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Eriosema kraussianum

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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 UUID643fdb5ce5c98564582045
Scientific name Eriosema kraussianum
Authority Meisn.
First published in London J. Bot.2: 91 (1843)

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
    • Southern Africa
      • Cape Provinces
      • Free State
      • Kwazulu-Natal
      • Northern Provinces

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000195450
Tropicos 13030139
KEW urn:lsid:ipni.org:names:494076-1
The Plant List ild-42038
Open Tree Of Life 3922287
NCBI Taxonomy 2730163
IPNI 494076-1
iNaturalist 139158
GBIF 5349171
EOL 646458
USDA GRIN 436179

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
Medicinal Plants Used for the Treatment of Erectile Dysfunction in Ethiopia: A Systematic Review Asmerom D, Kalay TH, Araya TY, Desta DM, Wondafrash DZ, Tafere GG Biomed Res Int 07-Jun-2021
PMCID:PMC8205584
doi:10.1155/2021/6656406
PMID:34212038
The Genus Eriosema (Fabaceae): From the Ethnopharmacology to an Evidence-Based Phytotherapeutic Perspective? Ateba SB, Njamen D, Krenn L Front Pharmacol 07-May-2021
PMCID:PMC8138667
doi:10.3389/fphar.2021.641225
PMID:34025412
In silico Targeting, inhibition and analysis of polyketide synthase enzyme in Aspergillus ssp Labib MM, Amin MK, Alzohairy AM, Elashtokhy MM, Samir O, Saleh I, Arif IA, Osman GH, Hassanein SE Saudi J Biol Sci 27-Oct-2020
PMCID:PMC7715038
doi:10.1016/j.sjbs.2020.10.012
PMID:33304124
African traditional medicines for erectile dysfunction: elusive dream or imminent reality? Ojewole JA Cardiovasc J Afr 01-Jul-2007
PMCID:PMC4170225
PMID:17940663
Vasodilatory and hypoglycaemic effects of two pyrano-isoflavone extractives from Eriosema kraussianum N. E. Br. [Fabaceae] rootstock in experimental rat models. Ojewole JA, Drewes SE, Khan F Phytochemistry 01-Mar-2006
doi:10.1016/J.PHYTOCHEM.2005.11.019
PMID:16434072
Minor pyrano-isoflavones from Eriosema kraussianum: activity-, structure-, and chemical reaction studies. Drewes SE, Horn MM, Khan F, Munro OQ, Dhlamini JT, Rakuambo C, Meyer JJ Phytochemistry 01-Jul-2004
doi:10.1016/J.PHYTOCHEM.2004.04.030
PMID:15280002
Pyrano-isoflavones with erectile-dysfunction activity from Eriosema kraussianum. Drewes SE, Horn MM, Munro OQ, Dhlamini JT, Meyer JJ, Rakuambo NC Phytochemistry 01-Apr-2002
doi:10.1016/S0031-9422(02)00035-3
PMID:11909631

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 / Isoflavans / Isoflavanones / 3-prenylated isoflavanones
(1R,14R)-11,14-dihydroxy-7,7,20,20-tetramethyl-2,6,21,25-tetraoxahexacyclo[12.11.0.03,12.05,10.015,24.017,22]pentacosa-3(12),4,8,10,15(24),16,18,22-octaen-13-one 162891490 Click to see CC1(C=CC2=CC3=C(C=C2O1)OC4C3(C(=O)C5=C(O4)C=C6C(=C5O)C=CC(O6)(C)C)O)C 434.40 unknown https://doi.org/10.1016/S0031-9422(02)00035-3
(1S,13R)-1,17,19-trihydroxy-7,7-dimethyl-18-(3-methylbut-2-enyl)-8,12,14-trioxapentacyclo[11.8.0.02,11.04,9.015,20]henicosa-2(11),3,5,9,15(20),16,18-heptaen-21-one 163078594 Click to see CC(=CCC1=C(C2=C(C=C1O)OC3C(C2=O)(C4=C(O3)C=C5C(=C4)C=CC(O5)(C)C)O)O)C 436.50 unknown https://doi.org/10.1016/S0031-9422(02)00035-3
(1S,14S)-11,14-dihydroxy-7,7,20,20-tetramethyl-2,6,21,25-tetraoxahexacyclo[12.11.0.03,12.05,10.015,24.017,22]pentacosa-3(12),4,8,10,15(24),16,18,22-octaen-13-one 162891488 Click to see CC1(C=CC2=CC3=C(C=C2O1)OC4C3(C(=O)C5=C(O4)C=C6C(=C5O)C=CC(O6)(C)C)O)C 434.40 unknown https://doi.org/10.1016/S0031-9422(02)00035-3
1,17,19-Trihydroxy-7,7-dimethyl-18-(3-methylbut-2-enyl)-8,12,14-trioxapentacyclo[11.8.0.02,11.04,9.015,20]henicosa-2(11),3,5,9,15(20),16,18-heptaen-21-one 5318853 Click to see CC(=CCC1=C(C2=C(C=C1O)OC3C(C2=O)(C4=C(O3)C=C5C(=C4)C=CC(O5)(C)C)O)O)C 436.50 unknown https://doi.org/10.1016/S0031-9422(02)00035-3
https://doi.org/10.1016/J.PHYTOCHEM.2004.04.030
Kraussianone 4 5318852 Click to see CC1(C=CC2=CC3=C(C=C2O1)OC4C3(C(=O)C5=C(O4)C=C6C(=C5O)C=CC(O6)(C)C)O)C 434.40 unknown https://doi.org/10.1016/S0031-9422(02)00035-3
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavans / Isoflavanones / 6-prenylated isoflavanones
(3R)-3,5-dihydroxy-7-(7-hydroxy-2,2-dimethylchromen-6-yl)-2,2-dimethyl-3,4-dihydropyrano[3,2-g]chromen-6-one 162897018 Click to see CC1(C=CC2=CC(=C(C=C2O1)O)C3=COC4=CC5=C(CC(C(O5)(C)C)O)C(=C4C3=O)O)C 436.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.04.030
(3S)-3,5-dihydroxy-7-(7-hydroxy-2,2-dimethylchromen-6-yl)-2,2-dimethyl-3,4-dihydropyrano[3,2-g]chromen-6-one 162897017 Click to see CC1(C=CC2=CC(=C(C=C2O1)O)C3=COC4=CC5=C(CC(C(O5)(C)C)O)C(=C4C3=O)O)C 436.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.04.030
3,5-Dihydroxy-7-(7-hydroxy-2,2-dimethylchromen-6-yl)-2,2-dimethyl-3,4-dihydropyrano[3,2-g]chromen-6-one 12997538 Click to see CC1(C=CC2=CC(=C(C=C2O1)O)C3=COC4=CC5=C(CC(C(O5)(C)C)O)C(=C4C3=O)O)C 436.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.04.030
5-Hydroxy-7-(7-hydroxy-2,2-dimethylchromen-6-yl)-2,2-dimethylpyrano[3,2-g]chromen-6-one 5318848 Click to see CC1(C=CC2=CC(=C(C=C2O1)O)C3=COC4=CC5=C(C=CC(O5)(C)C)C(=C4C3=O)O)C 418.40 unknown https://doi.org/10.1016/S0031-9422(02)00035-3
https://doi.org/10.1016/J.PHYTOCHEM.2005.11.019
5,7-Dihydroxy-3-(7-hydroxy-2,2-dimethylchromen-6-yl)-6-(2-hydroxy-3-methylbut-3-enyl)chromen-4-one 12997539 Click to see CC(=C)C(CC1=C(C2=C(C=C1O)OC=C(C2=O)C3=C(C=C4C(=C3)C=CC(O4)(C)C)O)O)O 436.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.04.030
5,7-Dihydroxy-3-(7-hydroxy-2,2-dimethylchromen-6-yl)-6-(3-hydroxy-3-methylbutyl)chromen-4-one 5318851 Click to see CC1(C=CC2=CC(=C(C=C2O1)O)C3=COC4=C(C3=O)C(=C(C(=C4)O)CCC(C)(C)O)O)C 438.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.04.030
https://doi.org/10.1016/S0031-9422(02)00035-3
5,7-Dihydroxy-3-(7-hydroxy-2,2-dimethylchromen-6-yl)-6-(3-methylbut-2-enyl)chromen-4-one 5318849 Click to see CC(=CCC1=C(C2=C(C=C1O)OC=C(C2=O)C3=C(C=C4C(=C3)C=CC(O4)(C)C)O)O)C 420.50 unknown https://doi.org/10.1016/S0031-9422(02)00035-3
https://doi.org/10.1016/J.PHYTOCHEM.2004.04.030
https://doi.org/10.1016/J.PHYTOCHEM.2005.11.019
5,7-dihydroxy-3-(7-hydroxy-2,2-dimethylchromen-6-yl)-6-[(2R)-2-hydroxy-3-methylbut-3-enyl]chromen-4-one 162994578 Click to see CC(=C)C(CC1=C(C2=C(C=C1O)OC=C(C2=O)C3=C(C=C4C(=C3)C=CC(O4)(C)C)O)O)O 436.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.04.030
5,7-dihydroxy-3-(7-hydroxy-2,2-dimethylchromen-6-yl)-6-[(2S)-2-hydroxy-3-methylbut-3-enyl]chromen-4-one 162994579 Click to see CC(=C)C(CC1=C(C2=C(C=C1O)OC=C(C2=O)C3=C(C=C4C(=C3)C=CC(O4)(C)C)O)O)O 436.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.04.030
5,8-Dihydroxy-3-(7-hydroxy-2,2-dimethylchromen-6-yl)-6-(3-hydroxy-3-methylbutyl)chromen-4-one 102510321 Click to see CC1(C=CC2=CC(=C(C=C2O1)O)C3=COC4=C(C=C(C(=C4C3=O)O)CCC(C)(C)O)O)C 438.50 unknown https://doi.org/10.1016/S0031-9422(02)00035-3
5,8-Dihydroxy-3-(7-hydroxy-2,2-dimethylchromen-6-yl)-6-(3-methylbut-2-enyl)chromen-4-one 102510322 Click to see CC(=CCC1=CC(=C2C(=C1O)C(=O)C(=CO2)C3=C(C=C4C(=C3)C=CC(O4)(C)C)O)O)C 420.50 unknown https://doi.org/10.1016/S0031-9422(02)00035-3

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