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Angelica archangelica

Angelica archangelica - 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 UUID644009612dd5f050249838
Scientific name Angelica archangelica
Authority L.
First published in Sp. Pl. : 250 (1753)

Description Top

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Angelica archangelica, also known as garden angelica, wild celery, and Norwegian angelica, is a biennial plant from the Apiaceae family. It is cultivated for its sweetly scented edible stems and roots, but caution should be taken as it resembles poisonous species. It grows up to 2.5 meters in height and has small yellowish or greenish flowers that bloom in July. Angelica is native to northern European countries and is also commercially grown in France. It has a long history of use as a vegetable and medicinal plant, and is commonly used to flavor liqueurs, omelettes, and jams. The roots are a popular botanical used in gin distillation and other alcoholic beverages. Angelica has a unique aroma and its essential oil contains over eighty different compounds. Its name is derived from the Latin word for "angel-like" and the Greek word for "chief angel."

Synonyms Top

Scientific name Authority First published in
Ligusticum angelica Stokes Bot. Mat. Med. 2: 96 (1812)
Selinum archangelica Vest Man. Bot. : 501 (1805)
Angelica archangelica subsp. norwegica (Rupr.) Nordh. Bergens Mus. Årbog (Årbok) 7: ??. 1936
Angelica commutata (C.A.Mey. ex Rupr.) M.Hiroe Umbell. World : 1430 (1979)
Angelica discocarpa (Fries) M.Hiroe Umbell. World : 1430 (1979)
Angelica intermedia Schult. ex Steud. Nomencl. Bot. 1: 49 (1821)
Angelica major Gilib. Fl. Lit. Inch. ii. 24. 1782
Angelica norwegica (Rupr.) Nyman Syll. Fl. Eur. , Suppl.: 26 (1865)
Angelica officinalis Moench Methodus : 81 (1794)
Angelica procera Salisb. Prodr. Stirp. Chap. Allerton : 164 (1796)
Angelica sativa Mill. Gard. Dict. ed. 8 : n.º 1 (1768)
Archangelica archangelica H.Karst. Deut. Fl. (Karsten) 843. 1882 [Sep 1882]
Archangelica commutata C.A.Mey. ex Rupr. Beitr. Pflanzenk. Russ. Reiches 11: 13 (1859)
Archangelica discocarpa Fries Bot. Not. 1857: 50 (1857)
Archangelica littoralis Agardh ex DC. Prodr. 4: 170 (1830)
Archangelica norwegica Rupr. Beitr. Pflanzenk. Russ. Reiches 2: 37 (1845)
Archangelica officinalis Hoffm. Gen. Pl. Umbell. : 162 (1814)
Archangelica officinalis subsp. litoralis DC. J.Dostál Folia Mus. Rerum Nat. Bohemiae Occid., Bot. 21: 9 (1984)
Archangelica sativa Besser Enum. Pl. Volh. : 13 (1821)
Archangelica slavica Reuss Kvetena Slov. : 184 (1853)
Archangelica spuria Wahlenb. Fl. Carpat. Princ. : 84 (1814)

Common names Top

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Language Common/alternative name
English garden angelica
English norwegian angelica
English holy ghost
English wild celery
Afrikaans engelkruid
Arabic انجليكا أرخانجيلكا
Arabic حشيشة الملاك
Azerbaijani dərman tütəkcəsi
Azerbaijani dərman cəbrayılotu
Belarusian Дзягіль лекавы
Bulgarian лечебна пищялка
Catalan herba de l'esperit sant
Catalan herba de l’esperit sant
Czech andělika lékařská
Czech děhel lékařský
Welsh llysiau`r-angel pêr
Danish kvan
German engelwurz
German echte engelwurz
German angelika
German erzengelwurz
German küsten-arznei-engelwurz
German arznei-engelwurz
diq helerg
Greek Αγγελική αρχαγγελική
Esperanto angeliko
Esperanto Ĝardenangeliko
Estonian harilik kikkaputk
Basque aingeru-belar landatu
Persian آنژلیک
Persian انژلیک
Persian حشیشه الملائک
Persian حشیشهٔ الملائک
Persian سنبل خطایی
Finnish väinönputki
Faroese hvonn (planta)
French angélique vraie
French angelique officinale
French angélique officinale
Galician anxélica
Hindi गार्डन एंजेलिका
Hindi एंजेलिका आर्चएंजेलिका
Croatian anđelika
Hungarian angyalgyökér
Hungarian orvosi angyalgyökér
Icelandic englahvönn
Icelandic englarót
Icelandic erkihvönn
Icelandic höfuðhvönn
Icelandic Ætihvönn
Japanese セイヨウトウキ
Kazakh Аю балдырған
kl kuanneq
lb angelique
lb leinskraut
Lithuanian vaistinė šventagaršvė
Macedonian Благ боз
Norwegian Bokmål fjellkvann
Norwegian Bokmål strandkvann
Norwegian Bokmål vossakvann
Norwegian Bokmål kvann
Dutch grote engelwortel
Dutch aartsengelwortel
Norwegian Nynorsk kvanne
Norwegian Nynorsk kvann
pam garden angelica
Polish archangelica
Polish arcydzięgiel
Polish arcydzięgiel lekarski
Polish arcydzięgiel litwor
Polish litwor
Polish dzięgiel litwor
Romanian aglică
Romanian angelină
Romanian anghelică
Romanian antonică
Romanian buciniş
Romanian buciniș
Romanian cucută mare
Romanian angelică
Russian Дягиль
Russian Дудник лекарственный
Russian Дягиль лекарственный
se boska
se fádnu
se olbmoborranrássi
Serbo-Croatian angelika
Serbo-Croatian anđelika
Slovak archangelika lekárska
Slovenian gozdni koren
Slovenian zdravilni gozdni koren
smn puurrâmrääsi
sms poorrâmrääʹss
Serbian Анђеоски корен
Serbian Анђелика
Swedish bosko
Swedish fjällkvanne
Swedish havssträtta
Swedish påsko
Swedish strandkvanne
Swedish kvanne
Ukrainian Дзенгель
Ukrainian Дудник лікарський
Ukrainian Дягиль лікарський
Ukrainian Дягіль лікарський
Ukrainian Дяглиця
Ukrainian Дягель лікарський
vep joršibut'k
vep zell'joršibut'k
Chinese 挪威当归
Chinese 欧白芷
Chinese 药用当归
Chinese 藥用當歸
Chinese 歐白芷

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Angelica archangelica subsp. decurrens (Ledeb.) Kuvaev Bot. Zhurn. (Moscow & Leningrad) 66: 952 (1981)
Angelica archangelica subsp. litoralis (Wahlenb.) Thell. Ill. Fl. Mitt.-Eur. 5(2): 1342. 1926 (1926)

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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Sow seeds at 20°C, expecting germination within 3 months without further temperature treatment.
Requires Light or Surface Sowing: These seeds need light to germinate and should not be covered with soil or only very lightly. They are often very small and sown directly on the surface of the growing medium.

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-0000536100
UNII S7E6K05K7Z
Canadensys 2533
USDA Plants ANAR9
Tropicos 1701408
INPN 82705
KEW urn:lsid:ipni.org:names:837560-1
The Plant List kew-2638995
Missouri Botanical Garden 276039
PFAF Angelica archangelica
Open Tree Of Life 428208
Observations.org 6430
NCBI Taxonomy 40949
NBN Atlas NBNSYS0000003704
Nature Serve 2.131325
IPNI 838181-1
iNaturalist 62336
GBIF 5371808
Freebase /m/03f_f_
EPPO ANKAR
EOL 581752
Elurikkus 2775
USDA GRIN 3415
Wikipedia Angelica_archangelica
CMAUP NPO6190
CMAUP NPO662
Plantarium 3519

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
Full-Length Transcriptome Sequencing and RNA-Seq Analysis Offer Insights into Terpenoid Biosynthesis in Blumea balsamifera (L.) DC. Ju Z, Liang L, Zheng Y, Shi H, Zhao W, Sun W, Pang Y Genes (Basel) 24-Feb-2024
PMCID:PMC10970515
doi:10.3390/genes15030285
PMID:38540346
The Meaning of Plants' Names: A New Discovering Approach to Its Medicinal and/or Toxic Properties dos Santos Dantas Lima L, Felipe Domingues Passero L, Indriunas A, de Souza Santos I, Francisco Uchôa Coqueiro L, Alexandre Souza da Cruz K, Batista de Almeida A, Carlos Fernandes Galduróz J, Rodrigues E Evid Based Complement Alternat Med 19-Feb-2024
PMCID:PMC10896657
doi:10.1155/2024/6678557
PMID:38410808
Methoxyfuranocoumarins of Natural Origin–Updating Biological Activity Research and Searching for New Directions—A Review Bartnik M Curr Issues Mol Biol 19-Jan-2024
PMCID:PMC10813879
doi:10.3390/cimb46010055
PMID:38275669
Bioactivity and toxicity of coumarins from African medicinal plants Anywar G, Muhumuza E Front Pharmacol 10-Jan-2024
PMCID:PMC10809390
doi:10.3389/fphar.2023.1231006
PMID:38273831
Anthocyanin Production from Plant Cell and Organ Cultures In Vitro Murthy HN, Joseph KS, Paek KY, Park SY Plants (Basel) 31-Dec-2023
PMCID:PMC10780419
doi:10.3390/plants13010117
PMID:38202425
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
Plant Extracts as Skin Care and Therapeutic Agents Michalak M Int J Mol Sci 22-Oct-2023
PMCID:PMC10607442
doi:10.3390/ijms242015444
PMID:37895122
Innovative Bioactive Nanofibrous Materials Combining Medicinal and Aromatic Plant Extracts and Electrospinning Method Stoyanova N, Nachev N, Spasova M Membranes (Basel) 21-Oct-2023
PMCID:PMC10608671
doi:10.3390/membranes13100840
PMID:37888012
The most polyphagous insect herbivore? Host plant associations of the Meadow spittlebug, Philaenus spumarius (L.) Thompson V, Harkin C, Stewart AJ PLoS One 04-Oct-2023
PMCID:PMC10602594
doi:10.1371/journal.pone.0291734
PMID:37792900
New Plants, New Resources, New Knowledge: Early Introductions of Exotic Plants to Indigenous Territories in Northwestern North America Turner NJ Plants (Basel) 28-Aug-2023
PMCID:PMC10490097
doi:10.3390/plants12173087
PMID:37687334
Unveiling the antitumor potential of novel N-(substituted-phenyl)-8-methoxycoumarin-3-carboxamides as dual inhibitors of VEGFR2 kinase and cytochrome P450 for targeted treatment of hepatocellular carcinoma Radwan EM, Abo-Elabass E, Abd El-Baky AE, Alshwyeh HA, Almaimani RA, Almaimani G, Ibrahim IA, Albogami A, Jaremko M, Alshawwa SZ, Saied EM Front Chem 04-Aug-2023
PMCID:PMC10436493
doi:10.3389/fchem.2023.1231030
PMID:37601910
Recent Updates on Viral Oncogenesis: Available Preventive and Therapeutic Entities Chowdhary S, Deka R, Panda K, Kumar R, Solomon AD, Das J, Kanoujiya S, Gupta AK, Sinha S, Ruokolainen J, Kesari KK, Gupta PK Mol Pharm 24-Jul-2023
PMCID:PMC10410670
doi:10.1021/acs.molpharmaceut.2c01080
PMID:37486263
Fungistatic Effect of Phthalide Lactones on Rhodotorula mucilaginosa Gach J, Olejniczak T, Pannek J, Boratyński F Molecules 15-Jul-2023
PMCID:PMC10384090
doi:10.3390/molecules28145423
PMID:37513295
Behavioral, Electrophysiological, and Toxicological Responses of Plutella xylostella to Extracts from Angelica pubescens Zheng R, Zhao J, Ma L, Qie X, Yan X, Hao C Insects 06-Jul-2023
PMCID:PMC10380822
doi:10.3390/insects14070613
PMID:37504619
Network pharmacology-based research on the effect of angelicin on osteosarcoma and the underlying mechanism Zhang Y, Wei J, Kong L, Song M, Zhang Y, Xiao X, Cao H, Li Z, Yang N, Jin Y Aging (Albany NY) 10-Jun-2023
PMCID:PMC10292874
doi:10.18632/aging.204786
PMID:37301545

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
> Alkaloids and derivatives / Gelsemium alkaloids
(Spiro(3H-indole-3,7'(6'H)-(3,) (6)methano(1H)oxepino(4,3-b)pyrrol)-2(1H)-one,) 2'-ethyl-2',3',3'a, 4',8',8'a-hexahydro-1-methoxy- 21589070 Click to see CCC1C2CC3C4(CC(C2CO3)N1)C5=CC=CC=C5N(C4=O)OC 328.40 unknown https://doi.org/10.1055/S-2006-961461
https://doi.org/10.1002/PCA.2800030108
https://doi.org/10.1016/S0021-9673(00)00321-6
> Alkaloids and derivatives / Tropane alkaloids
CID 6540490 6540490 Click to see CC=C(C)C(=O)OC1CC2CCC(C1)N2C 223.31 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Phenylpropanes
2-(4-Methylphenyl)propan-2-ol 14529 Click to see CC1=CC=C(C=C1)C(C)(C)O 150.22 unknown https://doi.org/10.1021/JF00046A030
> Hydrocarbons / Unsaturated hydrocarbons / Enynes
Undec-5-en-3-yne 53083 Click to see CCCCCC=CC#CCC 150.26 unknown https://doi.org/10.1021/JF00046A030
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Branched fatty acids / Methyl-branched fatty acids
(R)-2-Methylbutanoic acid 6950479 Click to see CCC(C)C(=O)O 102.13 unknown https://doi.org/10.1002/CBER.189602902124
2-Butenoic acid, 2-methyl- 6656 Click to see CC=C(C)C(=O)O 100.12 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.17-1161
2-Methylbutanoic acid 8314 Click to see CCC(C)C(=O)O 102.13 unknown https://doi.org/10.1002/CBER.189602902124
2,3-Dimethylacrylic acid, (E)- 125468 Click to see CC=C(C)C(=O)O 100.12 unknown via CMAUP database
2,3-Dimethylacrylic acid, (Z)- 643915 Click to see CC=C(C)C(=O)O 100.12 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.17-1161
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
15-Hydroxypentadecanoic acid 78360 Click to see C(CCCCCCCO)CCCCCCC(=O)O 258.40 unknown https://doi.org/10.1002/CBER.189602902124
Palmitic Acid 985 Click to see CCCCCCCCCCCCCCCC(=O)O 256.42 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.17-1161
https://doi.org/10.1080/10412905.1993.9698257
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Very long-chain fatty acids
Behenic Acid 8215 Click to see CCCCCCCCCCCCCCCCCCCCCC(=O)O 340.60 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.17-1161
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohol esters
Heptadecyl acetate 69967 Click to see CCCCCCCCCCCCCCCCCOC(=O)C 298.50 unknown https://doi.org/10.1021/JF00046A030
Tetradecyl acetate 12531 Click to see CCCCCCCCCCCCCCOC(=O)C 256.42 unknown https://doi.org/10.1021/JF00046A030
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols / Long-chain fatty alcohols
1-Tridecanol 8207 Click to see CCCCCCCCCCCCCO 200.36 unknown https://doi.org/10.1021/JF00046A030
Cetyl Alcohol 2682 Click to see CCCCCCCCCCCCCCCCO 242.44 unknown https://doi.org/10.1021/JF00046A030
Stearyl Alcohol 8221 Click to see CCCCCCCCCCCCCCCCCCO 270.50 unknown https://doi.org/10.1021/JF00046A030
> Lipids and lipid-like molecules / Fatty Acyls / Fatty aldehydes
Pentadecanal 17697 Click to see CCCCCCCCCCCCCCC=O 226.40 unknown https://doi.org/10.1021/JF00046A030
Tetradecanal 31291 Click to see CCCCCCCCCCCCCC=O 212.37 unknown https://doi.org/10.1021/JF00046A030
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
beta-OCIMENE, (3E)- 5281553 Click to see CC(=CCC=C(C)C=C)C 136.23 unknown https://doi.org/10.1021/JF00046A030
Myrcene 31253 Click to see CC(=CCCC(=C)C=C)C 136.23 unknown https://doi.org/10.1021/JF00046A030
https://doi.org/10.1002/(SICI)1099-1026(199711/12)12:6<397::AID-FFJ670>3.0.CO;2-Z
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
4-Isopropylbenzyl alcohol 325 Click to see CC(C)C1=CC=C(C=C1)CO 150.22 unknown https://doi.org/10.1021/JF00046A030
p-CYMENE 7463 Click to see CC1=CC=C(C=C1)C(C)C 134.22 unknown https://doi.org/10.1021/JF00046A030
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-alpha-Pinene 440968 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown https://doi.org/10.1002/(SICI)1099-1026(199711/12)12:6<397::AID-FFJ670>3.0.CO;2-Z
(+)-alpha-Pinene 82227 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown https://doi.org/10.1002/(SICI)1099-1026(199711/12)12:6<397::AID-FFJ670>3.0.CO;2-Z
(1R)-2-methyl-5-propan-2-ylbicyclo[3.1.0]hex-2-ene 6451618 Click to see CC1=CCC2(C1C2)C(C)C 136.23 unknown https://doi.org/10.1021/JF00046A030
1,7,7-Trimethylbicyclo[2.2.1]heptan-2-ol 64685 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown https://doi.org/10.1021/JF00046A030
3-Carene 26049 Click to see CC1=CCC2C(C1)C2(C)C 136.23 unknown https://doi.org/10.1021/JF00046A030
alpha-PINENE 6654 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown https://doi.org/10.1021/JF00046A030
beta-Pinene 14896 Click to see CC1(C2CCC(=C)C1C2)C 136.23 unknown https://doi.org/10.1021/JF00046A030
Bicyclo[3.1.0]hex-2-ene, 2-methyl-5-(1-methylethyl)- 17868 Click to see CC1=CCC2(C1C2)C(C)C 136.23 unknown https://doi.org/10.1021/JF00046A030
Bornyl acetate 6448 Click to see CC(=O)OC1CC2CCC1(C2(C)C)C 196.29 unknown https://doi.org/10.1021/JF00046A030
Camphene 6616 Click to see CC1(C2CCC(C2)C1=C)C 136.23 unknown https://doi.org/10.1021/JF00046A030
cis-Thujenol 91746682 Click to see CC1=CC(C2(C1C2)C(C)C)O 152.23 unknown https://doi.org/10.1021/JF00046A030
Sabinen 18818 Click to see CC(C)C12CCC(=C)C1C2 136.23 unknown https://doi.org/10.1021/JF00046A030
Sabinene 10887971 Click to see CC(C)C12CCC(=C)C1C2 136.23 unknown https://doi.org/10.1002/(SICI)1099-1026(199711/12)12:6<397::AID-FFJ670>3.0.CO;2-Z
> 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 via CMAUP database
(2S,4R)-p-Mentha-1(7),5-dien-2-ol 5319361 Click to see CC(C)C1CC(C(=C)C=C1)O 152.23 unknown https://doi.org/10.1002/HLCA.19790620703
3-Cyclohexen-1-ol,2-methylene-5-(1-methylethyl)-,(1S-trans)-(9CI) 11446451 Click to see CC(C)C1CC(C(=C)C=C1)O 152.23 unknown https://doi.org/10.1002/HLCA.19790620703
alpha-PHELLANDRENE 7460 Click to see CC1=CCC(C=C1)C(C)C 136.23 unknown https://doi.org/10.1021/JF00046A030
alpha-PHELLANDRENE, (-)- 442482 Click to see CC1=CCC(C=C1)C(C)C 136.23 unknown https://doi.org/10.1002/(SICI)1099-1026(199711/12)12:6<397::AID-FFJ670>3.0.CO;2-Z
Beta-Phellandrene 11142 Click to see CC(C)C1CCC(=C)C=C1 136.23 unknown https://doi.org/10.1021/JF00046A030
cis-1(7),5-p-Menthadien-2-ol 91753261 Click to see CC(C)C1CC(C(=C)C=C1)O 152.23 unknown https://doi.org/10.1002/HLCA.19790620703
gamma-Terpineol 11467 Click to see CC(=C1CCC(CC1)(C)O)C 154.25 unknown https://doi.org/10.1021/JF00046A030
Limonene, (-)- 439250 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1002/(SICI)1099-1026(199711/12)12:6<397::AID-FFJ670>3.0.CO;2-Z
Limonene, (+)- 440917 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1021/JF00046A030
Phellandral 89488 Click to see CC(C)C1CCC(=CC1)C=O 152.23 unknown https://doi.org/10.1021/JF00046A030
Terpinolene 11463 Click to see CC1=CCC(=C(C)C)CC1 136.23 unknown https://doi.org/10.1021/JF00046A030
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(+)-gamma-Cadinene 6432404 Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C 204.35 unknown https://doi.org/10.1021/JF00046A030
(1E,8E)-2,6,6,9-tetramethylcycloundeca-1,4,8-triene 134687947 Click to see CC1=CCC(C=CCC(=CCC1)C)(C)C 204.35 unknown https://doi.org/10.1021/JF00046A030
(1R,2S,7S,8S)-1,3-dimethyl-8-propan-2-yltricyclo[4.4.0.02,7]dec-3-ene 92042749 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown https://doi.org/10.1021/JF00046A030
(1S,2S,4R,5S,6R,7R)-2,8-dimethyl-5-propan-2-yltricyclo[4.4.0.02,7]dec-8-en-4-ol 162822888 Click to see CC1=CCC2C3C1C2(CC(C3C(C)C)O)C 220.35 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.29B-0999
(1S,5R,7S,10R)-4,10-dimethyl-7-propan-2-yltricyclo[4.4.0.01,5]dec-3-ene 134779875 Click to see CC1CCC(C2C13C2C(=CC3)C)C(C)C 204.35 unknown https://doi.org/10.1021/JF00046A030
(2S,4R,5S,6R,7R)-2,8-dimethyl-5-propan-2-yltricyclo[4.4.0.02,7]dec-8-en-4-ol 163187985 Click to see CC1=CCC2C3C1C2(CC(C3C(C)C)O)C 220.35 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.29B-0999
(R)-beta-bisabolene 68128 Click to see CC1=CCC(CC1)C(=C)CCC=C(C)C 204.35 unknown https://doi.org/10.1021/JF00046A030
2-[(1S,2S,3R,7S)-6,8-dimethyl-3-tricyclo[4.4.0.02,7]dec-8-enyl]propan-2-ol 101281096 Click to see CC1=CCC2C3C1C2(CCC3C(C)(C)O)C 220.35 unknown https://doi.org/10.1021/JF00046A030
8alpha-3-Copaen-8-ol 577203 Click to see CC1=CCC2C3C1C2(CC(C3C(C)C)O)C 220.35 unknown https://doi.org/10.1021/JF00046A030
alpha-Cubebene 442359 Click to see CC1CCC(C2C13C2C(=CC3)C)C(C)C 204.35 unknown https://doi.org/10.1021/JF00046A030
beta-Bisabolene 10104370 Click to see CC1=CCC(CC1)C(=C)CCC=C(C)C 204.35 unknown https://doi.org/10.1021/JF00046A030
beta-Farnesene, (6Z)- 5317319 Click to see CC(=CCCC(=CCCC(=C)C=C)C)C 204.35 unknown https://doi.org/10.1021/JF00046A030
Copaene 19725 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown https://doi.org/10.1021/JF00046A030
https://doi.org/10.1007/BF02066237
Copaene, (+)- 636457 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown https://doi.org/10.1007/BF02066237
https://doi.org/10.1021/JF00077A038
Cuparene 86895 Click to see CC1=CC=C(C=C1)C2(CCCC2(C)C)C 202.33 unknown https://doi.org/10.1021/JF00046A030
Cyclohexene, 4-ethenyl-4-methyl-3-(1-methylethenyl)-1-(1-methylethyl)-, (3R-trans)- 89316 Click to see CC(C)C1=CC(C(CC1)(C)C=C)C(=C)C 204.35 unknown https://doi.org/10.1021/JF00046A030
delta-Elemene 12309449 Click to see CC(C)C1=CC(C(CC1)(C)C=C)C(=C)C 204.35 unknown https://doi.org/10.1021/JF00046A030
gamma-Cadinene 15094 Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C 204.35 unknown https://doi.org/10.1021/JF00046A030
gamma-Muurolene 12313020 Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C 204.35 unknown https://doi.org/10.1021/JF00046A030
Humulene 5281520 Click to see CC1=CCC(C=CCC(=CCC1)C)(C)C 204.35 unknown https://doi.org/10.1021/JF00046A030
Isocaryophyllene 5281522 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1021/JF00046A030
Thujopsen 97829 Click to see CC1=CCC2(CCCC(C23C1C3)(C)C)C 204.35 unknown https://doi.org/10.1021/JF00046A030
Thujopsene 442402 Click to see CC1=CCC2(CCCC(C23C1C3)(C)C)C 204.35 unknown https://doi.org/10.1021/JF00046A030
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(1aS,4aS,7S,7aR,7bS)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol 97032059 Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C 220.35 unknown https://doi.org/10.1021/JF00046A030
(7aR)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol 5321422 Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C 220.35 unknown https://doi.org/10.1021/JF00046A030
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Bicyclogermacrane and isolepidozane sesquiterpenoids
(1S,2E,10R)-3,7,11,11-tetramethylbicyclo[8.1.0]undeca-2,6-diene 44583886 Click to see CC1=CCCC(=CC2C(C2(C)C)CC1)C 204.35 unknown https://doi.org/10.1021/JF00046A030
Bicyclogermacrene 5315347 Click to see CC1=CCCC(=CC2C(C2(C)C)CC1)C 204.35 unknown https://doi.org/10.1021/JF00046A030
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Cedrane and isocedrane sesquiterpenoids
(+)-beta-Cedrene 102432 Click to see CC1CCC2C13CCC(=C)C(C3)C2(C)C 204.35 unknown https://doi.org/10.1021/JF00046A030
beta-Cedrene 11106485 Click to see CC1CCC2C13CCC(=C)C(C3)C2(C)C 204.35 unknown https://doi.org/10.1021/JF00046A030
Cedrol 65575 Click to see CC1CCC2C13CCC(C(C3)C2(C)C)(C)O 222.37 unknown https://doi.org/10.1021/JF00046A030
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Elemane sesquiterpenoids
2-(4-Ethenyl-4-methyl-3-prop-1-en-2-ylcyclohexyl)propan-2-ol 547972 Click to see CC(=C)C1CC(CCC1(C)C=C)C(C)(C)O 222.37 unknown https://doi.org/10.1021/JF00046A030
Beta-Elemene 6918391 Click to see CC(=C)C1CCC(C(C1)C(=C)C)(C)C=C 204.35 unknown https://doi.org/10.1021/JF00046A030
Elemol 92138 Click to see CC(=C)C1CC(CCC1(C)C=C)C(C)(C)O 222.37 unknown https://doi.org/10.1021/JF00046A030
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
beta-EUDESMOL 91457 Click to see CC12CCCC(=C)C1CC(CC2)C(C)(C)O 222.37 unknown https://doi.org/10.1021/JF00046A030
beta-Selinene 442393 Click to see CC(=C)C1CCC2(CCCC(=C)C2C1)C 204.35 unknown https://doi.org/10.1021/JF00046A030
Dihydroeudesmol 44559303 Click to see CC1CCCC2(C1CC(CC2)C(C)(C)O)C 224.38 unknown https://doi.org/10.1021/JF00046A030
Rosifoliol 527256 Click to see CC1CCCC2(C1=CC(CC2)C(C)(C)O)C 222.37 unknown https://doi.org/10.1021/JF00046A030
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
(S,1Z,6Z)-8-Isopropyl-1-methyl-5-methylenecyclodeca-1,6-diene 91723653 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown https://doi.org/10.1021/JF00046A030
Germacrene D 5317570 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown https://doi.org/10.1021/JF00046A030
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
6-(3,7-Dimethylocta-2,6-dienyl)-7-hydroxychromen-2-one 5357655 Click to see CC(=CCCC(=CCC1=C(C=C2C(=C1)C=CC(=O)O2)O)C)C 298.40 unknown via CMAUP database
Umbelliprenin 1781413 Click to see CC(=CCCC(=CCCC(=CCOC1=CC2=C(C=C1)C=CC(=O)O2)C)C)C 366.50 unknown https://doi.org/10.1016/S0021-9673(00)00321-6
Xanthotoxol geranyl ether 5317564 Click to see CC(=CCCC(=CCOC1=C2C(=CC3=C1OC=C3)C=CC(=O)O2)C)C 338.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
CID 12310408 12310408 Click to see CC=C(C)C(=O)OC1CC2(C(O2)CC(C(=CC3C1C(=C)C(=O)O3)C)O)C 362.40 unknown https://doi.org/10.1016/0031-9422(83)83044-1
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
[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-yl] icosanoate 13828714 Click to see CCCCCCCCCCCCCCCCCCCC(=O)OC1CCC2(C3CCC4(C(C3CC=C2C1)CCC4C(C)CCC(CC)C(C)C)C)C 709.20 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.17-1161
beta-Sitosterol palmitate 13747834 Click to see CCCCCCCCCCCCCCCC(=O)OC1CCC2(C3CCC4(C(C3CC=C2C1)CCC4C(C)CCC(CC)C(C)C)C)C 653.10 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.17-1161
beta-Sitosteryl palmitate 9852570 Click to see CCCCCCCCCCCCCCCC(=O)OC1CCC2(C3CCC4(C(C3CC=C2C1)CCC4C(C)CCC(CC)C(C)C)C)C 653.10 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.17-1161
Stigmast-5-en-3beta-yl eicosanoate 13828717 Click to see CCCCCCCCCCCCCCCCCCCC(=O)OC1CCC2(C3CCC4(C(C3CC=C2C1)CCC4C(C)CCC(CC)C(C)C)C)C 709.20 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.17-1161
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Pregnane steroids / Gluco/mineralocorticoids, progestogins and derivatives
Pregnenolone 8955 Click to see CC(=O)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 316.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones / Cardenolides and derivatives
Digitoxigenin 4369270 Click to see CC12CCC(CC1CCC3C2CCC4(C3(CCC4C5=CC(=O)OC5)O)C)O 374.50 unknown via CMAUP database
Gitoxigenin 348482 Click to see CC12CCC(CC1CCC3C2CCC4(C3(CC(C4C5=CC(=O)OC5)O)O)C)O 390.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3S,8R,9R,10R,13R,14R,17R)-17-[(2R,5R)-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 11870456 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
> Nucleosides, nucleotides, and analogues / Purine nucleosides
Adenosine 60961 Click to see C1=NC(=C2C(=N1)N(C=N2)C3C(C(C(O3)CO)O)O)N 267.24 unknown https://doi.org/10.1016/0031-9422(83)83044-1
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-[5-[(E)-3-hydroxyprop-1-enyl]-2-methoxyphenoxy]oxane-3,4,5-triol 163190063 Click to see COC1=C(C=C(C=C1)C=CCO)OC2C(C(C(C(O2)CO)O)O)O 342.34 unknown https://doi.org/10.1016/0031-9422(83)83044-1
2-(Hydroxymethyl)-6-[5-(3-hydroxyprop-1-enyl)-2-methoxyphenoxy]oxane-3,4,5-triol 162888665 Click to see COC1=C(C=C(C=C1)C=CCO)OC2C(C(C(C(O2)CO)O)O)O 342.34 unknown https://doi.org/10.1016/0031-9422(83)83044-1
Coniferin 5280372 Click to see COC1=C(C=CC(=C1)C=CCO)OC2C(C(C(C(O2)CO)O)O)O 342.34 unknown https://doi.org/10.1016/0031-9422(83)83044-1
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Chromones
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 via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Chromones / Furanochromones
Angelicain 46240156 Click to see CC(C)(C1CC2=C(O1)C=C3C(=C2O)C(=O)C=C(O3)CO)O 292.28 unknown https://doi.org/10.3987/R-1986-02-0437
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
(2E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 54691413 Click to see COC1=C(C=CC(=C1)C=CC(=O)O)[O-] 193.18 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives
Osthol 10228 Click to see CC(=CCC1=C(C=CC2=C1OC(=O)C=C2)OC)C 244.28 unknown https://doi.org/10.1016/S0021-9673(00)00321-6
https://doi.org/10.1080/10412905.1993.9698257
https://doi.org/10.1002/PCA.2800030108
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Angular furanocoumarins
[(8R,9S)-8-[2-[(Z)-2-methylbut-2-enoyl]oxypropan-2-yl]-2-oxo-8,9-dihydrofuro[2,3-h]chromen-9-yl] (Z)-2-methylbut-2-enoate 133562226 Click to see CC=C(C)C(=O)OC1C(OC2=C1C3=C(C=C2)C=CC(=O)O3)C(C)(C)OC(=O)C(=CC)C 426.50 unknown https://doi.org/10.1055/S-2006-961461
https://doi.org/10.1002/PCA.2800030108
https://doi.org/10.1016/S0021-9673(00)00321-6
[(8S,9S)-8-[2-[(Z)-2-methylbut-2-enoyl]oxypropan-2-yl]-2-oxo-8,9-dihydrofuro[2,3-h]chromen-9-yl] (Z)-2-methylbut-2-enoate 163185718 Click to see CC=C(C)C(=O)OC1C(OC2=C1C3=C(C=C2)C=CC(=O)O3)C(C)(C)OC(=O)C(=CC)C 426.50 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.18-0932
[1-methyl-1-[(9R)-9-(3-methylbut-2-enoyloxy)-2-oxo-8,9-dihydrofuro[2,3-h]chromen-8-yl]ethyl] (E)-2-methylbut-2-enoate 53297351 Click to see CC=C(C)C(=O)OC(C)(C)C1C(C2=C(O1)C=CC3=C2OC(=O)C=C3)OC(=O)C=C(C)C 426.50 unknown via CMAUP database
[8-[2-(2-Methylbut-2-enoyloxy)propan-2-yl]-2-oxo-8,9-dihydrofuro[2,3-h]chromen-9-yl] 2-methylbut-2-enoate 3083773 Click to see CC=C(C)C(=O)OC1C(OC2=C1C3=C(C=C2)C=CC(=O)O3)C(C)(C)OC(=O)C(=CC)C 426.50 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.18-0932
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/10.1016/0031-9422(83)83044-1
Angelicin 10658 Click to see C1=CC2=C(C=CO2)C3=C1C=CC(=O)O3 186.16 unknown https://doi.org/10.1080/10412905.1993.9698257
https://doi.org/10.1016/S0021-9673(01)84214-X
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/10.1016/0031-9422(83)83044-1
Oroselone 74477 Click to see CC(=C)C1=CC2=C(O1)C=CC3=C2OC(=O)C=C3 226.23 unknown https://doi.org/10.1080/10412905.1993.9698257
Pimpinellin 4825 Click to see COC1=C(C2=C(C=CO2)C3=C1C=CC(=O)O3)OC 246.21 unknown https://doi.org/10.1016/S0021-9673(00)00321-6
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Linear furanocoumarins
9-Hydroxy-5,6-dihydrofuro[3,2-g]chromen-7-one 29920867 Click to see C1CC(=O)OC2=C1C=C3C=COC3=C2O 204.18 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens
(1'x,2S)-2-(1,2-Dihydroxy-1-methylethyl)-2,3-dihydro-7H-furo[3,2-g][1]benzopyran-7-one 2'-glucoside 131752523 Click to see CC(COC1C(C(C(C(O1)CO)O)O)O)(C2CC3=C(O2)C=C4C(=C3)C=CC(=O)O4)O 424.40 unknown https://doi.org/10.1016/0031-9422(83)83044-1
(2S)-2-[(2R)-2-hydroxy-1-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypropan-2-yl]-2,3-dihydrofuro[3,2-g]chromen-7-one 163084404 Click to see CC(COC1C(C(C(C(O1)CO)O)O)O)(C2CC3=C(O2)C=C4C(=C3)C=CC(=O)O4)O 424.40 unknown https://doi.org/10.1016/0031-9422(83)83044-1
4-(2,3-Dihydroxy-3-methylbutoxy)furo(3,2-g)chromen-7-one 483513 Click to see CC(C)(C(COC1=C2C=CC(=O)OC2=CC3=C1C=CO3)O)O 304.29 unknown via CMAUP database
4-[(3,3-Dimethyloxiran-2-yl)methoxy]furo[3,2-g]chromen-7-one 160544 Click to see CC1(C(O1)COC2=C3C=CC(=O)OC3=CC4=C2C=CO4)C 286.28 unknown via CMAUP database
5-[[(2S)-3,3-dimethyloxiran-2-yl]methoxy]furo[3,2-g]chromen-7-one 53316971 Click to see CC1(C(O1)COC2=CC(=O)OC3=C2C=C4C=COC4=C3)C 286.28 unknown via CMAUP database
Ammijin 216283 Click to see CC(C)(C1CC2=C(O1)C=C3C(=C2)C=CC(=O)O3)OC4C(C(C(C(O4)CO)O)O)O 408.40 unknown https://doi.org/10.1016/0031-9422(83)83044-1
Archangelin 177156 Click to see CC1=C(CCC(C1)(C)C)COC2=C3C=CC(=O)OC3=CC4=C2C=CO4 338.40 unknown https://doi.org/10.3987/R-1986-02-0437
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/10.1016/0031-9422(83)83044-1
Heraclenol 73253 Click to see CC(C)(C(COC1=C2C(=CC3=C1OC=C3)C=CC(=O)O2)O)O 304.29 unknown via CMAUP database
Heraclenol 3'-O-beta-D-glucopyranoside 21573687 Click to see CC(C)(C(COC1=C2C(=CC3=C1OC=C3)C=CC(=O)O2)O)OC4C(C(C(C(O4)CO)O)O)O 466.40 unknown https://doi.org/10.1016/0031-9422(83)80039-9
Isoimperatorin 68081 Click to see CC(=CCOC1=C2C=CC(=O)OC2=CC3=C1C=CO3)C 270.28 unknown https://doi.org/10.1016/S0021-9673(01)84214-X
https://doi.org/10.1007/BF02977004
https://doi.org/10.1016/S0021-9673(00)00321-6
https://doi.org/10.3987/R-1986-02-0437
https://doi.org/10.1002/PCA.2800030108
https://doi.org/10.1016/S0031-9422(00)81503-4
Isooxypeucedanin 625383 Click to see CC(C)C(=O)COC1=C2C=CC(=O)OC2=CC3=C1C=CO3 286.28 unknown via CMAUP database
Marmesin galactoside 611513 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/10.1016/0031-9422(83)83044-1
Ostruthol 6441273 Click to see CC=C(C)C(=O)OC(COC1=C2C=CC(=O)OC2=CC3=C1C=CO3)C(C)(C)O 386.40 unknown https://doi.org/10.1002/PCA.2800030108
https://doi.org/10.1016/S0021-9673(01)84214-X
Oxypeucedanin 928465 Click to see CC1(C(O1)COC2=C3C=CC(=O)OC3=CC4=C2C=CO4)C 286.28 unknown https://doi.org/10.1002/PCA.2800030108
https://doi.org/10.1016/S0021-9673(01)84214-X
Oxypeucedanin hydrate 17536 Click to see CC(C)(C(COC1=C2C=CC(=O)OC2=CC3=C1C=CO3)O)O 304.29 unknown via CMAUP database
Pentosalen 10212 Click to see CC(=CCOC1=C2C(=CC3=C1OC=C3)C=CC(=O)O2)C 270.28 unknown https://doi.org/10.3987/R-1986-02-0437
https://doi.org/10.1016/S0021-9673(01)84214-X
https://doi.org/10.1002/PCA.2800030108
https://doi.org/10.1016/S0021-9673(00)00321-6
https://doi.org/10.1002/JHRC.1240181213
https://doi.org/10.1007/BF02977004
Psoralen 6199 Click to see C1=CC(=O)OC2=CC3=C(C=CO3)C=C21 186.16 unknown https://doi.org/10.1002/PCA.2800030108
https://doi.org/10.1016/0098-8472(91)90043-N
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/10.1016/0031-9422(83)83044-1
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 5-hydroxypsoralens
Bergaptol 5280371 Click to see C1=CC(=O)OC2=CC3=C(C=CO3)C(=C21)O 202.16 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 5-methoxypsoralens
(R)-Byakangelicin 2'-glucoside 131752535 Click to see CC(C)(C(COC1=C2C(=C(C3=C1OC(=O)C=C3)OC)C=CO2)OC4C(C(C(C(O4)CO)O)O)O)O 496.50 unknown https://doi.org/10.1016/0031-9422(83)80039-9
(R)-Byakangelicin 3'-glucoside 131752534 Click to see CC(C)(C(COC1=C2C(=C(C3=C1OC(=O)C=C3)OC)C=CO2)O)OC4C(C(C(C(O4)CO)O)O)O 496.50 unknown https://doi.org/10.1016/0031-9422(83)80039-9
9-[(2R)-2-hydroxy-3-methyl-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutoxy]-4-methoxyfuro[3,2-g]chromen-7-one 101629717 Click to see CC(C)(C(COC1=C2C(=C(C3=C1OC(=O)C=C3)OC)C=CO2)O)OC4C(C(C(C(O4)CO)O)O)O 496.50 unknown https://doi.org/10.1016/0031-9422(83)80039-9
9-[(2R)-3-hydroxy-3-methyl-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutoxy]-4-methoxyfuro[3,2-g]chromen-7-one 101629718 Click to see CC(C)(C(COC1=C2C(=C(C3=C1OC(=O)C=C3)OC)C=CO2)OC4C(C(C(C(O4)CO)O)O)O)O 496.50 unknown https://doi.org/10.1016/0031-9422(83)80039-9
Bergapten 2355 Click to see COC1=C2C=CC(=O)OC2=CC3=C1C=CO3 216.19 unknown https://doi.org/10.1016/S0021-9673(01)84214-X
https://doi.org/10.1080/10412905.1993.9698257
https://doi.org/10.1002/PCA.2800030108
https://doi.org/10.1016/S0021-9673(00)00321-6
https://doi.org/10.1002/JHRC.1240181213
https://doi.org/10.1016/0098-8472(91)90043-N
Phellopterin 98608 Click to see CC(=CCOC1=C2C(=C(C3=C1OC(=O)C=C3)OC)C=CO2)C 300.30 unknown https://doi.org/10.1016/S0021-9673(00)00321-6
https://doi.org/10.1002/PCA.2800030108
> 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/S0021-9673(00)00321-6
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 8-methoxypsoralens
(R)-Isobyakangelicin 3'-glucoside 131752521 Click to see CC(C)(C(COC1=C2C=COC2=C(C3=C1C=CC(=O)O3)OC)O)OC4C(C(C(C(O4)CO)O)O)O 496.50 unknown https://doi.org/10.1016/0031-9422(83)80039-9
4-[(2R)-2-hydroxy-3-methyl-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutoxy]-9-methoxyfuro[3,2-g]chromen-7-one 163011361 Click to see CC(C)(C(COC1=C2C=COC2=C(C3=C1C=CC(=O)O3)OC)O)OC4C(C(C(C(O4)CO)O)O)O 496.50 unknown https://doi.org/10.1016/0031-9422(83)80039-9
Isopimpinellin 68079 Click to see COC1=C2C=COC2=C(C3=C1C=CC(=O)O3)OC 246.21 unknown https://doi.org/10.1016/S0021-9673(01)84214-X
https://doi.org/10.1080/10412905.1993.9698257
https://doi.org/10.1002/PCA.2800030108
https://doi.org/10.1016/S0021-9673(00)00321-6
https://doi.org/10.1016/S0031-9422(00)81503-4
Methoxsalen 4114 Click to see COC1=C2C(=CC3=C1OC=C3)C=CC(=O)O2 216.19 unknown https://doi.org/10.1016/S0021-9673(01)84214-X
https://doi.org/10.1002/PCA.2800030108
https://doi.org/10.1016/S0021-9673(00)00321-6
https://doi.org/10.1002/JHRC.1240181213
https://doi.org/10.1016/0098-8472(91)90043-N
https://doi.org/10.1016/S0031-9422(00)81503-4
> 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/S0021-9673(01)84214-X
Umbelliferone 5281426 Click to see C1=CC(=CC2=C1C=CC(=O)O2)O 162.14 unknown https://doi.org/10.1016/S0021-9673(01)84214-X
https://doi.org/10.1016/S0021-9673(00)00321-6
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Linear pyranocoumarins
Xanthoxyletin 66548 Click to see CC1(C=CC2=C(O1)C=C3C(=C2OC)C=CC(=O)O3)C 258.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Anthocyanins / Anthocyanidin-3-O-glycosides
Pelargonidin 3-O-sophoroside 23724704 Click to see C1=CC(=CC=C1C2=[O+]C3=CC(=CC(=C3C=C2OC4C(C(C(C(O4)CO)O)O)OC5C(C(C(C(O5)CO)O)O)O)O)O)O 595.50 unknown https://doi.org/10.1016/0031-9422(83)80039-9
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 3-prenylated chalcones
4-Hydroxyderricin 6438503 Click to see CC(=CCC1=C(C=CC(=C1O)C(=O)C=CC2=CC=C(C=C2)O)OC)C 338.40 unknown via CMAUP database
Xanthoangelol 643007 Click to see CC(=CCCC(=CCC1=C(C=CC(=C1O)C(=O)C=CC2=CC=C(C=C2)O)O)C)C 392.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Macrolides and analogues
1-Oxacyclononadec-10-en-2-one 78409344 Click to see C1CCCCOC(=O)CCCCCCCC=CCCC1 280.40 unknown https://doi.org/10.1080/10412905.1993.9698257
1-Oxacyclooctadeca-3,5-dien-2-one 163192801 Click to see C1CCCCCCOC(=O)C=CC=CCCCCC1 264.40 unknown https://doi.org/10.1080/10412905.1993.9698257
13-Methyloxacyclotetradecan-2-one 534607 Click to see CC1CCCCCCCCCCC(=O)OC1 226.35 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.29B-0637
https://doi.org/10.1021/JF00046A030
Oxacyclohexadecan-2-one 235414 Click to see C1CCCCCCCOC(=O)CCCCCC1 240.38 unknown https://doi.org/10.1021/JF00046A030
https://doi.org/10.1080/10412905.1993.9698257
Oxacyclotetradecan-2-one 15596 Click to see C1CCCCCCOC(=O)CCCCC1 212.33 unknown https://doi.org/10.1021/JF00046A030
Oxacyclotetradecan-2-one, 13-methyl-, (13R)- 10376424 Click to see CC1CCCCCCCCCCC(=O)OC1 226.35 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.29B-0637

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