Hypericum coris - Unknown
Part: Unknown
Author: Public Domain - WikiMedia

Hypericum coris - Unknown
Part: Unknown
Author: Public Domain - WikiMedia

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Details Top

Internal ID UUID6440214d5151c451407739
Scientific name Hypericum coris
Authority L.
First published in Sp. Pl. : 787 (1753)

Description Top

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Synonyms Top

Scientific name Authority First published in
Hypericum corifolium Salisb. Prodr. Stirp. Chap. Allerton : 369 (1796)
Hypericum multicaule Lam. Encycl. 4: 178 (1797)
Hypericum verticillatum Lam. Fl. Franç. 3: 149 (1779)

Common names Top

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Language Common/alternative name
German quirlblättriges johanniskraut

Subspecies (abbr. subsp./ssp.) Top

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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
  • Europe
    • Middle Europe
      • Switzerland
    • Northern Europe
      • Great Britain
    • Southeastern Europe
      • Italy
    • Southwestern Europe
      • France

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000727515
USDA Plants HYCO15
Tropicos 7800006
INPN 103260
Flora of Italy 1235
KEW urn:lsid:ipni.org:names:433340-1
The Plant List kew-2857961
Open Tree Of Life 295780
Observations.org 118890
NCBI Taxonomy 673923
IPNI 433340-1
iNaturalist 487459
GBIF 3713724
EPPO HYPCO
EOL 5707468
Elurikkus 400871
USDA GRIN 407263
Wikipedia Hypericum_coris

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)!
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Title Authors Publication Released IDs
Herbal Medicine for Oligomenorrhea and Amenorrhea: A Systematic Review of Ancient and Conventional Medicine Moini Jazani A, Hamdi K, Tansaz M, Nazemiyeh H, Sadeghi Bazargani H, Fazljou SM, Nasimi Doost Azgomi R Biomed Res Int 18-Mar-2018
PMCID:PMC5878906
doi:10.1155/2018/3052768
PMID:29744355
Anti-inflammatory phloroglucinol derivatives from Hypericum empetrifolium Crockett SL, Wenzig EM, Kunert O, Bauer R Phytochem Lett 15-Apr-2008
PMCID:PMC3000598
doi:10.1016/j.phytol.2007.12.003
PMID:21151761
Composition and antimicrobial activity of the essential oil of Hypericum coris. Schwob I, Bessiere JM, Dherbomez M, Viano J Fitoterapia 01-Oct-2002
doi:10.1016/S0367-326X(02)00171-5
PMID:12385876

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 / Benzoic acid esters
Benzyl Benzoate 2345 Click to see C1=CC=C(C=C1)COC(=O)C2=CC=CC=C2 212.24 unknown https://doi.org/10.1016/S0367-326X(02)00171-5
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Linalool, (+/-)- 6549 Click to see CC(=CCCC(C)(C=C)O)C 154.25 unknown https://doi.org/10.1016/S0367-326X(02)00171-5
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(-)-alpha-Curcumene 442360 Click to see CC1=CC=C(C=C1)C(C)CCC=C(C)C 202.33 unknown https://doi.org/10.1016/S0367-326X(02)00171-5
(+)-delta-Cadinene 441005 Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C 204.35 unknown https://doi.org/10.1016/S0367-326X(02)00171-5
(1R,4S,4aR)-1,6-dimethyl-4-propan-2-yl-3,4,4a,7,8,8a-hexahydro-2H-naphthalen-1-ol 5315592 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown https://doi.org/10.1016/S0367-326X(02)00171-5
1,6-Dimethyl-4-isopropyltetralin 10224 Click to see CC1CCC(C2=C1C=CC(=C2)C)C(C)C 202.33 unknown https://doi.org/10.1016/S0367-326X(02)00171-5
alpha-Cadinol 10398656 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown https://doi.org/10.1016/S0367-326X(02)00171-5
alpha-Curcumene 92139 Click to see CC1=CC=C(C=C1)C(C)CCC=C(C)C 202.33 unknown https://doi.org/10.1016/S0367-326X(02)00171-5
Cadina-1(10),4-diene 10223 Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C 204.35 unknown https://doi.org/10.1016/S0367-326X(02)00171-5
Calamenene 6429077 Click to see CC1CCC(C2=C1C=CC(=C2)C)C(C)C 202.33 unknown https://doi.org/10.1016/S0367-326X(02)00171-5
gamma-Muurolene 12313020 Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C 204.35 unknown https://doi.org/10.1016/S0367-326X(02)00171-5
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(1aS,4aS,7S,7aR,7bS)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol 97032059 Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C 220.35 unknown https://doi.org/10.1016/S0367-326X(02)00171-5
(7aR)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol 5321422 Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C 220.35 unknown https://doi.org/10.1016/S0367-326X(02)00171-5
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Himachalane and lippifoliane sesquiterpenoids
3,5,5,9-tetramethyl-2,4a,5,6,7,8-hexahydro-1H-benzo[7]annulene 15095 Click to see CC1=CC2C(=C(CCCC2(C)C)C)CC1 204.35 unknown https://doi.org/10.1016/S0367-326X(02)00171-5
beta-Himachalene 11586487 Click to see CC1=CC2C(=C(CCCC2(C)C)C)CC1 204.35 unknown https://doi.org/10.1016/S0367-326X(02)00171-5

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