Maclura pomifera - Fruit
Part: Fruit
Author: Sorin

Maclura pomifera - Leaf
Part: Leaf
Author: Sorin

Maclura pomifera - Aerial parts
Part: Aerial parts
Author: Sorin

Maclura pomifera - Bark
Part: Bark
Author: Sorin

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Details Top

Internal ID UUID643ffde30eadd331466520
Scientific name Maclura pomifera
Authority (Raf.) C.K.Schneid.
First published in Ill. Handb. Laubholzk. 1: 806 (1906)

Description Top

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Synonyms Top

Scientific name Authority First published in
Myroxylon abruptifolium Stokes Bot. Mat. Med. 2: 471 (1812)
Maclura aurantiaca Nutt. Gen. N. Amer. Pl. 2: 234 (1818)
Maclura pomifera var. inermis C.K.Schneid. Ill. Handb. Laubholzk. 2: 905 (1912)
Toxylon pomiferum Sarg. Silva 6: 89 (1895)
Toxylon maclura Raf. New Fl. 3: 43 (1838)
Ioxylon pomiferum Raf. Amer. Monthly Mag. & Crit. Rev. 2: 118 (1817)
Toxylon pomiferum Raf. Amer. Monthly Mag. & Crit. Rev. 2(2): 118, ex Sarg. 1817 [Dec 1817]
Joxylon pomiferum Raf.
Toxylon aurantiacum Raf. Med. Fl. 2: 268 (1830)
Maclura aurantiaca var. inermis André Rev. Hort. (Paris) 68: 33 (1896)

Common names Top

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Language Common/alternative name
English osage-orange
English bois d'arc
English bow-wood
English bodark
English yellowwood
English osage orange
English horse-apple
Afrikaans wildelemoen
Afrikaans indiaanse soetlemoen
Arabic عيش المسافر
Azerbaijani narıncı maklyura
Catalan bois d'arc
Czech maklura oranžová
German milchorange
German bois d'arc
German milchorangenbaum
German osagedorn
Basque osageen laranjondo
Persian توت آمریکایی
Finnish värimulperi
French maclure épineux
French maclura aurantiaca
French oranger des osages
French bois d'arc
Croatian maklura (biljna vrsta)
Hungarian narancseperfa
Hungarian maklúra
Hungarian oszázsnarancs
Hungarian narancseper
Armenian Մակլուրա նարնջագույն
Italian gelso degli osagi
Italian spino degli osagi
Japanese オセージ・オレンジ
Japanese アメリカハリグワ
Korean 오세이지뽕나무
Lithuanian obuolinė makliūra
Lithuanian makliūra
Lithuanian bois d'arc
Macedonian маклура
Dutch osagedoorn
Polish maklura
Polish żółtnica pomarańczowa
Portuguese laranja-de-osage
Portuguese laranjeira-dos-osage
Portuguese laranjeira-de-osage
Russian Маклюра оранжевая
Russian maclura aurantiaca
Russian Маклюра яблоконосная
Albanian maklura
Serbian Маклура
Serbian +maklurapomifera
Swedish bois d'arc
Turkish yalancı portakal ağacı
Turkish yalancı portakalağacı
Ukrainian Маклюра оранжева
Chinese 柘橙
Chinese 奧塞奇橙
Chinese 桑橙
Chinese 柘果
Chinese 拓果
Chinese 橙桑

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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Sow seeds at 20°C, expecting germination within 3 months without further temperature treatment.
Pulpy Coat Inhibits Germination: Seeds with a pulpy or fleshy outer coat need to have this material removed by soaking and rinsing in clean water daily for about a week. The inhibitory substances in the pulp are thus washed away, and germination rates improve.
wash and rinse daily in clean water for 1-5 days, then in detergent daily for about 2-5 days

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Europe
    • Eastern Europe
      • Krym
    • Middle Europe
      • Hungary
    • Southeastern Europe
      • Bulgaria
      • Greece
      • Italy
      • Romania
  • Northern America
    • North-central U.S.A.
      • Illinois
      • Iowa
      • Kansas
      • Missouri
      • Nebraska
      • Oklahoma
      • South Dakota
      • Wisconsin
    • Northeastern U.S.A.
      • Connecticut
      • Indiana
      • Massachusetts
      • Michigan
      • New Jersey
      • New York
      • Ohio
      • Pennsylvania
      • Rhode Island
      • West Virginia
    • Northwestern U.S.A.
      • Colorado
    • South-central U.S.A.
      • New Mexico
      • Texas
    • Southeastern U.S.A.
      • Alabama
      • Arkansas
      • Delaware
      • District Of Columbia
      • Florida
      • Georgia
      • Kentucky
      • Louisiana
      • Maryland
      • Mississippi
      • North Carolina
      • South Carolina
      • Tennessee
      • Virginia
    • Southwestern U.S.A.
      • California

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000447854
UNII 6PXR5N507N
Florida Plant Atlas 1893
Flora of Alabama 2679
Cornell Woody Plants 143
Canadensys 6675
USDA Plants MAPO
UConn 272
Tropicos 21300468
INPN 107130
Flora of Italy 292
KEW urn:lsid:ipni.org:names:148738-2
The Plant List kew-2501306
Missouri Botanical Garden 282737
PFAF Maclura pomifera
Open Tree Of Life 658498
Observations.org 139167
NCBI Taxonomy 3496
Nature Serve 2.134467
IUCN Red List 61886714
IPNI 148738-2
iNaturalist 58205
GBIF 2984580
Freebase /m/0g244
WisFlora 8330
FEIS plants/tree/macpom
EPPO MACPO
EOL 594618
Elurikkus 347964
Calflora (Californian flora) 5278
USDA GRIN 23061
Wikipedia Maclura_pomifera
CMAUP NPO27053

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
Proteolytic Activity of Silkworm Thorn (Cudrania tricuspidata) Fruit for Enzymatic Hydrolysis of Food Proteins Yang NE, Lee DH, Hwang J, Son WY, Kim KS, Kim GY, Kim HW Molecules 02-Feb-2024
PMCID:PMC10856028
doi:10.3390/molecules29030693
PMID:38338437
What Can Inflammation Tell Us about Therapeutic Strategies for Parkinson’s Disease? Xue J, Tao K, Wang W, Wang X Int J Mol Sci 29-Jan-2024
PMCID:PMC10855787
doi:10.3390/ijms25031641
PMID:38338925
Photoprotective Effects of Two New Morin-Schiff Base Derivatives on UVB-Irradiated HaCaT Cells García-Gil S, Rodríguez-Luna A, Ávila-Román J, Rodríguez-García G, del Río RE, Motilva V, Gómez-Hurtado MA, Talero E Antioxidants (Basel) 22-Jan-2024
PMCID:PMC10813227
doi:10.3390/antiox13010134
PMID:38275659
Critical Review on the Use of Extractives of Naturally Durable Woods as Natural Wood Protectants Kirker GT, Hassan B, Mankowski ME, Eller FJ Insects 18-Jan-2024
PMCID:PMC10816604
doi:10.3390/insects15010069
PMID:38249075
Comparison of the differentiation of ovine fetal bone-marrow mesenchymal stem cells towards osteocytes on chitosan/alginate/CuO-NPs and chitosan/alginate/FeO-NPs scaffolds Soltani L, Varmira K, Nazari M Sci Rep 02-Jan-2024
PMCID:PMC10762099
doi:10.1038/s41598-023-50664-6
PMID:38168144
Apoptosis-inducing anti-proliferative and quantitative phytochemical profiling with in silico study of antioxidant-rich Leea aequata L. leaves Mostofa MG, Reza AS, Khan Z, Munira MS, Khatoon MM, Kabir SR, Sadik MG, Ağagündüz D, Capasso R, Kazi M, Alam AK Heliyon 10-Dec-2023
PMCID:PMC10759211
doi:10.1016/j.heliyon.2023.e23400
PMID:38170014
Temporal variation of allergenic potential in urban parks during the vegetation period: a case study from Bratislava, Slovakia Zahradníková E, Rendeková A, Ščevková J Environ Sci Pollut Res Int 05-Dec-2023
PMCID:PMC10791852
doi:10.1007/s11356-023-31137-9
PMID:38052730
Virtual Screening-Accelerated Discovery of a Phosphodiesterase 9 Inhibitor with Neuroprotective Effects in the Kainate Toxicity In Vitro Model Landucci E, Ribaudo G, Anyanwu M, Oselladore E, Giannangeli M, Mazzantini C, Lana D, Giovannini MG, Memo M, Pellegrini-Giampietro DE, Gianoncelli A ACS Chem Neurosci 19-Sep-2023
PMCID:PMC10587872
doi:10.1021/acschemneuro.3c00431
PMID:37726213
The dual face of microglia (M1/M2) as a potential target in the protective effect of nutraceuticals against neurodegenerative diseases Darwish SF, Elbadry AM, Elbokhomy AS, Salama GA, Salama RM Front Aging 06-Sep-2023
PMCID:PMC10513083
doi:10.3389/fragi.2023.1231706
PMID:37744008
Native diversity buffers against severity of non-native tree invasions Delavaux CS, Crowther TW, Zohner CM, Robmann NM, Lauber T, van den Hoogen J, Kuebbing S, Liang J, de-Miguel S, Nabuurs GJ, Reich PB, Abegg M, Adou Yao YC, Alberti G, Almeyda Zambrano AM, Alvarado BV, Alvarez-Dávila E, Alvarez-Loayza P, Alves LF, Ammer C, Antón-Fernández C, Araujo-Murakami A, Arroyo L, Avitabile V, Aymard GA, Baker TR, Bałazy R, Banki O, Barroso JG, Bastian ML, Bastin JF, Birigazzi L, Birnbaum P, Bitariho R, Boeckx P, Bongers F, Bouriaud O, Brancalion PH, Brandl S, Brienen R, Broadbent EN, Bruelheide H, Bussotti F, Gatti RC, César RG, Cesljar G, Chazdon R, Chen HY, Chisholm C, Cho H, Cienciala E, Clark C, Clark D, Colletta GD, Coomes DA, Cornejo Valverde F, Corral-Rivas JJ, Crim PM, Cumming JR, Dayanandan S, de Gasper AL, Decuyper M, Derroire G, DeVries B, Djordjevic I, Dolezal J, Dourdain A, Engone Obiang NL, Enquist BJ, Eyre TJ, Fandohan AB, Fayle TM, Feldpausch TR, Ferreira LV, Fischer M, Fletcher C, Frizzera L, Gamarra JG, Gianelle D, Glick HB, Harris DJ, Hector A, Hemp A, Hengeveld G, Hérault B, Herbohn JL, Herold M, Hillers A, Honorio Coronado EN, Hui C, Ibanez TT, Amaral I, Imai N, Jagodziński AM, Jaroszewicz B, Johannsen VK, Joly CA, Jucker T, Jung I, Karminov V, Kartawinata K, Kearsley E, Kenfack D, Kennard DK, Kepfer-Rojas S, Keppel G, Khan ML, Killeen TJ, Kim HS, Kitayama K, Köhl M, Korjus H, Kraxner F, Laarmann D, Lang M, Lewis SL, Lu H, Lukina NV, Maitner BS, Malhi Y, Marcon E, Marimon BS, Marimon-Junior BH, Marshall AR, Martin EH, Martynenko O, Meave JA, Melo-Cruz O, Mendoza C, Merow C, Mendoza AM, Moreno VS, Mukul SA, Mundhenk P, Nava-Miranda MG, Neill D, Neldner VJ, Nevenic RV, Ngugi MR, Niklaus PA, Oleksyn J, Ontikov P, Ortiz-Malavasi E, Pan Y, Paquette A, Parada-Gutierrez A, Parfenova EI, Park M, Parren M, Parthasarathy N, Peri PL, Pfautsch S, Phillips OL, Picard N, Piedade MT, Piotto D, Pitman NC, Polo I, Poorter L, Poulsen AD, Pretzsch H, Ramirez Arevalo F, Restrepo-Correa Z, Rodeghiero M, Rolim SG, Roopsind A, Rovero F, Rutishauser E, Saikia P, Salas-Eljatib C, Saner P, Schall P, Schepaschenko D, Scherer-Lorenzen M, Schmid B, Schöngart J, Searle EB, Seben V, Serra-Diaz JM, Sheil D, Shvidenko AZ, Silva-Espejo JE, Silveira M, Singh J, Sist P, Slik F, Sonké B, Souza AF, Miscicki S, Stereńczak KJ, Svenning JC, Svoboda M, Swanepoel B, Targhetta N, Tchebakova N, ter Steege H, Thomas R, Tikhonova E, Umunay PM, Usoltsev VA, Valencia R, Valladares F, van der Plas F, Do TV, van Nuland ME, Vasquez RM, Verbeeck H, Viana H, Vibrans AC, Vieira S, von Gadow K, Wang HF, Watson JV, Werner GD, Wiser SK, Wittmann F, Woell H, Wortel V, Zagt R, Zawiła-Niedźwiecki T, Zhang C, Zhao X, Zhou M, Zhu ZX, Zo-Bi IC, Maynard DS Nature 23-Aug-2023
PMCID:PMC10533391
doi:10.1038/s41586-023-06440-7
PMID:37612513
The Therapeutic Potential of Natural Dietary Flavonoids against SARS-CoV-2 Infection Wang Z, Yang L Nutrients 03-Aug-2023
PMCID:PMC10421531
doi:10.3390/nu15153443
PMID:37571380
Altered profile of glycosylated proteins in serum samples obtained from patients with Hashimoto′s thyroiditis following depletion of highly abundant proteins Xu Y, Huo J, Nie R, Ge L, Xie C, Meng Y, Liu J, Wu L, Qin X Front Immunol 30-Jun-2023
PMCID:PMC10348014
doi:10.3389/fimmu.2023.1182842
PMID:37457741
A Review of Classification, Biosynthesis, Biological Activities and Potential Applications of Flavonoids Chen S, Wang X, Cheng Y, Gao H, Chen X Molecules 25-Jun-2023
PMCID:PMC10343696
doi:10.3390/molecules28134982
PMID:37446644
Deciphering Protein O-GalNAcylation: Method Development and Disease Implication Yue S, Wang X, Ge W, Li J, Yang C, Zhou Z, Zhang P, Yang X, Xiao W, Yang S ACS Omega 24-May-2023
PMCID:PMC10249083
doi:10.1021/acsomega.3c01653
PMID:37305274
Phytochemistry and pharmacology of natural prenylated flavonoids Lv HW, Wang QL, Luo M, Zhu MD, Liang HM, Li WJ, Cai H, Zhou ZB, Wang H, Tong SQ, Li XN Arch Pharm Res 14-Apr-2023
PMCID:PMC10101826
doi:10.1007/s12272-023-01443-4
PMID:37055613

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 / Benzene and substituted derivatives / Benzophenones
Maclurin 68213 Click to see C1=CC(=C(C=C1C(=O)C2=C(C=C(C=C2O)O)O)O)O 262.21 unknown https://doi.org/10.1007/BF02859211
> Benzenoids / Phenols / Benzenediols / Resorcinols
Resorcinol 5054 Click to see C1=CC(=CC(=C1)O)O 110.11 unknown https://doi.org/10.1007/BF02859211
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters / Fatty acid methyl esters
Methyl 14-oxooctadecanoate 13991164 Click to see CCCCC(=O)CCCCCCCCCCCCC(=O)OC 312.50 unknown https://doi.org/10.1016/S0031-9422(00)80492-6
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Palmitic Acid 985 Click to see CCCCCCCCCCCCCCCC(=O)O 256.42 unknown https://doi.org/10.1007/BF02859211
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Linoleic Acid 5280450 Click to see CCCCCC=CCC=CCCCCCCCC(=O)O 280.40 unknown https://doi.org/10.1093/JAOAC/55.3.645
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(-)-Butyrospermol 12302182 Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC3C2=CCC4C3(CCC(C4(C)C)O)C)C)C 426.70 unknown https://doi.org/10.1016/0031-9422(94)00971-U
https://doi.org/10.1071/CH9660175
(1R,3aS,5aS,5bR,7aS,9S,11aR,11bS,13aS,13bR)-3a,5a,5b,8,8,11a-hexamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-ol 163185435 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/10.1002/JCCS.196800006
(3R,4aR,6aR,6bS,8aS,11R,12S,12aS,14aR,14bR)-8a-(hydroxymethyl)-4,4,6a,6b,11,12,14b-heptamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picen-3-ol 293273 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)CO 442.70 unknown https://doi.org/10.1080/10575639708043746
(3S,10R,13R,14R,17R)-4,4,10,13,14-pentamethyl-17-[(2R)-6-methylhept-5-en-2-yl]-2,3,5,6,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-ol 102004740 Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC3C2=CCC4C3(CCC(C4(C)C)O)C)C)C 426.70 unknown https://doi.org/10.1016/0031-9422(94)00971-U
https://doi.org/10.1002/JPS.2600640121
https://doi.org/10.1016/S0031-9422(00)90379-0
(3S,5R,10R,13S,14S)-17-[(1R)-1,5-dimethylhex-4-enyl]-4,4,10,13,14-pentamethyl-2,3,5,6,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-ol 472759 Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC3C2=CCC4C3(CCC(C4(C)C)O)C)C)C 426.70 unknown https://doi.org/10.1016/0031-9422(94)00971-U
https://doi.org/10.1002/JPS.2600640121
https://doi.org/10.1016/S0031-9422(00)90379-0
[(1R,3aR,5aR,5bR,7aR,9S,11aR,11bS,13aR,13bR)-3a,5a,5b,8,8,11a-hexamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-yl] acetate 162942499 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)OC(=O)C)C)C 468.80 unknown https://doi.org/10.1002/JPS.2600640121
3alpha-Hydroxyfriedelane-2-one 14465808 Click to see CC1C(C(=O)CC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C)O 442.70 unknown via CMAUP database
Beta-Amyrin 73145 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 unknown https://doi.org/10.1007/BF02859211
Butyrospermol 12302181 Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC3C2=CCC4C3(CCC(C4(C)C)O)C)C)C 426.70 unknown https://doi.org/10.1016/0031-9422(94)00971-U
https://doi.org/10.1071/CH9660175
Butyrospermol acetate 6427349 Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC3C2=CCC4C3(CCC(C4(C)C)OC(=O)C)C)C)C 468.80 unknown https://doi.org/10.1016/S0031-9422(00)90379-0
Friedelin 91472 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C 426.70 unknown via CMAUP database
Lup-20(29)-en-3-ol, (3beta)- 521518 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/10.1071/CH9660175
https://doi.org/10.1002/JCCS.196800006
Lup-20(29)-en-3beta-ol, acetate 323074 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)OC(=O)C)C)C 468.80 unknown https://doi.org/10.1002/JPS.2600640121
Lupan-3beta,20-diol 10003607 Click to see CC1(C2CCC3(C(C2(CCC1O)C)CCC4C3(CCC5(C4C(CC5)C(C)(C)O)C)C)C)C 444.70 unknown https://doi.org/10.1002/JPS.2600640121
https://doi.org/10.1039/JR9590000073
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/10.1016/S0031-9422(00)90379-0
https://doi.org/10.1002/JCCS.196800006
https://doi.org/10.1002/JPS.2600640121
https://doi.org/10.1071/CH9660175
Monoginol A 15560607 Click to see CC1(C2CCC3(C(C2(CCC1O)C)CCC4C3(CCC5(C4C(CC5)C(C)(C)O)C)C)C)C 444.70 unknown https://doi.org/10.1002/JPS.2600640121
https://doi.org/10.1039/JR9590000073
Neoruscogenin 9910474 Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(C(CC(C5)O)O)C)C)OC16CCC(=C)CO6 428.60 unknown via CMAUP database
Ruscogenin 441893 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(C(CC(C6)O)O)C)C)C)OC1 430.60 unknown via CMAUP database
Uvaol 92802 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)CO 442.70 unknown https://doi.org/10.1080/10575639708043746
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Bile acids, alcohols and derivatives / Hydroxy bile acids, alcohols and derivatives / Dihydroxy bile acids, alcohols and derivatives
(22r)-22-Hydroxycholes-terol 13754059 Click to see CC(C)CCC(C(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)O 402.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins
(23S,25R)-23-[6-O-(beta-D-Glucopyranosyl)-beta-D-glucopyranosyloxy]spirosta-5-ene-3beta-ol 100982641 Click to see CC1CC(C2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)C)OC1)OC7C(C(C(C(O7)COC8C(C(C(C(O8)CO)O)O)O)O)O)O 754.90 unknown via CMAUP database
(23S)-1beta-[[2-O-[3-O-(beta-D-Glucopyranosyl)-alpha-L-rhamnopyranosyl]-alpha-L-arabinopyranosyl]oxy]-23-(beta-D-glucopyranosyloxy)spirosta-5,25(27)-diene-3beta-ol 10581939 Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(C(CC(C5)O)OC6C(C(C(CO6)O)O)OC7C(C(C(C(O7)C)O)OC8C(C(C(C(O8)CO)O)O)O)O)C)C)OC19C(CC(=C)CO9)OC1C(C(C(C(O1)CO)O)O)O 1047.10 unknown via CMAUP database
(25R)-1beta-(2-O-alpha-L-Rhamnopyranosyl-alpha-L-arabinopyranosyloxy)spirosta-5-ene-3beta-ol 44575746 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(C(CC(C6)O)OC7C(C(C(CO7)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C)C)OC1 708.90 unknown via CMAUP database
[(2S,3S,4R,5R,6S)-4,5-diacetyloxy-6-[(2S,3R,4S,5S)-2-[(1S,2S,3'S,4S,4'S,6S,7S,8R,9S,12S,13R,14R,16R)-4'-[[(2R,5S,6R,7R,8R,10R)-6,7-dihydroxy-2-[(2S)-2-hydroxybutan-2-yl]-10-methyl-3-oxo-1,4,9-trioxaspiro[4.5]decan-8-yl]oxy]-3',16-dihydroxy-7,9,13-trimethyl-5'-methylidenespiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-14-yl]oxy-4,5-dihydroxyoxan-3-yl]oxy-2-methyloxan-3-yl] acetate 21590070 Click to see CCC(C)(C1C(=O)OC2(O1)C(OC(C(C2O)O)OC3C(C4(C(C5C(O4)CC6C5(CCC7C6CC=C8C7(C(CC(C8)O)OC9C(C(C(CO9)O)O)OC1C(C(C(C(O1)C)OC(=O)C)OC(=O)C)OC(=O)C)C)C)C)OCC3=C)O)C)O 1139.20 unknown via CMAUP database
1beta-[(2-O-alpha-L-Rhamnopyranosyl-alpha-L-arabinopyranosyl)oxy]-26-(beta-D-glucopyranosyloxy)furosta-5,20(22),25(27)-trien-3beta-ol 44567205 Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CC(CC4=CCC5C(C34C)CCC6(C5CC7C6C(=C(O7)CCC(=C)COC8C(C(C(C(O8)CO)O)O)O)C)C)O)O)O)O)O)O 869.00 unknown via CMAUP database
1beta-[2-O-(3-O-beta-D-Glucopyranosyl-alpha-L-rhamnopyranosyl)-4-O-acetyl-alpha-L-arabinopyranosyloxy]spirosta-5,25(27)-dien-3beta-ol 101937241 Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(C(CC(C5)O)OC6C(C(C(CO6)OC(=O)C)O)OC7C(C(C(C(O7)C)O)OC8C(C(C(C(O8)CO)O)O)O)O)C)C)OC19CCC(=C)CO9 911.00 unknown via CMAUP database
Aculeoside B 154169 Click to see CC1CC(C2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(C(CC(C6)O)OC7C(C(C(C(O7)COC(=O)C)OC(=O)C)OC(=O)C)OC8C(C(C(C(O8)C)O)OC9C(C(C(C(O9)CO)O)O)O)O)C)C)C)OC1)OC1C(C(C(C(O1)CO)O)O)O 1205.30 unknown via CMAUP database
CID 10462472 10462472 Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(C(CC(C5)O)OC6C(C(C(CO6)O)O)OC7C(C(C(C(O7)C)O)O)O)C)C)OC18CCC(=C)CO8 706.90 unknown via CMAUP database
Ruscin(P) 13935613 Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(C(CC(C5)O)OC6C(C(C(CO6)O)O)OC7C(C(C(C(O7)C)O)OC8C(C(C(C(O8)CO)O)O)O)O)C)C)OC19CCC(=C)CO9 869.00 unknown via CMAUP database
Ruscoside [WHO-DD] 91936850 Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(C(CC(C5)O)OC6C(C(C(CO6)O)O)OC7C(C(C(C(O7)C)O)OC8C(C(C(C(O8)CO)O)O)O)O)C)C)OC1(CCC(=C)COC9C(C(C(C(O9)CO)O)O)O)O 1049.20 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3R,8R,9R,10S,13R,14R,17S)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 162965363 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1002/JCCS.196800006
(3S,8S,9S,10R,13R,14S,17S)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 122411793 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1002/JCCS.196800006
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/S0031-9422(00)90379-0
https://doi.org/10.1016/0031-9422(94)00971-U
https://doi.org/10.1080/10575639708043746
https://doi.org/10.1071/CH9660175
https://doi.org/10.1002/JCCS.196800006
24-Ethylcholest-5-en-3beta-ol 22012 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/S0031-9422(00)90379-0
https://doi.org/10.1080/10575639708043746
https://doi.org/10.1016/0031-9422(94)00971-U
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1071/CH9660175
https://doi.org/10.1016/0031-9422(94)00971-U
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 via CMAUP database
Stigmasterol 5280794 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1080/10575639708043746
> Organic nitrogen compounds / Organonitrogen compounds / Guanidines
1-{4-[(3-Aminopropyl)amino]butyl}guanidine 541551 Click to see C(CCN=C(N)N)CNCCCN 187.29 unknown https://doi.org/10.1016/0031-9422(94)00971-U
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols / Cyclohexanols
Inositol 892 Click to see C1(C(C(C(C(C1O)O)O)O)O)O 180.16 unknown https://doi.org/10.1016/S0031-9422(00)90379-0
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
Sucrose 5988 Click to see C(C1C(C(C(C(O1)OC2(C(C(C(O2)CO)O)O)CO)O)O)O)O 342.30 unknown https://doi.org/10.1007/BF02859211
https://doi.org/10.1016/S0031-9422(00)90379-0
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides
D-(-)-Fructose 5984 Click to see C(C(C(C(C(=O)CO)O)O)O)O 180.16 unknown https://doi.org/10.1016/S0031-9422(00)90379-0
D-Fructose 2723872 Click to see C1C(C(C(C(O1)(CO)O)O)O)O 180.16 unknown https://doi.org/10.1016/S0031-9422(00)90379-0
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Hexoses
(2R,3S,4R,5R)-2,3,4,5,6-pentahydroxyhexanal 107526 Click to see C(C(C(C(C(C=O)O)O)O)O)O 180.16 unknown https://doi.org/10.1016/S0031-9422(00)90379-0
D-Glucose 5793 Click to see C(C1C(C(C(C(O1)O)O)O)O)O 180.16 unknown https://doi.org/10.1016/S0031-9422(00)90379-0
> Organoheterocyclic compounds / Benzofurans
Euparone 104654 Click to see CC(=O)C1=CC2=CC(=C(C=C2O1)O)C(=O)C 218.20 unknown via CMAUP database
> Organoheterocyclic compounds / Benzofurans / Dibenzofurans
Ruscodibenzofuran 323624 Click to see CC1=C2C3=CC(=C(C=C3OC2=C(C=C1)C)O)C(=O)C 254.28 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
Toxyloxanthone C 5495919 Click to see CC1C(C2=C(O1)C=C3C(=C2O)C(=O)C4=C(O3)C(=C(C=C4)O)O)(C)C 328.30 unknown https://doi.org/10.1002/(SICI)1096-9888(200004)35:4<540::AID-JMS966>3.0.CO;2-Y
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / 8-prenylated xanthones
4,8,9-Trihydroxy-2,2,3,3-tetramethyl-6-(3-methylbut-2-enyl)furo[3,2-b]xanthen-5-one 162899948 Click to see CC(=CCC1=CC(=C(C2=C1C(=O)C3=C(C4=C(C=C3O2)OC(C4(C)C)(C)C)O)O)O)C 410.50 unknown https://doi.org/10.1016/S0031-9422(00)80492-6
4,8,9-trihydroxy-2,3,3-trimethyl-6-(3-methylbut-2-enyl)-2H-furo[3,2-b]xanthen-5-one 100960266 Click to see CC1C(C2=C(O1)C=C3C(=C2O)C(=O)C4=C(O3)C(=C(C=C4CC=C(C)C)O)O)(C)C 396.40 unknown https://doi.org/10.1016/S0031-9422(00)80492-6
https://doi.org/10.1002/(SICI)1096-9888(200004)35:4<540::AID-JMS966>3.0.CO;2-Y
Alvaxanthone 12305823 Click to see CC(=CCC1=CC(=C(C2=C1C(=O)C3=C(O2)C=C(C(=C3O)C(C)(C)C=C)O)O)O)C 396.40 unknown https://doi.org/10.1021/JO01026A040
https://doi.org/10.1021/JO01015A032
https://doi.org/10.1016/S0031-9422(00)80492-6
https://doi.org/10.1002/(SICI)1096-9888(200004)35:4<540::AID-JMS966>3.0.CO;2-Y
https://doi.org/10.1007/BF00597727
https://doi.org/10.1016/S0021-9673(98)00937-6
Prenylxanthone 67261294 Click to see CC(=CCC1=C2C(=CC=C1)OC3=CC=CC=C3C2=O)C 264.30 unknown https://doi.org/10.1002/(SICI)1096-9888(200004)35:4<540::AID-JMS966>3.0.CO;2-Y
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / Pyranoxanthones
6-Deoxyjacareubin 5281629 Click to see CC1(C=CC2=C(O1)C=C3C(=C2O)C(=O)C4=C(O3)C(=CC=C4)O)C 310.30 unknown https://doi.org/10.1007/BF02859211
https://doi.org/10.1007/BF00597727
Macluraxanthone 5281646 Click to see CC1(C=CC2=C(C3=C(C(=C2O1)C(C)(C)C=C)OC4=C(C3=O)C=CC(=C4O)O)O)C 394.40 unknown https://doi.org/10.1021/JO01026A041
https://doi.org/10.1021/JO01026A040
https://doi.org/10.1016/S0021-9673(98)00937-6
https://doi.org/10.1002/(SICI)1096-9888(200004)35:4<540::AID-JMS966>3.0.CO;2-Y
https://doi.org/10.1016/S0031-9422(00)80492-6
https://doi.org/10.1007/BF00597727
Osajaxanthone 6064803 Click to see CC1(C=CC2=C(O1)C=C3C(=C2O)C(=O)C4=C(O3)C=CC(=C4)O)C 310.30 unknown https://doi.org/10.1021/JO01026A040
https://doi.org/10.1016/S0031-9422(00)80492-6
https://doi.org/10.1021/JO01012A033
https://doi.org/10.1002/(SICI)1096-9888(200004)35:4<540::AID-JMS966>3.0.CO;2-Y
https://doi.org/10.1007/BF00597727
https://doi.org/10.1016/S0021-9673(98)00937-6
Tovoxanthone 12444404 Click to see CC1(C=CC2=C(O1)C(=CC3=C2C(=O)C4=C(C=CC=C4O3)O)O)C 310.30 unknown https://doi.org/10.1007/BF00597727
> Phenylpropanoids and polyketides / Coumarins and derivatives / Coumarin glycosides
Esculin 5281417 Click to see C1=CC(=O)OC2=CC(=C(C=C21)OC3C(C(C(C(O3)CO)O)O)O)O 340.28 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
(2S)-8-[(2S)-5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxo-2,3-dihydrochromen-8-yl]-5,7-dihydroxy-2-(4-hydroxyphenyl)-2,3-dihydrochromen-4-one 101324837 Click to see C1C(OC2=C(C(=CC(=C2C1=O)O)O)C3=C4C(=C(C=C3O)O)C(=O)CC(O4)C5=CC=C(C=C5)O)C6=CC=C(C=C6)O 542.50 unknown https://doi.org/10.1016/0031-9422(94)00971-U
8-[5,7-Dihydroxy-2-(4-hydroxyphenyl)-4-oxo-2,3-dihydrochromen-8-yl]-5,7-dihydroxy-2-(4-hydroxyphenyl)-2,3-dihydrochromen-4-one 162950592 Click to see C1C(OC2=C(C(=CC(=C2C1=O)O)O)C3=C4C(=C(C=C3O)O)C(=O)CC(O4)C5=CC=C(C=C5)O)C6=CC=C(C=C6)O 542.50 unknown https://doi.org/10.1016/0031-9422(94)00971-U
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 6-prenylated flavans / 6-prenylated flavanones
(S)-2-(2,4-dihydroxy-5-(3-methylbut-2-enyl)phenyl)-5,7-dihydroxy-6-(3-methylbut-2-enyl)chroman-4-one 44419446 Click to see CC(=CCC1=CC(=C(C=C1O)O)C2CC(=O)C3=C(O2)C=C(C(=C3O)CC=C(C)C)O)C 424.50 unknown https://doi.org/10.1016/S0031-9422(00)80492-6
5,7-Dihydroxy-2-(7-hydroxy-2,2-dimethylchromen-6-yl)-6-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one 14886039 Click to see CC(=CCC1=C(C2=C(C=C1O)OC(CC2=O)C3=C(C=C4C(=C3)C=CC(O4)(C)C)O)O)C 422.50 unknown https://doi.org/10.1016/S0031-9422(00)80492-6
Cajaflavanone 42607935 Click to see CC(=CCC1=C(C2=C(C3=C1OC(C=C3)(C)C)OC(CC2=O)C4=CC=C(C=C4)O)O)C 406.50 unknown https://doi.org/10.1016/0031-9422(94)00971-U
cudraflavanone A 21721847 Click to see CC(=CCC1=C(C2=C(C=C1O)OC(CC2=O)C3=C(C=C4C(=C3)C=CC(O4)(C)C)O)O)C 422.50 unknown https://doi.org/10.1016/S0031-9422(00)80492-6
Erythrisenegalone 15224381 Click to see CC(=CCC1=C(C2=C(C3=C1OC(C=C3)(C)C)OC(CC2=O)C4=CC=C(C=C4)O)O)C 406.50 unknown https://doi.org/10.1016/0031-9422(94)00971-U
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 8-prenylated flavans / 8-prenylated flavanones
2-(4-Hydroxyphenyl)-5-hydroxy-2,3-dihydro-10-(3-methyl-2-butenyl)-8,8-dimethyl-4H,8H-benzo[1,2-b:5,4-b']dipyran-4-one 13846826 Click to see CC(=CCC1=C2C(=C(C3=C1OC(CC3=O)C4=CC=C(C=C4)O)O)C=CC(O2)(C)C)C 406.50 unknown https://doi.org/10.1016/0031-9422(94)00971-U
8-Prenylnaringenin 480764 Click to see CC(=CCC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=CC=C(C=C3)O)C 340.40 unknown https://doi.org/10.1016/0031-9422(94)00971-U
CID 14542254 14542254 Click to see CC(=CCC1=CC(=C(C=C1O)O)C2CC(=O)C3=C(C=C(C(=C3O2)CC=C(C)C)O)O)C 424.50 unknown https://doi.org/10.1016/S0021-9673(98)00937-6
https://doi.org/10.1002/(SICI)1096-9888(200004)35:4<540::AID-JMS966>3.0.CO;2-Y
Euchrestaflavanone C 42608039 Click to see CC(=CCC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=C(C=C4C(=C3)C=CC(O4)(C)C)O)C 422.50 unknown https://doi.org/10.1016/S0021-9673(98)00937-6
https://doi.org/10.1002/(SICI)1096-9888(200004)35:4<540::AID-JMS966>3.0.CO;2-Y
Lupinifolin 10250777 Click to see CC(=CCC1=C2C(=C(C3=C1OC(CC3=O)C4=CC=C(C=C4)O)O)C=CC(O2)(C)C)C 406.50 unknown https://doi.org/10.1016/0031-9422(94)00971-U
Sophoraflavanone B 509245 Click to see CC(=CCC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=CC=C(C=C3)O)C 340.40 unknown https://doi.org/10.1016/0031-9422(94)00971-U
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(2R)-5,7-dihydroxy-2-(4-hydroxyphenyl)-2,3-dihydro-4H-chromen-4-one 667495 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O 272.25 unknown https://doi.org/10.1016/0031-9422(94)00971-U
(2S)-5,7,2',4'-tetrahydroxyflavanone 10356745 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=C(C=C(C=C3)O)O 288.25 unknown https://doi.org/10.1016/0031-9422(94)00971-U
5,7-Dihydroxy-2-(4-hydroxyphenyl)chroman-4-one 932 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O 272.25 unknown https://doi.org/10.1016/0031-9422(94)00971-U
Naringenin 439246 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O 272.25 unknown https://doi.org/10.1016/0031-9422(94)00971-U
Steppogenin 21596130 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=C(C=C(C=C3)O)O 288.25 unknown https://doi.org/10.1016/0031-9422(94)00971-U
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
(+/-)-Taxifolin 471 Click to see C1=CC(=C(C=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 304.25 unknown https://doi.org/10.1007/BF02859211
2-(2,4-Dihydroxyphenyl)-3,5,7-trihydroxy-2,3-dihydrochromen-4-one 362637 Click to see C1=CC(=C(C=C1O)O)C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O 304.25 unknown https://doi.org/10.1007/BF02859211
3,5,7-Trihydroxy-2-(4-hydroxyphenyl)-2,3-dihydrochromen-4-one 662 Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 288.25 unknown https://doi.org/10.1007/BF02859211
https://doi.org/10.1016/S0031-9422(00)81238-8
https://doi.org/10.1016/0031-9422(94)00971-U
Aromadendrin 122850 Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 288.25 unknown https://doi.org/10.1016/S0031-9422(00)81238-8
https://doi.org/10.1016/0031-9422(94)00971-U
Dihydromorin 5458714 Click to see C1=CC(=C(C=C1O)O)C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O 304.25 unknown https://doi.org/10.1016/S0031-9422(00)81238-8
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin 5280443 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 270.24 unknown https://doi.org/10.1016/S0031-9422(00)90379-0
https://doi.org/10.1016/0031-9422(94)00971-U
> Phenylpropanoids and polyketides / Flavonoids / Flavones / 6-prenylated flavones
(2R,3S)-4-hydroxy-7-(4-hydroxyphenyl)-2-(2-hydroxypropan-2-yl)-3-methyl-2,3-dihydrofuro[3,2-g]chromen-5-one 163007906 Click to see CC1C(OC2=C1C(=C3C(=C2)OC(=CC3=O)C4=CC=C(C=C4)O)O)C(C)(C)O 368.40 unknown https://doi.org/10.1016/S0031-9422(98)00380-X
5,7-dihydroxy-6-[(2S)-2-hydroxy-3-methylbut-3-enyl]-2-(4-hydroxyphenyl)chromen-4-one 162910873 Click to see CC(=C)C(CC1=C(C2=C(C=C1O)OC(=CC2=O)C3=CC=C(C=C3)O)O)O 354.40 unknown https://doi.org/10.1016/S0031-9422(98)00380-X
6-Prenylapigenin 10382485 Click to see CC(=CCC1=C(C2=C(C=C1O)OC(=CC2=O)C3=CC=C(C=C3)O)O)C 338.40 unknown https://doi.org/10.1016/S0031-9422(98)00380-X
https://doi.org/10.1016/S0031-9422(00)90379-0
Artocarpesin 399491 Click to see CC(=CCC1=C(C2=C(C=C1O)OC(=CC2=O)C3=C(C=C(C=C3)O)O)O)C 354.40 unknown https://doi.org/10.1016/S0031-9422(98)00380-X
https://doi.org/10.1016/0031-9422(94)00971-U
https://doi.org/10.1016/S0031-9422(00)90379-0
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol 5280863 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown https://doi.org/10.1007/BF02859211
Morin 5281670 Click to see C1=CC(=C(C=C1O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O 302.23 unknown https://doi.org/10.1016/0031-9422(94)00971-U
Quercetin 5280343 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 302.23 unknown https://doi.org/10.1007/BF02859211
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Rutin 5280805 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O 610.50 unknown https://doi.org/10.1007/BF02859211
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
(2S,3R)-3,5-dihydroxy-2-(4-hydroxyphenyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3-dihydrochromen-4-one 11155141 Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 450.40 unknown https://doi.org/10.1016/S0031-9422(00)90379-0
3,5-dihydroxy-2-(4-hydroxyphenyl)-7-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 25203835 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown https://doi.org/10.1055/S-0028-1099981
3,5-Dihydroxy-2-(4-hydroxyphenyl)-7-[(3,4,5-trihydroxy-6-methyltetrahydro-2H-pyran-2-yl)oxy]-4H-1-benzopyran-4-one 13940823 Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)O)C4=CC=C(C=C4)O)O)O)O)O 432.40 unknown https://doi.org/10.1007/S10600-009-9243-Z
3,5-Dihydroxy-2-(4-hydroxyphenyl)-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3-dihydrochromen-4-one 14282776 Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 450.40 unknown https://doi.org/10.1016/S0031-9422(00)90379-0
kaempferol 7-O-glucoside 10095180 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown https://doi.org/10.1016/S0031-9422(00)90379-0
Kaempferol-7-o-glucoside 5480982 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown https://doi.org/10.1016/S0031-9422(00)90379-0
https://doi.org/10.1055/S-0028-1099981
Kaempferol-7-rhamnoside 25079965 Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)O)C4=CC=C(C=C4)O)O)O)O)O 432.40 unknown https://doi.org/10.1007/S10600-009-9243-Z
> Phenylpropanoids and polyketides / Flavonoids / Pyranoflavonoids
(2S)-5-hydroxy-2-(4-hydroxyphenyl)-8,8-dimethyl-2,3-dihydropyrano[2,3-h]chromen-4-one 14187086 Click to see CC1(C=CC2=C(O1)C=C(C3=C2OC(CC3=O)C4=CC=C(C=C4)O)O)C 338.40 unknown https://doi.org/10.1016/0031-9422(94)00971-U
Carpachromene 10449654 Click to see CC1(C=CC2=C(O1)C=C3C(=C2O)C(=O)C=C(O3)C4=CC=C(C=C4)O)C 336.30 unknown https://doi.org/10.1016/S0031-9422(98)00380-X
Citflavanone 14187085 Click to see CC1(C=CC2=C(O1)C=C(C3=C2OC(CC3=O)C4=CC=C(C=C4)O)O)C 338.40 unknown https://doi.org/10.1016/0031-9422(94)00971-U
Cycloartocarpesin 15224382 Click to see CC1(C=CC2=C(O1)C=C3C(=C2O)C(=O)C=C(O3)C4=C(C=C(C=C4)O)O)C 352.30 unknown https://doi.org/10.1016/S0031-9422(98)00380-X
https://doi.org/10.1016/0031-9422(94)00971-U
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavans / Isoflavanones / 6-prenylated isoflavanones
(2R,3R)-4-hydroxy-6-(4-hydroxyphenyl)-2-(2-hydroxypropan-2-yl)-3-methoxy-2,3-dihydrofuro[3,2-g]chromen-5-one 124511655 Click to see CC(C)(C1C(C2=C(O1)C=C3C(=C2O)C(=O)C(=CO3)C4=CC=C(C=C4)O)OC)O 384.40 unknown https://doi.org/10.1016/S0031-9422(98)00380-X
3-(3,4-Dihydroxyphenyl)-5-hydroxy-6-(2-hydroxy-3-methylbut-3-enyl)-8,8-dimethylpyrano[2,3-h]chromen-4-one 101676241 Click to see CC(=C)C(CC1=C2C(=C3C(=C1O)C(=O)C(=CO3)C4=CC(=C(C=C4)O)O)C=CC(O2)(C)C)O 436.50 unknown https://doi.org/10.1016/S0031-9422(00)90379-0
3-(3,4-dihydroxyphenyl)-5-hydroxy-6-[(2R)-2-hydroxy-3-methylbut-3-enyl]-8,8-dimethylpyrano[2,3-h]chromen-4-one 162900031 Click to see CC(=C)C(CC1=C2C(=C3C(=C1O)C(=O)C(=CO3)C4=CC(=C(C=C4)O)O)C=CC(O2)(C)C)O 436.50 unknown https://doi.org/10.1016/S0031-9422(00)90379-0
5,7-dihydroxy-6-[(2R)-2-hydroxy-3-methylbut-3-enyl]-3-(4-hydroxyphenyl)chromen-4-one 26250194 Click to see CC(=C)C(CC1=C(C2=C(C=C1O)OC=C(C2=O)C3=CC=C(C=C3)O)O)O 354.40 unknown https://doi.org/10.1016/S0031-9422(98)00380-X
https://doi.org/10.1016/S0031-9422(00)90379-0
5,7-dihydroxy-6-[(2S)-2-hydroxy-3-methylbut-3-enyl]-3-(4-hydroxyphenyl)chromen-4-one 26250192 Click to see CC(=C)C(CC1=C(C2=C(C=C1O)OC=C(C2=O)C3=CC=C(C=C3)O)O)O 354.40 unknown https://doi.org/10.1016/S0031-9422(98)00380-X
Alpinumisoflavone 5490139 Click to see CC1(C=CC2=C(O1)C=C3C(=C2O)C(=O)C(=CO3)C4=CC=C(C=C4)O)C 336.30 unknown https://doi.org/10.1016/0031-9422(94)00971-U
Auriculasin 5358846 Click to see CC(=CCC1=C2C(=C(C3=C1OC=C(C3=O)C4=CC(=C(C=C4)O)O)O)C=CC(O2)(C)C)C 420.50 unknown https://doi.org/10.1016/S0031-9422(00)90379-0
Laburnetin 15237156 Click to see CC(=C)C(CC1=C(C2=C(C=C1O)OC=C(C2=O)C3=CC=C(C=C3)O)O)O 354.40 unknown https://doi.org/10.1016/S0031-9422(98)00380-X
https://doi.org/10.1016/S0031-9422(00)90379-0
Osajin 95168 Click to see CC(=CCC1=C2C(=C3C(=C1O)C(=O)C(=CO3)C4=CC=C(C=C4)O)C=CC(O2)(C)C)C 404.50 unknown https://doi.org/10.1007/S10600-009-9243-Z
https://doi.org/10.1007/BF00567305
https://doi.org/10.1021/JF0342369
https://doi.org/10.1016/0031-9422(94)00971-U
https://doi.org/10.1002/JPS.3030410912
https://doi.org/10.1002/JPS.2600640121
https://doi.org/10.1016/J.BMCL.2007.06.060
https://doi.org/10.1016/S0031-9422(00)90379-0
Pomiferin 4871 Click to see CC(=CCC1=C2C(=C3C(=C1O)C(=O)C(=CO3)C4=CC(=C(C=C4)O)O)C=CC(O2)(C)C)C 420.50 unknown https://doi.org/10.1021/JF0342369
https://doi.org/10.1007/S10600-009-9243-Z
https://doi.org/10.1002/JPS.3030410912
https://doi.org/10.1002/JPS.2600640121
https://doi.org/10.1016/J.BMCL.2007.06.060
https://doi.org/10.1016/S0031-9422(00)90379-0
Warangalone 5379679 Click to see CC(=CCC1=C2C(=C(C3=C1OC=C(C3=O)C4=CC=C(C=C4)O)O)C=CC(O2)(C)C)C 404.50 unknown https://doi.org/10.1016/0031-9422(94)00971-U
https://doi.org/10.1016/S0031-9422(00)90379-0
Wighteone 5281814 Click to see CC(=CCC1=C(C2=C(C=C1O)OC=C(C2=O)C3=CC=C(C=C3)O)O)C 338.40 unknown https://doi.org/10.1016/S0031-9422(98)00380-X
https://doi.org/10.1016/0031-9422(94)00971-U
> Phenylpropanoids and polyketides / Isoflavonoids / Pyranoisoflavonoids
Parvisoflavone A 11710066 Click to see CC1(C=CC2=C(O1)C=C(C3=C2OC=C(C3=O)C4=C(C=C(C=C4)O)O)O)C 352.30 unknown https://doi.org/10.1016/0031-9422(94)00971-U
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 3-prenylated chalcones
2-Propen-1-one, 1-[2,4-dihydroxy-3-(3-methyl-2-butenyl)phenyl]-3-(2,4-dihydroxyphenyl)-, (E)-; (2E)-1-[2,4-Dihydroxy-3-(3-methyl-2-buten-1-yl)phenyl]-3-(2,4-dihydroxyphenyl)-2-propen-1-one 69906284 Click to see CC(=CCC1=C(C=CC(=C1O)C(=O)C=CC2=C(C=C(C=C2)O)O)O)C 340.40 unknown https://doi.org/10.1016/0031-9422(94)00971-U
> Phenylpropanoids and polyketides / Stilbenes
1-[2-(2,4-Dimethoxyphenyl)ethenyl]-3,5-dimethoxybenzene 5491 Click to see COC1=CC(=C(C=C1)C=CC2=CC(=CC(=C2)OC)OC)OC 300.30 unknown https://doi.org/10.1016/S0031-9422(00)80492-6
1,3-Benzenediol, 5-[(1Z)-2-(4-hydroxyphenyl)ethenyl]- 5056 Click to see C1=CC(=CC=C1C=CC2=CC(=CC(=C2)O)O)O 228.24 unknown https://doi.org/10.1016/S0031-9422(00)81238-8
2,3',4,5'-Tetramethoxystilbene 5354004 Click to see COC1=CC(=C(C=C1)C=CC2=CC(=CC(=C2)OC)OC)OC 300.30 unknown https://doi.org/10.1016/S0031-9422(00)80492-6
CID 73197 73197 Click to see C1=CC(=C(C=C1O)O)C=CC2=CC(=CC(=C2)O)O 244.24 unknown https://doi.org/10.1016/S0031-9422(00)80492-6
Oxyresveratrol 5281717 Click to see C1=CC(=C(C=C1O)O)C=CC2=CC(=CC(=C2)O)O 244.24 unknown https://doi.org/10.1016/S0031-9422(00)81238-8
https://doi.org/10.2298/JSC0303235D
https://doi.org/10.1016/S0031-9422(00)80492-6
Resveratrol 445154 Click to see C1=CC(=CC=C1C=CC2=CC(=CC(=C2)O)O)O 228.24 unknown https://doi.org/10.1016/S0031-9422(00)81238-8

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