PU-11
PU-11 is a Hsp90α/Hsp90β inhibitor with IC50 values of 18.6 μM and 89.8 μM and Kd values of 2 and 4.2 μM. PU-11 binds to the ATP-binding pocket of Hsp90α and Hsp90β and displays selective binding preference for Hsp90α over Hsp90β, mediated by the nonconserved Hsp90α Ser52 residue. PU-11 can be used for the research of neurodegenerative disorders.
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研究用途以外に使用した場合、当社は一切の責任を負いかねます。
- CAS 番号: 1454619-18-1
- 分子式: C19H23N5O3
- 分子量:369.43
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保管条件:
Please store the product under the recommended conditions in the Certificate of Analysis.
生物活性
製品説明
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HSP90α 18.6 μM (IC50) |
HSP90β 89.8 μM (IC50) |
HSP90α 2 μM (Kd) |
HSP90β 4.2 μM (Kd) |
体外実験
PU-11 (Compound PU-11-trans) (30.1-50.7 μM) binds to purified human Hsp90α NTD with a Kd of 2.0 ± 0.14 μM and an IC50 of 18.6 μM, exhibiting selective affinity for this paralog[1].
PU-11 (93.3-97.8 μM) binds to purified human Hsp90β NTD with a Kd of 4.2 ± 0.74 μM and an IC50 of 89.8 μM, showing lower affinity than for Hsp90α[1].
PU-11 (33.0-41.8 μM) binds to purified human Hsp90αS52A mutant NTD with a Kd of 4.2 ± 0.03 μM, matching its affinity for wild-type Hsp90β[1].
PU-11 shows IC50 values of 111.4 ± 9.7 and 172.9 ± 7.3 μM for Grp94 and Trap-1[1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only. Further protocols information, click here.
化学情報
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CAS 番号 1454619-18-1
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分子量 369.43
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分子式 C19H23N5O3
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SMILES
C(/C=C/C)N1C=2C(N=C1CC3=CC(OC)=C(OC)C(OC)=C3)=C(N)N=CN2
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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.
プロトコル
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Cell Cytotoxicity Assay
Cytotoxicity assays are usually based on the assessment of cell membrane damage, which can also be indirectly detected by measuring cell viability. Detection methods include MTT assay, CKK-8 assay, LDH assay and ATP assay, etc.
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)