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Supplier NameMedChemExpress (MCE)
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Emailsales@medchemexpress.com; tech@medchemexpress.com
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Product Name4-Butylresorcinol
Synonyms4-Butylresorcinol
4-N-BUTYLRESORCINOL
4-Butylbenzene-1,3-diol
4-phenylbutane-1,3-diol
1,3-Benzenediol,4-butyl-
2,4-Dihydroxy-n-bytyl benzen
2,4-DIHYDROXY-N-BUTYL BENZEN

Synonyms

4-Butylresorcinol
4-N-BUTYLRESORCINOL
4-Butylbenzene-1,3-diol
4-phenylbutane-1,3-diol
1,3-Benzenediol,4-butyl-
2,4-Dihydroxy-n-bytyl benzen
2,4-DIHYDROXY-N-BUTYL BENZEN
2,4-DIHYDROXY-N-BUTYL BENZENE
4-06-00-06003 (Beilstein Handbook Reference
4-06-00-06003 (Beilstein Handbook Reference)
CAS18979-61-8
EINECS
Chemical FormulaC10H14O2
Molecular Weight166.22
inchiInChI=1/C10H14O2/c1-2-3-4-8-5-6-9(11)7-10(8)12/h5-7,11-12H,2-4H2,1H3
Package10 mM * 1 mL;25 mg;50 mg;100 mg
PriceEmail to quote
Descriptions4-Butylresorcinol

4-Butylresorcinol

MedChemExpress (MCE)

HY-107369

18979-61-8

Butylresorcinol

99.49%

Powder -20°C 3 years 4°C 2 years In solvent -80°C 2 years -20°C 1 year

Room temperature in continental US

Descriptions

4-Butylresorcinol

4-Butylresorcinol

MedChemExpress (MCE)

HY-107369

18979-61-8

Butylresorcinol

99.49%

Powder -20°C 3 years 4°C 2 years In solvent -80°C 2 years -20°C 1 year

Room temperature in continental US
may vary elsewhere.

4-Butylresorcinol is a phenol derivative which can inhibit tyrosinase with IC50 of 11.27 μM.

It shows that 4-Butylresorcinol (4-n-butylresorcinol) significantly inhibits melanin synthesis in a concentration-dependent manner. In addition, it is also found to inhibit the activity of tyrosinase, the rate-limiting melanogenic enzyme. 4-Butylresorcinol does not induce ERK, Akt activation, or MITF degradation, and has no effect on cAMP response element binding protein (CREB) phosphorylation, which stimulates MITF expression. 4-Butylresorcinol strongly reduces tyrosinase activity in a cell-free system. Moreover, 4-Butylresorcinol shows an additive effect in combination with hinokitiol, which reduces MITF expression[2].

Mel-Ab cell line is a mouse-derived spontaneously immortalized melanocyte cell line that produces large amounts of melanin. Mel-Ab cells are incubated in DMEM supplementing with 10% fetal bovine serum (FBS), 100 nM TPA, 1 nM CT, 50 μg/mL streptomycin, and 50 U/mL penicillin at 37 °C in 5% CO2. Cell viability is determined using a crystal violet assay. After incubating cells with test substances for 24 h, the medium is removed and stained with 0.1% crystal violet in 10% ethanol for 5 min at room temperature and then rinsed four times with distilled water[2].

Briefly, Mel-Ab cells are cultured in 60 mm dishes. After incubating with test substances (including 4-Butylresorcinol) in DMEM containing 2% FBS for 4d, the cells are washed with ice-cold PBS and lysed with phosphate buffer (pH 6.8) containing 1% Triton X-100. The cells are then disrupted by freeze-thawing, and lysates are clarified by centrifuging at 10000×g for 5 min. After quantifying protein levels and adjusting concentrations with lysis buffer, 90 μL of each lysate, is placed in a well of a 96-well plate, and 10 μL of 10 mM L-DOPA is then added. Control wells contain 90 μL of lysis buffer and 10 μL of 10mM L-DOPA[2].

IC50: 11.27 μM (4-Butylresorcinol)[1] In Vitro It shows that 4-Butylresorcinol (4-n-butylresorcinol) significantly inhibits melanin synthesis in a concentration-dependent manner. In addition, it is also found to inhibit the activity of tyrosinase, the rate-limiting melanogenic enzyme. 4-Butylresorcinol does not induce ERK, Akt activation, or MITF degradation, and has no effect on cAMP response element binding protein (CREB) phosphorylation, which stimulates MITF expression. 4-Butylresorcinol strongly reduces tyrosinase activity in a cell-free system. Moreover, 4-Butylresorcinol shows an additive effect in combination with hinokitiol, which reduces MITF expression[2]. MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only. 0 --> 4-Butylresorcinol Related Antibodies

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[1]. Jiang Y, et al. Synthesis and biological evaluation of unsymmetrical curcumin analogues as tyrosinaseinhibitors. Molecules. 2013 Apr 3
18(4):3948-61.
[Content Brief]

[2]. Kim DS, et al. Inhibitory effects of 4-n-butylresorcinol on tyrosinase activity and melanin synthesis. Biol Pharm Bull. 2005 Dec
28(12):2216-9.
[Content Brief]

Supplier Websitehttps://www.medchemexpress.com/4-Butylresorcinol.html
Last Update2025-05-21 16:50:25
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