2896-60-8
2896-60-8
Chemical Structure
4-Ethylresorcinol
- CAS No.: 2896-60-8
- Formula:C8H10O2
- Molecular Weight:138.17
IUPAC Name: 4-ethylbenzene-1,3-diol
InChIKey: VGMJYYDKPUPTID-UHFFFAOYSA-N
SMILES: OC1=CC=C(CC)C(O)=C1
Biological Activity: 4-Ethylresorcinol is a derivative of resorcinol and can serve as a substrate for tyrosinase. 4-Ethylresorcinol has anti-hyperpigmentation and antioxidant effects and can inhibit melanin synthesis. 4-Ethylresorcinol has potential whitening value[1][2].
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4-Ethylresorcinol | 99.71% | 4-Ethylresorcinol is a derivative of resorcinol and can serve as a substrate for tyrosinase. 4-Ethylresorcinol has anti-hyperpigmentation and antioxidant effects and can inhibit melanin synthesis. 4-Ethylresorcinol has potential whitening value. | ||||||||||||||||||||
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4-Ethylresorcinol (Standard) | ≥98% | 4-Ethylresorcinol (Standard) is the analytical standard of 4-Ethylresorcinol (HY-W015782). This product is intended for research and analytical applications. 4-Ethylresorcinol is a derivative of resorcinol and can serve as a substrate for tyrosinase. 4-Ethylresorcinol has anti-hyperpigmentation and antioxidant effects and can inhibit melanin synthesis. 4-Ethylresorcinol has potential whitening value. | ||||||||||||||||||||
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Structural Analogs
-
Similarity Score 0.91
HY-W265757R4-Ethylcatechol (Standard) -
Similarity Score 0.87
HY-W1677082-Ethyl-5-methylphenol -
Similarity Score 0.87
HY-1073694-Butylresorcinol -
Similarity Score 0.87
HY-W248907Gentisyl alcohol -
Similarity Score 0.85
HY-W012817Methylhydroquinone -
Similarity Score 0.84
HY-N0960(2,4-Dihydroxyphenyl)acetonitrile -
Similarity Score 0.84
HY-W1090384-Propylcatechol -
Similarity Score 0.83
HY-W0187593-Ethylphenol -
Similarity Score 0.82
HY-W0128144-Methylcatechol -
Explore the MedChemAI to find more analogs
References
- [1]. Jimenez AG, et, al. Characterization of the action of tyrosinase on resorcinols. Bioorg Med Chem. 2016 Sep 15;24(18):4434-4443. [Content Brief]
- [2]. Lam RYY, et, al. Mechanistic studies of anti-hyperpigmentary compounds: elucidating their inhibitory and regulatory actions. Int J Mol Sci. 2014 Aug 21;15(8):14649-68. [Content Brief]
