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

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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 pelagorium sidoides
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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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

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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-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
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
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
Changes in the Prescription of Antibiotics and Phytopharmaceuticals in Children Treated for Acute Upper and Lower Respiratory Tract Infections in Pediatric Practices in Germany in 2013, 2018, and 2022 Kostev K, van den Boom L, Tanislav C, Jacob L Antibiotics (Basel) 28-Sep-2023
PMCID:PMC10604680
doi:10.3390/antibiotics12101491
PMID:37887192
From Alpha to Omicron: How Different Variants of Concern of the SARS-Coronavirus-2 Impacted the World Andre M, Lau LS, Pokharel MD, Ramelow J, Owens F, Souchak J, Akkaoui J, Ales E, Brown H, Shil R, Nazaire V, Manevski M, Paul NP, Esteban-Lopez M, Ceyhan Y, El-Hage N Biology (Basel) 21-Sep-2023
PMCID:PMC10525159
doi:10.3390/biology12091267
PMID:37759666
The use of complementary and alternative medicine for the treatment of gastrointestinal symptoms in Long COVID: a systematic review Gawey B, Yang J, Bauer B, Song J, Wang XJ Ther Adv Chronic Dis 10-Aug-2023
PMCID:PMC10422885
doi:10.1177/20406223231190548
PMID:37577106
UHPLC-QQQ-MS and RP-HPLC Detection of Bioactive Alizarin and Scopoletin Metabolites from Morinda citrifolia Root Extracts and Their Antitubercular, Antibacterial, and Antioxidant Activities Sam-ang P, Phanumartwiwath A, Liana D, Sureram S, Hongmanee P, Kittakoop P ACS Omega 01-Aug-2023
PMCID:PMC10433487
doi:10.1021/acsomega.3c03656
PMID:37599981
In vitro and in vivo effects of Pelargonium sidoides DC. root extract EPs® 7630 and selected constituents against SARS-CoV-2 B.1, Delta AY.4/AY.117 and Omicron BA.2 Emanuel J, Papies J, Galander C, Adler JM, Heinemann N, Eschke K, Merz S, Pischon H, Rose R, Krumbholz A, Kulić Ž, Lehner MD, Trimpert J, Müller MA Front Pharmacol 26-Jul-2023
PMCID:PMC10410074
doi:10.3389/fphar.2023.1214351
PMID:37564181

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 / 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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