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Skimmia laureola

Skimmia laureola - 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 UUID644056ba8d3f5384324472
Scientific name Skimmia laureola
Authority (DC.) Decne.
First published in Voy. Inde 4: 180 (1844)

Description Top

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Synonyms Top

Scientific name Authority First published in
Limonia laureola Griff. Posth. Pap. (Itin. not.) 156: 783 1848

Common names Top

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Language Common/alternative name
Chinese 月桂茵芋

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

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-0001253537
UNII MPN9B74283
KEW urn:lsid:ipni.org:names:775241-1
The Plant List tro-50171940
Open Tree Of Life 186515
NCBI Taxonomy 354518
iNaturalist 602039
GBIF 7269594
Freebase /m/043mh3f
EPPO SKMLA
USDA GRIN 34487
Wikipedia Skimmia_laureola
PaleoBotany 42459

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
Exploring the benefits of wild plants in dietary nutrition: investigating perspectives, choices, health impacts and sustainable practices Anwar T, Qureshi H, Shahzadi S, Siddiqi EH, Ali HM, Abdelhamid MM, Nazim M BMC Complement Med Ther 14-Feb-2024
PMCID:PMC10865668
doi:10.1186/s12906-024-04379-4
PMID:38355544
The local medicinal plant knowledge in Kashmir Western Himalaya: a way to foster ecological transition via community-centred health seeking strategies Manzoor M, Ahmad M, Zafar M, Gillani SW, Shaheen H, Pieroni A, Al-Ghamdi AA, Elshikh MS, Saqib S, Makhkamov T, Khaydarov K J Ethnobiol Ethnomed 30-Nov-2023
PMCID:PMC10688143
doi:10.1186/s13002-023-00631-2
PMID:38037066
Review green synthesis of silver nanoparticles by using plant extracts and their antimicrobial activity Abada E, Mashraqi A, Modafer Y, Al Abboud MA, El-Shabasy A Saudi J Biol Sci 26-Nov-2023
PMCID:PMC10749906
doi:10.1016/j.sjbs.2023.103877
PMID:38148949
A Review of Sustainable Use of Biogenic Nanoscale Agro-Materials to Enhance Stress Tolerance and Nutritional Value of Plants Giri VP, Shukla P, Tripathi A, Verma P, Kumar N, Pandey S, Dimkpa CO, Mishra A Plants (Basel) 11-Feb-2023
PMCID:PMC9967242
doi:10.3390/plants12040815
PMID:36840163
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
Silver Nanoparticles: Bactericidal and Mechanistic Approach against Drug Resistant Pathogens More PR, Pandit S, Filippis AD, Franci G, Mijakovic I, Galdiero M Microorganisms 01-Feb-2023
PMCID:PMC9961011
doi:10.3390/microorganisms11020369
PMID:36838334
Functional silver nanoparticles synthesis from sustainable point of view: 2000 to 2023 ‒ A review on game changing materials Hasan KM, Xiaoyi L, Shaoqin Z, Horváth PG, Bak M, Bejó L, Sipos G, Alpár T Heliyon 10-Dec-2022
PMCID:PMC9800342
doi:10.1016/j.heliyon.2022.e12322
PMID:36590481
Green synthesized silver nanoparticles: Optimization, characterization, antimicrobial activity, and cytotoxicity study by hemolysis assay Liaqat N, Jahan N, Khalil-ur-Rahman, Anwar T, Qureshi H Front Chem 29-Aug-2022
PMCID:PMC9465387
doi:10.3389/fchem.2022.952006
PMID:36105303
A Critical Review of the Antimicrobial and Antibiofilm Activities of Green-Synthesized Plant-Based Metallic Nanoparticles Luzala MM, Muanga CK, Kyana J, Safari JB, Zola EN, Mbusa GV, Nuapia YB, Liesse JM, Nkanga CI, Krause RW, Balčiūnaitienė A, Memvanga PB Nanomaterials (Basel) 27-May-2022
PMCID:PMC9182092
doi:10.3390/nano12111841
PMID:35683697
Microencapsulation of Essential Oils: A Review Sousa VI, Parente JF, Marques JF, Forte MA, Tavares CJ Polymers (Basel) 23-Apr-2022
PMCID:PMC9099681
doi:10.3390/polym14091730
PMID:35566899
Medicinal plants mediated the green synthesis of silver nanoparticles and their biomedical applications Habeeb Rahuman HB, Dhandapani R, Narayanan S, Palanivel V, Paramasivam R, Subbarayalu R, Thangavelu S, Muthupandian S IET Nanobiotechnol 15-Apr-2022
PMCID:PMC9114445
doi:10.1049/nbt2.12078
PMID:35426251
Iron Oxide Nanoparticles-Plant Insignia Synthesis with Favorable Biomedical Activities and Less Toxicity, in the “Era of the-Green”: A Systematic Review Hamdy NM, Boseila AA, Ramadan A, Basalious EB Pharmaceutics 12-Apr-2022
PMCID:PMC9026296
doi:10.3390/pharmaceutics14040844
PMID:35456678
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
Multifarious global flora fabricated phytosynthesis of silver nanoparticles: a green nanoweapon for antiviral approach including SARS-CoV-2 Karthik C, Punnaivalavan KA, Prabha SP, Caroline DG Int Nano Lett 12-Feb-2022
PMCID:PMC8853038
doi:10.1007/s40089-022-00367-z
PMID:35194512
Inventorization of traditional ethnobotanical uses of wild plants of Dawarian and Ratti Gali areas of District Neelum, Azad Jammu and Kashmir Pakistan Ajaib M, Ishtiaq M, Bhatti KH, Hussain I, Maqbool M, Hussain T, Mushtaq W, Ghani A, Azeem M, Khan SM, Thind S, Bashir R PLoS One 29-Jul-2021
PMCID:PMC8321310
doi:10.1371/journal.pone.0255010
PMID:34324561

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 / Benzenediols / Catechols
Methyl 2-(2,5-dibromo-3,4-dihydroxyphenyl)acetate 71579763 Click to see COC(=O)CC1=CC(=C(C(=C1Br)O)O)Br 339.96 unknown https://doi.org/10.1515/ZNB-2009-0418
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols / Long-chain fatty alcohols
2-methylpropyl (2S)-2-hydroxy-19-(4-hydroxyphenyl)nonadecanoate 11662642 Click to see CC(C)COC(=O)C(CCCCCCCCCCCCCCCCCC1=CC=C(C=C1)O)O 462.70 unknown https://doi.org/10.1515/ZNB-2005-1111
2-Methylpropyl 2-hydroxy-19-(4-hydroxyphenyl)nonadecanoate 73046162 Click to see CC(C)COC(=O)C(CCCCCCCCCCCCCCCCCC1=CC=C(C=C1)O)O 462.70 unknown https://doi.org/10.1515/ZNB-2005-1111
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Linalool, (-)- 443158 Click to see CC(=CCCC(C)(C=C)O)C 154.25 unknown https://doi.org/10.1002/PRAC.19361470117
Linalool, (+/-)- 6549 Click to see CC(=CCCC(C)(C=C)O)C 154.25 unknown https://doi.org/10.1002/PRAC.19361470117
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(+)-beta-Phellandrene 442484 Click to see CC(C)C1CCC(=C)C=C1 136.23 unknown https://doi.org/10.1002/PRAC.19361470117
Beta-Phellandrene 11142 Click to see CC(C)C1CCC(=C)C=C1 136.23 unknown https://doi.org/10.1002/PRAC.19361470117
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids / Scalarane sesterterpenoids
(4aR,6aR,6aS,8aR,12aS,14aR,14bR)-4,4,6a,6a,8a,11,11,14b-octamethyl-2,4a,5,6,8,9,10,12,12a,13,14,14a-dodecahydro-1H-picen-3-one 392170 Click to see CC1(CCC2(CC=C3C4(CCC5C(C(=O)CCC5(C4CCC3(C2C1)C)C)(C)C)C)C)C 424.70 unknown https://doi.org/10.1080/10575639808048294
Taraxerol 92097 Click to see CC1(CCC2(CC=C3C4(CCC5C(C(CCC5(C4CCC3(C2C1)C)C)O)(C)C)C)C)C 426.70 unknown https://doi.org/10.1080/10575639808048294
https://doi.org/10.1016/0031-9422(88)80473-4
Taraxerone 92785 Click to see CC1(CCC2(CC=C3C4(CCC5C(C(=O)CCC5(C4CCC3(C2C1)C)C)(C)C)C)C)C 424.70 unknown https://doi.org/10.1080/10575639808048294
> 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/S0031-9422(00)81759-8
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/S0031-9422(00)81759-8
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(3S,5R,8R,9S,10R,13R,14S,17R)-17-[(2R,5S)-5-hydroxy-5,6-dimethylhept-6-en-2-yl]-4,4,10,13,14-pentamethyl-2,3,5,6,7,8,9,11,12,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 163038816 Click to see CC(CCC(C)(C(=C)C)O)C1CCC2(C1(CCC3C2CCC4C3(CCC(C4(C)C)O)C)C)C 458.80 unknown https://doi.org/10.1515/ZNB-2009-0418
[(1R,3aR,5aR,5bR,7aR,8R,11aR,11bR,13aR,13bS)-1-(3-hydroxyprop-1-en-2-yl)-3a,5a,5b,8,11a-pentamethyl-9-oxo-2,3,4,5,6,7,7a,10,11,11b,12,13,13a,13b-tetradecahydro-1H-cyclopenta[a]chrysen-8-yl]methyl acetate 21582880 Click to see CC(=O)OCC1(C2CCC3(C(C2(CCC1=O)C)CCC4C3(CCC5(C4C(CC5)C(=C)CO)C)C)C)C 498.70 unknown https://doi.org/10.1016/0031-9422(88)80473-4
[(1R,3aR,5aR,5bR,7aR,8R,11aR,11bR,13aR,13bS)-3a,5a,5b,8,11a-pentamethyl-9-oxo-1-(3-oxoprop-1-en-2-yl)-2,3,4,5,6,7,7a,10,11,11b,12,13,13a,13b-tetradecahydro-1H-cyclopenta[a]chrysen-8-yl]methyl acetate 21582879 Click to see CC(=O)OCC1(C2CCC3(C(C2(CCC1=O)C)CCC4C3(CCC5(C4C(CC5)C(=C)C=O)C)C)C)C 496.70 unknown https://doi.org/10.1016/0031-9422(88)80473-4
[(1R,3aR,5aR,5bR,7aR,8R,9S,11aR,11bR,13aR,13bS)-9-acetyloxy-3a,5a,5b,8,11a-pentamethyl-1-(3-oxoprop-1-en-2-yl)-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-8-yl]methyl acetate 21582892 Click to see CC(=O)OCC1(C2CCC3(C(C2(CCC1OC(=O)C)C)CCC4C3(CCC5(C4C(CC5)C(=C)C=O)C)C)C)C 540.80 unknown https://doi.org/10.1016/0031-9422(88)80473-4
[1-(3-hydroxyprop-1-en-2-yl)-3a,5a,5b,8,11a-pentamethyl-9-oxo-2,3,4,5,6,7,7a,10,11,11b,12,13,13a,13b-tetradecahydro-1H-cyclopenta[a]chrysen-8-yl]methyl acetate 14136897 Click to see CC(=O)OCC1(C2CCC3(C(C2(CCC1=O)C)CCC4C3(CCC5(C4C(CC5)C(=C)CO)C)C)C)C 498.70 unknown https://doi.org/10.1016/0031-9422(88)80473-4
[3a,5a,5b,8,11a-pentamethyl-9-oxo-1-(3-oxoprop-1-en-2-yl)-2,3,4,5,6,7,7a,10,11,11b,12,13,13a,13b-tetradecahydro-1H-cyclopenta[a]chrysen-8-yl]methyl acetate 14136893 Click to see CC(=O)OCC1(C2CCC3(C(C2(CCC1=O)C)CCC4C3(CCC5(C4C(CC5)C(=C)C=O)C)C)C)C 496.70 unknown https://doi.org/10.1016/0031-9422(88)80473-4
[9-Acetyloxy-3a,5a,5b,8,11a-pentamethyl-1-(3-oxoprop-1-en-2-yl)-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-8-yl]methyl acetate 14136895 Click to see CC(=O)OCC1(C2CCC3(C(C2(CCC1OC(=O)C)C)CCC4C3(CCC5(C4C(CC5)C(=C)C=O)C)C)C)C 540.80 unknown https://doi.org/10.1016/0031-9422(88)80473-4
17-(5-hydroxy-5,6-dimethylhept-6-en-2-yl)-4,4,10,13,14-pentamethyl-2,3,5,6,7,8,9,11,12,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 163038815 Click to see CC(CCC(C)(C(=C)C)O)C1CCC2(C1(CCC3C2CCC4C3(CCC(C4(C)C)O)C)C)C 458.80 unknown https://doi.org/10.1515/ZNB-2009-0418
Lup-20(29)-en-3-ol, (3beta)- 521518 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1016/0031-9422(88)80473-4
Lup-20(29)-en-3-one 323075 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)C)C)C 424.70 unknown https://doi.org/10.1016/0031-9422(88)80473-4
Lupenone 92158 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)C)C)C 424.70 unknown https://doi.org/10.1016/0031-9422(88)80473-4
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1016/0031-9422(88)80473-4
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cycloartanols and derivatives
O-Methyl cyclolaudenol 139076664 Click to see CC(CCC(C)C(=C)C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)OC)C)C 454.80 unknown https://doi.org/10.1080/10575630290020613
> 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/S0031-9422(00)81759-8
Beta-Sitosterol 222284 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/S0031-9422(00)81759-8
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Chromones
5-hydroxy-7-methoxy-2-methyl-6-(3-methylbut-2-enyloxy)-4H-chromen-4-one 13845711 Click to see CC1=CC(=O)C2=C(C(=C(C=C2O1)OC)OCC=C(C)C)O 290.31 unknown https://doi.org/10.1016/S0031-9422(00)81759-8
Chromone, 5-hydroxy-7-methoxy-2-methyl-6-(3-methyl-2-butenyl)- 615800 Click to see CC1=CC(=O)C2=C(C(=C(C=C2O1)OC)CC=C(C)C)O 274.31 unknown https://doi.org/10.1016/S0031-9422(00)81759-8
Peucenin 68477 Click to see CC1=CC(=O)C2=C(O1)C=C(C(=C2O)CC=C(C)C)O 260.28 unknown https://doi.org/10.1016/S0031-9422(00)81759-8
> Organoheterocyclic compounds / Quinolines and derivatives / Dihydrofuranoquinolines
2-(2-Methoxypropan-2-yl)-9-methyl-2,3-dihydrofuro[2,3-b]quinolin-4-one 73233008 Click to see CC(C)(C1CC2=C(O1)N(C3=CC=CC=C3C2=O)C)OC 273.33 unknown https://doi.org/10.1515/ZNB-2009-0418
Methyl isoplatydesmine, 4 16072115 Click to see CC(C)(C1CC2=C(O1)N(C3=CC=CC=C3C2=O)C)OC 273.33 unknown https://doi.org/10.1515/ZNB-2009-0418
> Organoheterocyclic compounds / Quinolines and derivatives / Furanoquinolines
Dictamnine 68085 Click to see COC1=C2C=COC2=NC3=CC=CC=C31 199.20 unknown https://doi.org/10.1515/ZNB-2009-0418
> Organoheterocyclic compounds / Quinolines and derivatives / Quinolones and derivatives / Hydroquinolones
[(2S,3S)-3-hydroxy-1-(4-methoxy-1-methyl-2-oxoquinolin-3-yl)butan-2-yl] acetate 162888257 Click to see CC(C(CC1=C(C2=CC=CC=C2N(C1=O)C)OC)OC(=O)C)O 319.40 unknown https://doi.org/10.1515/ZNB-2009-0418
[(2S)-1-(4-methoxy-1-methyl-2-oxoquinolin-3-yl)-3-methylbut-3-en-2-yl] acetate 10663149 Click to see CC(=C)C(CC1=C(C2=CC=CC=C2N(C1=O)C)OC)OC(=O)C 315.40 unknown https://doi.org/10.1021/NP970409A
https://doi.org/10.1515/ZNB-2009-0418
[(2S)-3-hydroxy-1-(4-methoxy-1-methyl-2-oxoquinolin-3-yl)-3-methylbutan-2-yl] acetate 10592757 Click to see CC(=O)OC(CC1=C(C2=CC=CC=C2N(C1=O)C)OC)C(C)(C)O 333.40 unknown https://doi.org/10.1021/NP970409A
[1-(4-Methoxy-1-methyl-2-oxoquinolin-3-yl)-3-methylbut-3-en-2-yl] acetate 85223963 Click to see CC(=C)C(CC1=C(C2=CC=CC=C2N(C1=O)C)OC)OC(=O)C 315.40 unknown https://doi.org/10.1021/NP970409A
https://doi.org/10.1515/ZNB-2009-0418
[3-Hydroxy-1-(4-methoxy-1-methyl-2-oxoquinolin-3-yl)butan-2-yl] acetate 162888256 Click to see CC(C(CC1=C(C2=CC=CC=C2N(C1=O)C)OC)OC(=O)C)O 319.40 unknown https://doi.org/10.1515/ZNB-2009-0418
3-(2-Hydroxy-3-methylbut-3-enyl)-4-methoxy-1-methylquinolin-2-one 24812693 Click to see CC(=C)C(CC1=C(C2=CC=CC=C2N(C1=O)C)OC)O 273.33 unknown https://doi.org/10.1021/NP970409A
https://doi.org/10.1515/ZNB-2009-0418
3-[(2S)-2-hydroxy-3-methylbut-3-enyl]-4-methoxy-1-methylquinolin-2-one 10730970 Click to see CC(=C)C(CC1=C(C2=CC=CC=C2N(C1=O)C)OC)O 273.33 unknown https://doi.org/10.1515/ZNB-2009-0418
https://doi.org/10.1021/NP970409A
Orijanone 10778640 Click to see CC(C)C(=O)CC1=C(C2=CC=CC=C2N(C1=O)C)OC 273.33 unknown https://doi.org/10.1021/NP970409A
https://doi.org/10.1515/ZNB-2009-0418
> Organoheterocyclic compounds / Quinolines and derivatives / Quinolones and derivatives / Pyranoquinolines
(3R)-3-hydroxy-2,2,10-trimethyl-9-(3-methylbut-2-enoxy)-3,4-dihydropyrano[2,3-b]quinolin-5-one 101390172 Click to see CC(=CCOC1=CC=CC2=C1N(C3=C(C2=O)CC(C(O3)(C)C)O)C)C 343.40 unknown https://doi.org/10.1515/ZNB-2005-1111
2,2,6-Trimethyl-3,4,5,6-tetrahydro-2H-pyrano[3,2-c]quinoline-5-one, 2 57340431 Click to see CC1(C(CC2=C(O1)C3=CC=CC=C3N(C2=O)C)O)C 259.30 unknown https://doi.org/10.1515/ZNB-2009-0418
3-Hydroxy-10-methyl-2,3,4,6,7,10-hexahydropyrano[3,2-c]quinolin-5-one 162877226 Click to see CC1C=CCC2=C1C3=C(CC(CO3)O)C(=O)N2 233.26 unknown https://doi.org/10.1515/ZNB-2009-0418
3-Hydroxy-2,2,10-trimethyl-9-(3-methylbut-2-enoxy)-3,4-dihydropyrano[2,3-b]quinolin-5-one 162897479 Click to see CC(=CCOC1=CC=CC2=C1N(C3=C(C2=O)CC(C(O3)(C)C)O)C)C 343.40 unknown https://doi.org/10.1515/ZNB-2005-1111
3-Hydroxy-2,2,6-trimethyl-3,4-dihydropyrano[3,2-c]quinolin-5-one 10729985 Click to see CC1(C(CC2=C(O1)C3=CC=CC=C3N(C2=O)C)O)C 259.30 unknown https://doi.org/10.1515/ZNB-2009-0418
> Phenylpropanoids and polyketides / Coumarins and derivatives
2H-1-Benzopyran-2-one, 7-methoxy-6-(3-methyl-2-oxobutyl)- 605135 Click to see CC(C)C(=O)CC1=C(C=C2C(=C1)C=CC(=O)O2)OC 260.28 unknown https://doi.org/10.1515/ZNB-2009-0418
https://doi.org/10.1080/10575630290020613
6-(2,3-Dihydroxy-3-methylbutyl)-7-methoxycoumarin 605103 Click to see CC(C)(C(CC1=C(C=C2C(=C1)C=CC(=O)O2)OC)O)O 278.30 unknown https://doi.org/10.1515/ZNB-2009-0418
6-(3-Hydroxy-2-methoxy-3-methylbutyl)-7-methoxychromen-2-one 162970298 Click to see CC(C)(C(CC1=C(C=C2C(=C1)C=CC(=O)O2)OC)OC)O 292.33 unknown https://doi.org/10.1515/ZNB-2009-0418
6-[(2R)-3-hydroxy-2-methoxy-3-methyl-butyl]-7-methoxy-chromen-2-one 91511982 Click to see CC(C)(C(CC1=C(C=C2C(=C1)C=CC(=O)O2)OC)OC)O 292.33 unknown https://doi.org/10.1515/ZNB-2009-0418
7,8-Dimethoxycoumarin 142768 Click to see COC1=C(C2=C(C=C1)C=CC(=O)O2)OC 206.19 unknown https://doi.org/10.1016/S0031-9422(00)81759-8
8-(4-Hydroxy-3-methylbutoxy)-7-methoxychromen-2-one 13845712 Click to see CC(CCOC1=C(C=CC2=C1OC(=O)C=C2)OC)CO 278.30 unknown https://doi.org/10.1016/S0031-9422(00)81759-8
8-[(3S)-4-hydroxy-3-methylbutoxy]-7-methoxychromen-2-one 163031881 Click to see CC(CCOC1=C(C=CC2=C1OC(=O)C=C2)OC)CO 278.30 unknown https://doi.org/10.1016/S0031-9422(00)81759-8
Osthol 10228 Click to see CC(=CCC1=C(C=CC2=C1OC(=O)C=C2)OC)C 244.28 unknown https://doi.org/10.1016/S0031-9422(00)81759-8
Scoparone 8417 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)OC 206.19 unknown https://doi.org/10.1016/S0031-9422(00)81759-8
Ulopterol 176475 Click to see CC(C)(C(CC1=C(C=C2C(=C1)C=CC(=O)O2)OC)O)O 278.30 unknown https://doi.org/10.1515/ZNB-2009-0418
https://doi.org/10.1080/10575630290020613
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens
(-)-Heraclenol 40429858 Click to see CC(C)(C(COC1=C2C(=CC3=C1OC=C3)C=CC(=O)O2)O)O 304.29 unknown https://doi.org/10.1016/S0031-9422(00)81759-8
https://doi.org/10.1080/10575630290020613
9-(2,3-Dihydroxy-3-methylbutoxy)furo[3,2-g]chromen-7-one 328236 Click to see CC(C)(C(COC1=C2C(=CC3=C1OC=C3)C=CC(=O)O2)O)O 304.29 unknown https://doi.org/10.1515/ZNB-2009-0418
https://doi.org/10.1016/S0031-9422(00)81759-8
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/10.1515/ZNB-2009-0418
Heraclenin 458010 Click to see CC1(C(O1)COC2=C3C(=CC4=C2OC=C4)C=CC(=O)O3)C 286.28 unknown https://doi.org/10.1016/S0031-9422(00)81759-8
Heraclenol 73253 Click to see CC(C)(C(COC1=C2C(=CC3=C1OC=C3)C=CC(=O)O2)O)O 304.29 unknown https://doi.org/10.1080/10575630290020613
https://doi.org/10.1515/ZNB-2009-0418
https://doi.org/10.1016/S0031-9422(00)81759-8
Isogosferol 148619 Click to see CC(=C)C(COC1=C2C(=CC3=C1OC=C3)C=CC(=O)O2)O 286.28 unknown https://doi.org/10.1515/ZNB-2009-0418
https://doi.org/10.1080/10575630290020613
Isooxypeucedanin 625383 Click to see CC(C)C(=O)COC1=C2C=CC(=O)OC2=CC3=C1C=CO3 286.28 unknown https://doi.org/10.1016/S0031-9422(00)81759-8
Oxyimperatorin 182251 Click to see CC1(C(O1)COC2=C3C(=CC4=C2OC=C4)C=CC(=O)O3)C 286.28 unknown https://doi.org/10.1016/S0031-9422(00)81759-8
Pentosalen 10212 Click to see CC(=CCOC1=C2C(=CC3=C1OC=C3)C=CC(=O)O2)C 270.28 unknown https://doi.org/10.1016/S0031-9422(00)81759-8
Prangenin 17897 Click to see CC1(C(O1)COC2=C3C(=CC4=C2OC=C4)C=CC(=O)O3)C 286.28 unknown https://doi.org/10.1016/S0031-9422(00)81759-8
Psoralen 6199 Click to see C1=CC(=O)OC2=CC3=C(C=CO3)C=C21 186.16 unknown https://doi.org/10.1016/S0031-9422(00)81759-8
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 5-hydroxypsoralens
Alloisoimperatorin 5317436 Click to see CC(=CCC1=C2C(=C(C3=C1OC=C3)O)C=CC(=O)O2)C 270.28 unknown https://doi.org/10.1016/S0031-9422(00)81759-8
Bergaptol 5280371 Click to see C1=CC(=O)OC2=CC3=C(C=CO3)C(=C21)O 202.16 unknown https://doi.org/10.1016/S0031-9422(00)81759-8
> 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/S0031-9422(00)81759-8
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 8-hydroxypsoralens
Alloimperatorin 69502 Click to see CC(=CCC1=C2C=CC(=O)OC2=C(C3=C1C=CO3)O)C 270.28 unknown https://doi.org/10.1016/S0031-9422(00)81759-8
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/S0031-9422(00)81759-8
> 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 https://doi.org/10.1016/S0031-9422(00)81759-8
Methoxsalen 4114 Click to see COC1=C2C(=CC3=C1OC=C3)C=CC(=O)O2 216.19 unknown https://doi.org/10.1016/S0031-9422(00)81759-8
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins
Isoscopoletin 69894 Click to see COC1=C(C=C2C=CC(=O)OC2=C1)O 192.17 unknown https://doi.org/10.1016/S0031-9422(00)81759-8
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 6,7-dihydroxycoumarins
Esculetin 5281416 Click to see C1=CC(=O)OC2=CC(=C(C=C21)O)O 178.14 unknown https://doi.org/10.1016/S0031-9422(00)81759-8
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Scopoletin 5280460 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)O 192.17 unknown https://doi.org/10.1016/S0031-9422(00)81759-8
Umbelliferone 5281426 Click to see C1=CC(=CC2=C1C=CC(=O)O2)O 162.14 unknown https://doi.org/10.1016/S0031-9422(00)81759-8

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