Details Top

Internal ID UUID643fd92edd993834845617
Scientific name Senna petersiana
Authority (Bolle) Lock
First published in Kew Bull.43: 340 (1988)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Cassia petersiana Bolle W.C.H.Peters, Naturw. Reise Mossambique6(1): 13 (1861)
Cassia delagoensis Harv. W.H.Harvey & auct. suc. (eds.), Fl. Cap.2: 272 (1862)
Cassia petersiana var. tomentosa Baker f. Legum. Trop. Africa3: 634 (1930)

Common names Top

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Language Common/alternative name
Afrikaans apiespeul

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
    • East Tropical Africa
      • Kenya
      • Tanzania
      • Uganda
    • Northeast Tropical Africa
      • Ethiopia
      • Sudan
    • South Tropical Africa
      • Malawi
      • Mozambique
      • Zambia
      • Zimbabwe
    • Southern Africa
      • Kwazulu-Natal
      • Northern Provinces
      • Swaziland
    • West-central Tropical Africa
      • Cameroon
      • Central African Republic
      • Rwanda
    • Western Indian Ocean
      • Madagascar

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000184159
USDA Plants SEPE9
Tropicos 13071414
KEW urn:lsid:ipni.org:names:945428-1
The Plant List ild-30188
Open Tree Of Life 389395
NCBI Taxonomy 992784
IUCN Red List 146208340
IPNI 945428-1
iNaturalist 340244
GBIF 2957867
Freebase /m/0ktxt6f
EOL 418441
USDA GRIN 403746
Wikipedia Senna_petersiana

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
Ethnoveterinary medicinal plants and their utilization by indigenous and local communities of Dugda District, Central Rift Valley, Ethiopia Oda BK, Lulekal E, Warkineh B, Asfaw Z, Debella A J Ethnobiol Ethnomed 09-Mar-2024
PMCID:PMC10924356
doi:10.1186/s13002-024-00665-0
PMID:38461267
Ethnobotanical study of wild edible plants in Dibatie district, Metekel zone, Benishangul Gumuz Regional State, western Ethiopia Anbessa B, Lulekal E, Getachew P, Hymete A J Ethnobiol Ethnomed 27-Feb-2024
PMCID:PMC10900549
doi:10.1186/s13002-024-00671-2
PMID:38413982
In-silico and in-vitro assessments of some fabaceae, rhamnaceae, apocynaceae, and anacardiaceae species against Mycobacterium tuberculosis H37Rv and triple-negative breast cancer cells Nyambo K, Adu-Amankwaah F, Tapfuma KI, Baatjies L, Julius L, Smith L, Ngxande M, Govender K, Mabasa L, Traore A, Masiphephethu MV, Niang IS, Mavumengwana V BMC Complement Med Ther 01-Jul-2023
PMCID:PMC10314437
doi:10.1186/s12906-023-04041-5
PMID:37393246
Phytochemical Content, Antibacterial Activity, and Antioxidant, Anti-Inflammatory, and Cytotoxic Effects of Traditional Medicinal Plants against Respiratory Tract Bacterial Pathogens Matotoka MM, Mashabela GT, Masoko P Evid Based Complement Alternat Med 31-May-2023
PMCID:PMC10247327
doi:10.1155/2023/1243438
PMID:37293600
Season, storage and extraction method impact on the phytochemical profile of Terminalia ivorensis Moomin A, Russell WR, Knott RM, Scobbie L, Mensah KB, Adu-Gyamfi PK, Duthie SJ BMC Plant Biol 25-Mar-2023
PMCID:PMC10039578
doi:10.1186/s12870-023-04144-8
PMID:36964494
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
Therapeutic Potential of Phenolic Compounds in Medicinal Plants—Natural Health Products for Human Health Sun W, Shahrajabian MH Molecules 15-Feb-2023
PMCID:PMC9960276
doi:10.3390/molecules28041845
PMID:36838831
An Inventory of Anthelmintic Plants across the Globe Ahmed H, Kilinc SG, Celik F, Kesik HK, Simsek S, Ahmad KS, Afzal MS, Farrakh S, Safdar W, Pervaiz F, Liaqat S, Zhang J, Cao J Pathogens 13-Jan-2023
PMCID:PMC9866317
doi:10.3390/pathogens12010131
PMID:36678480
An Inventory of South African Medicinal Plants Used in the Management of Sexually Transmitted and Related Opportunistic Infections: An Appraisal and Some Scientific Evidence (1990–2020) Mongalo NI, Raletsena MV Plants (Basel) 25-Nov-2022
PMCID:PMC9738887
doi:10.3390/plants11233241
PMID:36501281
Woody species diversity and carbon stock of church forests along age gradient in Dangila district, Awi-zone, Ethiopia Sewagegn GB, Abate DF, Yohannis Gebremariam Girma Heliyon 05-Sep-2022
PMCID:PMC9463591
doi:10.1016/j.heliyon.2022.e10491
PMID:36097492
Plant diversity and community analysis of Sele-Nono forest, Southwest Ethiopia: implication for conservation planning Kefalew A, Soromessa T, Demissew S Bot Stud 19-Jul-2022
PMCID:PMC9294133
doi:10.1186/s40529-022-00353-w
PMID:35851664
Structural Elucidation of an Atropisomeric Entcassiflavan-(4β→8)-Epicatechin Isolated from Dalbergia monetaria L.f. Based on NMR and ECD Calculations in Comparison to Experimental Data de Moura PH, Brandt W, Porzel A, Martins RC, Leal IC, Wessjohann LA Molecules 13-Apr-2022
PMCID:PMC9028727
doi:10.3390/molecules27082512
PMID:35458711
Metabolomic profile of medicinal plants with anti-RVFV activity More GK, Vervoort J, Steenkamp PA, Prinsloo G Heliyon 12-Feb-2022
PMCID:PMC8857432
doi:10.1016/j.heliyon.2022.e08936
PMID:35243061
A Review of Recent Studies on the Antioxidant and Anti-Infectious Properties of Senna Plants Alshehri MM, Quispe C, Herrera-Bravo J, Sharifi-Rad J, Tutuncu S, Aydar EF, Topkaya C, Mertdinc Z, Ozcelik B, Aital M, Kumar NV, Lapava N, Rajkovic J, Ertani A, Nicola S, Semwal P, Painuli S, González-Contreras C, Martorell M, Butnariu M, Bagiu IC, Bagiu RV, Barbhai MD, Kumar M, Daştan SD, Calina D, Cho WC Oxid Med Cell Longev 04-Feb-2022
PMCID:PMC8837466
doi:10.1155/2022/6025900
PMID:35154569
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

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 / Anthracenes / Anthraquinones
Aloe emodin 10207 Click to see 270.24 unknown https://doi.org/10.1016/S0367-326X(00)00155-6
Physcion 10639 Click to see 284.26 unknown https://doi.org/10.1016/S0367-326X(00)00155-6
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Octacosanol 68406 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCO 410.80 unknown https://doi.org/10.1016/S0367-326X(00)00155-6
1-Triacontanol 68972 Click to see 438.80 unknown https://doi.org/10.1016/S0367-326X(00)00155-6
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(3R,4aR,6aR,9aS,9bR)-3-ethenyl-3,4a,7,7,9a-pentamethyl-2,5,6,6a,9,9b-hexahydro-1H-cyclopenta[f]chromen-8-one 101603220 Click to see 290.40 unknown https://doi.org/10.1055/S-2007-969643
Alpha-Amyrin 73170 Click to see 426.70 unknown https://doi.org/10.1016/S0367-326X(00)00155-6
Beta-Amyrin 73145 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 unknown https://doi.org/10.1016/S0367-326X(00)00155-6
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
(24R)-5-Ergosten-3beta-ol 312822 Click to see 400.70 unknown https://doi.org/10.1016/S0367-326X(00)00155-6
(3S,8S,9S,14S,17R)-17-[(2R,5R)-5,6-dimethylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 134766514 Click to see 400.70 unknown https://doi.org/10.1016/S0367-326X(00)00155-6
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Stigmasterol 5280794 Click to see 412.70 unknown https://doi.org/10.1016/S0367-326X(00)00155-6
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
(2R,3R)-2-(3,4-dihydroxyphenyl)-6-[(2S,4S)-7-hydroxy-2-(4-hydroxyphenyl)-3,4-dihydro-2H-chromen-4-yl]-3,4-dihydro-2H-chromene-3,5,7-triol 163191145 Click to see 530.50 unknown https://doi.org/10.1016/0031-9422(95)00656-7
(2R,3R)-2-(3,4-dihydroxyphenyl)-8-[(2R,4R)-7-hydroxy-2-(4-hydroxyphenyl)-3,4-dihydro-2H-chromen-4-yl]-3,4-dihydro-2H-chromene-3,5,7-triol 163021686 Click to see C1C(C2=C(C=C(C=C2)O)OC1C3=CC=C(C=C3)O)C4=C(C=C(C5=C4OC(C(C5)O)C6=CC(=C(C=C6)O)O)O)O 530.50 unknown https://doi.org/10.1016/0031-9422(95)00656-7
(2R,3R)-2-(3,4-dihydroxyphenyl)-8-[(2S,4R)-2-(3,4-dihydroxyphenyl)-7-hydroxy-3,4-dihydro-2H-chromen-4-yl]-3,4-dihydro-2H-chromene-3,5,7-triol 100945224 Click to see C1C(C2=C(C=C(C=C2)O)OC1C3=CC(=C(C=C3)O)O)C4=C(C=C(C5=C4OC(C(C5)O)C6=CC(=C(C=C6)O)O)O)O 546.50 unknown https://doi.org/10.1016/0031-9422(95)00656-7
(2R,3R)-2-(3,4-dihydroxyphenyl)-8-[(2S,4R)-7-hydroxy-2-(4-hydroxyphenyl)-3,4-dihydro-2H-chromen-4-yl]-3,4-dihydro-2H-chromene-3,5,7-triol 163021685 Click to see C1C(C2=C(C=C(C=C2)O)OC1C3=CC=C(C=C3)O)C4=C(C=C(C5=C4OC(C(C5)O)C6=CC(=C(C=C6)O)O)O)O 530.50 unknown https://doi.org/10.1016/0031-9422(95)00656-7
(2R,3R)-2-(3,4-dihydroxyphenyl)-8-[(2S,4S)-2-(3,4-dihydroxyphenyl)-7-hydroxy-3,4-dihydro-2H-chromen-4-yl]-3,4-dihydro-2H-chromene-3,5,7-triol 100945226 Click to see C1C(C2=C(C=C(C=C2)O)OC1C3=CC(=C(C=C3)O)O)C4=C(C=C(C5=C4OC(C(C5)O)C6=CC(=C(C=C6)O)O)O)O 546.50 unknown https://doi.org/10.1016/0031-9422(95)00656-7
(2R,3R)-2-(3,4-dihydroxyphenyl)-8-[(2S,4S)-7-hydroxy-2-(4-hydroxyphenyl)-3,4-dihydro-2H-chromen-4-yl]-3,4-dihydro-2H-chromene-3,5,7-triol 163021687 Click to see C1C(C2=C(C=C(C=C2)O)OC1C3=CC=C(C=C3)O)C4=C(C=C(C5=C4OC(C(C5)O)C6=CC(=C(C=C6)O)O)O)O 530.50 unknown https://doi.org/10.1016/0031-9422(95)00656-7
(2R,3R)-8-[(2S,4R)-2-(3,4-dihydroxyphenyl)-7-hydroxy-3,4-dihydro-2H-chromen-4-yl]-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-chromene-3,5,7-triol 162941611 Click to see 562.50 unknown https://doi.org/10.1016/0031-9422(95)00656-7
(2R,3R)-8-[(2S,4R)-7-hydroxy-2-(4-hydroxyphenyl)-3,4-dihydro-2H-chromen-4-yl]-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-chromene-3,5,7-triol 162949649 Click to see 546.50 unknown https://doi.org/10.1016/0031-9422(95)00656-7
(2R,3R)-8-[(2S,4S)-7-hydroxy-2-(4-hydroxyphenyl)-3,4-dihydro-2H-chromen-4-yl]-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-chromene-3,5,7-triol 162949648 Click to see 546.50 unknown https://doi.org/10.1016/0031-9422(95)00656-7
(2R,3S)-8-[(2S,4R)-7-hydroxy-2-(4-hydroxyphenyl)-3,4-dihydro-2H-chromen-4-yl]-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-chromene-3,5,7-triol 102334782 Click to see 546.50 unknown https://doi.org/10.1016/0031-9422(95)00656-7
2-(3,4-dihydroxyphenyl)-6-[7-hydroxy-2-(4-hydroxyphenyl)-3,4-dihydro-2H-chromen-4-yl]-3,4-dihydro-2H-chromene-3,5,7-triol 163076549 Click to see 530.50 unknown https://doi.org/10.1016/0031-9422(95)00656-7
2-(3,4-dihydroxyphenyl)-8-[2-(3,4-dihydroxyphenyl)-7-hydroxy-3,4-dihydro-2H-chromen-4-yl]-3,4-dihydro-2H-chromene-3,5,7-triol 73161111 Click to see C1C(C2=C(C=C(C=C2)O)OC1C3=CC(=C(C=C3)O)O)C4=C(C=C(C5=C4OC(C(C5)O)C6=CC(=C(C=C6)O)O)O)O 546.50 unknown https://doi.org/10.1016/0031-9422(95)00656-7
2-(3,4-dihydroxyphenyl)-8-[7-hydroxy-2-(4-hydroxyphenyl)-3,4-dihydro-2H-chromen-4-yl]-3,4-dihydro-2H-chromene-3,5,7-triol 85164210 Click to see 530.50 unknown https://doi.org/10.1016/0031-9422(95)00656-7
8-[2-(3,4-dihydroxyphenyl)-7-hydroxy-3,4-dihydro-2H-chromen-4-yl]-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-chromene-3,5,7-triol 162941610 Click to see 562.50 unknown https://doi.org/10.1016/0031-9422(95)00656-7
8-[7-hydroxy-2-(4-hydroxyphenyl)-3,4-dihydro-2H-chromen-4-yl]-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-chromene-3,5,7-triol 162949647 Click to see 546.50 unknown https://doi.org/10.1016/0031-9422(95)00656-7

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