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Erythrina bidwillii

Erythrina bidwillii - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
Erythrina bidwillii - 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 UUID643fd8b2d37de181077760
Scientific name Erythrina bidwillii
Authority Lindl.

Description Top

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Synonyms Top

No known synonyms.

Common names Top

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Language Common/alternative name
Chinese 珊瑚刺桐

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

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

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000180554
KEW urn:lsid:ipni.org:names:494362-1
The Plant List ild-2675
Missouri Botanical Garden 280457
IPNI 494362-1
iNaturalist 356027
GBIF 5349503
Freebase /m/09gm5gw
EPPO ERZBI
EOL 644108
Wikipedia Erythrina_%C3%97_bidwillii
PFAF Erythrina x bidwillii

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)!
Title Authors Publication Released IDs
Phenolic Compounds in Erythrina x bidwilli and Their Activity Against Oral Microbial Organisms Munekazu Iinuma, Yasutoshi Okawa, Toshiyuki Tanaka, Yasuko Kobayashi, Ken-ichi Miyauchi The Japan Institute of Heterocyclic Chemistry 01-Apr-2009
doi:10.3987/COM-94-S(B)60
Two New Erythrinan Alkaloids from Erythrina x bidwillii Hitoshi Tanaka, Toshihiro Tanaka, Hideo Etoh, Sachiko Goto, Yukimasa Terada The Japan Institute of Heterocyclic Chemistry 12-Mar-2009
doi:10.3987/COM-99-8686
Erythrinan alkaloid from Erythrina x bidwillii Hitoshi Tanaka, Toshihiro Tanaka, Hideo Etoh Elsevier BV 23-Apr-2003
doi:10.1016/S0031-9422(98)00132-0
An isoflavan from Erythrina x bidwillii Hitoshi Tanaka, Toshihiro Tanaka, Ayako Hosoya, Yukio Kitade, Hideo Etoh Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(97)00732-2
Alkaloid constituents fromErythrina xbidwillii flowers Amrik Singh Chawla, Ashwani Sood, Manoi Kumar, Anthony H. Jackson Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(91)83084-X
Phenolic constituents in Erythrina x bidwilli and their activity against oral microbial organisms. Iinuma M, Tanaka T, Mizuno M, Yamamoto H, Kobayashi Y, Yonemori S Chem Pharm Bull (Tokyo) 01-Oct-1992
doi:10.1248/CPB.40.2749
PMID:1464104

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
(1S,11R,19R)-11-hydroxy-19-methoxy-5,7-dioxa-13-azapentacyclo[11.7.0.01,16.02,10.04,8]icosa-2,4(8),9,15,17-pentaen-14-one 101042366 Click to see COC1CC23C(=CC(=O)N2CC(C4=CC5=C(C=C34)OCO5)O)C=C1 327.30 unknown https://doi.org/10.3987/COM-99-8686
(1S,12R,19R)-12-hydroxy-19-methoxy-5,7-dioxa-13-azapentacyclo[11.7.0.01,16.02,10.04,8]icosa-2,4(8),9,15,17-pentaen-11-one 102438648 Click to see COC1CC23C(=CCN2C(C(=O)C4=CC5=C(C=C34)OCO5)O)C=C1 327.30 unknown https://doi.org/10.1016/S0031-9422(98)00132-0
https://doi.org/10.3987/COM-99-8686
(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/10.1016/0031-9422(91)83084-X
(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/10.1016/S0031-9422(98)00132-0
(2S,9S,13bS)-2,9,11,12-tetramethoxy-7-oxido-2,6,8,9-tetrahydro-1H-indolo[7a,1-a]isoquinolin-7-ium 102506563 Click to see COC1CC23C(=CC[N+]2(CC(C4=CC(=C(C=C34)OC)OC)OC)[O-])C=C1 359.40 unknown https://doi.org/10.1016/0031-9422(91)83084-X
12-Hydroxy-19-methoxy-5,7-dioxa-13-azapentacyclo[11.7.0.01,16.02,10.04,8]icosa-2,4(8),9,15,17-pentaen-11-one 163052368 Click to see COC1CC23C(=CCN2C(C(=O)C4=CC5=C(C=C34)OCO5)O)C=C1 327.30 unknown https://doi.org/10.1016/S0031-9422(98)00132-0
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/10.1016/S0031-9422(98)00132-0
8-Oxoerythraline 21599256 Click to see COC1CC23C(=CC(=O)N2CCC4=CC5=C(C=C34)OCO5)C=C1 311.30 unknown https://doi.org/10.3987/COM-99-8686
Erysodine 169017 Click to see COC1CC23C(=CCN2CCC4=CC(=C(C=C34)OC)O)C=C1 299.40 unknown https://doi.org/10.1016/S0031-9422(98)00132-0
https://doi.org/10.3987/COM-99-8686
Erysotramidine 11034782 Click to see COC1CC23C(=CC(=O)N2CCC4=CC(=C(C=C34)OC)OC)C=C1 327.40 unknown https://doi.org/10.1016/0031-9422(91)83084-X
Erysotrine 442219 Click to see COC1CC23C(=CCN2CCC4=CC(=C(C=C34)OC)OC)C=C1 313.40 unknown https://doi.org/10.1016/0031-9422(91)83084-X
Erythraline 5317205 Click to see COC1CC23C(=CCN2CCC4=CC5=C(C=C34)OCO5)C=C1 297.30 unknown https://doi.org/10.1016/S0031-9422(98)00132-0
https://doi.org/10.3987/COM-99-8686
Erythrartine 11336443 Click to see COC1CC23C(=CCN2CC(C4=CC(=C(C=C34)OC)OC)O)C=C1 329.40 unknown https://doi.org/10.1016/0031-9422(91)83084-X
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/S0031-9422(98)00132-0
https://doi.org/10.3987/COM-99-8686
Erythrinine 3084503 Click to see COC1CC23C(=CCN2CC(C4=CC5=C(C=C34)OCO5)O)C=C1 313.30 unknown https://doi.org/10.3987/COM-99-8686
https://doi.org/10.1016/S0031-9422(98)00132-0
> 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/10.1016/S0031-9422(98)00132-0
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
2-[4-Hydroxy-2-methoxy-3-(3-methylbut-2-enyl)phenyl]-1-benzofuran-6-ol 10019143 Click to see CC(=CCC1=C(C=CC(=C1OC)C2=CC3=C(O2)C=C(C=C3)O)O)C 324.40 unknown https://doi.org/10.3987/COM-94-S(B)60
> Phenylpropanoids and polyketides / Isoflavonoids / Furanoisoflavonoids / Pterocarpans
(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/10.1248/CPB.40.2749
9-methoxy-10-(3-methylbut-2-enyl)-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromen-3-ol 392464 Click to see CC(=CCC1=C(C=CC2=C1OC3C2COC4=C3C=CC(=C4)O)OC)C 338.40 unknown https://doi.org/10.1016/S0031-9422(97)00732-2
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/10.1248/CPB.40.2749
Erycristagallin 10362969 Click to see CC(=CCC1=CC2=C(C=C1O)OCC3=C2OC4=C3C=CC(=C4CC=C(C)C)O)C 390.50 unknown https://doi.org/10.3987/COM-94-S(B)60
Sandwicensin 467498 Click to see CC(=CCC1=C(C=CC2=C1OC3C2COC4=C3C=CC(=C4)O)OC)C 338.40 unknown https://doi.org/10.1016/S0031-9422(97)00732-2
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
8-Prenyldaidzein 14841119 Click to see CC(=CCC1=C(C=CC2=C1OC=C(C2=O)C3=CC=C(C=C3)O)O)C 322.40 unknown https://doi.org/10.1248/CPB.40.2749
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavans / Isoflavanones / 6-prenylated isoflavanones
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/10.1248/CPB.40.2749
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavans / Isoflavanones / 8-prenylated isoflavanones
(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/10.1248/CPB.40.2749
(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/10.1248/CPB.40.2749
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/10.1248/CPB.40.2749
Bidwillon B 10046930 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/10.1248/CPB.40.2749
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 2-O-methylated isoflavonoids
(3S)-3-[4-hydroxy-2-methoxy-3-(3-methylbut-2-enyl)phenyl]-3,4-dihydro-2H-chromen-7-ol 154495967 Click to see CC(=CCC1=C(C=CC(=C1OC)C2CC3=C(C=C(C=C3)O)OC2)O)C 340.40 unknown https://doi.org/10.1016/S0031-9422(97)00732-2
Bidwillol A 10042759 Click to see CC(=CCC1=C(C=CC(=C1OC)C2=CC3=C(C=C(C=C3)O)OC2)O)C 338.40 unknown https://doi.org/10.3987/COM-94-S(B)60
> Phenylpropanoids and polyketides / Isoflavonoids / Pyranoisoflavonoids
(3S)-3-(5-methoxy-2,2-dimethylchromen-6-yl)-3,4-dihydro-2H-chromen-7-ol 157675084 Click to see CC1(C=CC2=C(O1)C=CC(=C2OC)C3CC4=C(C=C(C=C4)O)OC3)C 338.40 unknown https://doi.org/10.1016/S0031-9422(97)00732-2
3-(4-Hydroxyphenyl)-8,8-dimethylpyrano[2,3-f]chromen-4-one 9996115 Click to see CC1(C=CC2=C(O1)C=CC3=C2OC=C(C3=O)C4=CC=C(C=C4)O)C 320.30 unknown https://doi.org/10.3987/COM-94-S(B)60
8-[(3S)-7-hydroxy-3,4-dihydro-2H-chromen-3-yl]-2,2-dimethylchromen-5-ol 162946117 Click to see CC1(C=CC2=C(C=CC(=C2O1)C3CC4=C(C=C(C=C4)O)OC3)O)C 324.40 unknown https://doi.org/10.1016/S0031-9422(97)00732-2
Erythbidin A 15391906 Click to see CC1(C=CC2=C(C=CC(=C2O1)C3CC4=C(C=C(C=C4)O)OC3)O)C 324.40 unknown https://doi.org/10.1016/S0031-9422(97)00732-2
Phaseollinisoflavan 162412 Click to see CC1(C=CC2=C(O1)C=CC(=C2O)C3CC4=C(C=C(C=C4)O)OC3)C 324.40 unknown https://doi.org/10.1016/S0031-9422(97)00732-2

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