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Heracleum candicans

Heracleum candicans - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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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 UUID644046ecf17d1041042704
Scientific name Heracleum candicans
Authority Wall. ex DC.
First published in Prodr. 4: 192 (1830)

Description Top

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No description added yet. Help us by writing one.

Synonyms Top

Scientific name Authority First published in
Tetrataenium candicans (Wall. ex DC.) Manden. Zametki Sist. Geogr. Rast. 41: 44 (1986)

Common names Top

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Language Common/alternative name
Chinese 藏当归
Chinese 白亮独活
Chinese 白独活
Chinese 白羌活

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
Heracleum candicans var. obtusifolium (Wall. ex DC.) F.T.Pu & M.F.Watson Acta Phytotax. Sin. 42: 562 (2004)

Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • East Himalaya
      • Nepal
      • Pakistan
      • West Himalaya
    • Indo-China
      • Myanmar

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001067675
Tropicos 1700133
KEW urn:lsid:ipni.org:names:842985-1
The Plant List tro-1700133
Open Tree Of Life 122459
NCBI Taxonomy 99506
IPNI 842985-1
iNaturalist 1062751
GBIF 6026415
USDA GRIN 18894

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
Analysis of Free Amino Acid Composition and Honey Plant Species in Seven Honey Species in China Yang J, Liu Y, Cui Z, Wang T, Liu T, Liu G Foods 29-Mar-2024
PMCID:PMC11011401
doi:10.3390/foods13071065
PMID:38611369
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
Plant Coumarins with Anti-HIV Activity: Isolation and Mechanisms of Action Sharapov AD, Fatykhov RF, Khalymbadzha IA, Zyryanov GV, Chupakhin ON, Tsurkan MV Int J Mol Sci 02-Feb-2023
PMCID:PMC9917851
doi:10.3390/ijms24032839
PMID:36769163
An ethnobotanical study on wild plants used by Tibetan people in Gyirong Valley, Tibet, China Guo CA, Ding X, Hu H, Zhang Y, Yang H, Wang Y J Ethnobiol Ethnomed 18-Nov-2022
PMCID:PMC9675253
doi:10.1186/s13002-022-00565-1
PMID:36401315
Quantitative ethnoveterinary study on plant resource utilization by indigenous communities in high-altitude regions Haq SM, Yaqoob U, Majeed M, Amjad MS, Hassan M, Ahmad R, Waheed M, Bussmann RW, Calixto ES, Proćków J, de la Lastra JM, Morales-de la Nuez A Front Vet Sci 06-Oct-2022
PMCID:PMC9583879
doi:10.3389/fvets.2022.944046
PMID:36277063
Climate change‐induced distributional change of medicinal and aromatic plants in the Nepal Himalaya Shrestha UB, Lamsal P, Ghimire SK, Shrestha BB, Dhakal S, Shrestha S, Atreya K Ecol Evol 15-Aug-2022
PMCID:PMC9379350
doi:10.1002/ece3.9204
PMID:35991283
Market survey on the traditional medicine of the Lijiang area in Yunnan Province, China Zhang M, Li H, Wang J, Tang M, Zhang X, Yang S, Liu J, Li Y, Huang X, Li Z, Huang L J Ethnobiol Ethnomed 23-May-2022
PMCID:PMC9125852
doi:10.1186/s13002-022-00532-w
PMID:35606860
A Cross-Cultural Analysis of Plant Resources among Five Ethnic Groups in the Western Himalayan Region of Jammu and Kashmir Haq SM, Hassan M, Bussmann RW, Calixto ES, Rahman IU, Sakhi S, Ijaz F, Hashem A, Al-Arjani AB, Almutairi KF, Abd_Allah EF, Aziz MA, Ali N Biology (Basel) 23-Mar-2022
PMCID:PMC9032642
doi:10.3390/biology11040491
PMID:35453691
Environmental variables drive plant species composition and distribution in the moist temperate forests of Northwestern Himalaya, Pakistan Rahman IU, Hart RE, Ijaz F, Afzal A, Iqbal Z, Calixto ES, Abd_Allah EF, Alqarawi AA, Hashem A, Al-Arjani AB, Kausar R, Haq SM PLoS One 24-Feb-2022
PMCID:PMC8870539
doi:10.1371/journal.pone.0260687
PMID:35202409
Comparison of Herbal Medicines Used for Women’s Menstruation Diseases in Different Areas of the World Jiao M, Liu X, Ren Y, Wang Y, Cheng L, Liang Y, Li Y, Zhang T, Wang W, Mei Z Front Pharmacol 04-Feb-2022
PMCID:PMC8854496
doi:10.3389/fphar.2021.751207
PMID:35185533
Classification and Characterization of the Manoor Valley’s (Lesser Himalaya) Vegetation from the Subtropical-Temperate Ecotonal Forests to the Alpine Pastures along Ecological Variables Rahman IU, Afzal A, Iqbal Z, Alzain MN, Al-Arjani AB, Alqarawi AA, Abd_Allah EF, Ali N, Sakhi S, Khan MA, Khan U, Ijaz F, Mumtaz S, Calixto ES Plants (Basel) 28-Dec-2021
PMCID:PMC8747448
doi:10.3390/plants11010087
PMID:35009089
Impact of Genomic and Transcriptomic Resources on Apiaceae Crop Breeding Strategies Palumbo F, Vannozzi A, Barcaccia G Int J Mol Sci 08-Sep-2021
PMCID:PMC8465131
doi:10.3390/ijms22189713
PMID:34575872
Plant Resources Utilization among Different Ethnic Groups of Ladakh in Trans-Himalayan Region Haq SM, Yaqoob U, Calixto ES, Rahman IU, Hashem A, Abd_Allah EF, Alakeel MA, Alqarawi AA, Abdalla M, Hassan M, Bussmann RW, Abbasi AM, Ur Rahman S, Ijaz F Biology (Basel) 26-Aug-2021
PMCID:PMC8468708
doi:10.3390/biology10090827
PMID:34571704
Wild plants used by the Lhoba people in Douyu Village, characterized by high mountains and valleys, in southeastern Tibet, China Chen WY, Yang T, Yang J, Qiu ZC, Ding XY, Wang YH, Wang YH J Ethnobiol Ethnomed 23-Jul-2021
PMCID:PMC8305498
doi:10.1186/s13002-021-00472-x
PMID:34301287
Hepatoprotective Effects of Heracleum candicans Against Carbon Tetrachloride-Induced Acute Liver Injury in Rats Li J, Song D, Zhang B, Guo J, Li W, Zhang X, Zhao Q Dose Response 12-Jul-2021
PMCID:PMC8278464
doi:10.1177/15593258211029510
PMID:34290575

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
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Stearic Acid 5281 Click to see CCCCCCCCCCCCCCCCCC(=O)O 284.50 unknown https://doi.org/10.1016/S0040-4020(01)82304-8
> 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 https://doi.org/10.1007/S11418-008-0266-8
(9E,11S,16S)-octadeca-9,17-dien-12,14-diyne-1,11,16-triol 86311066 Click to see C=CC(C#CC#CC(C=CCCCCCCCCO)O)O 290.40 unknown https://doi.org/10.1007/S11418-008-0266-8
Falcarindiol 5281148 Click to see CCCCCCCC=CC(C#CC#CC(C=C)O)O 260.40 unknown https://doi.org/10.1007/S11418-008-0266-8
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
9-[(3,7-Dimethyl-2,6-octadien-1-yl)oxy]-7H-furo[3,2-g][1]benzopyran-7-one 155658 Click to see CC(=CCCC(=CCOC1=C2C(=CC3=C1OC=C3)C=CC(=O)O2)C)C 338.40 unknown https://doi.org/10.1016/S0040-4020(01)82304-8
Xanthotoxol geranyl ether 5317564 Click to see CC(=CCCC(=CCOC1=C2C(=CC3=C1OC=C3)C=CC(=O)O2)C)C 338.40 unknown https://doi.org/10.1016/S0040-4020(01)82304-8
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
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 https://doi.org/10.1016/S0040-4020(01)82304-8
> Organic nitrogen compounds / Organonitrogen compounds / Amines / Tertiary amines / Tertiary alkylarylamines / Dialkylarylamines
Dipyridamole 3108 Click to see C1CCN(CC1)C2=NC(=NC3=C2N=C(N=C3N4CCCCC4)N(CCO)CCO)N(CCO)CCO 504.60 unknown https://doi.org/10.1007/S11418-008-0266-8
> Phenylpropanoids and polyketides / Coumarins and derivatives
8-[(2R)-2,3-dihydroxy-3-methylbutyl]-7-methoxychromen-2-one 821433 Click to see CC(C)(C(CC1=C(C=CC2=C1OC(=O)C=C2)OC)O)O 278.30 unknown https://doi.org/10.1007/S11418-008-0266-8
Osthol 10228 Click to see CC(=CCC1=C(C=CC2=C1OC(=O)C=C2)OC)C 244.28 unknown https://doi.org/10.1007/S11418-008-0266-8
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Angular furanocoumarins
Angelicin 10658 Click to see C1=CC2=C(C=CO2)C3=C1C=CC(=O)O3 186.16 unknown https://doi.org/10.1016/S0040-4020(01)82304-8
Columbianetin 92201 Click to see CC(C)(C1CC2=C(O1)C=CC3=C2OC(=O)C=C3)O 246.26 unknown https://doi.org/10.1007/S11418-008-0266-8
Pimpinellin 4825 Click to see COC1=C(C2=C(C=CO2)C3=C1C=CC(=O)O3)OC 246.21 unknown https://doi.org/10.1007/S11418-008-0266-8
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens
(+)-9-(3-Chloro-2-hydroxy-3-methylbutoxy)-7H-furo[3,2-g][1]benzopyran-7-one; 8-(3-Chloro-2-hydroxy-3-methylbutoxy)psoralen; 8-(3-Chloro-2-hydroxy-3-methylbutyloxy)psoralen 91885198 Click to see CC(C)(C(COC1=C2C(=CC3=C1OC=C3)C=CC(=O)O2)O)Cl 322.74 unknown https://doi.org/10.1007/S11418-008-0266-8
[(2R)-3-hydroxy-3-methyl-1-(7-oxofuro[3,2-g]chromen-9-yl)oxybutan-2-yl] (1S,3R,4R,5R)-1,3,4-trihydroxy-5-[(E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxycyclohexane-1-carboxylate 101502035 Click to see CC(C)(C(COC1=C2C(=CC3=C1OC=C3)C=CC(=O)O2)OC(=O)C4(CC(C(C(C4)OC(=O)C=CC5=CC(=C(C=C5)O)OC)O)O)O)O 654.60 unknown https://doi.org/10.1007/S11418-010-0394-9
[(2R)-3-hydroxy-3-methyl-1-(7-oxofuro[3,2-g]chromen-9-yl)oxybutan-2-yl] (E)-3-[7-[(2R)-2,3-dihydroxy-3-methylbutoxy]-6-hydroxy-1-benzofuran-5-yl]prop-2-enoate 101502036 Click to see CC(C)(C(COC1=C2C(=CC(=C1O)C=CC(=O)OC(COC3=C4C(=CC5=C3OC=C5)C=CC(=O)O4)C(C)(C)O)C=CO2)O)O 608.60 unknown https://doi.org/10.1007/S11418-010-0394-9
[3-Hydroxy-3-methyl-1-(7-oxofuro[3,2-g]chromen-9-yl)oxybutan-2-yl] 1,3,4-trihydroxy-5-[3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyloxy]cyclohexane-1-carboxylate 162992027 Click to see CC(C)(C(COC1=C2C(=CC3=C1OC=C3)C=CC(=O)O2)OC(=O)C4(CC(C(C(C4)OC(=O)C=CC5=CC(=C(C=C5)O)OC)O)O)O)O 654.60 unknown https://doi.org/10.1007/S11418-010-0394-9
[3-Hydroxy-3-methyl-1-(7-oxofuro[3,2-g]chromen-9-yl)oxybutan-2-yl] 3-[7-(2,3-dihydroxy-3-methylbutoxy)-6-hydroxy-1-benzofuran-5-yl]prop-2-enoate 162890531 Click to see CC(C)(C(COC1=C2C(=CC(=C1O)C=CC(=O)OC(COC3=C4C(=CC5=C3OC=C5)C=CC(=O)O4)C(C)(C)O)C=CO2)O)O 608.60 unknown https://doi.org/10.1007/S11418-010-0394-9
9-[(2R)-2-hydroxy-3-[(2R)-3-methoxy-3-methyl-1-(7-oxofuro[3,2-g]chromen-9-yl)oxybutan-2-yl]oxy-3-methylbutoxy]furo[3,2-g]chromen-7-one 163191385 Click to see CC(C)(C(COC1=C2C(=CC3=C1OC=C3)C=CC(=O)O2)O)OC(COC4=C5C(=CC6=C4OC=C6)C=CC(=O)O5)C(C)(C)OC 604.60 unknown https://doi.org/10.1007/S11418-010-0394-9
9-[(2R)-2-hydroxy-3-methylbut-3-enoxy]furo[3,2-g]chromen-7-one 131636642 Click to see CC(=C)C(COC1=C2C(=CC3=C1OC=C3)C=CC(=O)O2)O 286.28 unknown https://doi.org/10.1007/S11418-008-0266-8
9-[(2S)-2-[(3R)-3-hydroxy-2-methyl-4-(7-oxofuro[3,2-g]chromen-9-yl)oxybutan-2-yl]oxy-3-methylbut-3-enoxy]furo[3,2-g]chromen-7-one 163032400 Click to see CC(=C)C(COC1=C2C(=CC3=C1OC=C3)C=CC(=O)O2)OC(C)(C)C(COC4=C5C(=CC6=C4OC=C6)C=CC(=O)O5)O 572.60 unknown https://doi.org/10.1007/S11418-008-0266-8
9-[[(2R,4R)-9'-[(2R)-2-hydroxy-3-methoxy-3-methylbutoxy]-5,5-dimethylspiro[1,3-dioxolane-2,7'-furo[3,2-g]chromene]-4-yl]methoxy]furo[3,2-g]chromen-7-one 101502038 Click to see CC1(C(OC2(O1)C=CC3=C(O2)C(=C4C(=C3)C=CO4)OCC(C(C)(C)OC)O)COC5=C6C(=CC7=C5OC=C7)C=CC(=O)O6)C 604.60 unknown https://doi.org/10.1007/S11418-010-0394-9
9-[[(2R,4R)-9'-[(2R)-2-hydroxy-3-methyl-3-[(2S)-3-methyl-1-(7-oxofuro[3,2-g]chromen-9-yl)oxybut-3-en-2-yl]oxybutoxy]-5,5-dimethylspiro[1,3-dioxolane-2,7'-furo[3,2-g]chromene]-4-yl]methoxy]furo[3,2-g]chromen-7-one 162899757 Click to see CC(=C)C(COC1=C2C(=CC3=C1OC=C3)C=CC(=O)O2)OC(C)(C)C(COC4=C5C(=CC6=C4OC7(C=C6)OC(C(O7)(C)C)COC8=C9C(=CC1=C8OC=C1)C=CC(=O)O9)C=CO5)O 858.80 unknown https://doi.org/10.1007/S11418-008-0266-8
9-[[(2S,4R)-9'-[(2R)-2-hydroxy-3-methoxy-3-methylbutoxy]-5,5-dimethylspiro[1,3-dioxolane-2,7'-furo[3,2-g]chromene]-4-yl]methoxy]furo[3,2-g]chromen-7-one 101502039 Click to see CC1(C(OC2(O1)C=CC3=C(O2)C(=C4C(=C3)C=CO4)OCC(C(C)(C)OC)O)COC5=C6C(=CC7=C5OC=C7)C=CC(=O)O6)C 604.60 unknown https://doi.org/10.1007/S11418-010-0394-9
9-[[(2S,4R)-9'-[(2R)-2-hydroxy-3-methyl-3-[(2R)-3-methyl-1-(7-oxofuro[3,2-g]chromen-9-yl)oxybut-3-en-2-yl]oxybutoxy]-5,5-dimethylspiro[1,3-dioxolane-2,7'-furo[3,2-g]chromene]-4-yl]methoxy]furo[3,2-g]chromen-7-one 162899758 Click to see CC(=C)C(COC1=C2C(=CC3=C1OC=C3)C=CC(=O)O2)OC(C)(C)C(COC4=C5C(=CC6=C4OC7(C=C6)OC(C(O7)(C)C)COC8=C9C(=CC1=C8OC=C1)C=CC(=O)O9)C=CO5)O 858.80 unknown https://doi.org/10.1007/S11418-010-0394-9
9-[[(2S,4R)-9'-[(2R)-2-hydroxy-3-methyl-3-[(2S)-3-methyl-1-(7-oxofuro[3,2-g]chromen-9-yl)oxybut-3-en-2-yl]oxybutoxy]-5,5-dimethylspiro[1,3-dioxolane-2,7'-furo[3,2-g]chromene]-4-yl]methoxy]furo[3,2-g]chromen-7-one 162899756 Click to see CC(=C)C(COC1=C2C(=CC3=C1OC=C3)C=CC(=O)O2)OC(C)(C)C(COC4=C5C(=CC6=C4OC7(C=C6)OC(C(O7)(C)C)COC8=C9C(=CC1=C8OC=C1)C=CC(=O)O9)C=CO5)O 858.80 unknown https://doi.org/10.1007/S11418-008-0266-8
9-[[(2S,4S)-9'-[(2R)-2,3-dihydroxy-3-methylbutoxy]-5,5-dimethylspiro[1,3-dioxolane-2,7'-furo[3,2-g]chromene]-4-yl]methoxy]furo[3,2-g]chromen-7-one 15816834 Click to see CC1(C(OC2(O1)C=CC3=C(O2)C(=C4C(=C3)C=CO4)OCC(C(C)(C)O)O)COC5=C6C(=CC7=C5OC=C7)C=CC(=O)O6)C 590.60 unknown https://doi.org/10.1007/S11418-008-0266-8
9-[[9'-(2-Hydroxy-3-methoxy-3-methylbutoxy)-5,5-dimethylspiro[1,3-dioxolane-2,7'-furo[3,2-g]chromene]-4-yl]methoxy]furo[3,2-g]chromen-7-one 163101556 Click to see CC1(C(OC2(O1)C=CC3=C(O2)C(=C4C(=C3)C=CO4)OCC(C(C)(C)OC)O)COC5=C6C(=CC7=C5OC=C7)C=CC(=O)O6)C 604.60 unknown https://doi.org/10.1007/S11418-010-0394-9
9-[[9'-[2-Hydroxy-3-methyl-3-[3-methyl-1-(7-oxofuro[3,2-g]chromen-9-yl)oxybut-3-en-2-yl]oxybutoxy]-5,5-dimethylspiro[1,3-dioxolane-2,7'-furo[3,2-g]chromene]-4-yl]methoxy]furo[3,2-g]chromen-7-one 85254796 Click to see CC(=C)C(COC1=C2C(=CC3=C1OC=C3)C=CC(=O)O2)OC(C)(C)C(COC4=C5C(=CC6=C4OC7(C=C6)OC(C(O7)(C)C)COC8=C9C(=CC1=C8OC=C1)C=CC(=O)O9)C=CO5)O 858.80 unknown https://doi.org/10.1007/S11418-010-0394-9
9-[2-Hydroxy-3-[3-methoxy-3-methyl-1-(7-oxofuro[3,2-g]chromen-9-yl)oxybutan-2-yl]oxy-3-methylbutoxy]furo[3,2-g]chromen-7-one 163045355 Click to see CC(C)(C(COC1=C2C(=CC3=C1OC=C3)C=CC(=O)O2)O)OC(COC4=C5C(=CC6=C4OC=C6)C=CC(=O)O5)C(C)(C)OC 604.60 unknown https://doi.org/10.1007/S11418-010-0394-9
9-[3-[6-[[3,4-Dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-2-hydroxy-3-methylbutoxy]furo[3,2-g]chromen-7-one 73088243 Click to see CC(C)(C(COC1=C2C(=CC3=C1OC=C3)C=CC(=O)O2)O)OC4C(C(C(C(O4)COC5C(C(CO5)(CO)O)O)O)O)O 598.50 unknown https://doi.org/10.1007/S11418-010-0394-9
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 https://doi.org/10.1007/S11418-008-0266-8
DecurosideV 73834427 Click to see CC(C)(C1C(C2=C(O1)C=C3C(=C2)C=CC(=O)O3)O)OC4C(C(C(C(O4)CO)O)O)O 424.40 unknown https://doi.org/10.1007/S11418-010-0394-9
Heraclenol 3'-O-[beta-D-apiofuranosyl-(1-6)-beta-D-glucopyranoside] 11758254 Click to see CC(C)(C(COC1=C2C(=CC3=C1OC=C3)C=CC(=O)O2)O)OC4C(C(C(C(O4)COC5C(C(CO5)(CO)O)O)O)O)O 598.50 unknown https://doi.org/10.1007/S11418-010-0394-9
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/S11418-008-0266-8
Pentosalen 10212 Click to see CC(=CCOC1=C2C(=CC3=C1OC=C3)C=CC(=O)O2)C 270.28 unknown https://doi.org/10.1016/S0040-4020(01)82304-8
Rivulobirin C 10745970 Click to see CC1(C(OC2(O1)C=CC3=C(O2)C(=C4C(=C3)C=CO4)OCC(C(C)(C)O)O)COC5=C6C(=CC7=C5OC=C7)C=CC(=O)O6)C 590.60 unknown https://doi.org/10.1007/S11418-008-0266-8
Rivulobirin E 10674926 Click to see CC(C)(C(COC1=C2C(=CC3=C1OC=C3)C=CC(=O)O2)O)OC(COC4=C5C(=CC6=C4OC=C6)C=CC(=O)O5)C(C)(C)O 590.60 unknown https://doi.org/10.1007/S11418-008-0266-8
Smyrindioloside 10836072 Click to see CC(C)(C1C(C2=C(O1)C=C3C(=C2)C=CC(=O)O3)O)OC4C(C(C(C(O4)CO)O)O)O 424.40 unknown https://doi.org/10.1007/S11418-010-0394-9
> 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/S0040-4020(01)82304-8
Psoralen, 8-geranyl-5-methoxy- 6442182 Click to see CC(=CCCC(=CCOC1=C2C(=C(C3=C1OC(=O)C=C3)OC)C=CO2)C)C 368.40 unknown https://doi.org/10.1007/S11418-008-0266-8
> 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/10.1007/S11418-008-0266-8
Osthenol 5320318 Click to see CC(=CCC1=C(C=CC2=C1OC(=O)C=C2)O)C 230.26 unknown https://doi.org/10.1007/S11418-008-0266-8
Umbelliferone 5281426 Click to see C1=CC(=CC2=C1C=CC(=O)O2)O 162.14 unknown https://doi.org/10.1007/S11418-008-0266-8

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