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形式
powder
质量水平
储存条件
protect from light
颜色
white to beige
溶解性
DMSO: ≥20 mg/mL
储存温度
−20°C
SMILES字符串
CCCCCCCCCCCCCCCc1cccc(O)c1C(O)=O
InChI
1S/C22H36O3/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-16-19-17-15-18-20(23)21(19)22(24)25/h15,17-18,23H,2-14,16H2,1H3,(H,24,25)
InChI key
ADFWQBGTDJIESE-UHFFFAOYSA-N
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应用
漆树酸已：
- 用作组蛋白乙酰化酶(HAT)抑制剂，以研究其对大鼠皮层神经元的影响
- 用作体外乙酰化试验的阳性对照
- 用作乙酰化酶抑制剂，以研究其对转染人胚胎肾细胞的核糖核酸输出1 (Rae-1)蛋白乙酰化的影响
生化/生理作用
漆树酸是一种从腰果果壳中提取的天然生物活性化合物。它具有抗真菌、抗菌、抗白蚁和杀软体动物的活性。漆树酸作为一种治疗剂，可对抗肥胖、癌症、炎症疾病和氧化损伤。它作为各种酶的抑制剂，如脂氧合酶(LOX-1)、黄嘌呤氧化酶、核因子κ B (NFκB)激酶、酪氨酸酶和脲酶。
漆树酸是 HAT（组蛋白乙酰转移酶）抑制剂。
特点和优势
这种化合物是基因调控研究的特色产品。点击此处发现更多特色基因调控产品。在sigma.com/discover-bsm可了解更多关于生物活性小分子的其他研究领域。
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
Mingxi Li et al.
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 877(30), 3885-3892 (2009-10-16)
Global histone modifications and their putative relevance to short and long term cellular programming have drawn substantial interest in the study of chromatin. Here we describe the use of reverse-phase liquid chromatography coupled to Linear Ion Trap-Fourier Transform Mass Spectrometry
Mahadevappa Hemshekhar et al.
Basic & clinical pharmacology & toxicology, 110(2), 122-132 (2011-11-23)
Anacardic acid (AA) is a bioactive phytochemical found in nutshell of Anacardium occidentale. Chemically, it is a mixture of several closely related organic compounds, each consisting of salicylic acid substituted with an alkyl chain. The traditional Ayurveda depicts nutshell oil
ZhenHua Ni et al.
Respiratory research, 12, 47-47 (2011-04-15)
"Phosphatase and tensin homolog deleted on chromosome 10" (PTEN) is mostly considered to be a cancer-related gene, and has been suggested to be a new pathway of pathogenesis of asthma. The purpose of this study was to investigate the effects
Massimo Ghizzoni et al.
European journal of medicinal chemistry, 47(1), 337-344 (2011-11-22)
Histone acetyltransferases are important enzymes that regulate various cellular functions, such as epigenetic control of DNA transcription. Development of HAT inhibitors with high selectivity and potency will provide powerful mechanistic tools for the elucidation of the biological functions of HATs
Valentina Izzo et al.
Cell cycle (Georgetown, Tex.), 16(3), 271-279 (2017-01-07)
Phase II clinical trials indicate that the combination of cysteamine plus epigallocatechin gallate (EGCG) is effective against cystic fibrosis in patients bearing the most frequent etiological mutation (CFTRΔF508). Here, we investigated the interaction between both agents on cultured respiratory epithelia
商品
We offer a variety of small molecule research tools, such as transcription factor modulators, inhibitors of chromatin modifying enzymes, and agonists/antagonists for target identification and validation in gene regulation research; a selection of these research tools is shown below.
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