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Lasiosiphon kraussianus

Lasiosiphon kraussianus - 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 UUID643ffd9ea7f91905229815
Scientific name Lasiosiphon kraussianus
Authority (Meisn.) Hutch. & Dalziel
First published in Prodr. 14: 596 (1857)

Description Top

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Synonyms Top

Scientific name Authority First published in
Lasiosiphon villosus Burtt Davy Man. Pl. Transvaal 1: 46 (1926)
Lasiosiphon djuricus Gilg Bot. Jahrb. Syst. 19: 269 (1894)
Gnidia djurica Gilg Bot. Jahrb. Syst. 19: 268 (1894)
Gnidia hoepfneriana Gilg Bot. Jahrb. Syst. 19: 268 (1894)
Gnidia kerstingii Gilg ex Engl. Veg. Erde 9(III 2): 636 (1921)
Gnidia kraussiana Meisn. London J. Bot. 2: 552 (1843)
Gnidia passargei Gilg Bot. Jahrb. Syst. 23: 206 (1896)
Gnidia rorida (S.Moore) Eyles Trans. Roy. Soc. South Africa 5: 425 (1916)
Gnidia usinjensis Gilg Bot. Jahrb. Syst. 19: 269 (1894)
Gnidia kraussiana var. glabrata Meisn. London J. Bot. 2: 553 1843
Gnidia kraussiana var. pubescens Meisn. London J. Bot. 2: 553 1843
Lasiosiphon hoepfnerianus Vatke ex Gilg Bot. Jahrb. Syst. 19(2-3): 268. 1894 [21 Aug 1894]
Lasiosiphon kraussii Meisn. Prodr. [A. P. de Candolle] 14(2): 596. 1857 [late Nov 1857]
Lasiosiphon kerstingii H.Pearson Bull. Misc. Inform. Kew 1910: 338 (1910)
Lasiosiphon passargei H.Pearson Fl. Trop. Afr. 6(1): 232 (1910)
Lasiosiphon roridus S.Moore J. Linn. Soc., Bot. 40: 187 (1911)
Lasiosiphon affinis Kotschy & Peyr. Pl. Tinn. : 39 (1867)
Lasiosiphon kraussii var. pubescens (Meisn.) Meisn. Prodr. 14(2): 596 1857
Lasiosiphon kraussii var. glabratus (Meisn.) Meisn. Prodr. 14(2): 596 1857
Lasiosiphon kraussii var. angustifolius Meisn. Prodr. 14(2): 596 1857
Lasiosiphon kraussii var. villosus Burtt Davy Man. Pl. Transvaal 1: 207 1926

Common names Top

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Language Common/alternative name
English lesser yellow-head
Shona katupa

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
      • Chad
      • Sudan
    • South Tropical Africa
      • Angola
      • Malawi
      • Mozambique
      • Zambia
      • Zimbabwe
    • Southern Africa
      • Botswana
      • Cape Provinces
      • Free State
      • Kwazulu-Natal
      • Lesotho
      • Namibia
      • Northern Provinces
      • Swaziland
    • West Tropical Africa
      • Benin
      • Burkina
      • Ghana
      • Guinea
      • Guinea-Bissau
      • Mali
      • Nigeria
      • Togo
    • West-central Tropical Africa
      • Burundi
      • Cameroon
      • Central African Republic
      • Rwanda
      • Zaïre

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000445417
Tropicos 50039447
KEW urn:lsid:ipni.org:names:832128-1
NCBI Taxonomy 142746
IPNI 832128-1
iNaturalist 588737
GBIF 5524499
USDA GRIN 418421
CMAUP NPO22176

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
A Review of Ethnomedicinal Plants as Potential Anthelmintic Agents to Alternatively Control Gastrointestinal Nematodes of Ruminants in South Africa Mhlongo LC, Mseleku C, Tenza T, Fomum SW, McGaw LJ, Hassen A, Nsahlai IV J Parasitol Res 16-Jan-2024
PMCID:PMC10805549
doi:10.1155/2024/7955692
PMID:38268708
Hydromethanolic Root Extract of Gnidia Kraussiana Demonstrates Anti-Inflammatory Effect Through Anti-Oxidant Activity Enhancement in a Rodent Model of Gout Dadaya E, Koubala B, Ndjonka D, Zingué S, Laya A, Atsang G Dose Response 29-Jan-2023
PMCID:PMC9893086
doi:10.1177/15593258221148015
PMID:36743195
Traditional knowledge of plants used in hunting and fishing practices among Baka hunter-gatherers of eastern Cameroon Fongnzossie EF, Ngansop MT, Oishi T, Biwole AB, Biye EH, Ichikawa M J Ethnobiol Ethnomed 03-Jan-2023
PMCID:PMC9808952
doi:10.1186/s13002-022-00571-3
PMID:36597154
Medicinal plants used for the management of respiratory diseases in Zimbabwe: Review and perspectives potential management of COVID-19 Nyagumbo E, Pote W, Shopo B, Nyirenda T, Chagonda I, Mapaya RJ, Maunganidze F, Mavengere WN, Mawere C, Mutasa I, Kademeteme E, Maroyi A, Taderera T, Bhebhe M Phys Chem Earth (2002) 21-Sep-2022
PMCID:PMC9489988
doi:10.1016/j.pce.2022.103232
PMID:36161239
Medicinal Plants for Mitigating Pain and Inflammatory-Related Conditions: An Appraisal of Ethnobotanical Uses and Patterns in South Africa Aremu AO, Pendota SC Front Pharmacol 22-Oct-2021
PMCID:PMC8569556
doi:10.3389/fphar.2021.758583
PMID:34744737
Antiplasmodial, antimalarial activities and toxicity of African medicinal plants: a systematic review of literature Tajbakhsh E, Kwenti TE, Kheyri P, Nezaratizade S, Lindsay DS, Khamesipour F Malar J 25-Aug-2021
PMCID:PMC8390284
doi:10.1186/s12936-021-03866-0
PMID:34433465
Fractionated Extracts From Gnidia kraussiana (Malvales: Thymeleaceae) as Bioactive Phytochemicals for Effective Management of Callosobruchus maculatus (Coleoptera: Chrysomelidae) in Stored Vigna unguiculata (Fabales: Fabaceae) Seeds Kosini D, Nukenine EN, Agbor GA, Tchinda AT, Abdou JP, Yaya JA, Kowa TK J Insect Sci 15-Feb-2021
PMCID:PMC7882871
doi:10.1093/jisesa/ieab006
PMID:33585925
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
Exploring African Medicinal Plants for Potential Anti-Diabetic Compounds with the DIA-DB Inverse Virtual Screening Web Server Pereira AS, den Haan H, Peña-García J, Moreno MM, Pérez-Sánchez H, Apostolides Z Molecules 24-May-2019
PMCID:PMC6571761
doi:10.3390/molecules24102002
PMID:31137754
Medicinal Plants for the Treatment of Local Tissue Damage Induced by Snake Venoms: An Overview from Traditional Use to Pharmacological Evidence Félix-Silva J, Silva-Junior AA, Zucolotto SM, Fernandes-Pedrosa MD Evid Based Complement Alternat Med 21-Aug-2017
PMCID:PMC5585606
doi:10.1155/2017/5748256
PMID:28904556
Potential of Traditional Knowledge of Plants in the Management of Arthropods in Livestock Industry with Focus on (Acari) Ticks Wanzala W Evid Based Complement Alternat Med 17-Jul-2017
PMCID:PMC5536150
doi:10.1155/2017/8647919
PMID:28798806
From Traditional Usage to Pharmacological Evidence: Systematic Review of Gunnera perpensa L. Maroyi A Evid Based Complement Alternat Med 07-Dec-2016
PMCID:PMC5174174
doi:10.1155/2016/1720123
PMID:28053640
Dominant viral pathologies in the extensive and semi-intensive animal breeding and their treatment mode in ethno veterinary medicine in Benin Kpodékon TM, Ogni CA, Dassou H, Dougnon TJ, Boko C, Koutinhouin GB, Goussanou JS, Akoegninou A, Youssao I Vet World 23-Dec-2015
PMCID:PMC4774822
doi:10.14202/vetworld.2015.1424-1434
PMID:27047056
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
Ethnobotanical survey of medicinal plants used in the treatment of animal diarrhoea in Plateau State, Nigeria Offiah NV, Makama S, Elisha IL, Makoshi MS, Gotep JG, Dawurung CJ, Oladipo OO, Lohlum AS, Shamaki D BMC Vet Res 11-Jul-2011
PMCID:PMC3162497
doi:10.1186/1746-6148-7-36
PMID:21745405

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
3,4-Dihydroxybenzoic acid 72 Click to see C1=CC(=C(C=C1C(=O)O)O)O 154.12 unknown via CMAUP database
4-Hydroxybenzoic acid 135 Click to see C1=CC(=CC=C1C(=O)O)O 138.12 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Rhamnofolane and daphnane diterpenoids
(1R,2S,6S,7S,8R,10S,11S,12R,14S,16R,18R)-6,7-dihydroxy-8-(hydroxymethyl)-4,18-dimethyl-14-[(1E,3E)-nona-1,3-dienyl]-16-prop-1-en-2-yl-9,13,15,19-tetraoxahexacyclo[12.4.1.01,11.02,6.08,10.012,16]nonadec-3-en-5-one 162983869 Click to see CCCCCC=CC=CC12OC3C4C5C(O5)(C(C6(C(C4(O1)C(CC3(O2)C(=C)C)C)C=C(C6=O)C)O)O)CO 528.60 unknown https://doi.org/10.1002/(SICI)1096-9063(199907)55:7<745::AID-PS15>3.0.CO;2-0
(1R,2S,6S,7S,8R,10S,11S,12R,14S,16R,18R)-6,7-dihydroxy-8-(hydroxymethyl)-4,18-dimethyl-14-nonyl-16-prop-1-en-2-yl-9,13,15,19-tetraoxahexacyclo[12.4.1.01,11.02,6.08,10.012,16]nonadec-3-en-5-one 98055399 Click to see CCCCCCCCCC12OC3C4C5C(O5)(C(C6(C(C4(O1)C(CC3(O2)C(=C)C)C)C=C(C6=O)C)O)O)CO 532.70 unknown https://doi.org/10.1002/(SICI)1096-9063(199907)55:7<745::AID-PS15>3.0.CO;2-0
[(1R,2R,4R,5R,6S,7S,9R,10S,11S,12S,13S,14S,15R,22R,23R,25R)-10,11,22-trihydroxy-9-(hydroxymethyl)-2,13,15-trimethyl-4-prop-1-en-2-yl-8,24,26,27-tetraoxaheptacyclo[12.10.1.14,23.15,23.01,6.07,9.011,25]heptacosan-12-yl] benzoate 102402651 Click to see CC1CCCCCCC(C23OC4C5C6C(O6)(C(C7(C(C1C(C7OC(=O)C8=CC=CC=C8)C)C5(O2)C(CC4(O3)C(=C)C)C)O)O)CO)O 654.80 unknown https://doi.org/10.1021/NP50032A006
https://doi.org/10.1055/S-2007-969366
[10,11,22-Trihydroxy-9-(hydroxymethyl)-2,13,15-trimethyl-4-prop-1-en-2-yl-8,24,26,27-tetraoxaheptacyclo[12.10.1.14,23.15,23.01,6.07,9.011,25]heptacosan-12-yl] benzoate 435021 Click to see CC1CCCCCCC(C23OC4C5C6C(O6)(C(C7(C(C1C(C7OC(=O)C8=CC=CC=C8)C)C5(O2)C(CC4(O3)C(=C)C)C)O)O)CO)O 654.80 unknown https://doi.org/10.1021/NP50032A006
https://doi.org/10.1055/S-2007-969366
22,23,24,25-Tetradehydro-simplexin 118701523 Click to see CCCCCC=CC=CC12OC3C4C5C(O5)(C(C6(C(C4(O1)C(CC3(O2)C(=C)C)C)C=C(C6=O)C)O)O)CO 528.60 unknown https://doi.org/10.1021/NP50032A006
6,7-Dihydroxy-8-(hydroxymethyl)-4,18-dimethyl-14-nona-1,3-dienyl-16-prop-1-en-2-yl-9,13,15,19-tetraoxahexacyclo[12.4.1.01,11.02,6.08,10.012,16]nonadec-3-en-5-one 182701 Click to see CCCCCC=CC=CC12OC3C4C5C(O5)(C(C6(C(C4(O1)C(CC3(O2)C(=C)C)C)C=C(C6=O)C)O)O)CO 528.60 unknown https://doi.org/10.1002/(SICI)1096-9063(199907)55:7<745::AID-PS15>3.0.CO;2-0
Excoecariatoxin 5281400 Click to see CCCCCC=CC=CC12OC3C4C5C(O5)(C(C6(C(C4(O1)C(CC3(O2)C(=C)C)C)C=C(C6=O)C)O)O)CO 528.60 unknown https://doi.org/10.1021/NP50032A006
Gnidilatin 44575850 Click to see CCCCCCCCCC12OC3C4C5C(O5)(C(C6(C(C4(O1)C(C(C3(O2)C(=C)C)OC(=O)C7=CC=CC=C7)C)C=C(C6=O)C)O)O)CO 652.80 unknown https://doi.org/10.1021/NP50032A006
Gnidilatin 320169 Click to see CCCCCCCCCC12OC3C4C5C(O5)(C(C6(C(C4(O1)C(C(C3(O2)C(=C)C)OC(=O)C7=CC=CC=C7)C)C=C(C6=O)C)O)O)CO 652.80 unknown https://doi.org/10.1021/NP50032A006
Pimelea factor P1 434096 Click to see CCCCCCCCCC12OC3C4C5C(O5)(C(C6(C(C4(O1)C(CC3(O2)C(=C)C)C)C=C(C6=O)C)O)O)CO 532.70 unknown https://doi.org/10.1002/(SICI)1096-9063(199907)55:7<745::AID-PS15>3.0.CO;2-0
Yuanhuacin 6440205 Click to see CCCCCC=CC=CC12OC3C4C5C(O5)(C(C6(C(C4(O1)C(C(C3(O2)C(=C)C)OC(=O)C7=CC=CC=C7)C)C=C(C6=O)C)O)O)CO 648.70 unknown https://doi.org/10.1021/NP50032A006
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
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
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown via CMAUP database
> Phenylpropanoids and polyketides / 3,4-dihydrocoumarins
6,7-Dihydroxy-3,4-dihydro-2H-1-benzopyran-2-one 14701353 Click to see C1CC(=O)OC2=CC(=C(C=C21)O)O 180.16 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
3-(3-Hydroxy-4-methoxy-phenyl)-acrylic acid 92126 Click to see COC1=C(C=C(C=C1)C=CC(=O)O)O 194.18 unknown via CMAUP database
3-(4-Hydroxy-3-methoxyphenyl)prop-2-enoic acid 709 Click to see COC1=C(C=CC(=C1)C=CC(=O)O)O 194.18 unknown via CMAUP database
3,4-Dihydroxy cinnamic acid 2518 Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O 180.16 unknown via CMAUP database
4-Hydroxycinnamic acid 322 Click to see C1=CC(=CC=C1C=CC(=O)O)O 164.16 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
Taxifolin 439533 Click to see C1=CC(=C(C=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 304.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol 5280863 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown via CMAUP database
Myricetin 5281672 Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O 318.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid 3-O-p-coumaroyl glycosides
Helichrysoside 5317991 Click to see C1=CC(=CC=C1C=CC(=O)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 610.50 unknown via CMAUP database
isorhamnetin 3-O-(6"-O-feruloyl)-glucoside 90657785 Click to see COC1=C(C=CC(=C1)C=CC(=O)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)OC)O)O)O)O 654.60 unknown via CMAUP database
isorhamnetin 3-O-(6"-O-p-coumaroyl)-glucoside 44429737 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)COC(=O)C=CC5=CC=C(C=C5)O)O)O)O)O 624.50 unknown via CMAUP database
Quercetin 3-(6''-ferulylglucoside) 11114901 Click to see COC1=C(C=CC(=C1)C=CC(=O)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 640.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
[(2R,3S,4S,5R,6S)-6-[5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-4-oxochromen-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl acetate 44429735 Click to see CC(=O)OCC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)OC)O)O)O 520.40 unknown via CMAUP database
6''-O-Acetylastragalin 10435673 Click to see CC(=O)OCC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)O)O)O 490.40 unknown via CMAUP database
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
Narcissin 5481663 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)OC)O)O)O)O)O)O 624.50 unknown via CMAUP database
Quercetin 3-O-(6''-acetyl-glucoside) 10006384 Click to see CC(=O)OCC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 506.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
3,3'-Di-O-methylellagic acid 5488919 Click to see COC1=C(C=C2C3=C1OC(=O)C4=CC(=C(C(=C43)OC2=O)OC)O)O 330.24 unknown via CMAUP database
Ellagic Acid 5281855 Click to see C1=C2C3=C(C(=C1O)O)OC(=O)C4=CC(=C(C(=C43)OC2=O)O)O 302.19 unknown via CMAUP database
Flavogallonic acid 14503023 Click to see C1=C2C3=C(C(=C1O)O)OC(=O)C4=C3C(=C(C(=C4C5=C(C(=C(C=C5C(=O)O)O)O)O)O)O)OC2=O 470.30 unknown via CMAUP database

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