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Hypericum elegans

Hypericum elegans - 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 UUID644021502b339838093977
Scientific name Hypericum elegans
Authority Stephan ex Willd.
First published in Sp. Pl., ed. 4 , 3: 1469 (1803)

Description Top

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Synonyms Top

Scientific name Authority First published in
Hypericum anagallidifolium C.Presl Delic. Prag. : 22 (1822)
Hypericum hyssopifolium var. pauciglandulosum Choisy Prodr. [A. P. de Candolle] 1: 552. 1824
Hypericum kohlianum Spreng. Fl. Hal. Tent. Nov. : 214 (1806)
Hypericum kotoliani Bellardi ex Colla Herb. Pedem. 1: 464 (1833)
Hypericum elegans var. pectinatum Celak. Oesterr. Bot. Z. 24: 140. 1874
Hypericum elegans var. stepposum Savul. & Rayss Mat. Fl. Basarab. 3: 175. 1934

Common names Top

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Language Common/alternative name
Belarusian Святаяннік зграбны
Czech třezalka ozdobná
German zierliches hartheu
German zierliches johanniskraut
Upper Sorbian lepy křižomnik
Hungarian karcsú orbáncfű
Polish dziurawiec wytworny
Romanian floare-de-friguri
Romanian ţintaura

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
  • Asia-temperate
    • Caucasus
      • North Caucasus
      • Transcaucasus
    • Siberia
      • Altay
      • Krasnoyarsk
      • West Siberia
    • Western Asia
      • Turkey
  • Europe
    • Eastern Europe
      • Belarus
      • Central European Russia
      • East European Russia
      • South European Russia
      • Ukraine
    • Middle Europe
      • Czechoslovakia
      • Germany
      • Hungary
      • Poland
    • Southeastern Europe
      • Bulgaria
      • Romania
      • Yugoslavia

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000727585
Tropicos 100347900
KEW urn:lsid:ipni.org:names:433393-1
The Plant List kew-2858056
Open Tree Of Life 4730076
Observations.org 124229
NCBI Taxonomy 1321328
IPNI 433393-1
GBIF 3713091
EPPO HYPEL
EOL 5707528
Elurikkus 650263
USDA GRIN 460046
Wikipedia Hypericum_elegans

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
New Enlightenment of Skin Cancer Chemoprevention through Phytochemicals: In Vitro and In Vivo Studies and the Underlying Mechanisms Singh M, Suman S, Shukla Y Biomed Res Int 17-Mar-2014
PMCID:PMC3976810
doi:10.1155/2014/243452
PMID:24757666
Benzophenones from Hypericum elegans with antioxidant and acetylcholinesterase inhibitory potential Zheleva-Dimitrova D, Nedialkov P, Momekov G Pharmacogn Mag 01-Oct-2013
PMCID:PMC3798133
doi:10.4103/0973-1296.117846
PMID:24143038
Norathyriol suppresses solar UV-induced skin cancer by targeting ERKs Li J, Malakhova M, Mottamal M, Reddy K, Kurinov I, Carper A, Langfald A, Oi N, Kim MO, Zhu F, Sosa CP, Zhou K, Bode AM, Dong Z Cancer Res 14-Nov-2011
PMCID:PMC3251698
doi:10.1158/0008-5472.CAN-11-2596
PMID:22084399
Elegaphenone and 7-epi-clusianone, the major cytotoxic constituents of Hypericum elegans. Nedialkov PT, Zheleva-Dimitrova D, Momekov G, Karlov K, Girreser U, Kitanov GM Nat Prod Res 01-Oct-2011
doi:10.1080/14786419.2010.524647
PMID:21707255
Bioactive xanthones from the roots of Hypericum perforatum (common St John’s wort) Crockett SL, Poller B, Tabanca N, Pferschy-Wenzig EM, Kunert O, Wedge DE, Bucar F J Sci Food Agric 27-Oct-2010
PMCID:PMC3318991
doi:10.1002/jsfa.4202
PMID:21218475
Radical scavenging and antioxidant activities of methanolic extracts from Hypericum species growing in Bulgaria Zheleva-Dimitrova D, Nedialkov P, Kitanov G Pharmacogn Mag 05-May-2010
PMCID:PMC2900065
doi:10.4103/0973-1296.62889
PMID:20668569
Benzophenone O-glycosides from Hypericum elegans. Nedialkov PT, Zheleva-Dimitrova D, Girreser U, Kitanov GM Nat Prod Res 01-Jan-2009
doi:10.1080/14786410802278327
PMID:19731135
Subject Index N/A 01-Jan-2005
PMCID:PMC7148952
doi:10.1016/S1572-5995(05)80049-3

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-(3,7-Dimethylocta-2,6-dienoxy)-4,6-dihydroxyphenyl]-phenylmethanone 123591898 Click to see CC(=CCCC(=CCOC1=CC(=CC(=C1C(=O)C2=CC=CC=C2)O)O)C)C 366.40 unknown https://doi.org/10.1080/14786419.2010.524647
[2-[(2E)-3,7-dimethylocta-2,6-dienoxy]-4,6-dihydroxyphenyl]-phenylmethanone 101480931 Click to see CC(=CCCC(=CCOC1=CC(=CC(=C1C(=O)C2=CC=CC=C2)O)O)C)C 366.40 unknown https://doi.org/10.1080/14786419.2010.524647
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
[6-acetyloxy-7-(acetyloxymethyl)-4-[[3,5-dihydroxy-6-(hydroxymethyl)-4-oxooxan-2-yl]oxymethyl]-7-hydroxy-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-1-yl] 3-methylbutanoate 14414533 Click to see CC(C)CC(=O)OC1C2C(CC(C2(COC(=O)C)O)OC(=O)C)C(=CO1)COC3C(C(=O)C(C(O3)CO)O)O 560.50 unknown https://doi.org/10.1080/14786419.2010.524647
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(2R,3S,4S,5S,6R)-2-[[(3R,4S,5R,6S)-3-[[(1R,2S,3R,4R,5R)-2,3-dihydroxy-5-(hydroxymethyl)-4-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycyclohexyl]amino]-4,5,6-trihydroxycyclohexen-1-yl]methoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 139589202 Click to see C1C(C(C(C(C1NC2C=C(C(C(C2O)O)O)COC3C(C(C(C(O3)CO)O)O)O)O)O)OC4C(C(C(C(O4)CO)O)O)O)CO 659.60 unknown https://doi.org/10.1080/14786419.2010.524647
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(3,5-Dihydroxyphenyl)-[2-hydroxy-4-methoxy-6-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyphenyl]methanone 162848648 Click to see CC1C(C(C(C(O1)OC2=CC(=CC(=C2C(=O)C3=CC(=CC(=C3)O)O)O)OC)O)O)O 422.40 unknown https://doi.org/10.1080/14786410802278327
(3,5-dihydroxyphenyl)-[2-hydroxy-4-methoxy-6-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyphenyl]methanone 162848649 Click to see CC1C(C(C(C(O1)OC2=CC(=CC(=C2C(=O)C3=CC(=CC(=C3)O)O)O)OC)O)O)O 422.40 unknown https://doi.org/10.1080/14786410802278327
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
Norathyriol 5281656 Click to see C1=C(C=C2C(=C1O)C(=O)C3=CC(=C(C=C3O2)O)O)O 260.20 unknown https://doi.org/10.1080/14786410802278327
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
Amentoflavone 5281600 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4=C(C=CC(=C4)C5=CC(=O)C6=C(C=C(C=C6O5)O)O)O)O 538.50 unknown https://doi.org/10.1080/14786410802278327
> 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 https://doi.org/10.1080/14786410802278327
Quercetin 5280343 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 302.23 unknown https://doi.org/10.1080/14786410802278327
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-Dihydroxy-phenyl)-5,7-dihydroxy-3-(3,4,5-trihydroxy-6-methyl-tetrahydro-pyran-2-yloxy)-chromen-4-one 5353915 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 448.40 unknown https://doi.org/10.1080/14786410802278327
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 5378597 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown https://doi.org/10.1080/14786410802278327
3-[5-(1,2-Dihydroxyethyl)-3,4-dihydroxyoxolan-2-yl]oxy-2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromen-4-one 13179952 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(O4)C(CO)O)O)O)O)O 464.40 unknown https://doi.org/10.1080/14786410802278327
Hyperoside 5281643 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown https://doi.org/10.1080/14786410802278327
Isoquercitrin 5484006 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(O4)C(CO)O)O)O)O)O 464.40 unknown https://doi.org/10.1080/14786410802278327
Quercitrin 5280459 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 448.40 unknown https://doi.org/10.1080/14786410802278327
Rutin 5280805 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)O)O)O)O)O)O)O 610.50 unknown https://doi.org/10.1080/14786410802278327
Vitamin P 5293655 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)O)O)O)O)O)O)O 610.50 unknown https://doi.org/10.1080/14786410802278327

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