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Artemisia vulgaris

Artemisia vulgaris - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
Artemisia vulgaris - 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 UUID643fd1771e5fa967170973
Scientific name Artemisia vulgaris
Authority L.
First published in Sp. Pl. : 848 (1753)

Description Top

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No description added yet. Help us by writing one.

Synonyms Top

Scientific name Authority First published in
Artemisia vulgaris Burm.f. Fl. Ind. (N. L. Burman) 177. 1768 [1 Mar-6 Apr 1768]
Artemisia michauxii Besser Fl. Bor.-Amer. 1: 324 (1833)
Artemisia vulgaris var. latiloba Ledeb. Flora Altaica 4: 83 1833
Artemisia dubia var. septentrionalis Pamp. Nuovo Giorn. Bot. Ital., n.s., 36: 439 (1930)
Artemisia vulgaris var. selengensis (Turcz. ex Besser) Maxim. Bulletin de l'Academie Imperiale des Sciences de St-Petersbourg 8: 536 1872
Artemisia vulgaris var. vulgaris L.
Artemisia ludoviciana Besser Nouv. Mém. Soc. Imp. Naturalistes Moscou 3: 38. 1834
Absinthium vulgare (L.) Dulac Fl. Hautes-Pyrénées : 502 (1867)

Common names Top

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Language Common/alternative name
English mugwort
English common wormwood
Spanish madra
Spanish artamisa
Spanish artamisia
Spanish artemega
Spanish artemisa comun
Spanish artemisa común
Spanish artemisa vulgar
Spanish hierba del caminante
Spanish madre yerba
Spanish tomaraja
Spanish tomarajas
Arabic نبات الشيح الدارج
Arabic برنجاسف
Arabic حبق الراعي
Arabic شوبلاء
Arabic شيح الدارج
Azerbaijani adi yovşan
azb عادی یووشان
bcl artamisa
Belarusian быліца
Belarusian бульняк
Belarusian быльнік
Belarusian быльняк
Belarusian забудкі
Belarusian чарнабыль
Belarusian чарнабыльнік
Belarusian чарнобыль
Belarusian чорнабыль
Belarusian палын звычайны
Bulgarian див пелин
Catalan artemisa vulgar
Catalan altimira
Czech pelyněk černobýl
Czech Černobýl
cv Хура эрĕм
Welsh y feidiog lwyd
Welsh gwrysgen lwyd
Welsh llysiau llywyd
Danish grå bynke
Danish grå-bynke
German gemeiner beifuss
German beifuss
German fliegenkraut
German gänsekraut
German gemeiner beifuß
German gewöhnlicher beifuss
German gewöhnlicher beifuß
German gewürzbeifuß
German johannesgürtelkraut
German jungfernkraut
German sonnenwendkraut
German weiberkraut
German werzwisch
German wilder wermut
German beifuß
Estonian harilik puju
Basque artemisia min
Persian برنجاسف
Finnish pujo
French armoise commune
French armoise vulgaire
frr grä jüden
frr bifut
Irish mongach meisce
Galician herba de nosa señora
Manx bollan bane
Croatian divlji pelin
ht amwaz
Hungarian feketeürömfű
Hungarian közönséges üröm
Hungarian fekete üröm
Japanese オウシュウヨモギ
Georgian მამულა
Kabyle alala
Kazakh Қараермен
Kannada ಮಾಚಿಪತ್ರೆ
Korean 불가리스쑥
Cornish les loos
lb bäifouss
lb wëlle batteralzem
lb bäibes
li bijvoet
li aels
lmo Èrba lègn
Lithuanian paprastasis kietis
Latvian parastā vībotne
Latvian vībotne
Macedonian Див пелин
Malay baru cina
Malay daun hian
Malay daun manis
Malay daun sundamala
Malay hia
myv Чульматикше
nap matrëcana
Norwegian Bokmål burot
Nepali तितेपाती
Dutch bijvoet
Dutch moxa
Norwegian Nynorsk burot
pam dikut-maria
pcd Àrmòze
pcd béldanme
pcd bon·nës-danmes
pcd crizintinme soevåjhe
pcd iérpe-às-chin·nes
pcd iérpe-éd-fabrique
pcd toubacq éd bòn·nës-finmes
pcd toubacq-sint-piére
pcd iérpe-éd-sint-jin
pdc aldi fraa
Polish bylica pospolita
Portuguese amunimuyê
Portuguese balainho de velho
Portuguese balainho-de-velho
Portuguese centhratherum punctatum
Romanian pelin
Russian чернобыльник
Russian полынь обыкновенная
Samogitian kėitis
Slovak palina obyčajná
Slovenian navadni pelin
Serbian Дивљи пелин
stq muugerk
su lokatmala
Swedish gråbo
Swedish bönrot
Swedish gråböna
Swedish gråbynke
Tamil மாசிபத்திரி
Telugu మాచీపత్రం
Telugu మాచిపత్రి
tg Биринҷосан
Thai โกฐจุฬาลัมพาไทย
Turkish bayağı yavşan
Ukrainian чорнобиль
Ukrainian полин звичайний
vec sinsioło
Vietnamese co linh li
Vietnamese ngải diệp
Vietnamese nhả ngải
Vietnamese quá sú
Vietnamese thuốc cứu
Vietnamese ngải cứu
Chinese 白蒿
Chinese 野艾
Chinese 毛莲蒿
Chinese 北艾
Chinese 细叶艾
Chinese 艾叶
Chinese 艾

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Artemisia vulgaris subsp. inundata Darijma Byull. Moskovsk. Obshch. Isp. Prir., Otd. Biol. 97(5): 68 (1992) (1992)
Artemisia vulgaris subsp. vulgaris Unknown

Varieties (abbr. var.) Top

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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-0000115588
UNII JDR81QW9ZQ
Florida Plant Atlas 1805
Flora of Alabama 526
Canadensys 2918
USDA Plants ARVU
Tropicos 2700154
INPN 84061
Flora of Italy 5704
KEW urn:lsid:ipni.org:names:20812-2
The Plant List gcc-77033
Missouri Botanical Garden 256948
PFAF Artemisia vulgaris
PaleoBotany 10301
Open Tree Of Life 1092844
Observations.org 6376
NCBI Taxonomy 4220
NBN Atlas NBNSYS0000004469
Nature Serve 2.137181
IPNI 180284-1
iNaturalist 52856
GBIF 3120946
Freebase /m/02j28w
WisFlora 2633
EPPO ARTVU
EOL 850415
Elurikkus 2912
Calflora (Californian flora) 8472
USDA GRIN 4190
Wikipedia Artemisia_vulgaris

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
Therapeutic efficacy of acupuncture point stimulation for stomach cancer pain: a systematic review and meta-analysis Zhou X, Zhang J, Jiang L, Zhang S, Gu Y, Tang J, Pu T, Quan X, Chi H, Huang S Front Neurol 04-Apr-2024
PMCID:PMC11024429
doi:10.3389/fneur.2024.1334657
PMID:38638316
Incidence of grass and weed sensitization in Bangkok, Thailand: a clinical study Aud-in S, Juprasong Y, Pinkaew B, Talek K, Tantilipikorn P, Songnuan W Front Public Health 28-Mar-2024
PMCID:PMC11007029
doi:10.3389/fpubh.2024.1301095
PMID:38605873
Bois noir management in vineyard: a review on effective and promising control strategies Pierro R, Moussa A, Mori N, Marcone C, Quaglino F, Romanazzi G Front Plant Sci 27-Mar-2024
PMCID:PMC11004249
doi:10.3389/fpls.2024.1364241
PMID:38601314
Synthesis of eco-friendly layered double hydroxide and nanoemulsion for jasmine and peppermint oils and their larvicidal activities against Culex pipiens Linnaeus Radwan IT, Khater HF, Mohammed SH, Khalil A, Farghali MA, Mahmoud MG, Selim A, Manaa EA, Bagato N, Baz MM Sci Rep 22-Mar-2024
PMCID:PMC10959945
doi:10.1038/s41598-024-56802-y
PMID:38519561
Higher Plant-Derived Biostimulants: Mechanisms of Action and Their Role in Mitigating Plant Abiotic Stress Martínez-Lorente SE, Martí-Guillén JM, Pedreño MÁ, Almagro L, Sabater-Jara AB Antioxidants (Basel) 06-Mar-2024
PMCID:PMC10967762
doi:10.3390/antiox13030318
PMID:38539851
Novel adjuvants in allergen-specific immunotherapy: where do we stand? Lin YJ, Zimmermann J, Schülke S Front Immunol 23-Feb-2024
PMCID:PMC10920236
doi:10.3389/fimmu.2024.1348305
PMID:38464539
Use of Essential Oils to Counteract the Phenomena of Antimicrobial Resistance in Livestock Species Lupia C, Castagna F, Bava R, Naturale MD, Zicarelli L, Marrelli M, Statti G, Tilocca B, Roncada P, Britti D, Palma E Antibiotics (Basel) 07-Feb-2024
PMCID:PMC10885947
doi:10.3390/antibiotics13020163
PMID:38391549
Rumen fermentation and microbiota in Shami goats fed on condensed tannins or herbal mixture Rabee AE, Mohamed M. Ghandour M, Sallam A, Elwakeel EA, Mohammed RS, Sabra EA, Abdel-Wahed AM, Mourad DM, Hamed AA, Hafez OR BMC Vet Res 31-Jan-2024
PMCID:PMC10829277
doi:10.1186/s12917-024-03887-2
PMID:38297287
Influence of meteorological and ambient air quality factors on Artemisia pollen counts in Urumqi, Northwest China Jiapaer K, Halik Ü, Keyimu M, Bilal I, Shi L, Mumin R Heliyon 26-Jan-2024
PMCID:PMC10847607
doi:10.1016/j.heliyon.2024.e25124
PMID:38327407
In vitro inhibition of biofilm and virulence factor production in azole-resistant strains of Candida albicans isolated from diabetic foot by Artemisia vulgaris stabilized tin (IV) oxide nanoparticles Zubair M, Husain FM, Al-Amri M, Hasan I, Hassan I, Albalawi T, Fatima F, Khan A, Arshad M, Alam P, Ahmad N, Alatawy R, Begum S, Mir R, Alshadfan H, Ansari AA, Al-Anazi AB Front Cell Infect Microbiol 25-Jan-2024
PMCID:PMC10850385
doi:10.3389/fcimb.2023.1322778
PMID:38332949
Pest categorisation of Pratylenchus loosi Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Migheli Q, Vloutoglou I, Gobbi A, Maiorano A, Pautasso M, Reignault PL EFSA J 16-Jan-2024
PMCID:PMC10790189
doi:10.2903/j.efsa.2024.8548
PMID:38229874
The use of inhibition assay in Api g 7 suspected allergy in a female patient with anaphylaxis: A case report Ukleja-Sokołowska N, Lis K, Graczyk M, Bartuzi M, Bartuzi Z Int J Immunopathol Pharmacol 13-Jan-2024
PMCID:PMC10788074
doi:10.1177/03946320231223004
PMID:38217433
Commodity risk assessment of Corylus avellana plants from the UK Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Civera AV, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Faccoli M, Mikulová A, Mosbach‐Schulz O, Stergulc F, Streissl F, Gonthier P EFSA J 12-Jan-2024
PMCID:PMC10784871
doi:10.2903/j.efsa.2024.8495
PMID:38222930
Assessment of antimalarial activity of crude extract of Chan-Ta-Lee-La and Pra-Sa-Chan-Dang formulations and their plant ingredients for new drug candidates of malaria treatment: In vitro and in vivo experiments Chaniad P, Phuwajaroanpong A, Plirat W, Konyanee A, Septama AW, Punsawad C PLoS One 11-Jan-2024
PMCID:PMC10783769
doi:10.1371/journal.pone.0296756
PMID:38206944
Boesenbergia rotunda and Its Pinostrobin for Atopic Dermatitis: Dual 5-Lipoxygenase and Cyclooxygenase-2 Inhibitor and Its Mechanistic Study through Steady-State Kinetics and Molecular Modeling Liana D, Eurtivong C, Phanumartwiwath A Antioxidants (Basel) 05-Jan-2024
PMCID:PMC10812521
doi:10.3390/antiox13010074
PMID:38247498

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 / Methoxyphenols
Eugenol 3314 Click to see COC1=C(C=CC(=C1)CC=C)O 164.20 unknown https://doi.org/10.1021/NP50047A038
> Hydrocarbons / Unsaturated hydrocarbons / Enynes
(3E,5Z)-1,3,5-Tridecatriene-7,9,11-triyne 5322029 Click to see CC#CC#CC#CC=CC=CC=C 166.22 unknown https://doi.org/10.1016/S0031-9422(00)91232-9
(all-E)-1,7,9-Heptadecatriene-11,13,15-triyne 14409592 Click to see CC#CC#CC#CC=CC=CCCCCC=C 222.32 unknown https://doi.org/10.1016/S0031-9422(00)91232-9
https://doi.org/10.1016/S0031-9422(00)98068-3
Heptadeca-1,7,9-trien-11,13,15-triyne 72731071 Click to see CC#CC#CC#CC=CC=CCCCCC=C 222.32 unknown https://doi.org/10.1016/S0031-9422(00)91232-9
https://doi.org/10.1016/S0031-9422(00)98068-3
Trideca-1,3,5-trien-7,9,11-triyne 528756 Click to see CC#CC#CC#CC=CC=CC=C 166.22 unknown https://doi.org/10.1016/S0031-9422(00)91232-9
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters
2-Decene-4,6,8-triynoic acid, methyl ester, (Z)- 5281309 Click to see CC#CC#CC#CC=CC(=O)OC 172.18 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.04-1567
https://doi.org/10.1002/CBER.19550880320
https://doi.org/10.1016/S0031-9422(00)91232-9
Dehydromatricaria ester 5281146 Click to see CC#CC#CC#CC=CC(=O)OC 172.18 unknown https://doi.org/10.1016/S0031-9422(00)91232-9
Methyl 2-decene-4,6,8-triynoate 75958 Click to see CC#CC#CC#CC=CC(=O)OC 172.18 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.04-1567
https://doi.org/10.1002/CBER.19550880320
https://doi.org/10.1016/S0031-9422(00)91232-9
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Palmitic Acid 985 Click to see CCCCCCCCCCCCCCCC(=O)O 256.42 unknown https://doi.org/10.1080/10412905.1999.9701189
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohol esters
[(E)-3-oxotetradec-6-en-8,10,12-triynyl] 3-methylbutanoate 14409595 Click to see CC#CC#CC#CC=CCCC(=O)CCOC(=O)CC(C)C 298.40 unknown https://doi.org/10.1016/S0031-9422(00)98068-3
3-Oxotetradec-6-en-8,10,12-triynyl 3-methylbutanoate 162985929 Click to see CC#CC#CC#CC=CCCC(=O)CCOC(=O)CC(C)C 298.40 unknown https://doi.org/10.1016/S0031-9422(00)98068-3
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols / Long-chain fatty alcohols
(4E,6E)-tetradeca-4,6-dien-8,10,12-triyn-1-ol 14194106 Click to see CC#CC#CC#CC=CC=CCCCO 198.26 unknown https://doi.org/10.1016/S0031-9422(00)91232-9
Stearyl Alcohol 8221 Click to see CCCCCCCCCCCCCCCCCCO 270.50 unknown https://doi.org/10.1080/10412905.1999.9701189
Tetradeca-4,6-dien-8,10,12-triyn-1-ol 71353587 Click to see CC#CC#CC#CC=CC=CCCCO 198.26 unknown https://doi.org/10.1016/S0031-9422(00)91232-9
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Acyclic diterpenoids
3,7,11,15-Tetramethyl-2-hexadecen-1-OL 5366244 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C 296.50 unknown https://doi.org/10.1080/10412905.1999.9701189
Phytol 5280435 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C 296.50 unknown https://doi.org/10.1080/10412905.1999.9701189
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Geraniol 637566 Click to see CC(=CCCC(=CCO)C)C 154.25 unknown https://doi.org/10.1021/NP50047A038
Linalool, (+/-)- 6549 Click to see CC(=CCCC(C)(C=C)O)C 154.25 unknown https://doi.org/10.1080/10412905.1992.9698101
https://doi.org/10.1021/NP50047A038
Myrcene 31253 Click to see CC(=CCCC(=C)C=C)C 136.23 unknown https://doi.org/10.1007/BF01024117
https://doi.org/10.1055/S-0028-1097719
https://doi.org/10.1021/NP50047A038
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
p-CYMENE 7463 Click to see CC1=CC=C(C=C1)C(C)C 134.22 unknown https://doi.org/10.1055/S-0028-1097719
https://doi.org/10.1021/NP50047A038
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-beta-Pinene 440967 Click to see CC1(C2CCC(=C)C1C2)C 136.23 unknown https://doi.org/10.1055/S-0028-1097719
(-)-Camphene 440966 Click to see CC1(C2CCC(C2)C1=C)C 136.23 unknown https://doi.org/10.1055/S-0028-1097719
(-)-Camphor 444294 Click to see CC1(C2CCC1(C(=O)C2)C)C 152.23 unknown https://doi.org/10.1007/BF01024117
(+)-3-Carene 443156 Click to see CC1=CCC2C(C1)C2(C)C 136.23 unknown https://doi.org/10.1007/BF00600857
(+)-alpha-Pinene 82227 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown https://doi.org/10.1055/S-0028-1097719
(+)-alpha-Thujone 12304612 Click to see CC1C2CC2(CC1=O)C(C)C 152.23 unknown https://doi.org/10.1055/S-0028-1097719
(+)-Camphene 92221 Click to see CC1(C2CCC(C2)C1=C)C 136.23 unknown https://doi.org/10.1007/BF00600857
(+)-Isoborneol 6973640 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown https://doi.org/10.1007/BF01024117
(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/NP50047A038
(1S,3S,4R)-2,2,3-Trimethylbicyclo[2.2.1]heptane 71418467 Click to see CC1C2CCC(C2)C1(C)C 138.25 unknown https://doi.org/10.1007/BF00600857
(5S)-4-methylidene-1-propan-2-ylbicyclo[3.1.0]hexane 6429260 Click to see CC(C)C12CCC(=C)C1C2 136.23 unknown https://doi.org/10.1080/10412905.1999.9701189
[(1S,2R,3S,4R)-3-hydroxy-1,7,7-trimethyl-2-bicyclo[2.2.1]heptanyl] acetate 162914132 Click to see CC(=O)OC1C(C2CCC1(C2(C)C)C)O 212.28 unknown https://doi.org/10.1055/S-0028-1097719
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/10.1055/S-0028-1097719
https://doi.org/10.1007/BF01024117
https://doi.org/10.1021/NP50047A038
https://doi.org/10.1080/10412905.1992.9698101
3-Carene 26049 Click to see CC1=CCC2C(C1)C2(C)C 136.23 unknown https://doi.org/10.1007/BF00600857
3-Thujanone 11027 Click to see CC1C2CC2(CC1=O)C(C)C 152.23 unknown https://doi.org/10.1055/S-0028-1097719
https://doi.org/10.1021/NP50047A038
https://doi.org/10.1007/BF01024117
alpha-PINENE 6654 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown https://doi.org/10.1080/10412905.1992.9698101
https://doi.org/10.1055/S-0028-1097719
https://doi.org/10.1021/NP50047A038
beta-Pinene 14896 Click to see CC1(C2CCC(=C)C1C2)C 136.23 unknown https://doi.org/10.1007/BF01024117
https://doi.org/10.1080/10412905.1992.9698101
https://doi.org/10.1055/S-0028-1097719
https://doi.org/10.1021/NP50047A038
beta-Thujone 91456 Click to see CC1C2CC2(CC1=O)C(C)C 152.23 unknown https://doi.org/10.1021/NP50047A038
https://doi.org/10.1007/BF01024117
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/NP50047A038
Borneol 6552009 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown https://doi.org/10.1055/S-0028-1097719
https://doi.org/10.1007/BF01024117
Bornyl acetate 6448 Click to see CC(=O)OC1CC2CCC1(C2(C)C)C 196.29 unknown https://doi.org/10.1055/S-0028-1097719
https://doi.org/10.1021/NP50047A038
https://doi.org/10.1007/BF01024117
Bornyl acetate, (-)- 93009 Click to see CC(=O)OC1CC2CCC1(C2(C)C)C 196.29 unknown https://doi.org/10.1055/S-0028-1097719
Camphene 6616 Click to see CC1(C2CCC(C2)C1=C)C 136.23 unknown https://doi.org/10.1007/BF00600857
https://doi.org/10.1055/S-0028-1097719
https://doi.org/10.1021/NP50047A038
Camphor 2537 Click to see CC1(C2CCC1(C(=O)C2)C)C 152.23 unknown https://doi.org/10.1055/S-0028-1097719
https://doi.org/10.1007/BF01024117
https://doi.org/10.1021/NP50047A038
https://doi.org/10.1080/10412905.1992.9698101
Camphor (synthetic) 159055 Click to see CC1(C2CCC1(C(=O)C2)C)C 152.23 unknown https://doi.org/10.1007/BF01024117
https://doi.org/10.1055/S-0028-1097719
cis-Sabinene hydrate 11744854 Click to see CC(C)C12CCC(C1C2)(C)O 154.25 unknown https://doi.org/10.1007/BF00600857
Isocamphane 296894 Click to see CC1C2CCC(C2)C1(C)C 138.25 unknown https://doi.org/10.1007/BF00600857
Sabinen 18818 Click to see CC(C)C12CCC(=C)C1C2 136.23 unknown https://doi.org/10.1055/S-0028-1097719
https://doi.org/10.1021/NP50047A038
Sabinene 10887971 Click to see CC(C)C12CCC(=C)C1C2 136.23 unknown https://doi.org/10.1055/S-0028-1097719
Sabinene hydrate 62367 Click to see CC(C)C12CCC(C1C2)(C)O 154.25 unknown https://doi.org/10.1007/BF00600857
Thujone 261491 Click to see CC1C2CC2(CC1=O)C(C)C 152.23 unknown https://doi.org/10.1021/NP50047A038
https://doi.org/10.1007/BF01024117
trans-Borneol 44630107 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown https://doi.org/10.1021/NP50047A038
https://doi.org/10.1080/10412905.1992.9698101
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(-)-trans-Carveol 94221 Click to see CC1=CCC(CC1O)C(=C)C 152.23 unknown https://doi.org/10.1080/10412905.1992.9698101
(+)-alpha-Terpineol 442501 Click to see CC1=CCC(CC1)C(C)(C)O 154.25 unknown https://doi.org/10.1055/S-0028-1097719
(+)-Terpinen-4-ol 2724161 Click to see CC1=CCC(CC1)(C(C)C)O 154.25 unknown https://doi.org/10.1055/S-0028-1097719
4-Terpineol, (+/-)- 11230 Click to see CC1=CCC(CC1)(C(C)C)O 154.25 unknown https://doi.org/10.1055/S-0028-1097719
https://doi.org/10.1007/BF01024117
https://doi.org/10.1080/10412905.1999.9701189
https://doi.org/10.1021/NP50047A038
https://doi.org/10.1080/10412905.1992.9698101
alpha-PHELLANDRENE 7460 Click to see CC1=CCC(C=C1)C(C)C 136.23 unknown https://doi.org/10.1080/10412905.1992.9698101
alpha-Terpinene 7462 Click to see CC1=CC=C(CC1)C(C)C 136.23 unknown https://doi.org/10.1007/BF01024117
Alpha-Terpineol 17100 Click to see CC1=CCC(CC1)C(C)(C)O 154.25 unknown https://doi.org/10.1080/10412905.1992.9698101
https://doi.org/10.1055/S-0028-1097719
https://doi.org/10.1021/NP50047A038
Limonene, (+)- 440917 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1007/BF01024117
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1021/NP50047A038
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(+)-beta-Caryophyllene 20831623 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1055/S-0028-1097719
(+)-gamma-Cadinene 6432404 Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C 204.35 unknown https://doi.org/10.1021/NP50047A038
(1R,2S,6S,7S,8R)-1,3-dimethyl-8-propan-2-yltricyclo[4.4.0.02,7]dec-3-ene 50919054 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown https://doi.org/10.1055/S-0028-1097719
(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/10.1080/10412905.1992.9698101
(1R,4aS,8aS)-1,6-dimethyl-4-propan-2-yl-1,2,4a,5,8,8a-hexahydronaphthalene 10375656 Click to see CC1CC=C(C2C1CC=C(C2)C)C(C)C 204.35 unknown https://doi.org/10.1055/S-0028-1097719
(2R,4aR,5S,8aS)-1,2,3,4,4a,5,8,8a-Octahydro-5-hydroxy-4a-methyl-alpha,8-bis(methylene)-2-naphthaleneacetic acid 163041330 Click to see CC12CCC(CC1C(=C)C=CC2O)C(=C)C(=O)O 248.32 unknown https://doi.org/10.1016/0031-9422(91)83661-4
(E)-beta-farnesene 10407 Click to see CC(=CCCC(=CCCC(=C)C=C)C)C 204.35 unknown https://doi.org/10.1007/BF00600857
1,4,8-Cycloundecatriene, 2,6,6,9-tetramethyl-, (1E,4E,8E)- 23204 Click to see CC1=CCC(C=CCC(=CCC1)C)(C)C 204.35 unknown https://doi.org/10.1007/BF00600857
1alpha-1-Hydroxy-2,4(18),11(13)-eudesmatrien-12-oic acid 14864221 Click to see CC12CCC(CC1C(=C)C=CC2O)C(=C)C(=O)O 248.32 unknown https://doi.org/10.1016/0031-9422(91)83661-4
2-Isopropenyl-1-methyl-4-(1-methylethylidene)-1-vinylcyclohexane 6432312 Click to see CC(=C1CCC(C(C1)C(=C)C)(C)C=C)C 204.35 unknown https://doi.org/10.1080/10412905.1992.9698101
4-Isopropyl-1,6-dimethyl-1,2,4a,5,8,8a-hexahydronaphthalene 85125935 Click to see CC1CC=C(C2C1CC=C(C2)C)C(C)C 204.35 unknown https://doi.org/10.1055/S-0028-1097719
alpha-Cadinol 10398656 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown https://doi.org/10.1080/10412905.1992.9698101
beta-CARYOPHYLLENE OXIDE 1742210 Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C 220.35 unknown https://doi.org/10.1080/10412905.1999.9701189
https://doi.org/10.1007/S11418-008-0253-0
https://doi.org/10.1080/10412905.1992.9698101
beta-Cubebene 93081 Click to see CC1CCC(C2C13C2C(=C)CC3)C(C)C 204.35 unknown https://doi.org/10.1080/10412905.1992.9698101
beta-Farnesene 5281517 Click to see CC(=CCCC(=CCCC(=C)C=C)C)C 204.35 unknown https://doi.org/10.1007/BF00600857
Bicyclo[7.2.0]undec-4-ene, 4,11,11-trimethyl-8-methylene-, (1S,4E,9R)- 26318 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1055/S-0028-1097719
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1080/10412905.1992.9698101
https://doi.org/10.1021/NP50047A038
Caryophyllene epoxide 14350 Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C 220.35 unknown https://doi.org/10.1080/10412905.1999.9701189
Caryophyllene,alpha + beta mixt. 5354499 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1021/NP50047A038
Copaene 19725 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown https://doi.org/10.1055/S-0028-1097719
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/10.1080/10412905.1999.9701189
delta-Cadinol 3084311 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown https://doi.org/10.1080/10412905.1992.9698101
delta-Elemene 12309449 Click to see CC(C)C1=CC(C(CC1)(C)C=C)C(=C)C 204.35 unknown https://doi.org/10.1080/10412905.1999.9701189
gamma-Cadinene 15094 Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C 204.35 unknown https://doi.org/10.1021/NP50047A038
gamma-Muurolene 12313020 Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C 204.35 unknown https://doi.org/10.1080/10412905.1992.9698101
Humulene 5281520 Click to see CC1=CCC(C=CCC(=CCC1)C)(C)C 204.35 unknown https://doi.org/10.1007/BF00600857
https://doi.org/10.1080/10412905.1992.9698101
T-Muurolol 3084331 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown https://doi.org/10.1080/10412905.1999.9701189
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(1aR,4aR,7S,7aS,7bR)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol 13854258 Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C 220.35 unknown https://doi.org/10.1055/S-0028-1097719
(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/10.1055/S-0028-1097719
alpha-Gurjunene 15560276 Click to see CC1CCC2C(C2(C)C)C3=C(CCC13)C 204.35 unknown https://doi.org/10.1080/10412905.1992.9698101
> 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/10.1080/10412905.1999.9701189
Bicyclogermacrene 5315347 Click to see CC1=CCCC(=CC2C(C2(C)C)CC1)C 204.35 unknown https://doi.org/10.1080/10412905.1999.9701189
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Elemane sesquiterpenoids
Beta-Elemene 6918391 Click to see CC(=C)C1CCC(C(C1)C(=C)C)(C)C=C 204.35 unknown https://doi.org/10.1080/10412905.1999.9701189
https://doi.org/10.1080/10412905.1992.9698101
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
2-[(2R,4aS)-4a,8-dimethyl-7-oxo-1,2,3,4-tetrahydronaphthalen-2-yl]prop-2-enoic acid 10900924 Click to see CC1=C2CC(CCC2(C=CC1=O)C)C(=C)C(=O)O 246.30 unknown https://doi.org/10.1016/0031-9422(91)83661-4
3-Oxo-1,4,11(13)-eudesmatrien-12-oic acid 14864220 Click to see CC1=C2CC(CCC2(C=CC1=O)C)C(=C)C(=O)O 246.30 unknown https://doi.org/10.1016/0031-9422(91)83661-4
Platambin 613194 Click to see CC(C)C1CCC2(C(CCC(=C)C2C1O)O)C 238.37 unknown https://doi.org/10.1016/0031-9422(91)83661-4
Voleneol 14137570 Click to see CC(C)C1CCC2(C(CCC(=C)C2C1O)O)C 238.37 unknown https://doi.org/10.1016/0031-9422(91)83661-4
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids
(1S,2R,5S,8S,9S,12S,13R,14R,15R,16R,17S,19S,22S,23S,26S,27R)-12,16-dihydroxy-3,8,12,17,19,23-hexamethyl-6,18,25-trioxaoctacyclo[13.11.1.01,17.02,14.04,13.05,9.019,27.022,26]heptacos-3-ene-7,24-dione 102054563 Click to see CC1C2CCC(C3C4C5C6C7(CCC8C(C(=O)OC8C6(C4C(=C3C2OC1=O)C)C(C5O)(O7)C)C)C)(C)O 512.60 unknown https://doi.org/10.1016/0031-9422(79)80167-3
> Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids / Carotenoids / Carotenes
(6Z,8E,10Z,12E,14E,16E,18E,20E,22E,24E,26E)-2,6,10,14,19,23,27,31-octamethyldotriaconta-2,6,8,10,12,14,16,18,20,22,24,26,30-tridecaene 101764622 Click to see CC(=CCCC(=CC=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC=C(C)CCC=C(C)C)C)C)C)C 536.90 unknown https://doi.org/10.1016/S0031-9422(00)98068-3
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(3S,4aS,6aR,6aR,6bR,8aR,11R,12S,12aR,14aR,14bS)-4,4,6a,6b,8a,11,12,14b-octamethyl-2,3,4a,5,6,6a,7,8,9,10,11,12,12a,14a-tetradecahydro-1H-picen-3-ol 163023159 Click to see CC1CCC2(CCC3(C(C2C1C)C=CC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C)C 426.70 unknown https://doi.org/10.1055/S-0028-1097719
[(3S,6aR,8aR,12S,14bR)-4,4,6a,6b,8a,11,12,14b-octamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picen-3-yl] acetate 5318295 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC(=O)C)C)C)C2C1C)C)C 468.80 unknown https://doi.org/10.1055/S-0028-1097719
alpha-Amyrenyl acetate 92842 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC(=O)C)C)C)C2C1C)C)C 468.80 unknown https://doi.org/10.1055/S-0028-1097719
Fernenol 12305178 Click to see CC(C)C1CCC2C1(CCC3(C2(CC=C4C3CCC5C4(CCC(C5(C)C)O)C)C)C)C 426.70 unknown https://doi.org/10.1016/S0040-4039(00)70236-X
Sorghumol 621134 Click to see CC(C)C1CCC2C1(CCC3(C2(CC=C4C3CCC5C4(CCC(C5(C)C)O)C)C)C)C 426.70 unknown https://doi.org/10.1016/S0040-4039(00)70236-X
Squalene 638072 Click to see CC(=CCCC(=CCCC(=CCCC=C(C)CCC=C(C)CCC=C(C)C)C)C)C 410.70 unknown https://doi.org/10.1007/S11418-008-0253-0
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3S,8S,9S,10R,13R,14S,17R)-17-[(E,2S,5S)-5-Ethyl-6-methylhept-3-en-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 12314479 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1007/S11418-008-0253-0
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/10.1007/S11418-008-0253-0
> Organic acids and derivatives / Carboxylic acids and derivatives / Carboxylic acid derivatives / Carboxylic acid esters
(4-Ethenyl-2,5-dimethylhexa-2,5-dienyl) acetate 78409237 Click to see CC(=C)C(C=C)C=C(C)COC(=O)C 194.27 unknown https://doi.org/10.1002/HLCA.19810640519
(4-Ethenyl-2,5-dimethylhexa-2,5-dienyl) propanoate 163023580 Click to see CCC(=O)OCC(=CC(C=C)C(=C)C)C 208.30 unknown https://doi.org/10.1002/HLCA.19810640519
(S)-Neolyratyl acetate 101413630 Click to see CC(=CC(C=C)C(=C)COC(=O)C)C 194.27 unknown https://doi.org/10.1002/HLCA.19810640519
(S)-Santolina acetate 21630872 Click to see CC(=CC(C=C)C(C)(C)OC(=O)C)C 196.29 unknown https://doi.org/10.1002/HLCA.19810640519
[(2E,4S)-4-ethenyl-2,5-dimethylhexa-2,5-dienyl] propanoate 101415510 Click to see CCC(=O)OCC(=CC(C=C)C(=C)C)C 208.30 unknown https://doi.org/10.1002/HLCA.19810640519
[(2Z,4R)-4-ethenyl-2,5-dimethylhexa-2,5-dienyl] acetate 162943768 Click to see CC(=C)C(C=C)C=C(C)COC(=O)C 194.27 unknown https://doi.org/10.1002/HLCA.19810640519
[(3S,4R)-3-ethenyl-4-hydroxy-2,5-dimethylhex-5-en-2-yl] acetate 163190325 Click to see CC(=C)C(C(C=C)C(C)(C)OC(=O)C)O 212.28 unknown https://doi.org/10.1002/HLCA.19810640519
[(3S)-3-ethenyl-2,5-dimethylhex-4-en-2-yl] acetate 101413931 Click to see CC(=CC(C=C)C(C)(C)OC(=O)C)C 196.29 unknown https://doi.org/10.1002/HLCA.19810640519
[(3S)-3-ethenyl-5-methyl-2-methylidenehex-4-enyl] acetate 163044311 Click to see CC(=CC(C=C)C(=C)COC(=O)C)C 194.27 unknown https://doi.org/10.1002/HLCA.19810640519
[(4S)-3,3,6-trimethylhepta-1,5-dien-4-yl] propanoate 163043628 Click to see CCC(=O)OC(C=C(C)C)C(C)(C)C=C 210.31 unknown https://doi.org/10.1002/HLCA.19810640519
3-Ethenyl-4-hydroxy-2,5-dimethylhex-5-en-2-yl acetate 121015983 Click to see CC(=C)C(C(C=C)C(C)(C)OC(=O)C)O 212.28 unknown https://doi.org/10.1002/HLCA.19810640519
Artemisyl propionate 101415797 Click to see CCC(=O)OC(C=C(C)C)C(C)(C)C=C 210.31 unknown https://doi.org/10.1002/HLCA.19810640519
> Organic acids and derivatives / Carboxylic acids and derivatives / Dicarboxylic acids and derivatives
CID 163049495 163049495 Click to see CC(=O)OC1C2C(CCC3(C(O3)CCC2=C)C)C(=CO1)C(CC=C=C)OC(=O)C 402.50 unknown https://doi.org/10.1016/S0031-9422(00)98068-3
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Cyanogenic glycosides
Prunasin 119033 Click to see C1=CC=C(C=C1)C(C#N)OC2C(C(C(C(O2)CO)O)O)O 295.29 unknown https://doi.org/10.1093/OXFORDJOURNALS.JBCHEM.A022468
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Alpha,beta-unsaturated ketones / Alpha-branched alpha,beta-unsaturated ketones
[(3R)-3-ethenyl-2,5-dimethyl-4-oxohex-5-en-2-yl] acetate 162950046 Click to see CC(=C)C(=O)C(C=C)C(C)(C)OC(=O)C 210.27 unknown https://doi.org/10.1002/HLCA.19810640519
3-Ethenyl-2,5-dimethyl-4-oxohex-5-en-2-yl acetate 21630871 Click to see CC(=C)C(=O)C(C=C)C(C)(C)OC(=O)C 210.27 unknown https://doi.org/10.1002/HLCA.19810640519
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Alpha,beta-unsaturated ketones / Enones
3,3,6-Trimethylhepta-1,5-dien-4-one 68346 Click to see CC(=CC(=O)C(C)(C)C=C)C 152.23 unknown https://doi.org/10.1016/S0031-9422(00)98068-3
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
(E)-tetradec-6-en-8,10,12-triyn-3-one 6244989 Click to see CCC(=O)CCC=CC#CC#CC#CC 198.26 unknown https://doi.org/10.1016/S0031-9422(00)91232-9
https://doi.org/10.3891/ACTA.CHEM.SCAND.04-1567
1-[(2S)-3,3-dimethyloxiran-2-yl]-2,2-dimethylbut-3-en-1-one 163189390 Click to see CC1(C(O1)C(=O)C(C)(C)C=C)C 168.23 unknown https://doi.org/10.1002/HLCA.19810640519
2-Heptadecanone 18027 Click to see CCCCCCCCCCCCCCCC(=O)C 254.50 unknown https://doi.org/10.1080/10412905.1999.9701189
3-Nonanone 61235 Click to see CCCCCCC(=O)CC 142.24 unknown https://doi.org/10.1007/BF01024117
Epoxyartemisia ketone 11816089 Click to see CC1(C(O1)C(=O)C(C)(C)C=C)C 168.23 unknown https://doi.org/10.1002/HLCA.19810640519
Tetradec-6-en-8,10,12-triyn-3-one 100451 Click to see CCC(=O)CCC=CC#CC#CC#CC 198.26 unknown https://doi.org/10.1016/S0031-9422(00)91232-9
https://doi.org/10.3891/ACTA.CHEM.SCAND.04-1567
> Organoheterocyclic compounds / Epoxides
(1R,11S)-1,5,5,8-tetramethyl-12-oxabicyclo[9.1.0]dodeca-3,7-diene 132587053 Click to see CC1=CCC(C=CCC2(C(O2)CC1)C)(C)C 220.35 unknown https://doi.org/10.1080/10412905.1999.9701189
Humulene epoxyde 5463721 Click to see CC1=CCC(C=CCC2(C(O2)CC1)C)(C)C 220.35 unknown https://doi.org/10.1080/10412905.1999.9701189
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
Artabsin 442146 Click to see CC1C2CCC(C3=CCC(=C3C2OC1=O)C)(C)O 248.32 unknown https://doi.org/10.1016/0031-9422(79)80167-3
> Organoheterocyclic compounds / Pyrans / Pyranones and derivatives / Dihydropyranones
6-hydroxy-3-methyl-7-propan-2-yl-5,6,7,7a-tetrahydro-4aH-cyclopenta[b]pyran-2-one 162891700 Click to see CC1=CC2CC(C(C2OC1=O)C(C)C)O 210.27 unknown https://doi.org/10.1016/S0031-9422(00)91232-9
6-methyl-7-propan-2-yl-5,6,7,7a-tetrahydro-4aH-cyclopenta[b]pyran-2-one 162884128 Click to see CC1CC2C=CC(=O)OC2C1C(C)C 194.27 unknown https://doi.org/10.1016/S0031-9422(00)91232-9
> Phenylpropanoids and polyketides / Coumarins and derivatives
7-Methoxy-2,4,11-trioxatricyclo[7.3.1.05,10]trideca-1(13),5(10),6,8-tetraen-12-one 163189849 Click to see COC1=CC2=C3C(=C1)C=C(C(=O)O3)OCO2 220.18 unknown https://doi.org/10.1021/NP50045A040
7,8-Methylenedioxy-6-methoxycoumarin 5319474 Click to see COC1=C2C(=C3C(=C1)C=CC(=O)O3)OCO2 220.18 unknown https://doi.org/10.1021/NP50045A040
Coumarin 323 Click to see C1=CC=C2C(=C1)C=CC(=O)O2 146.14 unknown https://doi.org/10.1007/BF00574599
> Phenylpropanoids and polyketides / Coumarins and derivatives / Coumarin glycosides
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/10.1007/BF00574599
> 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/10.1007/BF00574599
> 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/10.1007/BF00574599
Umbelliferone 5281426 Click to see C1=CC(=CC2=C1C=CC(=O)O2)O 162.14 unknown https://doi.org/10.1007/BF00574599
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(+/-)-Eriodictyol 11095 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)O)O 288.25 unknown https://doi.org/10.1021/JF9801264
Eriodictyol 440735 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)O)O 288.25 unknown https://doi.org/10.1021/JF9801264
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin 5280443 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 270.24 unknown https://doi.org/10.1021/JF9801264
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown https://doi.org/10.1021/JF9801264
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Isorhamnetin 5281654 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 316.26 unknown https://doi.org/10.1021/JF9801264
Quercetin 5280343 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 302.23 unknown https://doi.org/10.1021/JF9801264
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
5,7-dihydroxy-2-(4-hydroxyphenyl)-8-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one 5378180 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(C(O4)CO)O)O)O)O 432.40 unknown https://doi.org/10.1021/JF9801264
Vitexin 5280441 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(C(O4)CO)O)O)O)O 432.40 unknown https://doi.org/10.1021/JF9801264
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-Dihydroxyphenyl)-5,7-Dihydroxy-3-[(2S,3R,4S,5R,6R)-3,4,5-Trihydroxy-6-(Hydroxymethyl)Oxan-2-yl]Oxy-Chromen-4-one 12304323 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/JF9801264
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/JF9801264
5,7-Dihydroxy-2-(4-hydroxyphenyl)-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 5462193 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown https://doi.org/10.1021/JF9801264
5,7-Dihydroxy-2-(4-hydroxyphenyl)-3-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxymethyl]oxan-2-yl]oxychromen-4-one 12313332 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 https://doi.org/10.1021/JF9801264
Astragalin 5282102 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown https://doi.org/10.1021/JF9801264
Hyperoside 5281643 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/JF9801264
kaempferol-3-O-alpha-L-rhamnoside 15558501 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)O)O)O 432.40 unknown https://doi.org/10.1021/JF9801264
Kaempferol-3-O-rhamnoside 5835713 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)O)O)O 432.40 unknown https://doi.org/10.1021/JF9801264
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 https://doi.org/10.1021/JF9801264
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/JF9801264
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/JF9801264
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
2-(3,4-dihydroxyphenyl)-5-hydroxy-7-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 13093776 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown https://doi.org/10.1021/JF9801264
3,5-dihydroxy-2-(4-hydroxyphenyl)-7-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 25203835 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown https://doi.org/10.1021/JF9801264
Kaempferol-7-o-glucoside 5480982 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown https://doi.org/10.1021/JF9801264
Luteolin 7-galactoside 5291488 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown https://doi.org/10.1021/JF9801264
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Chryseriol 5280666 Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 300.26 unknown https://doi.org/10.1021/JF9801264
Homoeriodictyol 73635 Click to see COC1=C(C=CC(=C1)C2CC(=O)C3=C(C=C(C=C3O2)O)O)O 302.28 unknown https://doi.org/10.1021/JF9801264
Homoeriodictyol (+/-)- 3512637 Click to see COC1=C(C=CC(=C1)C2CC(=O)C3=C(C=C(C=C3O2)O)O)O 302.28 unknown https://doi.org/10.1021/JF9801264
Tricin 5281702 Click to see COC1=CC(=CC(=C1O)OC)C2=CC(=O)C3=C(C=C(C=C3O2)O)O 330.29 unknown https://doi.org/10.1021/JF9801264
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
Diosmetin 5281612 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 300.26 unknown https://doi.org/10.1021/JF9801264
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
Eupafolin 5317284 Click to see COC1=C(C2=C(C=C1O)OC(=CC2=O)C3=CC(=C(C=C3)O)O)O 316.26 unknown https://doi.org/10.1021/JF9801264
Jaceosidin 5379096 Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(O2)C=C(C(=C3O)OC)O)O 330.29 unknown https://doi.org/10.1021/JF9801264

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