TP-472
CAS No. 2079895-62-6
TP-472 ( TP472 )
产品货号. M13237 CAS No. 2079895-62-6
TP-472 是一种新型 BRD9/7 化学探针,具有优异的效力(ITC 测定的 BRD9 KD=33nM;BRD7 KD=340 nM)。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 5MG | ¥4541 | 有现货 |
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| 500MG | 获取报价 | 有现货 |
|
| 1G | 获取报价 | 有现货 |
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生物学信息
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产品名称TP-472
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注意事项本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
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产品简述TP-472 是一种新型 BRD9/7 化学探针,具有优异的效力(ITC 测定的 BRD9 KD=33nM;BRD7 KD=340 nM)。
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产品描述TP-472 is a novel BRD9/7 chemical probe that has excellent potency (BRD9 KD=33nM; BRD7 KD=340 nM by ITC), >30 fold selectivity over all other bromodomain family members except BRD7 and is cell active (EC50 320 nM in a BRD9 NanoBRET assay); has a good PK profile and is suitable for in vivo applications.
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体外实验TP-472 (1 μM, 3 μM; 24-216 hours) yields concentration-dependent growth defects in ESCs.TP-472 (0.1-10 μM; 24 h) effectively inhibits the growth of both the BRAF mutant melanoma cell lines at 5 and 10 μM concentrations.TP-472 (for 2 weeks) also strongly inhibits the long-term survival of multiple melanoma cell lines (M14, SKMEL-28, A375, and A2058) at concentrations of 5 and 10 μM.TP-472 (5-10 μM; 24 h) treatment downregulates genes encoding various extracellular matrix (ECM) proteins, including integrins, collagens, and fibronectins in A375 cells.TP-472 (0.1-10 μM; 24 h) results in the upregulation of pro-apoptotic genes (BAX, MDM2, CDKN1A) in A375 cells.Cell Viability Assay Cell Line:Embryonic stem cells Concentration:1 μM, 3 μM Incubation Time:24 hours, 72 hours, 120 hours, 168 hours, 216 hours Result:Yields concentration-dependent growth defects in ESCs.Cell Proliferation Assay Cell Line:M14 and SKMEL-28 cells Concentration:0.1 μM, 0.5 μM, 1 μM, 2 μM, 5 μM, 10 μM Incubation Time:24 h Result:Effectively inhibited the growth of both the BRAF mutant melanoma cell lines.Western Blot Analysis Cell Line:A375 cells Concentration:10 μM Incubation Time:24 h Result:Resulted in the upregulation of pro-apoptotic genes.
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体内实验TP-472 (20 mg/kg; i.p.; three times a week; for 5 weeks) significantly inhibits the subcutaneous tumor growth in melanoma xenograft mouse model. Animal Model:NSG mice injected with A375-MA2 cells (male five- to six-week-old) Dosage:20 mg/kg Administration:i.p.; three times a week; for 5 weeks Result:Significantly inhibited the subcutaneous tumor growth in melanoma xenograft mouse model.
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同义词TP472
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通路Chromatin/Epigenetic
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靶点Bromodomain
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受体Bromodomain
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研究领域——
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适应症——
化学信息
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CAS Number2079895-62-6
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分子量333.391
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分子式C20H19N3O2
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纯度>98% (HPLC)
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溶解度In Vitro:?DMSO : 100 mg/mL (299.96 mM)
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SMILESCC1=C(C=C(C=C1)C(=O)NC2CC2)C3=C4N=CC=CN4C(=C3)C(=O)C
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化学全称3-(6-acetylpyrrolo[1,2-a]pyrimidin-8-yl)-N-cyclopropyl-4-methylbenzamide
运输与储存
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储存条件(-20℃)
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运输条件With Ice Pack
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稳定性≥ 2 years
参考文献
1. Pérez-Salvia M, et al. Epigenetics. 2017 May 4;12(5):323-339.
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