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Tofacitinib citrate

产品号 S5001 公司名称 Selleck Chemicals
CAS号 540737-29-9 公司网站 http://www.selleckchem.com
分子式 C22H28N6O8 电 话 (877) 796-6397
分子量 504.49312 传 真 (832) 582-8590
纯 度 电子邮件 sales@selleckchem.com
保 存 -20°C Chembase数据库ID: 73080

产品价格信息

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产品别名

标题
Tofacitinib citrate
IUPAC标准名
2-hydroxypropane-1,2,3-tricarboxylic acid; 3-[(3R,4R)-4-methyl-3-[methyl({7H-pyrrolo[2,3-d]pyrimidin-4-yl})amino]piperidin-1-yl]-3-oxopropanenitrile
IUPAC传统名
citro; tofacitinib
别名
CP-690550

产品登记号

CAS号 540737-29-9

产品性质

作用靶点 JAK
成盐信息 citrate
溶解度 DMSO
保存条件 -20°C

产品详细信息

详细说明 (English)
Protocol
Kinase Assay [1]
Enzyme assays The JAK1, JAK2, and JAK3 kinase assays utilize a protein expressed in baculovirus-infected SF9 cells (a fusion protein of GST and the catalytic domain of human JAK enzyme) purified by affinity chromatography on glutathione?Sepharose. The substrate for the reaction is polyglutamic acid-tyrosine [PGT (4:1)], coated onto Nunc Maxi Sorp plates at 100 μg/mL overnight at 37 °C. The plates are washed three times, and JAK enzyme is added to the wells, which contained 100 μL of kinase buffer (50 mM HEPES, pH 7.3, 125 mM NaCl, 24 mM MgCl2) + ATP + 1 mM sodium orthovanadate). For Tofacitinib citrate, it is also added for kinase assay at different doses. After incubation at room temperature for 30 min, the plates are washed three times. The level of phosphorylated tyrosine in a given well is determined by standard ELISA assay utilizing an anti-phosphotyrosine antibody.
Cell Assay [2]
Cell Lines FDCP-EpoR JAK2WT and JAK2V617F cell lines
Concentrations 0-4 μM
Incubation Time 72 hours
Methods Determination of growth inhibition by Tofacitinib citrate is performed using identical culture conditions for both FDCP-EpoR JAK2WT and JAK2V617F cell lines. Briefly, 1 × 105 cells/mL are cultured in 96-well flat-bottom plates at 37 °C in a humidified 5% CO2 atmosphere using RPMI 1640 supplemented with 1.25% FCS, and 5% WEHI supernatant. Decreased FCS concentration is necessary to prevent binding between Tofacitinib citrate and serum proteins. Growth inhibition assays are terminated by addition of 20 μL CellTiter96 One Solution Reagent. Flat-bottom plates are incubated for an additional 3 hours for MTT assay. Absorbance is determined at 595 nm on a BioTek Synergy-HT microplate reader. Results are the average ± standard deviation of three independent determinations.
Animal Study [2]
Animal Models Mauritius-origin adult cynomolgus monkeys
Formulation 0.5% methylcellulose in distilled water
Doses 10, 30 mg/kg/d
Administration Oral gavage
References
[1] Flanagan ME, et al. J Med Chem, 2010, 53(24), 8468-8484.
[2] Manshouri T, et al. Cancer Sci, 2008, 99(6), 1265-1273.
[3] Conklyn M, et al. J Leukoc Biol, 2004, 76(6), 1248-1255.