Tropolone (Standard)
Tropolone is a seven-membered non-benzenoid aromatic compound, which is the precursor of many Azulene derivatives. Tropolone is a potent mushroom tyrosinase inhibitor with an IC50 value of 0.4 μM. Its inhibitory effect can be achieved by dialysis or excess CU2+ Reversa. Tropolone exhibits broad anti-viral and anti-fungal activity and is synergistic upon co-treatment with nucleos(t)ide analog drugs. Tropolone is a promising candidate for research in osteosarcoma.
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- Pureté : 98%
- CAS No.: 533-75-5
- Formule: C7H6O2
- Masse moléculaire:122.12
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Stockage:
Please store the product under the recommended conditions in the Certificate of Analysis.
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Product Information
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Chemical Information
- Pureté et documentation
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Help & FAQs
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HY-N7135
TropoloneTropone Derivatives; Tyrosinase Inhibitor; Virus Inhibitor; Funga Inhibitor -
HY-N0322
Cholesterol (from animal)ERRα Agonist -
HY-N0322R
Cholesterol (Standard) -
HY-B0350A
Sodium butyrateHDAC Inhibitor -
HY-N0192
ArbutinEndogenous Metabolite -
HY-N0322E
Cholesterol (synthetic)ERRα Agonist -
HY-N0616
TrifolirhizinPterocarpan Flavonoid -
HY-N0192R
Arbutin (Standard)Endogenous Metabolite -
HY-W003607
3-O-Ethyl-L-ascorbic acidVitamin C Derivative -
HY-N3266
Methyl rosmarinateHydroxycinnamic Acid -
HY-N2278
Kushenol ATyrosinase Inhibitor -
HY-N1238
β-SitostenoneTyrosinase/COX Inhibitor
Product Information
Information
Application
The compound is the grade of analytical standard, which is the reference standard supplied assay. It is commonly used in qualitative, quantitative and methodological research experiments in HPLC, GC and MS.
Chemical Information
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CAS No. 533-75-5
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Masse moléculaire 122.12
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Formule C7H6O2
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SMILES
O=C1C(O)=CC=CC=C1
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Structure Classification
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Initial Source
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Livraison
Room temperature in continental US; may vary elsewhere.
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Stockage
Please store the product under the recommended conditions in the Certificate of Analysis.
Pureté et documentation
Références
[1]. Woodson ME, et al. In vitro evaluation of tropolone absorption, metabolism, and clearance. Antiviral Res. 2023 Dec;220:105762. [Content Brief]
[2]. Haney SL, et al. Investigation of the activity of a novel tropolone in osteosarcoma. Drug Dev Res. 2024 Feb;85(1):e22129. [Content Brief]
[3]. Donald D Nolting,et al. Synthesis of bicyclo[5.3.0]azulene derivatives. Nat Protoc. 2009; 4(8): 1113–1117. [Content Brief]
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
Tropolone (Standard) Related Classifications
HY-N7135R Related Classifications
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