SKLB70326
SKLB70326 is a small molecule inhibitor of cell cycle progression that induces cell cycle arrest and apoptosis in human hepatocellular carcinoma cells. SKLB70326 is involved in downregulating cyclin-dependent kinase (CDK) 2, CDK4, and CDK6, while also activating PARP, caspase-3, caspase-9, and Bax, and downregulating Bcl-2.
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: 1257317-77-3
- 分子式: C15H13N3O2S
- 分子量:299.35
-
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
製品説明
Cellular Effect
|
Cell Line
|
Type | Value | Description | References |
|---|---|---|---|---|
| A-431 | IC50 |
>100 μM
Compound: 1g
|
Cytotoxicity against human A431 cells after 48 hrs by MTT assay
Cytotoxicity against human A431 cells after 48 hrs by MTT assay
|
[PMID: 20846862] |
| A549 | IC50 |
>100 μM
Compound: 1g
|
Cytotoxicity against human A549 cells after 48 hrs by MTT assay
Cytotoxicity against human A549 cells after 48 hrs by MTT assay
|
[PMID: 20846862] |
| Bel-7402 | IC50 |
7.4 μM
Compound: 1g
|
Cytotoxicity against human Bel7402 cells after 48 hrs by MTT assay
Cytotoxicity against human Bel7402 cells after 48 hrs by MTT assay
|
[PMID: 20846862] |
| HCT-116 | IC50 |
>100 μM
Compound: 1g
|
Cytotoxicity against human HCT116 cells after 48 hrs by MTT assay
Cytotoxicity against human HCT116 cells after 48 hrs by MTT assay
|
[PMID: 20846862] |
| HepG2 | IC50 |
0.016 μM
Compound: 1g
|
Cytotoxicity against human HepG2 cells after 48 hrs by MTT assay
Cytotoxicity against human HepG2 cells after 48 hrs by MTT assay
|
[PMID: 20846862] |
| Huh-7 | CC50 |
<0.4 μM
Compound: 13f
|
Cytotoxicity against human HuH7 cells after 72 hrs by MTT assay
Cytotoxicity against human HuH7 cells after 72 hrs by MTT assay
|
[PMID: 24529869] |
| Huh-7 | EC50 |
>20 μM
Compound: 13f
|
Antiviral activity against HCV genotype 1b infected in human HuH7 cells assessed as inhibition of viral RNA replication after 72 hrs by luciferase reporter gene assay
Antiviral activity against HCV genotype 1b infected in human HuH7 cells assessed as inhibition of viral RNA replication after 72 hrs by luciferase reporter gene assay
|
[PMID: 24529869] |
| MCF7 | IC50 |
>100 μM
Compound: 1g
|
Cytotoxicity against human MCF7 cells after 48 hrs by MTT assay
Cytotoxicity against human MCF7 cells after 48 hrs by MTT assay
|
[PMID: 20846862] |
| PC-3 | IC50 |
>100 μM
Compound: 1g
|
Cytotoxicity against human PC3 cells after 48 hrs by MTT assay
Cytotoxicity against human PC3 cells after 48 hrs by MTT assay
|
[PMID: 20846862] |
| RAW264.7 | IC50 |
3.3 μM
Compound: 1f
|
Antiinflammatory activity in mouse RAW264.7 cells assessed as inhibition of LPS-induced nitric oxide production incubated for 1 hr prior to LPS challenge measured after 24 hrs by Griess assay
Antiinflammatory activity in mouse RAW264.7 cells assessed as inhibition of LPS-induced nitric oxide production incubated for 1 hr prior to LPS challenge measured after 24 hrs by Griess assay
|
[PMID: 23499235] |
| SMMC-7721 | IC50 |
0.9 μM
Compound: 1g
|
Cytotoxicity against human SMMC7721 cells after 48 hrs by MTT assay
Cytotoxicity against human SMMC7721 cells after 48 hrs by MTT assay
|
[PMID: 20846862] |
化学情報
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CAS 番号 1257317-77-3
-
分子量 299.35
-
分子式 C15H13N3O2S
-
SMILES
O=C(N)C1=C(C2=CC=C(N=C2S1)C3=CC=CC(OC)=C3)N
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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)