Scientific name	Authority	First published in
Pimpinella capillacea	Poit. ex Urb.	Fl. Bras. 11(1): 342 (1879)
Pimpinella lateriflora	Link	Enum. Hort. Berol. Alt. 1: 285 (1821)
Visnaga vulgaris	Bubani	Fl. Pyren. 2: 350 (1899)
Sison pumilum	Brot.	Fl. Lusit. 1: 425 (1804)
Sison majus	Eaton & Wright	Man. Bot. , ed. 8: 429 (1840)
Sison lateriflorum	Bertol.	Fl. Ital. 3: 283 (1838)
Aethusa ammi	(L.) Spreng.	Mag. Neuesten Entdeck. Gesammten Naturk. Ges. Naturf. Freunde Berlin 6: 260 (1812)
Ammi boeberi	Hell. ex Hoffm.	Gen. Pl. Umbell. XVIII. 1814
Ammi broussonetii	DC.	Prodr. 4: 113 (1830)
Ammi cicutifolium	Willd. ex Roem. & Schult.	Syst. Veg., ed. 15 bis 6: 531 (1820)
Ammi elatum	Salisb.	Prodr. Stirp. Chap. Allerton : 162 (1796)
Ammi glaucifolium	L.	Sp. Pl. : 243 (1753)
Ammi intermedium	DC.	Prodr. 4: 113 (1830)
Ammi majus var. isophyllum	Lowe	Man. Fl. Madeira 1: 351 1864
Ammi majus var. tenuifolium	Lowe	Man. Fl. Madeira 1: 351 1864
Ammi pauciradiatum	Hochst. ex A.Rich.	Tent. Fl. Abyss. 1: 322 (1848)
Ammi pumilum	DC.	Prodr. 4: 113 (1830)
Ammi topalii	Beauverd	Candollea 7: 264 (1937)
Anethum pinnatum	Ruiz & Pav. ex Urb.	Fl. Bras. 11(1): 342 (1879)
Apium ammi	Crantz	Stirp. Austr. Fasc. iii. 109; ed. II. 217.
Apium ammi-maius	Crantz	Cl. Umbell. Emend. : 103 (1767)
Apium candollei	M.Hiroe	Umbell. World : 860 (1979)
Apium elatum	Calest.	Bull. Soc. Bot. Ital. 1905: 284 (1905)
Apium petraeum	Crantz	Cl. Umbell. Emend. : 104 (1767)
Apium pumilum	Calest.	in Martelli, Webbia 175.
Carum majus	Koso-Pol.	Bull. Soc. Imp. Naturalistes Moscou , n.s., 29: 198 (1915 publ. 1916)
Cuminum aethiopicum	Royle	Ill. Bot. Himal. Mts. : 230 (1835)
Cuminum regium	Royle	Ill. Bot. Himal. Mts. : 230 (1835)
Daucus glaber	Parsa	Kew Bull. 3(2): 199. 1948 [20 Nov 1948]
Daucus parsae	M.Hiroe	Umbell. World : 595 (1979)
Helosciadium lateriflorum	(Link) W.D.J.Koch	Nova Acta Phys.-Med. Acad. Caes. Leop.-Carol. Nat. Cur. 12(1): 126 (1824)
Ammi majus var. glaucifolium	(L.) Mérat	Nouv. Fl. Env. Paris 107 1812
Ammi majus var. heterophyllum	Lowe	Man. Fl. Madeira 1: 350 1864
Ammi majus var. intermedium	(DC.) Gren. & Godr.	Fl. France 1: 732 1849
Ammi majus var. laciniatum	Godr.	Fl. Lorraine 274 1843
Ammi majus var. serratum	Mutel	Fl. Dauphiné ed. 2: 241 1848
Ammi majus var. tenue	Ball	Spic. Moroc. 468 1878
Ammi majus var. glaucifolium	(L.) Noulet
Selinum ammoides	E.H.L.Krause	Deutschl. Fl. Abbild. , ed. 2, 12: 43 (1904)
Visnaga major	(L.) J.Vick	Vick's Ill. Cat. Fl. Guide : 54 (1866)

Common names Top

Add a new one! Suggest a correction!

Filter by language:

Language	Common/alternative name
English	bishopís weed
English	bishopis weed
English	large bullwort
English	lady’s lace
English	greater ammi
English	laceflower
English	bishopsweed
Spanish	ameo mayor
Spanish	aneo bastardo
Spanish	apio cimarrón
Spanish	espuma del mar
Spanish	hinojo borde
Spanish	sistra
Spanish	ammi majus var apiifolium
Spanish	ammi majus var genuinum
Spanish	encaje
Spanish	jistra
Spanish	ammi majus var glaucifolium
Spanish	ammi vulgar
Spanish	ammi majus var. serratum
Spanish	ammi majus var. intermedium
Spanish	ammi majus var. glaucifolium
Spanish	ammi majus var. apiifolium
Spanish	ammi majus var serratum
Spanish	ammi majus var intermedium
Arabic	خلة شيطانية
Azerbaijani	böyük dişqurtlayan
Azerbaijani	may dişqurtlayanı
Azerbaijani	ammi glaucifolium
Catalan	siscla
Czech	morač větší
Czech	pakmín větší
Welsh	esgoblys
German	bischofskraut
German	große knorpelmöhre
German	großes ammei
Estonian	suur ammi
Finnish	isosudenporkkana
French	ammi élevé
French	ammi eleve
French	ammi officinal
French	ammi inodore
French	ammi Élevé
French	ammi commun
Hebrew	אמיתה גדולה
Malayalam	അമ്മി മാജസ്
Dutch	groot akkerscherm
os	Æхсæнпъæз
Polish	ammi maius
Polish	aminek większy
Russian	Амми большая
Swedish	slöjsilja
Turkish	yabani diş otu
Chinese	大阿米芹

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!

Name	Authority	First published in
Ammi majus subsp. procerum	(Lowe) Menezes	Fl. Madeira 76. 1914 (1914)

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

Suggest a correction or add new data!

Sow seeds at 20°C, expecting germination within 3 months without further temperature treatment.

Requires Darkness: These seeds need to be covered with soil or otherwise kept in the dark to germinate properly. Light inhibits their germination process.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Africa click to expand
- East Tropical Africa
  - Kenya
- Macaronesia
  - Azores
  - Canary Islands
  - Madeira
  - Selvagens
- Northeast Tropical Africa
  - Eritrea
  - Ethiopia
- Northern Africa
  - Algeria
  - Egypt
  - Libya
  - Morocco
  - Tunisia
- Southern Africa
  - Cape Provinces
  - Free State
  - Kwazulu-Natal
  - Northern Provinces

Asia-temperate click to expand
- Arabian Peninsula
  - Gulf States
  - Kuwait
  - Oman
  - Saudi Arabia
  - Yemen
- China
  - China Southeast
- Eastern Asia
  - Japan
- Middle Asia
  - Tadzhikistan
- Western Asia
  - Cyprus
  - East Aegean Islands
  - Iran
  - Iraq
  - Lebanon-Syria
  - Palestine
  - Sinai
  - Turkey

Asia-tropical click to expand
- Indian Subcontinent
  - Pakistan

Australasia click to expand
- Australia
  - Tasmania
- New Zealand
  - New Zealand North
  - New Zealand South

Europe click to expand
- Middle Europe
  - Belgium
  - Czechoslovakia
- Northern Europe
  - Denmark
  - Finland
  - Great Britain
  - Ireland
  - Norway
  - Sweden
- Southeastern Europe
  - Albania
  - Greece
  - Italy
  - Kriti
  - Sicilia
  - Turkey-in-Europe
  - Yugoslavia
- Southwestern Europe
  - Baleares
  - Corse
  - France
  - Portugal
  - Sardegna
  - Spain

Northern America click to expand
- Mexico
  - Mexico Central
  - Mexico Southwest
- North-central U.S.A.
  - Missouri
  - South Dakota
- Northeastern U.S.A.
  - Pennsylvania
- Northwestern U.S.A.
  - Oregon
- South-central U.S.A.
  - Texas
- Southeastern U.S.A.
  - Alabama
  - Florida
  - Georgia
  - Louisiana
  - Mississippi
  - South Carolina
- Southwestern U.S.A.
  - Arizona
  - California

Pacific click to expand
- South-central Pacific
  - Tubuai Islands
- Southwestern Pacific
  - New Caledonia

Southern America click to expand
- Brazil
  - Brazil South
- Caribbean
  - Bahamas
  - Bermuda
  - Cuba
  - Dominican Republic
  - Haiti
- Central America
  - Costa Rica
  - El Salvador
  - Guatemala
  - Honduras
- Southern South America
  - Argentina Northeast
  - Argentina Northwest
  - Argentina South
  - Chile South
  - Uruguay
- Western South America
  - Colombia

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000531157
UNII	0Q7F804ETV
Florida Plant Atlas	1749
Flora of Alabama	321
USDA Plants	AMMA
Tropicos	1700290
INPN	82130
Flora of Italy	3589
KEW	urn:lsid:ipni.org:names:837486-1
The Plant List	kew-2633874
Open Tree Of Life	1074876
Observations.org	6411
NCBI Taxonomy	48026
NBN Atlas	NBNSYS0000003675
Nature Serve	2.131144
IPNI	837486-1
iNaturalist	75417
GBIF	3034182
Freebase	/m/02pp1xc
EPPO	AMIMA
EOL	584988
Elurikkus	2738
Calflora (Californian flora)	308
USDA GRIN	2899
Wikipedia	Ammi_majus
CMAUP	NPO7090

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

Impact of Heavy Metal Pollution in the Environment on the Metabolic Profile of Medicinal Plants and Their Therapeutic Potential

Asiminicesei DM, Fertu DI, Gavrilescu M

Plants (Basel)

21-Mar-2024

PMCID:	PMC10976221
doi:	10.3390/plants13060913
PMID:	38592933

Achieving agricultural sustainability through soybean production in Iran: Potential and challenges

Majidian P, Ghorbani HR, Farajpour M

Heliyon

16-Feb-2024

PMCID:	PMC10884498
doi:	10.1016/j.heliyon.2024.e26389
PMID:	38404839

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

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

Ultra-Performance Liquid Chromatography Coupled with Mass Metabolic Profiling of Ammi majus Roots as Waste Product with Isolation and Assessment of Oral Mucosal Toxicity of Its Psoralen Component Xanthotoxin

Fathallah N, El Deeb M, Rabea AA, Almehmady AM, Alkharobi H, Elhady SS, Khalil N

Metabolites

29-Sep-2023

PMCID:	PMC10608439
doi:	10.3390/metabo13101044
PMID:	37887369

The Application of Arbuscular Mycorrhizal Fungi as Microbial Biostimulant, Sustainable Approaches in Modern Agriculture

Sun W, Shahrajabian MH

Plants (Basel)

29-Aug-2023

PMCID:	PMC10490045
doi:	10.3390/plants12173101
PMID:	37687348

Furoquinoline Alkaloids: Insights into Chemistry, Occurrence, and Biological Properties

Szewczyk A, Pęczek F

Int J Mol Sci

15-Aug-2023

PMCID:	PMC10454094
doi:	10.3390/ijms241612811
PMID:	37628986

Prevalence, motivation, and associated factors of medicinal herbs consumption in pregnant women from Eastern Mediterranean Regional Office: a systematic review

Bouqoufi A, Lahlou L, Ait El Hadj F, Abdessadek M, Obtel M, Khabbal Y

Pharm Biol

14-Jul-2023

PMCID:	PMC10351469
doi:	10.1080/13880209.2023.2229388
PMID:	37452524

Photodynamic Therapy: From the Basics to the Current Progress of N-Heterocyclic-Bearing Dyes as Effective Photosensitizers

Lima E, Reis LV

Molecules

29-Jun-2023

PMCID:	PMC10343694
doi:	10.3390/molecules28135092
PMID:	37446758

Apiaceae Medicinal Plants in China: A Review of Traditional Uses, Phytochemistry, Bolting and Flowering (BF), and BF Control Methods

Li M, Li M, Wang L, Li M, Wei J

Molecules

27-May-2023

PMCID:	PMC10254214
doi:	10.3390/molecules28114384
PMID:	37298861

Allelopathy: an alternative tool for sustainable agriculture

Ain Q, Mushtaq W, Shadab M, Siddiqui MB

Physiol Mol Biol Plants

24-Apr-2023

PMCID:	PMC10172429
doi:	10.1007/s12298-023-01305-9
PMID:	37187777

African eggplant-associated virus: Characterization of a novel tobamovirus identified from Solanum macrocarpon and assessment of its potential impact on tomato and pepper crops

Giesbers AK, Roenhorst A, Schenk MF, Westenberg M, Botermans M

PLoS One

13-Apr-2023

PMCID:	PMC10101479
doi:	10.1371/journal.pone.0277840
PMID:	37053240

Review of natural compounds for potential psoriasis treatment

Elkhawaga OY, Ellety MM, Mofty SO, Ghanem MS, Mohamed AO

Inflammopharmacology

30-Mar-2023

PMCID:	PMC10229448
doi:	10.1007/s10787-023-01178-0
PMID:	36995575

Therapeutic Effects of Coumarins with Different Substitution Patterns

Flores-Morales V, Villasana-Ruíz AP, Garza-Veloz I, González-Delgado S, Martinez-Fierro ML

Molecules

06-Mar-2023

PMCID:	PMC10005689
doi:	10.3390/molecules28052413
PMID:	36903660

Molecular phylogenetic study of flavonoids in medicinal plants: a case study family Apiaceae

Youssef D, El-Bakatoushi R, Elframawy A, El-Sadek L, Badan GE

J Plant Res

28-Feb-2023

PMCID:	PMC10126080
doi:	10.1007/s10265-023-01442-y
PMID:	36853579

Phytochemical Profile Top

Add a new one!

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
Arhimachalene	11458355	Click to see CC1CCCC(C2=C1C=CC(=C2)C)(C)C	202.33	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Methoxybenzenes / Dimethoxybenzenes
3-(3',4'-Dimethoxyphenyl)prop-2-enyl isovalerate	6442914	Click to see CC(C)CC(=O)OCC=CC1=CC(=C(C=C1)OC)OC	278.34	unknown	via CMAUP database
3,4-Dimethoxycinnamyl alcohol	5387770	Click to see COC1=C(C=C(C=C1)C=CCO)OC	194.23	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Styrenes
Cinnamyl isovalerate	5355855	Click to see CC(C)CC(=O)OCC=CC1=CC=CC=C1	218.29	unknown	via CMAUP database
> Benzenoids / Naphthalenes / Naphthalenecarboxylic acids and derivatives / Naphthalenecarboxylic acids
(7S,8R)-6-Methylidene-5-oxo-8-(3,4,5-trimethoxyphenyl)-7,8-dihydrobenzo[f][1,3]benzodioxole-7-carboxylic acid	11144085	Click to see COC1=CC(=CC(=C1OC)OC)C2C(C(=C)C(=O)C3=CC4=C(C=C23)OCO4)C(=O)O	412.40	unknown	via CMAUP database
> Benzenoids / Phenol ethers / Anisoles
3',4',5'-Trimethoxycinnamylisovalerate	6442915	Click to see CC(C)CC(=O)OCC=CC1=CC(=C(C(=C1)OC)OC)OC	308.40	unknown	via CMAUP database
> Hydrocarbon derivatives / Tropones / Tropolones
Nootkatin	238797	Click to see CC(C)C1=CC(=O)C(=CC=C1CC=C(C)C)O	232.32	unknown	via CMAUP database
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
alpha-Duprezianene	101985700	Click to see CC1CCC2C13CCC(C2(C)C)C(=C3)C	204.35	unknown	via CMAUP database
beta-Duprezianane	91750164	Click to see CC1CCC2C13CCC(C2(C)C)C(=C)C3	204.35	unknown	via CMAUP database
Pseudowiddrene	15409431	Click to see CC1=CCC2(C(=CCCC2(C)C)CC1)C	204.35	unknown	via CMAUP database
> Lignans, neolignans and related compounds / Aryltetralin lignans
(5R)-5,6,7,8-Tetrahydro-5beta-(3,4,5-trimethoxyphenyl)-7alpha-(hydroxymethyl)naphtho[2,3-d]-1,3-dioxole-6beta-carboxylic acid methyl ester	101618918	Click to see COC1=CC(=CC(=C1OC)OC)C2C(C(CC3=CC4=C(C=C23)OCO4)CO)C(=O)OC	430.40	unknown	via CMAUP database
> Lignans, neolignans and related compounds / Aryltetralin lignans / 9,9p-dihydroxyaryltetralin lignans
Podophyllinic acid	134632	Click to see COC1=CC(=CC(=C1OC)OC)C2C(C(C(C3=CC4=C(C=C23)OCO4)O)CO)C(=O)O	432.40	unknown	via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans
(-)-Sesamin	382073	Click to see C1C2C(COC2C3=CC4=C(C=C3)OCO4)C(O1)C5=CC6=C(C=C5)OCO6	354.40	unknown	via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 7,9-epoxylignans
[(2R,3S,4S)-2-(1,3-benzodioxol-5-yl)-4-(1,3-benzodioxol-5-ylmethyl)oxolan-3-yl]methanol	11653313	Click to see C1C(C(C(O1)C2=CC3=C(C=C2)OCO3)CO)CC4=CC5=C(C=C4)OCO5	356.40	unknown	via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 9,9-epoxylignans / Dibenzylbutyrolactone lignans
(3E,4R)-4-(1,3-Benzodioxol-5-ylmethyl)-3-[(3,4,5-trimethoxyphenyl)methylidene]oxolan-2-one	11165431	Click to see COC1=CC(=CC(=C1OC)OC)C=C2C(COC2=O)CC3=CC4=C(C=C3)OCO4	398.40	unknown	via CMAUP database
(3S,4R)-4-(1,3-benzodioxol-5-ylmethyl)-3-[(R)-hydroxy-(3,4,5-trimethoxyphenyl)methyl]oxolan-2-one	173676	Click to see COC1=CC(=CC(=C1OC)OC)C(C2C(COC2=O)CC3=CC4=C(C=C3)OCO4)O	416.40	unknown	via CMAUP database
Hinokinin	442879	Click to see C1C(C(C(=O)O1)CC2=CC3=C(C=C2)OCO3)CC4=CC5=C(C=C4)OCO5	354.40	unknown	via CMAUP database
Podorhizol	9931715	Click to see COC1=CC(=CC(=C1OC)OC)C(C2C(COC2=O)CC3=CC4=C(C=C3)OCO4)O	416.40	unknown	via CMAUP database
Savinin	5281867	Click to see C1C(C(=CC2=CC3=C(C=C2)OCO3)C(=O)O1)CC4=CC5=C(C=C4)OCO5	352.30	unknown	via CMAUP database
Yatein	442835	Click to see COC1=CC(=CC(=C1OC)OC)CC2C(COC2=O)CC3=CC4=C(C=C3)OCO4	400.40	unknown	via CMAUP database
> Lignans, neolignans and related compounds / Lignan lactones
beta-Peltatin A methyl ether	159962	Click to see COC1=CC(=CC(=C1OC)OC)C2C3C(CC4=C(C5=C(C=C24)OCO5)OC)COC3=O	428.40	unknown	via CMAUP database
Deoxypicropodophyllotoxin	11711021	Click to see COC1=CC(=CC(=C1OC)OC)C2C3C(CC4=CC5=C(C=C24)OCO5)COC3=O	398.40	unknown	via CMAUP database
Deoxypodophyllotoxin	345501	Click to see COC1=CC(=CC(=C1OC)OC)C2C3C(CC4=CC5=C(C=C24)OCO5)COC3=O	398.40	unknown	via CMAUP database
> Lignans, neolignans and related compounds / Lignan lactones / Podophyllotoxins
Epipicropodophyllotoxin acetate	14160031	Click to see CC(=O)OC1C2COC(=O)C2C(C3=CC4=C(C=C13)OCO4)C5=CC(=C(C(=C5)OC)OC)OC	456.40	unknown	via CMAUP database
Picropodophyllin	72435	Click to see COC1=CC(=CC(=C1OC)OC)C2C3C(COC3=O)C(C4=CC5=C(C=C24)OCO5)O	414.40	unknown	via CMAUP database
Podofilox	10607	Click to see COC1=CC(=CC(=C1OC)OC)C2C3C(COC3=O)C(C4=CC5=C(C=C24)OCO5)O	414.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
7-hydroxy-8-[(E)-3-methyl-4-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybut-2-enyl]chromen-2-one	163194486	Click to see CC(=CCC1=C(C=CC2=C1OC(=O)C=C2)O)COC3C(C(C(C(O3)CO)O)O)O	408.40	unknown	https://doi.org/10.1016/0031-9422(93)85365-X
7-hydroxy-8-[(E)-3-methyl-4-[(3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybut-2-enyl]chromen-2-one	162944476	Click to see CC(=CCC1=C(C=CC2=C1OC(=O)C=C2)O)COC3C(C(C(C(O3)CO)O)O)O	408.40	unknown	https://doi.org/10.1016/0031-9422(93)85365-X
7-Hydroxy-8-[3-methyl-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybut-2-enyl]chromen-2-one	162944475	Click to see CC(=CCC1=C(C=CC2=C1OC(=O)C=C2)O)COC3C(C(C(C(O3)CO)O)O)O	408.40	unknown	https://doi.org/10.1016/0031-9422(93)85365-X
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohol esters
(2E,4Z)-Deca-2,4-dienyl isovalerate	6436644	Click to see CCCCCC=CC=CCOC(=O)CC(C)C	238.37	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(13E)-15-Hydroxylabda-8(20),13-dien-19-oic acid methyl ester	14060410	Click to see CC(=CCO)CCC1C(=C)CCC2C1(CCCC2(C)C(=O)OC)C	334.50	unknown	via CMAUP database
(1R,4abeta)-Decahydro-1beta-[(E)-5-hydroxy-3-methyl-3-pentenyl]-2,5,5,8abeta-tetramethylnaphthalen-2alpha-ol	12306731	Click to see CC(=CCO)CCC1C2(CCCC(C2CCC1(C)O)(C)C)C	308.50	unknown	via CMAUP database
(1S,4R,5S,9S,10R,12S)-16-(2-hydroperoxypropan-2-yl)-5,9-dimethyl-13,14-dioxatetracyclo[10.2.2.01,10.04,9]hexadec-15-ene-5-carboxylic acid	97044524	Click to see CC12CCCC(C1CCC34C2CC(C(=C3)C(C)(C)OO)OO4)(C)C(=O)O	366.40	unknown	via CMAUP database
15-Hydroperoxy-8alpha,12alpha-epidioxyabieta-13-ene-19-oic acid methyl ester	12149368	Click to see CC12CCCC(C1CCC34C2CC(C(=C3)C(C)(C)OO)OO4)(C)C(=O)OC	380.50	unknown	via CMAUP database
15-Hydroxy-8alpha,12alpha-epidioxyabieta-13-ene-19-oic acid methyl ester	12149369	Click to see CC12CCCC(C1CCC34C2CC(C(=C3)C(C)(C)O)OO4)(C)C(=O)OC	364.50	unknown	via CMAUP database
4-Epiabietic acid	6973653	Click to see CC(C)C1=CC2=CCC3C(C2CC1)(CCCC3(C)C(=O)O)C	302.50	unknown	via CMAUP database
4-Epicommunic acid	12303810	Click to see CC(=CCC1C(=C)CCC2C1(CCCC2(C)C(=O)O)C)C=C	302.50	unknown	via CMAUP database
Abietal	443479	Click to see CC(C)C1=CC2=CCC3C(CCCC3(C2CC1)C)(C)C=O	286.50	unknown	via CMAUP database
Abietic acid	10569	Click to see CC(C)C1=CC2=CCC3C(C2CC1)(CCCC3(C)C(=O)O)C	302.50	unknown	via CMAUP database
Abietyl alcohol	443474	Click to see CC(C)C1=CC2=CCC3C(CCCC3(C2CC1)C)(C)CO	288.50	unknown	via CMAUP database
Dehydroabietal	11694869	Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2)(C)C=O)C	284.40	unknown	via CMAUP database
Isopimaric acid	442048	Click to see CC1(CCC2C(=CCC3C2(CCCC3(C)C(=O)O)C)C1)C=C	302.50	unknown	via CMAUP database
Isopimarinol	15586712	Click to see CC1(CCC2C(=CCC3C2(CCCC3(C)CO)C)C1)C=C	288.50	unknown	via CMAUP database
Sandaracopimaradienediol	12313649	Click to see CC1(CCC2C(=C1)CCC3C2(CCC(C3(C)CO)O)C)C=C	304.50	unknown	via CMAUP database
Sandaracopimaric acid	221580	Click to see CC1(CCC2C(=C1)CCC3C2(CCCC3(C)C(=O)O)C)C=C	302.50	unknown	via CMAUP database
Sandaracopimarinol	12314286	Click to see CC1(CCC2C(=C1)CCC3C2(CCCC3(C)CO)C)C=C	288.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
(+)-Linalyl acetate	6999980	Click to see CC(=CCCC(C)(C=C)OC(=O)C)C	196.29	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1aR,4aS,8aS)-4a,8,8-trimethyl-1,1a,4,5,6,7-hexahydrocyclopropa[j]naphthalene-2-carbaldehyde	12444332	Click to see CC1(CCCC2(C13CC3C(=CC2)C=O)C)C	218.33	unknown	via CMAUP database
[S,(+)]-2-Methyl-6-p-tolylheptane	101694025	Click to see CC1=CC=C(C=C1)C(C)CCCC(C)C	204.35	unknown	via CMAUP database
15,16-Dinor-13-oxolabda-8(17)-ene-19-oic acid methyl ester	11255232	Click to see CC(=O)CCC1C(=C)CCC2C1(CCCC2(C)C(=O)OC)C	306.40	unknown	via CMAUP database
Cuparene	86895	Click to see CC1=CC=C(C=C1)C2(CCCC2(C)C)C	202.33	unknown	via CMAUP database
Thujopsene	442402	Click to see CC1=CCC2(CCCC(C23C1C3)(C)C)C	204.35	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Cedrane and isocedrane sesquiterpenoids
(1R,2R,5S,7R)-2,6,6-Trimethyl-8-methylidenetricyclo[5.3.1.01,5]undecane	16213223	Click to see CC1CCC2C13CCC(=C)C(C3)C2(C)C	204.35	unknown	via CMAUP database
(1S,2R,5S,7S)-2,6,6,8-tetramethyltricyclo[5.3.1.01,5]undec-8-en-4-one	12308772	Click to see CC1CC(=O)C2C13CC=C(C(C3)C2(C)C)C	218.33	unknown	via CMAUP database
(3R,8abeta)-3alpha,8,8-Trimethyl-6-methylenedecahydro-3aalpha,7alpha-methanoazulene-2-one	21576983	Click to see CC1C(=O)CC2C13CCC(=C)C(C3)C2(C)C	218.33	unknown	via CMAUP database
(3R)-3alpha,6,8,8-Tetramethyl-2,3,4,7,8,8abeta-hexahydro-3aalpha,7alpha-methanoazulene-2(1H)-one	21576982	Click to see CC1C(=O)CC2C13CC=C(C(C3)C2(C)C)C	218.33	unknown	via CMAUP database
(3R)-3beta,8,8-Trimethyl-6-methylene-3,3a,4,5,6,7,8,8abeta-octahydro-3aalpha,7alpha-methanoazulene-1(2H)-one	12308774	Click to see CC1CC(=O)C2C13CCC(=C)C(C3)C2(C)C	218.33	unknown	via CMAUP database
[(1S,2R,5R,6S,7S)-2,6,8-trimethyl-6-tricyclo[5.3.1.01,5]undec-8-enyl]methanol	22211622	Click to see CC1CCC2C13CC=C(C(C3)C2(C)CO)C	220.35	unknown	via CMAUP database
3beta-Hydroxycedrene	15215015	Click to see CC1C(CC2C13CC=C(C(C3)C2(C)C)C)O	220.35	unknown	via CMAUP database
alpha-Cedrene	6431015	Click to see CC1CCC2C13CC=C(C(C3)C2(C)C)C	204.35	unknown	via CMAUP database
beta-Cedrene	11106485	Click to see CC1CCC2C13CCC(=C)C(C3)C2(C)C	204.35	unknown	via CMAUP database
Cedrenone	13335685	Click to see CC1CCC2C13CC(C2(C)C)C(=CC3=O)C	218.33	unknown	via CMAUP database
Cedrol	65575	Click to see CC1CCC2C13CCC(C(C3)C2(C)C)(C)O	222.37	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Elemane sesquiterpenoids
8-Acetoxyelemol	14138886	Click to see CC(=C)C1CC(C(CC1(C)C=C)OC(=O)C)C(C)(C)O	280.40	unknown	via CMAUP database
8-Hydroxyelemol	14138884	Click to see CC(=C)C1CC(C(CC1(C)C=C)O)C(C)(C)O	238.37	unknown	via CMAUP database
Elemol	92138	Click to see CC(=C)C1CC(CCC1(C)C=C)C(C)(C)O	222.37	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
3-Hydroxyolean-12-en-28-oic acid	619166	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C	456.70	unknown	https://doi.org/10.1016/0031-9422(93)85365-X
Oleanolic Acid	10494	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C	456.70	unknown	https://doi.org/10.1016/0031-9422(93)85365-X
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Hydroxysteroids
3beta-Hydroxyisopimaric acid	102193489	Click to see CC1(CCC2C(=CCC3C2(CCC(C3(C)C(=O)O)O)C)C1)C=C	318.40	unknown	via CMAUP database
3beta-Hydroxysandaracopimaric acid	101200911	Click to see CC1(CCC2C(=C1)CCC3C2(CCC(C3(C)C(=O)O)O)C)C=C	318.40	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclic alcohols and derivatives
(1R,2R,5R,7R,8S)-2,6,6,8-tetramethyltricyclo[6.2.1.01,5]undecan-7-ol	101985389	Click to see CC1CCC2C13CCC(C3)(C(C2(C)C)O)C	222.37	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
Widdrol	94334	Click to see CC1(CCCC2(C1=CCC(CC2)(C)O)C)C	222.37	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
Cnidioside B	24148534	Click to see COC1=C2C(=CC(=C1OC3C(C(C(C(O3)CO)O)O)O)CCC(=O)O)C=CO2	398.40	unknown	https://doi.org/10.1080/10575639308043865
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Sugar alcohols
Mannitol	6251	Click to see C(C(C(C(C(CO)O)O)O)O)O	182.17	unknown	https://doi.org/10.1016/0031-9422(93)85365-X
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones
(3R)-3alpha,7,7-Trimethyl-5-methylene-3a,4,5,6,7,7abeta-hexahydro-3aalpha,6alpha-ethano-1H-indene-2(3H)-one	21576981	Click to see CC1C(=O)CC2C13CCC(C2(C)C)C(=C)C3	218.33	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
(1R,2R,5R,8S)-2,6,6,8-tetramethyltricyclo[6.2.1.01,5]undecan-7-one	21576985	Click to see CC1CCC2C13CCC(C3)(C(=O)C2(C)C)C	220.35	unknown	via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Chromones / Furanochromones
Ammiol	621572	Click to see COC1=C2C(=O)C=C(OC2=C(C3=C1C=CO3)OC)CO	276.24	unknown	https://doi.org/10.1016/0031-9422(93)85365-X
> Phenylpropanoids and polyketides / Cinnamyl alcohols
3,4,5-Trimethoxycinnamyl alcohol	6436306	Click to see COC1=CC(=CC(=C1OC)OC)C=CCO	224.25	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives
7-(3-Methylbuta-1,3-dienoxy)chromen-2-one	72733137	Click to see CC(=C)C=COC1=CC2=C(C=C1)C=CC(=O)O2	228.24	unknown	https://doi.org/10.1016/0031-9422(90)85418-F
7-(4-Hydroxy-3-methylbut-1-enoxy)chromen-2-one	162886885	Click to see CC(CO)C=COC1=CC2=C(C=C1)C=CC(=O)O2	246.26	unknown	https://doi.org/10.1016/0031-9422(90)85418-F
7-[(E,3R)-4-hydroxy-3-methylbut-1-enoxy]chromen-2-one	163185356	Click to see CC(CO)C=COC1=CC2=C(C=C1)C=CC(=O)O2	246.26	unknown	https://doi.org/10.1016/0031-9422(90)85418-F
7-Methoxycoumarin	10748	Click to see COC1=CC2=C(C=C1)C=CC(=O)O2	176.17	unknown	https://doi.org/10.1016/0031-9422(90)85418-F
7-Prenyloxycoumarin	320362	Click to see CC(=CCOC1=CC2=C(C=C1)C=CC(=O)O2)C	230.26	unknown	https://doi.org/10.1016/0031-9422(90)85418-F
Coumarin B	14585499	Click to see CC(=C)C=COC1=CC2=C(C=C1)C=CC(=O)O2	228.24	unknown	https://doi.org/10.1016/0031-9422(90)85418-F
> Phenylpropanoids and polyketides / Coumarins and derivatives / Coumarin glycosides
8-(4-Hydroxy-3-methylbut-2-enyl)-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-2-one	74096941	Click to see CC(=CCC1=C(C=CC2=C1OC(=O)C=C2)OC3C(C(C(C(O3)CO)O)O)O)CO	408.40	unknown	https://doi.org/10.1016/0031-9422(93)85365-X
8-[(E)-4-hydroxy-3-methylbut-2-enyl]-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-2-one	23958167	Click to see CC(=CCC1=C(C=CC2=C1OC(=O)C=C2)OC3C(C(C(C(O3)CO)O)O)O)CO	408.40	unknown	https://doi.org/10.1016/0031-9422(93)85365-X
8-[(E)-4-hydroxy-3-methylbut-2-enyl]-7-[(3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-2-one	163050307	Click to see CC(=CCC1=C(C=CC2=C1OC(=O)C=C2)OC3C(C(C(C(O3)CO)O)O)O)CO	408.40	unknown	https://doi.org/10.1016/0031-9422(93)85365-X
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Angular furanocoumarins
(8R)-8-prop-1-en-2-yl-8,9-dihydrofuro[2,3-h]chromen-2-one	51520705	Click to see CC(=C)C1CC2=C(O1)C=CC3=C2OC(=O)C=C3	228.24	unknown	https://doi.org/10.1002/JPS.2600600528
> 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
(2S)-9-hydroxy-2-prop-1-en-2-yl-2,3-dihydrofuro[3,2-g]chromen-7-one	139088001	Click to see CC(=C)C1CC2=C(O1)C(=C3C(=C2)C=CC(=O)O3)O	244.24	unknown	https://doi.org/10.1016/0031-9422(93)85365-X
(R)-Apiumetin	131752966	Click to see CC(=C)C1CC2=C(O1)C(=C3C(=C2)C=CC(=O)O3)O	244.24	unknown	https://doi.org/10.1016/0031-9422(93)85365-X
(R)-Pabulenol	511358	Click to see CC(=C)C(COC1=C2C=CC(=O)OC2=CC3=C1C=CO3)O	286.28	unknown	https://doi.org/10.1021/JF60220A023
[3-Hydroxy-3-methyl-1-(7-oxofuro[3,2-g]chromen-9-yl)oxybutan-2-yl] acetate	13845714	Click to see CC(=O)OC(COC1=C2C(=CC3=C1OC=C3)C=CC(=O)O2)C(C)(C)O	346.30	unknown	https://doi.org/10.1016/0031-9422(93)85365-X
2-(2-Hydroxypropan-2-yl)-2,3-dihydrofuro[3,2-g]chromen-7-one	604512	Click to see CC(C)(C1CC2=C(O1)C=C3C(=C2)C=CC(=O)O3)O	246.26	unknown	https://doi.org/10.1016/0031-9422(90)85418-F https://doi.org/10.1021/JO01060A039
2-Isopropenyl-2,3-dihydrofuro[3,2-g]chromen-7-one	611672	Click to see CC(=C)C1CC2=C(O1)C=C3C(=C2)C=CC(=O)O3	228.24	unknown	https://doi.org/10.1016/0031-9422(90)85418-F
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/10.1021/JO01105A632 https://doi.org/10.1021/JO01060A039
Ammirin	759292	Click to see CC(=C)C1CC2=C(O1)C=C3C(=C2)C=CC(=O)O3	228.24	unknown	https://doi.org/10.1016/0031-9422(90)85418-F
Heraclenin	458010	Click to see CC1(C(O1)COC2=C3C(=CC4=C2OC=C4)C=CC(=O)O3)C	286.28	unknown	https://doi.org/10.1021/JF60220A023 https://doi.org/10.1038/182054A0 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3349536/
Isoimperatorin	68081	Click to see CC(=CCOC1=C2C=CC(=O)OC2=CC3=C1C=CO3)C	270.28	unknown	https://doi.org/10.1002/RECL.19680870808 https://doi.org/10.1021/JF60220A023
Marmesin	334704	Click to see CC(C)(C1CC2=C(O1)C=C3C(=C2)C=CC(=O)O3)O	246.26	unknown	https://doi.org/10.1021/JO01060A039 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3349536/ https://doi.org/10.1002/RECL.19680870808 https://doi.org/10.1111/J.1432-1033.1988.TB13800.X https://doi.org/10.1016/0031-9422(90)85418-F
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/10.1021/JO01105A632
Nodakenetin	26305	Click to see CC(C)(C1CC2=C(O1)C=C3C(=C2)C=CC(=O)O3)O	246.26	unknown	https://doi.org/10.1021/JO01060A039
Oxypeucedanin	928465	Click to see CC1(C(O1)COC2=C3C=CC(=O)OC3=CC4=C2C=CO4)C	286.28	unknown	https://doi.org/10.1021/JF60220A023
Pabulenol	3009225	Click to see CC(=C)C(COC1=C2C=CC(=O)OC2=CC3=C1C=CO3)O	286.28	unknown	https://doi.org/10.1021/JF60220A023
Pentosalen	10212	Click to see CC(=CCOC1=C2C(=CC3=C1OC=C3)C=CC(=O)O2)C	270.28	unknown	https://doi.org/10.1002/RECL.19680870808 https://doi.org/10.1021/JA01166A523
Prangenin	17897	Click to see CC1(C(O1)COC2=C3C(=CC4=C2OC=C4)C=CC(=O)O3)C	286.28	unknown	https://doi.org/10.1038/182054A0
Psoralen	6199	Click to see C1=CC(=O)OC2=CC3=C(C=CO3)C=C21	186.16	unknown	https://doi.org/10.1002/(SICI)1521-3773(19990201)38:3<400::AID-ANIE400>3.0.CO;2-K
Saxalin	182277	Click to see CC(C)(C(COC1=C2C=CC(=O)OC2=CC3=C1C=CO3)O)Cl	322.74	unknown	https://doi.org/10.1021/JF60220A023
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 5-methoxypsoralens
8-Hydroxybergapten	3083726	Click to see COC1=C2C=COC2=C(C3=C1C=CC(=O)O3)O	232.19	unknown	https://doi.org/10.1016/0031-9422(93)85365-X
Bergapten	2355	Click to see COC1=C2C=CC(=O)OC2=CC3=C1C=CO3	216.19	unknown	https://doi.org/10.1002/RECL.19680870808 https://doi.org/10.1055/S-2006-961168 https://doi.org/10.1016/0031-9422(90)85418-F https://doi.org/10.1021/JF60220A023
> 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	via CMAUP database
> 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/10.1002/RECL.19680870808 https://doi.org/10.1016/0031-9422(90)85418-F https://doi.org/10.1021/JF60220A023
Methoxsalen	4114	Click to see COC1=C2C(=CC3=C1OC=C3)C=CC(=O)O2	216.19	unknown	https://doi.org/10.1002/RECL.19680870808 https://doi.org/10.1016/S0168-9452(01)00597-0 https://doi.org/10.1055/S-2006-958144 https://doi.org/10.1021/JA01166A523 https://doi.org/10.1021/JF60220A023 https://doi.org/10.1111/J.2042-7158.1950.TB12975.X
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins
6-Hydroxy-7-methoxy-4-methyl-2H-chromen-2-one	238946	Click to see CC1=CC(=O)OC2=CC(=C(C=C12)O)OC	206.19	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3349536/
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
7-Hydroxy-8-(4-hydroxy-3-methylbut-2-enyl)chromen-2-one	74315868	Click to see CC(=CCC1=C(C=CC2=C1OC(=O)C=C2)O)CO	246.26	unknown	https://doi.org/10.1016/0031-9422(93)85365-X
7-hydroxy-8-[(E)-4-hydroxy-3-methylbut-2-enyl]chromen-2-one	14102503	Click to see CC(=CCC1=C(C=CC2=C1OC(=O)C=C2)O)CO	246.26	unknown	https://doi.org/10.1016/0031-9422(93)85365-X
Scopoletin	5280460	Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)O	192.17	unknown	https://doi.org/10.1016/0031-9422(93)85365-X
Umbelliferone	5281426	Click to see C1=CC(=CC2=C1C=CC(=O)O2)O	162.14	unknown	https://doi.org/10.1016/0031-9422(90)85418-F https://doi.org/10.1016/S0168-9452(00)00381-2 https://doi.org/10.1055/S-2006-961168
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Angular pyranocoumarins
(8R)-8-(hydroxymethyl)-8-methyl-9,10-dihydropyrano[2,3-h]chromen-2-one	162895159	Click to see CC1(CCC2=C(O1)C=CC3=C2OC(=O)C=C3)CO	246.26	unknown	https://doi.org/10.1016/0031-9422(93)85365-X
2H,8H-Benzo[1,2-b:3,4-b']dipyran-2-one, 9,10-dihydro-9-hydroxy-8,8-dimethyl-, (R)-	759302	Click to see CC1(C(CC2=C(O1)C=CC3=C2OC(=O)C=C3)O)C	246.26	unknown	https://doi.org/10.1016/0031-9422(93)85365-X
8-(Hydroxymethyl)-8-methyl-9,10-dihydropyrano[2,3-h]chromen-2-one	162895158	Click to see CC1(CCC2=C(O1)C=CC3=C2OC(=O)C=C3)CO	246.26	unknown	https://doi.org/10.1016/0031-9422(93)85365-X
Lomatin	600670	Click to see CC1(C(CC2=C(O1)C=CC3=C2OC(=O)C=C3)O)C	246.26	unknown	https://doi.org/10.1016/0031-9422(93)85365-X
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Linear pyranocoumarins
Dihydroxanthyletin	10466390	Click to see CC1(CCC2=C(O1)C=C3C(=C2)C=CC(=O)O3)C	230.26	unknown	https://doi.org/10.1016/0031-9422(93)85365-X
> Phenylpropanoids and polyketides / Flavonoids / Flavones
5,6,7-Trihydroxy-2-(2,4,5-trihydroxyphenyl)-4H-1-benzopyran-4-one	71331302	Click to see C1=C(C(=CC(=C1O)O)O)C2=CC(=O)C3=C(O2)C=C(C(=C3O)O)O	318.23	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
[(2R,3S,4R,5S,6S)-6-[(3S,4R,5R,6S)-2-[5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-4-oxochromen-3-yl]oxy-4,5-dihydroxy-6-[[(3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-3-yl]oxy-4,5-dihydroxy-2-methyloxan-3-yl] acetate	162891879	Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)OC)COC6C(C(C(C(O6)CO)O)O)O)O)O)O)O)OC(=O)C	828.70	unknown	https://doi.org/10.1016/S0031-9422(98)00417-8
[(2R,3S,4R,5S,6S)-6-[(3S,4R,5R,6S)-2-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-4,5-dihydroxy-6-[[(3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-3-yl]oxy-4,5-dihydroxy-2-methyloxan-3-yl] acetate	163092975	Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)COC6C(C(C(C(O6)CO)O)O)O)O)O)O)O)OC(=O)C	798.70	unknown	https://doi.org/10.1016/S0031-9422(98)00417-8
[(2S,3R,4R,5S,6S)-6-[(2S,3R,4S,5S,6R)-2-[5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-4-oxochromen-3-yl]oxy-4,5-dihydroxy-6-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-3-yl]oxy-4,5-dihydroxy-2-methyloxan-3-yl] acetate	162891880	Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)OC)COC6C(C(C(C(O6)CO)O)O)O)O)O)O)O)OC(=O)C	828.70	unknown	https://doi.org/10.1016/S0031-9422(98)00417-8
[(2S,3R,4R,5S,6S)-6-[(2S,3S,4S,5S,6R)-2-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-4,5-dihydroxy-6-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-3-yl]oxy-4,5-dihydroxy-2-methyloxan-3-yl] acetate	163092974	Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)COC6C(C(C(C(O6)CO)O)O)O)O)O)O)O)OC(=O)C	798.70	unknown	https://doi.org/10.1016/S0031-9422(98)00417-8
5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-3-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	51402809	Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O	478.40	unknown	https://doi.org/10.1016/S0031-9422(98)00417-8
5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-3-[(2S,3S,4R,5R,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one	154496793	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)OC)O)O)O)O)O)O	624.50	unknown	https://doi.org/10.1016/S0031-9422(98)00417-8
5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-3-[(2S,4S,5S)-3,4,5-trihydroxy-6-[[(2R,3S,5R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one	162995386	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)OC)O)O)O)O)O)O	624.50	unknown	https://doi.org/10.1016/S0031-9422(98)00417-8
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/10.1016/S0031-9422(98)00417-8

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