Scientific name	Authority	First published in
Chirocalyx latifolius	(Schumach. & Thonn.) Walp.	Flora36: 148 (1853)
Erythrina guineensis	G.Don	Gen. Hist.2: 371 (1832)
Erythrina latifolia	Schumach. & Thonn.	C.F.Schumacher, Beskr. Guin. Pl.: 333 (1827)
Macrocymbium vogelii	Walp.	Flora36: 149 (1853)
Duchassaingia senegalensis	(DC.) Hassk.	Hort. Bogor. Descr. 194 1858
Corallodendron senegalense	(DC.) Kuntze	Revis. Gen. Pl.1: 173 (1891)
Erythrina senegalensis var. camerounensis	Aubrév.	Notul. Syst. (Paris)14: 58 (1950)

Common names Top

Add a new one! Suggest a correction!

Filter by language:

Language	Common/alternative name
Arabic	حمرية سنغالية
Bambara	ntenbilen
dag	taŋjibga
Chinese	塞内加尔刺桐

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!

No subspecies added yet.

Varieties (abbr. var.) Top

Add a new one! Suggest a correction!

No variety added yet.

Subvarieties (abbr. subvar.) Top

Add a new one! Suggest a correction!

No subvariety added yet.

Forms (abbr. f.) Top

Add a new one! Suggest a correction!

No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!

No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Africa click to expand
- Northeast Tropical Africa
  - Chad
- West Tropical Africa
  - Benin
  - Burkina
  - Gambia
  - Ghana
  - Guinea
  - Guinea-Bissau
  - Ivory Coast
  - Liberia
  - Mali
  - Mauritania
  - Niger
  - Nigeria
  - Senegal
  - Sierra Leone
  - Togo
- West-central Tropical Africa
  - Cameroon
  - Equatorial Guinea
  - Gulf Of Guinea Islands

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000181131
UNII	001P21T3RG
Tropicos	13030278
KEW	urn:lsid:ipni.org:names:494578-1
The Plant List	ild-2729
Open Tree Of Life	1095837
Observations.org	395296
NCBI Taxonomy	157649
IUCN Red List	19892718
IPNI	494578-1
iNaturalist	139167
GBIF	5349683
EPPO	ERZSE
EOL	644439
Elurikkus	524584
USDA GRIN	15765
Wikipedia	Erythrina_senegalensis

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

Comprehensive Review of Epidemiology and Treatment of Snakebite Envenomation in West Africa: Case of Benin

Dossou AJ, Fandohan AB, Omara T, Chippaux JP

J Trop Med

08-Apr-2024

PMCID:	PMC11018376
doi:	10.1155/2024/8357312
PMID:	38623180

In vitro activities and mechanisms of action of anti-cancer molecules from African medicinal plants: a systematic review

Adico MD, Bayala B, Zoure AA, Lagarde A, Bazie JT, Traore L, Buñay J, Yonli AT, Djigma F, Bambara HA, Baron S, Simporé J, Lobaccaro JM

Am J Cancer Res

15-Mar-2024

PMCID:	PMC10998760
doi:	10.62347/AUHB5811
PMID:	38590420

Medicinal herbs and their metabolites with biological potential to protect and combat liver toxicity and its disorders: A review

Islam Shawon S, Nargis Reyda R, Qais N

Heliyon

01-Feb-2024

PMCID:	PMC10864916
doi:	10.1016/j.heliyon.2024.e25340
PMID:	38356556

Antimicrobial, antioxidant and antiproliferative activities of a galactose-binding seed lectin from Manilkara zapota

Podder MK, Hossain MM, Kabir SR, Asaduzzaman AK, Hasan I

Heliyon

17-Jan-2024

PMCID:	PMC10835259
doi:	10.1016/j.heliyon.2024.e24592
PMID:	38312555

Medical Ethnobotany of the Bissau-Guinean Community of Migrants Living in Northern Italy and Comparison with the Ethnopharmacology of Guinea-Bissau

Sambù A, Cornara L, Catarino L, Indjai B, Biagi M, Giordani P

Plants (Basel)

08-May-2023

PMCID:	PMC10181441
doi:	10.3390/plants12091909
PMID:	37176967

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

Metabolite profiling, antifungal, biofilm formation prevention and disruption of mature biofilm activities of Erythrina senegalensis stem bark extract against Candida albicans and Candida glabrata

Harley BK, Quagraine AM, Neglo D, Aggrey MO, Orman E, Mireku-Gyimah NA, Amengor CD, Jato J, Saaka Y, Fleischer TC

PLoS One

28-Nov-2022

PMCID:	PMC9704668
doi:	10.1371/journal.pone.0278096
PMID:	36441750

“A Review of Parquetina nigrescens (Afzel.) Bullock, A Plant for Traditional Medicine: Phytochemical and Pharmacological Properties”

Adase E, Ankutse P, Kumadoh D, Archer MA, Kyene MO, Yeboah GN, Asamoah Agyare DO

Evid Based Complement Alternat Med

16-Nov-2022

PMCID:	PMC9683991
doi:	10.1155/2022/6076707
PMID:	36437836

The potential of plant extracts in cell therapy

Li C, Cui Z, Deng S, Chen P, Li X, Yang H

Stem Cell Res Ther

14-Sep-2022

PMCID:	PMC9476258
doi:	10.1186/s13287-022-03152-z
PMID:	36104798

Exploring the Phytochemicals and Anti-Cancer Potential of the Members of Fabaceae Family: A Comprehensive Review

Usman M, Khan WR, Yousaf N, Akram S, Murtaza G, Kudus KA, Ditta A, Rosli Z, Rajpar MN, Nazre M

Molecules

16-Jun-2022

PMCID:	PMC9230627
doi:	10.3390/molecules27123863
PMID:	35744986

Ethnopharmacological Study of Medicinal Plants Used for the Treatment of Cardiovascular Diseases and Their Associated Risk Factors in sub-Saharan Africa

Odukoya JO, Odukoya JO, Mmutlane EM, Ndinteh DT

Plants (Basel)

23-May-2022

PMCID:	PMC9143319
doi:	10.3390/plants11101387
PMID:	35631812

In Vitro Antioxidant and Anticancer Properties of Various E. senegalensis Extracts

Fofana S, Delporte C, Calvo Esposito R, Ouédraogo M, Van Antwerpen P, Guissou IP, Semdé R, Mathieu V

Molecules

16-Apr-2022

PMCID:	PMC9025838
doi:	10.3390/molecules27082583
PMID:	35458781

Ethnobotanical Survey of Local Flora Used for Medicinal Purposes among Indigenous People in Five Areas in Lagos State, Nigeria

Lawal IO, Rafiu BO, Ale JE, Majebi OE, Aremu AO

Plants (Basel)

25-Feb-2022

PMCID:	PMC8912796
doi:	10.3390/plants11050633
PMID:	35270103

Local perception of ecosystem services and their conservation in Sudanian savannas of Burkina Faso (West Africa)

Nabaloum A, Goetze D, Ouédraogo A, Porembski S, Thiombiano A

J Ethnobiol Ethnomed

19-Feb-2022

PMCID:	PMC8858500
doi:	10.1186/s13002-022-00508-w
PMID:	35183193

Green Carbon Nanostructures for Functional Composite Materials

Barra A, Nunes C, Ruiz-Hitzky E, Ferreira P

Int J Mol Sci

06-Feb-2022

PMCID:	PMC8836917
doi:	10.3390/ijms23031848
PMID:	35163770

Phytochemical Profile Top

Add a new one!

Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.

Name	PubChem ID	Canonical SMILES	MW	Found in	Proof
> Alkaloids and derivatives / Erythrina alkaloids / Erythrinanes
(2R,3R,4S,5S,6R)-2-[[(2R,13bS)-11-hydroxy-12-methoxy-2,6,8,9-tetrahydro-1H-indolo[7a,1-a]isoquinolin-2-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol	163103757	Click to see COC1=C(C=C2CCN3CC=C4C3(C2=C1)CC(C=C4)OC5C(C(C(C(O5)CO)O)O)O)O	447.50	unknown	https://doi.org/10.1016/0031-9422(94)00779-S
2-[(2,12-dimethoxy-2,6,8,9-tetrahydro-1H-indolo[7a,1-a]isoquinolin-11-yl)oxy]-6-(hydroxymethyl)oxane-3,4,5-triol	3792560	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/10.1016/0031-9422(94)00779-S
Erysodine	169017	Click to see COC1CC23C(=CCN2CCC4=CC(=C(C=C34)OC)O)C=C1	299.40	unknown	https://doi.org/10.1016/0031-9422(94)00779-S
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/10.1016/0031-9422(94)00779-S
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/10.1016/0031-9422(94)00779-S
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohol esters
Triacontan-4-yl 3-phenylprop-2-enoate	163194009	Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCC(CCC)OC(=O)C=CC1=CC=CC=C1	569.00	unknown	https://doi.org/10.1021/NP50072A004
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(3S,4aR,6aR,6bS,8S,8aS,12aR,14aR,14bS)-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene-3,8-diol	154496975	Click to see CC1(CCC2(C(C1)C3=CCC4C5(CCC(C(C5CCC4(C3(CC2O)C)C)(C)C)O)C)C)C	442.70	unknown	https://doi.org/10.1016/0031-9422(94)00671-F
(3S,4aS,6aR,6aR,6bR,8aR,12aS,14aR,14bS)-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,6a,7,8,9,10,12,12a,14a-tetradecahydropicen-3-ol	154497735	Click to see CC1(CCC2(CCC3(C(C2C1)C=CC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C)C)C	426.70	unknown	https://doi.org/10.1016/0031-9422(94)00671-F
(3S,4aS,6aR,6bS,8aS,12aR,14aR,14bR)-8a-(hydroxymethyl)-4,4,6a,6b,11,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-ol	154496541	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)CO)C	442.70	unknown	https://doi.org/10.1016/0031-9422(94)00671-F
(4aR,6aR,6aR,6bR,8aR,10S,12aS,14bR)-10-hydroxy-2,2,4a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-6a-carboxylic acid	163075254	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C(=O)O)C)C	456.70	unknown	https://doi.org/10.1016/0031-9422(94)00671-F
(4aS,6aS,6aS,6bR,8aS,10S,12aR,14bR)-10-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid	51892422	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C	456.70	unknown	https://doi.org/10.1016/0031-9422(94)00671-F
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/10.1016/0031-9422(94)00671-F
Beta-Peltoboykinolic Acid	12016584	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C(=O)O)C)C	456.70	unknown	https://doi.org/10.1016/0031-9422(94)00671-F
Erythrodiol	101761	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)CO)C	442.70	unknown	https://doi.org/10.1016/0031-9422(94)00671-F
Maniladiol	397934	Click to see CC1(CCC2(C(C1)C3=CCC4C5(CCC(C(C5CCC4(C3(CC2O)C)C)(C)C)O)C)C)C	442.70	unknown	https://doi.org/10.1016/0031-9422(94)00671-F
Oleanolic Acid	10494	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C	456.70	unknown	https://doi.org/10.1016/0031-9422(94)00671-F
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids
3-(1H-indol-3-yl)-2-(trimethylazaniumyl)propanoate	3861164	Click to see C[N+](C)(C)C(CC1=CNC2=CC=CC=C21)C(=O)[O-]	246.30	unknown	https://doi.org/10.1016/0031-9422(94)00779-S
> 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/10.1016/0031-9422(94)00779-S
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
Ferulic acid	445858	Click to see COC1=C(C=CC(=C1)C=CC(=O)O)O	194.18	unknown	https://doi.org/10.1021/NP50072A004
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 6-prenylated flavans / 6-prenylated flavanones
Cajaflavanone	42607935	Click to see CC(=CCC1=C(C2=C(C3=C1OC(C=C3)(C)C)OC(CC2=O)C4=CC=C(C=C4)O)O)C	406.50	unknown	https://doi.org/10.1016/0031-9422(85)80067-4
Erythrisenegalone	15224381	Click to see CC(=CCC1=C(C2=C(C3=C1OC(C=C3)(C)C)OC(CC2=O)C4=CC=C(C=C4)O)O)C	406.50	unknown	https://doi.org/10.1016/0031-9422(85)80067-4 https://doi.org/10.1016/S0031-9422(00)80645-7 https://doi.org/10.1055/S-2006-959446
> 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/10.1055/S-2006-959446
5,7-Dihydroxy-2-(4-hydroxyphenyl)-6,8-bis(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one	3951	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/10.1055/S-2006-946674
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/10.1055/S-2006-959446 https://doi.org/10.1021/NP50072A004 https://doi.org/10.1021/NP50053A025
Lupinifolin	10250777	Click to see CC(=CCC1=C2C(=C(C3=C1OC(CC3=O)C4=CC=C(C=C4)O)O)C=CC(O2)(C)C)C	406.50	unknown	https://doi.org/10.1055/S-2006-959446
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
6-(2,4-Dihydroxyphenyl)-4-hydroxy-9-(3-methylbut-2-enyl)furo[3,2-g]chromen-5-one	101922023	Click to see CC(=CCC1=C2C(=C(C3=C1OC=C(C3=O)C4=C(C=C(C=C4)O)O)O)C=CO2)C	378.40	unknown	https://doi.org/10.1016/0031-9422(94)00671-F
Tectorigenin	5281811	Click to see COC1=C(C2=C(C=C1O)OC=C(C2=O)C3=CC=C(C=C3)O)O	300.26	unknown	https://doi.org/10.1080/10826079208016365
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavans / Isoflavanones / 6-prenylated isoflavanones
(2R)-6-(2,4-dihydroxyphenyl)-4-hydroxy-2-(2-hydroxypropan-2-yl)-9-(3-methylbut-2-enyl)-2,3-dihydrofuro[3,2-g]chromen-5-one	163060823	Click to see CC(=CCC1=C2C(=C(C3=C1OC=C(C3=O)C4=C(C=C(C=C4)O)O)O)CC(O2)C(C)(C)O)C	438.50	unknown	https://doi.org/10.1055/S-2006-959446
(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/10.1055/S-2006-959446
(2S)-6-(2,4-dihydroxyphenyl)-4-hydroxy-2-(2-hydroxypropan-2-yl)-9-(3-methylbut-2-enyl)-2,3-dihydrofuro[3,2-g]chromen-5-one	163060822	Click to see CC(=CCC1=C2C(=C(C3=C1OC=C(C3=O)C4=C(C=C(C=C4)O)O)O)CC(O2)C(C)(C)O)C	438.50	unknown	https://doi.org/10.1055/S-2006-959446
(3S)-7-(2,4-dihydroxyphenyl)-3,5-dihydroxy-2,2-dimethyl-10-(3-methylbut-2-enyl)-3,4-dihydropyrano[3,2-g]chromen-6-one	162857939	Click to see CC(=CCC1=C2C(=C(C3=C1OC=C(C3=O)C4=C(C=C(C=C4)O)O)O)CC(C(O2)(C)C)O)C	438.50	unknown	https://doi.org/10.1055/S-2006-959446
(9R)-3-(2,4-dihydroxyphenyl)-5,9-dihydroxy-8,8-dimethyl-6-(3-methylbut-2-enyl)-9,10-dihydropyrano[2,3-h]chromen-4-one	163088636	Click to see CC(=CCC1=C2C(=C3C(=C1O)C(=O)C(=CO3)C4=C(C=C(C=C4)O)O)CC(C(O2)(C)C)O)C	438.50	unknown	https://doi.org/10.1016/S0031-9422(99)00171-5
(9S)-3-(2,4-dihydroxyphenyl)-5,9-dihydroxy-8,8-dimethyl-6-(3-methylbut-2-enyl)-9,10-dihydropyrano[2,3-h]chromen-4-one	49768587	Click to see CC(=CCC1=C2C(=C3C(=C1O)C(=O)C(=CO3)C4=C(C=C(C=C4)O)O)CC(C(O2)(C)C)O)C	438.50	unknown	https://doi.org/10.1016/S0031-9422(99)00171-5
10-[(3,3-Dimethyloxiran-2-yl)methyl]-5-hydroxy-7-(4-hydroxyphenyl)-2,2-dimethylpyrano[3,2-g]chromen-6-one	101663499	Click to see CC1(C=CC2=C(C3=C(C(=C2O1)CC4C(O4)(C)C)OC=C(C3=O)C5=CC=C(C=C5)O)O)C	420.50	unknown	https://doi.org/10.1016/S0031-9422(00)86896-X
10-[[(2R)-3,3-dimethyloxiran-2-yl]methyl]-5-hydroxy-7-(4-hydroxyphenyl)-2,2-dimethylpyrano[3,2-g]chromen-6-one	163015442	Click to see CC1(C=CC2=C(C3=C(C(=C2O1)CC4C(O4)(C)C)OC=C(C3=O)C5=CC=C(C=C5)O)O)C	420.50	unknown	https://doi.org/10.1016/S0031-9422(00)86896-X
3-(2,4-Dihydroxyphenyl)-5,7-dihydroxy-6-(3-methylbut-2-enyl)-8-(3-methylbut-3-enyl)chromen-4-one	162988666	Click to see CC(=CCC1=C(C2=C(C(=C1O)CCC(=C)C)OC=C(C2=O)C3=C(C=C(C=C3)O)O)O)C	422.50	unknown	https://doi.org/10.1016/S0031-9422(00)86896-X
3-(2,4-dihydroxyphenyl)-5,7-dihydroxy-6-[(2R)-2-hydroxy-3-methylbut-3-enyl]-8-(3-methylbut-2-enyl)chromen-4-one	163090353	Click to see CC(=CCC1=C(C(=C(C2=C1OC=C(C2=O)C3=C(C=C(C=C3)O)O)O)CC(C(=C)C)O)O)C	438.50	unknown	https://doi.org/10.1016/S0031-9422(99)00171-5
3-(2,4-dihydroxyphenyl)-5,7-dihydroxy-8-[(2R)-2-hydroxy-3-methylbut-3-enyl]-6-(3-methylbut-2-enyl)chromen-4-one	162875224	Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)C(=CO2)C3=C(C=C(C=C3)O)O)CC(C(=C)C)O)O)C	438.50	unknown	https://doi.org/10.1016/S0031-9422(99)00171-5 https://doi.org/10.1016/S0031-9422(00)86896-X
3-(2,4-Dihydroxyphenyl)-5,9-dihydroxy-8,8-dimethyl-6-(3-methylbut-2-enyl)-9,10-dihydropyrano[2,3-h]chromen-4-one	15479577	Click to see CC(=CCC1=C2C(=C3C(=C1O)C(=O)C(=CO3)C4=C(C=C(C=C4)O)O)CC(C(O2)(C)C)O)C	438.50	unknown	https://doi.org/10.1016/S0031-9422(99)00171-5
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/10.1055/S-2006-959446
5-hydroxy-10-[(2R)-2-hydroxy-3-methylbut-3-enyl]-7-(4-hydroxyphenyl)-2,2-dimethylpyrano[3,2-g]chromen-6-one	163186580	Click to see CC(=C)C(CC1=C2C(=C(C3=C1OC=C(C3=O)C4=CC=C(C=C4)O)O)C=CC(O2)(C)C)O	420.50	unknown	https://doi.org/10.1016/0031-9422(94)00779-S
5,7-Dihydroxy-3-(4-hydroxyphenyl)-6-(3-methylbut-2-enyl)-8-(3-methylbut-3-enyl)chromen-4-one	162910624	Click to see CC(=CCC1=C(C2=C(C(=C1O)CCC(=C)C)OC=C(C2=O)C3=CC=C(C=C3)O)O)C	406.50	unknown	https://doi.org/10.1016/S0031-9422(00)86896-X
5,7-dihydroxy-8-[(2R)-2-hydroxy-3-methylbut-3-enyl]-3-(4-hydroxyphenyl)-6-(3-methylbut-2-enyl)chromen-4-one	124355949	Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)C(=CO2)C3=CC=C(C=C3)O)CC(C(=C)C)O)O)C	422.50	unknown	https://doi.org/10.1016/S0031-9422(00)86896-X
5,7-dihydroxy-8-[(2S)-2-hydroxy-3-methylbut-3-enyl]-3-(4-hydroxyphenyl)-6-(3-methylbut-2-enyl)chromen-4-one	124355950	Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)C(=CO2)C3=CC=C(C=C3)O)CC(C(=C)C)O)O)C	422.50	unknown	https://doi.org/10.1016/S0031-9422(00)86896-X
6-(2,4-Dihydroxyphenyl)-4-hydroxy-2-(2-hydroxypropan-2-yl)-9-(3-methylbut-2-enyl)-2,3-dihydrofuro[3,2-g]chromen-5-one	101663504	Click to see CC(=CCC1=C2C(=C(C3=C1OC=C(C3=O)C4=C(C=C(C=C4)O)O)O)CC(O2)C(C)(C)O)C	438.50	unknown	https://doi.org/10.1055/S-2006-959446
6,8-Diprenylgenistein	480783	Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)C(=CO2)C3=CC=C(C=C3)O)CC=C(C)C)O)C	406.50	unknown	https://doi.org/10.1016/S0031-9422(99)00171-5
7-(2,4-Dihydroxyphenyl)-10-[(3,3-dimethyloxiran-2-yl)methyl]-5-hydroxy-2,2-dimethylpyrano[3,2-g]chromen-6-one	101663498	Click to see CC1(C=CC2=C(C3=C(C(=C2O1)CC4C(O4)(C)C)OC=C(C3=O)C5=C(C=C(C=C5)O)O)O)C	436.50	unknown	https://doi.org/10.1016/S0031-9422(00)86896-X
7-(2,4-dihydroxyphenyl)-10-[[(2R)-3,3-dimethyloxiran-2-yl]methyl]-5-hydroxy-2,2-dimethylpyrano[3,2-g]chromen-6-one	162939222	Click to see CC1(C=CC2=C(C3=C(C(=C2O1)CC4C(O4)(C)C)OC=C(C3=O)C5=C(C=C(C=C5)O)O)O)C	436.50	unknown	https://doi.org/10.1016/S0031-9422(00)86896-X
7-(2,4-dihydroxyphenyl)-10-[[(2S)-3,3-dimethyloxiran-2-yl]methyl]-5-hydroxy-2,2-dimethylpyrano[3,2-g]chromen-6-one	162939221	Click to see CC1(C=CC2=C(C3=C(C(=C2O1)CC4C(O4)(C)C)OC=C(C3=O)C5=C(C=C(C=C5)O)O)O)C	436.50	unknown	https://doi.org/10.1016/S0031-9422(00)86896-X
7-(2,4-Dihydroxyphenyl)-3,5-dihydroxy-2,2-dimethyl-10-(3-methylbut-2-enyl)-3,4-dihydropyrano[3,2-g]chromen-6-one	101663505	Click to see CC(=CCC1=C2C(=C(C3=C1OC=C(C3=O)C4=C(C=C(C=C4)O)O)O)CC(C(O2)(C)C)O)C	438.50	unknown	https://doi.org/10.1055/S-2006-959446
7-(2,4-dihydroxyphenyl)-5-hydroxy-10-[(2R)-2-hydroxy-3-methylbut-3-enyl]-2,2-dimethylpyrano[3,2-g]chromen-6-one	163087297	Click to see CC(=C)C(CC1=C2C(=C(C3=C1OC=C(C3=O)C4=C(C=C(C=C4)O)O)O)C=CC(O2)(C)C)O	436.50	unknown	https://doi.org/10.1016/0031-9422(94)00779-S
8-Prenylluteone	471687	Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)C(=CO2)C3=C(C=C(C=C3)O)O)CC=C(C)C)O)C	422.50	unknown	https://doi.org/10.1016/S0031-9422(00)90543-0
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(99)00171-5
Auriculatin	5358847	Click to see CC(=CCC1=C2C(=C(C3=C1OC=C(C3=O)C4=C(C=C(C=C4)O)O)O)C=CC(O2)(C)C)C	420.50	unknown	https://doi.org/10.1021/NP50046A019 https://doi.org/10.1016/S0031-9422(00)86896-X https://doi.org/10.1055/S-2006-959446 https://doi.org/10.1016/S0031-9422(99)00171-5
Erysenegalensein D	25256865	Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)C(=CO2)C3=C(C=C(C=C3)O)O)CC(C(=C)C)O)O)C	438.50	unknown	https://doi.org/10.1016/S0031-9422(99)00171-5 https://doi.org/10.1016/S0031-9422(00)86896-X https://doi.org/10.1016/S0031-9422(00)90543-0
erysenegalensein E	15478903	Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)C(=CO2)C3=CC=C(C=C3)O)CC(C(=C)C)O)O)C	422.50	unknown	https://doi.org/10.1016/S0031-9422(00)90543-0 https://doi.org/10.1016/S0031-9422(00)86896-X
Erysenegalensein L	15235622	Click to see CC(=C)C(CC1=C2C(=C(C3=C1OC=C(C3=O)C4=C(C=C(C=C4)O)O)O)C=CC(O2)(C)C)O	436.50	unknown	https://doi.org/10.1016/0031-9422(94)00779-S
Erysenegalensein N	49768588	Click to see CC(=CCC1=C(C(=C(C2=C1OC=C(C2=O)C3=C(C=C(C=C3)O)O)O)CC(C(=C)C)O)O)C	438.50	unknown	https://doi.org/10.1016/S0031-9422(99)00171-5
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/NP50072A004 https://doi.org/10.1055/S-2006-959446
Euchrenone b8	14704591	Click to see CC(=C)C(CC1=C2C(=C(C3=C1OC=C(C3=O)C4=CC=C(C=C4)O)O)C=CC(O2)(C)C)O	420.50	unknown	https://doi.org/10.1016/0031-9422(94)00779-S
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(85)80067-4 https://doi.org/10.1016/S0031-9422(00)86896-X
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavans / Isoflavanones / 8-prenylated isoflavanones
(3R,11R)-3,7,21-trihydroxy-17,17-dimethyl-14-(3-methylbut-2-enyl)-10,12,16-trioxapentacyclo[11.8.0.03,11.04,9.015,20]henicosa-1(13),4(9),5,7,14,18,20-heptaen-2-one	51542657	Click to see CC(=CCC1=C2C(=C(C3=C1OC4C(C3=O)(C5=C(O4)C=C(C=C5)O)O)O)C=CC(O2)(C)C)C	436.50	unknown	https://doi.org/10.1016/0031-9422(94)00671-F
(3S)-5,7-dihydroxy-6,8-bis(3-methylbut-2-enyl)-3-(2,4,5-trihydroxyphenyl)-2,3-dihydrochromen-4-one	162933392	Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)C(CO2)C3=CC(=C(C=C3O)O)O)CC=C(C)C)O)C	440.50	unknown	https://doi.org/10.1021/NP50115A013
(7S)-7-(2,4-dihydroxy-5-methoxyphenyl)-5-hydroxy-2,2-dimethyl-10-(3-methylbut-2-enyl)-7,8-dihydropyrano[3,2-g]chromen-6-one	163104313	Click to see CC(=CCC1=C2C(=C(C3=C1OCC(C3=O)C4=CC(=C(C=C4O)O)OC)O)C=CC(O2)(C)C)C	452.50	unknown	https://doi.org/10.1021/NP50115A013
5,7-Dihydroxy-6,8-bis(3-methylbut-2-enyl)-3-(2,4,5-trihydroxyphenyl)-2,3-dihydrochromen-4-one	10478410	Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)C(CO2)C3=CC(=C(C=C3O)O)O)CC=C(C)C)O)C	440.50	unknown	https://doi.org/10.1021/NP50115A013
7-(2,4-Dihydroxy-5-methoxyphenyl)-5-hydroxy-2,2-dimethyl-10-(3-methylbut-2-enyl)-7,8-dihydropyrano[3,2-g]chromen-6-one	101916981	Click to see CC(=CCC1=C2C(=C(C3=C1OCC(C3=O)C4=CC(=C(C=C4O)O)OC)O)C=CC(O2)(C)C)C	452.50	unknown	https://doi.org/10.1021/NP50115A013
Erysenegalensein J	51136516	Click to see CC(=CCC1=C2C(=C(C3=C1OC4C(C3=O)(C5=C(O4)C=C(C=C5)O)O)O)C=CC(O2)(C)C)C	436.50	unknown	https://doi.org/10.1016/0031-9422(94)00671-F
> Phenylpropanoids and polyketides / Isoflavonoids / Pyranoisoflavonoids
3-(2,4-Dihydroxyphenyl)-10-hydroxy-7,7-dimethyl-5-(3-methylbut-2-enyl)pyrano[2,3-g]chromen-4-one	163030793	Click to see CC(=CCC1=C2C(=C(C3=C1C(=O)C(=CO3)C4=C(C=C(C=C4)O)O)O)C=CC(O2)(C)C)C	420.50	unknown	https://doi.org/10.1016/S0031-9422(99)00171-5
> Phenylpropanoids and polyketides / Neoflavonoids / Neoflavones
5,7-Dimethoxy-4-phenylchromen-2-one	701671	Click to see COC1=CC2=C(C(=CC(=O)O2)C3=CC=CC=C3)C(=C1)OC	282.29	unknown	https://doi.org/10.1016/S0031-9422(99)00171-5

Biological Material Top

Contributors Top

No known contributors. Be the first!

Collections Top

In private collections	0
In public collections	0

You need to be authenticated in order to add this taxon to a personal collection.

Erythrina senegalensis

Table of Contents

Details Top

Description Top

Synonyms Top

Common names Top

Subspecies (abbr. subsp./ssp.) Top

Varieties (abbr. var.) Top

Subvarieties (abbr. subvar.) Top

Forms (abbr. f.) Top

Germination/Propagation Top

Distribution (via POWO/KEW) Top

Links to other databases Top

Genomes (via NCBI) Top

Scientific Literature Top

Phytochemical Profile Top

Biological Material Top

Contributors Top

Collections Top