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Echinops setifer

Echinops setifer - 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 UUID643fc9a0f2424391199005
Scientific name Echinops setifer
Authority Iljin
First published in Bot. Mater. Gerb. Glavn. Bot. Sada R.S.F.S.R. 4: 108 (1923)

Description Top

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Synonyms Top

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Common names Top

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Language Common/alternative name
Japanese ヒゴタイ
Korean 절굿대
Chinese 糙毛蓝刺头

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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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • China North-central
      • China Southeast
    • Eastern Asia
      • Japan
      • Korea

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000032146
Tropicos 50044439
KEW urn:lsid:ipni.org:names:202671-1
The Plant List gcc-131086
PFAF Echinops setifer
Open Tree Of Life 507188
NCBI Taxonomy 406080
IPNI 202671-1
iNaturalist 475874
GBIF 5392732
EPPO ECPSE
USDA GRIN 460193
Wikipedia Echinops_setifer
CMAUP NPO22699

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
Effect of Malva neglecta and lactulose on survival of Lactobacillus fermentum and textural properties of synbiotic stirred yogurt Jooyandeh H, Momenzadeh S, Alizadeh Behbahani B, Barzegar H J Food Sci Technol 20-Jan-2023
PMCID:PMC9998791
doi:10.1007/s13197-023-05667-6
PMID:36908339
Ecosystem changes following the 2016 Kumamoto earthquakes in Japan: Future perspectives Sidle RC, Gomi T, Akasaka M, Koyanagi K Ambio 29-Dec-2017
PMCID:PMC6131130
doi:10.1007/s13280-017-1005-8
PMID:29288415

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
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(10R)-10-hydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid 45358157 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown via CMAUP database
(1S,2R,4aR,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-hydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid 45483617 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown via CMAUP database
Arjunic acid 15385516 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1O)C)C(=O)O)C 488.70 unknown via CMAUP database
Pomolic acid 382831 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1(C)O)C)C(=O)O 472.70 unknown via CMAUP database
Tormentic acid 73193 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1(C)O)C)C(=O)O 488.70 unknown via CMAUP database
Ursolic Acid 64945 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Bile acids, alcohols and derivatives / Hydroxy bile acids, alcohols and derivatives
(2S,3R,5R,10R,13R,14S,17S)-2,3,14-trihydroxy-10,13-dimethyl-17-[(2R)-1,2,5-trihydroxy-1,5-dimethyl-hexyl]-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-6-one 118701161 Click to see CC12CCC3C(=CC(=O)C4C3(CC(C(C4)O)O)C)C1(CCC2C(C)(C(CCC(C)(C)O)O)O)O 480.60 unknown via CMAUP database
(2S,3R,5R,10R,13R,14S,17S)-2,3,14-trihydroxy-10,13-dimethyl-17-[(3R)-2,3,6-trihydroxy-6-methylheptan-2-yl]-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-6-one 439770 Click to see CC12CCC3C(=CC(=O)C4C3(CC(C(C4)O)O)C)C1(CCC2C(C)(C(CCC(C)(C)O)O)O)O 480.60 unknown via CMAUP database
(2S,3R,5R,10R,13R,14S)-2,3,14-trihydroxy-10,13-dimethyl-17-[(2R,3R)-2,3,6-trihydroxy-6-methylheptan-2-yl]-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-6-one 44143979 Click to see CC12CCC3C(=CC(=O)C4C3(CC(C(C4)O)O)C)C1(CCC2C(C)(C(CCC(C)(C)O)O)O)O 480.60 unknown via CMAUP database
(2S,3R,5R,10R,13R)-2,3,14-trihydroxy-10,13-dimethyl-17-[(2R)-2,3,6-trihydroxy-6-methylheptan-2-yl]-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-6-one 5459151 Click to see CC12CCC3C(=CC(=O)C4C3(CC(C(C4)O)O)C)C1(CCC2C(C)(C(CCC(C)(C)O)O)O)O 480.60 unknown via CMAUP database
(2S,3R,9R,10R,13R,14S,17S)-2,3,14-trihydroxy-10,13-dimethyl-17-[(2S,3R)-2,3,6-trihydroxy-6-methylheptan-2-yl]-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-6-one 101778163 Click to see CC12CCC3C(=CC(=O)C4C3(CC(C(C4)O)O)C)C1(CCC2C(C)(C(CCC(C)(C)O)O)O)O 480.60 unknown via CMAUP database
2,3,14-trihydroxy-10,13-dimethyl-17-(2,3,6-trihydroxy-6-methylheptan-2-yl)-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-6-one 271605 Click to see CC12CCC3C(=CC(=O)C4C3(CC(C(C4)O)O)C)C1(CCC2C(C)(C(CCC(C)(C)O)O)O)O 480.60 unknown via CMAUP database
20-Hydroxyecdysone 5459840 Click to see CC12CCC3C(=CC(=O)C4C3(CC(C(C4)O)O)C)C1(CCC2C(C)(C(CCC(C)(C)O)O)O)O 480.60 unknown via CMAUP database
5-beta-Cholest-7-en-6-one, 2-beta,3-beta,14,20,22,25-hexahydroxy-, (22R)- 3032482 Click to see CC12CCC3C(=CC(=O)C4C3(CC(C(C4)O)O)C)C1(CCC2C(C)(C(CCC(C)(C)O)O)O)O 480.60 unknown via CMAUP database
> Organoheterocyclic compounds / Bi- and oligothiophenes
2,2':5',2''-Terthiophene 65067 Click to see C1=CSC(=C1)C2=CC=C(S2)C3=CC=CS3 248.40 unknown via CMAUP database
5-(3-Buten-1-ynyl)-2,2'-bithiophene 70813 Click to see C=CC#CC1=CC=C(S1)C2=CC=CS2 216.30 unknown via CMAUP database
5-(4-Hydroxybut-1-ynyl)-2,2'-bithiophene 440357 Click to see C1=CSC(=C1)C2=CC=C(S2)C#CCCO 234.30 unknown via CMAUP database
Arctic acid 182071 Click to see CC#CC1=CC=C(S1)C2=CC=C(S2)C(=O)O 248.30 unknown via CMAUP database
Arctinal 13779265 Click to see CC#CC1=CC=C(S1)C2=CC=C(S2)C=O 232.30 unknown via CMAUP database
Arctinol B 46842526 Click to see CC#CC1=CC=C(S1)C2=CC=C(S2)C(CO)O 264.40 unknown via CMAUP database
Arctinone B 10014817 Click to see CC#CC1=CC=C(S1)C2=CC=C(S2)C(=O)C 246.40 unknown via CMAUP database
> Organoheterocyclic compounds / Thiophenes / 2,5-disubstituted thiophenes
Echinoynethiophene A 10263246 Click to see CC#CC1=CC=C(S1)C#CC#CC(CO)O 230.28 unknown via CMAUP database

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