Xanthocercis zambesiaca - Unknown
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Internal ID UUID643fdead2806b861721613
Scientific name Xanthocercis zambesiaca
Authority (Baker) Dumaz-le-Grand
First published in Bull. Soc. Bot. France99: 314 (1953)

Description Top

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Xanthocercis zambesiaca, also known as the nyala tree or mshatu, is a legume species found in the southern subtropics of Africa. It grows in hot, low-lying river valleys in countries such as Botswana, Malawi, Mozambique, South Africa, Zambia, and Zimbabwe. These trees thrive in areas with plentiful moisture and deep, fertile soil, often growing on alluvium or termite mounds. While they are sparsely found in the eastern lowveld of Southern Africa, they are more abundant in the Limpopo valley and along the Shashe River in the Tuli Block, where they are known as mshatu trees. The foliage and fruit of the nyala tree provide food for various vertebrates during autumn and winter. Additionally, the nyala tree is a phreatophyte, meaning it indicates the presence of ground water. The wood of the nyala tree can be worked and has a smooth appearance, but the process can cause irritation to the nose and throat.

Synonyms Top

Scientific name Authority First published in
Pseudocadia zambesiaca (Baker) Harms H.G.A.Engler & O.Drude, Veg. Erde9(III 1): 524 (1915)
Sophora zambesiaca Baker D.Oliver & auct. suc. (eds.), Fl. Trop. Afr.2: 253 (1871)

Common names Top

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Language Common/alternative name
Afrikaans njalaboom

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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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Africa
    • South Tropical Africa
      • Malawi
      • Mozambique
      • Zambia
      • Zimbabwe
    • Southern Africa
      • Botswana
      • Northern Provinces

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000212102
Tropicos 13062380
KEW urn:lsid:ipni.org:names:525829-1
The Plant List ild-7179
Open Tree Of Life 980886
NCBI Taxonomy 53932
IUCN Red List 146210831
IPNI 525829-1
iNaturalist 340321
GBIF 2975473
Freebase /m/080mbtk
EOL 704219
USDA GRIN 101974
Wikipedia Xanthocercis_zambesiaca
CMAUP NPO21156

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
Fiber-like Action of d-Fagomine on the Gut Microbiota and Body Weight of Healthy Rats Ramos-Romero S, Ponomarenko J, Amézqueta S, Hereu M, Miralles-Pérez B, Romeu M, Méndez L, Medina I, Torres JL Nutrients 03-Nov-2022
PMCID:PMC9657608
doi:10.3390/nu14214656
PMID:36364917
Chromosomal-level genome assembly of the orchid tree Bauhinia variegata (Leguminosae; Cercidoideae) supports the allotetraploid origin hypothesis of Bauhinia Zhong Y, Chen Y, Zheng D, Pang J, Liu Y, Luo S, Meng S, Qian L, Wei D, Dai S, Zhou R DNA Res 19-Apr-2022
PMCID:PMC9052405
doi:10.1093/dnares/dsac012
PMID:35438173
Evolution of the Anther Gland in Early-Branching Papilionoids (ADA Clade, Papilionoideae, Leguminosae) Leite VG, Teixeira SP, Sartori ÂL, Mansano VF Plants (Basel) 22-Mar-2022
PMCID:PMC9002870
doi:10.3390/plants11070835
PMID:35406815
A Review of Ethnoveterinary Knowledge, Biological Activities and Secondary Metabolites of Medicinal Woody Plants Used for Managing Animal Health in South Africa Selogatwe KM, Asong JA, Struwig M, Ndou RV, Aremu AO Vet Sci 12-Oct-2021
PMCID:PMC8537377
doi:10.3390/vetsci8100228
PMID:34679058
Isolation and elucidation of two isoflavonoids from an American Indian plant, Amorpha canescens Pursh, using Magnetic Microbead Affinity Selection Screening (MagMASS) for estrogen receptor alpha ligands Burton TC, Lankin DC, Nikolic D, Guo B, Ju J, Dietz BM, Che CT, Soejarto DD, van Breemen RB Phytochem Lett 18-Aug-2021
PMCID:PMC9032482
doi:10.1016/j.phytol.2021.07.018
PMID:35465454
Reference transcriptomes and comparative analyses of six species in the threatened rosewood genus Dalbergia Hung TH, So T, Sreng S, Thammavong B, Boounithiphonh C, Boshier DH, MacKay JJ Sci Rep 20-Oct-2020
PMCID:PMC7576600
doi:10.1038/s41598-020-74814-2
PMID:33082403
The traditional use of southern African medicinal plants in the treatment of viral respiratory diseases: A review of the ethnobotany and scientific evaluations Cock IE, Van Vuuren SF J Ethnopharmacol 27-Jul-2020
PMCID:PMC7384428
doi:10.1016/j.jep.2020.113194
PMID:32730880
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
Legume Cytosolic and Plastid Acetyl-Coenzyme—A Carboxylase Genes Differ by Evolutionary Patterns and Selection Pressure Schemes Acting before and after Whole-Genome Duplications Szczepaniak A, Książkiewicz M, Podkowiński J, Czyż KB, Figlerowicz M, Naganowska B Genes (Basel) 21-Nov-2018
PMCID:PMC6265850
doi:10.3390/genes9110563
PMID:30469317
Antidiabetic phytoconstituents and their mode of action on metabolic pathways Bharti SK, Krishnan S, Kumar A, Kumar A Ther Adv Endocrinol Metab 12-Feb-2018
PMCID:PMC5813859
doi:10.1177/2042018818755019
PMID:29492244
Ethnoveterinary plants and practices used for ecto-parasite control in semi-arid smallholder farming areas of Zimbabwe Nyahangare ET, Mvumi BM, Mutibvu T J Ethnobiol Ethnomed 30-Apr-2015
PMCID:PMC4449613
doi:10.1186/s13002-015-0006-6
PMID:25925402
Multiple Polyploidy Events in the Early Radiation of Nodulating and Nonnodulating Legumes Cannon SB, McKain MR, Harkess A, Nelson MN, Dash S, Deyholos MK, Peng Y, Joyce B, Stewart CN Jr, Rolf M, Kutchan T, Tan X, Chen C, Zhang Y, Carpenter E, Wong GK, Doyle JJ, Leebens-Mack J Mol Biol Evol 27-Oct-2014
PMCID:PMC4271530
doi:10.1093/molbev/msu296
PMID:25349287
Isoflavones from Calpurnia Aurea subsp. Aurea and Their Anticancer Activity Korir E, Kiplimo JJ, Crouch NR, Moodley N, Koorbanally NA Afr J Tradit Complement Altern Med 23-Aug-2014
PMCID:PMC4202514
doi:10.4314/ajtcam.v11i5.5
PMID:25395701
An Isoflavone from Dipteryx alata Vogel is Active against the in Vitro Neuromuscular Paralysis of Bothrops jararacussu Snake Venom and Bothropstoxin I, and Prevents Venom-Induced Myonecrosis Ferraz MC, Yoshida EH, Tavares RV, Cogo JC, Cintra AC, Dal Belo CA, Franco LM, dos Santos MG, Resende FA, Varanda EA, Hyslop S, Puebla P, San Feliciano A, Oshima-Franco Y Molecules 06-May-2014
PMCID:PMC6271625
doi:10.3390/molecules19055790
PMID:24806579
The role of biocatalysis in the asymmetric synthesis of alkaloids Schrittwieser JH, Resch V RSC Adv 07-Aug-2013
PMCID:PMC4285126
doi:10.1039/c3ra42123f
PMID:25580241

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
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Canophyllol 7330581 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)CO)C)C)C)C 442.70 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(2R,3R,4S,5S,6R)-2-[(2R,3R,4R)-3-hydroxy-2-(hydroxymethyl)piperidin-4-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 10852369 Click to see C1CNC(C(C1OC2C(C(C(C(O2)CO)O)O)O)O)CO 309.31 unknown https://doi.org/10.1021/NP960646Y
(2R,3R,4S,5S,6R)-2-[(2R,3R,4R)-4-hydroxy-2-(hydroxymethyl)piperidin-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 21591966 Click to see C1CNC(C(C1O)OC2C(C(C(C(O2)CO)O)O)O)CO 309.31 unknown https://doi.org/10.1021/NP960646Y
(2S,3R,4S,5R,6R)-2-[(2R,3R,4R)-3-hydroxy-2-(hydroxymethyl)piperidin-4-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 162845022 Click to see C1CNC(C(C1OC2C(C(C(C(O2)CO)O)O)O)O)CO 309.31 unknown https://doi.org/10.1021/NP960646Y
(2S,3R,4S,5R,6R)-2-[(2R,3R,4R)-4-hydroxy-2-(hydroxymethyl)piperidin-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 162865026 Click to see C1CNC(C(C1O)OC2C(C(C(C(O2)CO)O)O)O)CO 309.31 unknown https://doi.org/10.1021/NP960646Y
2-[3-Hydroxy-2-(hydroxymethyl)piperidin-4-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 85079512 Click to see C1CNC(C(C1OC2C(C(C(C(O2)CO)O)O)O)O)CO 309.31 unknown https://doi.org/10.1021/NP960646Y
Fagomine Glucoside 354149 Click to see C1CNC(C(C1O)OC2C(C(C(C(O2)CO)O)O)O)CO 309.31 unknown https://doi.org/10.1021/NP960646Y
> Organoheterocyclic compounds / Indolizidines
Castanospermine 54445 Click to see C1CN2CC(C(C(C2C1O)O)O)O 189.21 unknown via CMAUP database
> Organoheterocyclic compounds / Piperidines
(2R,3S,4S)-2-(hydroxymethyl)piperidine-3,4-diol 10678391 Click to see C1CNC(C(C1O)O)CO 147.17 unknown https://doi.org/10.1021/NP960646Y
1-Deoxynojirimycin 29435 Click to see C1C(C(C(C(N1)CO)O)O)O 163.17 unknown via CMAUP database
3-Epi-fagomine 10290867 Click to see C1CNC(C(C1O)O)CO 147.17 unknown https://doi.org/10.1021/NP960646Y
3,4-Dihydroxy-2-piperidinemethanol 3553645 Click to see C1CNC(C(C1O)O)CO 147.17 unknown https://doi.org/10.1021/NP960646Y
Fagomine 72259 Click to see C1CNC(C(C1O)O)CO 147.17 unknown https://doi.org/10.1021/NP960646Y
> Organoheterocyclic compounds / Pyrrolidines
2,5-Dideoxy-2,5-imino-D-mannitol 124702 Click to see C(C1C(C(C(N1)CO)O)O)O 163.17 unknown via CMAUP database
> Phenylpropanoids and polyketides / Aurone flavonoids / Auronols
(2S)-2-[(3,4-dihydroxyphenyl)methyl]-2,6-dihydroxy-1-benzofuran-3-one 163025545 Click to see C1=CC(=C(C=C1CC2(C(=O)C3=C(O2)C=C(C=C3)O)O)O)O 288.25 unknown https://doi.org/10.1016/0031-9422(88)80154-7
2,6,3',4'-Tetrahydroxy-2-benzylcoumaranone 42607788 Click to see C1=CC(=C(C=C1CC2(C(=O)C3=C(O2)C=C(C=C3)O)O)O)O 288.25 unknown https://doi.org/10.1016/0031-9422(88)80154-7
Carasinaurone 101767761 Click to see COC1=CC(=CC2=C1C(=O)C(O2)(CC3=CC=C(C=C3)O)O)O 302.28 unknown https://doi.org/10.1016/0031-9422(88)80154-7
Carpusin 134369 Click to see COC1=CC(=CC2=C1C(=O)C(O2)(CC3=CC=C(C=C3)O)O)O 302.28 unknown https://doi.org/10.1016/0031-9422(88)80154-7
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Fisetin 5281614 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(O2)C=C(C=C3)O)O)O)O 286.24 unknown https://doi.org/10.1016/0031-9422(88)80154-7
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 3-hydroxy,4-methoxyisoflavonoids
3'-Hydroxy-8-O-methylretusin 44257262 Click to see COC1=C(C=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3OC)O)O 314.29 unknown https://doi.org/10.1016/0031-9422(88)80154-7
7,8,3'-Trihydroxy-4'-methoxyisoflavone 44257264 Click to see COC1=C(C=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3O)O)O 300.26 unknown https://doi.org/10.1016/0031-9422(88)80154-7
8-(3-Hydroxy-4-methoxyphenyl)-3-(4-hydroxy-3-methoxyphenyl)-2-(hydroxymethyl)-2,3-dihydropyrano[3,2-h][1,4]benzodioxin-7-one 14058045 Click to see COC1=C(C=C(C=C1)C2=COC3=C(C2=O)C=CC4=C3OC(C(O4)C5=CC(=C(C=C5)O)OC)CO)O 478.40 unknown https://doi.org/10.1016/0031-9422(88)80154-7
https://doi.org/10.1039/P19880001237
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 4-O-methylisoflavones
7-Hydroxy-8,3',4'-trimethoxyisoflavone 44257263 Click to see COC1=C(C=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3OC)O)OC 328.30 unknown https://doi.org/10.1016/0031-9422(88)80154-7
8-O-methylretusin 5319771 Click to see COC1=CC=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3OC)O 298.29 unknown https://doi.org/10.1016/0031-9422(88)80154-7
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Cinnamylphenols
(1R)-1-hydroxy-1-(4-hydroxy-2-methoxyphenyl)-3-(4-hydroxyphenyl)propan-2-one 86310826 Click to see COC1=C(C=CC(=C1)O)C(C(=O)CC2=CC=C(C=C2)O)O 288.29 unknown https://doi.org/10.1016/0031-9422(88)80154-7
(2R)-2-hydroxy-1-(4-hydroxy-2-methoxyphenyl)-3-(4-hydroxyphenyl)propan-1-one 162851350 Click to see COC1=C(C=CC(=C1)O)C(=O)C(CC2=CC=C(C=C2)O)O 288.29 unknown https://doi.org/10.1016/0031-9422(88)80154-7
(2R)-3-(3,4-dihydroxyphenyl)-2-hydroxy-1-(4-hydroxy-2-methoxyphenyl)propan-1-one 162933739 Click to see COC1=C(C=CC(=C1)O)C(=O)C(CC2=CC(=C(C=C2)O)O)O 304.29 unknown https://doi.org/10.1016/0031-9422(88)80154-7
1-(2-Methoxy-4-hydroxyphenyl)-3-(4-hydroxy-phenyl)propan-2-one 14160604 Click to see COC1=C(C=CC(=C1)O)CC(=O)CC2=CC=C(C=C2)O 272.29 unknown https://doi.org/10.1016/0031-9422(88)80154-7
1-Hydroxy-1-(4-hydroxy-2-methoxyphenyl)-3-(4-hydroxyphenyl)propan-2-one 14160605 Click to see COC1=C(C=CC(=C1)O)C(C(=O)CC2=CC=C(C=C2)O)O 288.29 unknown https://doi.org/10.1016/0031-9422(88)80154-7
3,4,4',alpha-Tetrahydroxy-2'-methoxydihydrochalcone 42607725 Click to see COC1=C(C=CC(=C1)O)C(=O)C(CC2=CC(=C(C=C2)O)O)O 304.29 unknown https://doi.org/10.1016/0031-9422(88)80154-7
4,4',alpha-Trihydroxy-2'-methoxydihydrochalcone 14160611 Click to see COC1=C(C=CC(=C1)O)C(=O)C(CC2=CC=C(C=C2)O)O 288.29 unknown https://doi.org/10.1016/0031-9422(88)80154-7

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