Atranorin
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IUPAC name
(3-hydroxy-4-methoxycarbonyl-2,5-dimethylphenyl) 3-formyl-2,4-dihydroxy-6-methylbenzoate
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Other names | |
Identifiers | |
3D model (
JSmol ) |
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ChEBI | |
ChEMBL | |
ChemSpider | |
ECHA InfoCard
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100.006.844 |
EC Number |
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PubChem CID
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UNII | |
CompTox Dashboard (EPA)
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Properties | |
C19H18O8 | |
Molar mass | 374.345 g·mol−1 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Atranorin is a chemical substance produced by some species of
allergic reaction to atranorin.[8]
References
- ^ a b "Atranorin (CAS 479-20-9)". www.caymanchem.com.
- ^ "479-20-9 | Atranorin | Atranorine; NSC 249980; NSC 685591; NSC 87512; Parmelin; Parmelin Acid; Usnarin; Usnarin Acid | C
19G
18O
8 | TRC". www.trc-canada.com. - PMID 21111802.
- ^ a b Jaeck, Andreas. "Atranorin". www.internetchemie.info.
- ^ PMID 28443519.
- PMID 28811522.
- PMID 21111802.
- ^ "Allergen Atranorin Allergie Allergologie". www.alles-zur-allergologie.de.
Further reading
- Zeitschrift Für Naturforschung: A journal of chemical sciences. B (in German). Verlag der Zeitschrift für Naturforschung.
- Jahresbericht über die Fortschritte der Chemie und verwandter Theile anderer Wissenschaften (in German). Friedrich Vieweg Und Sohn.
- Vos, Carlo; Mckinney, Phillip; Pearson, Colby; Heiny, Erik; Gunawardena, Gamini; Holt, Emily A. (2018). "The optimal extraction and stability of atranorin from lichens, in relation to solvent and pH". The Lichenologist. 50 (4): 499–512. S2CID 91786583.
- Harikrishnan, Adhikesavan; Veena, V.; Lakshmi, B.; Shanmugavalli, R.; Theres, Sonia; Prashantha, C. N.; Shah, Tanya; Oshin, K.; Togam, Ringu; Nandi, Sisir (4 March 2021). "Atranorin, an antimicrobial metabolite from lichen Parmotrema rampoddense exhibited in vitro anti-breast cancer activity through interaction with Akt activity". Journal of Biomolecular Structure and Dynamics. 39 (4): 1248–1258. S2CID 211475842.