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Centaurea amanicola

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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 UUID643fcecc3740d134881886
Scientific name Centaurea amanicola
Authority Hub.-Mor.
First published in Bauhinia iii. 322 (1967).

Description Top

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Synonyms Top

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Common names Top

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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-0000084682
KEW urn:lsid:ipni.org:names:189859-1
The Plant List gcc-41119
Open Tree Of Life 3894338
IPNI 189859-1
GBIF 3127664
EOL 6215606

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)!
Title Authors Publication Released IDs
Chemical constituents of Centaurea cadmea C. Karamenderes, E. Bedir, H. Abou-Gazar, I. A. Khan Springer Science and Business Media LLC 23-Feb-2008
doi:10.1007/S10600-007-0232-9

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 / Hydroxybenzoic acid derivatives
4-Hydroxybenzoic acid 135 Click to see C1=CC(=CC=C1C(=O)O)O 138.12 unknown https://doi.org/10.1007/S10600-007-0232-9
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Vanillic Acid 8468 Click to see COC1=C(C=CC(=C1)C(=O)O)O 168.15 unknown https://doi.org/10.1007/S10600-007-0232-9
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
Benzyl beta-d-glucopyranoside 188977 Click to see C1=CC=C(C=C1)COC2C(C(C(C(O2)CO)O)O)O 270.28 unknown https://doi.org/10.1007/S10600-007-0232-9
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
4-Heptanoylbenzaldehyde 85800353 Click to see CCCCCCC(=O)C1=CC=C(C=C1)C=O 218.29 unknown https://doi.org/10.1007/S10600-007-0232-9
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Scopoletin 5280460 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)O 192.17 unknown https://doi.org/10.1007/S10600-007-0232-9
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin 5280443 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 270.24 unknown https://doi.org/10.1007/S10600-007-0232-9

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Contributors Top

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Collections Top

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