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GNE-064

GNE-064 (compound 5) 是一种选择性的,具有口服活性的以及高可溶性的 SMARCA4,SMARCA2 和 PBRM1 bromodomains 5 抑制剂。GNE-064 对 SMARCA4 具有抑制作用,其 IC50 值为 0.035 μM,对 SMARCA2 也具有抑制作用,其 EC50 值为 0.10 μM。GNE-064 对 SMARCA4,SMARCA2,PBRM1 bromodomains 5 和 PBRM1 bromodomains 2 的 Kd 值为 0.01,0.016

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GNE-064的二维码
  • 库存: 现货
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  • 包装
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  • 5mg
    ¥3262.00
    2610.00
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  • 10mg
    ¥5175.00
    4140.00
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  • 25mg
    ¥10250.00
    8200.00
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  • 50mg
    ¥15487.00
    12390.00
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  • 货号: ajcf18588
  • CAS: 1997321-20-6
  • 别名:
  • 分子式: C17H21N5O2
  • 分子量: 327.38
  • 纯度: >98%
  • 溶解度: DMSO : ≥ 125 mg/mL (381.82 mM)
  • 储存: Store at -20°C
  • 库存: 现货

Background

IC50: 0.035 μM (SMARCA4)[1]


GNE-064 (compound 5) is a selective, orally active and highly soluble inhibitor of SMARCA4, SMARCA2 and PBRM1 bromodomains 5. GNE-064 inhibits SMARCA4 with an IC50 of 0.035 μM and inhibits SMARCA2 with an EC50 of 0.10 μM. GNE-064 possess Kds with 0.01, 0.016, 0.018 and 0.049 μM for SMARCA4, SMARCA2, PBRM1 bromodomains 5 and PBRM1 bromodomains 2, repectively. GNE-064 can be used as a chemical probe for the research of drug synthesis[1].


GNE-064 (0-0.5 μM; 1 h) inhibits SMARCA2 in ZsGreen-SMARCA2 BD-expressing U2OS cells[1].

Cell Viability Assay[1]

Cell Line: ZsGreen-SMARCA2 BD-expressing U2OS cells
Concentration: 0-0.5 μM
Incubation Time: 1 hour
Result: Inhibited SMARCA2 in ZsGreen-SMARCA2 BD-expressing U2OS cells with an EC50 of 0.1 μM.


GNE-064 (compound 5) (0.5 and 1.0 mg/kg; i.v. and p.o. once ) exibits ideal pharmacokinetics value in female CD-1 mice [1].

Animal Model: Female CD-1 mice[1]
Dosage: 0.5 mg/kg (i.v.) and 1.0 mg/kg (p.o.)
Administration: Intravenous injection and oral gavage; 0.5 mg/kg and 1.0 mg/kg once
Result: Showed a low unbound plasma clearance with 16 mL/min/kg, a reasonable half-life of 1.1 h and good oral bioavailability of 59%.


[1]. Taylor AM, et al. GNE-064: A Potent, Selective, and Orally Bioavailable Chemical Probe for the Bromodomains of SMARCA2 and SMARCA4 and the Fifth Bromodomain of PBRM1. J Med Chem. 2022 Aug 5.

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