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Erythrina suberosa

Erythrina suberosa - 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 UUID643fd9527cb8e864033938
Scientific name Erythrina suberosa
Authority Roxb.
First published in Fl. Ind. ed. 1832, 3: 253 (1832)

Description Top

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Synonyms Top

Scientific name Authority First published in
Erythrina glabrescens (Prain) R.Parker
Erythrina stricta var. suberosa (Roxb.) Niyomdham Nordic J. Bot.12: 342 (1992)
Erythrina sublobata Roxb. Fl. Ind. ed. 1832, 3: 254 (1832)
Erythrina suberosa var. glabrescens Prain J. Asiat. Soc. Bengal, Pt. 2, Nat. Hist.66: 410 (1897)
Micropteryx suberosa (Roxb.) Walp. Linnaea23: 740 (1851)
Micropteryx sublobata (Roxb.) Walp. Linnaea23: 740 (1851)
Erythrina maxima Roxb. ex Wight & Arn. Prodr. Fl. Ind. Orient.1: 261 (1834)
Erythrina bisetosa Griff. Not. Pl. Asiat.4: 441 (1854)
Erythrina hamiltoniana Steud. Nomencl. Bot., ed. 2, 1: 596 (1840)
Erythrina glabrescens (Prain) R.Parker Indian Forester46: 647 (1920)
Erythrina suberosa var. sublobata Roxb. ex Haines Bot. Bihar Orissa: 285 (1925)
Erythrina suberosa var. glabrescens Haines Bot. Bihar & Orissa 1: 285 1925
Corallodendron suberosum (Roxb.) Kuntze Revis. Gen. Pl.1: 173 (1891)

Common names Top

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Language Common/alternative name
Nepali फलेदो

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

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000185019
Tropicos 13030287
KEW urn:lsid:ipni.org:names:494598-1
The Plant List ild-31145
Open Tree Of Life 583667
NCBI Taxonomy 1288013
iNaturalist 461918
GBIF 5349546
EOL 643183
USDA GRIN 15768
Wikipedia Erythrina_suberosa

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
Recent updates on nano-phyto-formulations based therapeutic intervention for cancer treatment WAHI A, BISHNOI M, RAINA N, SINGH MA, VERMA P, GUPTA PK, KAUR G, TULI HS, GUPTA M Oncol Res 15-Nov-2023
PMCID:PMC10767243
doi:10.32604/or.2023.042228
PMID:38188681
Implementation of machine learning in DNA barcoding for determining the plant family taxonomy Riza LS, Zain MI, Izzuddin A, Prasetyo Y, Hidayat T, Abu Samah KA Heliyon 21-Sep-2023
PMCID:PMC10520734
doi:10.1016/j.heliyon.2023.e20161
PMID:37767518
Ethnoveterinary practises of medicinal plants used for the treatment of different cattle diseases: A case study in East Khasi Hill district of Meghalaya, North East India Bhat NA, Jeri L, Karmakar D, Mipun P, Bharali P, Sheikh N, Nongkynrih CJ, Kumar Y Heliyon 13-Jul-2023
PMCID:PMC10368863
doi:10.1016/j.heliyon.2023.e18214
PMID:37501975
Phytochemical-Mediated Biosynthesis of Silver Nanoparticles from Strobilanthes glutinosus: Exploring Biological Applications Javed R, Ijaz S, Hameed H, Nazish M, Sharif MS, Afreen A, Alarjani KM, Elshikh MS, Mehboob S, Abdul Razak S, Waheed A, Ahmed R, Tariq M Micromachines (Basel) 04-Jul-2023
PMCID:PMC10386440
doi:10.3390/mi14071372
PMID:37512683
Terminalia chebula-Assisted Silver Nanoparticles: Biological Potential, Synthesis, Characterization, and Ecotoxicity Tharani M, Rajeshkumar S, Al-Ghanim KA, Nicoletti M, Sachivkina N, Govindarajan M Biomedicines 18-May-2023
PMCID:PMC10216392
doi:10.3390/biomedicines11051472
PMID:37239143
Development of a risk score to identify patients at high risk for a severe course of COVID-19. Jacob J, Tesch F, Wende D, Batram M, Loser F, Weidinger O, Roessler M, Seifert M, Risch L, Nagel O, König C, Jucknewitz R, Treskova-Schwarzbach M, Hertle D, Scholz S, Stern S, Ballesteros P, Baßler S, Bertele B, Repschläger U, Richter N, Riederer C, Sobik F, Schramm A, Schulte C, Walker J, Schmitt J Z Gesundh Wiss 22-Mar-2023
PMCID:PMC10032626
doi:10.1007/978-0-85729-323-7_1884
PMID:37361269
Beneficial Effect of Wound Dressings Containing Silver and Silver Nanoparticles in Wound Healing—From Experimental Studies to Clinical Practice Rybka M, Mazurek Ł, Konop M Life (Basel) 26-Dec-2022
PMCID:PMC9864212
doi:10.3390/life13010069
PMID:36676019
Biological synthesis of hybrid silver nanoparticles by Periploca aphylla Dcne. From nanotechnology to biotechnology applications Arshad S, Anwar N, Rauf M, Anwar Z, Shah M, Hamayun M, Ud-Din J, Gul H, Nasim S, Lee IJ, Arif M Front Chem 23-Nov-2022
PMCID:PMC9727244
doi:10.3389/fchem.2022.994895
PMID:36505740
Green nanopriming: responses of alfalfa (Medicago sativa L.) seedlings to alfalfa extracts capped and light-induced silver nanoparticles Song K, Zhao D, Sun H, Gao J, Li S, Hu T, He X BMC Plant Biol 05-Jul-2022
PMCID:PMC9254587
doi:10.1186/s12870-022-03692-9
PMID:35790925
Recent Advances in Green Synthesis of Ag NPs for Extenuating Antimicrobial Resistance Parmar S, Kaur H, Singh J, Matharu AS, Ramakrishna S, Bechelany M Nanomaterials (Basel) 28-Mar-2022
PMCID:PMC9000675
doi:10.3390/nano12071115
PMID:35407234
Traditional and Phytochemical Bases of Herbs, Shrubs, Climbers, and Trees from Ethiopia for Their Anticancer Response Abate L, Tadesse MG, Bachheti A, Bachheti RK Biomed Res Int 03-Feb-2022
PMCID:PMC8831057
doi:10.1155/2022/1589877
PMID:35155671
Sustainable phyto-fabrication of silver nanoparticles using Gmelina arborea exhibit antimicrobial and biofilm inhibition activity Chandrasekharan S, Chinnasamy G, Bhatnagar S Sci Rep 07-Jan-2022
PMCID:PMC8742086
doi:10.1038/s41598-021-04025-w
PMID:34997051
Phytoantioxidant Functionalized Nanoparticles: A Green Approach to Combat Nanoparticle-Induced Oxidative Stress Balkrishna A, Kumar A, Arya V, Rohela A, Verma R, Nepovimova E, Krejcar O, Kumar D, Thakur N, Kuca K Oxid Med Cell Longev 26-Oct-2021
PMCID:PMC8563134
doi:10.1155/2021/3155962
PMID:34737844
Study on potential applications and toxicity analysis of green synthesized nanoparticles GARG R, RANI P, GARG R, EDDY NO Turk J Chem 27-Sep-2021
PMCID:PMC10734732
doi:10.3906/kim-2106-59
PMID:38144602
Multi-Gene Phylogeny and Morphology Reveal Haplohelminthosporium gen. nov. and Helminthosporiella gen. nov. Associated with Palms in Thailand and A Checklist for Helminthosporium Reported Worldwide Konta S, Hyde KD, Karunarathna SC, Mapook A, Senwanna C, Dauner LA, Nanayakkara CM, Xu J, Tibpromma S, Lumyong S Life (Basel) 19-May-2021
PMCID:PMC8161214
doi:10.3390/life11050454
PMID:34069619

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name PubChem ID Canonical SMILES MW Found in Proof
> Alkaloids and derivatives / Erythrina alkaloids / Erythrinanes
19-Methoxy-5,7-dioxa-13-azapentacyclo[11.7.0.0^{1,16}.0^{2,10}.0^{4,8}]icosa-2(10),3,8,15,17-pentaene 12308897 Click to see COC1CC23C(=CCN2CCC4=CC5=C(C=C34)OCO5)C=C1 297.30 unknown https://doi.org/10.1002/JPS.2600590828
2,11,12-trimethoxy-2,6,8,9-tetrahydro-1H-indolo[7a,1-a]isoquinoline 3472080 Click to see COC1CC23C(=CCN2CCC4=CC(=C(C=C34)OC)OC)C=C1 313.40 unknown https://doi.org/10.1002/JPS.2600590828
Erysodine 169017 Click to see COC1CC23C(=CCN2CCC4=CC(=C(C=C34)OC)O)C=C1 299.40 unknown https://doi.org/10.1002/JPS.2600590828
Erysotrine 442219 Click to see COC1CC23C(=CCN2CCC4=CC(=C(C=C34)OC)OC)C=C1 313.40 unknown https://doi.org/10.1002/JPS.2600590828
Erythraline 5317205 Click to see COC1CC23C(=CCN2CCC4=CC5=C(C=C34)OCO5)C=C1 297.30 unknown https://doi.org/10.1002/JPS.2600590828
Erythrinan-16-ol, 1,2,6,7-tetradehydro-3,15-dimethoxy-, (3beta)- 622748 Click to see COC1CC23C(=CCN2CCC4=CC(=C(C=C34)OC)O)C=C1 299.40 unknown https://doi.org/10.1002/JPS.2600590828
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Arachidic Acid 10467 Click to see CCCCCCCCCCCCCCCCCCCC(=O)O 312.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10032626/
Myristic Acid 11005 Click to see CCCCCCCCCCCCCC(=O)O 228.37 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10032626/
Oleic Acid 445639 Click to see CCCCCCCCC=CCCCCCCCC(=O)O 282.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10032626/
Palmitic Acid 985 Click to see CCCCCCCCCCCCCCCC(=O)O 256.42 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10032626/
Stearic Acid 5281 Click to see CCCCCCCCCCCCCCCCCC(=O)O 284.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10032626/
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Very long-chain fatty acids
Behenic Acid 8215 Click to see CCCCCCCCCCCCCCCCCCCCCC(=O)O 340.60 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10032626/
> 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://www.ncbi.nlm.nih.gov/pmc/articles/PMC10032626/
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids / L-alpha-amino acids
Hypaphorine 442106 Click to see C[N+](C)(C)C(CC1=CNC2=CC=CC=C21)C(=O)[O-] 246.30 unknown https://doi.org/10.1007/BF01897872
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 2-prenylated flavans / 2-prenylated flavanones
(2R)-2-[3,4-dihydroxy-2-(3-methylbut-2-enyl)phenyl]-5,7-dihydroxy-2,3-dihydrochromen-4-one 162934902 Click to see CC(=CCC1=C(C=CC(=C1O)O)C2CC(=O)C3=C(C=C(C=C3O2)O)O)C 356.40 unknown https://doi.org/10.1055/S-2006-962680
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 8-prenylated flavans / 8-prenylated flavanones
Lonchocarpol A 124035 Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)CC(O2)C3=CC=C(C=C3)O)CC=C(C)C)O)C 408.50 unknown https://doi.org/10.1021/NP0101696
> Phenylpropanoids and polyketides / Isoflavonoids / Furanoisoflavonoids / Pterocarpans
(2R,11R,16S)-17,17-dimethyl-8-(3-methylbut-2-enyl)-4,12,18-trioxapentacyclo[11.8.0.02,11.05,10.014,19]henicosa-1(13),5(10),6,8,14(19),20-hexaene-7,16-diol 162946150 Click to see CC(=CCC1=CC2=C(C=C1O)OCC3C2OC4=C3C=CC5=C4CC(C(O5)(C)C)O)C 408.50 unknown https://doi.org/10.1016/S0031-9422(00)00441-6
(6aR,11aR)-2,10-bis(3-methylbut-2-enyl)-6,11a-dihydro-[1]benzofuro[3,2-c]chromene-3,6a,9-triol 163001878 Click to see CC(=CCC1=CC2=C(C=C1O)OCC3(C2OC4=C3C=CC(=C4CC=C(C)C)O)O)C 408.50 unknown https://doi.org/10.1016/S0031-9422(00)00441-6
(6aR,11aR)-9-hydroxy-3-methoxy-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromene-2-carbaldehyde 12051845 Click to see COC1=CC2=C(C=C1C=O)C3C(CO2)C4=C(O3)C=C(C=C4)O 298.29 unknown https://doi.org/10.1016/S0031-9422(00)00441-6
https://doi.org/10.3987/COM-98-8334
(6aS,11aS)-2,10-bis(3-methylbut-2-enyl)-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromene-3,9-diol 124351123 Click to see CC(=CCC1=CC2=C(C=C1O)OCC3C2OC4=C3C=CC(=C4CC=C(C)C)O)C 392.50 unknown https://doi.org/10.1016/S0031-9422(00)00441-6
17,17-Dimethyl-8-(3-methylbut-2-enyl)-4,12,18-trioxapentacyclo[11.8.0.02,11.05,10.014,19]henicosa-1(13),5(10),6,8,14(19),15,20-heptaene-2,7-diol 22297563 Click to see CC(=CCC1=CC2=C(C=C1O)OCC3(C2OC4=C3C=CC5=C4C=CC(O5)(C)C)O)C 406.50 unknown https://doi.org/10.1016/S0031-9422(00)00441-6
17,17-Dimethyl-8-(3-methylbut-2-enyl)-4,12,18-trioxapentacyclo[11.8.0.02,11.05,10.014,19]henicosa-1(13),5(10),6,8,14(19),20-hexaene-7,16-diol 85433283 Click to see CC(=CCC1=CC2=C(C=C1O)OCC3C2OC4=C3C=CC5=C4CC(C(O5)(C)C)O)C 408.50 unknown https://doi.org/10.1016/S0031-9422(00)00441-6
2-Prenyl-6a-hydroxyphaseollidin 44257484 Click to see CC(=CCC1=CC2=C(C=C1O)OCC3(C2OC4=C3C=CC(=C4CC=C(C)C)O)O)C 408.50 unknown https://doi.org/10.1016/S0031-9422(00)00441-6
2,10-Di-(gamma,gamma-dimethylallyl)-glycinol 10341413 Click to see CC(=CCC1=CC2=C(C=C1O)OCC3(C2OC4=C3C=CC(=C4CC=C(C)C)O)O)C 408.50 unknown https://doi.org/10.1016/S0031-9422(00)00441-6
3,6a-Dihydroxy-9-methoxy-10-prenylpterocarpan 3559400 Click to see CC(=CCC1=C(C=CC2=C1OC3C2(COC4=C3C=CC(=C4)O)O)OC)C 354.40 unknown https://doi.org/10.1016/S0031-9422(00)00441-6
9-hydroxy-3-methoxy-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromene-2-carbaldehyde 162844124 Click to see COC1=CC2=C(C=C1C=O)C3C(CO2)C4=C(O3)C=C(C=C4)O 298.29 unknown https://doi.org/10.1016/S0031-9422(00)00441-6
CID 10408212 10408212 Click to see CC(=CCC1=CC2=C(C=C1O)OCC3C2OC4=C3C=CC(=C4CC=C(C)C)O)C 392.50 unknown https://doi.org/10.1016/S0031-9422(00)00441-6
Cristacarpin 126540 Click to see CC(=CCC1=C(C=CC2=C1OC3C2(COC4=C3C=CC(=C4)O)O)OC)C 354.40 unknown https://doi.org/10.1016/S0031-9422(00)00441-6
https://doi.org/10.3987/COM-98-8334
Erystagallin A 10410005 Click to see CC(=CCC1=CC2=C(C=C1O)OCC3(C2OC4=C3C=CC(=C4CC=C(C)C)OC)O)C 422.50 unknown https://doi.org/10.1016/S0031-9422(00)00441-6
erysubin D 12051846 Click to see CC(=CCC1=CC2=C(C=C1O)OCC3C2OC4=C3C=CC5=C4CC(C(O5)(C)C)O)C 408.50 unknown https://doi.org/10.1016/S0031-9422(00)00441-6
Erysubin E 637080 Click to see CC(=CCC1=CC2=C(C=C1O)OCC3(C2OC4=C3C=CC5=C4C=CC(O5)(C)C)O)C 406.50 unknown https://doi.org/10.1016/S0031-9422(00)00441-6
Erythrabyssin II 5086400 Click to see CC(=CCC1=CC2=C(C=C1O)OCC3C2OC4=C3C=CC(=C4CC=C(C)C)O)C 392.50 unknown https://doi.org/10.1016/S0031-9422(00)00441-6
Phaseolin 91572 Click to see CC1(C=CC2=C(O1)C=CC3=C2OC4C3COC5=C4C=CC(=C5)O)C 322.40 unknown https://doi.org/10.1016/S0031-9422(00)00441-6
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
Erysubin A 15838885 Click to see CC(C)(C1=CC2=C(C3=C(C=C2O1)OC=C(C3=O)C4=CC=C(C=C4)O)O)O 352.30 unknown https://doi.org/10.3987/COM-98-8334
Erysubin F 12051847 Click to see CC(=CCC1=C(C=CC(=C1)C2=COC3=C(C2=O)C=CC(=C3CC=C(C)C)O)O)C 390.50 unknown https://doi.org/10.1016/S0031-9422(00)00441-6
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavans / Isoflavanones / 6-prenylated isoflavanones
(2S)-4-hydroxy-6-(4-hydroxyphenyl)-2-(2-hydroxypropan-2-yl)-9-(3-methylbut-2-enyl)-2,3-dihydrofuro[3,2-g]chromen-5-one 162842930 Click to see CC(=CCC1=C2C(=C(C3=C1OC=C(C3=O)C4=CC=C(C=C4)O)O)CC(O2)C(C)(C)O)C 422.50 unknown https://doi.org/10.3987/COM-01-9346
(2S)-5-hydroxy-2-(hydroxymethyl)-7-(4-hydroxyphenyl)-2-methylpyrano[3,2-g]chromen-6-one 92446140 Click to see CC1(C=CC2=C(O1)C=C3C(=C2O)C(=O)C(=CO3)C4=CC=C(C=C4)O)CO 352.30 unknown https://doi.org/10.3987/COM-98-8334
(3S)-3,5-dihydroxy-7-(4-hydroxyphenyl)-2,2-dimethyl-3,4-dihydropyrano[3,2-g]chromen-6-one 163014258 Click to see CC1(C(CC2=C(O1)C=C3C(=C2O)C(=O)C(=CO3)C4=CC=C(C=C4)O)O)C 354.40 unknown https://doi.org/10.3987/COM-98-8334
3,5-Dihydroxy-7-(4-hydroxyphenyl)-2,2-dimethyl-3,4-dihydropyrano[3,2-g]chromen-6-one 11988359 Click to see CC1(C(CC2=C(O1)C=C3C(=C2O)C(=O)C(=CO3)C4=CC=C(C=C4)O)O)C 354.40 unknown https://doi.org/10.3987/COM-98-8334
4-Hydroxy-6-(4-hydroxyphenyl)-2-(2-hydroxypropan-2-yl)-9-(3-methylbut-2-enyl)-2,3-dihydrofuro[3,2-g]chromen-5-one 195652 Click to see CC(=CCC1=C2C(=C(C3=C1OC=C(C3=O)C4=CC=C(C=C4)O)O)CC(O2)C(C)(C)O)C 422.50 unknown https://doi.org/10.3987/COM-01-9346
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/10.3987/COM-98-8334
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/10.1021/NP0101696
https://doi.org/10.3987/COM-98-8334
https://doi.org/10.1016/S0031-9422(00)00441-6
Erysubin B 10760434 Click to see CC1(C=CC2=C(O1)C=C3C(=C2O)C(=O)C(=CO3)C4=CC=C(C=C4)O)CO 352.30 unknown https://doi.org/10.3987/COM-98-8334
Erythrinin C 44257283 Click to see CC(C)(C1CC2=C(O1)C=C3C(=C2O)C(=O)C(=CO3)C4=CC=C(C=C4)O)O 354.40 unknown https://doi.org/10.3987/COM-98-8334
Euchrenone b10 402594 Click to see CC(=CCC1=C2C(=C3C(=C1O)C(=O)C(=CO3)C4=CC=C(C=C4)O)CC(O2)C(C)(C)O)C 422.50 unknown https://doi.org/10.1021/NP0101696
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/10.3987/COM-98-8334
https://doi.org/10.1021/NP0101696
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/10.3987/COM-98-8334
https://doi.org/10.1016/S0031-9422(00)00441-6
https://doi.org/10.1021/NP0101696
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavans / Isoflavanones / 8-prenylated isoflavanones
(3R)-3-(2,4-dihydroxyphenyl)-3,7-dihydroxy-6,8-bis(3-methylbut-2-enyl)-2H-chromen-4-one 162941344 Click to see CC(=CCC1=CC2=C(C(=C1O)CC=C(C)C)OCC(C2=O)(C3=C(C=C(C=C3)O)O)O)C 424.50 unknown https://doi.org/10.1016/S0031-9422(00)00441-6
(3R)-3-(2,4-dihydroxyphenyl)-7-hydroxy-6,8-bis(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one 26238931 Click to see CC(=CCC1=CC2=C(C(=C1O)CC=C(C)C)OCC(C2=O)C3=C(C=C(C=C3)O)O)C 408.50 unknown https://doi.org/10.1016/S0031-9422(00)00441-6
(7S)-7-(2,4-dihydroxyphenyl)-2,2-dimethyl-10-(3-methylbut-2-enyl)-7,8-dihydropyrano[3,2-g]chromen-6-one 162911740 Click to see CC(=CCC1=C2C(=CC3=C1OCC(C3=O)C4=C(C=C(C=C4)O)O)C=CC(O2)(C)C)C 406.50 unknown https://doi.org/10.1016/S0031-9422(00)00441-6
3-(2,4-Dihydroxyphenyl)-7-hydroxy-6,8-bis(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one 10001497 Click to see CC(=CCC1=CC2=C(C(=C1O)CC=C(C)C)OCC(C2=O)C3=C(C=C(C=C3)O)O)C 408.50 unknown https://doi.org/10.1016/S0031-9422(00)00441-6

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