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Jurinea maxima

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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 UUID643fcf3b916ee742782926
Scientific name Jurinea maxima
Authority C.Winkl.
First published in Trudy Imp. S.-Peterburgsk. Bot. Sada xi. (1890) 336.

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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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-0000088503
Tropicos 2731629
KEW urn:lsid:ipni.org:names:227005-1
The Plant List gcc-44835
Open Tree Of Life 7612155
Observations.org 133731
NCBI Taxonomy 2893678
IPNI 227005-1
GBIF 5392467
CMAUP NPO6834

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
The structure of maximolide S. Kh. Zakirov, Sh. Z. Kasymov, N. D. Abdullaev, G. P. Sidyakin Springer Science and Business Media LLC 09-Jul-2008
doi:10.1007/BF00570698
Structure and configuration of jurmolide S. Kh. Zakirov, Sh. Z. Kasymov, G. P. Sidyakin Springer Science and Business Media LLC 20-Nov-2004
doi:10.1007/BF00567826
Sesquiterpene lactones fromJurinea maxima S. Kh. Zakirov, Sh. Z. Kasymov, G. P. Sidyakin Springer Science and Business Media LLC 20-Nov-2004
doi:10.1007/BF00567721
Sesquiterpene lactones from Viguiera hypargyrea L Alvarez Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)80616-0

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
Syringic acid 10742 Click to see COC1=CC(=CC(=C1O)OC)C(=O)O 198.17 unknown via CMAUP database
> 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 via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
Syringaldehyde 8655 Click to see COC1=CC(=CC(=C1O)OC)C=O 182.17 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans
Syringaresinol, (+)- 443023 Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)O)OC 418.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
(3aR,4S,6E,10Z,11aR)-3a,4,5,8,9,11a-Hexahydro-4-hydroxy-10-(hydroxymethyl)-6-methyl-3-methylenecyclodeca[b]furan-2(3H)-one 3488096 Click to see CC1=CCCC(=CC2C(C(C1)O)C(=C)C(=O)O2)CO 264.32 unknown https://doi.org/10.1007/BF00567721
Salonitenolide 5281498 Click to see CC1=CCCC(=CC2C(C(C1)O)C(=C)C(=O)O2)CO 264.32 unknown https://doi.org/10.1007/BF00567721
https://doi.org/10.1016/S0031-9422(00)80616-0
https://doi.org/10.1007/BF00567826
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Guaianolides and derivatives
(3,9-dimethyl-6-methylidene-2,8-dioxo-3a,4,5,6a,7,9,9a,9b-octahydro-3H-azuleno[4,5-b]furan-4-yl) acetate 162996208 Click to see CC1C2C(CC1=O)C(=C)CC(C3C2OC(=O)C3C)OC(=O)C 306.40 unknown https://doi.org/10.1007/BF00567826
Isoamberboin 14589063 Click to see CC1C2C(CC1=O)C(=C)CC(C3C2OC(=O)C3C)O 264.32 unknown https://doi.org/10.1007/BF00570698
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
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
> Organoheterocyclic compounds / Azolidines / Imidazolidines / Hydantoins
(5E)-5-[[(3R,4S)-4-ethyl-5-oxooxolan-3-yl]methylidene]-1-methylimidazolidine-2,4-dione 11499651 Click to see CCC1C(COC1=O)C=C2C(=O)NC(=O)N2C 238.24 unknown via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Furanoquinolines
Dictamnine 68085 Click to see COC1=C2C=COC2=NC3=CC=CC=C31 199.20 unknown via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Quinolones and derivatives / Hydroquinolones
4-Methoxy-1-methylquinolin-2-one 182073 Click to see CN1C2=CC=CC=C2C(=CC1=O)OC 189.21 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Angular furanocoumarins
(8S)-5-hydroxy-8-prop-1-en-2-yl-8,9-dihydrofuro[2,3-h]chromen-2-one 44310181 Click to see CC(=C)C1CC2=C(O1)C=C(C3=C2OC(=O)C=C3)O 244.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
3-(1,1-Dimethylallyl)scopoletin 5377569 Click to see CC(C)(C=C)C1=CC2=CC(=C(C=C2OC1=O)O)OC 260.28 unknown via CMAUP database
Scopoletin 5280460 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)O 192.17 unknown via CMAUP database

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