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Entada goetzei

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID68f90d82e2709090978287
Scientific name Entada goetzei
Authority (Harms) S.A.O’Donnell & G.P.Lewis
First published in PhytoKeys 205: 119 (2022)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Piptadenia goetzei Harms Bot. Jahrb. Syst.28: 397 (1900)
Elephantorrhiza goetzei (Harms) Harms Veg. Erde 9(III 1): 400 (1915)

Common names Top

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Language Common/alternative name
English false sumach bean
English narrow-pod elephant root
Afrikaans basterbasboontjie
Afrikaans smalpeulbasboontjie

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Entada goetzei subsp. goetzei
Entada goetzei subsp. lata (Brenan & Brummitt) S.A.O’Donnell & G.P.Lewis PhytoKeys 205: 120 (2022)

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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Distribution (via POWO/KEW) Top

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Links to other databases Top

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Database ID/link to page
Tropicos 13057149
KEW urn:lsid:ipni.org:names:493741-1
The Plant List ild-41
Open Tree Of Life 1076015
NCBI Taxonomy 992692
IUCN Red List 144301554
IPNI 493741-1
iNaturalist 584446
GBIF 2933005
EOL 686791
World Flora Online wfo-1000040053

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 Uses of the Fabaceae Family in Zimbabwe: A Review Maroyi A Plants (Basel) 10-Mar-2023
PMCID:PMC10051751
doi:10.3390/plants12061255
PMID:36986943
Traditional Kenyan Herbal Medicine: Exploring Natural Products Therapeutics against Schistosomiasis Ndegwa FK, Kondam C, Aboagye SY, Esan TE, Waxali ZS, Miller ME, Gikonyo NK, Mbugua PK, Okemo PO, Williams DL, Hagen TJ J Helminthol 03-Mar-2022
PMCID:PMC10030042
doi:10.1017/S0022149X22000074
PMID:35238288
PZQ Therapy: How Close are we in the Development of Effective Alternative Anti-schistosomal Drugs? Aruleba RT, Adekiya TA, Oyinloye BE, Masamba P, Mbatha LS, Pretorius A, Kappo AP Infect Disord Drug Targets 01-Dec-2019
PMCID:PMC7046992
doi:10.2174/1871526519666181231153139
PMID:30599112
Diversification of African Tree Legumes in Miombo–Mopane Woodlands Maquia I, Catarino S, Pena AR, Brito DR, Ribeiro NS, Romeiras MM, Ribeiro-Barros AI Plants (Basel) 20-Jun-2019
PMCID:PMC6631767
doi:10.3390/plants8060182
PMID:31226765
Conservation and sustainable use of the medicinal Leguminosae plants from Angola Catarino S, Duarte MC, Costa E, Carrero PG, Romeiras MM PeerJ 23-May-2019
PMCID:PMC6535223
doi:10.7717/peerj.6736
PMID:31198619
Plants Used by Bapedi Traditional Healers to Treat Asthma and Related Symptoms in Limpopo Province, South Africa Semenya SS, Maroyi A Evid Based Complement Alternat Med 19-Jul-2018
PMCID:PMC6077574
doi:10.1155/2018/2183705
PMID:30108649
Anti-HIV activity of southern African plants: Current developments, phytochemistry and future research Prinsloo G, Marokane CK, Street RA J Ethnopharmacol 12-Aug-2017
PMCID:PMC7125770
doi:10.1016/j.jep.2017.08.005
PMID:28807850
Traditional use of medicinal plants in south-central Zimbabwe: review and perspectives Maroyi A J Ethnobiol Ethnomed 04-May-2013
PMCID:PMC3653698
doi:10.1186/1746-4269-9-31
PMID:23642285
Phytoliths in woody plants from the Miombo woodlands of Mozambique Mercader J, Bennett T, Esselmont C, Simpson S, Walde D Ann Bot 09-May-2009
PMCID:PMC2706725
doi:10.1093/aob/mcp097
PMID:19429923
A new flavan from Elephantorrhiza goetzei Fortune Moyo, Berhanu A. Gashe, Runner R.T. Majinda Elsevier BV 25-Jul-2002
doi:10.1016/S0367-326X(99)00068-4
A new stilbene glycoside from Elephantorrhiza goetzei. Wanjala CC, Majinda RR Fitoterapia 01-Aug-2001
doi:10.1016/S0367-326X(01)00295-7
PMID:11543962

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 / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Gallic acids
Gallic Acid 370 Click to see 170.12 unknown https://doi.org/10.1016/S0367-326X(01)00295-7
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Galloyl esters
Methyl Gallate 7428 Click to see 184.15 unknown https://doi.org/10.1016/S0367-326X(99)00068-4
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
[3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl] 10,11-dihydroxy-9,9-bis(hydroxymethyl)-2,2,6a,6b,12a-pentamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 162946076 Click to see 666.80 unknown https://doi.org/10.1016/S0367-326X(01)00295-7
Bellericoside 101425822 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(CO)CO)O)O)C)C)C2C1)C)C(=O)OC6C(C(C(C(O6)CO)O)O)O)C 666.80 unknown https://doi.org/10.1016/S0367-326X(01)00295-7
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
[3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl] 1,10,11-trihydroxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 14658049 Click to see 666.80 unknown https://doi.org/10.1016/S0367-326X(01)00295-7
Arjungenin 12444386 Click to see 504.70 unknown https://doi.org/10.1016/S0367-326X(01)00295-7
Sericoside 76972524 Click to see 666.80 unknown https://doi.org/10.1016/S0367-326X(01)00295-7
Tomentosic acid 622032 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1O)C)C(=O)O)C 504.70 unknown https://doi.org/10.1016/S0367-326X(01)00295-7
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
(2S,3R)-2-(3,4-dihydroxyphenyl)-3,4-dihydro-2H-chromene-3,5,6,7,8-pentol 154496500 Click to see 322.27 unknown https://doi.org/10.1016/S0367-326X(99)00068-4
2-(3,4-dihydroxyphenyl)-3,4-dihydro-2H-1-benzopyran-3,5,7-triol 1203 Click to see 290.27 unknown https://doi.org/10.1016/S0367-326X(01)00295-7
Catechin 9064 Click to see 290.27 unknown https://doi.org/10.1016/S0367-326X(99)00068-4
https://doi.org/10.1016/S0367-326X(01)00295-7
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Epigallocatechins
(-)-Gallocatechin 9882981 Click to see 306.27 unknown https://doi.org/10.1016/S0367-326X(01)00295-7
Flavan-3,3',4',5,5',7-hexol 1249 Click to see 306.27 unknown https://doi.org/10.1016/S0367-326X(01)00295-7
> Phenylpropanoids and polyketides / Stilbenes
5-(2-(4-Hydroxyphenyl)Ethenyl)Benzene-1,3-Diol 5056 Click to see 228.24 unknown https://doi.org/10.1016/S0367-326X(01)00295-7
Resveratrol 445154 Click to see 228.24 unknown https://doi.org/10.1016/S0367-326X(01)00295-7
> Phenylpropanoids and polyketides / Stilbenes / Stilbene glycosides
(2S,3R,4R,5R,6R)-2-methyl-6-[[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[3-[(E)-2-(4-hydroxyphenyl)ethenyl]-5-methoxyphenoxy]oxan-2-yl]methoxy]oxane-3,4,5-triol 11168830 Click to see 550.60 unknown https://doi.org/10.1016/S0367-326X(01)00295-7
(2S,3R,4R,5R,6R)-2-methyl-6-[[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[3-hydroxy-5-[(E)-2-(4-hydroxyphenyl)ethenyl]phenoxy]oxan-2-yl]methoxy]oxane-3,4,5-triol 45481958 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=CC(=C3)O)C=CC4=CC=C(C=C4)O)O)O)O)O)O)O 536.50 unknown https://doi.org/10.1016/S0367-326X(01)00295-7
2-Methyl-6-[[3,4,5-trihydroxy-6-[3-[2-(4-hydroxyphenyl)ethenyl]-5-methoxyphenoxy]oxan-2-yl]methoxy]oxane-3,4,5-triol 85422700 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=CC(=C3)OC)C=CC4=CC=C(C=C4)O)O)O)O)O)O)O 550.60 unknown https://doi.org/10.1016/S0367-326X(01)00295-7
2-Methyl-6-[[3,4,5-trihydroxy-6-[3-hydroxy-5-[2-(4-hydroxyphenyl)ethenyl]phenoxy]oxan-2-yl]methoxy]oxane-3,4,5-triol 163005573 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=CC(=C3)O)C=CC4=CC=C(C=C4)O)O)O)O)O)O)O 536.50 unknown https://doi.org/10.1016/S0367-326X(01)00295-7

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