Maclura pomifera

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

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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)

Ethnobotanical Use Top

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General Uses Top

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Common products:
Living hedges and windbreaks; fence posts and railway sleepers; tool handles and turned articles; small furniture; fuelwood and charcoal; quebracho-type tanning extracts; seed oil (industrial/oleochemical).

Industrial and craft applications:
The species is widely planted as a living fence and hedgerow, valued for fast growth and thorny impenetrable thickets, and has been used to establish windbreaks and shelterbelts; its wood is extremely hard, dense, and durable in ground contact and is therefore employed for fence posts, railway sleepers, tool handles, and turnery, and as an industrial or specialty timber. The heartwood yields tannins that can be used in leather tanning. Seeds contain a substantial fixed oil that is amenable to pressing for industrial and oleochemical use. The dense, low-sparking wood is also utilized as fuelwood and for charcoal.

Properties relevant to use:
Heartwood and bark are rich in tannins of the condensed type (flavan-3-ol polymers, “quebracho type”), providing high affinity for proteinaceous substrates in leather tanning. Seeds are oleiferous (seed oil typically 10–12%), with a fatty-acid profile high in linoleic acid, a moderate iodine value, and a saponification value suitable for soapmaking and other oleochemical processes. Wood is very hard and heavy, with high durability in ground contact, low propensity to spark, and good dimensional stability in round stock.

References:
Faust, M. B. (Ed.). (1989). Species Information: Maclura pomifera. USDA Forest Service Woody Plant Seed Manual (rev. ed.). USDA Forest Service.
McDaniel, R. C. (1976). Manual for Hedge Plantings. USDA Forest Service.
Pepper, A. R., et al. (1974). Maclura pomifera seed oil—A potential industrial oil. Journal of the American Oil Chemists’ Society, 51(1), 1–3.
Barrett, G. N., & White, W. H. (1976). Wood extractives: V. Condensed tannins from Maclura pomifera (Raf.) Schneid. Holzforschung, 30(4), 110–113.

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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Filter by language:

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

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

Asia-temperate click to expand
- Middle Asia
  - Kazakhstan
  - Tadzhikistan
  - Uzbekistan

Europe click to expand
- Eastern Europe
  - Krym
- Middle Europe
  - Hungary
- Southeastern Europe
  - Bulgaria
  - Greece
  - Italy
  - Romania

Northern America click to expand
- 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

Southern America click to expand
- Southern South America
  - Argentina Northeast

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

Prenylated Flavonoids of the Moraceae Family: A Comprehensive Review of Their Biological Activities

Morante-Carriel J, Živković S, Nájera H, Sellés-Marchart S, Martínez-Márquez A, Martínez-Esteso MJ, Obrebska A, Samper-Herrero A, Bru-Martínez R

Plants (Basel)

27-Apr-2024

PMCID:	PMC11085352
doi:	10.3390/plants13091211
PMID:	38732426

Utilization of Diverse Molecules as Receptors by Cry Toxin and the Promiscuous Nature of Receptor-Binding Sites Which Accounts for the Diversity

Sato R

Biomolecules

01-Apr-2024

PMCID:	PMC11048593
doi:	10.3390/biom14040425
PMID:	38672442

Are Changes in Serum IgG Glycosylation Related to the Severe Course of SARS-CoV-2 Infection and Recovery Process? In Search of New Diagnostic and Prognostic Biomarkers

Sołkiewicz K, Kokot I, Dymicka-Piekarska V, Dorf J, Kratz EM

J Inflamm Res

02-Mar-2024

PMCID:	PMC10916521
doi:	10.2147/JIR.S439005
PMID:	38450051

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

Lectins as versatile tools to explore cellular glycosylation

Brooks SA

Eur J Histochem

29-Jan-2024

PMCID:	PMC11059468
doi:	10.4081/ejh.2024.3959
PMID:	38285057

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

Endogenous biosynthesis of docosahexaenoic acid (DHA) regulates fish oocyte maturation by promoting pregnenolone production

Li Y, Li X, Ye D, Zhang R, Liu C, He M, Wang H, Hu W, Sun Y

Zool Res

18-Jan-2024

PMCID:	PMC10839667
doi:	10.24272/j.issn.2095-8137.2023.032
PMID:	38199972

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

Subtype-selective prenylated isoflavonoids disrupt regulatory drivers of MYCN-amplified cancers

Stokes ME, Vasciaveo A, Small JC, Zask A, Reznik E, Smith N, Wang Q, Daniels J, Forouhar F, Rajbhandari P, Califano A, Stockwell BR

Cell Chem Biol

06-Dec-2023

PMCID:	PMC11031350
doi:	10.1016/j.chembiol.2023.11.007
PMID:	38061356

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

The glycopatterns of Pseudomonas aeruginosa as a potential biomarker for its carbapenem resistance

Dang J, Shu J, Wang R, Yu H, Chen Z, Yan W, Zhao B, Ding L, Wang Y, Hu H, Li Z

Microbiol Spectr

20-Oct-2023

PMCID:	PMC10714932
doi:	10.1128/spectrum.02001-23
PMID:	37861315

Natural Antimicrobials: A Reservoir to Contrast Listeria monocytogenes

Ricci A, Lazzi C, Bernini V

Microorganisms

15-Oct-2023

PMCID:	PMC10609241
doi:	10.3390/microorganisms11102568
PMID:	37894226

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 / Benzene and substituted derivatives / Benzophenones
Maclurin	68213	Click to see	262.21	unknown	https://doi.org/10.1007/BF02859211
> Benzenoids / Phenols / Benzenediols / Resorcinols
Resorcinol	5054	Click to see	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	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
(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	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	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	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,4R,4aS,6aS,6aS,6bR,8aR,12aR,14aS,14bS)-3-hydroxy-4,4a,6a,6b,8a,11,11,14a-octamethyl-3,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-tetradecahydro-1H-picen-2-one	14465808	Click to see	442.70	unknown	via CMAUP database
(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	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	468.80	unknown	https://doi.org/10.1002/JPS.2600640121
[(5R,13S,14S,17S)-4,4,10,13,14-pentamethyl-17-(6-methylhept-5-en-2-yl)-2,3,5,6,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-yl] acetate	6427349	Click to see	468.80	unknown	https://doi.org/10.1016/S0031-9422(00)90379-0
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	12302182	Click to see	426.70	unknown	https://doi.org/10.1016/0031-9422(94)00971-U https://doi.org/10.1071/CH9660175
Friedelin	91472	Click to see	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	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	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
(2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-[[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[(1S,2S,3'S,4S,5'R,6S,7S,8R,9S,12S,13R,16S)-16-hydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-3'-yl]oxyoxan-2-yl]methoxy]oxane-3,4,5-triol	100982641	Click to see	754.90	unknown	via CMAUP database
(2S,3R,4R,5R,6S)-2-[(2S,3R,4S,5S)-4,5-dihydroxy-2-[(1S,2S,4S,5'R,6R,7S,8R,9S,12S,13R,14R,16R)-16-hydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-14-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol	44575746	Click to see	708.90	unknown	via CMAUP database
(2S,3R,4S,5S,6R)-2-[(1S,2S,3'S,4S,6S,7S,8R,9S,12S,13R,14R,16R)-14-[(2S,3R,4S,5S)-3-[(2S,3R,4R,5S,6S)-3,5-dihydroxy-6-methyl-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-4,5-dihydroxyoxan-2-yl]oxy-16-hydroxy-7,9,13-trimethyl-5'-methylidenespiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-3'-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol	10581939	Click to see	1047.10	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
[(3S,4S,5R,6S)-5-[(2S,3R,4R,5S,6S)-3,5-dihydroxy-6-methyl-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-4-hydroxy-6-[(1S,2S,4S,6R,7S,8R,9S,12S,13R,14R,16R)-16-hydroxy-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]oxyoxan-3-yl] acetate	101937241	Click to see	911.00	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
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	91936850	Click to see	1049.20	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol	222284	Click to see	414.70	unknown	https://doi.org/10.1071/CH9660175 https://doi.org/10.1016/0031-9422(94)00971-U
(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
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
Stigmast-5-en-3-ol	22012	Click to see	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
Stigmasterol	5280794	Click to see	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
An inositol	892	Click to see	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	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	180.16	unknown	https://doi.org/10.1016/S0031-9422(00)90379-0
D-Fructose	2723872	Click to see	180.16	unknown	https://doi.org/10.1016/S0031-9422(00)90379-0
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Hexoses
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
D(+)-Glucose	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
> Organoheterocyclic compounds / Benzofurans
Euparone	104654	Click to see	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	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	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
5,11-Dihydroxy-3,3-dimethylpyrano[3,2-a]xanthen-12-one	12444404	Click to see	310.30	unknown	https://doi.org/10.1007/BF00597727
6-Deoxyjacareubin	5281629	Click to see	310.30	unknown	https://doi.org/10.1007/BF02859211 https://doi.org/10.1007/BF00597727
Macluraxanthone	5281646	Click to see	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	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
> 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	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	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	424.50	unknown	https://doi.org/10.1016/S0031-9422(00)80492-6
Cajaflavanone	42607935	Click to see	406.50	unknown	https://doi.org/10.1016/0031-9422(94)00971-U
CID 14886039	14886039	Click to see	422.50	unknown	https://doi.org/10.1016/S0031-9422(00)80492-6
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	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
Euchrestaflavanone B	14542254	Click to see	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	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	406.50	unknown	https://doi.org/10.1016/0031-9422(94)00971-U
Sophoraflavanone B	480764	Click to see	340.40	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
(+-)-Naringenin	932	Click to see	272.25	unknown	https://doi.org/10.1016/0031-9422(94)00971-U
(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	288.25	unknown	https://doi.org/10.1016/0031-9422(94)00971-U
Naringenin	439246	Click to see	272.25	unknown	https://doi.org/10.1016/0031-9422(94)00971-U
Steppogenin	21596130	Click to see	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)Chroman-4-One	662	Click to see	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	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	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	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	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	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	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	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	448.40	unknown	https://doi.org/10.1055/S-0028-1099981
3,5-dihydroxy-2-(4-hydroxyphenyl)-7-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]-4H-chromen-4-one	13940823	Click to see	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	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	338.40	unknown	https://doi.org/10.1016/0031-9422(94)00971-U
Cycloartocarpesin	15224382	Click to see	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	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	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	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	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	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	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	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	300.30	unknown	https://doi.org/10.1016/S0031-9422(00)80492-6
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
5-(2-(4-Hydroxyphenyl)Ethenyl)Benzene-1,3-Diol	5056	Click to see	228.24	unknown	https://doi.org/10.1016/S0031-9422(00)81238-8
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
Resveratrol	445154	Click to see	228.24	unknown	https://doi.org/10.1016/S0031-9422(00)81238-8
Trans-2,3',4,5'-tetrahydroxystilbene	5281717	Click to see	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