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Psephellus dealbatus

Psephellus dealbatus - 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 UUID643fd25b6e914811177219
Scientific name Psephellus dealbatus
Authority K.Koch
First published in Linnaea 24: 438 (1851)

Description Top

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Synonyms Top

Scientific name Authority First published in
Psephellus lactiflorus g.kos ex A.N.Tsukhukidze Zametki Sist. Geogr. Rast. 32: 69 (1976)
Centaurea tschuchrukidzei Czerep. Sosud. Rast. SSSR 54 (1981), nom. nov. (1981)
Psephellus sosnowskyi Chukhr. in Izvest. Akad. Nauk Gruz. SSR, 1(56): 444 (1976)
Psephellus nogmovii g.kos ex A.N.Tsukhukidze Zametki Sist. Geogr. Rast. 32: 68 (1976)
Centaurea procumbens Hablitz Reise Russland 4: 167 (1784)
Centaurea nogmovii (Koss ex Tschuchr.) Czerep. Sosud. Rast. SSSR 53 (1981): (1981)
Psephellus calocephalus Cass. Dict. Sci. Nat., ed. 2. 43: 488 (1826)
Psephellus sosnowskyi Tschuchr. Izvest. Akad. Nauk Gruz. SSR 1(56): 444. 1976
Psephellus kacheticus Rehmann ex Boiss. Fl. Orient. 3: 608 (1875)
Psephellus cabardensis Koss ex Tschuchr. Zametki Sist. Geogr. Rast. 32: 69. 1976
Psephellus nogmovii Koss ex Tschuchr. Zametki Sist. Geogr. Rast. 32: 68. 1976
Centaurea cabardensis (Koss ex Tschuchr.) Czerep. Sosud. Rast. SSSR 52 (1981): (1981)
Psephellus cabardensis g.kos ex A.N.Tsukhukidze Zametki Sist. Geogr. Rast. 32: 69 (1976)
Centaurea kachetica (Rehmann ex Boiss.) Czerep. Sosud. Rast. SSSR 52 (1981):.
Psephellus lazicus Boiss. Fl. Orient. 3: 608 (1875)
Psephellus lactiflorus Koss ex Tschuchr. Zametki Sist. Geogr. Rast. 32: 69 (1976)
Centaurea dealbata Willd. Sp. Pl., ed. 4 , 3: 2295 (1803)
Centaurea baksanica Czerep. Sosud. Rast. SSSR 51 (1981), nom. nov. (1981)

Common names Top

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Language Common/alternative name
Azerbaijani ağımtıl psefellus
Czech chrpinec bělavý
Finnish huoparuusukaunokki
Norwegian Bokmål filtknoppurt
Russian василёк подбелённый
Russian Псефеллюс беловатый
Russian Псефеллюс подбелённый
Chinese 白粉矢车菊
Chinese 粉绒矢车菊

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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Sow seeds at 20°C, expecting germination within 3 months without further temperature treatment.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • Caucasus
      • North Caucasus
      • Transcaucasus
    • Western Asia
      • Turkey
  • Europe
    • Eastern Europe
      • Baltic States
    • Middle Europe
      • Austria
      • Belgium
      • Czechoslovakia
      • Germany
      • Poland
    • Northern Europe
      • Great Britain

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000122956
INPN 717860
KEW urn:lsid:ipni.org:names:239761-1
The Plant List gcc-84107
Plantarium 48015
IPNI 239761-1
iNaturalist 522029
GBIF 3137829
USDA GRIN 462375
Wikipedia Psephellus_dealbatus
CMAUP NPO7401

Genomes (via NCBI) Top

No reference genome is available on NCBI yet. We are constantly monitoring for new data.

Scientific Literature Top

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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 / Gallic acid and derivatives
[(1R,2R)-1-(7-methoxy-1,3-benzodioxol-5-yl)-2-methyl-3-oxobutyl] 3,4,5-trimethoxybenzoate 11859073 Click to see CC(C(C1=CC2=C(C(=C1)OC)OCO2)OC(=O)C3=CC(=C(C(=C3)OC)OC)OC)C(=O)C 446.40 unknown via CMAUP database
[(1S,2R)-2-methyl-3-oxo-1-(3,4,5-trimethoxyphenyl)butyl] 7-methoxy-1,3-benzodioxole-5-carboxylate 11859072 Click to see CC(C(C1=CC(=C(C(=C1)OC)OC)OC)OC(=O)C2=CC3=C(C(=C2)OC)OCO3)C(=O)C 446.40 unknown via CMAUP database
Tsangin C 56661913 Click to see CC(C(C1=CC(=C(C(=C1)OC)OC)OC)OC(=O)C2=CC(=C(C(=C2)OC)OC)OC)C(=O)C 462.50 unknown via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
Vanillin 1183 Click to see COC1=C(C=CC(=C1)C=O)O 152.15 unknown via CMAUP database
> Lignans, neolignans and related compounds / Dibenzylbutane lignans
4Alpha,5Alpha-Epoxybeilschmin A 71454057 Click to see CC1C(OC2(C1(O2)C)C3=CC4=C(C(=C3)OC)OCO4)C5=CC(=C(C(=C5)OC)OC)OC 430.40 unknown via CMAUP database
4Alpha,5Alpha-Epoxybeilschmin B 71459474 Click to see CC1C(OC2(C1(O2)C)C3=CC(=C(C(=C3)OC)OC)OC)C4=CC(=C(C(=C4)OC)OC)OC 446.50 unknown via CMAUP database
Beilschmin D 71455792 Click to see CC1C(OC2(C1(O2)C)C3=CC4=C(C(=C3)OC)OCO4)C5=CC6=C(C(=C5)OC)OCO6 414.40 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 7,7-epoxylignans
Beilschmin A 22297613 Click to see CC1C(C(OC1C2=CC3=C(C(=C2)OC)OCO3)C4=CC(=C(C(=C4)OC)OC)OC)C 416.50 unknown via CMAUP database
Beilschmin B 14352170 Click to see CC1C(C(OC1C2=CC(=C(C(=C2)OC)OC)OC)C3=CC(=C(C(=C3)OC)OC)OC)C 432.50 unknown via CMAUP database
beilschminol A, rel- 54671632 Click to see CC1C(C(OC1C2=CC(=C(C(=C2)OC)OC)O)C3=CC4=C(C(=C3)OC)OCO4)C 402.40 unknown via CMAUP database
rel-(7S,8S,7'R,8'R)-3,3',4,4',5,5'-hexamethoxy-7.O.7',8.8'-lignan 21827796 Click to see CC1C(C(OC1C2=CC(=C(C(=C2)OC)OC)OC)C3=CC(=C(C(=C3)OC)OC)OC)C 432.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Methyl linoleate 5284421 Click to see CCCCCC=CCC=CCCCCCCCC(=O)OC 294.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
alpha-Tocopherolquinone 2734086 Click to see CC1=C(C(=O)C(=C(C1=O)C)CCC(C)(CCCC(C)CCCC(C)CCCC(C)C)O)C 446.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Tanacetene 5321610 Click to see CC(=CCCC=C(C)CCC=C(C)C)C 206.37 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids
alpha-Tocospiro-B 21674157 Click to see CC1=C(C(C2(C1=O)CCC(O2)(C)CCCC(C)CCCC(C)CCCC(C)C)(C(=O)C)O)C 462.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Squalene 638072 Click to see CC(=CCCC(=CCCC(=CCCC=C(C)CCC=C(C)CCC=C(C)C)C)C)C 410.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
Ergosta-4,6,8(14),22-tetraen-3-one 6441416 Click to see CC(C)C(C)C=CC(C)C1CCC2=C3C=CC4=CC(=O)CCC4(C3CCC12C)C 392.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
3-Hydroxystigmast-5-en-7-one 160608 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2C(=O)C=C4C3(CCC(C4)O)C)C)C(C)C 428.70 unknown via CMAUP database
6alpha-Hydroxystigmast-4-en-3-one 9867274 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC(C4=CC(=O)CCC34C)O)C)C(C)C 428.70 unknown via CMAUP database
6beta-Hydroxystigmast-4-en-3-one 9823926 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC(C4=CC(=O)CCC34C)O)C)C(C)C 428.70 unknown via CMAUP database
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
Stigmast-4-en-3-one 5484202 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CCC4=CC(=O)CCC34C)C)C(C)C 412.70 unknown via CMAUP database
Stigmast-4-ene-3,6-dione 5490007 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC(=O)C4=CC(=O)CCC34C)C)C(C)C 426.70 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzaldehydes / Hydroxybenzaldehydes
4-Hydroxybenzaldehyde 126 Click to see C1=CC(=CC=C1C=O)O 122.12 unknown via CMAUP database
> Organoheterocyclic compounds / Benzodioxoles
Endiandramide A 54669853 Click to see CC(C)CNC(=O)C1C=CC2CC3C(C4C3C2C1C=C4)CC5=CC6=C(C=C5)OCO6 405.50 unknown via CMAUP database
tsangibeilin A, rac- 54671628 Click to see C1C2C=CC(C3C2C4C1C(C4C=C3)CCCC5=CC6=C(C=C5)OCO6)C(=O)O 378.50 unknown via CMAUP database
tsangibeilin B, rel- 54671629 Click to see C1C2C=CC(C3C2C4C1C(C4C=C3)CC5=CC6=C(C=C5)OCO6)C(=O)O 350.40 unknown via CMAUP database

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