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Hypericum roeperianum

Hypericum roeperianum - 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 UUID6440216c2c03e198356832
Scientific name Hypericum roeperianum
Authority G.W.Schimp. ex A.Rich.
First published in Tent. Fl. Abyss. 1: 96 (1847)

Description Top

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Synonyms Top

Scientific name Authority First published in
Hypericum conrauanum Engl. Bot. Jahrb. Syst. 40: 555 (1908)
Hypericum riparium A.Chev. Mém. Soc. Bot. France 8: 8 (1907)
Hypericum schimperi Hochst. Flora 24(1, Intelligenzbl.): 29 (1841); et ex A. Rich. Tent. Fl. Abyss. 1: 97.
Hypericum schimperi var. huillense Hiern Cat. Afr. Pl. 1: 56. 1896
Hypericum quartinianum subsp. roeperianum (Schimp. ex A.Rich.) Engl. Abh. Königl. Akad. Wiss. Berlin 1891: 307 1892
Hypericum schimperi var. angustisepalum Engl. Abh. Königl. Akad. Wiss. Berlin 1891: 307. 1892
Hypericum roeperianum var. schimperi (Hochst. ex A.Rich.) Moggi & Pisacchi Webbia 22: 249. 1967

Common names Top

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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
    • East Tropical Africa
      • Kenya
      • Tanzania
      • Uganda
    • Northeast Tropical Africa
      • Ethiopia
      • Sudan
    • South Tropical Africa
      • Angola
      • Mozambique
      • Zambia
      • Zimbabwe
    • Southern Africa
      • Northern Provinces
    • West Tropical Africa
      • Guinea
      • Nigeria
    • West-central Tropical Africa
      • Cameroon
      • Zaïre

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000728241
USDA Plants HYRO8
Tropicos 7800909
KEW urn:lsid:ipni.org:names:433810-1
The Plant List kew-2858864
Open Tree Of Life 905362
Observations.org 330502
NCBI Taxonomy 269018
IUCN Red List 146447898
IPNI 433810-1
iNaturalist 587653
GBIF 3712122
EOL 5708155
Elurikkus 400520
USDA GRIN 407281

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
Phytochemicals: potential alternative strategy to fight Salmonella enterica serovar Typhimurium Almuzaini AM Front Vet Sci 16-May-2023
PMCID:PMC10228746
doi:10.3389/fvets.2023.1188752
PMID:37261108
Plant Coumarins with Anti-HIV Activity: Isolation and Mechanisms of Action Sharapov AD, Fatykhov RF, Khalymbadzha IA, Zyryanov GV, Chupakhin ON, Tsurkan MV Int J Mol Sci 02-Feb-2023
PMCID:PMC9917851
doi:10.3390/ijms24032839
PMID:36769163
Anthelmintic Agents from African Medicinal Plants: Review and Prospects Jato J, Orman E, Duah Boakye Y, Oppong Bekoe E, Oppong Bekoe S, Asare-Nkansah S, Spiegler V, Hensel A, Liebau E, Agyare C Evid Based Complement Alternat Med 31-Dec-2022
PMCID:PMC9825222
doi:10.1155/2022/8023866
PMID:36624864
Phytochemical profile and antimicrobial activity of the leaves and stem bark of Symphonia globulifera L.f. and Allophylus abyssinicus (Hochst.) Radlk Lukubye B, Ajayi CO, Wangalwa R, Kagoro-Rugunda G BMC Complement Med Ther 23-Aug-2022
PMCID:PMC9396842
doi:10.1186/s12906-022-03692-0
PMID:35999537
Natural Products-Based Metallic Nanoparticles as Antimicrobial Agents Susanti D, Haris MS, Taher M, Khotib J Front Pharmacol 02-Jun-2022
PMCID:PMC9205242
doi:10.3389/fphar.2022.895616
PMID:35721199
Natural Compounds With Antimicrobial and Antiviral Effect and Nanocarriers Used for Their Transportation Stan D, Enciu AM, Mateescu AL, Ion AC, Brezeanu AC, Stan D, Tanase C Front Pharmacol 06-Sep-2021
PMCID:PMC8450524
doi:10.3389/fphar.2021.723233
PMID:34552489
A Review of Plant-Based Therapies for the Treatment of Urinary Tract Infections in Traditional Southern African Medicine Cock I, Mavuso N, Van Vuuren S Evid Based Complement Alternat Med 29-Jul-2021
PMCID:PMC8346297
doi:10.1155/2021/7341124
PMID:34367307
African Herbal Medicines: Adverse Effects and Cytotoxic Potentials with Different Therapeutic Applications Okaiyeto K, Oguntibeju OO Int J Environ Res Public Health 02-Jun-2021
PMCID:PMC8199769
doi:10.3390/ijerph18115988
PMID:34199632
Cytotoxic Constituents of the Bark of Hypericum roeperianum towards Multidrug-Resistant Cancer Cells Guefack MG, Damen F, Mbaveng AT, Tankeo SB, Bitchagno GT, Çelik İ, Simo Mpetga JD, Kuete V Evid Based Complement Alternat Med 25-Sep-2020
PMCID:PMC7532997
doi:10.1155/2020/4314807
PMID:33062009
The traditional use of southern African medicinal plants for the treatment of bacterial respiratory diseases: A review of the ethnobotany and scientific evaluations Cock IE, Van Vuuren SF J Ethnopharmacol 27-Jul-2020
PMCID:PMC7383173
doi:10.1016/j.jep.2020.113204
PMID:32730881
Tamarix arabica and Salvadora persica as antibacterial agents Al-Judaibi AA AIMS Microbiol 18-May-2020
PMCID:PMC7326732
doi:10.3934/microbiol.2020008
PMID:32617445
Plant-Based Natural Products for the Discovery and Development of Novel Anthelmintics against Nematodes Liu M, Panda SK, Luyten W Biomolecules 09-Mar-2020
PMCID:PMC7175113
doi:10.3390/biom10030426
PMID:32182910
Acetone leaf extracts of some South African trees with high activity against Escherichia coli also have good antimycobacterial activity and selectivity index Elisha IL, Botha FS, Madikizela B, McGaw LJ, Eloff JN BMC Complement Altern Med 19-Jun-2017
PMCID:PMC5477271
doi:10.1186/s12906-017-1831-z
PMID:28629354
The antibacterial activity of extracts of nine plant species with good activity against Escherichia coli against five other bacteria and cytotoxicity of extracts Elisha IL, Botha FS, McGaw LJ, Eloff JN BMC Complement Altern Med 28-Feb-2017
PMCID:PMC5329917
doi:10.1186/s12906-017-1645-z
PMID:28241818
Potency and selectivity indices of acetone leaf extracts of nine selected South African trees against six opportunistic Enterobacteriaceae isolates from commercial chicken eggs Elisha IL, Jambalang AR, Botha FS, Buys EM, McGaw LJ, Eloff JN BMC Complement Altern Med 02-Feb-2017
PMCID:PMC5289020
doi:10.1186/s12906-017-1597-3
PMID:28148263

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 / Benzophenones
[3-(3,7-Dimethyl-2,6-octadienyl)-2,4,6-trihydroxyphenyl]phenylmethanone 497548 Click to see CC(=CCCC(=CCC1=C(C(=C(C=C1O)O)C(=O)C2=CC=CC=C2)O)C)C 366.40 unknown https://doi.org/10.1016/J.BMC.2015.08.028
3-Geranyl-2,4,6-trihydroxybenzophenone 6477676 Click to see CC(=CCCC(=CCC1=C(C(=C(C=C1O)O)C(=O)C2=CC=CC=C2)O)C)C 366.40 unknown https://doi.org/10.1016/J.BMC.2015.08.028
> Benzenoids / Benzene and substituted derivatives / Butyrophenones
Empetrikarinol B 71458439 Click to see CCC(C)C(=O)C1=C(C=C(C2=C1OC(C(C2)O)(C)CCC=C(C)C)O)O 362.50 unknown https://doi.org/10.1016/J.BMC.2015.08.028
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Pentadecanoic acid 13849 Click to see CCCCCCCCCCCCCCC(=O)O 242.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2014.05.008
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Monocyclic monoterpenoids
3-Geranyl-1-(3-methylbutanoyl)phloroglucinol 129737718 Click to see CC(C)CC(=O)C1(CC(CC(=C1)O)(CC=C(C)CCC=C(C)C)O)O 350.50 unknown https://doi.org/10.1016/J.BMC.2015.08.028
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
1-[3-(3,7-Dimethylocta-2,6-dienyl)-2,4,6-trihydroxyphenyl]-2-methylpropan-1-one 85140047 Click to see CC(C)C(=O)C1=C(C=C(C(=C1O)CC=C(C)CCC=C(C)C)O)O 332.40 unknown https://doi.org/10.1016/J.BMC.2015.08.028
1-[3-[(2E)-3,7-dimethylocta-2,6-dienyl]-2,4,6-trihydroxy-phenyl]-2-methyl-butan-1-one 14282627 Click to see CCC(C)C(=O)C1=C(C=C(C(=C1O)CC=C(C)CCC=C(C)C)O)O 346.50 unknown https://doi.org/10.1016/J.BMC.2015.08.028
2-Geranyl-4-isobutyrylphloroglucinol 10426888 Click to see CC(C)C(=O)C1=C(C=C(C(=C1O)CC=C(C)CCC=C(C)C)O)O 332.40 unknown https://doi.org/10.1016/J.BMC.2015.08.028
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans
Madeleinol B 78073027 Click to see CC(C)C(=O)C1=C(C=C(C2=C1OC(C(C2)O)(C)CCC=C(C)C)O)O 348.40 unknown https://doi.org/10.1016/J.BMC.2015.08.028
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / 2,2-dimethyl-1-benzopyrans
1,5,5-Trimethyl-8-propan-2-yl-6,15-dioxatetracyclo[9.3.1.04,13.07,12]pentadeca-7,9,11-trien-9-ol 122189282 Click to see CC(C)C1=C2C3=C(C=C1O)OC4(CCC(C3C4)C(O2)(C)C)C 302.40 unknown https://doi.org/10.1016/J.BMC.2015.08.028
Empetrifranzinan B 71495029 Click to see CC(C)C(=O)C1=C2C3=C(C=C1O)OC(C4C3CC(O2)(CC4)C)(C)C 330.40 unknown https://doi.org/10.1016/J.BMC.2015.08.028
Empetrifranzinan C 71449450 Click to see CCC(C)C(=O)C1=C2C3=C(C=C1O)OC4(CCC(C3C4)C(O2)(C)C)C 344.40 unknown https://doi.org/10.1016/J.BMC.2015.08.028
Empetrifranzinan D 122189281 Click to see CCC(C)C(=O)C1=C2C3=C(C=C1O)OC(C4C3CC(O2)(CC4)C)(C)C 344.40 unknown https://doi.org/10.1016/J.BMC.2015.08.028
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthenes
Madeleinol A 122189280 Click to see CC(C)C(=O)C1=C(C=C(C2=C1OC3(CCC(C(C3C2)(C)C)O)C)O)O 348.40 unknown https://doi.org/10.1016/J.BMC.2015.08.028
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
2-Hydroxyxanthone 74708 Click to see C1=CC=C2C(=C1)C(=O)C3=C(O2)C=CC(=C3)O 212.20 unknown https://doi.org/10.1016/0031-9422(96)00284-1
5-Hydroxy-2-methoxyxanthone 53873221 Click to see COC1=CC2=C(C=C1)OC3=C(C2=O)C=CC=C3O 242.23 unknown https://doi.org/10.1016/0031-9422(96)00284-1
5-O-demethylpaxanthonin 15958474 Click to see CC(=C)C1CC(C(C1)(C)C)C2=C(C3=C(C=C2O)OC4=C(C3=O)C=CC(=C4O)O)O 396.40 unknown https://doi.org/10.1016/0031-9422(96)00284-1
5,9,10-trihydroxy-1,1,2-trimethyl-2H-furo[2,3-c]xanthen-6-one 10336602 Click to see CC1C(C2=C(O1)C=C(C3=C2OC4=C(C3=O)C=CC(=C4O)O)O)(C)C 328.30 unknown https://doi.org/10.1016/0031-9422(96)00284-1
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / 4-prenylated xanthones
1,3,5,6-Tetrahydroxy-4-(5-methyl-2-prop-1-en-2-ylhex-4-enyl)xanthen-9-one 10000814 Click to see CC(=CCC(CC1=C2C(=C(C=C1O)O)C(=O)C3=C(O2)C(=C(C=C3)O)O)C(=C)C)C 396.40 unknown https://doi.org/10.1016/0031-9422(96)00284-1
4-[(4E)-5,9-dimethyl-2-prop-1-en-2-yldeca-4,9-dienyl]-1,3,5,6-tetrahydroxyxanthen-9-one 102000289 Click to see CC(=C)CCCC(=CCC(CC1=C2C(=C(C=C1O)O)C(=O)C3=C(O2)C(=C(C=C3)O)O)C(=C)C)C 464.50 unknown https://doi.org/10.1016/0031-9422(96)00284-1
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / Pyranoxanthones
Isojacareubin 9996463 Click to see CC1(C=CC2=C(O1)C=C(C3=C2OC4=C(C3=O)C=CC(=C4O)O)O)C 326.30 unknown https://doi.org/10.1016/0031-9422(96)00284-1

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