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Aegle marmelos

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 UUID6440078f0135e122058924
Scientific name Aegle marmelos
Authority (L.) Corrêa
First published in Trans. Linn. Soc. London 5: 223 (1800)

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.

Aegle marmelos, commonly called bael, has a long history of use in South Asian folk medicine. In Ayurvedic practice, the fruit pulp is steeped in hot water to produce a mild tea that is taken for cough, sore throat, and mild fever; the leaves are similarly decocted for digestive complaints and for treating skin eruptions (Sharma et al., 2015). In Bangladesh, the bark is macerated in alcohol to make a tincture that is applied topically as a poultice for wounds and ulcers, while the fruit is boiled into a decoction to relieve dysentery and diarrhea (Khan et al., 2018). Nepalese healers also prepare a leaf infusion to soothe menstrual cramps and to reduce inflammation in arthritis (Bhandari et al., 2019). These preparations all involve infusions, decoctions, tinctures, or poultices, and they illustrate the plant’s versatility across three distinct cultural traditions.

A simple, safe tea can be made from fresh bael fruit. Take 1 cup (≈ 250 mL) of boiling water and add the pulp of one medium fruit, or 1 tablespoon of finely chopped leaves. Let the mixture steep for 5–7 minutes, then strain. Drink one cup twice daily. The tea is generally well tolerated, but pregnant women should avoid large quantities of the fruit pulp because of its mild emmenagogue activity. If you have a history of kidney stones, consult a healthcare provider before using bael regularly, as the fruit contains oxalates.

The therapeutic effects of bael are linked to several well‑documented phytochemicals. The fruit pulp is rich in flavonoids such as quercetin and kaempferol, which have antioxidant and anti‑inflammatory properties. The bark contains alkaloids like bael alkaloid and coumarins such as esculetin, which contribute to its antimicrobial and antidiarrheal actions. Phenolic acids, including gallic acid, are also present and help to soothe irritated mucous membranes. These constituents provide a biochemical basis for the plant’s traditional uses in treating respiratory, digestive, and skin ailments.

Modern research continues to validate bael’s medicinal potential. Recent studies in the Journal of Ethnopharmacology have confirmed its antibacterial activity against common gastrointestinal pathogens, and commercial herbal vendors now offer bael fruit tea, dried leaf powders, and standardized bark extracts. The plant remains an integral part of contemporary Ayurvedic formulations and is still widely used by rural communities in India, Bangladesh, and Nepal for everyday health maintenance.

General Uses Top

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Common products:
Fruit pulp is processed into beverages, syrups, and confectionery products; it is also used as a flavoring agent in non-medicinal formulations and as a natural acidulant. Established products include “bael” fruit beverages and preserves. The fruit rind yields pectin used as a gelling agent in jams and jellies.

Industrial and craft applications:
Wood is used locally for agricultural implements, tool handles, and furniture. The tree yields a gum/resin that functions as a non-medicinal adhesive and coating binder; it is compatible with natural dyes and acts as a fixative in craft applications. Natural-dye processes employ the fruit pulp or rind as a brown dye for protein fibers such as wool and silk.

Food and beverages (non-medicinal):
Pulp is processed into drinks and syrups; candied pulp and fruit leather are produced. The rind’s pectin is used as a food gelling agent; total soluble solids and acidity make it suitable for syrup and beverage bases. Bael essential oil is used by the flavor and fragrance industry for citrus-like aromatic notes.

Colorants and tanning:
Fruit pulp/rind provide brown natural dyes for textiles, notably protein fibers. Leather tanning with the fruit is reported historically; tannins in the pulp contribute to the dye/tanning effect and fix colors.

Wood and fiber:
Wood is used in rural construction and tool-making; specific gravity and durability are suitable for such applications. No bast-fiber or commercial fiber use is documented.

Fragrance and cosmetics:
Bael leaf and fruit essential oils are used in perfumery and as fragrance components in non-medicinal cosmetic bases.

Properties relevant to use:
Acidity and pectin content in the pulp enable beverage and confectionery processing; the essential oil’s composition yields citrus-aromatic notes. Tannins in the pulp contribute to dyeing and tanning; the gum provides adhesive/coating functionality.

Scientific/model-organism use:
The species is used in agronomic and genetic studies; it is represented in national germplasm repositories and referenced in databases (e.g., GBIF) to support taxonomy and conservation resources. No standardized model-organism protocols are established.

Standards and regulation:
Food-grade pectin production follows national and international food additive standards (e.g., purity criteria and heavy-metal limits). Flavor/fragrance uses are subject to relevant safety and quality standards (e.g., FEMA/GRAS status for flavoring materials, ISO/ASTM methods for fragrance evaluation).

Sustainability and sourcing:
As a hardy tree adapted to semi-arid and tropical conditions, it is cultivated in India and neighboring regions; wild harvesting remains significant in some areas. Sustainable practices include on-farm processing of pulp/gum to reduce waste and support rural livelihoods.

Synonyms Top

Scientific name Authority First published in
Aegle marmelos var. mahurensis Zate Indian J. Forest. 5: 36 (1982)
Belou marmelos (L.) A.Lyons Pl. Nam. , ed. 2: 69 (1907)
Bilacus marmelos Kuntze Revis. Gen. Pl. 1: 99 (1891)
Crateva marmelos L. Sp. Pl. : 444 (1753)
Crateva religiosa Ainslie Mat. Med. Hind. 124.
Feronia pellucida Roth Nov. Pl. Sp. : 384 (1821)
Aegle marmelos var. tamilnadensis (S.A.Kader) D.D.Pramanick & Mastakar Fl. Pl. India Annot. Checkl. 1: 225. 2020
Aegle tamilnadensis S.A.Kader J. Econ. Taxon. Bot. 39: 544. 2016 [dt. 2015; publ. 30 Jun 2016]

Common names Top

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Language Common/alternative name
English indian bael
English japanese bitter orange
English bael fruit
English bengal quince
English golden apple
English stone apple
English wood apple
English bel fruit
English bael fruit of india
Spanish membrillo de bengala
Spanish aegle marmelos var. mahurensis
Spanish feronia pellucida
Spanish crateva marmelos
Spanish belou marmelos
Spanish bilacus marmelos
Spanish crateva religiosa
ace bi
Arabic قثاء هندي
Arabic بل
Assamese বেল
ban bila
Bulgarian бенгалска дюля
bho श्रीफल
Bengali বিল্ব
Bengali শ্রীফল
Bengali বেল
Catalan bael
Czech oslizák líbezný
German belbaum
German bilva
German madjobaum
German bengalische quitte
Greek αίγλη
Greek ιαπωνική πικροπορτοκαλιά
Greek κυδωνιά της Βεγγάλης
Greek μπάελ
Greek μπελ
Greek μπίλι
Greek ξυλομηλιά
Greek πετρομηλιά
Greek χρυσό μήλο
Greek αίγλη η μάρμελος
Persian بکرایی
Finnish belahedelmä
French arbre bael
Gujarati બીલી
Hindi बेल
Hindi बेल फल
Hindi श्री फल
Hindi बिल्व
Indonesian maja
Japanese マトゥーム
Japanese ベルノキ
jv maja
Khmer ដើមព្នៅ
Kannada ಅಜೆಲ್ ಮರ್ಮೆಲಸ್
Kannada ಬಿಲ್ವಪತ್ರೆ ಮರ
koi Баиль
kv Баиль
lbe Баиль
mad billâ gheḍḍhâng
mad billâ paè'
mad billâ
mai बेल
Malayalam bael
Malayalam കൂവളം
mnw ဗဳ၊ တၞံ
Marathi बेल
mrj Баиль
Malay pokok maja
Burmese ဥသျှစ်
Burmese ဥသျှစ်ပင်
Nepali बेल
Dutch madja
Dutch bael
Dutch slijmappelboom
Dutch slijmappel
Dutch crateva marmelos
Oriya ବେଲ
Punjabi ਬਿਲ
pam bael
Polish bilwa
Polish klejowiec jadalny
Polish kleiszcze smakowite
Punjab بیل گری
Portuguese bael
Russian Бильва
Russian Баиль
sa अश्वत्थः
sa बिल्वम्
sa बिल्वः
sat ᱥᱤ.ᱡᱚ
sat ᱥᱤᱧᱡᱟᱹ
sd بيل ڦل
su maja
Swedish marmeladträd
Swedish marmeladträdssläktet
Swedish indiskt marmeladträd
Tamil வில்வ மரம்
Tamil வில்வம்
tcy ಬಿಲ್ವ ಪತ್ರೆ
Telugu ఎగెల్
Telugu బిల్వ
Telugu బిల్వపత్రం
Telugu బిల్వము
Telugu మారేడు
Thai มะตูม
udm Баиль
Urdu بیلگری
Uzbek bael
Chinese 箭杆七
Chinese 印度枳
Chinese 木橘
Chinese 硬皮橘
Chinese 孟加拉苹果

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • Bangladesh
      • East Himalaya
      • India
      • Nepal
      • Pakistan
      • Sri Lanka
      • West Himalaya
    • Indo-China
      • Andaman Islands
      • Cambodia
      • Laos
      • Myanmar
      • Vietnam
    • Malesia
      • Lesser Sunda Islands
      • Sulawesi

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000521533
UNII D556G3D4C5
USDA Plants AEMA3
Tropicos 28100016
INPN 705775
KEW urn:lsid:ipni.org:names:770819-1
The Plant List kew-2623456
PFAF Aegle marmelos
Open Tree Of Life 490374
NCBI Taxonomy 68527
IUCN Red List 156233789
IPNI 770819-1
iNaturalist 325928
GBIF 5421195
Freebase /m/06f1wh
EPPO AELMA
EOL 483583
US Library of Congress sh85010929
USDA GRIN 1560
Wikipedia Aegle_marmelos
CMAUP NPO5045

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_030449875.1 ASM3044987v1 Contig Huazhong Agricultural University 2023-07-13 150 263.21 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
Detection and molecular characterization of ‘Candidatus Phytoplasma australasiaticum’ in Aegle marmelos: a fruit of high medicinal values in India Singh SK, Ranebennur H, Gupta S, Pandey H, Singh V, Rao GP 3 Biotech 03-May-2024
PMCID:PMC11068701
doi:10.1007/s13205-024-03995-8
PMID:38706929
Efficacy and safety of the Ayurvedic herbal preparation Maharishi Amrit Kalash: a systematic review of randomized controlled trials Koch AK, Patel M, Gupta S, Wullenkord R, Jeitler M, Kessler CS Front Med (Lausanne) 16-Apr-2024
PMCID:PMC11058942
doi:10.3389/fmed.2024.1325037
PMID:38690176
Physiological and molecular insights into the allelopathic effects on agroecosystems under changing environmental conditions Kumar N, Singh H, Giri K, Kumar A, Joshi A, Yadav S, Singh R, Bisht S, Kumari R, Jeena N, Khairakpam R, Mishra G Physiol Mol Biol Plants 06-Apr-2024
PMCID:PMC11018569
doi:10.1007/s12298-024-01440-x
PMID:38633277
Mitigation Potential of Herbal Extracts and Constituent Bioactive Compounds on Salmonella in Meat-Type Poultry Orimaye OE, Ekunseitan DA, Omaliko PC, Fasina YO Animals (Basel) 03-Apr-2024
PMCID:PMC11011123
doi:10.3390/ani14071087
PMID:38612326
Systematic Evaluation of Aegle marmelos-Derived Compounds: Potential Therapeutic Agents Against Inflammation and Oxidative Stress Sankirtha H, Thirumani L, Alex A, Neha B, Vimal S, Madar IH Cureus 03-Apr-2024
PMCID:PMC11066703
doi:10.7759/cureus.57499
PMID:38706993
Extracting bioactive compounds and proteins from Bacopa monnieri using natural deep eutectic solvents Vo TP, Nguyen TH, Nguyen VK, Dang TC, Nguyen LG, Chung TQ, Vo TT, Nguyen DQ PLoS One 29-Mar-2024
PMCID:PMC10980249
doi:10.1371/journal.pone.0300969
PMID:38551952
Overview of Ethnobotanical–Pharmacological Studies Carried Out on Medicinal Plants from the Serra da Estrela Natural Park: Focus on Their Antidiabetic Potential Lahlou RA, Carvalho F, Pereira MJ, Lopes J, Silva LR Pharmaceutics 25-Mar-2024
PMCID:PMC11054966
doi:10.3390/pharmaceutics16040454
PMID:38675115
An Alarming Decline in the Nutritional Quality of Foods: The Biggest Challenge for Future Generations’ Health Bhardwaj RL, Parashar A, Parewa HP, Vyas L Foods 14-Mar-2024
PMCID:PMC10969708
doi:10.3390/foods13060877
PMID:38540869
Cosmeceuticals: A transit state from synthetic to natural Sathyaseelan S, Rao BH, Anushmati S Indian J Pharmacol 08-Mar-2024
PMCID:PMC11001171
doi:10.4103/ijp.ijp_244_21
PMID:38454588
Syrupy herbal formulation of green bean pod extract of Phaseolus vulgaris L.: Formulation optimization by central composite design, and evaluation for anti-urolithiatic activity Noorulla KM, Doyo Dalecha D, Jemal Haji M, S R, Arumugam M, Zafar A, Gadisa Gobena W, Mekit S, Haji Negawo H, Hussein M, Fekadu Demessie H, Yasir M Heliyon 29-Feb-2024
PMCID:PMC10943400
doi:10.1016/j.heliyon.2024.e27330
PMID:38495171
Development and Assessment of SNP Genotyping Arrays for Citrus and Its Close Relatives Hiraoka Y, Ferrante SP, Wu GA, Federici CT, Roose ML Plants (Basel) 29-Feb-2024
PMCID:PMC10935022
doi:10.3390/plants13050691
PMID:38475537
Use of Medicinal Plants in the Process of Wound Healing: A Literature Review Cedillo-Cortezano M, Martinez-Cuevas LR, López JA, Barrera López IL, Escutia-Perez S, Petricevich VL Pharmaceuticals (Basel) 27-Feb-2024
PMCID:PMC10975678
doi:10.3390/ph17030303
PMID:38543089
Scopoletin: a review of its pharmacology, pharmacokinetics, and toxicity Gao XY, Li XY, Zhang CY, Bai CY Front Pharmacol 23-Feb-2024
PMCID:PMC10923241
doi:10.3389/fphar.2024.1268464
PMID:38464713
Use of checkerboard assay to determine the synergy between essential oils extracted from leaves of Aegle marmelos (L.) Correa and nystatin against Candida albicans Kamble PA, Phadke M Ayu 21-Feb-2024
PMCID:PMC10946663
doi:10.4103/ayu.ayu_397_21
PMID:38505112
An integrative ayurvedic approach in management of breast abscess – A case report Jaivarshaa GV P, Dasar D, Biswas S, Kumar A J Ayurveda Integr Med 21-Feb-2024
PMCID:PMC10897883
doi:10.1016/j.jaim.2024.100890
PMID:38387146

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Alkaloids and derivatives
(-)-Montanine 11087935 Click to see COC1C=C2C(CC1O)N3CC2C4=CC5=C(C=C4C3)OCO5 301.34 unknown https://doi.org/10.1080/14786410310001608037
> Alkaloids and derivatives / Protopine alkaloids
Allocryptopine 98570 Click to see 369.40 unknown https://doi.org/10.1039/JR9590001922
> Benzenoids / Anthracenes / Anthraquinones
1-Methyl-2-(3-methylbut-2-enoxy)anthracene-9,10-dione 46201020 Click to see 306.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.10.013
2-Isopropenyl-4-methyl-1-oxa-cyclopenta[b]anthracene-5,10-dione 45103626 Click to see 302.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.10.013
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzamides
N-[(2S)-2-hydroxy-2-(4-methoxyphenyl)ethyl]benzamide 6482976 Click to see 271.31 unknown https://doi.org/10.1016/J.BMCL.2008.08.024
Tembamide 177583 Click to see COC1=CC=C(C=C1)C(CNC(=O)C2=CC=CC=C2)O 271.31 unknown https://doi.org/10.1016/J.BMCL.2008.08.024
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acids
Valencic Acid 267137 Click to see CC(=CCOC1=CC=C(C=C1)C(=O)O)C 206.24 unknown https://doi.org/10.1016/J.PHYTOCHEM.2011.11.018
https://doi.org/10.1080/14786410310001608037
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / P-methoxybenzoic acids and derivatives
4-Methoxybenzoic Acid 7478 Click to see 152.15 unknown https://doi.org/10.1080/14786410310001608037
> Benzenoids / Benzene and substituted derivatives / Benzylethers
(E)-N-[(2S)-2-ethoxy-2-(4-methoxyphenyl)ethyl]-3-phenylprop-2-enamide 163186897 Click to see 325.40 unknown https://doi.org/10.1016/S0031-9422(00)88714-2
(E)-N-[(2S)-2-methoxy-2-[4-(3-methylbut-2-enoxy)phenyl]ethyl]-3-phenylprop-2-enamide 163185622 Click to see 365.50 unknown https://doi.org/10.1016/S0031-9422(00)88714-2
N-[2-methoxy-2-(4-methoxyphenyl)ethyl]-3-phenylprop-2-enamide 400060 Click to see COC1=CC=C(C=C1)C(CNC(=O)C=CC2=CC=CC=C2)OC 311.40 unknown https://doi.org/10.1016/J.BMCL.2008.08.024
https://doi.org/10.1016/S0031-9422(00)88714-2
https://doi.org/10.1016/J.TET.2008.11.088
> Benzenoids / Benzene and substituted derivatives / Benzyloxycarbonyls
[(1R)-1-[4-(3-methylbut-2-enoxy)phenyl]-2-[[(E)-3-phenylprop-2-enoyl]amino]ethyl] acetate 163189088 Click to see CC(=CCOC1=CC=C(C=C1)C(CNC(=O)C=CC2=CC=CC=C2)OC(=O)C)C 393.50 unknown https://doi.org/10.1016/J.TET.2008.11.088
[1-[4-(3-Methylbut-2-enoxy)phenyl]-2-(3-phenylprop-2-enoylamino)ethyl] acetate 162970094 Click to see CC(=CCOC1=CC=C(C=C1)C(CNC(=O)C=CC2=CC=CC=C2)OC(=O)C)C 393.50 unknown https://doi.org/10.1016/J.TET.2008.11.088
> Benzenoids / Benzene and substituted derivatives / Phenylpropanes
2-Tert-Butylphenol 6923 Click to see 150.22 unknown https://doi.org/10.1078/094471103322004794
> Benzenoids / Benzene and substituted derivatives / Styrenes
N-[2-hydroxy-2-(4-hydroxyphenyl)ethyl]-3-phenylprop-2-enamide 73115961 Click to see 283.32 unknown https://doi.org/10.1016/S0031-9422(00)86977-0
> Benzenoids / Naphthalenes / Naphthoquinones
Plumbagin 10205 Click to see 188.18 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.10.013
> Benzenoids / Phenol ethers
(E)-N-[(2R)-2-hydroxy-2-[4-(3-methylbut-2-enoxy)phenyl]ethyl]-3-phenylprop-2-enamide 163187632 Click to see 351.40 unknown https://doi.org/10.1016/S0031-9422(00)86977-0
https://doi.org/10.1016/0031-9422(81)83112-3
https://doi.org/10.1016/J.PHYTOCHEM.2011.11.018
(E)-N-[(2R)-2-hydroxy-2-[4-[(2S)-2-hydroxy-3-methylbut-3-enoxy]phenyl]ethyl]-3-phenylprop-2-enamide 163188272 Click to see 367.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2011.11.018
Marmeline 131750977 Click to see 351.40 unknown https://doi.org/10.1016/S0031-9422(00)86977-0
N-[2-[4-(3-methylbut-2-enoxy)phenyl]ethenyl]-3-phenylprop-2-enamide 75050399 Click to see CC(=CCOC1=CC=C(C=C1)C=CNC(=O)C=CC2=CC=CC=C2)C 333.40 unknown https://doi.org/10.1016/J.BMCL.2008.08.024
N-[2-[4-(3-methylbut-2-enoxy)phenyl]ethyl]-3-phenylprop-2-enamide 75050400 Click to see 335.40 unknown https://doi.org/10.1016/S0031-9422(00)86977-0
https://doi.org/10.1016/J.BMCL.2008.08.024
> Benzenoids / Phenol ethers / Anisoles
(5R)-5-(4-methoxyphenyl)-2-[(E)-2-phenylethenyl]-4,5-dihydro-1,3-oxazole 102034873 Click to see 279.30 unknown https://doi.org/10.1016/J.TET.2008.11.088
(5S)-5-(4-methoxyphenyl)-2-phenyl-4,5-dihydro-1,3-oxazole 163072561 Click to see 253.29 unknown https://doi.org/10.1590/S0103-50532011000100024
5-(4-Methoxyphenyl)-2-(2-phenylethenyl)-4,5-dihydro-1,3-oxazole 74433641 Click to see 279.30 unknown https://doi.org/10.1016/J.TET.2008.11.088
N-[2-(4-methoxyphenyl)ethenyl]-3-phenylprop-2-enamide 73187989 Click to see 279.30 unknown https://doi.org/10.1016/S0031-9422(00)86977-0
https://doi.org/10.1016/J.BMCL.2008.08.024
> Benzenoids / Phenols / Methoxyphenols
Npc482626 24667 Click to see 360.50 unknown https://doi.org/10.1078/094471103322004794
Vanillin 1183 Click to see COC1=C(C=CC(=C1)C=O)O 152.15 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.10.013
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
Gamma-Terpinene 7461 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1995.9698520
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 7,9-epoxylignans
(+)-9'-Isovaleroxylariciresinol 46211187 Click to see 444.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3602229/
> Lignans, neolignans and related compounds / Lignan glycosides
(-)-2|A-O-(|A-D-Glucopyranosyl)lyoniresinol 10438246 Click to see COC1=CC(=CC(=C1O)OC)C2C(C(CC3=CC(=C(C(=C23)OC)O)OC)COC4C(C(C(C(O4)CO)O)O)O)CO 582.60 unknown https://doi.org/10.1248/CPB.42.1924
(+)-Lyoniresinol 3alpha-O-beta-D-glucopyranoside 10483388 Click to see 582.60 unknown https://doi.org/10.1248/CPB.42.1924
(+)-Lyoniresinol 9-glucoside 74256819 Click to see 582.60 unknown https://doi.org/10.1248/CPB.42.1924
(2R,3R,4S,5S,6R)-2-(((1R,2R,3R)-7-hydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)-3-(hydroxymethyl)-6,8-dimethoxy-1,2,3,4-tetrahydronaphthalen-2-yl)methoxy)-6-(hydroxymethyl)oxane-3,4,5-triol 10348278 Click to see 582.60 unknown https://doi.org/10.1248/CPB.42.1924
(2R,3R,4S,5S,6R)-2-[[(1R,2S,3S)-7-hydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)-3-(hydroxymethyl)-6,8-dimethoxy-1,2,3,4-tetrahydronaphthalen-2-yl]methoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 10031185 Click to see COC1=CC(=CC(=C1O)OC)C2C(C(CC3=CC(=C(C(=C23)OC)O)OC)CO)COC4C(C(C(C(O4)CO)O)O)O 582.60 unknown https://doi.org/10.1248/CPB.42.1924
2-((7-Hydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)-3-(hydroxymethyl)-6,8-dimethoxy-1,2,3,4-tetrahydronaphthalen-2-yl)methoxy)-6-(hydroxymethyl)oxane-3,4,5-triol 14521083 Click to see 582.60 unknown https://doi.org/10.1248/CPB.42.1924
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Palmitic Acid 985 Click to see 256.42 unknown https://doi.org/10.1078/094471103322004794
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
7-[(E,4R,6R)-4,7-dihydroxy-3,7-dimethyl-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoct-2-enoxy]chromen-2-one 11813223 Click to see 510.50 unknown https://doi.org/10.1246/CL.1995.881
7-[[(2E,4R,6R)-6-(I(2)-D-Glucopyranosyloxy)-4,7-dihydroxy-3,7-dimethyl-2-octen-1-yl]oxy]-2H-1-benzopyran-2-one 73113622 Click to see 510.50 unknown https://doi.org/10.1246/CL.1995.881
Aegelinoside A 44579743 Click to see 459.50 unknown https://doi.org/10.1016/J.BMCL.2008.08.024
Aegelinoside B 44579744 Click to see 459.50 unknown https://doi.org/10.1016/J.BMCL.2008.08.024
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
[(E,3R)-2-hydroxy-2,6-dimethyl-8-(2-oxochromen-7-yl)oxyoct-6-en-3-yl] octadeca-9,12-dienoate 163003104 Click to see CCCCCC=CCC=CCCCCCCCC(=O)OC(CCC(=CCOC1=CC2=C(C=C1)C=CC(=O)O2)C)C(C)(C)O 594.80 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3602229/
Methyl 9,12-octadecadienoate 8203 Click to see 294.50 unknown https://doi.org/10.1078/094471103322004794
Methyl linoleate 5284421 Click to see 294.50 unknown https://doi.org/10.1078/094471103322004794
R-(+)-Marmin-6'-Linoleate 71584690 Click to see 594.80 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3602229/
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
beta-Ocimene, (3Z)- 5320250 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1995.9698520
Linalool 6549 Click to see 154.25 unknown https://doi.org/10.1080/10412905.1995.9698520
Myrcene 31253 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1995.9698520
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(+-)-alpha-Pinene 6654 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1995.9698520
(+-)-Myrtenol 10582 Click to see 152.23 unknown https://doi.org/10.1080/10412905.1995.9698520
(3R)-4-methylidene-1-(propan-2-yl)bicyclo[3.1.0]hexan-3-ol 42626428 Click to see 152.23 unknown https://doi.org/10.1080/10412905.1995.9698520
Beta-Pinene 14896 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1995.9698520
Sabinene 18818 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1995.9698520
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(-)-cis-Carveol 330573 Click to see CC1=CCC(CC1O)C(=C)C 152.23 unknown https://doi.org/10.1080/10412905.1995.9698520
(-)-trans-Carveol 94221 Click to see CC1=CCC(CC1O)C(=C)C 152.23 unknown https://doi.org/10.1080/10412905.1995.9698520
(+-)-Piperitone 6987 Click to see 152.23 unknown https://doi.org/10.1080/10412905.1995.9698520
4-Terpineol, (+/-)- 11230 Click to see CC1=CCC(CC1)(C(C)C)O 154.25 unknown https://doi.org/10.1080/10412905.1995.9698520
alpha-PHELLANDRENE 7460 Click to see CC1=CCC(C=C1)C(C)C 136.23 unknown https://doi.org/10.1021/JF00108A040
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1080/10412905.1995.9698520
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
alpha-Elemene 80048 Click to see CC(C)C1=CC(=C(C)C)CCC1(C)C=C 204.35 unknown https://doi.org/10.1080/10412905.1995.9698520
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1080/10412905.1995.9698520
Caryophyllene oxide 1742210 Click to see 220.35 unknown https://doi.org/10.1080/10412905.1995.9698520
Curcumene 92139 Click to see 202.33 unknown https://doi.org/10.1080/10412905.1995.9698520
Humulene 5281520 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1995.9698520
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Illudanes and illudins / Melleolides and analogues
Melledonal C 189493 Click to see CC1=C(C(=CC(=C1Cl)OC)O)C(=O)OC2CC3(C2(C(=CC4(C3C(C(C4)(C)C)O)O)C=O)O)C 480.90 unknown https://doi.org/10.1246/CL.1995.881
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
2H-1-Benzopyran-2-one, 7-[[(2E)-3,7-dimethyl-2,6-octadienyl]oxy]- 400073 Click to see CC(=CCCC(=CCOC1=CC2=C(C=C1)C=CC(=O)O2)C)C 298.40 unknown https://doi.org/10.1590/S0103-50532011000100024
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3602229/
7-((2E)-3,7-Dimethylocta-2,6-Dienoxy)-6-Methoxychromen-2-One 5319406 Click to see 328.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3602229/
Auraptene 1550607 Click to see 298.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3602229/
https://doi.org/10.1590/S0103-50532011000100024
https://doi.org/10.1055/S-2006-960014
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Betulinic Acid 64971 Click to see 456.70 unknown https://doi.org/10.1080/14786410310001608037
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1055/S-2006-960014
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids / Limonoids
[(1S,2R,3R,5R,7R,10S,11R,14R,15S)-15-[(2R,3S,5R)-5-[(2S)-3,3-dimethyloxiran-2-yl]-2-hydroxyoxolan-3-yl]-3-hydroxy-2,6,6,10-tetramethyl-7-pentacyclo[12.3.1.01,14.02,11.05,10]octadecanyl] 3-methylbutanoate 163078747 Click to see CC(C)CC(=O)OC1CCC2(C3CCC45CC4(C3(C(CC2C1(C)C)O)C)CCC5C6CC(OC6O)C7C(O7)(C)C)C 572.80 unknown https://doi.org/10.1055/S-0031-1273558
[15-[5-(3,3-Dimethyloxiran-2-yl)-2-hydroxyoxolan-3-yl]-3-hydroxy-2,6,6,10-tetramethyl-7-pentacyclo[12.3.1.01,14.02,11.05,10]octadecanyl] 3-methylbutanoate 14165901 Click to see CC(C)CC(=O)OC1CCC2(C3CCC45CC4(C3(C(CC2C1(C)C)O)C)CCC5C6CC(OC6O)C7C(O7)(C)C)C 572.80 unknown https://doi.org/10.1055/S-0031-1273558
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 Click to see 414.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.10.013
17-(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 122544 Click to see 412.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.10.013
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.10.013
beta-Sitosterol 3-O-beta-D-galactopyranoside 296119 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.10.013
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.10.013
Stigmasterol 5280794 Click to see 412.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.10.013
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
(1S,2Z,4Z,6Z)-1,5-dimethylcycloocta-2,4,6-trien-1-ol 162878378 Click to see 150.22 unknown https://doi.org/10.1271/BBB1961.46.1873
1,5-Dimethylcycloocta-2,4,6-trien-1-ol 162878377 Click to see 150.22 unknown https://doi.org/10.1271/BBB1961.46.1873
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glucuronides / O-glucuronides
3-O-beta-D-Galactopyranuronosyl-D-galactose 13915951 Click to see C(C1C(C(C(C(O1)O)O)OC2C(C(C(C(O2)C(=O)O)O)O)O)O)O 356.28 unknown https://doi.org/10.1016/S0008-6215(00)85922-4
3-O-beta-D-Glucopyranuronosyl-beta-D-galactopyranose 5288377 Click to see 356.28 unknown https://doi.org/10.1016/S0008-6215(00)85922-4
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
2-O-(alpha-L-rhamnopyranosyl)-alpha-L-rhamnopyranose 46224590 Click to see 310.30 unknown https://doi.org/10.1016/S0008-6215(00)85922-4
3-O-beta-D-galactopyranosyl-beta-D-galactopyranose 5288340 Click to see 342.30 unknown https://doi.org/10.1016/S0008-6215(00)85922-4
6-(Hydroxymethyl)-4-(3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl)oxyoxane-2,3,5-triol 4195243 Click to see 342.30 unknown https://doi.org/10.1016/S0008-6215(00)85922-4
GlyTouCan:G50656OG 14585977 Click to see 310.30 unknown https://doi.org/10.1016/S0008-6215(00)85922-4
N-[(2S)-2-(4-methoxyphenyl)-2-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyethyl]-3-phenylprop-2-enamide 162867348 Click to see 459.50 unknown https://doi.org/10.1016/J.BMCL.2008.08.024
N-[2-(4-methoxyphenyl)-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyethyl]-3-phenylprop-2-enamide 75050411 Click to see 459.50 unknown https://doi.org/10.1016/J.BMCL.2008.08.024
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
beta-D-Glucopyranoside, 2-(hydroxymethyl)phenyl 5145 Click to see 286.28 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.10.013
Salicin 439503 Click to see 286.28 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.10.013
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
6-deoxy-Hex(?1-2)6-deoxy-Hex(?1-5)Penf 163025007 Click to see 442.40 unknown https://doi.org/10.1016/S0008-6215(00)85922-4
Gal(b1-3)[GlcA(b1-6)]Gal(b1-3)b-Gal 162983832 Click to see 680.60 unknown https://doi.org/10.1016/S0008-6215(00)85922-4
GlcA(b1-3)Gal(b1-2)a-Rha 162913077 Click to see 502.40 unknown https://doi.org/10.1016/S0008-6215(00)85922-4
GlcA(b1-3)Gal(b1-3)[GlcA(b1-6)]b-Gal 163015292 Click to see 694.50 unknown https://doi.org/10.1016/S0008-6215(00)85922-4
GlcA(b1-3)Gal(b1-3)b-Gal 163190772 Click to see 518.40 unknown https://doi.org/10.1016/S0008-6215(00)85922-4
Hex(?1-3)[HexA(?1-6)]Hex(?1-3)Hex 162983831 Click to see C(C1C(C(C(C(O1)O)O)OC2C(C(C(C(O2)COC3C(C(C(C(O3)C(=O)O)O)O)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 680.60 unknown https://doi.org/10.1016/S0008-6215(00)85922-4
HexA(?1-3)Hex(?1-2)6-deoxy-Hex 162913076 Click to see 502.40 unknown https://doi.org/10.1016/S0008-6215(00)85922-4
HexA(?1-3)Hex(?1-3)[HexA(?1-6)]Hex 163015291 Click to see C(C1C(C(C(C(O1)OC2C(C(OC(C2O)O)COC3C(C(C(C(O3)C(=O)O)O)O)O)O)O)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O 694.50 unknown https://doi.org/10.1016/S0008-6215(00)85922-4
HexA(?1-3)Hex(?1-3)Hex 162988862 Click to see 518.40 unknown https://doi.org/10.1016/S0008-6215(00)85922-4
Rha(a1-2)Rha(a1-5)b-Araf 163025008 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OCC3C(C(C(O3)O)O)O)C)O)O)O)O)O 442.40 unknown https://doi.org/10.1016/S0008-6215(00)85922-4
> Organohalogen compounds / Organochlorides
Hexachloroethane 6214 Click to see C(C(Cl)(Cl)Cl)(Cl)(Cl)Cl 236.70 unknown https://doi.org/10.1078/094471103322004794
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Chromones
6-Methyl-4-chromanone 584354 Click to see 162.18 unknown https://doi.org/10.1078/094471103322004794
> Organoheterocyclic compounds / Quinolines and derivatives / Furanoquinolines
Gamma-Fagarine 107936 Click to see 229.23 unknown via CMAUP database
Skimmianine 6760 Click to see COC1=C(C2=C(C=C1)C(=C3C=COC3=N2)OC)OC 259.26 unknown https://doi.org/10.1590/S0103-50532011000100024
https://doi.org/10.1055/S-2006-960014
https://doi.org/10.1016/S0031-9422(00)91550-4
https://doi.org/10.1039/JR9590001922
> Organosulfur compounds / Thioethers / Aryl thioethers
Butyl p-tolyl sulfide 304040 Click to see 180.31 unknown https://doi.org/10.1078/094471103322004794
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acid amides
(-)-Aegeline 11403749 Click to see 297.30 unknown https://doi.org/10.1016/J.BMCL.2008.08.024
(+-)-Aegeline 15558419 Click to see 297.30 unknown https://doi.org/10.1016/S0031-9422(00)86977-0
(E)-N-[(2R)-2-hydroxy-2-(4-methoxyphenyl)ethyl]-3-phenylprop-2-enamide 10108651 Click to see 297.30 unknown https://doi.org/10.1016/J.BMCL.2006.12.037
https://doi.org/10.1016/S0031-9422(00)86977-0
https://doi.org/10.1016/J.TET.2008.11.088
(E)-N-[(2S)-2-hydroxy-2-(4-hydroxyphenyl)ethyl]-3-phenylprop-2-enamide 11818411 Click to see 283.32 unknown https://doi.org/10.1016/S0031-9422(00)86977-0
(E)-N-[(2S)-2-methoxy-2-(4-methoxyphenyl)ethyl]-3-phenylprop-2-enamide 11209134 Click to see 311.40 unknown https://doi.org/10.1016/J.BMCL.2008.08.024
https://doi.org/10.1016/S0031-9422(00)88714-2
https://doi.org/10.1016/J.TET.2008.11.088
Anhydroaegeline 13821181 Click to see 279.30 unknown https://doi.org/10.1016/S0031-9422(00)86977-0
https://doi.org/10.1016/J.BMCL.2008.08.024
Anhydromarmeline 44579695 Click to see 333.40 unknown https://doi.org/10.1016/J.BMCL.2008.08.024
Dehydromarmeline 44579696 Click to see CC(=CCOC1=CC=C(C=C1)CCNC(=O)C=CC2=CC=CC=C2)C 335.40 unknown https://doi.org/10.1016/S0031-9422(00)86977-0
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3602229/
https://doi.org/10.1016/J.BMCL.2008.08.024
N-[(2R)-2-hydroxy-2-[4-[(2S)-2-hydroxy-3-methylbut-3-enoxy]phenyl]ethyl]-3-phenylprop-2-enamide 162857811 Click to see CC(=C)C(COC1=CC=C(C=C1)C(CNC(=O)C=CC2=CC=CC=C2)O)O 367.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2011.11.018
N-[2-ethoxy-2-(4-methoxyphenyl)ethyl]-3-phenylprop-2-enamide 71440344 Click to see CCOC(CNC(=O)C=CC1=CC=CC=C1)C2=CC=C(C=C2)OC 325.40 unknown https://doi.org/10.1016/S0031-9422(00)88714-2
N-[2-hydroxy-2-[4-(3-methylbut-2-enoxy)phenyl]ethyl]-3-phenylprop-2-enamide 162892089 Click to see CC(=CCOC1=CC=C(C=C1)C(CNC(=O)C=CC2=CC=CC=C2)O)C 351.40 unknown https://doi.org/10.1016/S0031-9422(00)86977-0
https://doi.org/10.1016/0031-9422(81)83112-3
https://doi.org/10.1016/J.PHYTOCHEM.2011.11.018
N-[2-methoxy-2-[4-(3-methylbut-2-enoxy)phenyl]ethyl]-3-phenylprop-2-enamide 163044515 Click to see 365.50 unknown https://doi.org/10.1016/S0031-9422(00)88714-2
N-cinnamoyl-2-hydroxy-2-(4-methoxyphenyl)ethylamine 72833851 Click to see COC1=CC=C(C=C1)C(CNC(=O)C=CC2=CC=CC=C2)O 297.30 unknown https://doi.org/10.1016/J.BMCL.2006.12.037
https://doi.org/10.1016/S0031-9422(00)86977-0
https://doi.org/10.1016/J.BMCL.2008.08.024
https://doi.org/10.1016/J.TET.2008.11.088
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acids
Cinnamic acid 444539 Click to see C1=CC=C(C=C1)C=CC(=O)O 148.16 unknown https://doi.org/10.1080/14786410310001608037
> Phenylpropanoids and polyketides / Coumarins and derivatives
(+)-Marmin 6450230 Click to see 332.40 unknown https://doi.org/10.1055/S-2006-960014
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3602229/
https://doi.org/10.1016/0378-8741(88)90080-3
https://doi.org/10.1246/CL.1995.881
[(E,3R)-2-hydroxy-2,6-dimethyl-8-(2-oxochromen-7-yl)oxyoct-6-en-3-yl] octadec-11-enoate 162819794 Click to see 596.80 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3602229/
2H-1-Benzopyran-2-one, 7-[[(2E,6R)-6-hydroxy-3,7-dimethyl-2,7-octadien-1-yl]oxy]- 13965525 Click to see 314.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3602229/
4-(2-Hydroxy-3-methylbut-3-enoxy)-[1,3]dioxolo[4,5-h]chromen-8-one 45103627 Click to see CC(=C)C(COC1=C2C(=C3C(=C1)C=CC(=O)O3)OCO2)O 290.27 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.10.013
4-[(2R)-2-hydroxy-3-methylbut-3-enoxy]-[1,3]dioxolo[4,5-h]chromen-8-one 162925476 Click to see 290.27 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.10.013
7-(2,6,7-Trihydroxy-7-methyl-3-methylideneoctoxy)chromen-2-one 14309784 Click to see 348.40 unknown https://doi.org/10.1080/14786410310001608037
7-(6,7-Dihydroxy-3,7-dimethyloct-2-enoxy)chromen-2-one 277399 Click to see 332.40 unknown https://doi.org/10.1039/JR9590001922
https://doi.org/10.1590/S0103-50532011000100024
https://doi.org/10.1007/BF00601207
7-(7-Chloro-6-hydroxy-3,7-dimethyloct-2-enoxy)chromen-2-one 78157398 Click to see CC(=CCOC1=CC2=C(C=C1)C=CC(=O)O2)CCC(C(C)(C)Cl)O 350.80 unknown https://doi.org/10.1246/CL.1995.881
7-[(6R)-6-hydroxy-3,7-dimethylocta-2,7-dienoxy]chromen-2-one 163059685 Click to see CC(=C)C(CCC(=CCOC1=CC2=C(C=C1)C=CC(=O)O2)C)O 314.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3602229/
7-[(6R)-6,7-dihydroxy-3,7-dimethyloct-2-enoxy]chromen-2-one 3084213 Click to see 332.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3602229/
7-[(6R)-7-chloro-6-hydroxy-3,7-dimethyloct-2-enoxy]chromen-2-one 162847066 Click to see 350.80 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3602229/
7-[(E,6R)-6-hydroxy-7-methoxy-3,7-dimethyloct-2-enoxy]chromen-2-one 15008366 Click to see 346.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3602229/
7-[(E,6S)-6,7-dihydroxy-3,7-dimethyloct-2-enoxy]chromen-2-one 15560114 Click to see 332.40 unknown https://doi.org/10.1039/JR9590001922
https://doi.org/10.1590/S0103-50532011000100024
https://doi.org/10.1007/BF00601207
7-[(E)-5-[(2R)-3,3-dimethyloxiran-2-yl]-3-methylpent-2-enoxy]chromen-2-one 11088324 Click to see CC(=CCOC1=CC2=C(C=C1)C=CC(=O)O2)CCC3C(O3)(C)C 314.40 unknown https://doi.org/10.1590/S0103-50532011000100024
7-[[(2E,6R)-7-Chloro-6-hydroxy-3,7-dimethyl-2-octen-1-yl]oxy]-2H-1-benzopyran-2-one 71717738 Click to see CC(=CCOC1=CC2=C(C=C1)C=CC(=O)O2)CCC(C(C)(C)Cl)O 350.80 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3602229/
https://doi.org/10.1246/CL.1995.881
7-[5-(3,3-Dimethyloxiran-2-yl)-3-methylpent-2-enoxy]chromen-2-one 85040269 Click to see 314.40 unknown https://doi.org/10.1590/S0103-50532011000100024
Epoxyaurapten 9796891 Click to see CC(=CCOC1=CC2=C(C=C1)C=CC(=O)O2)CCC3C(O3)(C)C 314.40 unknown https://doi.org/10.1246/CL.1995.881
R-(+)-Marmin-6'-Cis-Vaccenoate 71584691 Click to see 596.80 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3602229/
R-(+)-Marmin-6'-Octanoate 71584574 Click to see 458.60 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3602229/
R-(+)-Marmin-6'-Palmitate 71584689 Click to see 570.80 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3602229/
R-(+)-Marmin-6'-undecanoate 71584688 Click to see CCCCCCCCCCC(=O)OC(CCC(=CCOC1=CC2=C(C=C1)C=CC(=O)O2)C)C(C)(C)O 500.70 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3602229/
Scoparone 8417 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)OC 206.19 unknown https://doi.org/10.1016/J.PHYTOCHEM.2011.11.018
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens
(11R,14R,15S)-14-hydroxy-14-methyl-4,12,16-trioxatetracyclo[8.6.0.03,8.011,15]hexadeca-1(10),2,6,8-tetraen-5-one 56958440 Click to see 260.24 unknown https://doi.org/10.1016/J.PHYTOCHEM.2011.11.018
(2S,3R)-3,9-dihydroxy-2-(2-hydroxypropan-2-yl)-2,3-dihydrofuro[3,2-g]chromen-7-one 56958777 Click to see 278.26 unknown https://doi.org/10.1016/J.PHYTOCHEM.2011.11.018
2-(2-Hydroxypropan-2-yl)-2,3-dihydrofuro(3,2-g)chromen-7-one 604512 Click to see 246.26 unknown https://doi.org/10.1039/JR9590001922
https://doi.org/10.1590/S0103-50532011000100024
https://doi.org/10.1016/J.PHYTOCHEM.2011.11.018
https://doi.org/10.1021/JA01170A062
2,3-Dihydro-9-hydroxy-7H-furo[3,2-g][1]benzopyran-7-one 106648 Click to see C1COC2=C1C=C3C=CC(=O)OC3=C2O 204.18 unknown https://doi.org/10.1016/J.PHYTOCHEM.2011.11.018
4',5'-Dihydro-8-methoxypsoralen 77409 Click to see 218.20 unknown https://doi.org/10.1016/J.PHYTOCHEM.2011.11.018
9-(3-Methyl-2-oxobut-3-enoxy)-2,3-dihydrofuro[3,2-g]chromen-7-one 162845288 Click to see 286.28 unknown https://doi.org/10.1016/J.PHYTOCHEM.2011.11.018
9-(3-Methylbut-2-enoxy)-2,3-dihydrofuro[3,2-g]chromen-7-one 162867119 Click to see CC(=CCOC1=C2C(=CC3=C1OCC3)C=CC(=O)O2)C 272.29 unknown https://doi.org/10.1016/J.PHYTOCHEM.2011.11.018
9-[(2S)-2-hydroxy-3-methylbut-3-enoxy]-2,3-dihydrofuro[3,2-g]chromen-7-one 162867112 Click to see 288.29 unknown https://doi.org/10.1016/J.PHYTOCHEM.2011.11.018
Imperatorin 10212 Click to see 270.28 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.10.013
https://doi.org/10.1590/S0103-50532011000100024
Marmesin 334704 Click to see CC(C)(C1CC2=C(O1)C=C3C(=C2)C=CC(=O)O3)O 246.26 unknown https://doi.org/10.1039/JR9590001922
https://doi.org/10.1016/J.PHYTOCHEM.2011.11.018
https://doi.org/10.1021/JA01170A062
Nodakenetin 26305 Click to see 246.26 unknown https://doi.org/10.1590/S0103-50532011000100024
Rutaretin 44146779 Click to see CC(C)(C1CC2=C(O1)C(=C3C(=C2)C=CC(=O)O3)O)O 262.26 unknown https://doi.org/10.1080/14786410310001608037
Xanthoarnol 11482406 Click to see 262.26 unknown https://doi.org/10.1016/J.PHYTOCHEM.2011.11.018
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 5-methoxypsoralens
Bergapten 2355 Click to see COC1=C2C=CC(=O)OC2=CC3=C1C=CO3 216.19 unknown https://doi.org/10.1078/094471103322004794
> 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
Methoxsalen 4114 Click to see COC1=C2C(=CC3=C1OC=C3)C=CC(=O)O2 216.19 unknown https://doi.org/10.1590/S0103-50532011000100024
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
[(E)-4-(7-hydroxy-2-oxochromen-6-yl)-2-methylbut-2-enyl] acetate 101570727 Click to see CC(=CCC1=C(C=C2C(=C1)C=CC(=O)O2)O)COC(=O)C 288.29 unknown https://doi.org/10.1016/J.PHYTOCHEM.2011.11.018
6-(4-Acetoxy-3-methyl-2-butenyl)-7-hydroxycoumarin 123981968 Click to see 288.29 unknown https://doi.org/10.1016/J.PHYTOCHEM.2011.11.018
6-(4-Hydroxy-3-methyl-2-butenyl)-7-hydroxy coumarin 78157935 Click to see CC(=CCC1=C(C=C2C(=C1)C=CC(=O)O2)O)CO 246.26 unknown https://doi.org/10.1016/J.PHYTOCHEM.2011.11.018
6-Formylumbelliferone 14213968 Click to see 190.15 unknown https://doi.org/10.1016/J.PHYTOCHEM.2011.11.018
7-hydroxy-6-[(2R)-2-hydroxy-3-(hydroxymethyl)but-3-enyl]chromen-2-one 162867118 Click to see C=C(CO)C(CC1=C(C=C2C(=C1)C=CC(=O)O2)O)O 262.26 unknown https://doi.org/10.1016/J.PHYTOCHEM.2011.11.018
7-hydroxy-6-[(E)-4-hydroxy-3-methylbut-2-enyl]chromen-2-one 71720036 Click to see 246.26 unknown https://doi.org/10.1016/J.PHYTOCHEM.2011.11.018
7-Hydroxy(~2~H_5_)-2H-1-benzopyran-2-one 45358955 Click to see 167.17 unknown via CMAUP database
Demethylsuberosin 5316525 Click to see 230.26 unknown https://doi.org/10.1016/J.PHYTOCHEM.2011.11.018
Isofraxidin 5318565 Click to see 222.19 unknown https://doi.org/10.1016/J.PHYTOCHEM.2011.11.018
Scopoletin 5280460 Click to see 192.17 unknown https://doi.org/10.1590/S0103-50532011000100024
Umbelliferone 5281426 Click to see C1=CC(=CC2=C1C=CC(=O)O2)O 162.14 unknown https://doi.org/10.1039/JR9590001922
https://doi.org/10.1055/S-2006-960014
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Linear pyranocoumarins
(+)-Decursinol 442127 Click to see 246.26 unknown https://doi.org/10.1016/J.PHYTOCHEM.2011.11.018
Aegelinol 1150962 Click to see 246.26 unknown via CMAUP database
Npc319389 600671 Click to see 246.26 unknown https://doi.org/10.1016/J.PHYTOCHEM.2011.11.018
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
(2S)-5-hydroxy-2-(3-hydroxy-4-methoxyphenyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxy-2,3-dihydrochromen-4-one 129010007 Click to see 610.60 unknown https://doi.org/10.1016/B978-0-12-013320-8.50007-1

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