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Internal ID UUID643fcd9ba5675640161004
Scientific name Hieracium gymnocephalum
Authority Griseb. ex Pant.
First published in Oesterr. Bot. Z. 23: 266 (1873)

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Synonyms Top

Scientific name Authority First published in
Hieracium waldsteinii subsp. orieni (A.Kern.) Freyn 652 1895
Hieracium gymnocephalum subsp. orieni (A.Kern.) Murr & Zahn 114 1907

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Name Authority First published in
Hieracium gymnocephalum subsp. gymnocephalum Pant.

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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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000073830
KEW urn:lsid:ipni.org:names:218182-1
The Plant List gcc-30574
Open Tree Of Life 38237
Observations.org 127410
NCBI Taxonomy 546191
IPNI 218182-1
GBIF 3136593
EOL 6222275

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
Antiulcer Agents: From Plant Extracts to Phytochemicals in Healing Promotion Sharifi-Rad M, Fokou PV, Sharopov F, Martorell M, Ademiluyi AO, Rajkovic J, Salehi B, Martins N, Iriti M, Sharifi-Rad J Molecules 17-Jul-2018
PMCID:PMC6100067
doi:10.3390/molecules23071751
PMID:30018251
Intra-individual polymorphism in diploid and apomictic polyploid hawkweeds (Hieracium, Lactuceae, Asteraceae): disentangling phylogenetic signal, reticulation, and noise Fehrer J, Krak K, Chrtek J Jr BMC Evol Biol 22-Sep-2009
PMCID:PMC2759941
doi:10.1186/1471-2148-9-239
PMID:19772642
A taraxasterol derivative and phenolic compounds from Hieracium gymnocephalum S.D Petrović, M.S Gorunović, V Wray, I Merfort Elsevier BV 26-Jul-2002
doi:10.1016/S0031-9422(98)00536-6
Flavonoid and phenolic acid patterns in seven Hieracium species Silvana D. Petrovic, Ralf Löscher, Momcilo S. Gorunovic, Irmgard Merfort Elsevier BV 25-Jul-2002
doi:10.1016/S0305-1978(98)00128-8

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 / Anthracenes
8-Hydroxy-9,10-dimethoxyanthracene-2-carbaldehyde 163029200 Click to see COC1=C2C=CC(=CC2=C(C3=C1C=CC=C3O)OC)C=O 282.29 unknown https://doi.org/10.1016/S0031-9422(98)00536-6
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(3S,4aR,6aR,6aR,6bR,8aS,10R,12S,12aR,14aR,14bR)-4,4,6a,6b,8a,12,14b-heptamethyl-11-methylidene-1,2,3,4a,5,6,6a,7,8,9,10,12,12a,13,14,14a-hexadecahydropicene-3,10-diol 100987455 Click to see CC1C2C3CCC4C5(CCC(C(C5CCC4(C3(CCC2(CC(C1=C)O)C)C)C)(C)C)O)C 442.70 unknown https://doi.org/10.1016/S0031-9422(98)00536-6
alpha-Amyrin 73170 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(98)00536-6
Beta-Amyrin 73145 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(98)00536-6
Olean-12-en-3beta-ol 225689 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(98)00536-6
Urs-12-en-3beta-ol 225688 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(98)00536-6
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
3-[3-(3,4-Dihydroxyphenyl)prop-2-enoyloxy]-1,4,5-trihydroxy-cyclohexanecarboxylic acid 348159 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown https://doi.org/10.1016/S0031-9422(98)00536-6
3,5-Dicaffeoyl-epi-quinic acid 60150332 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)OC(=O)C=CC3=CC(=C(C=C3)O)O 516.40 unknown https://doi.org/10.1016/S0031-9422(98)00536-6
Chlorogenic Acid 1794427 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown https://doi.org/10.1016/S0031-9422(98)00536-6
https://doi.org/10.1016/S0305-1978(98)00128-8
Isochlorogenic acid A 6474310 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)OC(=O)C=CC3=CC(=C(C=C3)O)O 516.40 unknown https://doi.org/10.1016/S0305-1978(98)00128-8
> Organoheterocyclic compounds / Isoquinolines and derivatives / Isoquinolones and derivatives
5-Chloro-7-hydroxy-2-(2-hydroxyethyl)-7-methyl-3-(3-methylpent-1-enyl)isoquinoline-6,8-dione 78108622 Click to see CCC(C)C=CC1=CC2=C(C(=O)C(C(=O)C2=CN1CCO)(C)O)Cl 351.80 unknown https://doi.org/10.1016/S0031-9422(98)00536-6
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown https://doi.org/10.1016/S0031-9422(98)00536-6
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
2-(3,4-Dihydroxyphenyl)-5-hydroxy-7-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxymethyl]oxan-2-yl]oxychromen-4-one 12315422 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O)O 594.50 unknown https://doi.org/10.1016/S0031-9422(98)00536-6
2-(3,4-Dihydroxyphenyl)-5-hydroxy-7-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxyoxan-2-yl)oxymethyl]oxan-2-yl]oxychromen-4-one 12302232 Click to see C1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O)O 580.50 unknown https://doi.org/10.1016/S0031-9422(98)00536-6
Apigenin 7-O-glucoside 5385553 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O 432.40 unknown https://doi.org/10.1016/S0031-9422(98)00536-6
Apigetrin 5280704 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O 432.40 unknown https://doi.org/10.1016/S0305-1978(98)00128-8
https://doi.org/10.1016/S0031-9422(98)00536-6
Caesiosid 12302233 Click to see C1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O)O 580.50 unknown https://doi.org/10.1016/S0031-9422(98)00536-6
Luteolin 7-galactoside 5291488 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown https://doi.org/10.1016/S0031-9422(98)00536-6
Luteolin 7-O-glucoside 5280637 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown https://doi.org/10.1016/S0031-9422(98)00536-6
Luteolin 7-rutinoside 10461109 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O)O 594.50 unknown https://doi.org/10.1016/S0031-9422(98)00536-6

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