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Lessertia frutescens

Lessertia frutescens - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
Lessertia frutescens - 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 UUID6440590981fa3797079393
Scientific name Lessertia frutescens
Authority (L.) Goldblatt & J.C.Manning
First published in Strelitzia9: 708 (2000)

Description Top

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Synonyms Top

Scientific name Authority First published in
Sutherlandia frutescens (L.) W.T.Aiton Hortus Kew.4: 327 (1812)
Colutea frutescens L. Sp. Pl.: 723 (1753)
Colutia frutescens (L.) Medik. Philos. Bot.1: 210 (1789)

Common names Top

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Language Common/alternative name
Afrikaans kankerbossie
German ballonerbse
Japanese レッセルティア・フルテスセンス
Russian Сутерландия кустарниковая
Chinese 纸荚豆

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Lessertia frutescens subsp. frutescens Unknown
Lessertia frutescens subsp. microphylla (Burch. ex DC.) J.C.Manning & Boatwr. Strelitzia29: 804 (2012)
Lessertia frutescens subsp. speciosa (E.Phillips & R.A.Dyer) J.C.Manning & Boatwr. Strelitzia29: 804 (2012)

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

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
    • East Tropical Africa
      • Kenya
    • Southern Africa
      • Botswana
      • Cape Provinces
      • Free State
      • Kwazulu-Natal
      • Lesotho
      • Namibia
      • Northern Provinces
  • Australasia
    • Australia
      • New South Wales
      • South Australia
      • Victoria
      • Western Australia

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001274560
Tropicos 50273408
KEW urn:lsid:ipni.org:names:1017425-1
The Plant List tro-50273408
Open Tree Of Life 611053
NCBI Taxonomy 47091
IPNI 1017425-1
iNaturalist 589008
GBIF 5633333
Freebase /m/027_nb6
USDA GRIN 446528
Wikipedia Sutherlandia_frutescens
CMAUP NPO6779

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 against Viral Infections: A Review of Metabolomics Evidence for the Antiviral Properties and Potentials in Plant Sources Adeosun WB, Loots DT Viruses 31-Jan-2024
PMCID:PMC10892737
doi:10.3390/v16020218
PMID:38399995
Bioprospecting for Rhizobacteria with the Ability to Enhance Drought Tolerance in Lessertia frutescens Hlongwane MM, Dakora FD, Mohammed M, Mokgalaka-Fleischmann NS Int J Mol Sci 18-Dec-2023
PMCID:PMC10743902
doi:10.3390/ijms242417585
PMID:38139414
Abiotic Stress Tolerance in Crop and Medicinal Plants Dobrikova AG Plants (Basel) 15-Dec-2023
PMCID:PMC10746992
doi:10.3390/plants12244167
PMID:38140494
Moringa oleifera: A Review on the Antiproliferative Potential in Breast Cancer Cells Moremane MM, Abrahams B, Tiloke C Curr Issues Mol Biol 18-Aug-2023
PMCID:PMC10453312
doi:10.3390/cimb45080434
PMID:37623253
Phenolic Compounds and Antioxidant and Anti-Enzymatic Activities of Selected Adaptogenic Plants from South America, Asia, and Africa Gębalski J, Małkowska M, Graczyk F, Słomka A, Piskorska E, Gawenda-Kempczyńska D, Kondrzycka-Dąda A, Bogucka-Kocka A, Strzemski M, Sowa I, Wójciak M, Grzyb S, Krolik K, Ptaszyńska AA, Załuski D Molecules 10-Aug-2023
PMCID:PMC10457937
doi:10.3390/molecules28166004
PMID:37630255
Fascinating Furanosteroids and Their Pharmacological Profile Dembitsky VM Molecules 26-Jul-2023
PMCID:PMC10419491
doi:10.3390/molecules28155669
PMID:37570639
Plants, Cells, Algae, and Cyanobacteria In Vitro and Cryobank Collections at the Institute of Plant Physiology, Russian Academy of Sciences—A Platform for Research and Production Center Yuorieva N, Sinetova M, Messineva E, Kulichenko I, Fomenkov A, Vysotskaya O, Osipova E, Baikalova A, Prudnikova O, Titova M, Nosov AV, Popova E Biology (Basel) 09-Jun-2023
PMCID:PMC10295647
doi:10.3390/biology12060838
PMID:37372123
Effects of natural products on skin inflammation caused by abnormal hormones secreted by the adrenal gland Xie W, Zhang C, Wang T, Wang J, Fu F Front Pharmacol 03-May-2023
PMCID:PMC10188947
doi:10.3389/fphar.2023.1156271
PMID:37205913
Ethnobotanical survey of medicinal plants used by indigenous knowledge holders to manage healthcare needs in children Ndhlovu PT, Asong JA, Omotayo AO, Otang-Mbeng W, Aremu AO PLoS One 27-Mar-2023
PMCID:PMC10042359
doi:10.1371/journal.pone.0282113
PMID:36972257
The molecular interplay of known phytochemicals as Culex pipiens and Rift Valley fever virus inhibitors through molecular docking Abutaha N, AL-Mekhlafi FA, Wadaan MA, Moustafa Rady A, Baabbad AA, Al-Khalifa MS Saudi J Biol Sci 01-Mar-2023
PMCID:PMC10036733
doi:10.1016/j.sjbs.2023.103611
PMID:36970253
High nitrogen inhibits biomass and saponins accumulation in a medicinal plant Panax notoginseng Cun Z, Wu HM, Zhang JY, Shuang SP, Hong J, An TX, Chen JW PeerJ 21-Feb-2023
PMCID:PMC9951802
doi:10.7717/peerj.14933
PMID:36846464
Bibliometric Study of Adaptogens in Dermatology: Pharmacophylogeny, Phytochemistry, and Pharmacological Mechanisms Liu XX, Chen CY, Li L, Guo MM, He YF, Meng H, Dong YM, Xiao PG, Yi F Drug Des Devel Ther 06-Feb-2023
PMCID:PMC9912821
doi:10.2147/DDDT.S395256
PMID:36776447
The Potential of Rhizobacteria to Mitigate Abiotic Stress in Lessertia frutescens Hlongwane MM, Mohammed M, Mokgalaka NS, Dakora FD Plants (Basel) 03-Jan-2023
PMCID:PMC9824651
doi:10.3390/plants12010196
PMID:36616325
Effect of Soil Type and In Vitro Proliferation Conditions on Acclimation and Growth of Willow Shoots Micropropagated in Continuous Immersion Bioreactors Trasar-Cepeda C, Sánchez C, Casalderrey M, Bello D, Vielba JM, Rico S, Aldrey A, Vidal N Plants (Basel) 27-Dec-2022
PMCID:PMC9823317
doi:10.3390/plants12010132
PMID:36616261
Antimicrobial Effects of Gum Arabic-Silver Nanoparticles against Oral Pathogens Ahmed O, Sibuyi NR, Fadaka AO, Madiehe AM, Maboza E, Olivier A, Meyer M, Geerts G Bioinorg Chem Appl 13-Dec-2022
PMCID:PMC9767746
doi:10.1155/2022/9602325
PMID:36561898

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / p-Hydroxybenzoic acid esters / p-Hydroxybenzoic acid alkyl esters
Methylparaben 7456 Click to see COC(=O)C1=CC=C(C=C1)O 152.15 unknown https://doi.org/10.1016/S0378-8741(04)00117-5
Propylparaben 7175 Click to see CCCOC(=O)C1=CC=C(C=C1)O 180.20 unknown https://doi.org/10.1016/S0378-8741(04)00117-5
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Ethane 6324 Click to see CC 30.07 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 9,9-epoxylignans / Dibenzylbutyrolactone lignans
Arctigenin 64981 Click to see COC1=C(C=C(C=C1)CC2COC(=O)C2CC3=CC(=C(C=C3)O)OC)OC 372.40 unknown via CMAUP database
> Lignans, neolignans and related compounds / Lignan glycosides
Arctiin 100528 Click to see COC1=C(C=C(C=C1)CC2COC(=O)C2CC3=CC(=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)OC)OC 534.60 unknown via CMAUP database
Matairesinoside 486612 Click to see COC1=C(C=CC(=C1)CC2COC(=O)C2CC3=CC(=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)OC)O 520.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Palmitic Acid 985 Click to see CCCCCCCCCCCCCCCC(=O)O 256.42 unknown https://doi.org/10.1016/S0378-8741(04)00117-5
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Diterpene glycosides
2-[6-(16,18-Dihydroxy-6,10,15,15-tetramethyl-19-oxapentacyclo[10.6.1.01,14.03,11.06,10]nonadec-3-en-7-yl)-3-hydroxy-2-methylheptan-2-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 74393053 Click to see CC(CCC(C(C)(C)OC1C(C(C(C(O1)CO)O)O)O)O)C2CCC3(C2(CC=C4C3C5CC6C(C(CC(C6(C4)O5)O)O)(C)C)C)C 652.90 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3457064/
Sutherlandioside A 25137460 Click to see CC(CCC(C(C)(C)OC1C(C(C(C(O1)CO)O)O)O)O)C2CCC3(C2(CC=C4C3C5CC6C(C(CC(C6(C4)O5)O)O)(C)C)C)C 652.90 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3457064/
https://doi.org/10.1055/S-0036-1578788
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
(1S)-1alpha-(beta-D-Glucopyranosyloxy)-1,4aalpha,5,6,7,7aalpha-hexahydrocyclopenta[c]pyran-4,7alpha-dicarboxylic acid 4-beta-D-glucopyranosyl 7-methyl ester 101673970 Click to see COC(=O)C1CCC2C1C(OC=C2C(=O)OC3C(C(C(C(O3)CO)O)O)O)OC4C(C(C(C(O4)CO)O)O)O 566.50 unknown via CMAUP database
(1S)-1alpha-(beta-D-Glucopyranosyloxy)-1,4aalpha,5,6,7,7aalpha-hexahydrocyclopenta[c]pyran-4,7alpha-dicarboxylic acid 4-beta-D-glucopyranosyl ester 101673969 Click to see C1CC(C2C1C(=COC2OC3C(C(C(C(O3)CO)O)O)O)C(=O)OC4C(C(C(C(O4)CO)O)O)O)C(=O)O 552.50 unknown via CMAUP database
(1S)-1alpha-(beta-D-Glucopyranosyloxy)-1,4aalpha,5,6,7,7aalpha-hexahydrocyclopenta[c]pyran-4,7alpha-dicarboxylic acid 7-methyl ester 101673972 Click to see COC(=O)C1CCC2C1C(OC=C2C(=O)O)OC3C(C(C(C(O3)CO)O)O)O 404.40 unknown via CMAUP database
(1S)-1alpha-(beta-D-Glucopyranosyloxy)-1,4aalpha,5,6,7,7aalpha-hexahydrocyclopenta[c]pyran-4,7alpha-dicarboxylic acid dimethyl ester 101673971 Click to see COC(=O)C1CCC2C1C(OC=C2C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O 418.40 unknown via CMAUP database
Adoxosidic acid 13892717 Click to see C1CC2C(C1CO)C(OC=C2C(=O)O)OC3C(C(C(C(O3)CO)O)O)O 376.36 unknown via CMAUP database
Forsythide 15559328 Click to see C1CC(C2C1C(=COC2OC3C(C(C(C(O3)CO)O)O)O)C(=O)O)C(=O)O 390.34 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
10-Hydroxy-15-[5-hydroxy-6-methyl-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyheptan-2-yl]-7,7,12,16-tetramethylpentacyclo[9.7.0.01,3.03,8.012,16]octadec-5-en-4-one 74393052 Click to see CC(CCC(C(C)(C)OC1C(C(C(C(O1)CO)O)O)O)O)C2CCC3(C2(CCC45C3C(CC6C4(C5)C(=O)C=CC6(C)C)O)C)C 634.80 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3457064/
Sutherlandioside D 25137459 Click to see CC(CCC(C(C)(C)OC1C(C(C(C(O1)CO)O)O)O)O)C2CCC3(C2(CCC45C3C(CC6C4(C5)C(=O)C=CC6(C)C)O)C)C 634.80 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3457064/
https://doi.org/10.1055/S-0036-1578788
Ursolic Acid 64945 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cycloartanols and derivatives
6-Hydroxy-15-[5-hydroxy-6-methyl-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyheptan-2-yl]-7,7,12,16-tetramethylpentacyclo[9.7.0.01,3.03,8.012,16]octadecane-4,18-dione 74393132 Click to see CC(CCC(C(C)(C)OC1C(C(C(C(O1)CO)O)O)O)O)C2CCC3(C2(CC(=O)C45C3CCC6C4(C5)C(=O)CC(C6(C)C)O)C)C 650.80 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3457064/
6,10-Dihydroxy-15-[5-hydroxy-6-methyl-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyheptan-2-yl]-7,7,12,16-tetramethylpentacyclo[9.7.0.01,3.03,8.012,16]octadecan-4-one 74393051 Click to see CC(CCC(C(C)(C)OC1C(C(C(C(O1)CO)O)O)O)O)C2CCC3(C2(CCC45C3C(CC6C4(C5)C(=O)CC(C6(C)C)O)O)C)C 652.90 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3457064/
Sutherlandioside B 25137458 Click to see CC(CCC(C(C)(C)OC1C(C(C(C(O1)CO)O)O)O)O)C2CCC3(C2(CCC45C3C(CC6C4(C5)C(=O)CC(C6(C)C)O)O)C)C 652.90 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3457064/
https://doi.org/10.1055/S-0036-1578788
Sutherlandioside C 25137617 Click to see CC(CCC(C(C)(C)OC1C(C(C(C(O1)CO)O)O)O)O)C2CCC3(C2(CC(=O)C45C3CCC6C4(C5)C(=O)CC(C6(C)C)O)C)C 650.80 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3457064/
https://doi.org/10.1055/S-0036-1578788
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3S)-17-[(5S)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 6745 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/S0378-8741(04)00117-5
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
Clionasterol 457801 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/S0378-8741(04)00117-5
Stigmast-4-en-3-one 5484202 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CCC4=CC(=O)CCC34C)C)C(C)C 412.70 unknown https://doi.org/10.1016/S0378-8741(04)00117-5
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
Forsythoside F 6442994 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)COC4C(C(C(CO4)O)O)O)OCCC5=CC(=C(C=C5)O)O)O)O)O)O 756.70 unknown via CMAUP database
Forsythoside G 101231533 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)COC4C(C(CO4)(CO)O)OC)OCCC5=CC(=C(C=C5)O)O)O)O)O)O 770.70 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
Verbascoside 5281800 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)CO)OCCC4=CC(=C(C=C4)O)O)O)O)O)O 624.60 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Astragalin 5282102 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown via CMAUP database
Isoquercetin 5280804 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown via CMAUP database
Rutin 5280805 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O 610.50 unknown via CMAUP database

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