HS-438
HS-438 is a potent and selective BCR-ABL inhibitor. HS-438 shows antiproliferative activity. HS-438 decreases the expression of phosphorylation of BCR-ABL (Tyr177). HS-438 induces apoptosis and cell cycle arrest at G0/G1 phase. HS-438 shows antitumor activity. HS-438 has the potential for the research of chronic myeloid leukemia (CML).
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: 1430720-10-7
- 分子式: C17H17N3O3S
- 分子量:343.40
-
保管条件:
Please store the product under the recommended conditions in the Certificate of Analysis.
生物活性
|
Cell Line
|
Type | Value | Description | References |
|---|---|---|---|---|
| BaF3 | IC50 |
>10 μM
Compound: 10b
|
Cytotoxicity against mouse BA/F3 cells after 48 hrs by XTT assay
Cytotoxicity against mouse BA/F3 cells after 48 hrs by XTT assay
|
[PMID: 23600806] |
| BaF3 | IC50 |
0.089 μM
Compound: 10b
|
Cytotoxicity against mouse BA/F3 cells transfected with wild type Bcr-Abl after 48 hrs by XTT assay
Cytotoxicity against mouse BA/F3 cells transfected with wild type Bcr-Abl after 48 hrs by XTT assay
|
[PMID: 23600806] |
| BaF3 | IC50 |
0.14 μM
Compound: 10b
|
Cytotoxicity against mouse BA/F3 cells transfected with Bcr-Abl T315I mutant after 48 hrs by XTT assay
Cytotoxicity against mouse BA/F3 cells transfected with Bcr-Abl T315I mutant after 48 hrs by XTT assay
|
[PMID: 23600806] |
| K562 | IC50 |
0.12 μM
Compound: 10b
|
Cytotoxicity against human K562 cells
Cytotoxicity against human K562 cells
|
[PMID: 23600806] |
化学情報
-
CAS 番号 1430720-10-7
-
分子量 343.40
-
分子式 C17H17N3O3S
-
SMILES
O=C(NCCO)NC1=NC2=CC=C(C=C2S1)C3=CC=CC=C3OC
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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)