2174-64-3
2174-64-3
Chemical Structure
5-Methoxyresorcinol
- CAS No.: 2174-64-3
- Formula:C7H8O3
- Molecular Weight:140.14
IUPAC Name: 5-methoxybenzene-1,3-diol
InChIKey: HDVRLUFGYQYLFJ-UHFFFAOYSA-N
SMILES: COC1=CC(O)=CC(O)=C1
Biological Activity: 5-Methoxyresorcinol is a model molecule of the A ring of flavonoids, specifically simulating the chemical behavior of the resorcinol-type A ring found in catechins. 5-Methoxyresorcinol exhibits extremely low reactivity of tocopherol. 5-Methoxyresorcinol hardly inhibits cholesteryl ester transfer protein (CETP)[1][2].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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5-Methoxyresorcinol | 99.63% | 5-Methoxyresorcinol is a model molecule of the A ring of flavonoids, specifically simulating the chemical behavior of the resorcinol-type A ring found in catechins. 5-Methoxyresorcinol exhibits extremely low reactivity of tocopherol. 5-Methoxyresorcinol hardly inhibits cholesteryl ester transfer protein (CETP). | ||||||||||||||||||||
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5-Methoxyresorcinol (Standard) | ≥98% | 5-Methoxyresorcinol (Standard) is an analytical standard for 5-Methoxyresorcinol (HY-W015752). This product is intended for research and analytical applications. 5-Methoxyresorcinol is a model molecule for the A ring of flavonoids, specifically mimicking the chemical behavior of the resorcinol-type A ring in catechins. 5-Methoxyresorcinol exhibits very low tocopherol regeneration activity. 5-Methoxyresorcinol shows little inhibition of cholesteryl ester transfer protein (CETP). | ||||||||||||||||||||
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Structural Analogs
-
Similarity Score 0.85
HY-W0136752-Methoxyhydroquinone -
Similarity Score 0.85
HY-W001117R3,5-Dimethoxyphenol (Standard) -
Similarity Score 0.84
HY-D0168Orcinol -
Similarity Score 0.84
HY-W0157155-Methylresorcinol monohydrate -
Similarity Score 0.82
HY-13938Iretol -
Similarity Score 0.81
HY-W0074163,5-Dihydroxybenzaldehyde -
Similarity Score 0.81
HY-Y18403-Methoxyphenol -
Similarity Score 0.80
HY-W1165763-Methoxycatechol -
Explore the MedChemAI to find more analogs
References
- [1]. Mukai K, et al. Structure-activity relationship of the tocopherol-regeneration reaction by catechins. Free Radic Biol Med. 2005 May 1;38(9):1243-56. [Content Brief]
- [2]. Hirata H, et al. Xanthohumol, a prenylated chalcone from Humulus lupulus L., inhibits cholesteryl ester transfer protein. Food Chem. 2012 Oct 1;134(3):1432-7. [Content Brief]
