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Artocarpus nobilis

Artocarpus nobilis - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID64400aed173ea958061245
Scientific name Artocarpus nobilis
Authority Thwaites
First published in Enum. Pl. Zeyl. : 282 (1861)

Description Top

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Synonyms Top

Scientific name Authority First published in
Saccus nobilis Kuntze Revis. Gen. Pl. 2: 633. 1891 [5 Nov 1891]
Artocarpus pubescens Moon Cat. Pl. Ceylon. 61. 1824

Common names Top

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Language Common/alternative name
Dutch වල් දෙල් හෙවත් බැදි දෙල්
Sinhala වල් දෙල් හෙවත් බැදි දෙල්

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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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000550554
Tropicos 100293254
KEW urn:lsid:ipni.org:names:850421-1
The Plant List kew-2654041
Open Tree Of Life 6107972
NCBI Taxonomy 2290778
IUCN Red List 30865
IPNI 850421-1
iNaturalist 189500
GBIF 3764420
Freebase /m/02x821d
EOL 7211999
USDA GRIN 474664
Wikipedia Artocarpus_nobilis

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
Adsorption of Chromium and Nickel Ions on Commercial Activated Carbon—An Analysis of Adsorption Kinetics and Statics Lach J, Okoniewska E Molecules 03-Nov-2023
PMCID:PMC10650461
doi:10.3390/molecules28217413
PMID:37959832
The significance of essential oils and their antifungal properties in the food industry: A systematic review Abdi-Moghadam Z, Mazaheri Y, Rezagholizade-shirvan A, Mahmoudzadeh M, Sarafraz M, Mohtashami M, Shokri S, Ghasemi A, Nickfar F, Darroudi M, Hossieni H, Hadian Z, Shamloo E, Rezaei Z Heliyon 29-Oct-2023
PMCID:PMC10637975
doi:10.1016/j.heliyon.2023.e21386
PMID:37954273
Valorization of Fibrous Plant-Based Food Waste as Biosorbents for Remediation of Heavy Metals from Wastewater—A Review Karim A, Raji Z, Karam A, Khalloufi S Molecules 20-May-2023
PMCID:PMC10221818
doi:10.3390/molecules28104205
PMID:37241944
Removal of heavy metals from binary and multicomponent adsorption systems using various adsorbents – a systematic review Bayuo J, Rwiza MJ, Sillanpää M, Mtei KM RSC Adv 28-Apr-2023
PMCID:PMC10140672
doi:10.1039/d3ra01660a
PMID:37124024
Assessing diversity and phylogeny of Indonesian breadfruit (Artocarpus spp.) using internal transcribed spacer (ITS) region and leaf morphology Mursyidin DH, Setiawan A J Genet Eng Biotechnol 09-Feb-2023
PMCID:PMC9911577
doi:10.1186/s43141-023-00476-y
PMID:36757524
Novel eco-friendly [1,2,4]triazolo[3,4-a]isoquinoline chalcone derivatives efficiency against fungal deterioration of ancient Egyptian mummy cartonnage, Egypt Geweely NS, Soliman MM, Ali RA, Hassaneen HM, Abdelhamid IA Arch Microbiol 07-Jan-2023
PMCID:PMC9825552
doi:10.1007/s00203-022-03395-7
PMID:36609727
Advances in the Removal of Cr(III) from Spent Industrial Effluents—A Review Staszak K, Kruszelnicka I, Ginter-Kramarczyk D, Góra W, Baraniak M, Lota G, Regel-Rosocka M Materials (Basel) 30-Dec-2022
PMCID:PMC9822515
doi:10.3390/ma16010378
PMID:36614717
Homo sapiens lithic technology and microlithization in the South Asian rainforest at Kitulgala Beli-lena (c. 45 – 8,000 years ago) Picin A, Wedage O, Blinkhorn J, Amano N, Deraniyagala S, Boivin N, Roberts P, Petraglia M PLoS One 13-Oct-2022
PMCID:PMC9560501
doi:10.1371/journal.pone.0273450
PMID:36227910
Phenolic Profile, Antioxidant, Anti-Enzymatic and Cytotoxic Activity of the Fruits and Roots of Eleutherococcus senticosus (Rupr. et Maxim.) Maxim Graczyk F, Gębalski J, Makuch-Kocka A, Gawenda-Kempczyńska D, Ptaszyńska AA, Grzyb S, Bogucka-Kocka A, Załuski D Molecules 30-Aug-2022
PMCID:PMC9457789
doi:10.3390/molecules27175579
PMID:36080343
Global Perspective of Plant-Based Cosmetic Industry and Possible Contribution of Sri Lanka to the Development of Herbal Cosmetics Nadeeshani Dilhara Gamage DG, Dharmadasa RM, Chandana Abeysinghe D, Saman Wijesekara RG, Prathapasinghe GA, Someya T Evid Based Complement Alternat Med 04-Mar-2022
PMCID:PMC8916882
doi:10.1155/2022/9940548
PMID:35280508
Chalcone Scaffolds, Bioprecursors of Flavonoids: Chemistry, Bioactivities, and Pharmacokinetics Rudrapal M, Khan J, Dukhyil AA, Alarousy RM, Attah EI, Sharma T, Khairnar SJ, Bendale AR Molecules 26-Nov-2021
PMCID:PMC8659147
doi:10.3390/molecules26237177
PMID:34885754
Chalcones: Synthetic Chemistry Follows Where Nature Leads Jasim HA, Nahar L, Jasim MA, Moore SA, Ritchie KJ, Sarker SD Biomolecules 13-Aug-2021
PMCID:PMC8392591
doi:10.3390/biom11081203
PMID:34439870
Ethnopharmacological Survey on Medicinal Plants Used for Cosmetic Treatments in Traditional and Ayurveda Systems of Medicine in Sri Lanka Gamage DG, Dharmadasa RM, Abeysinghe DC, Wijesekara RG, Prathapasinghe GA, Someya T Evid Based Complement Alternat Med 26-Jun-2021
PMCID:PMC8257331
doi:10.1155/2021/5599654
PMID:34257686
An extensive review on chromium (vi) removal using natural and agricultural wastes materials as alternative biosorbents Bayuo J J Environ Health Sci Eng 10-Mar-2021
PMCID:PMC8172654
doi:10.1007/s40201-021-00641-w
PMID:34150305
Scientific opinion on the import of Musa fruits as a pathway for the entry of non‐EU Tephritidae into the EU territory Bragard C, Dehnen‐Schmutz K, Di Serio F, Gonthier P, Jacques M, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Thulke H, Vicent Civera A, Yuen J, Zappalà L, Papadopoulos N, Papanastasiou S, Czwienczek E, Kertész V, MacLeod A EFSA J 08-Mar-2021
PMCID:PMC7938759
doi:10.2903/j.efsa.2021.6426
PMID:33732390

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
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(4,4,6a,6b,8a,11,11,14b-Octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl) acetate 345510 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4CC(CC5)(C)C)C)C)C)C 468.80 unknown https://doi.org/10.1016/J.PHYTOL.2010.07.008
beta-Amyrin acetate 92156 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4CC(CC5)(C)C)C)C)C)C 468.80 unknown https://doi.org/10.1016/J.PHYTOL.2010.07.008
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/10.1016/J.PHYTOL.2010.07.008
Lupeol Acetate 92157 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/10.1016/J.PHYTOL.2010.07.008
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cycloartanols and derivatives
(1S,3R,6S,8S,11R,12S,15R,16R)-7,7,12,16-tetramethyl-15-[(2S)-6-methylhept-5-en-2-yl]pentacyclo[9.7.0.01,3.03,8.012,16]octadecan-6-ol 162953296 Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C 426.70 unknown https://doi.org/10.1016/0031-9422(73)85088-5
(1S,3R,8S,11S,12S,15R,16R)-7,7,12,16-tetramethyl-15-[(2R)-6-methylhept-5-en-2-yl]pentacyclo[9.7.0.01,3.03,8.012,16]octadecan-6-one 163000436 Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(=O)C5(C)C)C)C 424.70 unknown https://doi.org/10.1016/0031-9422(73)85088-5
[(1S,3R,6S,8R,11S,12S,15R,16R)-7,7,12,16-tetramethyl-15-[(2S)-6-methylhept-5-en-2-yl]-6-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl] acetate 162935455 Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)OC(=O)C)C)C 468.80 unknown https://doi.org/10.1016/0031-9422(73)85088-5
[15-(5,6-Dimethylhept-6-en-2-yl)-7,7,12,16-tetramethyl-6-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl] acetate 14312788 Click to see CC(CCC(C)C(=C)C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)OC(=O)C)C)C 482.80 unknown https://doi.org/10.1016/J.PHYTOL.2010.07.008
9,19-Cyclo-9beta-lanost-24-en-3beta-ol 500213 Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C 426.70 unknown https://doi.org/10.1016/0031-9422(73)85088-5
9,19-Cyclolanost-24-en-3-ol, acetate, (3beta)- 518616 Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)OC(=O)C)C)C 468.80 unknown https://doi.org/10.1016/0031-9422(73)85088-5
CID 348093 348093 Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(=O)C5(C)C)C)C 424.70 unknown https://doi.org/10.1016/0031-9422(73)85088-5
Cyclolaudenyl acetate 14312790 Click to see CC(CCC(C)C(=C)C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)OC(=O)C)C)C 482.80 unknown https://doi.org/10.1016/J.PHYTOL.2010.07.008
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid esters
[(1S,3S,6S,11S,12S,15S,16R)-15-acetyl-7,7,12,16-tetramethyl-6-pentacyclo[9.7.0.01,3.03,8.012,16]octadec-8-enyl] acetate 16112793 Click to see CC(=O)C1CCC2(C1(CCC34C2CC=C5C3(C4)CCC(C5(C)C)OC(=O)C)C)C 398.60 unknown https://doi.org/10.1515/ZNB-2007-0222
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / Pyranoxanthones
(17R)-12,21,23-trihydroxy-8,8,18,18-tetramethyl-3,9,19-trioxahexacyclo[15.6.1.02,15.04,13.05,10.020,24]tetracosa-1(24),2(15),4(13),5(10),6,11,20,22-octaen-14-one 162872214 Click to see CC1(C=CC2=C(O1)C=C(C3=C2OC4=C(C3=O)CC5C6=C4C(=CC(=C6OC5(C)C)O)O)O)C 434.40 unknown https://doi.org/10.1016/0031-9422(89)80059-7
(17S)-12,21,23-trihydroxy-8,8,18,18-tetramethyl-3,9,19-trioxahexacyclo[15.6.1.02,15.04,13.05,10.020,24]tetracosa-1(24),2(15),4(13),5(10),6,11,20,22-octaen-14-one 46887867 Click to see CC1(C=CC2=C(O1)C=C(C3=C2OC4=C(C3=O)CC5C6=C4C(=CC(=C6OC5(C)C)O)O)O)C 434.40 unknown https://doi.org/10.1016/0031-9422(89)80059-7
https://doi.org/10.1016/J.FITOTE.2007.07.014
Artobiloxanthoe 10071572 Click to see CC(=C)C1CC2=C(C3=C1C(=C(C=C3O)O)O)OC4=C(C2=O)C(=CC5=C4C=CC(O5)(C)C)O 434.40 unknown https://doi.org/10.1016/J.FITOTE.2007.07.014
https://doi.org/10.1016/J.PHYTOL.2010.07.008
https://doi.org/10.1016/0031-9422(89)80059-7
Artobiloxanthone 46887866 Click to see CC(=C)C1CC2=C(C3=C1C(=C(C=C3O)O)O)OC4=C(C2=O)C(=CC5=C4C=CC(O5)(C)C)O 434.40 unknown https://doi.org/10.1016/J.FITOTE.2007.07.014
https://doi.org/10.1016/J.PHYTOL.2010.07.008
https://doi.org/10.1016/0031-9422(89)80059-7
CID 21672553 21672553 Click to see CC(=C)C1CC2=C(C3=C1C(=C(C=C3O)O)O)OC4=C(C2=O)C(=CC5=C4C=CC(O5)(C)C)O 434.40 unknown https://doi.org/10.1016/0031-9422(89)80059-7
Cycloartobiloxanthone 10342859 Click to see CC1(C=CC2=C(O1)C=C(C3=C2OC4=C(C3=O)CC5C6=C4C(=CC(=C6OC5(C)C)O)O)O)C 434.40 unknown https://doi.org/10.1016/J.FITOTE.2007.07.014
https://doi.org/10.1016/0031-9422(89)80059-7
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 3-prenylated flavans / 3-prenylated flavanones
(2R)-2-[3-[(2E)-3,7-dimethylocta-2,6-dienyl]-4-hydroxyphenyl]-5,7-dihydroxy-2,3-dihydrochromen-4-one 162955077 Click to see CC(=CCCC(=CCC1=C(C=CC(=C1)C2CC(=O)C3=C(C=C(C=C3O2)O)O)O)C)C 408.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.04.011
2-[3-(3,7-Dimethylocta-2,6-dienyl)-4-hydroxyphenyl]-5,7-dihydroxy-2,3-dihydrochromen-4-one 66839797 Click to see CC(=CCCC(=CCC1=C(C=CC(=C1)C2CC(=O)C3=C(C=C(C=C3O2)O)O)O)C)C 408.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.04.011
2-[3-(3,7-Dimethylocta-2,6-dienyl)-4,5-dihydroxyphenyl]-5,7-dihydroxy-2,3-dihydrochromen-4-one 66839910 Click to see CC(=CCCC(=CCC1=C(C(=CC(=C1)C2CC(=O)C3=C(C=C(C=C3O2)O)O)O)O)C)C 424.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.04.011
Isonymphaeol B 10070991 Click to see CC(=CCCC(=CCC1=C(C(=CC(=C1)C2CC(=O)C3=C(C=C(C=C3O2)O)O)O)O)C)C 424.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.04.011
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 8-prenylated flavans / 8-prenylated flavanones
(2S)-7,4'-Dihydroxy-8-geranylflavanone 42607813 Click to see CC(=CCCC(=CCC1=C(C=CC2=C1OC(CC2=O)C3=CC=C(C=C3)O)O)C)C 392.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.04.011
8-(3,7-Dimethylocta-2,6-dienyl)-7-hydroxy-2-(4-hydroxyphenyl)-2,3-dihydrochromen-4-one 74819339 Click to see CC(=CCCC(=CCC1=C(C=CC2=C1OC(CC2=O)C3=CC=C(C=C3)O)O)C)C 392.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.04.011
> Phenylpropanoids and polyketides / Flavonoids / Flavones / 3-prenylated flavones
2-(4,5-Dihydroxy-2-methoxyphenyl)-5-hydroxy-8,8-dimethyl-3-(3-methylbut-2-enyl)pyrano[2,3-h]chromen-4-one 163049420 Click to see CC(=CCC1=C(OC2=C(C1=O)C(=CC3=C2C=CC(O3)(C)C)O)C4=CC(=C(C=C4OC)O)O)C 450.50 unknown https://doi.org/10.1016/J.FITOTE.2007.07.014
8-(4,5-Dihydroxy-2-methoxyphenyl)-5-hydroxy-2,2-dimethyl-7-(3-methylbut-2-enyl)pyrano[3,2-g]chromen-6-one 162870414 Click to see CC(=CCC1=C(OC2=CC3=C(C=CC(O3)(C)C)C(=C2C1=O)O)C4=CC(=C(C=C4OC)O)O)C 450.50 unknown https://doi.org/10.1016/J.FITOTE.2007.07.014
Artobilichromene 14259062 Click to see CC(=CCC1=C(C(=CC(=C1O)O)C2=CC(=O)C3=C(C4=C(C=C3O2)OC(C=C4)(C)C)O)O)C 436.50 unknown https://doi.org/10.1016/0031-9422(89)80059-7
Artonin E 5481962 Click to see CC(=CCC1=C(OC2=C(C1=O)C(=CC3=C2C=CC(O3)(C)C)O)C4=CC(=C(C=C4O)O)O)C 436.50 unknown https://doi.org/10.1016/J.FITOTE.2007.07.014
https://doi.org/10.1016/J.PHYTOL.2010.07.008
> Phenylpropanoids and polyketides / Flavonoids / Flavones / 6-prenylated flavones
2-(4,5-Dihydroxy-2-methoxyphenyl)-5,7-dihydroxy-3,6-bis(3-methylbut-2-enyl)chromen-4-one 162944028 Click to see CC(=CCC1=C(C2=C(C=C1O)OC(=C(C2=O)CC=C(C)C)C3=CC(=C(C=C3OC)O)O)O)C 452.50 unknown https://doi.org/10.1016/J.FITOTE.2007.07.014
> Phenylpropanoids and polyketides / Flavonoids / Flavones / 8-prenylated flavones
2-(3,4-Dihydroxyphenyl)-8-(3,7-dimethylocta-2,6-dienyl)-7-hydroxychromen-4-one 73236019 Click to see CC(=CCCC(=CCC1=C(C=CC2=C1OC(=CC2=O)C3=CC(=C(C=C3)O)O)O)C)C 406.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.04.011
2-(3,4-dihydroxyphenyl)-8-[(2E)-3,7-dimethylocta-2,6-dienyl]-7-hydroxychromen-4-one 16081691 Click to see CC(=CCCC(=CCC1=C(C=CC2=C1OC(=CC2=O)C3=CC(=C(C=C3)O)O)O)C)C 406.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.04.011
2-(4,5-Dihydroxy-2-methoxyphenyl)-5,7-dihydroxy-3,8-bis(3-methylbut-2-enyl)chromen-4-one 163010099 Click to see CC(=CCC1=C2C(=C(C=C1O)O)C(=O)C(=C(O2)C3=CC(=C(C=C3OC)O)O)CC=C(C)C)C 452.50 unknown https://doi.org/10.1016/J.FITOTE.2007.07.014
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
[(2R,3S,4S,5R,6S)-6-[(2S,3R,4S,5R,6S)-6-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-4,5-dihydroxy-2-methyloxan-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl acetate 5319939 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)O)O)OC5C(C(C(C(O5)COC(=O)C)O)O)O 636.60 unknown https://doi.org/10.1016/J.PHYTOL.2010.07.008
[(2R,3S,4S,5R,6S)-6-[(2S,3R,4S,5R)-6-[5,7-Dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-4,5-dihydroxy-2-methyloxan-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl acetate 73981677 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)O)O)OC5C(C(C(C(O5)COC(=O)C)O)O)O 636.60 unknown https://doi.org/10.1016/J.PHYTOL.2010.07.008
> Phenylpropanoids and polyketides / Flavonoids / Pyranoflavonoids
(6S)-3,8,10-trihydroxy-6-(2-methylprop-1-enyl)-6H-chromeno[4,3-b]chromen-7-one 124303545 Click to see CC(=CC1C2=C(C3=C(O1)C=C(C=C3)O)OC4=CC(=CC(=C4C2=O)O)O)C 352.30 unknown https://doi.org/10.1016/J.PHYTOL.2010.07.008
Cyclocommunol 10315987 Click to see CC(=CC1C2=C(C3=C(O1)C=C(C=C3)O)OC4=CC(=CC(=C4C2=O)O)O)C 352.30 unknown https://doi.org/10.1016/J.PHYTOL.2010.07.008
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
(3E)-1-[(S)-5-Hydroxy-2-methyl-2-(4-methyl-3-pentenyl)-2H-1-benzopyran-6-yl]-3-(4-hydroxyphenyl)-2-propene-1-one 101505024 Click to see CC(=CCCC1(C=CC2=C(O1)C=CC(=C2O)C(=O)C=CC3=CC=C(C=C3)O)C)C 390.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.04.011
(E)-1-[(2R,3R)-3,5-dihydroxy-2-methyl-2-(4-methylpent-3-enyl)-3,4-dihydrochromen-6-yl]-3-(4-hydroxyphenyl)prop-2-en-1-one 163038236 Click to see CC(=CCCC1(C(CC2=C(O1)C=CC(=C2O)C(=O)C=CC3=CC=C(C=C3)O)O)C)C 408.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.04.011
1-[3,5-Dihydroxy-2-methyl-2-(4-methylpent-3-enyl)-3,4-dihydrochromen-6-yl]-3-(4-hydroxyphenyl)prop-2-en-1-one 73236018 Click to see CC(=CCCC1(C(CC2=C(O1)C=CC(=C2O)C(=O)C=CC3=CC=C(C=C3)O)O)C)C 408.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.04.011
5-Hydroxy-6-(4-hydroxycinnamoyl)-2-methyl-2-(4-methyl-3-pentenyl)-2h-1-benzopyran 74037136 Click to see CC(=CCCC1(C=CC2=C(O1)C=CC(=C2O)C(=O)C=CC3=CC=C(C=C3)O)C)C 390.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.04.011
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 3-prenylated chalcones
(E)-1-[2,4-dihydroxy-3-[(2E,5S)-5-methoxy-3,7-dimethylocta-2,6-dienyl]phenyl]-3-(4-hydroxyphenyl)prop-2-en-1-one 163195552 Click to see CC(=CC(CC(=CCC1=C(C=CC(=C1O)C(=O)C=CC2=CC=C(C=C2)O)O)C)OC)C 422.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.04.011
(E)-1-[2,4-dihydroxy-3-[(2E,6R)-6-hydroxy-3,7-dimethylocta-2,7-dienyl]phenyl]-3-(3,4-dihydroxyphenyl)prop-2-en-1-one 163193457 Click to see CC(=C)C(CCC(=CCC1=C(C=CC(=C1O)C(=O)C=CC2=CC(=C(C=C2)O)O)O)C)O 424.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.03.033
(E)-1-[2,4-dihydroxy-3-[(2E,6R)-6-hydroxy-3,7-dimethylocta-2,7-dienyl]phenyl]-3-(4-hydroxyphenyl)prop-2-en-1-one 162964110 Click to see CC(=C)C(CCC(=CCC1=C(C=CC(=C1O)C(=O)C=CC2=CC=C(C=C2)O)O)C)O 408.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.04.011
https://doi.org/10.1016/J.PHYTOCHEM.2004.03.033
(E)-1-[2,4-dihydroxy-3-[(2E,6S)-6-hydroxy-3,7-dimethylocta-2,7-dienyl]phenyl]-3-(4-hydroxyphenyl)prop-2-en-1-one 162964112 Click to see CC(=C)C(CCC(=CCC1=C(C=CC(=C1O)C(=O)C=CC2=CC=C(C=C2)O)O)C)O 408.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.04.011
(E)-1-[2,4-dihydroxy-3-[(2R)-2-hydroxy-7-methyl-3-methylideneoct-6-enyl]phenyl]-3-(4-hydroxyphenyl)prop-2-en-1-one 122398175 Click to see CC(=CCCC(=C)C(CC1=C(C=CC(=C1O)C(=O)C=CC2=CC=C(C=C2)O)O)O)C 408.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.03.033
1-[2,4-Dihydroxy-3-(5-methoxy-3,7-dimethylocta-2,6-dienyl)phenyl]-3-(4-hydroxyphenyl)prop-2-en-1-one 73236020 Click to see CC(=CC(CC(=CCC1=C(C=CC(=C1O)C(=O)C=CC2=CC=C(C=C2)O)O)C)OC)C 422.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.04.011
1-[2,4-Dihydroxy-3-(6-hydroxy-3,7-dimethylocta-2,7-dienyl)phenyl]-3-(3,4-dihydroxyphenyl)prop-2-en-1-one 72967248 Click to see CC(=C)C(CCC(=CCC1=C(C=CC(=C1O)C(=O)C=CC2=CC(=C(C=C2)O)O)O)C)O 424.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.03.033
1-[3-(3,7-Dimethylocta-2,6-dienyl)-2,4-dihydroxyphenyl]-3-(4-hydroxyphenyl)prop-2-en-1-one 124949 Click to see CC(=CCCC(=CCC1=C(C=CC(=C1O)C(=O)C=CC2=CC=C(C=C2)O)O)C)C 392.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.04.011
https://doi.org/10.1016/J.PHYTOCHEM.2004.03.033
2',4',4-Trihydroxy-3'-[2-hydroxy-7-methyl-3-methylene-6-octaenyl]chalcone 72812157 Click to see CC(=CCCC(=C)C(CC1=C(C=CC(=C1O)C(=O)C=CC2=CC=C(C=C2)O)O)O)C 408.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.03.033
2',4',4-Trihydroxy-3'-[6-hydroxy-3,7-dimethyl-2,7-octadienyl]chalcone 85134973 Click to see CC(=C)C(CCC(=CCC1=C(C=CC(=C1O)C(=O)C=CC2=CC=C(C=C2)O)O)C)O 408.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.03.033
https://doi.org/10.1016/J.PHYTOCHEM.2006.04.011
3-(3,4-Dihydroxyphenyl)-1-[3-(3,7-dimethylocta-2,6-dienyl)-2,4-dihydroxyphenyl]prop-2-en-1-one 54453233 Click to see CC(=CCCC(=CCC1=C(C=CC(=C1O)C(=O)C=CC2=CC(=C(C=C2)O)O)O)C)C 408.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.04.011
https://doi.org/10.1016/J.PHYTOCHEM.2004.03.033
3'-Geranyl-2',3,4,4'-tetrahydroxychalcone 11742190 Click to see CC(=CCCC(=CCC1=C(C=CC(=C1O)C(=O)C=CC2=CC(=C(C=C2)O)O)O)C)C 408.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.04.011
Xanthoangelol 643007 Click to see CC(=CCCC(=CCC1=C(C=CC(=C1O)C(=O)C=CC2=CC=C(C=C2)O)O)C)C 392.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.04.011
https://doi.org/10.1016/J.PHYTOCHEM.2004.03.033

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