Camelliquercetiside D
Camelliquercetiside D is a natural product. Camelliquercetiside D can be isolated from the leaves of Camellia sinensis. Camelliquercetiside D inhibits alcohol dehydrogenase, with an IC50 of 41.5 μM against yeast ADH. Camelliquercetiside D exhibits scavenging activity against DPPH.
For research use only. We do not sell to patients.
- CAS No.: 194292-73-4
- Formula: C36H36O18
- Molecular Weight:756.66
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Storage:
Please store the product under the recommended conditions in the Certificate of Analysis.
Biological Activity
Camelliquercetiside D inhibits alcohol dehydrogenase derived from Saccharomyces cerevisiae, with an IC50 value of 41.5 μM[1].
Camelliquercetiside D scavenges DPPH free radicals with an IC50 value of 29.2 μM[1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
Chemical Information
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CAS No. 194292-73-4
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Molecular Weight 756.66
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Formula C36H36O18
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SMILES
O=C(C(O[C@H]1[C@@H]([C@H]([C@@H]([C@H](O1)CO[C@H]2[C@@H]([C@@H]([C@H]([C@@H](O2)C)O)O)O)O)O)OC(/C=C/C3=CC=C(C=C3)O)=O)=C(C4=CC(O)=C(C=C4)O)OC5=CC(O)=C6)C5=C6O
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Structure Classification
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Initial Source
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Shipping
Room temperature in continental US; may vary elsewhere.
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Storage
Please store the product under the recommended conditions in the Certificate of Analysis.
Purity & Documentation
References
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)