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Erythrina addisoniae

Erythrina addisoniae - 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 UUID643fd8b19de7b869835352
Scientific name Erythrina addisoniae
Authority Hutch. & Dalziel
First published in Fl. W. Trop. Afr.1: 406 (1928)

Description Top

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Synonyms Top

No known synonyms.

Common names Top

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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
    • West Tropical Africa
      • Ghana
      • Guinea
      • Ivory Coast
      • Liberia
      • Nigeria
      • Sierra Leone
    • West-central Tropical Africa
      • Congo

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000180521
Tropicos 13043726
KEW urn:lsid:ipni.org:names:494342-1
The Plant List ild-2672
Open Tree Of Life 3921548
NCBI Taxonomy 2590682
IPNI 494342-1
GBIF 5349697
EOL 644088

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
Phytochemistry and pharmacology of natural prenylated flavonoids Lv HW, Wang QL, Luo M, Zhu MD, Liang HM, Li WJ, Cai H, Zhou ZB, Wang H, Tong SQ, Li XN Arch Pharm Res 14-Apr-2023
PMCID:PMC10101826
doi:10.1007/s12272-023-01443-4
PMID:37055613
In Vivo Bioactivities of Hoya parasitica (Wall.) and In Silico Study against Cyclooxygenase Enzymes Sarkar KK, Mitra T, Rahman MA, Raja IM, Aktaruzzaman M, Abid MA, Zilani MN, Roy DN Biomed Res Int 28-Apr-2022
PMCID:PMC9071894
doi:10.1155/2022/1331758
PMID:35528171
Targeting Breast Cancer and Their Stem Cell Population through AMPK Activation: Novel Insights Uprety B, Abrahamse H Cells 07-Feb-2022
PMCID:PMC8834477
doi:10.3390/cells11030576
PMID:35159385
A study on catalytic and non-catalytic sites of H5N1 and H1N1 neuraminidase as the target for chalcone inhibitors Hariyono P, Kotta JC, Adhipandito CF, Aprilianto E, Candaya EJ, Wahab HA, Hariono M Appl Biol Chem 17-Sep-2021
PMCID:PMC8445792
doi:10.1186/s13765-021-00639-w
PMID:34549099
Quantum Mechanical Predictions of the Antioxidant Capability of Moracin C Isomers Parise A, De Simone BC, Marino T, Toscano M, Russo N Front Chem 21-Apr-2021
PMCID:PMC8097241
doi:10.3389/fchem.2021.666647
PMID:33968905
A review of Cameroonian medicinal plants with potentials for the management of the COVID-19 pandemic Fongnzossie Fedoung E, Biwole AB, Nyangono Biyegue CF, Ngansop Tounkam M, Akono Ntonga P, Nguiamba VP, Essono DM, Forbi Funwi P, Tonga C, Nguenang GM, Kemeuze V, Sonwa DJ, Tsabang N, Bouelet IS, Tize Z, Boum AT, Momo Solefack MC, Betti JL, Nouga Bissoue A, Lehman LG, Mapongmetsem PM, Nneme Nneme L, Ngono Ngane RA, Ngogang Yonkeu J 26-Mar-2021
PMCID:PMC7994110
doi:10.1007/s13596-021-00567-6
Osteoarthritis Is a Low-Grade Inflammatory Disease: Obesity's Involvement and Herbal Treatment Zeddou M Evid Based Complement Alternat Med 04-Nov-2019
PMCID:PMC6874989
doi:10.1155/2019/2037484
PMID:31781260
Effect of Double Bond Position on 2-Phenyl-benzofuran Antioxidants: A Comparative Study of Moracin C and Iso-Moracin C Li X, Xie H, Zhan R, Chen D Molecules 24-Mar-2018
PMCID:PMC6017532
doi:10.3390/molecules23040754
PMID:29587376
An Integrated Computational Approach for Plant-Based Protein Tyrosine Phosphatase Non-Receptor Type 1 Inhibitors Bibi S, Sakata K Curr Comput Aided Drug Des 01-Dec-2017
PMCID:PMC5744427
doi:10.2174/1573409913666170406145607
PMID:28382867
New prenylated isoflavonoids as protein tyrosine phosphatase 1B (PTP1B) inhibitors from Erythrina addisoniae. Nguyen PH, Sharma G, Dao TT, Uddin MN, Kang KW, Ndinteh DT, Mbafor JT, Oh WK Bioorg Med Chem 01-Nov-2012
doi:10.1016/J.BMC.2012.08.024
PMID:23022281
Identification of Novel Human Dipeptidyl Peptidase-IV Inhibitors of Natural Origin (Part II): In Silico Prediction in Antidiabetic Extracts Guasch L, Sala E, Ojeda MJ, Valls C, Bladé C, Mulero M, Blay M, Ardévol A, Garcia-Vallvé S, Pujadas G PLoS One 21-Sep-2012
PMCID:PMC3448616
doi:10.1371/journal.pone.0044972
PMID:23028712
Natural products possessing protein tyrosine phosphatase 1B (PTP1B) inhibitory activity found in the last decades Jiang CS, Liang LF, Guo YW Acta Pharmacol Sin 03-Sep-2012
PMCID:PMC4002712
doi:10.1038/aps.2012.90
PMID:22941286
New stilbenoid with inhibitory activity on viral neuraminidases from Erythrina addisoniae. Nguyen PH, Na M, Dao TT, Ndinteh DT, Mbafor JT, Park J, Cheong H, Oh WK Bioorg Med Chem Lett 15-Nov-2010
doi:10.1016/J.BMCL.2010.09.077
PMID:20934335
Cameroonian Medicinal Plants: Pharmacology and Derived Natural Products Kuete V, Efferth T Front Pharmacol 25-Oct-2010
PMCID:PMC3153003
doi:10.3389/fphar.2010.00123
PMID:21833168
Prenylated flavonoid derivatives from the bark of Erythrina addisoniae. Wätjen W, Suckow-Schnitker AK, Rohrig R, Kulawik A, Addae-Kyereme J, Wright CW, Passreiter CM J Nat Prod 01-Apr-2008
doi:10.1021/NP070417J
PMID:18302333

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
> Benzenoids / Naphthalenes / Naphthalenecarboxylic acids and derivatives / Naphthalenecarboxylic acids
Fisheacid 139583718 Click to see C1C(C(=CC2=CC=CC=C21)C3=CC4=CC=CC=C4CC3C(=O)O)C(=O)O 346.40 unknown https://doi.org/10.1080/10826079208016365
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
2'-O-Demethylbidwillol B 23655080 Click to see CC(=CCC1=C(C=CC(=C1O)C2=CC3=C(O2)C=C(C=C3)O)O)C 310.30 unknown https://doi.org/10.1016/J.BMCL.2007.05.005
Addisofuran A 44432363 Click to see CC(=CCC1=CC(=C(C=C1O)OC)C2=CC3=C(O2)C=C(C=C3)O)C 324.40 unknown https://doi.org/10.1016/J.BMCL.2007.05.005
Addisofuran B 44432364 Click to see CC(=CCC1=C(C=C2C(=C1)C=C(O2)C3=C(C=C(C=C3)O)OC)O)C 324.40 unknown https://doi.org/10.1016/J.BMCL.2007.05.005
Glabrocoumarone A 10542808 Click to see CC1(C=CC2=C(C=CC(=C2O1)C3=CC4=C(O3)C=C(C=C4)O)O)C 308.30 unknown https://doi.org/10.1016/J.BMCL.2007.05.005
Glabrocoumarone B 15233562 Click to see CC1(C=CC2=C(O1)C=CC(=C2O)C3=CC4=C(O3)C=C(C=C4)O)C 308.30 unknown https://doi.org/10.1016/J.BMCL.2007.05.005
Vignafuran 441958 Click to see COC1=CC2=C(C=C1)C=C(O2)C3=C(C=C(C=C3)O)OC 270.28 unknown https://doi.org/10.1016/J.BMCL.2007.05.005
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acid amides
N-[2-hydroxy-2-[4-(3-methylbut-2-enoxy)phenyl]ethyl]-3-phenylprop-2-enamide 162892089 Click to see CC(=CCOC1=CC=C(C=C1)C(CNC(=O)C=CC2=CC=CC=C2)O)C 351.40 unknown https://doi.org/10.1016/J.BMCL.2010.09.077
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 3-prenylated flavans / 3-prenylated flavanones
(2R)-7-hydroxy-2-[4-hydroxy-3,5-bis(3-methylbut-2-enyl)phenyl]-2,3-dihydrochromen-4-one 7021184 Click to see CC(=CCC1=CC(=CC(=C1O)CC=C(C)C)C2CC(=O)C3=C(O2)C=C(C=C3)O)C 392.50 unknown https://doi.org/10.1021/NP070417J
(2S)-5,7-dihydroxy-2-[3-[(2R)-2-hydroxy-3-methylbut-3-enyl]-4-methoxy-5-(3-methylbut-2-enyl)phenyl]-2,3-dihydrochromen-4-one 162852553 Click to see CC(=CCC1=C(C(=CC(=C1)C2CC(=O)C3=C(C=C(C=C3O2)O)O)CC(C(=C)C)O)OC)C 438.50 unknown https://doi.org/10.1021/NP070417J
(2S)-5,7-dihydroxy-2-[4-hydroxy-3-[(2R)-2-hydroxy-3-methylbut-3-enyl]-5-(3-methylbut-2-enyl)phenyl]-2,3-dihydrochromen-4-one 163024985 Click to see CC(=CCC1=C(C(=CC(=C1)C2CC(=O)C3=C(C=C(C=C3O2)O)O)CC(C(=C)C)O)O)C 424.50 unknown https://doi.org/10.1021/NP070417J
(2S)-7-hydroxy-2-[4-hydroxy-3-[(2R)-2-hydroxy-3-methylbut-3-enyl]-5-(3-methylbut-2-enyl)phenyl]-2,3-dihydrochromen-4-one 162901131 Click to see CC(=CCC1=C(C(=CC(=C1)C2CC(=O)C3=C(O2)C=C(C=C3)O)CC(C(=C)C)O)O)C 408.50 unknown https://doi.org/10.1021/NP070417J
5,7-Dihydroxy-2-[3-(2-hydroxy-3-methylbut-3-enyl)-4-methoxy-5-(3-methylbut-2-enyl)phenyl]-2,3-dihydrochromen-4-one 74336649 Click to see CC(=CCC1=C(C(=CC(=C1)C2CC(=O)C3=C(C=C(C=C3O2)O)O)CC(C(=C)C)O)OC)C 438.50 unknown https://doi.org/10.1021/NP070417J
5,7-Dihydroxy-2-[4-hydroxy-3-(2-hydroxy-3-methylbut-3-enyl)-5-(3-methylbut-2-enyl)phenyl]-2,3-dihydrochromen-4-one 73316641 Click to see CC(=CCC1=C(C(=CC(=C1)C2CC(=O)C3=C(C=C(C=C3O2)O)O)CC(C(=C)C)O)O)C 424.50 unknown https://doi.org/10.1021/NP070417J
5,7-Dihydroxy-2-[4-hydroxy-3,5-bis(3-methylbut-2-enyl)phenyl]-2,3-dihydrochromen-4-one 101203 Click to see CC(=CCC1=CC(=CC(=C1O)CC=C(C)C)C2CC(=O)C3=C(C=C(C=C3O2)O)O)C 408.50 unknown https://doi.org/10.1021/NP070417J
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/10.1021/NP070417J
7-Hydroxy-2-[4-hydroxy-3-(2-hydroxy-3-methylbut-3-enyl)-5-(3-methylbut-2-enyl)phenyl]-2,3-dihydrochromen-4-one 74336650 Click to see CC(=CCC1=C(C(=CC(=C1)C2CC(=O)C3=C(O2)C=C(C=C3)O)CC(C(=C)C)O)O)C 408.50 unknown https://doi.org/10.1021/NP070417J
abyssinoflavanone VII 16737250 Click to see CC(=CCC1=C(C(=CC(=C1)C2CC(=O)C3=C(C=C(C=C3O2)O)O)CC(C(=C)C)O)O)C 424.50 unknown https://doi.org/10.1021/NP070417J
Abyssinone IV 4063835 Click to see CC(=CCC1=CC(=CC(=C1O)CC=C(C)C)C2CC(=O)C3=C(O2)C=C(C=C3)O)C 392.50 unknown https://doi.org/10.1021/NP070417J
Abyssinone V 442153 Click to see CC(=CCC1=CC(=CC(=C1O)CC=C(C)C)C2CC(=O)C3=C(C=C(C=C3O2)O)O)C 408.50 unknown https://doi.org/10.1021/NP070417J
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/10.1021/NP070417J
abyssinone-IV 7330513 Click to see CC(=CCC1=CC(=CC(=C1O)CC=C(C)C)C2CC(=O)C3=C(O2)C=C(C=C3)O)C 392.50 unknown https://doi.org/10.1021/NP070417J
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Anthocyanins / Anthocyanidin-5-O-glycosides
Cyanin 441688 Click to see C1=CC(=C(C=C1C2=C(C=C3C(=CC(=CC3=[O+]2)O)OC4C(C(C(C(O4)CO)O)O)O)OC5C(C(C(C(O5)CO)O)O)O)O)O 611.50 unknown https://doi.org/10.1080/10826079208016365
> Phenylpropanoids and polyketides / Isoflavonoids / Furanoisoflavonoids / Pterocarpans
17,17-Dimethyl-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 15382623 Click to see CC1(C=CC2=CC3=C(C=C2O1)OCC4C3OC5=C4C=CC(=C5)O)C 322.40 unknown https://doi.org/10.1016/J.TOX.2007.09.010
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.TOX.2007.09.010
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.TOX.2007.09.010
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
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/J.BMC.2012.08.024
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavans / Isoflavanones / 3-prenylated isoflavanones
erythraddison III 71454955 Click to see CC(=CCC1=C(C=CC(=C1)C2COC3=CC(=CC(=C3C2=O)O)O)OC)C 354.40 unknown https://doi.org/10.1016/J.BMC.2012.08.024
erythraddison IV 52325746 Click to see CC1(C=CC2=CC(=C(C=C2O1)OC)C3COC4=CC(=CC(=C4C3=O)O)O)C 368.40 unknown https://doi.org/10.1016/J.BMC.2012.08.024
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavans / Isoflavanones / 6-prenylated isoflavanones
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/10.1016/J.BMC.2012.08.024
5-Hydroxy-3-(4-methoxyphenyl)-8,8-dimethyl-10-(3-methylbut-2-en-1-yl)pyrano[3,2-g]chromen-4(8H)-one 5379768 Click to see CC(=CCC1=C2C(=C(C3=C1OC=C(C3=O)C4=CC=C(C=C4)OC)O)C=CC(O2)(C)C)C 418.50 unknown https://doi.org/10.1055/S-2006-946674
Erythraddison A 50899658 Click to see CC1(C=CC2=C(C3=C(C(=C2O1)CO)OC=C(C3=O)C4=CC=C(C=C4)O)O)C 366.40 unknown https://doi.org/10.1016/J.BMCL.2010.09.077
Erythraddison I 71460437 Click to see CC1(C=CC2=C(C3=C(C(=C2O1)C(C(C(C)(C)O)O)OC)OC=C(C3=O)C4=CC=C(C=C4)O)O)C 468.50 unknown https://doi.org/10.1016/J.BMC.2012.08.024
erythraddison II 38361391 Click to see CC(=CCC1=CC2=C(C(=C1O)CC=C(C)C)OC=C(C2=O)C3=C(C=C(C=C3)O)O)C 406.50 unknown https://doi.org/10.1016/J.BMC.2012.08.024
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/10.1021/NP020599B
https://doi.org/10.1055/S-2006-946674
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavans / Isoflavanones / 8-prenylated isoflavanones
(3S)-3-(2,4-dihydroxyphenyl)-5-hydroxy-8,8-dimethyl-6-(3-methylbut-2-enyl)-2,3-dihydropyrano[2,3-h]chromen-4-one 97423597 Click to see CC(=CCC1=C(C2=C(C3=C1OC(C=C3)(C)C)OCC(C2=O)C4=C(C=C(C=C4)O)O)O)C 422.50 unknown https://doi.org/10.1055/S-2006-946674
(3S)-3-(2,4-dihydroxyphenyl)-5,7-dihydroxy-6,8-bis(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one 26213317 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 424.50 unknown https://doi.org/10.1055/S-2006-946674
(7R)-7-(2,4-dihydroxyphenyl)-5-hydroxy-2,2-dimethyl-10-(3-methylbut-2-enyl)-7,8-dihydropyrano[3,2-g]chromen-6-one 163044003 Click to see CC(=CCC1=C2C(=C(C3=C1OCC(C3=O)C4=C(C=C(C=C4)O)O)O)C=CC(O2)(C)C)C 422.50 unknown https://doi.org/10.1055/S-2006-946674
2,3-Dihydroauriculatin 163749 Click to see CC(=CCC1=C2C(=C(C3=C1OCC(C3=O)C4=C(C=C(C=C4)O)O)O)C=CC(O2)(C)C)C 422.50 unknown https://doi.org/10.1055/S-2006-946674
3-(2,4-Dihydroxyphenyl)-5-hydroxy-8,8-dimethyl-6-(3-methylbut-2-enyl)-2,3-dihydropyrano[2,3-h]chromen-4-one 11964495 Click to see CC(=CCC1=C(C2=C(C3=C1OC(C=C3)(C)C)OCC(C2=O)C4=C(C=C(C=C4)O)O)O)C 422.50 unknown https://doi.org/10.1055/S-2006-946674
3-(2,4-Dihydroxyphenyl)-5,7-dihydroxy-6,8-bis(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one 11964494 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 424.50 unknown https://doi.org/10.1055/S-2006-946674
> Phenylpropanoids and polyketides / Stilbenes
2-(2-Hydroxy-4-methoxyphenyl)-3-(4-hydroxy-2-methoxyphenyl)prop-2-enal 75576265 Click to see COC1=CC(=C(C=C1)C(=CC2=C(C=C(C=C2)O)OC)C=O)O 300.30 unknown https://doi.org/10.1016/J.BMCL.2010.09.077

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