420119 Sigma-AldrichJNK Inhibitor II - CAS 129-56-6 - Calbiochem
JNK Inhibitor II, CAS 129-56-6, is a cell-permeable, potent, selective, ATP-competitive, and reversible inhibitor of c-Jun N-terminal kinase (IC50 = 40 nM for JNK-1 & 2 & 90 nM for JNK-3).
More>> JNK Inhibitor II, CAS 129-56-6, is a cell-permeable, potent, selective, ATP-competitive, and reversible inhibitor of c-Jun N-terminal kinase (IC50 = 40 nM for JNK-1 & 2 & 90 nM for JNK-3). Less<<JNK Inhibitor II - CAS 129-56-6 - Calbiochem: のSDS（安全データシート）、CoA（試験成績書）およびCoQ（品質証明書）、カタログなど製品関連の技術資料を入手いただけます。
同義語: Anthra[1,9-cd]pyrazol-6(2H)-one, 1,9-pyrazoloanthrone, SP600125, SAPK Inhibitor II
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概要
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主要スペック表
| CAS # | Empirical Formula |
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| 129-56-6 | C₁₄H₈N₂O |
価格＆在庫状況
| カタログ番号 | 在庫状況 | 包装 | Qty/Pk | 価格 | 数量 | |
|---|---|---|---|---|---|---|
| 420119-25MGCN |
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樹脂ｱﾝﾌﾟﾙ | 25 mg |
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— | |
| 420119-50MGCN |
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樹脂ｱﾝﾌﾟﾙ | 50 mg |
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— | |
| 420119-5MGCN |
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樹脂ｱﾝﾌﾟﾙ | 5 mg |
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| Description | |
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| Overview | A potent, cell-permeable, selective, and reversible inhibitor of c-Jun N-terminal kinase (JNK) (IC50 = 40 nM for JNK-1 and JNK-2 and 90 nM for JNK-3). The inhibition is competitive with respect to ATP. Exhibits over 300-fold greater selectivity for JNK as compared to ERK1 and p38-2 MAP kinases. Inhibits the phosphorylation of c-Jun and blocks cellular expression of IL-2, IFN-γ, TNF-α, and COX-2. Blocks IL-1-induced accumulation of phospho-Jun and induction of c-Jun transcription. A 50 mM (5 mg/454 µl) solution of JNK Inhibitor II (Cat. No. 420128) in DMSO is also available. |
| Catalogue Number | 420119 |
| Brand Family | Calbiochem® |
| Synonyms | Anthra[1,9-cd]pyrazol-6(2H)-one, 1,9-pyrazoloanthrone, SP600125, SAPK Inhibitor II |
| References | |
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| References | Shin, M., and Boyd, Y.D. 2002. Biochim. Biophys. Acta 1589, 311. Bennett, B.L., et al. 2001. Proc. Natl. Acad. Sci. USA 98, 13681. Han, Z., et al. 2001. J. Clin. Invest. 108, 73. |
| Product Information | |
|---|---|
| CAS number | 129-56-6 |
| ATP Competitive | Y |
| Form | Yellowish orange solid |
| Hill Formula | C₁₄H₈N₂O |
| Chemical formula | C₁₄H₈N₂O |
| Reversible | Y |
| Structure formula Image | |
| Quality Level | MQ200 |
| Biological Information | |
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| Primary Target | JNK 1, JNK 2, JNK 3 |
| Primary Target IC<sub>50</sub> | 40 nM for JNK-1 and JNK-2 and 90 nM for JNK-3 |
| Purity | ≥98% by HPLC |
| Physicochemical Information | |
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| Cell permeable | Y |
| Dimensions |
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| Materials Information |
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| Toxicological Information |
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| Safety Information according to GHS | |
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| RTECS | CB4585000 |
| Safety Information |
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| Product Usage Statements |
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| Packaging Information | |
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| Packaged under inert gas | Packaged under inert gas |
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| Supplemental Information |
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| Specifications |
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| Global Trade Item Number | |
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| カタログ番号 | GTIN |
| 420119-25MGCN | 04055977187977 |
| 420119-50MGCN | 04055977187991 |
| 420119-5MGCN | 07790788050092 |
Documentation
JNK Inhibitor II - CAS 129-56-6 - Calbiochem (M)SDS
| タイトル |
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JNK Inhibitor II - CAS 129-56-6 - Calbiochem 試験成績書（CoA）
| タイトル | ロット番号 |
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| 420119 |
参考資料
| 参考資料の概要 |
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| Shin, M., and Boyd, Y.D. 2002. Biochim. Biophys. Acta 1589, 311. Bennett, B.L., et al. 2001. Proc. Natl. Acad. Sci. USA 98, 13681. Han, Z., et al. 2001. J. Clin. Invest. 108, 73. |
Posters
| タイトル |
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| Human Kinome & InhibitorSelect™ Libraries |
引用
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Note that this data sheet is not lot-specific and is representative of the current specifications for this product. Please consult the vial label and the certificate of analysis for information on specific lots. Also note that shipping conditions may differ from storage conditions.
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