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1、Hotline: 400-820-3792Inhibitors Agonists Screening Librarieswww.MedChemETapinarofCat. No.: HY-109044CAS No.: 79338-84-4Synonyms: WBI 1001; Benvitimod; GSK2894512分式: CHO分量: 254.32作靶點: Aryl Hydrocarbon Receptor作通路: Immunology/Inflammation儲存式: 4C, protect from light* In solvent : -80C, 6 months; -20C,
2、1 month (protect fromlight)溶解性數(shù)據(jù)體外實驗 DMSO : 125 mg/mL (491.51 mM)* means soluble, but saturation unknown.Mass Solvent1 mg 5 mg 10 mg Concentration制備儲備液1 mM 3.9321 mL 19.6603 mL 39.3205 mL5 mM 0.7864 mL 3.9321 mL 7.8641 mL10 mM 0.3932 mL 1.9660 mL 3.9321 mL請根據(jù)產(chǎn)品在不同溶劑中的溶解度,選擇合適的溶劑配制儲備液,并請注意儲備液的保存式和期限。
3、體內(nèi)實驗請根據(jù)您的實驗動物和給藥式選擇適當?shù)娜芙獍?,配制前請先配制澄清的儲備液,再依次添加助溶?為保證實驗結(jié)果的可靠性,體內(nèi)實驗的作液,建議您現(xiàn)現(xiàn)配,當天使;澄清的儲備液可以根據(jù)儲存條件,適當保存;以下溶劑前的百分 指該溶劑在您配制終溶液中的體積占):1. 請依序添加每種溶劑: 10% DMSO 40% PEG300 5% Tween-80 45% salineSolubility: 2.5 mg/mL (9.83 mM); Clear solution2. 請依序添加每種溶劑: 10% DMSO 90% (20% SBE-CD in saline)Solubility: 2.5 mg/mL
4、 (9.83 mM); Clear solution3. 請依序添加每種溶劑: 10% DMSO 90% corn oil1/2 Master of Small Molecules 您邊的抑制劑師www.MedChemESolubility: 2.5 mg/mL (9.83 mM); Clear solutionBIOLOGICAL ACTIVITY物活性 Tapinarof種天然的芳烴受體 (AhR) 激動劑,EC50 為 13 nM。IC50 & Target EC50: 13 nM (AhR) 1體外研究 Tapinarof activates the AhR pathway throu
5、gh direct binding. Tapinarof dose-dependently induces nucleartranslocation of AhR in immortalized keratinocytes (HaCaT) (EC50=0.16 nM) 1.體內(nèi)研究 Tapinarof acts through AhR to reduce inflammation in IMQ-treated mice. AhR-sufficient mice on a C57Bl/6background exhibit a reduced clinical score after treat
6、ment with Tapinarof or 6-formylindolo(3,2-b)carbazole(FICZ). In contrast, AhR KO mice do not respond to the anti-inflammatory effects of Tapinarof. FICZ is usedas a comparator in these studies and yields similar results, with dramatically reduced inflammatoryresponses in wild-type, but not AhR KO mi
7、ce 1.PROTOCOLCell Assay 1 HaCaT cells (10,000 cells/well) are cultured in 96-well Greiner CLEAR plates in 100 L DMEM with HEPES,Glutamax and 10% fetal bovine serum to confluence. Media is replaced with 100 L media containing 0.2%heat-inactivated, charcoal-stripped fetal bovine serum and incubated ov
8、ernight. Titrating concentrations ofTapinarof (10-8 M ,10-6 M, 10-4 M, 0.01 M, and 1 M) are added for 30 minutes followed by washingand fixing in ice-cold methanol:acetone (50:50). Samples are blocked with 3% BSA for 1 hour, and thenwashed again in phosphate buffered saline with 0.1% Tween-20. Next,
9、 cells are stained with 50 L of 1:50dilution anti-AhR antibody in 3% BSA, followed by 50 L secondary antibody (1:500 dilution chicken anti-rabbit AlexaFluor488 and 1:2,000 dilution Hoechst 33342) in 3% BSA/phosphate buffered saline. Images areacquired on InCell 2000 and/or Opera. Image analysis is p
10、erformed using InCell Analyzer Workstation and/orColumbus 1.MCE has not independently confirmed the accuracy of these methods. They are for reference only.Animal Mice 1Administration 1 Female BALB/c mice (BALB/cByJRj) are used. Studies are performed using 100 L of Tapinarof (1%) orFICZ (0.01%, at th
11、e limit of solubility) in 60% ethanol: 40% water 1.MCE has not independently confirmed the accuracy of these methods. They are for reference only.REFERENCES1. Smith SH, et al. Tapinarof Is a Natural AhR Agonist that Resolves Skin Inflammation in Mice and Humans. J Invest Dermatol. 2017Oct;137(10):2110-2119.McePdfHeight2/2 Master of Small Molecules 您邊的抑制劑師www.MedChemECaution: Product has n
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