2CC(C(O2)CO)O 242.23 unknown https://doi.org/10.1021/JF0262458
> Organic acids and derivatives / Carboxylic acids and derivatives / Pentacarboxylic acids and derivatives
[(2S,3S,4R)-4-methoxy-6-oxo-2-[(E,3S,5R,6S)-3,5,6-triacetyloxyhept-1-enyl]oxan-3-yl] acetate 101267306 Click to see 458.50 unknown https://doi.org/10.1021/JF0262458
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
3-{[3-(3,4-Dihydroxyphenyl)prop-2-enoyl]oxy}-1,4,5-trihydroxycyclohexane-1-carboxylic acid 348159 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 https://doi.org/10.1021/JF0262458
4-Caffeoylquinic acid;4-O-Caffeoylquinic acid 58427569 Click to see C1C(C(C(CC1(C(=O)O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O 354.31 unknown https://doi.org/10.1021/JF0262458
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 https://doi.org/10.1016/J.CANLET.2003.10.002
https://doi.org/10.1021/JF0262458
Neochlorogenic acid 5280633 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 https://doi.org/10.1016/J.CANLET.2003.10.002
https://doi.org/10.1021/JF0262458
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols / Cyclohexanols
An inositol 892 Click to see 180.16 unknown https://doi.org/10.1007/BF02975882
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(2R,3R,4S,5S,6R)-2-[(2R)-3-hydroxy-2-(4-hydroxy-3-methoxyphenyl)propoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 38363186 Click to see COC1=C(C=CC(=C1)C(CO)COC2C(C(C(C(O2)CO)O)O)O)O 360.36 unknown https://doi.org/10.1021/JF0349127
2-(Hydroxymethyl)-6-[2-(4-hydroxyphenyl)ethoxy]oxane-3,4,5-triol 4961358 Click to see C1=CC(=CC=C1CCOC2C(C(C(C(O2)CO)O)O)O)O 300.30 unknown https://doi.org/10.1021/JF0349127
2-[3-Hydroxy-2-(4-hydroxy-3-methoxyphenyl)propoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 75130902 Click to see 360.36 unknown https://doi.org/10.1021/JF0349127
Salidroside 159278 Click to see 300.30 unknown https://doi.org/10.1021/JF0349127
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
3-[4-hydroxy-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]propanoic acid 11427899 Click to see 344.31 unknown https://doi.org/10.1021/JF0349127
3-[4-Hydroxy-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]propanoic acid 72957555 Click to see C1=CC(=C(C=C1O)OC2C(C(C(C(O2)CO)O)O)O)CCC(=O)O 344.31 unknown https://doi.org/10.1021/JF0349127
3-[6-[3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1-benzofuran-5-yl]propanoic acid 73809260 Click to see 368.30 unknown https://doi.org/10.1021/JF0262458
Cnidioside A 21592256 Click to see C1=COC2=CC(=C(C=C21)CCC(=O)O)OC3C(C(C(C(O3)CO)O)O)O 368.30 unknown https://doi.org/10.1021/JF0262458
methyl 3-[4-hydroxy-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]propanoate 11314328 Click to see COC(=O)CCC1=C(C=C(C=C1)O)OC2C(C(C(C(O2)CO)O)O)O 358.34 unknown https://doi.org/10.1021/JF0349127
Methyl 3-[4-hydroxy-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]propanoate 72797587 Click to see 358.34 unknown https://doi.org/10.1021/JF0349127
> Organoheterocyclic compounds / Azolidines / Imidazolidines / Hydantoins / Phenylhydantoins
Bsh5HY4acu 76966547 Click to see CCC1(C(=O)NC(=O)N1C)C2=CC=CC=C2 218.25 unknown https://doi.org/10.1016/0031-9422(95)00625-7
Methetoin 21908 Click to see CCC1(C(=O)NC(=O)N1C)C2=CC=CC=C2 218.25 unknown https://doi.org/10.1016/0031-9422(95)00625-7
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Chromones
Eugenin 10189 Click to see 206.19 unknown https://doi.org/10.1016/0031-9422(95)00625-7
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Chromones / Furanochromones
Visammiol 5315249 Click to see 276.28 unknown https://doi.org/10.1016/0031-9422(95)00625-7
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Pyranochromenes
Hamaudol 164722 Click to see 276.28 unknown https://doi.org/10.1016/0031-9422(95)00625-7
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / Pyranoxanthones
(Z)-4-[(1R,2R,17R,19S)-12-hydroxy-8,8,21,21-tetramethyl-5-(3-methylbut-2-enyl)-14,18-dioxo-3,7,20-trioxahexacyclo[15.4.1.02,15.02,19.04,13.06,11]docosa-4(13),5,9,11,15-pentaen-19-yl]-2-methylbut-2-enoic acid 102533562 Click to see 560.60 unknown https://doi.org/10.1016/0031-9422(95)00625-7
> Organoheterocyclic compounds / Diazines / Pyrimidines and pyrimidine derivatives / Pyrimidones
Uracil 1174 Click to see 112.09 unknown https://doi.org/10.1021/JF0262458
> Organoheterocyclic compounds / Indoles and derivatives / Indolyl carboxylic acids and derivatives
Dl-Tryptophan 1148 Click to see 204.22 unknown https://doi.org/10.1021/JF0262458
Tryptophan 6305 Click to see C1=CC=C2C(=C1)C(=CN2)CC(C(=O)O)N 204.22 unknown https://doi.org/10.1021/JF0262458
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(5R)-5-[(Z)-hex-4-en-2-ynyl]oxolan-2-one 162852891 Click to see CC=CC#CCC1CCC(=O)O1 164.20 unknown https://doi.org/10.1021/JF0262458
> Phenylpropanoids and polyketides / Coumarins and derivatives
Ulopterol 176475 Click to see 278.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Coumarin glycosides
6-(2,3-Dihydroxy-3-methylbutyl)-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-2-one 74933426 Click to see 426.40 unknown https://doi.org/10.1016/S0031-9422(06)80121-4
7-[(2S,3R,4S,5S,6R)-6-[[(2R,3R,4S)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-6-[(2S)-2,3-dihydroxy-3-methylbutyl]chromen-2-one 163046588 Click to see CC(C)(C(CC1=C(C=C2C(=C1)C=CC(=O)O2)OC3C(C(C(C(O3)COC4C(C(CO4)(CO)O)O)O)O)O)O)O 558.50 unknown https://doi.org/10.1016/S0031-9422(06)80121-4
7-[6-[[3,4-Dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-6-(2,3-dihydroxy-3-methylbutyl)chromen-2-one 197658 Click to see 558.50 unknown https://doi.org/10.1016/S0031-9422(06)80121-4
7-Hydroxy-6-(3,4,5-Trihydroxy-6-(Hydroxymethyl)Oxan-2-Yl)Oxychromen-2-One 5351506 Click to see 340.28 unknown https://doi.org/10.1021/JF0262458
Esculin 5281417 Click to see C1=CC(=O)OC2=CC(=C(C=C21)OC3C(C(C(C(O3)CO)O)O)O)O 340.28 unknown https://doi.org/10.1021/JF0262458
Peucedanol 7-O-glucoside 44144279 Click to see 426.40 unknown https://doi.org/10.1016/S0031-9422(06)80121-4
Peujaponiside 101665120 Click to see 558.50 unknown https://doi.org/10.1016/S0031-9422(06)80121-4
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Angular furanocoumarins
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 https://doi.org/10.1021/JF0262458
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 https://doi.org/10.1021/JF0262458
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens
(-)-Deltoin 906525 Click to see 328.40 unknown https://doi.org/10.1016/0031-9422(95)00625-7
(R)-(+)-Oxypeucedanin Hydrate 53319618 Click to see 322.31 unknown via CMAUP database
Imperatorin 10212 Click to see 270.28 unknown https://doi.org/10.1016/0031-9422(95)00625-7
Isoimperatorin 68081 Click to see 270.28 unknown https://doi.org/10.1016/0031-9422(95)00625-7
Marmesin 334704 Click to see CC(C)(C1CC2=C(O1)C=C3C(=C2)C=CC(=O)O3)O 246.26 unknown https://doi.org/10.1016/0031-9422(95)00625-7
Nodakenetin 26305 Click to see 246.26 unknown via CMAUP database
Oxypeucedanin hydrate 17536 Click to see CC(C)(C(COC1=C2C=CC(=O)OC2=CC3=C1C=CO3)O)O 304.29 unknown https://doi.org/10.1016/0031-9422(95)00625-7
Psoralen 6199 Click to see 186.16 unknown https://doi.org/10.1016/0031-9422(95)00625-7
https://doi.org/10.1007/BF02976373
> 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 https://doi.org/10.1016/0031-9422(95)00625-7
https://doi.org/10.1007/BF02976373
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 8-hydroxypsoralens
Xanthotoxol 65090 Click to see 202.16 unknown https://doi.org/10.1016/0031-9422(95)00625-7
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 8-methoxypsoralens
8-Methoxypsoralen 4114 Click to see 216.19 unknown https://doi.org/10.1016/0031-9422(95)00625-7
https://doi.org/10.1007/BF02976373
Cnidilin 821449 Click to see 300.30 unknown https://doi.org/10.1016/0031-9422(95)00625-7
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
(+)-Peusedanol 15296614 Click to see 264.27 unknown https://doi.org/10.1016/S0031-9422(06)80121-4
https://doi.org/10.1248/YAKUSHI1947.88.5_513
https://doi.org/10.1016/0031-9422(93)85132-B
2H-1-Benzopyran-2-one, 6-(2,3-dihydroxy-3-methylbutyl)-7-hydroxy- 5374451 Click to see 264.27 unknown https://doi.org/10.1016/S0031-9422(06)80121-4
https://doi.org/10.1248/YAKUSHI1947.88.5_513
https://doi.org/10.1016/0031-9422(93)85132-B
https://doi.org/10.1016/0031-9422(95)00625-7
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Angular pyranocoumarins
(-)-Isosamidin 5089290 Click to see 386.40 unknown https://doi.org/10.1016/0031-9422(95)00625-7
(-)-Praeruptorin A 9821539 Click to see 386.40 unknown https://doi.org/10.1055/S-2002-34934
(-)-Praeruptorin B 25717254 Click to see 426.50 unknown https://doi.org/10.1016/0031-9422(92)80463-O
((9R,10R)-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 5319252 Click to see 426.50 unknown https://doi.org/10.1016/0031-9422(92)80463-O
(+)-cis-4-Tigloylkhellactone 102110083 Click to see 344.40 unknown https://doi.org/10.1016/0031-9422(95)00625-7
(+)-Praeruptorin A 73189387 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 https://doi.org/10.1055/S-2002-34934
https://doi.org/10.1016/0031-9422(92)83160-Z
https://doi.org/10.1016/0031-9422(91)85156-T
(+)-Pteryxin 511787 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 https://doi.org/10.1016/0031-9422(95)00625-7
(+)-trans-Khellactone 11436940 Click to see 262.26 unknown https://doi.org/10.1016/0031-9422(91)85156-T
(10-Acetyloxy-8,8-dimethyl-2-oxo-9,10-dihydropyrano[2,3-f]chromen-9-yl) 2-methylbutanoate 10157 Click to see 388.40 unknown https://doi.org/10.1016/0031-9422(92)80463-O
(10-Hydroxy-8,8-dimethyl-2-oxo-9,10-dihydropyrano[2,3-f]chromen-9-yl) 3-methylbut-2-enoate 511784 Click to see 344.40 unknown https://doi.org/10.1016/0031-9422(93)85132-B
(8,8-dimethyl-2-oxo-9,10-dihydropyrano[2,3-h]chromen-9-yl) (E)-2-methylbut-2-enoate 5367834 Click to see CC=C(C)C(=O)OC1CC2=C(C=CC3=C2OC(=O)C=C3)OC1(C)C 328.40 unknown https://doi.org/10.1016/0031-9422(95)00625-7
(9-Hydroxy-8,8-dimethyl-2-oxo-9,10-dihydropyrano[2,3-f]chromen-10-yl) 2-methylbut-2-enoate 511782 Click to see 344.40 unknown https://doi.org/10.1016/0031-9422(95)00625-7
(9-Hydroxy-8,8-dimethyl-2-oxo-9,10-dihydropyrano[2,3-f]chromen-10-yl) 3-methylbut-2-enoate 13964643 Click to see 344.40 unknown https://doi.org/10.1016/0031-9422(93)85132-B
[(9R,10S)-9-acetyloxy-8,8-dimethyl-2-oxo-9,10-dihydropyrano[2,3-f]chromen-10-yl] (E)-2-methylbut-2-enoate 6861381 Click to see 386.40 unknown https://doi.org/10.1016/0031-9422(95)00625-7
[(9R,10S)-9-acetyloxy-8,8-dimethyl-2-oxo-9,10-dihydropyrano[2,3-f]chromen-10-yl] 3-methylbut-2-enoate 13592766 Click to see 386.40 unknown https://doi.org/10.1016/0031-9422(95)00625-7
[(9S,10R)-10-acetyloxy-8,8-dimethyl-2-oxo-9,10-dihydropyrano[2,3-f]chromen-9-yl] (E)-2-methylbut-2-enoate 13964642 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 https://doi.org/10.1016/0031-9422(91)85156-T
[(9S,10R)-10-acetyloxy-8,8-dimethyl-2-oxo-9,10-dihydropyrano[2,3-f]chromen-9-yl] 2-methylbut-2-enoate 126969610 Click to see 386.40 unknown https://doi.org/10.1007/BF02976373
[(9S,10S)-10-acetyloxy-8,8-dimethyl-2-oxo-9,10-dihydropyrano[2,3-f]chromen-9-yl] (2R)-2-methylbutanoate 1150983 Click to see 388.40 unknown https://doi.org/10.1016/0031-9422(92)80463-O
[(9S,10S)-8,8-dimethyl-9-(3-methylbut-2-enoyloxy)-2-oxo-9,10-dihydropyrano[2,3-f]chromen-10-yl] 3-methylbutanoate 10342527 Click to see CC(C)CC(=O)OC1C(C(OC2=C1C3=C(C=C2)C=CC(=O)O3)(C)C)OC(=O)C=C(C)C 428.50 unknown https://doi.org/10.1016/0031-9422(92)80463-O
[(9S,10S)-9-acetyloxy-8,8-dimethyl-2-oxo-9,10-dihydropyrano[2,3-f]chromen-10-yl] (E)-2-methylbut-2-enoate 1150979 Click to see 386.40 unknown https://doi.org/10.1016/0031-9422(95)00625-7
[(9S,10S)-9-hydroxy-8,8-dimethyl-2-oxo-9,10-dihydropyrano[2,3-f]chromen-10-yl] 3-methylbut-2-enoate 51669197 Click to see CC(=CC(=O)OC1C(C(OC2=C1C3=C(C=C2)C=CC(=O)O3)(C)C)O)C 344.40 unknown https://doi.org/10.1016/0031-9422(93)85132-B
[(9S)-8,8-dimethyl-2-oxo-9,10-dihydropyrano[2,3-h]chromen-9-yl] 3-methylbut-2-enoate 101049705 Click to see CC(=CC(=O)OC1CC2=C(C=CC3=C2OC(=O)C=C3)OC1(C)C)C 328.40 unknown https://doi.org/10.1016/0031-9422(93)85132-B
[8,8-Dimethyl-9-(2-methylbut-2-enoyloxy)-2-oxo-9,10-dihydropyrano[2,3-f]chromen-10-yl] 2-methylbut-2-enoate 163334 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 https://doi.org/10.1016/0031-9422(92)80463-O
[8,8-Dimethyl-9-(3-methylbut-2-enoyloxy)-2-oxo-9,10-dihydropyrano[2,3-f]chromen-10-yl] 3-methylbutanoate 72665212 Click to see 428.50 unknown https://doi.org/10.1016/0031-9422(92)80463-O
[8,8-dimethyl-9-[(Z)-2-methylbut-2-enoyl]oxy-2-oxo-9,10-dihydropyrano[2,3-f]chromen-10-yl] (Z)-2-methylbut-2-enoate 6450453 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 https://doi.org/10.1016/0031-9422(92)80463-O
[9-[(Z)-but-2-enyl]-8,8-dimethyl-2-oxo-9,10-dihydropyrano[2,3-f]chromen-10-yl] acetate 5320690 Click to see 342.40 unknown https://doi.org/10.1007/BF02976373
10-Hydroxy-8,8-dimethyl-9-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-9,10-dihydropyrano[2,3-f]chromen-2-one 23540036 Click to see 424.40 unknown https://doi.org/10.1021/JF0262458
2-Butenoic acid, 3-methyl-, 9,10-dihydro-10-hydroxy-8,8-dimethyl-2-oxo-2H,8H-benzo[1,2-b:3,4-ba(2)]dipyran-9-yl ester, cis- 162927134 Click to see CC(=CC(=O)OC1C(C2=C(C=CC3=C2OC(=O)C=C3)OC1(C)C)O)C 344.40 unknown https://doi.org/10.1016/0031-9422(93)85132-B
3-Methyl-2-butenoic acid (9S,10S)-8,8-dimethyl-9-(3-methylbutyryloxy)-2-oxo-9,10-dihydro-2H,8H-benzo[1,2-b:3,4-b']dipyran-10-yl ester 10477665 Click to see CC(C)CC(=O)OC1C(C2=C(C=CC3=C2OC(=O)C=C3)OC1(C)C)OC(=O)C=C(C)C 428.50 unknown via CMAUP database
cis-3'-Acetyl-4'-angeloylkhellactone 1549023 Click to see 386.40 unknown https://doi.org/10.1016/0031-9422(95)00625-7
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
d-Laserpitin 51396729 Click to see 344.40 unknown https://doi.org/10.1016/0031-9422(93)85132-B
Jatamansin 668081 Click to see 328.40 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 https://doi.org/10.1016/0031-9422(92)83160-Z
https://doi.org/10.1016/0031-9422(91)85156-T
Khellactone, cis-(-)- 11097348 Click to see CC1(C(C(C2=C(O1)C=CC3=C2OC(=O)C=C3)O)O)C 262.26 unknown https://doi.org/10.1016/0031-9422(92)83160-Z
Peucedanocoumarin III 1032882 Click to see 386.40 unknown via CMAUP database
Praeroside II 24066895 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 https://doi.org/10.1021/JF0262458
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 https://doi.org/10.1021/JF0262458
Praeruptorin A 38347607 Click to see 386.40 unknown https://doi.org/10.1016/0031-9422(91)85156-T
https://doi.org/10.1016/0031-9422(92)83160-Z
Praeruptorin D 1070682 Click to see 426.50 unknown https://doi.org/10.1016/0031-9422(92)80463-O
Pteryxin 5281425 Click to see 386.40 unknown via CMAUP database
Samidin 442150 Click to see 386.40 unknown https://doi.org/10.1016/0031-9422(92)80463-O
Selinidin 668079 Click to see 328.40 unknown via CMAUP database
Visnadine 442151 Click to see 388.40 unknown https://doi.org/10.1016/0031-9422(92)80463-O
> Phenylpropanoids and polyketides / Flavonoids / Flavones / 8-prenylated flavones
Rhynchospermin 13896029 Click to see 398.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-Dihydroxyphenyl)-5,7-Dihydroxy-3-(3,4,5-Trihydroxy-6-(Hydroxymethyl)Oxan-2-Yl)Oxychromen-4-One 5378597 Click to see 464.40 unknown https://doi.org/10.1021/JF0262458
Isoquercetin 5280804 Click to see 464.40 unknown https://doi.org/10.1021/JF0262458
Kaempferol-3-O-Rutinoside 5318767 Click to see 594.50 unknown via CMAUP database
Rutin 5280805 Click to see 610.50 unknown https://doi.org/10.1021/JF0262458
Vitamin P 5293655 Click to see 610.50 unknown https://doi.org/10.1021/JF0262458

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