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T-5224

货号 T5416Cas号 530141-72-1 一键复制产品信息纯度: 99.29%
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T-5224 是选择性的转录因子 c-Fos/activator protein (AP)-1 抑制剂,具有抗炎作用。T-5224 能够特异性抑制 c-Fos/c-Jun 的 DNA 结合活性,抑制 IL-1β 诱导的 Mmp-3、Mmp-13、Adamts-5 转录上调,但对其他转录因子的结合活性无影响。T-5224 可用于类风湿关节炎、骨关节炎、软骨退变研究。

T-5224

一键复制产品信息
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纯度: 99.29%

货号 T5416Cas号 530141-72-1

T-5224 是选择性的转录因子 c-Fos/activator protein (AP)-1 抑制剂,具有抗炎作用。T-5224 能够特异性抑制 c-Fos/c-Jun 的 DNA 结合活性,抑制 IL-1β 诱导的 Mmp-3、Mmp-13、Adamts-5 转录上调,但对其他转录因子的结合活性无影响。T-5224 可用于类风湿关节炎、骨关节炎、软骨退变研究。

T-5224
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规格价格库存数量
1 mg
¥ 378
现货
2 mg
¥ 548
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5 mg
¥ 888
现货
10 mg
¥ 1,330
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25 mg
¥ 2,250
现货
50 mg
¥ 3,280
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100 mg
¥ 4,890
现货
500 mg
¥ 9,870
现货
1 mL x 10 mM (in DMSO)
¥ 987
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TargetMol的所有产品仅用作科学研究或药证申报,不能被用于人体,我们不向个人提供产品和服务。请您遵守承诺用途,不得违反法律法规规定用于任何其他用途。

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选择批次:
纯度: 99.15%
颜色: 白色
资源下载: COA LCMS HNMR产品操作手册

产品介绍


生物活性
产品描述
T-5224 is a selective inhibitor of the transcription factor c-Fos/activator protein (AP)-1 with anti-inflammatory effects. T-5224 specifically suppresses the DNA-binding activity of c-Fos/c-Jun, thereby inhibiting IL-1β-induced transcriptional upregulation of Mmp-3, Mmp-13, and Adamts-5, without affecting the binding activity of other transcription factors. T-5224 can be used in research on rheumatoid arthritis, osteoarthritis, and cartilage degeneration.
靶点活性
AP-1 (NIH3T3 cells):10 μM, MMP1 (SW982 cells):10 μM, β-hexosaminidase (RBL-2H3 cells):18.30 ± 1.48 µM
体外活性

方法:人表皮角质形成细胞 NHEKs 加入 0.1-1 μM 浓度的 T-5224 ,处理 24 小时后,MTT 法检测细胞活力。
结果:该浓度范围内 T-5224 无细胞毒性、不影响细胞增殖。[1]
方法:HSC-3-M3, OSC-19 中加入梯度浓度 T-5224 (0, 20, 40, 80 μM),划痕后 24 小时测量细胞迁移面积。
结果:T-5224 呈剂量依赖性抑制两种细胞的迁移,80 μM 时迁移几乎被完全抑制。[2]

体内活性

方法:8~10 周雌性 BALB/c 小鼠构建 DNFB 模型,模型构建成功后,给药 1% T-5224/1% baricitinib/1% T-5224+1% baricitinib 软膏,每侧耳 25mg,1 次 / 天,共 8 天。
结果:T-5224 显著抑制炎症、恢复 Flg 表达,T-5224 可恢复 Elovl6;T-5224抑制 Il17a/Il17f 。[1]
方法:BALB/c 裸鼠,将 HSC-3-M3 细胞(1×10⁵)注射入舌部,建立原位移植瘤模型,从肿瘤接种后第 1 天开始口服灌胃 T-5224 (150 mg/kg/天),每日一次,连续给药 4 周。
结果:两组间原发肿瘤体积无显著差异,T-5224 对体重也无明显影响。 颈淋巴结转移率,对照组为 74.1% (20/27),T-5224 治疗组为 40.0% (12/30),差异显著。[2]

激酶实验
The DNA binding activity of transcription factors was measured using the TransAM kits. Nuclear extracts containing factors such as c-Fos/AP-1, c-Jun/AP-1, ATF-2, C/EBPa, MyoD, Sp-1 or NF-kB/p65 and various concentrations of T-5224 were added in the multi-well plates precoated with respective consensus double-stranded (ds)DNA oligomers. After incubation for 1 h, the transcription factor bound to its respective consensus dsDNA sequences was detected by using antibodies reactive against the respective transcription factors according to the manufacturer's protocol [1].
细胞实验
NIH/3T3 cells were transiently transfected with the luciferase reporter plasmids pAP-1-Luc (× 7 TGACTAA), pNF-kB-Luc (× 5 TGGGGACTTTCCGC) or control phRL-TK, and cultured overnight. Cells were incubated in 0.5% FBS/DMEM containing T-5224 for 1 h, and then stimulated with PMA (10 ng/ml) or TNFa (10 ng/ml), and then cultured for 3 h, followed by measurement of lysate by using dual-luciferase reporter assay system [1].
动物实验
Mice were housed in an SPF (specific pathogen-free) grade environment and provided food and water ad libitum with a 12 h:12 h light/dark cycle. Male 8-week-old DBA/1J mice were immunized with bovine type II collagen emulsified in Freund's complete adjuvant on days 0 and 21. T-5224, MTX and LEF were orally administered once per day. Arthritis was assessed in a blind fashion for four paws per mouse using the following score: 0, uninvolved; 1, swelling of ≤2 toes or slight swelling in ankles and wrists; 2, swelling of ≥3 toes or moderate swelling in ankles and wrists; 3, extensive swelling of total paw. X-ray films of four paws taken using Softex were assessed for joint destruction in 2nd to 5th proximal interphalangeal joints and five metatarsophalangeal joints of four paws, the carpal joints of the forepaws, and the tarsal and calcaneal joints of the hind paws. Score was: 0, no change; 1, partial erosion; 2, complete erosion for joints; and 0, negative; 0.5, positive for osteoporosis. IL-1β (500 ng per unilateral hind paw) was administered into the footpads. The mice with ≥1 arthritis score were treated with either anti-TNFα antibody at 50 or 250 μg/mouse, intraperitoneally (i.p.) twice a week and/or with 3 mg/kg T-5224, orally once daily [1].
化学信息
分子量517.53
分子式C29H27NO8
CAS No.530141-72-1
SmilesOC(=O)CCc1cc(ccc1OCc1ccc2c(c1)o[nH]c2=O)C(=O)c1ccc(OC2CCCC2)cc1O
密度1.376 g/cm3 (Predicted)
储存&溶解度
存储

Store at low temperature Powder: -20°C for 3 years | In solvent: -80°C for 1 year Shipping with blue ice/Shipping at ambient temperature.

实际储存温度请以COA为准

溶解度信息
H2O: Insoluble
DMSO: 240 mg/mL (463.74 mM), Sonication is recommended.
体内实验配方
10% DMSO+40% PEG300+5% Tween 80+45% Saline: 5 mg/mL (9.66 mM), Suspension.
请按顺序添加溶剂,在添加下一种溶剂之前,尽可能使溶液澄清。如有必要,可通过加热、超声、涡旋处理进行溶解。工作液建议现配现用。以上配方仅供参考,体内配方并不是绝对的,请根据不同情况进行调整。
溶液配制表
DMSO
1mg5mg10mg50mg
1 mM1.9323 mL9.6613 mL19.3226 mL96.6128 mL
5 mM0.3865 mL1.9323 mL3.8645 mL19.3226 mL
10 mM0.1932 mL0.9661 mL1.9323 mL9.6613 mL
20 mM0.0966 mL0.4831 mL0.9661 mL4.8306 mL
50 mM0.0386 mL0.1932 mL0.3865 mL1.9323 mL
100 mM0.0193 mL0.0966 mL0.1932 mL0.9661 mL
该溶液配制表仅适用于固体产品。对于液体产品,请根据标明的浓度或密度计算稀释方案。

计算器

  • 摩尔浓度 计算器
  • 稀释 计算器
  • 配液 计算器
  • 分子量 计算器

体内实验配液计算器

请在以下方框中输入您的动物实验信息后点击计算,可以得到母液配置方法和体内配方的制备方法:
比如您的给药剂量是10 mg/kg,每只动物体重20 g,给药体积100 μL, 一共给药动物10只,您使用的配方为 10% DMSO + 40% PEG300 + 5% Tween 80 + 45% Saline / PBS / ddH2O, 那么您的工作液浓度为2 mg/mL
母液配置方法:2 mg 药物溶于 100 μL DMSO ( 母液浓度为 20 mg/mL ), 如您需要配置的浓度超过该产品的溶解度,请先与我们联系。
体内配方的制备方法:100 μL DMSO 母液, 添加 400 μL PEG300 混匀澄清, 再加 50 μL Tween 80, 混匀澄清, 再加 450 μL Saline / PBS / ddH2O 混匀澄清
以上为“体内实验配液计算器”的使用方法举例,并不是具体某个化合物的推荐配制方式,请根据您的实验动物和给药方式选择适当的溶解方案。
方案所需的各类助溶剂如: DMSOPEG300PEG400Tween 80SBE-β-CD玉米油等, 均可在TargetMol网站点击购买。
1 请输入动物实验的基本信息
mg/kg
g
μL
2 请输入动物体内配方组成,不同的产品配方组成不同,如有配方需求,可先联系我们提供正确的体内配方。
% DMSO
%
% Tween 80
% Saline/PBS/ddH2O

剂量转换

对于不同动物的给药剂量换算,您也可以参考 更多

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