
PCI-29732
CAS No. 330786-25-9
PCI-29732 ( PCI29732 | PCI 29732 )
产品货号. M14102 CAS No. 330786-25-9
一种选择性且不可逆的 Btk 抑制剂,生化 Ki 为 8.2 nM。
纯度: >98% (HPLC)






规格 | 价格/人民币 | 库存 | 数量 |
2MG | ¥389 | 有现货 |
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5MG | ¥648 | 有现货 |
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10MG | ¥1037 | 有现货 |
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25MG | ¥2041 | 有现货 |
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50MG | ¥3637 | 有现货 |
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100MG | ¥5338 | 有现货 |
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200MG | 获取报价 | 有现货 |
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500MG | 获取报价 | 有现货 |
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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PCI-29732
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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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产品简述一种选择性且不可逆的 Btk 抑制剂,生化 Ki 为 8.2 nM。
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产品描述A selective and irreversible Btk inhibitor with biochemical Ki of 8.2 nM; also inhibits Lck and Lyn with Ki of 4.6 and 2.5 nM.(In Vitro):PCI29732 shows cytotoxicity in different cells. The IC50 values are 7.94 μM for S1, 7.79 μM for S1-MI-80, 6.55 μM for H460, 6.34 μM for H460/MX20, 6.14 μM for KB, 6.02 μM for KBv200, 12.45 μM for HEK293/pcDNA3, 14.58 μM for HEK293-ABCG2-482-R2, and 13.24 μM for HEK293-ABCG2-482-T7 cells.PCI-29732 blocks the transcriptional up-regulation of a panel of B-cell activation genes in human CD20+ B cells stimulated at the B-cell antigen receptor (BCR).(In Vivo):PCI 29732 inhibits the function of ABCG2 by competitively binding to the ATP-binding site of ABCG2 and enhances the anti-tumor efficacy of substrate chemotherapeutic agents.PCI 29732 (20 mg/kg; p.o.; every 3 d × 5 times) enhances the anticancer efficacy of Topotecan in the H460/MX20 cell xenograft nude mice model.
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体外实验PCI29732 shows cytotoxicity in different cells. The IC50 values are 7.94 μM for S1, 7.79 μM for S1-MI-80, 6.55 μM for H460, 6.34 μM for H460/MX20, 6.14 μM for KB, 6.02 μM for KBv200, 12.45 μM for HEK293/pcDNA3, 14.58 μM for HEK293-ABCG2-482-R2, and 13.24 μM for HEK293-ABCG2-482-T7 cells.PCI-29732 blocks the transcriptional up-regulation of a panel of B-cell activation genes in human CD20+ B cells stimulated at the B-cell antigen receptor (BCR).
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体内实验PCI 29732 inhibits the function of ABCG2 by competitively binding to the ATP-binding site of ABCG2 and enhances the anti-tumor efficacy of substrate chemotherapeutic agents.PCI 29732 (20 mg/kg; p.o.; every 3 d × 5 times) enhances the anticancer efficacy of Topotecan in the H460/MX20 cell xenograft nude mice model. Animal Model:5-6 weeks old athymic nude mice (bearing H460/MX20 cells)Dosage:20 mg/kg (combination with Topotecan; every 3 d × 5 times, i.p., 3 mg/kg; topotecan was given 1 h after PCI29732 administration)Administration:P.o.; every 3 d × 5 times Result:Significant reductions in tumor weight and volume were observed in the group treated with PCI29732 in combination with Topotecan.
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同义词PCI29732 | PCI 29732
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通路Tyrosine Kinase
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靶点BTK
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受体BTK|Itk
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研究领域Inflammation/Immunology
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适应症——
化学信息
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CAS Number330786-25-9
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分子量371.435
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分子式C22H21N5O
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纯度>98% (HPLC)
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溶解度DMSO: ≥ 53 mg/mL
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SMILESNC1=C2C(N(C3CCCC3)N=C2C4=CC=C(OC5=CC=CC=C5)C=C4)=NC=N1
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化学全称1H-Pyrazolo[3,4-d]pyrimidin-4-amine, 1-cyclopentyl-3-(4-phenoxyphenyl)-
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. Pan Z, et al. ChemMedChem. 2007 Jan;2(1):58-61.
2. Honigberg LA, et al. Proc Natl Acad Sci U S A. 2010 Jul 20;107(29):13075-80.
产品手册




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