HTT-D3
HTT-D3 is an orally active, blood-brain barrier penetrant splicing modulator of huntingtin (HTT). HTT-D3 promotes the inclusion of a pseudo-exon containing a premature termination codon into HTT pre-mRNA, triggers nonsense-mediated mRNA degradation and reduces HTT protein levels. HTT-D3 induces dose-dependent, comparable reductions in mutant HTT protein in both the brain and peripheral tissues of transgenic mouse models. HTT-D3 can be used for the research of Huntington's disease.
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- CAS 番号: 2254502-89-9
- 分子式: C23H25FN6
- 分子量:404.48
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保管条件:
Please store the product under the recommended conditions in the Certificate of Analysis.
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生物活性
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化学情報
- 純度とドキュメンテーション
- 参考文献
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Help & FAQs
生物活性
HTT-D3 (10 μM; 1 h) exhibits reduced P-gp substrate activity in MDCK-MDR1 cells[1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
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Animal Model:BACHD mice (6-10 weeks old, female); Hu97/18 mice (2-4 months old, both sexes)[1]
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Dosage:1, 3, 10 mg/kg for BACHD mice; 2, 6, 12 mg/kg for Hu97/18 mice;
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Administration:Oral gavage, once daily, for 21 consecutive days
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Result:Induced dose-dependent and approximately equivalent mHTT protein lowering in brain and peripheral tissues, uniform mHTT reduction was observed in striatum and cortex of Hu97/18 mice, and significant positive correlations were detected between mHTT levels in cortex, striatum, plasma and CSF in Hu97/18 mice.
化学情報
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CAS 番号 2254502-89-9
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分子量 404.48
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分子式 C23H25FN6
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SMILES
FC1=CC(C2=NN3C(C(C)=C2)=NC(C)=C3)=CC4=NN=C(C5CCN(CC)CC5)C=C14
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輸送条件
Room temperature in continental US; may vary elsewhere.
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保管条件
Please store the product under the recommended conditions in the Certificate of Analysis.
純度とドキュメンテーション
参考文献
Calculators
濃度 (開始) × 体積 (開始) = 濃度 (終了) × 体積 (終了)
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