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Peucedanum japonicum

Peucedanum japonicum - Unknown
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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

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]

Description Top

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Peucedanum japonicum, also known as coastal hog fennel, is a species of the Peucedanum genus, which is known for its many medicinal species in the parsley family. It was first described by Thunberg in 1784. This plant has a stout stem and glabrous leaves, with 1-2 ternate leaflets. It can be found in coastal areas and seashores below 100 meters, primarily in China, Japan, Korea, and the Philippines. In Korean cuisine, the leaves are used fresh or pickled, while in Japan it is known as the "longevity herb" and is used in traditional dishes. In China, it is used as a medicinal herb, but it is believed to cause delirium if consumed in large quantities. However, it has been found to have potential anti-obesity properties in mice. Overall, Peucedanum japonicum is a versatile plant with both culinary and medicinal uses in various cultures.

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
Korean 갯기름나물
Chinese 滨海前胡
Chinese 日本前胡

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)

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

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

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-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!
You can also contribute to this by clicking here.
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 C1=CC(=CC=C1C(CO)O)O 154.16 unknown https://doi.org/10.1021/JF0349127
> Benzenoids / Phenols / Methoxyphenols
Junipediol A 86072622 Click to see COC1=C(C=CC(=C1)C(CO)CO)O 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
CID 15628135 15628135 Click to see CC(=O)C=C=C1C(CC(CC1(C)O)OC2C(C(C(C(O2)CO)O)O)O)(C)C 386.40 unknown https://doi.org/10.1021/JF0349127
Icariside B1 15628136 Click to see CC(=O)C=C=C1C(CC(CC1(C)O)OC2C(C(C(C(O2)CO)O)O)O)(C)C 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 C1=NC2=C(N1C3C(C(C(O3)CO)O)O)NC(=NC2=O)N 283.24 unknown https://doi.org/10.1021/JF0262458
CID 765 765 Click to see C1=NC2=C(N1C3C(C(C(O3)CO)O)O)NC(=NC2=O)N 283.24 unknown https://doi.org/10.1021/JF0262458
> Nucleosides, nucleotides, and analogues / Pyrimidine nucleosides
Uridine 6029 Click to see C1=CN(C(=O)NC1=O)C2C(C(C(O2)CO)O)O 244.20 unknown https://doi.org/10.1021/JF0262458
> Nucleosides, nucleotides, and analogues / Pyrimidine nucleosides / Pyrimidine 2-deoxyribonucleosides
1-[4-Hydroxy-5-(hydroxymethyl)oxolan-2-yl]-5-methylpyrimidine-2,4-dione 1134 Click to see CC1=CN(C(=O)NC1=O)C2CC(C(O2)CO)O 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 CC(C(CC(C=CC1C(C(CC(=O)O1)OC)OC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C 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
Inositol 892 Click to see C1(C(C(C(C(C1O)O)O)O)O)O 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 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
Salidroside 159278 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
> 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 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-[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 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
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 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
> 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 CC1=CC(=O)C2=C(C=C(C=C2O1)OC)O 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 CC1=CC(=O)C2=C(C3=C(C=C2O1)OC(C3)C(C)(C)O)O 276.28 unknown https://doi.org/10.1016/0031-9422(95)00625-7
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Pyranochromenes
Hamaudol 164722 Click to see CC1=CC(=O)C2=C(C3=C(C=C2O1)OC(C(C3)O)(C)C)O 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 CC(=CCC1=C2C(=C(C3=C1OC45C6CC(C=C4C3=O)C(=O)C5(OC6(C)C)CC=C(C)C(=O)O)O)C=CC(O2)(C)C)C 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 C1=CNC(=O)NC1=O 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 C1=CC=C2C(=C1)C(=CN2)CC(C(=O)O)N 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 CC(C)(C(CC1=C(C=C2C(=C1)C=CC(=O)O2)OC)O)O 278.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Coumarin glycosides
2H-1-Benzopyran-2-one, 6-(beta-D-glucopyranosyloxy)-7-hydroxy- 5351506 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
6-(2,3-Dihydroxy-3-methylbutyl)-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-2-one 74933426 Click to see CC(C)(C(CC1=C(C=C2C(=C1)C=CC(=O)O2)OC3C(C(C(C(O3)CO)O)O)O)O)O 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 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
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 CC(C)(C(CC1=C(C=C2C(=C1)C=CC(=O)O2)OC3C(C(C(C(O3)CO)O)O)O)O)O 426.40 unknown https://doi.org/10.1016/S0031-9422(06)80121-4
Peujaponiside 101665120 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
> 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
(R)-(+)-Oxypeucedanin Hydrate 53319618 Click to see CC(C)(C(COC1=C2C=CC(=O)OC2=CC3=C1C=CO3)O)O.O 322.31 unknown via CMAUP database
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 https://doi.org/10.1016/0031-9422(95)00625-7
Isoimperatorin 68081 Click to see CC(=CCOC1=C2C=CC(=O)OC2=CC3=C1C=CO3)C 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 CC(C)(C1CC2=C(O1)C=C3C(=C2)C=CC(=O)O3)O 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
Pentosalen 10212 Click to see CC(=CCOC1=C2C(=CC3=C1OC=C3)C=CC(=O)O2)C 270.28 unknown https://doi.org/10.1016/0031-9422(95)00625-7
Psoralen 6199 Click to see C1=CC(=O)OC2=CC3=C(C=CO3)C=C21 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 C1=CC(=O)OC2=C(C3=C(C=CO3)C=C21)O 202.16 unknown https://doi.org/10.1016/0031-9422(95)00625-7
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 8-methoxypsoralens
Cnidilin 821449 Click to see CC(=CCOC1=C2C=COC2=C(C3=C1C=CC(=O)O3)OC)C 300.30 unknown https://doi.org/10.1016/0031-9422(95)00625-7
Methoxsalen 4114 Click to see COC1=C2C(=CC3=C1OC=C3)C=CC(=O)O2 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 / Hydroxycoumarins / 7-hydroxycoumarins
(+)-Peusedanol 15296614 Click to see CC(C)(C(CC1=C(C=C2C(=C1)C=CC(=O)O2)O)O)O 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 CC(C)(C(CC1=C(C=C2C(=C1)C=CC(=O)O2)O)O)O 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
(-)-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 https://doi.org/10.1055/S-2002-34934
(+)-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 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(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 CCC(C)C(=O)OC1C(C2=C(C=CC3=C2OC(=O)C=C3)OC1(C)C)OC(=O)C 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 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
(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-Acetyloxy-8,8-dimethyl-2-oxo-9,10-dihydropyrano[2,3-f]chromen-10-yl) 3-methylbut-2-enoate 5089290 Click to see CC(=CC(=O)OC1C(C(OC2=C1C3=C(C=C2)C=CC(=O)O3)(C)C)OC(=O)C)C 386.40 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 CC=C(C)C(=O)OC1C(C(OC2=C1C3=C(C=C2)C=CC(=O)O3)(C)C)O 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 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-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 https://doi.org/10.1016/0031-9422(95)00625-7
[(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 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
[(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 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
[(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 CC(=CC(=O)OC1C(C(OC2=C1C3=C(C=C2)C=CC(=O)O3)(C)C)OC(=O)C)C 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 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/10.1007/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 CCC(C)C(=O)OC1C(C2=C(C=CC3=C2OC(=O)C=C3)OC1(C)C)OC(=O)C 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)-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 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 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
[(9S,10S)-9-hydroxy-8,8-dimethyl-2-oxo-9,10-dihydropyrano[2,3-f]chromen-10-yl] (E)-2-methylbut-2-enoate 102110083 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 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] (Z)-2-methylbut-2-enoate 668079 Click to see CC=C(C)C(=O)OC1CC2=C(C=CC3=C2OC(=O)C=C3)OC1(C)C 328.40 unknown via CMAUP database
[(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 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
[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 CC=CCC1C(C2=C(C=CC3=C2OC(=O)C=C3)OC1(C)C)OC(=O)C 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 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
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',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 CC=C(C)C(=O)OC1C(C(OC2=C1C3=C(C=C2)C=CC(=O)O3)(C)C)O 344.40 unknown https://doi.org/10.1016/0031-9422(93)85132-B
Jatamansin 668081 Click to see CC=C(C)C(=O)OC1CC2=C(C=CC3=C2OC(=O)C=C3)OC1(C)C 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 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 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 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
https://doi.org/10.1016/0031-9422(92)83160-Z
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 https://doi.org/10.1016/0031-9422(92)80463-O
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
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 https://doi.org/10.1016/0031-9422(92)80463-O
Visnadine 442151 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 https://doi.org/10.1016/0031-9422(92)80463-O
> Phenylpropanoids and polyketides / Flavonoids / Flavones / 8-prenylated flavones
Rhynchospermin 13896029 Click to see CC(=CCC1=C(C=C(C2=C1OC(=C(C2=O)O)C3=CC(=C(C=C3)OC)O)O)OC)C 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-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 5378597 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown https://doi.org/10.1021/JF0262458
Isoquercetin 5280804 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown https://doi.org/10.1021/JF0262458
Kaempferol-3-O-rutinoside 5318767 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)O)O)O)O)O)O 594.50 unknown via CMAUP database
Rutin 5280805 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O 610.50 unknown https://doi.org/10.1021/JF0262458
Vitamin P 5293655 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O 610.50 unknown https://doi.org/10.1021/JF0262458

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