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Pelargonium sidoides

Pelargonium sidoides - 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 UUID644053e0a65f9819683900
Scientific name Pelargonium sidoides
Authority DC.
First published in Prodr. 1: 680 (1824)

Description Top

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Synonyms Top

Scientific name Authority First published in
Pelargonium spectabile Sweet Geraniaceae : t. 136 (1822)
Cortusina sidifolia (Thunb.) Eckl. & Zeyh. Enum. Pl. Afric. Austral. : 77 (1835)
Geraniospermum sidifolium (Thunb.) Kuntze Revis. Gen. Pl. 3(2): 32 (1898)
Geranium sidifolium Thunb. Prodr. Pl. Cap. : 114 (1800)

Common names Top

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Language Common/alternative name
Arabic إبرة الراعي جنوب أفريقيا
Arabic لقلقي سيدي
Arabic لقلقي سيداوي
Hungarian fokföldi muskátli
Portuguese umckan
Turkish güney afrika sardunyası

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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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Africa
    • Southern Africa
      • Cape Provinces
      • Free State
      • Kwazulu-Natal
      • Lesotho
      • Northern Provinces
      • Swaziland

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001221559
UNII 4FY2944729
Tropicos 50009275
KEW urn:lsid:ipni.org:names:377008-1
The Plant List tro-50009275
Open Tree Of Life 5516854
NCBI Taxonomy 1417791
IUCN Red List 219273119
IPNI 377008-1
iNaturalist 568517
GBIF 3827581
Freebase /m/02pzryz
EOL 5016794
USDA GRIN 427633
Wikipedia Pelargonium_sidoides

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
Long-Lasting Silver Nanoparticles Synthesized with Tagetes erecta and Their Antibacterial Activity against Erwinia amylovora, a Serious Rosaceous Pathogen Zarate-Escobedo J, Zavaleta-Mancera HA, Soto-Hernández RM, Pérez-Rodríguez P, Vilchis-Nestor AR, Silva-Rojas HV, Trejo-Téllez LI Plants (Basel) 29-Mar-2024
PMCID:PMC11013423
doi:10.3390/plants13070981
PMID:38611509
Lactoferrins in Their Interactions with Molecular Targets: A Structure-Based Overview Piacentini R, Boffi A, Milanetti E Pharmaceuticals (Basel) 20-Mar-2024
PMCID:PMC10974892
doi:10.3390/ph17030398
PMID:38543184
Long-term benefits of EPs® 7630 in patients with acute sinusitis: a real-world cohort study Tisch M, Roháč L, Reineke T, Burkart M, Kostev K Front Pharmacol 18-Mar-2024
PMCID:PMC10982470
doi:10.3389/fphar.2024.1358879
PMID:38562459
Special Issue—“Natural Products That Might Change Society” Amen Y, Shimizu K Molecules 26-Feb-2024
PMCID:PMC10934775
doi:10.3390/molecules29051008
PMID:38474520
Identifying in-market application of Pelargonium root extract EPs 7630 for the treatment of COVID-19: analysis of pharmacovigilance data Malek FA, Funk P Front Pharmacol 23-Feb-2024
PMCID:PMC10920291
doi:10.3389/fphar.2024.1335309
PMID:38464728
Investigation on the Efficacy of Two Food Supplements Containing a Fixed Combination of Selected Probiotics and β-Glucans or Elderberry Extract for the Immune System: Modulation on Cytokines Expression in Human THP-1 and PBMC Cappellucci G, Baini G, Miraldi E, Pauletto L, De Togni H, Raso F, Biagi M Foods 01-Feb-2024
PMCID:PMC10855234
doi:10.3390/foods13030458
PMID:38338593
Proportion of Over-The-Counter Medicines Containing a Plant Component and Those with Synthetic Substances Administered among Children in a Bulgarian Population Hadzhieva B, Petkova-Dimitrova V Pharmaceuticals (Basel) 31-Jan-2024
PMCID:PMC10892009
doi:10.3390/ph17020192
PMID:38399407
Editorial: Global excellence in ethnopharmacology: europe Assimopoulou AN, Trifan A Front Pharmacol 30-Jan-2024
PMCID:PMC10861649
doi:10.3389/fphar.2024.1368610
PMID:38352147
A literature review of bioactive substances for the treatment of periodontitis: In vitro, in vivo and clinical studies Kim TH, Heo SY, Chandika P, Kim YM, Kim HW, Kang HW, Je JY, Qian ZJ, Kim N, Jung WK Heliyon 11-Jan-2024
PMCID:PMC10826675
doi:10.1016/j.heliyon.2024.e24216
PMID:38293511
Stevens’ Cure (Umckaloabo)—the vindication of a patent medicine Brendler T, Stander MA, van Wyk BE Front Pharmacol 03-Jan-2024
PMCID:PMC10791834
doi:10.3389/fphar.2023.1294997
PMID:38235116
Designing of Drug Delivery Systems to Improve the Antimicrobial Efficacy in the Periodontal Pocket Based on Biodegradable Polyesters Zięba M, Sikorska W, Musioł M, Janeczek H, Włodarczyk J, Pastusiak M, Gupta A, Radecka I, Parati M, Tylko G, Kowalczuk M, Adamus G Int J Mol Sci 29-Dec-2023
PMCID:PMC10778800
doi:10.3390/ijms25010503
PMID:38203673
Exploring the Sustainable Exploitation of Bioactive Compounds in Pelargonium sp.: Beyond a Fragrant Plant Roman S, Voaides C, Babeanu N Plants (Basel) 10-Dec-2023
PMCID:PMC10748180
doi:10.3390/plants12244123
PMID:38140450
Comment on Subhadra et al. Significant Broad-Spectrum Antiviral Activity of Bi121 against Different Variants of SARS-CoV-2. Viruses 2023, 15, 1299 Kulić Ž Viruses 17-Nov-2023
PMCID:PMC10675578
doi:10.3390/v15112268
PMID:38005944
Reply to Kulić, Ž. Comment on “Subhadra et al. Significant Broad-Spectrum Antiviral Activity of Bi121 against Different Variants of SARS-CoV-2. Viruses 2023, 15, 1299” Subhadra B, Agrawal R, Pal VK, Chenine AL, Mattathil JG, Singh A Viruses 17-Nov-2023
PMCID:PMC10674820
doi:10.3390/v15112269
PMID:38005945
Proposed mechanisms of action of herbal drugs and their biologically active constituents in the treatment of coughs: an overview Pourova J, Dias P, Pour M, Bittner Fialová S, Czigle S, Nagy M, Tóth J, Balázs VL, Horváth A, Csikós E, Farkas Á, Horváth G, Mladěnka P PeerJ 24-Oct-2023
PMCID:PMC10607228
doi:10.7717/peerj.16096
PMID:37901462

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 / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Gallic acids
Gallic Acid 370 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)O 170.12 unknown https://doi.org/10.1002/PTR.785
https://doi.org/10.1078/1433-187X-00307
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Galloyl esters
Methyl gallate 7428 Click to see COC(=O)C1=CC(=C(C(=C1)O)O)O 184.15 unknown https://doi.org/10.1002/PTR.785
> Nucleosides, nucleotides, and analogues / Purine nucleotides / Cyclic purine nucleotides / 3,5-cyclic purine nucleotides
2-amino-9-(2,7-dihydroxy-2-oxo-4a,6,7,7a-tetrahydro-4H-furo[3,2-d][1,3,2]dioxaphosphinin-6-yl)-1-methylpurin-6-one 75065095 Click to see CN1C(=O)C2=C(N=C1N)N(C=N2)C3C(C4C(O3)COP(=O)(O4)O)O 359.23 unknown https://doi.org/10.1055/S-0029-1186167
2-amino-9-(2,7-dihydroxy-2-oxo-4a,6,7,7a-tetrahydro-4H-furo[3,2-d][1,3,2]dioxaphosphinin-6-yl)-3H-purin-6-one 295 Click to see C1C2C(C(C(O2)N3C=NC4=C3NC(=NC4=O)N)O)OP(=O)(O1)O 345.21 unknown https://doi.org/10.1055/S-0029-1186167
9-[(4aR,6R,7R,7aS)-2,7-dihydroxy-2-oxo-4a,6,7,7a-tetrahydro-4H-furo[3,2-d][1,3,2]dioxaphosphinin-6-yl]-2-amino-3H-purin-6-one 24316 Click to see C1C2C(C(C(O2)N3C=NC4=C3NC(=NC4=O)N)O)OP(=O)(O1)O 345.21 unknown https://doi.org/10.1055/S-0029-1186167
Acrasin 274 Click to see C1C2C(C(C(O2)N3C=NC4=C(N=CN=C43)N)O)OP(=O)(O1)O 329.21 unknown https://doi.org/10.1055/S-0029-1186167
Adenosine cyclic phosphate 6076 Click to see C1C2C(C(C(O2)N3C=NC4=C(N=CN=C43)N)O)OP(=O)(O1)O 329.21 unknown https://doi.org/10.1055/S-0029-1186167
N(1)-methyl-cGMP 44755113 Click to see CN1C(=O)C2=C(N=C1N)N(C=N2)C3C(C4C(O3)COP(=O)(O4)O)O 359.23 unknown https://doi.org/10.1055/S-0029-1186167
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
Artelin 3085344 Click to see CC1C2C(CC(=C3C(C2OC1=O)C(=C(C3=O)O)C)C)O 278.30 unknown https://doi.org/10.1016/0031-9422(95)00166-5
CID 75579717 75579717 Click to see CC1C2C(CC(=C3C(C2OC1=O)C(=C(C3=O)O)C)C)O 278.30 unknown https://doi.org/10.1016/0031-9422(95)00166-5
> Phenylpropanoids and polyketides / Coumarins and derivatives
(5,6-Dimethoxy-2-oxochromen-7-yl) acetate 10400559 Click to see CC(=O)OC1=C(C(=C2C=CC(=O)OC2=C1)OC)OC 264.23 unknown https://doi.org/10.1016/0031-9422(95)00166-5
5,6-Dimethoxy-7-(sulfooxy)-2h-1-benzopyran-2-one 85779359 Click to see COC1=C2C=CC(=O)OC2=CC(=C1OC)OS(=O)(=O)O 302.26 unknown https://doi.org/10.1055/S-0029-1186167
5,6,7-Trimethoxycoumarin 148724 Click to see COC1=C(C(=C2C=CC(=O)OC2=C1)OC)OC 236.22 unknown https://doi.org/10.1016/0031-9422(95)00166-5
5,6,7,8-Tetramethoxycoumarin 151319 Click to see COC1=C(C(=C(C2=C1C=CC(=O)O2)OC)OC)OC 266.25 unknown https://doi.org/10.1016/0031-9422(95)00166-5
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins
6,8-Dihydroxy-5,7-dimethoxycoumarin 3025904 Click to see COC1=C(C(=C(C2=C1C=CC(=O)O2)O)OC)O 238.19 unknown https://doi.org/10.1016/0031-9422(95)00166-5
6,8-Dihydroxy-7-methoxycoumarin 928135 Click to see COC1=C(C=C2C=CC(=O)OC2=C1O)O 208.17 unknown https://doi.org/10.1016/0031-9422(95)00166-5
Isoscopoletin 69894 Click to see COC1=C(C=C2C=CC(=O)OC2=C1)O 192.17 unknown https://doi.org/10.1002/PTR.785
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 6,7-dihydroxycoumarins
(6,7-Dihydroxy-2-oxochromen-8-yl) hydrogen sulfate 87709239 Click to see C1=CC(=O)OC2=C(C(=C(C=C21)O)O)OS(=O)(=O)O 274.21 unknown https://doi.org/10.1055/S-0029-1186167
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7,8-dihydroxycoumarins
(7,8-Dihydroxy-2-oxochromen-6-yl) hydrogen sulfate 86088421 Click to see C1=CC(=O)OC2=C(C(=C(C=C21)OS(=O)(=O)O)O)O 274.21 unknown https://doi.org/10.1055/S-0029-1186167
7,8-Dihydroxy-5,6-dimethoxychromen-2-one 101726825 Click to see COC1=C(C(=C(C2=C1C=CC(=O)O2)O)O)OC 238.19 unknown https://doi.org/10.1055/S-0029-1186167
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
(7-Hydroxy-2-oxo-6-sulfooxychromen-8-yl) hydrogen sulfate 25051519 Click to see C1=CC(=O)OC2=C(C(=C(C=C21)OS(=O)(=O)O)O)OS(=O)(=O)O 354.30 unknown https://doi.org/10.1055/S-0029-1186167
5,6,7-Trihydroxycoumarin 91665193 Click to see C1=CC(=O)OC2=C1C(=C(C(=C2)O)O)O 194.14 unknown https://doi.org/10.1016/0031-9422(95)00166-5
5,7-Dihydroxy-6-methoxychromen-2-one 130034462 Click to see COC1=C(C2=C(C=C1O)OC(=O)C=C2)O 208.17 unknown https://doi.org/10.1016/0031-9422(95)00166-5
6,7,8-Trihydroxy-2H-1-benzopyran-2-one 11819936 Click to see C1=CC(=O)OC2=C(C(=C(C=C21)O)O)O 194.14 unknown https://doi.org/10.1055/S-0029-1186167
https://doi.org/10.1016/0031-9422(95)00166-5
7-Hydroxy-5,6-dimethoxy-8-(sulfooxy)-2h-1-benzopyran-2-one 25051520 Click to see COC1=C(C(=C(C2=C1C=CC(=O)O2)OS(=O)(=O)O)O)OC 318.26 unknown https://doi.org/10.1055/S-0029-1186167
Scopoletin 5280460 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)O 192.17 unknown https://doi.org/10.1016/0031-9422(95)00166-5
Umckalin 5316862 Click to see COC1=C(C(=CC2=C1C=CC(=O)O2)O)OC 222.19 unknown https://doi.org/10.1055/S-0029-1186167
https://doi.org/10.1016/0031-9422(95)00166-5
https://doi.org/10.1002/PTR.785
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Cianidanol 9064 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown https://doi.org/10.1002/PTR.785

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