PU24FCl
PU24FCl is a specific inhibitor of Hsp90. PU24FCl exhibits wide-ranging anti-cancer activities. PU24FCl accumulates in tumors while being rapidly cleared from normal tissue.
商品は「研究用試薬」です。人や動物の医療用・臨床診断用・食品用の製品ではありません。
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: 422508-46-1
- 分子式: C20H21ClFN5O3
- 分子量:433.86
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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
IC50 & Target
[1]|
HSP90 |
Cellular Effect
|
Cell Line
|
Type | Value | Description | References |
|---|---|---|---|---|
| HCT-116 | GI50 |
3.9 μM
Compound: 8
|
Cellular activity against human colon tumor cell line, HCT116
Cellular activity against human colon tumor cell line, HCT116
|
[PMID: 14698151] |
| MCF7 | IC50 |
1.2 μM
Compound: PUC24FCI
|
Antiproliferative activity against human MCF7 cells by MTS assay
Antiproliferative activity against human MCF7 cells by MTS assay
|
[PMID: 17488003] |
| MCF7 | IC50 |
1.7 μM
Compound: PUC24FCI
|
Inhibition of human recombinant HSP90 in MCF7 cells assessed as Her2 degradation
Inhibition of human recombinant HSP90 in MCF7 cells assessed as Her2 degradation
|
[PMID: 17488003] |
| MCF7 | IC50 |
2.5 μM
Compound: PUC24FCI
|
Binding affinity to human recombinant HSP90 in MCF7 cell lysates assessed as inhibition of biotinylated-geldanamycin binding
Binding affinity to human recombinant HSP90 in MCF7 cell lysates assessed as inhibition of biotinylated-geldanamycin binding
|
[PMID: 17488003] |
| MCF7 | IC50 |
7 μM
Compound: PUC24FCI
|
Selectivity for HSP90 in MCF7 cells over HSP90 in NDF cells
Selectivity for HSP90 in MCF7 cells over HSP90 in NDF cells
|
[PMID: 17488003] |
| MDA-MB-468 | EC50 |
0.23 μM
Compound: 4
|
Effective concentration against heat shock protein HSP90-alpha in MDA-MB-468 cells
Effective concentration against heat shock protein HSP90-alpha in MDA-MB-468 cells
|
[PMID: 15828828] |
| SK-BR-3 | IC50 |
0.66 μM
Compound: PU24FCl
|
Displacement of GM-cy3B from Hsp90 in human SKBR3 cells after 24 hrs by fluorescence polarization assay
Displacement of GM-cy3B from Hsp90 in human SKBR3 cells after 24 hrs by fluorescence polarization assay
|
[PMID: 24548207] |
| SK-BR-3 | IC50 |
1.8 μM
Compound: 4
|
Inhibitory concentration against SKBr3 cell line
Inhibitory concentration against SKBr3 cell line
|
[PMID: 15828828] |
| SK-BR-3 | IC50 |
2 μM
Compound: PU24FCl
|
Inhibition of Hsp70 in human SKBR3 cells assessed as HER2 protein degradation by Western blotting analysis
Inhibition of Hsp70 in human SKBR3 cells assessed as HER2 protein degradation by Western blotting analysis
|
[PMID: 24548207] |
| SK-BR-3 | IC50 |
2.5 μM
Compound: PU24FCl
|
Inhibition of Hsp70 in human SKBR3 cells assessed as RAF1 protein degradation by Western blotting analysis
Inhibition of Hsp70 in human SKBR3 cells assessed as RAF1 protein degradation by Western blotting analysis
|
[PMID: 24548207] |
| SK-BR-3 | IC50 |
2.9 μM
Compound: PU24FCl
|
Growth inhibition of human SKBR3 cells after 72 hrs by Alamar Blue assay
Growth inhibition of human SKBR3 cells after 72 hrs by Alamar Blue assay
|
[PMID: 24548207] |
化学情報
-
CAS 番号 422508-46-1
-
分子量 433.86
-
分子式 C20H21ClFN5O3
-
SMILES
FC1=NC2=C(N=C(CC3=CC(OC)=C(C(OC)=C3Cl)OC)N2CCCC#C)C(N)=N1
-
輸送条件
Room temperature in continental US; may vary elsewhere.
-
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)