Erythrina zeyheri

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Details Top

Internal ID	UUID643fd8cbdbd2a201687176
Scientific name	Erythrina zeyheri
Authority	Harv.
First published in	W.H.Harvey & auct. suc. (eds.), Fl. Cap.2: 236 (1862)

Description Top

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Synonyms Top

Scientific name	Authority	First published in
Corallodendron zeyheri	(Harv.) Kuntze	Revis. Gen. Pl.1: 173 (1891)

Common names Top

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Language	Common/alternative name
English	plough-breaker
Afrikaans	ploegbreker
Arabic	حمرية زايرية
Chinese	肉质刺桐

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

Africa click to expand
- South Tropical Africa
  - Zimbabwe
- Southern Africa
  - Botswana
  - Cape Provinces
  - Free State
  - Kwazulu-Natal
  - Lesotho
  - Northern Provinces

Links to other databases Top

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Database	ID/link to page
World Flora Online	wfo-0000181259
Tropicos	13030301
KEW	urn:lsid:ipni.org:names:494630-1
The Plant List	ild-2741
Open Tree Of Life	284186
NCBI Taxonomy	347911
IPNI	494630-1
iNaturalist	553421
GBIF	5349495
Freebase	/m/0pb5ztx
EOL	644571
USDA GRIN	15775
Wikipedia	Erythrina_zeyheri

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)!
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Title

Authors

Publication

Released

IDs

DNA Barcoding to Confirm the Morphological Identification of the Coral Trees (Erythrina spp., Fabaceae) in the Ancient Gardens of Naples (Campania, Italy)

De Luca A, Sibilio G, De Luca P, Del Guacchio E

Plants (Basel)

06-Jun-2018

PMCID:	PMC6027229
doi:	10.3390/plants7020043
PMID:	29882805

Antidiabetic Medicinal Plants Used by the Basotho Tribe of Eastern Free State: A Review

Balogun FO, Tshabalala NT, Ashafa AO

J Diabetes Res

29-Jun-2016

PMCID:	PMC4942634
doi:	10.1155/2016/4602820
PMID:	27437404

A natural history of botanical therapeutics

Schmidt B, Ribnicky DM, Poulev A, Logendra S, Cefalu WT, Raskin I

Metabolism

01-Jul-2008

PMCID:	PMC2981029
doi:	10.1016/j.metabol.2008.03.001
PMID:	18555851

Ethnopharmacological uses of Erythrina senegalensis: a comparison of three areas in Mali, and a link between traditional knowledge and modern biological science

Togola A, Austarheim I, Theïs A, Diallo D, Paulsen BS

J Ethnobiol Ethnomed

05-Mar-2008

PMCID:	PMC2278129
doi:	10.1186/1746-4269-4-6
PMID:	18321374

Isoflavonoids from roots of Erythrina zeyheri.

Tanaka H, Oh-Uchi T, Etoh H, Sako M, Asai F, Fukai T, Sato M, Murata J, Tateishi Y

Phytochemistry

01-Oct-2003

doi:	10.1016/S0031-9422(03)00390-X
PMID:	13679098

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
> Phenylpropanoids and polyketides / Isoflavonoids / Furanoisoflavonoids / Pterocarpans
(2S,11S)-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-heptaen-7-ol	161690659	Click to see CC(=CCC1=CC2=C(C=C1O)OCC3C2OC4=C3C=CC5=C4C=CC(O5)(C)C)C	390.50	unknown	https://doi.org/10.1016/S0031-9422(03)00390-X
(6aR,11aR)-10-(3-methylbut-2-enyl)-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromene-3,9-diol	5117820	Click to see CC(=CCC1=C(C=CC2=C1OC3C2COC4=C3C=CC(=C4)O)O)C	324.40	unknown	https://doi.org/10.1016/S0031-9422(03)00390-X
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-heptaen-7-ol	44257437	Click to see CC(=CCC1=CC2=C(C=C1O)OCC3C2OC4=C3C=CC5=C4C=CC(O5)(C)C)C	390.50	unknown	https://doi.org/10.1016/S0031-9422(03)00390-X
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/S0031-9422(03)00390-X
9-Methoxy-2,10-bis(3-methylbut-2-enyl)-6,11a-dihydro-[1]benzofuro[3,2-c]chromene-3,6a-diol	85135193	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(03)00390-X
9-Methoxy-4,10-bis(3-methylbut-2-enyl)-6,11a-dihydro-[1]benzofuro[3,2-c]chromene-3,6a-diol	22298401	Click to see CC(=CCC1=C(C=CC2=C1OCC3(C2OC4=C3C=CC(=C4CC=C(C)C)OC)O)O)C	422.50	unknown	https://doi.org/10.1016/S0031-9422(03)00390-X
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(03)00390-X
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/S0031-9422(03)00390-X
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(03)00390-X
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(03)00390-X
Eryzerin E	641707	Click to see CC(=CCC1=C(C=CC2=C1OCC3(C2OC4=C3C=CC(=C4CC=C(C)C)OC)O)O)C	422.50	unknown	https://doi.org/10.1016/S0031-9422(03)00390-X
Folitenol	15840592	Click to see CC(=CCC1=CC2=C(C=C1O)OCC3C2OC4=C3C=CC5=C4C=CC(O5)(C)C)C	390.50	unknown	https://doi.org/10.1016/S0031-9422(03)00390-X
Phaseollidin	119268	Click to see CC(=CCC1=C(C=CC2=C1OC3C2COC4=C3C=CC(=C4)O)O)C	324.40	unknown	https://doi.org/10.1016/S0031-9422(03)00390-X
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavans / Isoflavanols
4-[(3R)-7-hydroxy-6,8-bis(3-methylbut-2-enyl)-3,4-dihydro-2H-chromen-3-yl]benzene-1,3-diol	10092034	Click to see CC(=CCC1=C(C(=C2C(=C1)CC(CO2)C3=C(C=C(C=C3)O)O)CC=C(C)C)O)C	394.50	unknown	https://doi.org/10.1016/S0031-9422(03)00390-X
4-[(7R)-2,2-dimethyl-10-(3-methylbut-2-enyl)-7,8-dihydro-6H-pyrano[3,2-g]chromen-7-yl]benzene-1,3-diol	162891689	Click to see CC(=CCC1=C2C(=CC3=C1OC(C=C3)(C)C)CC(CO2)C4=C(C=C(C=C4)O)O)C	392.50	unknown	https://doi.org/10.1016/S0031-9422(03)00390-X
4-[(7S)-2,2-dimethyl-10-(3-methylbut-2-enyl)-7,8-dihydro-6H-pyrano[3,2-g]chromen-7-yl]benzene-1,3-diol	162891690	Click to see CC(=CCC1=C2C(=CC3=C1OC(C=C3)(C)C)CC(CO2)C4=C(C=C(C=C4)O)O)C	392.50	unknown	https://doi.org/10.1016/S0031-9422(03)00390-X
4-[2,2-dimethyl-10-(3-methylbut-2-enyl)-7,8-dihydro-6H-pyrano[3,2-g]chromen-7-yl]benzene-1,3-diol	11761017	Click to see CC(=CCC1=C2C(=CC3=C1OC(C=C3)(C)C)CC(CO2)C4=C(C=C(C=C4)O)O)C	392.50	unknown	https://doi.org/10.1016/S0031-9422(03)00390-X
4-[7-hydroxy-6,8-bis(3-methylbut-2-enyl)-3,4-dihydro-2H-chromen-3-yl]benzene-1,3-diol	21576519	Click to see CC(=CCC1=C(C(=C2C(=C1)CC(CO2)C3=C(C=C(C=C3)O)O)CC=C(C)C)O)C	394.50	unknown	https://doi.org/10.1016/S0031-9422(03)00390-X
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavans / Isoflavanones / 8-prenylated isoflavanones
(3R)-3-[2,4-dihydroxy-3-(3-methylbut-2-enyl)phenyl]-7-hydroxy-8-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one	101263233	Click to see CC(=CCC1=C(C=CC(=C1O)C2COC3=C(C2=O)C=CC(=C3CC=C(C)C)O)O)C	408.50	unknown	https://doi.org/10.1016/S0031-9422(03)00390-X
(3S)-3-[2,4-dihydroxy-3-(3-methylbut-2-enyl)phenyl]-7-hydroxy-8-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one	101263234	Click to see CC(=CCC1=C(C=CC(=C1O)C2COC3=C(C2=O)C=CC(=C3CC=C(C)C)O)O)C	408.50	unknown	https://doi.org/10.1016/S0031-9422(03)00390-X
3-[2,4-Dihydroxy-3-(3-methylbut-2-enyl)phenyl]-7-hydroxy-8-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one	10982434	Click to see CC(=CCC1=C(C=CC(=C1O)C2COC3=C(C2=O)C=CC(=C3CC=C(C)C)O)O)C	408.50	unknown	https://doi.org/10.1016/S0031-9422(03)00390-X
7-Hydroxy-3-(4-hydroxy-2-methoxyphenyl)-6,8-bis(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one	21576518	Click to see CC(=CCC1=CC2=C(C(=C1O)CC=C(C)C)OCC(C2=O)C3=C(C=C(C=C3)O)OC)C	422.50	unknown	https://doi.org/10.1016/S0031-9422(03)00390-X
Eryzerin B	10862753	Click to see CC(=CCC1=CC2=C(C(=C1O)CC=C(C)C)OCC(C2=O)C3=C(C=C(C=C3)O)OC)C	422.50	unknown	https://doi.org/10.1016/S0031-9422(03)00390-X

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Erythrina zeyheri

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