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Stizolophus balsamita

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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 UUID643fcc3a8f0cb202880297
Scientific name Stizolophus balsamita
Authority (Lam.) K.Koch
First published in K. Koch in Linnaea 24. 1851. 423 1851

Description Top

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Synonyms Top

Scientific name Authority First published in
Stizolophus balsamitella (Bornm.) Soják Novit. Bot. Delect. Seminum Horti Bot. Univ. Carol. Prag. 1962: 48 (1962) (1962)
Calcitrapa balsamita Sweet Hort. Brit. : 218 (1826)
Stizolophus balsamitifolius Cass. Dict. Sci. Nat., ed. 2. 51: 49, 50 (1827)
Centaurea balsamitella Bornm. Repert. Spec. Nov. Regni Veg. 24: 376 (1928)
Centaurea balsamita Lam. Encycl. 1: 667 (1785)

Common names Top

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Language Common/alternative name
Arabic ستيزولوفس بلسمي

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
  • Asia-temperate
    • Caucasus
      • Transcaucasus
    • Middle Asia
      • Kazakhstan
      • Kirgizstan
      • Tadzhikistan
      • Turkmenistan
      • Uzbekistan
    • Western Asia
      • Afghanistan
      • Iran
      • Iraq
      • Lebanon-Syria
      • Palestine
      • Turkey

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000060188
Tropicos 2703309
KEW urn:lsid:ipni.org:names:251693-1
The Plant List gcc-17248
Open Tree Of Life 1036518
NCBI Taxonomy 145830
IPNI 251693-1
iNaturalist 632895
GBIF 3141524

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
Benefits of topical natural ingredients in epidermal permeability barrier Lei D, Liu D, Zhang J, Zhang L, Man MQ Front Physiol 04-Jan-2024
PMCID:PMC10794395
doi:10.3389/fphys.2023.1275506
PMID:38239888
Medicinal Herbs in the Relief of Neurological, Cardiovascular, and Respiratory Symptoms after COVID-19 Infection A Literature Review Nawrot J, Gornowicz-Porowska J, Budzianowski J, Nowak G, Schroeder G, Kurczewska J Cells 11-Jun-2022
PMCID:PMC9220793
doi:10.3390/cells11121897
PMID:35741026
Taxifolin as a Promising Ingredient of Cosmetics for Adult Skin Micek I, Nawrot J, Seraszek-Jaros A, Jenerowicz D, Schroeder G, Spiżewski T, Suchan A, Pawlaczyk M, Gornowicz-Porowska J Antioxidants (Basel) 15-Oct-2021
PMCID:PMC8533573
doi:10.3390/antiox10101625
PMID:34679758
Biologically Active Compounds in Stizolophus balsamita Inflorescences: Isolation, Phytochemical Characterization and Effects on the Skin Biophysical Parameters Nawrot J, Budzianowski J, Nowak G, Micek I, Budzianowska A, Gornowicz-Porowska J Int J Mol Sci 23-Apr-2021
PMCID:PMC8122880
doi:10.3390/ijms22094428
PMID:33922647
Phytotherapy Perspectives for Treating Fungal Infections, Migraine, Sebhorreic Dermatitis and Hyperpigmentations with the Plants of the Centaureinae Subtribe (Asteraceae) Nawrot J, Gornowicz-Porowska J, Nowak G Molecules 15-Nov-2020
PMCID:PMC7696306
doi:10.3390/molecules25225329
PMID:33203185
Pharmaceutical resource discovery from traditional medicinal plants: Pharmacophylogeny and pharmacophylogenomics Hao DC, Xiao PG Chin Herb Med 12-Mar-2020
PMCID:PMC9476761
doi:10.1016/j.chmed.2020.03.002
PMID:36119793
The Anti-Serotonin Effect of Parthenolide Derivatives and Standardised Extract from the Leaves of Stizolophus balsamita Nawrot J, Napierała M, Kaczerowska-Pietrzak K, Florek E, Gornowicz-Porowska J, Pelant E, Nowak G Molecules 15-Nov-2019
PMCID:PMC6891796
doi:10.3390/molecules24224131
PMID:31731603
NMR data for the hydroxyl groups detected by NOESY spectra in sesquiterpene lactones Budzianowski J, Nawrot J, Nowak G Data Brief 12-Jul-2019
PMCID:PMC6661464
doi:10.1016/j.dib.2019.104246
PMID:31384644
Potential Use of Turkish Medicinal Plants in the Treatment of Various Diseases Ozkan G, Kamiloglu S, Ozdal T, Boyacioglu D, Capanoglu E Molecules 25-Feb-2016
PMCID:PMC6273156
doi:10.3390/molecules21030257
PMID:26927038
Detection Progress of Selected Drugs in TLC Pyka A Biomed Res Int 16-Jan-2014
PMCID:PMC3914296
doi:10.1155/2014/732078
PMID:24551853
Lessons from Plectocephalus (Compositae, Cardueae-Centaureinae): ITS disorientation in annuals and Beringian dispersal as revealed by molecular analyses Susanna A, Galbany-Casals M, Romaschenko K, Barres L, Martín J, Garcia-Jacas N Ann Bot 28-Jun-2011
PMCID:PMC3143048
doi:10.1093/aob/mcr138
PMID:21712295
Cirsimaritin from Stizolophus balsamita E. M. Suleimenov, V. A. Raldugin, S. M. Adekenov Springer Science and Business Media LLC 01-Oct-2008
doi:10.1007/S10600-008-9077-0
Sesquiterpene Lactones from Stizolophus balsamita and Their Biological Activity E. M. Suleimenov, O. V. Morozova, V. A. Raldugin, Yu. V. Gatilov, T. V. Rybalova, M. M. Shakirov, R. Seidakhmetov, R. M. Aksartov, S. M. Adekenov Springer Science and Business Media LLC 05-Jan-2006
doi:10.1007/S10600-005-0205-9
The sesquiterpene lactones ofStizolophus balsamita K. S. Rybalko, M. N. Mukhametzhanov, V. I. Sheichenko, O. A. Konovalova Springer Science and Business Media LLC 20-Nov-2004
doi:10.1007/BF00564798
Stizolin — A new sesquiterpene lactone fromStizolophus balsamita M. N. Mukhametzhanov, V. I. Sheichenko, A. I. Ban'kovskii, K. S. Rybalko, K. I. Boryaev Springer Science and Business Media LLC 20-Nov-2004
doi:10.1007/BF00564930

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
(1S,2S,4R,8E,10S,11S)-10-hydroxy-4,8-dimethyl-12-methylidene-3,14-dioxatricyclo[9.3.0.02,4]tetradec-8-en-13-one 162955779 Click to see CC1=CC(C2C(C3C(O3)(CCC1)C)OC(=O)C2=C)O 264.32 unknown https://doi.org/10.1007/BF00564930
10-Hydroxy-4,8-dimethyl-12-methylidene-3,14-dioxatricyclo[9.3.0.02,4]tetradec-8-en-13-one 162955778 Click to see CC1=CC(C2C(C3C(O3)(CCC1)C)OC(=O)C2=C)O 264.32 unknown https://doi.org/10.1007/BF00564930
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
(1S,2R,4R,7Z,10S,11R)-10-hydroxy-4,8-dimethyl-12-methylidene-3,14-dioxatricyclo[9.3.0.02,4]tetradec-7-en-13-one 14191293 Click to see CC1=CCCC2(C(O2)C3C(C(C1)O)C(=C)C(=O)O3)C 264.32 unknown https://doi.org/10.1016/0031-9422(92)83281-3
https://doi.org/10.1007/BF00564798
(1S,2R,4S,7Z,10S,11R)-10-hydroxy-4,8-dimethyl-12-methylidene-3,14-dioxatricyclo[9.3.0.02,4]tetradec-7-en-13-one 163011543 Click to see CC1=CCCC2(C(O2)C3C(C(C1)O)C(=C)C(=O)O3)C 264.32 unknown https://doi.org/10.1007/BF00564720
(1S,2S,4R,7E,10S,11R)-10-hydroxy-4,8-dimethyl-12-methylidene-3,14-dioxatricyclo[9.3.0.02,4]tetradec-7-en-13-one 88590525 Click to see CC1=CCCC2(C(O2)C3C(C(C1)O)C(=C)C(=O)O3)C 264.32 unknown https://doi.org/10.1007/BF01946442
[(1S,2R,4R,7Z,9R,10R,11R)-9-hydroxy-4,8-dimethyl-12-methylidene-13-oxo-3,14-dioxatricyclo[9.3.0.02,4]tetradec-7-en-10-yl] 3-methylbut-2-enoate 101306931 Click to see CC1=CCCC2(C(O2)C3C(C(C1O)OC(=O)C=C(C)C)C(=C)C(=O)O3)C 362.40 unknown https://doi.org/10.1016/0031-9422(92)83281-3
https://doi.org/10.1007/BF00564798
10-Hydroxy-4,8-dimethyl-12-methylidene-3,14-dioxatricyclo[9.3.0.02,4]tetradec-7-en-13-one 73097248 Click to see CC1=CCCC2(C(O2)C3C(C(C1)O)C(=C)C(=O)O3)C 264.32 unknown https://doi.org/10.1007/BF00564720
Stizolicin 15089249 Click to see CC1=CCCC2(C(O2)C3C(C(C1)OC(=O)C(=CCO)CO)C(=C)C(=O)O3)C 378.40 unknown https://doi.org/10.1007/BF01946442
https://doi.org/10.1016/0031-9422(92)83281-3
https://doi.org/10.1007/S10600-005-0205-9
https://doi.org/10.1007/BF00564798
> Phenylpropanoids and polyketides / Coumarins and derivatives
3-Hydroxy-9-[[6-hydroxy-2-(hydroxymethyl)-7-methoxy-2,3-dihydro-1-benzofuran-3-yl]oxy]-10-methoxybenzo[c]chromen-6-one 163009793 Click to see COC1=C(C=CC2=C1OC(C2OC3=C(C4=C(C=C3)C(=O)OC5=C4C=CC(=C5)O)OC)CO)O 452.40 unknown https://doi.org/10.1007/S10600-005-0205-9
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Cirsimaritin 188323 Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC=C(C=C3)O)O)OC 314.29 unknown https://doi.org/10.1007/S10600-008-9077-0

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