Hexylresorcinol
(Synonyms: 4-己基间苯二酚; 4-Hexylresorcinol) 目录号 : GC13621An alkylresorcinol
Cas No.:136-77-6
Sample solution is provided at 25 µL, 10mM.
Quality Control & SDS
- View current batch:
- Purity: >98.00%
- COA (Certificate Of Analysis)
- SDS (Safety Data Sheet)
- Datasheet
IC50: 1.24 μM
Hexylresorcinol is a mushroom tyrosinase inhibitor.
Tyrosinase, a copper-containing enzyme, is distributed in microorganisms, animals, and plants widely. Mushroom tyrosinase has been becoming popular due to its availability and usages in various applications.
In vitro: Previous results showed hexylresorcinol could inhibit both mono- and di-phenolase activity of mushroom tyrosinase. Moreover, hexylresorcinol at 2 μM lengthened the lag period from 98 s to 26. Hexylresorcinol could also display reversible inhibition of the enzyme. In addition, the kinetic analyses showed that hexylresorcinol was a competitive inhibitor with the apparent inhibition constant binding with free enzyme to be 0.443 μM for diphenolase [1].
In vivo: Previous in vivo study showed that hexylresorcinol could induce chromosome aberrations in mouse eukaryotic cells at doses of 0.5, 0.05, and 0.005 mg/g and the metabolic transformation of hexylresorcinol decreased its genotoxic effect in mice. Moreover, the mutagenic effect lasted for 3 days only at the highest dose of hexylresorcinol (0.5 mg/g). Thus, hexylresorcinol doses less than 0.5 mg/g were metabolized within two days to the extent of the cytotoxic effect. In addition, hexylresorcinol was transformed at a rate of 0.0025–0.025 mg/day after a single administration to mice [2].
Clinical trial: Hexylresorcinol is clinically available for topically use on small skin infections, or as an ingredient in throat lozenges. Johnson & Johnson has marketed hexylresorcinol in its skincare products as an anti-aging cream (https://en.wikipedia.org/wiki/Hexylresorcinol).
References:
[1] Chen QX,Ke LN,Song KK,Huang H,Liu XD. Inhibitory effects of hexylresorcinol and dodecylresorcinol on mushroom (Agaricus bisporus) tyrosinase. Protein J.2004 Feb;23(2):135-41.
[2] Margulis AB,Ozhiganova IV,Bushmanova OV,Kolpakov AI,Il'inskaia ON. Hexylresorcinol induces chromosome aberrations in mouse peripheral blood cells. Genetika. 2005 Aug;41(8):1045-8.
Cas No. | 136-77-6 | SDF | |
别名 | 4-己基间苯二酚; 4-Hexylresorcinol | ||
化学名 | 4-hexylbenzene-1,3-diol | ||
Canonical SMILES | CCCCCCC1=C(O)C=C(O)C=C1 | ||
分子式 | C12H18O2 | 分子量 | 194.27 |
溶解度 | DMSO : 38mg/mL | 储存条件 | Store at -20°C |
General tips | 请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效。 储备液的保存方式和期限:-80°C 储存时,请在 6 个月内使用,-20°C 储存时,请在 1 个月内使用。 为了提高溶解度,请将管子加热至37℃,然后在超声波浴中震荡一段时间。 |
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Shipping Condition | 评估样品解决方案:配备蓝冰进行发货。所有其他可用尺寸:配备RT,或根据请求配备蓝冰。 |
制备储备液 | |||
1 mg | 5 mg | 10 mg | |
1 mM | 5.1475 mL | 25.7374 mL | 51.4748 mL |
5 mM | 1.0295 mL | 5.1475 mL | 10.295 mL |
10 mM | 0.5147 mL | 2.5737 mL | 5.1475 mL |
第一步:请输入基本实验信息(考虑到实验过程中的损耗,建议多配一只动物的药量) | ||||||||||
给药剂量 | mg/kg | 动物平均体重 | g | 每只动物给药体积 | ul | 动物数量 | 只 | |||
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% DMSO % % Tween 80 % saline | ||||||||||
计算重置 |
计算结果:
工作液浓度: mg/ml;
DMSO母液配制方法: mg 药物溶于 μL DMSO溶液(母液浓度 mg/mL,
体内配方配制方法:取 μL DMSO母液,加入 μL PEG300,混匀澄清后加入μL Tween 80,混匀澄清后加入 μL saline,混匀澄清。
1. 首先保证母液是澄清的;
2.
一定要按照顺序依次将溶剂加入,进行下一步操作之前必须保证上一步操作得到的是澄清的溶液,可采用涡旋、超声或水浴加热等物理方法助溶。
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