Hypericum annulatum - Unknown
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Internal ID UUID644021463ce69055960864
Scientific name Hypericum annulatum
Authority Moris
First published in Stirp. Sard. Elench. 1: 9 (1827)

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Synonyms Top

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Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Hypericum annulatum subsp. afromontanum (Bullock) N.Robson Bull. Nat. Hist. Mus. (London), Bot. 23: 69 (1993)
Hypericum annulatum subsp. annulatum Unknown
Hypericum annulatum subsp. intermedium (Steud. ex A.Rich.) N.Robson Bull. Nat. Hist. Mus. (London), Bot. 23: 69 (1993)

Varieties (abbr. var.) 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
      • Eritrea
      • Ethiopia
      • Sudan
  • Europe
    • Middle Europe
      • Czechoslovakia
      • Switzerland
    • Southeastern Europe
      • Albania
      • Bulgaria
      • Greece
      • Yugoslavia
    • Southwestern Europe
      • Sardegna

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000727348
Tropicos 7800025
Flora of Italy 1241
KEW urn:lsid:ipni.org:names:433193-1
Open Tree Of Life 541328
Observations.org 118864
NCBI Taxonomy 708052
IPNI 433193-1
GBIF 7329869
EPPO HYPNN
Elurikkus 589389
USDA GRIN 408292
Wikipedia Hypericum_annulatum

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
Potential Implications of Hyperoside on Oxidative Stress-Induced Human Diseases: A Comprehensive Review Wang K, Zhang H, Yuan L, Li X, Cai Y J Inflamm Res 13-Oct-2023
PMCID:PMC10581022
doi:10.2147/JIR.S418222
PMID:37854313
Cytotoxic and Antibacterial Prenylated Acylphloroglucinols from Hypericum olympicum L. Ilieva Y, Momekov G, Zaharieva MM, Marinov T, Kokanova-Nedialkova Z, Najdenski H, Nedialkov PT Plants (Basel) 29-Mar-2023
PMCID:PMC10097024
doi:10.3390/plants12071500
PMID:37050127
Xanthone Biosynthetic Pathway in Plants: A Review Remali J, Sahidin I, Aizat WM Front Plant Sci 08-Apr-2022
PMCID:PMC9024401
doi:10.3389/fpls.2022.809497
PMID:35463410
Cytotoxic and Anti-Inflammatory Activities of Dihydroisocoumarin and Xanthone Derivatives from Garcinia picrorhiza Sukandar ER, Kaennakam S, Raab P, Nöst X, Rassamee K, Bauer R, Siripong P, Ersam T, Tip-pyang S, Chavasiri W Molecules 01-Nov-2021
PMCID:PMC8587515
doi:10.3390/molecules26216626
PMID:34771035
Xanthone Glucosides: Isolation, Bioactivity and Synthesis Huang Q, Wang Y, Wu H, Yuan M, Zheng C, Xu H Molecules 14-Sep-2021
PMCID:PMC8465223
doi:10.3390/molecules26185575
PMID:34577044
Recent Applications of Capillary Electrophoresis in the Determination of Active Compounds in Medicinal Plants and Pharmaceutical Formulations Gackowski M, Przybylska A, Kruszewski S, Koba M, Mądra-Gackowska K, Bogacz A Molecules 07-Jul-2021
PMCID:PMC8307982
doi:10.3390/molecules26144141
PMID:34299418
Antiproliferative Effects of St. John’s Wort, Its Derivatives, and Other Hypericum Species in Hematologic Malignancies Allegra A, Tonacci A, Spagnolo EV, Musolino C, Gangemi S Int J Mol Sci 25-Dec-2020
PMCID:PMC7795730
doi:10.3390/ijms22010146
PMID:33375664
Comparative Transcriptome Reconstruction of Four Hypericum Species Focused on Hypericin Biosynthesis Soták M, Czeranková O, Klein D, Jurčacková Z, Li L, Čellárová E Front Plant Sci 13-Jul-2016
PMCID:PMC4942478
doi:10.3389/fpls.2016.01039
PMID:27468294
Effects of Aronia melanocarpa Fruit Juice on Isolated Rat Hepatocytes Kondeva-Burdina M, Valcheva-Kuzmanova S, Markova T, Mitcheva M, Belcheva A Pharmacogn Mag 01-Oct-2015
PMCID:PMC4787094
doi:10.4103/0973-1296.172967
PMID:27013800
An ethnobotanical study of medicinal plants used in Kilte Awulaelo District, Tigray Region of Ethiopia Teklay A, Abera B, Giday M J Ethnobiol Ethnomed 08-Sep-2013
PMCID:PMC3852788
doi:10.1186/1746-4269-9-65
PMID:24011232
Morphological and Phytochemical Diversity among Hypericum Species of the Mediterranean Basin Nürk NM, Crockett SL Med Aromat Plant Sci Biotechnol 01-Jan-2011
PMCID:PMC3364718
PMID:22662020
Simultaneous determination of benzophenones and gentisein in Hypericum annulatum Moris by high-performance liquid chromatography. Zheleva-Dimitrova D, Gevrenova R, Nedialkov P, Kitanov G Phytochem Anal 01-Jan-2007
doi:10.1002/PCA.940
PMID:17260692
Subject Index N/A 01-Jan-2005
PMCID:PMC7148952
doi:10.1016/S1572-5995(05)80049-3
Two benzophenone O-arabinosides and a chromone from Hypericum annulatum. Nedialkov PT, Kitanov GM Phytochemistry 01-Apr-2002
doi:10.1016/S0031-9422(01)00484-8
PMID:11937168
Benzophenone O-glucoside, a biogenic precursor of 1,3,7-trioxygenated xanthones in Hypericum annulatum. Kitanov GM, Nedialkov PT Phytochemistry 01-Aug-2001
doi:10.1016/S0031-9422(01)00194-7
PMID:11454351

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
(2,6-Dihydroxy-4-methoxyphenyl)(3,5-dihydroxyphenyl)methanone 71360772 Click to see COC1=CC(=C(C(=C1)O)C(=O)C2=CC(=CC(=C2)O)O)O 276.24 unknown https://doi.org/10.1016/S0031-9422(01)00194-7
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
[(2S,3R,4R,5S)-5-[2-(3,5-dihydroxybenzoyl)-3-hydroxy-5-methoxyphenoxy]-4-hydroxy-2-(hydroxymethyl)oxolan-3-yl] acetate 5315498 Click to see CC(=O)OC1C(OC(C1O)OC2=CC(=CC(=C2C(=O)C3=CC(=CC(=C3)O)O)O)OC)CO 450.40 unknown https://doi.org/10.1016/S0031-9422(01)00484-8
[(2S,3R,4R,5S)-5-[2-(3,5-dihydroxybenzoyl)-3-hydroxyphenoxy]-4-hydroxy-2-(hydroxymethyl)oxolan-3-yl] acetate 102463820 Click to see CC(=O)OC1C(OC(C1O)OC2=CC=CC(=C2C(=O)C3=CC(=CC(=C3)O)O)O)CO 420.40 unknown https://doi.org/10.1016/S0031-9422(01)00484-8
[2-[(2S,3R,4R,5S)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-6-hydroxy-4-methoxyphenyl]-(3,5-dihydroxyphenyl)methanone 5319218 Click to see COC1=CC(=C(C(=C1)OC2C(C(C(O2)CO)O)O)C(=O)C3=CC(=CC(=C3)O)O)O 408.40 unknown https://doi.org/10.1016/S0031-9422(01)00484-8
[2-[(2S,3R,4R,5S)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-6-hydroxyphenyl]-(3,5-dihydroxyphenyl)methanone 102463819 Click to see C1=CC(=C(C(=C1)OC2C(C(C(O2)CO)O)O)C(=O)C3=CC(=CC(=C3)O)O)O 378.30 unknown https://doi.org/10.1016/S0031-9422(01)00484-8
[2-[(2S,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-6-hydroxy-4-methoxyphenyl]-(3,5-dihydroxyphenyl)methanone 163032925 Click to see COC1=CC(=C(C(=C1)OC2C(C(C(O2)CO)O)O)C(=O)C3=CC(=CC(=C3)O)O)O 408.40 unknown https://doi.org/10.1016/S0031-9422(01)00484-8
[2-[3,4-Dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-6-hydroxy-4-methoxyphenyl]-(3,5-dihydroxyphenyl)methanone 22297159 Click to see COC1=CC(=C(C(=C1)OC2C(C(C(O2)CO)O)O)C(=O)C3=CC(=CC(=C3)O)O)O 408.40 unknown https://doi.org/10.1016/S0031-9422(01)00484-8
[5-[2-(3,5-Dihydroxybenzoyl)-3-hydroxy-5-methoxyphenoxy]-4-hydroxy-2-(hydroxymethyl)oxolan-3-yl] acetate 73981786 Click to see CC(=O)OC1C(OC(C1O)OC2=CC(=CC(=C2C(=O)C3=CC(=CC(=C3)O)O)O)OC)CO 450.40 unknown https://doi.org/10.1016/S0031-9422(01)00484-8
[5-hydroxy-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-(2,4,6-trihydroxyphenyl)methanone 102019362 Click to see C1=CC(=C(C=C1O)C(=O)C2=C(C=C(C=C2O)O)O)OC3C(C(C(C(O3)CO)O)O)O 424.40 unknown https://doi.org/10.1016/S0031-9422(01)00194-7
[5-Hydroxy-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-(2,4,6-trihydroxyphenyl)methanone 162922515 Click to see C1=CC(=C(C=C1O)C(=O)C2=C(C=C(C=C2O)O)O)OC3C(C(C(C(O3)CO)O)O)O 424.40 unknown https://doi.org/10.1016/S0031-9422(01)00194-7
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Chromones
5,7-Dihydroxy-3-methylchromone 22978769 Click to see CC1=COC2=CC(=CC(=C2C1=O)O)O 192.17 unknown https://doi.org/10.1016/S0031-9422(01)00484-8
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
Gentisein 5281635 Click to see C1=CC2=C(C=C1O)C(=O)C3=C(C=C(C=C3O2)O)O 244.20 unknown https://doi.org/10.1002/PCA.940

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