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Erythrina lysistemon

Erythrina lysistemon - 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 UUID643fd8c243540928044972
Scientific name Erythrina lysistemon
Authority Hutch.
First published in Bull. Misc. Inform. Kew1933: 422 (1933)

Description Top

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No description added yet. Help us by writing one.

Synonyms Top

Scientific name Authority First published in
Erythrina caffra var. mossambicensis Baker f. J. Bot.76: 238 (1938)

Common names Top

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Language Common/alternative name
English sacred coral-tree
English common coral tree
English lucky bean tree
Afrikaans koraalboom
Afrikaans kafferboom
nso mophete
st mokhungwane
tn mophete
ve muvhale
xh umsintsi
Chinese 黑刺桐
Zulu umsinsi

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Africa
    • East Tropical Africa
      • Kenya
      • Tanzania
    • Macaronesia
      • Madeira
    • Northeast Tropical Africa
      • Ethiopia
    • South Tropical Africa
      • Malawi
      • Mozambique
      • Zimbabwe
    • Southern Africa
      • Botswana
      • Cape Provinces
      • Kwazulu-Natal
      • Northern Provinces
      • Swaziland

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000180919
Tropicos 13043736
KEW urn:lsid:ipni.org:names:494491-1
The Plant List ild-2709
Open Tree Of Life 284184
NCBI Taxonomy 347910
IUCN Red List 146455940
IPNI 494491-1
iNaturalist 119673
GBIF 5349556
Freebase /m/027hffg
EPPO ERZLY
EOL 644356
USDA GRIN 15755
Wikipedia Erythrina_lysistemon

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
A comparison of freezer‐stored DNA and herbarium tissue samples for chloroplast assembly and genome skimming McAssey EV, Downs C, Yorkston M, Morden C, Heyduk K Appl Plant Sci 05-Jun-2023
PMCID:PMC10278930
doi:10.1002/aps3.11527
PMID:37342160
Antimicrobial activities and phylogenetic study of Erythrina senegalensis DC (Fabaceae) seed lectin Enoma S, Adewole TS, Agunbiade TO, Kuku A BioTechnologia (Pozn) 27-Mar-2023
PMCID:PMC10091453
doi:10.5114/bta.2023.125083
PMID:37064277
The Development of Pharmacophore Models for the Search of New Natural Inhibitors of SARS-CoV-2 Spike RBD–ACE2 Binding Interface Semenov VA, Krivdin LB Molecules 15-Dec-2022
PMCID:PMC9788546
doi:10.3390/molecules27248938
PMID:36558067
Prenylated Flavonoids in Topical Infections and Wound Healing Sychrová A, Škovranová G, Čulenová M, Bittner Fialová S Molecules 13-Jul-2022
PMCID:PMC9323352
doi:10.3390/molecules27144491
PMID:35889363
Antibacterial Effects of Flavonoids and Their Structure-Activity Relationship Study: A Comparative Interpretation Shamsudin NF, Ahmed QU, Mahmood S, Ali Shah SA, Khatib A, Mukhtar S, Alsharif MA, Parveen H, Zakaria ZA Molecules 09-Feb-2022
PMCID:PMC8879123
doi:10.3390/molecules27041149
PMID:35208939
Medicinal Plants for Mitigating Pain and Inflammatory-Related Conditions: An Appraisal of Ethnobotanical Uses and Patterns in South Africa Aremu AO, Pendota SC Front Pharmacol 22-Oct-2021
PMCID:PMC8569556
doi:10.3389/fphar.2021.758583
PMID:34744737
A Review of Ethnoveterinary Knowledge, Biological Activities and Secondary Metabolites of Medicinal Woody Plants Used for Managing Animal Health in South Africa Selogatwe KM, Asong JA, Struwig M, Ndou RV, Aremu AO Vet Sci 12-Oct-2021
PMCID:PMC8537377
doi:10.3390/vetsci8100228
PMID:34679058
Antiplasmodial, antimalarial activities and toxicity of African medicinal plants: a systematic review of literature Tajbakhsh E, Kwenti TE, Kheyri P, Nezaratizade S, Lindsay DS, Khamesipour F Malar J 25-Aug-2021
PMCID:PMC8390284
doi:10.1186/s12936-021-03866-0
PMID:34433465
A Review of Plant-Based Therapies for the Treatment of Urinary Tract Infections in Traditional Southern African Medicine Cock I, Mavuso N, Van Vuuren S Evid Based Complement Alternat Med 29-Jul-2021
PMCID:PMC8346297
doi:10.1155/2021/7341124
PMID:34367307
Natural and Historical Heritage of the Lisbon Botanical Gardens: An Integrative Approach with Tree Collections Cunha AR, Soares AL, Brilhante M, Arsénio P, Vasconcelos T, Espírito-Santo D, Duarte MC, Romeiras MM Plants (Basel) 04-Jul-2021
PMCID:PMC8309379
doi:10.3390/plants10071367
PMID:34371570
Chemical composition, antioxidant activities and antibacterial activities of essential oil from Erythrina caffra Thunb. growing in South Africa Wintola OA, Olajuyigbe AA, Afolayan AJ, Coopoosamy RM, Olajuyigbe OO Heliyon 07-Jun-2021
PMCID:PMC8213900
doi:10.1016/j.heliyon.2021.e07244
PMID:34179531
South Africa’s Best BARK Medicines Prescribed at the Johannesburg Muthi Markets for Skin, Gut, and Lung Infections: MIC’s and Brine Shrimp Lethality Khumalo GP, Sadgrove NJ, Van Vuuren SF, Van Wyk BE Antibiotics (Basel) 07-Jun-2021
PMCID:PMC8227155
doi:10.3390/antibiotics10060681
PMID:34200286
Accommodating receptor flexibility and free energy calculation to reduce false positive binders in the discovery of natural products blockers of SARS-COV-2 spike RBD-ACE2 interface Ogedjo M, Onoka I, Sahini M, Shadrack DM Biochem Biophys Rep 25-May-2021
PMCID:PMC8148615
doi:10.1016/j.bbrep.2021.101024
PMID:34056140
African Plant-Based Natural Products with Antivirulence Activities to the Rescue of Antibiotics Mahavy CE, Duez P, ElJaziri M, Rasamiravaka T Antibiotics (Basel) 19-Nov-2020
PMCID:PMC7699609
doi:10.3390/antibiotics9110830
PMID:33228261
Emerging paradigms of viral diseases and paramount role of natural resources as antiviral agents Sagaya Jansi R, Khusro A, Agastian P, Alfarhan A, Al-Dhabi NA, Arasu MV, Rajagopal R, Barcelo D, Al-Tamimi A Sci Total Environ 07-Nov-2020
PMCID:PMC7833357
doi:10.1016/j.scitotenv.2020.143539
PMID:33234268

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
(+)-alpha-Hydroxyerysotrine 11472951 Click to see COC1CC23C(=CCN2CC(C4=CC(=C(C=C34)OC)OC)O)C=C1 329.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.04.029
(+)-Erysotramidine 14589898 Click to see COC1CC23C(=CC(=O)N2CCC4=CC(=C(C=C34)OC)OC)C=C1 327.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.04.029
(+)-Erythristemine 14557990 Click to see COC1CC23C(=CCN2CC(C4=CC(=C(C=C34)OC)OC)OC)C=C1 343.40 unknown https://doi.org/10.1139/V81-400
https://doi.org/10.1016/J.PHYTOCHEM.2004.04.029
(1S,11R,19R)-11,19-dimethoxy-5,7-dioxa-13-azapentacyclo[11.7.0.01,16.02,10.04,8]icosa-2,4(8),9,15,17-pentaene 162983764 Click to see COC1CC23C(=CCN2CC(C4=CC5=C(C=C34)OCO5)OC)C=C1 327.40 unknown https://doi.org/10.1039/J39710000652
(2R,13bS)-2,11,12-trimethoxy-1,2-dihydroindolo[7a,1-a]isoquinolin-6-one 11347922 Click to see COC1CC23C(=CC(=O)N2C=CC4=CC(=C(C=C34)OC)OC)C=C1 325.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.04.029
(2R,13bS)-2,11,12-trimethoxy-7-oxido-2,6,8,9-tetrahydro-1H-indolo[7a,1-a]isoquinolin-7-ium 101851986 Click to see COC1CC23C(=CC[N+]2(CCC4=CC(=C(C=C34)OC)OC)[O-])C=C1 329.40 unknown https://doi.org/10.1021/NP50073A014
(2R,9R,13bS)-2,12-dimethoxy-2,6,8,9-tetrahydro-1H-indolo[7a,1-a]isoquinoline-9,11-diol 21679847 Click to see COC1CC23C(=CCN2CC(C4=CC(=C(C=C34)OC)O)O)C=C1 315.40 unknown https://doi.org/10.1002/OMR.1270210110
(2R,9R,13bS)-2,9,11,12-tetramethoxy-1,2,8,9-tetrahydroindolo[7a,1-a]isoquinolin-6-one 11394212 Click to see COC1CC23C(=CC(=O)N2CC(C4=CC(=C(C=C34)OC)OC)OC)C=C1 357.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.04.029
(2R,9R,13bS)-2,9,12-trimethoxy-2,6,8,9-tetrahydro-1H-indolo[7a,1-a]isoquinolin-11-ol 21679846 Click to see COC1CC23C(=CCN2CC(C4=CC(=C(C=C34)OC)O)OC)C=C1 329.40 unknown https://doi.org/10.1002/OMR.1270210110
(2R,9R,13bS)-9-hydroxy-2,11,12-trimethoxy-1,2,8,9-tetrahydroindolo[7a,1-a]isoquinolin-6-one 11484680 Click to see COC1CC23C(=CC(=O)N2CC(C4=CC(=C(C=C34)OC)OC)O)C=C1 343.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.04.029
(2R,9S,13bS)-2,12-dimethoxy-2,6,8,9-tetrahydro-1H-indolo[7a,1-a]isoquinoline-9,11-diol 10245165 Click to see COC1CC23C(=CCN2CC(C4=CC(=C(C=C34)OC)O)O)C=C1 315.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.04.029
https://doi.org/10.1002/OMR.1270210110
(2S,3R,4R,5R,6S)-2-[[(2R,13bS)-2,12-dimethoxy-2,6,8,9-tetrahydro-1H-indolo[7a,1-a]isoquinolin-11-yl]oxy]-6-methyloxane-3,4,5-triol 162949764 Click to see CC1C(C(C(C(O1)OC2=C(C=C3C(=C2)CCN4C35CC(C=CC5=CC4)OC)OC)O)O)O 445.50 unknown https://doi.org/10.1021/NP50073A014
11,19-Dimethoxy-5,7-dioxa-13-azapentacyclo[11.7.0.01,16.02,10.04,8]icosa-2,4(8),9,15,17-pentaene 162983763 Click to see COC1CC23C(=CCN2CC(C4=CC5=C(C=C34)OCO5)OC)C=C1 327.40 unknown https://doi.org/10.1039/J39710000652
2-[(2,12-dimethoxy-2,6,8,9-tetrahydro-1H-indolo[7a,1-a]isoquinolin-11-yl)oxy]-6-methyloxane-3,4,5-triol 162949763 Click to see CC1C(C(C(C(O1)OC2=C(C=C3C(=C2)CCN4C35CC(C=CC5=CC4)OC)OC)O)O)O 445.50 unknown https://doi.org/10.1021/NP50073A014
2,11,12-Trimethoxy-1,2-dihydroindolo[7a,1-a]isoquinolin-6-one 72811265 Click to see COC1CC23C(=CC(=O)N2C=CC4=CC(=C(C=C34)OC)OC)C=C1 325.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.04.029
2,11,12-trimethoxy-2,6,8,9-tetrahydro-1H-indolo[7a,1-a]isoquinolin-9-ol 72806502 Click to see COC1CC23C(=CCN2CC(C4=CC(=C(C=C34)OC)OC)O)C=C1 329.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.04.029
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/10.1016/J.PHYTOCHEM.2004.04.029
https://doi.org/10.1039/J39710000652
2,9,11,12-Tetramethoxy-1,2,8,9-tetrahydroindolo[7a,1-a]isoquinolin-6-one 14557989 Click to see COC1CC23C(=CC(=O)N2CC(C4=CC(=C(C=C34)OC)OC)OC)C=C1 357.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.04.029
2,9,12-trimethoxy-2,6,8,9-tetrahydro-1H-indolo[7a,1-a]isoquinolin-11-ol 73823603 Click to see COC1CC23C(=CCN2CC(C4=CC(=C(C=C34)OC)O)OC)C=C1 329.40 unknown https://doi.org/10.1002/OMR.1270210110
9-Hydroxy-2,11,12-trimethoxy-1,2,8,9-tetrahydroindolo[7a,1-a]isoquinolin-6-one 72979617 Click to see COC1CC23C(=CC(=O)N2CC(C4=CC(=C(C=C34)OC)OC)O)C=C1 343.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.04.029
Erysodine 169017 Click to see COC1CC23C(=CCN2CCC4=CC(=C(C=C34)OC)O)C=C1 299.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.04.029
https://doi.org/10.1021/NP50073A014
Erysotramidine 11034782 Click to see COC1CC23C(=CC(=O)N2CCC4=CC(=C(C=C34)OC)OC)C=C1 327.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.04.029
Erysotrine 442219 Click to see COC1CC23C(=CCN2CCC4=CC(=C(C=C34)OC)OC)C=C1 313.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.04.029
https://doi.org/10.1021/NP50073A014
https://doi.org/10.1039/J39710000652
Erythrartine 11336443 Click to see COC1CC23C(=CCN2CC(C4=CC(=C(C=C34)OC)OC)O)C=C1 329.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.04.029
Erythravine 11231853 Click to see COC1=C(C=C2C(=C1)CCN3C24CC(C=CC4=CC3)O)OC 299.40 unknown https://doi.org/10.1021/NP50073A014
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/10.1016/J.PHYTOCHEM.2004.04.029
Erythristemine 12143915 Click to see COC1CC23C(=CCN2CC(C4=CC(=C(C=C34)OC)OC)OC)C=C1 343.40 unknown https://doi.org/10.1021/NP50073A014
https://doi.org/10.1016/J.PHYTOCHEM.2004.04.029
Grycoerysodine 44570487 Click to see COC1CC23C(=CCN2CCC4=CC(=C(C=C34)OC)OC5C(C(C(C(O5)CO)O)O)O)C=C1 461.50 unknown https://doi.org/10.1021/NP50073A014
> Organoheterocyclic compounds / Tetrahydroisoquinolines
N-acetyl-MY336-A 139590323 Click to see CC1=CC2=C(C(N(C(C2)CO)C(=O)C)CO)C(=C1OC)O 295.33 unknown https://doi.org/10.1002/OMR.1270210110
https://doi.org/10.1016/J.PHYTOCHEM.2004.04.029
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 3-prenylated flavans / 3-prenylated flavanones
5,7-Dihydroxy-2-[3-(3-hydroxy-3-methylbut-1-enyl)-4-methoxy-5-(3-methylbut-2-enyl)phenyl]-2,3-dihydrochromen-4-one 402592 Click to see CC(=CCC1=C(C(=CC(=C1)C2CC(=O)C3=C(C=C(C=C3O2)O)O)C=CC(C)(C)O)OC)C 438.50 unknown https://doi.org/10.1016/S0031-9422(02)00202-9
5,7-Dihydroxy-2-[4-methoxy-3,5-bis-(3-methyl-but-2-enyl)-phenyl]-chroman-4-one 15382621 Click to see CC(=CCC1=CC(=CC(=C1OC)CC=C(C)C)C2CC(=O)C3=C(C=C(C=C3O2)O)O)C 422.50 unknown https://doi.org/10.1016/S0031-9422(02)00202-9
Abyssinone V 4'-methyl ether 6548074 Click to see CC(=CCC1=CC(=CC(=C1OC)CC=C(C)C)C2CC(=O)C3=C(C=C(C=C3O2)O)O)C 422.50 unknown https://doi.org/10.1016/S0031-9422(02)00202-9
Burttinone 42607959 Click to see CC(=CCC1=C(C(=CC(=C1)C2CC(=O)C3=C(C=C(C=C3O2)O)O)C=CC(C)(C)O)OC)C 438.50 unknown https://doi.org/10.1016/S0031-9422(02)00202-9
> Phenylpropanoids and polyketides / Isoflavonoids / Furanoisoflavonoids / Pterocarpans
(1R,14R,21R)-7,7,20,20-tetramethyl-6,12,19,25-tetraoxahexacyclo[12.11.0.02,11.05,10.015,24.018,23]pentacosa-2(11),3,5(10),8,15(24),16,18(23)-heptaen-21-ol 162863116 Click to see CC1(C=CC2=C(O1)C=CC3=C2OCC4C3OC5=C4C=CC6=C5CC(C(O6)(C)C)O)C 406.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.09.012
(1R,14R)-7,7,20,20-tetramethyl-6,12,19,25-tetraoxahexacyclo[12.11.0.02,11.05,10.015,24.018,23]pentacosa-2(11),3,5(10),8,15(24),16,18(23)-heptaen-21-ol 44606347 Click to see CC1(C=CC2=C(O1)C=CC3=C2OCC4C3OC5=C4C=CC6=C5CC(C(O6)(C)C)O)C 406.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.09.012
(1R,7R,12R)-7-(2-hydroxypropan-2-yl)-6,11,19-trioxapentacyclo[10.8.0.02,10.05,9.013,18]icosa-2(10),3,5(9),13(18),14,16-hexaen-16-ol 162954458 Click to see CC(C)(C1CC2=C(O1)C=CC3=C2OC4C3COC5=C4C=CC(=C5)O)O 340.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.09.012
(1S,13S)-7,7-dimethyl-8,12,20-trioxapentacyclo[11.8.0.02,11.04,9.014,19]henicosa-2(11),3,5,9,14(19),15,17-heptaen-17-ol 102484013 Click to see CC1(C=CC2=CC3=C(C=C2O1)OC4C3COC5=C4C=CC(=C5)O)C 322.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.09.012
(2R,10R)-17,17-dimethyl-5-(3-methylbut-2-enyl)-3,12,16-trioxapentacyclo[11.8.0.02,10.04,9.015,20]henicosa-1(13),4(9),5,7,14,18,20-heptaen-6-ol 15559470 Click to see CC(=CCC1=C(C=CC2=C1OC3C2COC4=C3C=C5C=CC(OC5=C4)(C)C)O)C 390.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.09.012
(2R,10R)-5-(3-methylbut-2-enyl)-3,12,17-trioxapentacyclo[11.7.0.02,10.04,9.014,18]icosa-1(13),4(9),5,7,14(18),15,19-heptaen-6-ol 44606348 Click to see CC(=CCC1=C(C=CC2=C1OC3C2COC4=C3C=CC5=C4C=CO5)O)C 348.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.09.012
(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/J.PHYTOCHEM.2009.09.012
(6aR,11aR)-3,9-dihydroxy-4,10-bis(3-methylbut-2-enyl)-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromene-8-carbaldehyde 44606521 Click to see CC(=CCC1=C(C=CC2=C1OCC3C2OC4=C3C=C(C(=C4CC=C(C)C)O)C=O)O)C 420.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.09.012
(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/J.PHYTOCHEM.2009.09.012
17,17-Dimethyl-5-(3-methylbut-2-enyl)-3,12,16-trioxapentacyclo[11.8.0.02,10.04,9.015,20]henicosa-1(13),4(9),5,7,14,18,20-heptaen-6-ol 15559469 Click to see CC(=CCC1=C(C=CC2=C1OC3C2COC4=C3C=C5C=CC(OC5=C4)(C)C)O)C 390.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.09.012
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/J.PHYTOCHEM.2009.09.012
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/J.PHYTOCHEM.2009.09.012
3,9-dihydroxy-4,10-bis(3-methylbut-2-enyl)-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromene-8-carbaldehyde 75080461 Click to see CC(=CCC1=C(C=CC2=C1OCC3C2OC4=C3C=C(C(=C4CC=C(C)C)O)C=O)O)C 420.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.09.012
4-Prenylphaseollidin 21141346 Click to see CC(=CCC1=C(C=CC2=C1OC3C2COC4=C3C=CC(=C4CC=C(C)C)O)O)C 392.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.09.012
5-(3-Methylbut-2-enyl)-3,12,17-trioxapentacyclo[11.7.0.02,10.04,9.014,18]icosa-1(13),4(9),5,7,14(18),15,19-heptaen-6-ol 75080361 Click to see CC(=CCC1=C(C=CC2=C1OC3C2COC4=C3C=CC5=C4C=CO5)O)C 348.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.09.012
7-(2-Hydroxypropan-2-yl)-6,11,19-trioxapentacyclo[10.8.0.02,10.05,9.013,18]icosa-2(10),3,5(9),13(18),14,16-hexaen-16-ol 162954457 Click to see CC(C)(C1CC2=C(O1)C=CC3=C2OC4C3COC5=C4C=CC(=C5)O)O 340.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.09.012
7,7,20,20-Tetramethyl-6,12,19,25-tetraoxahexacyclo[12.11.0.02,11.05,10.015,24.018,23]pentacosa-2(11),3,5(10),8,15(24),16,18(23)-heptaen-21-ol 75080360 Click to see CC1(C=CC2=C(O1)C=CC3=C2OCC4C3OC5=C4C=CC6=C5CC(C(O6)(C)C)O)C 406.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.09.012
Calocarpin 15382622 Click to see CC(=CCC1=CC2=C(C=C1O)OCC3C2OC4=C3C=CC(=C4)O)C 324.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.09.012
Calopocarpin 11709595 Click to see CC(=CCC1=CC2=C(C=C1O)OCC3C2OC4=C3C=CC(=C4)O)C 324.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.09.012
CID 821442 821442 Click to see CC1(C=CC2=CC3=C(C=C2O1)OC4C3COC5=C4C=CC(=C5)O)C 322.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.09.012
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/J.PHYTOCHEM.2009.09.012
Erybraedin A 362562 Click to see CC(=CCC1=C(C=CC2=C1OC3C2COC4=C3C=CC(=C4CC=C(C)C)O)O)C 392.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.09.012
eryvarin D 15546808 Click to see CC(=CCC1=C(C=CC2=C1OC3=C2COC4=C3C=CC(=C4)O)OC)C 336.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.09.012
Isoneorautenol 73649 Click to see CC1(C=CC2=CC3=C(C=C2O1)OC4C3COC5=C4C=CC(=C5)O)C 322.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.09.012
Orientanol C 42607512 Click to see CC(=CCC1=C(C=CC2=C1OC3(C2(COC4=C3C=C5C=CC(OC5=C4)(C)C)O)O)O)C 422.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.09.012
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/J.PHYTOCHEM.2009.09.012
Phaseolin; Phaseolin (phytoalexin) 4063834 Click to see CC1(C=CC2=C(O1)C=CC3=C2OC4C3COC5=C4C=CC(=C5)O)C 322.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.09.012
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavans / Isoflavanones / 3-prenylated isoflavanones
(3S)-5,7-dihydroxy-3-[2-hydroxy-4-methoxy-5-(3-methylbut-2-enyl)phenyl]-2,3-dihydrochromen-4-one 636604 Click to see CC(=CCC1=CC(=C(C=C1OC)O)C2COC3=CC(=CC(=C3C2=O)O)O)C 370.40 unknown https://doi.org/10.1016/S0031-9422(02)00202-9
5-Deoxyglyasperin F 1812 Click to see CC1(C=CC2=C(C=CC(=C2O1)C3COC4=C(C3=O)C=CC(=C4)O)O)C 338.40 unknown https://doi.org/10.1021/NP970031G
5-Deoxylicoisoflavanone 5352086 Click to see CC1(C=CC2=C(O1)C=CC(=C2O)C3COC4=C(C3=O)C=CC(=C4)O)C 338.40 unknown https://doi.org/10.1021/NP970031G
5,7-Dihydroxy-3-[2-hydroxy-4-methoxy-5-(3-methylbut-2-enyl)phenyl]-2,3-dihydrochromen-4-one 5319135 Click to see CC(=CCC1=CC(=C(C=C1OC)O)C2COC3=CC(=CC(=C3C2=O)O)O)C 370.40 unknown https://doi.org/10.1016/S0031-9422(02)00202-9
Glyasperin F 392442 Click to see CC1(C=CC2=C(C=CC(=C2O1)C3COC4=CC(=CC(=C4C3=O)O)O)O)C 354.40 unknown https://doi.org/10.1021/NP970031G
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavans / Isoflavanones / 6-prenylated isoflavanones
(8S)-5-hydroxy-3-(4-hydroxyphenyl)-8-(2-hydroxypropan-2-yl)-6-(3-methylbut-2-enyl)-8,9-dihydrofuro[2,3-h]chromen-4-one 162825860 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/10.1016/S0031-9422(02)00202-9
5,7-dihydroxy-6-[(2R)-2-hydroxy-3-methylbut-3-enyl]-3-(4-hydroxyphenyl)-8-(3-methylbut-2-enyl)chromen-4-one 124355947 Click to see CC(=CCC1=C(C(=C(C2=C1OC=C(C2=O)C3=CC=C(C=C3)O)O)CC(C(=C)C)O)O)C 422.50 unknown https://doi.org/10.1016/S0031-9422(02)00202-9
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/S0031-9422(02)00202-9
Isoerysenegalensein E 5318561 Click to see CC(=CCC1=C(C(=C(C2=C1OC=C(C2=O)C3=CC=C(C=C3)O)O)CC(C(=C)C)O)O)C 422.50 unknown https://doi.org/10.1016/S0031-9422(02)00202-9
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 4-O-methylisoflavones
5,7-Dihydroxy-3-[2-hydroxy-4-methoxy-5-(3-methylbut-2-enyl)phenyl]chromen-4-one 101213759 Click to see CC(=CCC1=CC(=C(C=C1OC)O)C2=COC3=CC(=CC(=C3C2=O)O)O)C 368.40 unknown https://doi.org/10.1016/S0031-9422(02)00202-9

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