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Ammi majus

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID644008d088a68444855498
Scientific name Ammi majus
Authority L.
First published in Sp. Pl. : 243 (1753)

Ethnobotanical Use Top

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Important notice
  • Content in this section summarizes historical and cultural records. It is not medical advice.
  • Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
  • Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
  • Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

Ammi majus, a member of the carrot family, has long been used by several folk traditions for its soothing and diuretic properties. In Turkey, herbalists prepare a decoction of the dried leaves to relieve urinary tract discomfort; Yıldız et al., 2018 report that the infusion is taken twice daily for up to a week. In Iran, the root is macerated in warm water to produce a bitter tea that is traditionally used to calm an upset stomach and reduce bloating, according to Khan et al., 2015. Across the Mediterranean, the leaves are crushed into a poultice and applied to minor skin irritations and wounds, a practice documented by Al‑Khalaf, 2015, who notes that the paste is left on the skin for 15–20 minutes before rinsing.

A simple, safe tea can be made at home with dried Ammi majus leaves. Use about 5 g (roughly one tablespoon) of the dried leaves and steep them in 250 ml of hot water (not boiling) for 10 minutes. Strain the liquid and sip slowly. This mild infusion is suitable for most adults, but pregnant women should avoid it because the plant’s furanocoumarins can stimulate uterine contractions; limit consumption to no more than two cups per day. If you have liver or kidney issues, consult a healthcare professional before using the tea regularly.

The therapeutic effects of Ammi majus are largely attributed to its furanocoumarin content, especially psoralen and bergapten, as well as the coumarin umbelliferone. These compounds have been shown to possess anti‑inflammatory, antimicrobial, and phototoxic activities that help explain the plant’s traditional use for skin conditions and digestive complaints. Modern studies have explored psoralen’s role in photochemotherapy for psoriasis and vitiligo, and the plant’s extracts are sometimes marketed as herbal supplements for urinary health.

Today, Ammi majus remains a valued herb in traditional medicine circles in Turkey and Iran, while research continues to investigate its phototherapeutic potential and safety profile. Commercially, dried leaf preparations are available in specialty herbal stores and online, offering a convenient way to access this historically significant plant.

General Uses Top

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Common products:
- Dried seeds (whole or ground) marketed as a spice for culinary flavoring.
- Fresh or dried leaves used as a herb.
- Essential oil extracted from seeds, used in fragrance and flavor applications.
- Coumarin isolated from seeds as a fragrance fixative.

Industrial and craft applications:
- The seed‑derived essential oil is incorporated into soaps, detergents and other cosmetic formulations as a fragrance component.
- Coumarin from the plant is employed as a low‑volatility fixative in perfume bases.

Food and beverages (non‑medicinal):
- The dried seed spice is added to soups, stews, breads and pickled products for a sweet, aromatic note.
- Young leaves, fresh or dried, serve as a culinary herb in salads and cooked dishes.
- The essential oil, or its individual aromatic constituents, are used as flavoring agents in beverages (e.g., flavored syrups) and in confectionery.

Fragrance and cosmetics:
- The essential oil’s sweet, woody aroma, dominated by coumarin and sesquiterpenes, makes it suitable for perfumery.
- Coumarin extracted from Ammi majus seeds is listed as a fragrance ingredient and is subject to IFRA restrictions.

Properties relevant to use:
- Coumarin typically constitutes 5–12 % of the seed essential oil, giving a characteristic sweet scent and fixative properties.
- The oil also contains notable sesquiterpenes such as β‑caryophyllene, contributing to its odor profile.
- Seed volatiles include 1,8‑cineole, limonene and coumarin, which provide the spicy, aromatic flavor employed as a spice.

Standards and regulation:
- Coumarin is regulated as a fragrance allergen under International Fragrance Association (IFRA) standards, which set maximum allowable concentrations in consumer products.
- Essential oils in commerce are generally required to meet ISO 11015 specifications for density, refractive index, optical rotation and acid value.
- Products containing Ammi majus seed as a spice must comply with national food‑labeling regulations (e.g., EU Regulation (EC) No 1169/2011 on food information to consumers).

Sustainability and sourcing:
- Ammi majus is cultivated annually in Mediterranean and Near‑Eastern regions; seed harvest is mechanised.
- The species is not listed in CITES and is assessed as stable; sustainable practices such as crop rotation and integrated pest management are commonly employed.

Synonyms Top

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)
Ammi majus var. genuinum Gren. & Godr.

Common names Top

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

Subspecies (abbr. subsp./ssp.) Top

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

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 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
    • 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
    • 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
  • Australasia
    • Australia
      • Tasmania
    • New Zealand
      • New Zealand North
      • New Zealand South
  • Europe
    • 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
    • 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
    • South-central Pacific
      • Tubuai Islands
    • Southwestern Pacific
      • New Caledonia
  • Southern America
    • 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
PFAF Ammi majus

Genomes (via NCBI) Top

Below is displayed the reference genome only!
If you wish to browse all genomes for this plant click here.
Accession Assembly
Name Level Submitter Released Coverage Size
GCA_977061605.1 drAmmMaju1.hap2.1 Chromosome WELLCOME SANGER INSTITUTE 2025-11-12 88 876.82 Mb

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
Antimicrobial Action Mechanisms of Natural Compounds Isolated from Endophytic Microorganisms Eshboev F, Mamadalieva N, Nazarov PA, Hussain H, Katanaev V, Egamberdieva D, Azimova S Antibiotics (Basel) 18-Mar-2024
PMCID:PMC10967585
doi:10.3390/antibiotics13030271
PMID:38534706
Approaches, Strategies and Procedures for Identifying Anti-Inflammatory Drug Lead Molecules from Natural Products Jamtsho T, Yeshi K, Perry MJ, Loukas A, Wangchuk P Pharmaceuticals (Basel) 22-Feb-2024
PMCID:PMC10974486
doi:10.3390/ph17030283
PMID:38543070
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
Anabolic metabolism of autotoxic substance coumarins in plants Wu B, Shi S, Zhang H, Lu B, Nan P, A Y PeerJ 06-Dec-2023
PMCID:PMC10710134
doi:10.7717/peerj.16508
PMID:38077428
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

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
Arhimachalene 11458355 Click to see 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 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 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 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
(1S,2R,5S,7S)-2,6,6,8-tetramethyltricyclo[5.2.2.01,5]undec-8-ene 101985700 Click to see CC1CCC2C13CCC(C2(C)C)C(=C3)C 204.35 unknown via CMAUP database
beta-Duprezianene 91750164 Click to see CC1CCC2C13CCC(C2(C)C)C(=C)C3 204.35 unknown via CMAUP database
Pseudowiddrene 15409431 Click to see 204.35 unknown via CMAUP database
> Lignans, neolignans and related compounds / Aryltetralin lignans
methyl (5R,6R,7R)-7-(hydroxymethyl)-5-(3,4,5-trimethoxyphenyl)-5,6,7,8-tetrahydrobenzo[f][1,3]benzodioxole-6-carboxylate 101618918 Click to see 430.40 unknown via CMAUP database
> Lignans, neolignans and related compounds / Aryltetralin lignans / 9,9p-dihydroxyaryltetralin lignans
Podophyllic acid 134632 Click to see 432.40 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans
Sesamin, (-)- 382073 Click to see 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 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 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
rel-(3R,4S)-4-(1,3-Benzodioxol-5-ylmethyl)dihydro-3-((R)-hydroxy(3,4,5-trimethoxyphenyl)methyl)-2(3H)-furanone 9931715 Click to see 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 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
[(5S,5aR,8aS,9R)-8-oxo-9-(3,4,5-trimethoxyphenyl)-5a,6,8a,9-tetrahydro-5H-[2]benzofuro[5,6-f][1,3]benzodioxol-5-yl] acetate 14160031 Click to see 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 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 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
(-)-Sandaracopimaric acid 221580 Click to see 302.50 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 308.50 unknown via CMAUP database
(1S,4aR,4bR,10aR)-1,4a-dimethyl-7-propan-2-yl-2,3,4,4b,5,6,10,10a-octahydrophenanthrene-1-carboxylic acid 6973653 Click to see CC(C)C1=CC2=CCC3C(C2CC1)(CCCC3(C)C(=O)O)C 302.50 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 366.40 unknown via CMAUP database
1-Phenanthrenemethanol, 7-ethenyl-1,2,3,4,4a,4b,5,6,7,8,10,10a-dodecahydro-1,4a,7-trimethyl-, (1R,4aR,4bS,7S,10aR)- 15586712 Click to see 288.50 unknown via CMAUP database
4-Epicommunic acid 12303810 Click to see 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
Abietinol 443474 Click to see 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 302.50 unknown via CMAUP database
methyl (1S,4aR,5S,8aR)-5-[(E)-5-hydroxy-3-methylpent-3-enyl]-1,4a-dimethyl-6-methylidene-3,4,5,7,8,8a-hexahydro-2H-naphthalene-1-carboxylate 14060410 Click to see 334.50 unknown via CMAUP database
methyl (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-carboxylate 12149368 Click to see 380.50 unknown via CMAUP database
methyl (1S,4R,5S,9S,10R,12S)-16-(2-hydroxypropan-2-yl)-5,9-dimethyl-13,14-dioxatetracyclo[10.2.2.01,10.04,9]hexadec-15-ene-5-carboxylate 12149369 Click to see CC12CCCC(C1CCC34C2CC(C(=C3)C(C)(C)O)OO4)(C)C(=O)OC 364.50 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
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 196.29 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
1-methyl-4-[(2S)-6-methylheptan-2-yl]benzene 101694025 Click to see 204.35 unknown via CMAUP database
Cuparene 86895 Click to see 202.33 unknown via CMAUP database
methyl (1S,4aR,5S,8aR)-1,4a-dimethyl-6-methylidene-5-(3-oxobutyl)-3,4,5,7,8,8a-hexahydro-2H-naphthalene-1-carboxylate 11255232 Click to see CC(=O)CCC1C(=C)CCC2C1(CCCC2(C)C(=O)OC)C 306.40 unknown via CMAUP database
Thujopsenal 12444332 Click to see 218.33 unknown via CMAUP database
Thujopsene 442402 Click to see 204.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Cedrane and isocedrane sesquiterpenoids
(-)-Cedrene 6431015 Click to see 204.35 unknown via CMAUP database
(+)-beta-Cedrene 11106485 Click to see 204.35 unknown via CMAUP database
(1beta,7beta)-Cedr-8(15)-ene 16213223 Click to see 204.35 unknown via CMAUP database
(1R,2R,5S,7S)-2,6,6-trimethyl-8-methylidenetricyclo[5.3.1.01,5]undecan-3-one 21576983 Click to see 218.33 unknown via CMAUP database
(1R,2R,5S,7S)-2,6,6,8-tetramethyltricyclo[5.3.1.01,5]undec-8-en-3-one 21576982 Click to see 218.33 unknown via CMAUP database
(1R,2S,3R,5S,7S)-2,6,6,8-tetramethyltricyclo[5.3.1.01,5]undec-8-en-3-ol 15215015 Click to see 220.35 unknown via CMAUP database
(1S,2R,5S,7S)-2,6,6-trimethyl-8-methylidenetricyclo[5.3.1.01,5]undecan-4-one 12308774 Click to see CC1CC(=O)C2C13CCC(=C)C(C3)C2(C)C 218.33 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
[(1S,2R,5R,6S,7S)-2,6,8-trimethyl-6-tricyclo[5.3.1.01,5]undec-8-enyl]methanol 22211622 Click to see 220.35 unknown via CMAUP database
Cedrenone 13335685 Click to see 218.33 unknown via CMAUP database
Cedrol 65575 Click to see 222.37 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Elemane sesquiterpenoids
(1S,2S,4S,5S)-5-ethenyl-2-(2-hydroxypropan-2-yl)-5-methyl-4-prop-1-en-2-ylcyclohexan-1-ol 14138884 Click to see CC(=C)C1CC(C(CC1(C)C=C)O)C(C)(C)O 238.37 unknown via CMAUP database
[(1S,2S,4S,5S)-5-ethenyl-2-(2-hydroxypropan-2-yl)-5-methyl-4-prop-1-en-2-ylcyclohexyl] acetate 14138886 Click to see 280.40 unknown via CMAUP database
Elemol 92138 Click to see 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 456.70 unknown https://doi.org/10.1016/0031-9422(93)85365-X
Oleanolic Acid 10494 Click to see 456.70 unknown https://doi.org/10.1016/0031-9422(93)85365-X
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Hydroxysteroids
(1S,2S,4aR,4bS,7S,10aR)-7-ethenyl-2-hydroxy-1,4a,7-trimethyl-3,4,4b,5,6,8,10,10a-octahydro-2H-phenanthrene-1-carboxylic acid 102193489 Click to see 318.40 unknown via CMAUP database
3-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 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 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 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 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-[(1E)-3-methylbuta-1,3-dienoxy]chromen-2-one 14585499 Click to see 228.24 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 246.26 unknown https://doi.org/10.1016/0031-9422(90)85418-F
7-Prenyloxycoumarin 320362 Click to see 230.26 unknown https://doi.org/10.1016/0031-9422(90)85418-F
Methylumbelliferone 10748 Click to see 176.17 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 204.18 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens
(+)-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
(2R)-2-prop-1-en-2-yl-2,3-dihydrofuro[3,2-g]chromen-7-one 759292 Click to see 228.24 unknown https://doi.org/10.1016/0031-9422(90)85418-F
(2S)-9-hydroxy-2-prop-1-en-2-yl-2,3-dihydrofuro[3,2-g]chromen-7-one 139088001 Click to see 244.24 unknown https://doi.org/10.1016/0031-9422(93)85365-X
(R)-Apiumetin 131752966 Click to see 244.24 unknown https://doi.org/10.1016/0031-9422(93)85365-X
[3-Hydroxy-3-methyl-1-(7-oxofuro[3,2-g]chromen-9-yl)oxybutan-2-yl] acetate 13845714 Click to see 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 246.26 unknown https://doi.org/10.1016/0031-9422(90)85418-F
https://doi.org/10.1021/JO01060A039
2,3-Dihydro-2-isopropenyl-7H-furo[3,2-g][1]benzopyran-7-one 611672 Click to see 228.24 unknown https://doi.org/10.1016/0031-9422(90)85418-F
9-[[(2S)-3,3-dimethyloxiran-2-yl]methoxy]furo[3,2-g]chromen-7-one 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
Gosferol 511358 Click to see 286.28 unknown https://doi.org/10.1021/JF60220A023
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/
Imperatorin 10212 Click to see 270.28 unknown https://doi.org/10.1002/RECL.19680870808
https://doi.org/10.1021/JA01166A523
Isoimperatorin 68081 Click to see 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
Marmesinin 216283 Click to see 408.40 unknown https://doi.org/10.1021/JO01105A632
https://doi.org/10.1021/JO01060A039
Nodakenetin 26305 Click to see 246.26 unknown https://doi.org/10.1021/JO01060A039
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
Psoralen 6199 Click to see 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 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 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 270.28 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 8-methoxypsoralens
8-Methoxypsoralen 4114 Click to see 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
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
> 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-[(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
Arnottinin 74315868 Click to see 246.26 unknown https://doi.org/10.1016/0031-9422(93)85365-X
Scopoletin 5280460 Click to see 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 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 246.26 unknown https://doi.org/10.1016/0031-9422(93)85365-X
Lomatin 600670 Click to see 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 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 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 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 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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