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| Product | Description | |
|---|---|---|
| Atranorin | Atranorin is a lichen secondary metabolite. Atranorin inhibits lung cancer cell motility and tumorigenesis by affecting AP-1, Wnt, and STAT signaling and suppressing RhoGTPase activity [1] [2]. Uses: Scientific research. Group: Natural products. CAS No. 479-20-9. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg. Product ID: HY-N2907. |  |
| Atranorin | Atranorin. Uses: Designed for use in research and industrial production. Additional or Alternative Names: PARMELIN;USNARIN;ATRANORIN;3-hydroxy-4-(methoxycarbonyl)-2,5-dimethylphenyl 3-formyl-2,4-dihydroxy-6-methylbenzoate;3-Formyl-2,4-dihydroxy-6-methylbenzoicacid3-hydroxy-4-(methoxycarbonyl)-2,5-dimethylphenylester;NSC-685591;ATRANORIN(P);Atrarin. Product Category: Heterocyclic Organic Compound. Appearance: White powder. CAS No. 479-20-9. Molecular formula: C19H18O8. Mole weight: 374.4. Purity: 0.98. IUPACName: (3-hydroxy-4-methoxycarbonyl-2,5-dimethylphenyl) 3-formyl-2,4-dihydroxy-6-methylbenzoate. Canonical SMILES: CC1=CC(=C(C(=C1C(=O)OC2=C(C(=C(C(=C2)C)C(=O)OC)O)C)O)C=O)O. Product ID: ACM479209. Alfa Chemistry ISO 9001:2015 Certified. |  |
| Atranorin | Atranorin, which can be found in the herbs of Parmelia tinctorum Despr, has a relevant redox-active action, acting as a pro-oxidant or antioxidant agent depending on the radical. Also, it will exert cytoprotective effects on cells under oxidative stress induced by H(2)O(2). It was found to be more efficient at equitoxic doses and correlated more strongly with an increased number of floating cells or a higher apoptotic index. It also exhibited significant anti-inflammatory activity in the acute model of inflammation (leukocyte migration to the peritoneal cavity), carrageenan- and arachidonic acid-induced hind paw edema in rats. Besides, Atranorin exhibited a dose-dependent antioxidant activity in vitro, as assessed by total radical-trapping antioxidant parameter and total antioxidant reactivity assays. Uses: Antinociceptive/antiinflammatory/antibacterial. Synonyms: Atranoric acid; Atranorine; Parmelin; Usnarin; Benzoic acid, 3-formyl-2,4-dihydroxy-6-methyl-, 3-hydroxy-4-(methoxycarbonyl)-2,5-dimethylphenyl ester. Grade: 98%. CAS No. 479-20-9. Molecular formula: C19H18O8. Mole weight: 374.34. |  |
| 2,4,5-Trichlorolichexanthone | 2,4,5-Trichlorolichexanthone, a new xanthones isolated from a Dimelaena Lichen, shows to cooccur with norstictic acid, connorstictic acid, atranorin and 2,4,5-trichlorolichexanthone in a Dimelaena lichen. Synonyms: 9H-Xanthen-9-one, 2,4,5-trichloro-1-hydroxy-3,6-dimethoxy-8-methyl-; 2,4,5-Trichloro-lichexanthone; 2,4,5-trichloro-1-hydroxy-3,6-dimethoxy-8-methylxanthen-9-one. CAS No. 69987-59-3. Molecular formula: C16H11Cl3O5. Mole weight: 389.61. | |
| Echinocarpic acid | It has been isolated from the lichen Pamelia norcrambidiocarpa together with atranorin and chloroatranorin. Synonyms: Benzoic acid, 2,4-dihydroxy-3,6-dimethyl-, (1,3-dihydro-1,4-dihydroxy-6-methoxy-3-oxo-5-isobenzofuranyl)methyl ester; 1',4'-dihydroxy-6'-methoxy-3'-oxo-1',3'-dihydroisobenzofuran-5'-ylmethyl 2,4-dihydroxy-3,6-dimethylbenzoate. CAS No. 79586-50-8. Molecular formula: C19H18O9. Mole weight: 390.34. | |
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