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Hypericum thasium

Hypericum thasium - 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 UUID64402171a94db147260868
Scientific name Hypericum thasium
Authority Griseb.
First published in Spic. Fl. Rumel. 1: 227 (1843)

Description Top

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Synonyms Top

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Common names Top

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Language Common/alternative name
Bulgarian тасоска звъника

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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000728391
KEW urn:lsid:ipni.org:names:433906-1
The Plant List kew-2859055
Open Tree Of Life 4730083
Observations.org 147593
NCBI Taxonomy 1321357
IPNI 433906-1
iNaturalist 194817
GBIF 3715326
EPPO HYPTH
EOL 5708320
Elurikkus 401250

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
MAO-A Inhibitory Potential of Terpene Constituents from Ginger Rhizomes—A Bioactivity Guided Fractionation Kukula-Koch W, Koch W, Czernicka L, Głowniak K, Asakawa Y, Umeyama A, Marzec Z, Kuzuhara T Molecules 29-May-2018
PMCID:PMC6099963
doi:10.3390/molecules23061301
PMID:29844252
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
Cellular reactive oxygen species inhibitory constituents of Hypericum thasium Griseb. Demirkiran O, Ahmed Mesaik M, Beynek H, Abbaskhan A, Iqbal Choudhary M Phytochemistry 01-Jan-2009
doi:10.1016/J.PHYTOCHEM.2008.10.006
PMID:19203769

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
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(3,5-Dihydroxyphenyl)-[2-hydroxy-4-methoxy-6-(3,4,5-trihydroxyoxan-2-yl)oxyphenyl]methanone 74817320 Click to see COC1=CC(=C(C(=C1)OC2C(C(C(CO2)O)O)O)C(=O)C3=CC(=CC(=C3)O)O)O 408.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.10.006
(3,5-dihydroxyphenyl)-[2-hydroxy-4-methoxy-6-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyphenyl]methanone 42603668 Click to see COC1=CC(=C(C(=C1)OC2C(C(C(CO2)O)O)O)C(=O)C3=CC(=CC(=C3)O)O)O 408.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.10.006
(3,5-Dihydroxyphenyl)-[2,4-dihydroxy-6-(3,4,5-trihydroxyoxan-2-yl)oxyphenyl]methanone 74817319 Click to see C1C(C(C(C(O1)OC2=CC(=CC(=C2C(=O)C3=CC(=CC(=C3)O)O)O)O)O)O)O 394.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.10.006
(3,5-dihydroxyphenyl)-[2,4-dihydroxy-6-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyphenyl]methanone 42603667 Click to see C1C(C(C(C(O1)OC2=CC(=CC(=C2C(=O)C3=CC(=CC(=C3)O)O)O)O)O)O)O 394.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.10.006
[(2S,3R,4R,5R)-5-[2-(3,5-dihydroxybenzoyl)-3,5-dihydroxyphenoxy]-4-hydroxy-2-(hydroxymethyl)oxolan-3-yl] acetate 162904363 Click to see CC(=O)OC1C(OC(C1O)OC2=CC(=CC(=C2C(=O)C3=CC(=CC(=C3)O)O)O)O)CO 436.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.10.006
[2,4-dihydroxy-6-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-phenylmethanone 101130544 Click to see C1=CC=C(C=C1)C(=O)C2=C(C=C(C=C2OC3C(C(C(C(O3)CO)O)O)O)O)O 392.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.10.006
[2,4-Dihydroxy-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-phenylmethanone 85362951 Click to see C1=CC=C(C=C1)C(=O)C2=C(C=C(C=C2OC3C(C(C(C(O3)CO)O)O)O)O)O 392.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.10.006
[5-[2-(3,5-Dihydroxybenzoyl)-3,5-dihydroxyphenoxy]-4-hydroxy-2-(hydroxymethyl)oxolan-3-yl] acetate 74817318 Click to see CC(=O)OC1C(OC(C1O)OC2=CC(=CC(=C2C(=O)C3=CC(=CC(=C3)O)O)O)O)CO 436.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.10.006
[6-[2-(3,5-Dihydroxybenzoyl)-3,5-dihydroxyphenoxy]-4,5-dihydroxyoxan-3-yl] acetate 74817321 Click to see CC(=O)OC1COC(C(C1O)O)OC2=CC(=CC(=C2C(=O)C3=CC(=CC(=C3)O)O)O)O 436.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.10.006
2-(3,5-dihydroxybenzoyl)-3,5-dihydroxyphenyl 4-O-acetyl-beta-d-xylopyranoside 42603669 Click to see CC(=O)OC1COC(C(C1O)O)OC2=CC(=CC(=C2C(=O)C3=CC(=CC(=C3)O)O)O)O 436.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.10.006
garcimangosone D 11003703 Click to see C1=CC=C(C=C1)C(=O)C2=C(C=C(C=C2OC3C(C(C(C(O3)CO)O)O)O)O)O 392.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.10.006
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
3,8'-Biapigenin 10414856 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4=C(OC5=CC(=CC(=C5C4=O)O)O)C6=CC=C(C=C6)O)O 538.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.10.006
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/10.1016/J.PHYTOCHEM.2008.10.006
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
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/10.1016/J.PHYTOCHEM.2008.10.006
> 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/10.1016/J.PHYTOCHEM.2008.10.006
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 51402807 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/10.1016/J.PHYTOCHEM.2008.10.006
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/10.1016/J.PHYTOCHEM.2008.10.006
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one 26339717 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/10.1016/J.PHYTOCHEM.2008.10.006
Isoquercetin 5280804 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/10.1016/J.PHYTOCHEM.2008.10.006
Quercetin 3-alloside 12304327 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/10.1016/J.PHYTOCHEM.2008.10.006
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/10.1016/J.PHYTOCHEM.2008.10.006

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