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Merck
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文件

SML1246

Sigma-Aldrich

JNK-IN-8

≥96% (HPLC)

别名:

3-[[4-(二甲基氨基)-1-氧代-2-丁烯-1-基)氨基)-N-(4-((4-(3-吡啶基)-2-嘧啶基)氨基)苯基)苯甲酰胺

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About This Item

经验公式（希尔记法）:
C29H29N7O2
CAS号:
1410880-22-6
分子量:
507.59
MDL號碼:
MFCD22124890
分類程式碼代碼:
12352200
PubChem物質ID:
329825741
NACRES:
NA.77

品質等級

100

化驗

≥96% (HPLC)

形狀

powder

顏色

white to beige

溶解度

DMSO: 20 mg/mL, clear

儲存溫度

2-8°C

SMILES 字串

O=C(C1=CC(NC(C=CCN(C)C)=O)=CC=C1)NC(C=C2C)=CC=C2NC3=NC=CC(C4=CC=CN=C4)=N3

InChI

1S/C29H29N7O2/c1-20-17-24(11-12-25(20)34-29-31-15-13-26(35-29)22-8-5-14-30-19-22)33-28(38)21-7-4-9-23(18-21)32-27(37)10-6-16-36(2)3/h4-15,17-19H,16H2,1-3H3,(H,32,37)(H,33,38)(H,31,34,35)

InChI 密鑰

GJFCSAPFHAXMSF-UHFFFAOYSA-N

應用

JNK-IN-8 已用作抑制剂来研究 JNK 信号转导在醉茄素 A（WFA）诱导的骨髓增生异常综合征（MDS）-L 细胞凋亡中的重要性。

生化／生理作用

JNK-IN-8 和拉帕替尼通过诱导凋亡协同降低人三阴性乳腺癌（TNBC）细胞系中的细胞活力。JNK-IN-8 和拉帕替尼导致细胞毒性氧化应激的积累。
JNK-IN-8 是有效的、选择性和不可逆的 JNK1/2/3 抑制剂，可抑制 c-Jun 的磷酸化。JNK-IN-8 与保守的半胱氨酸残基形成共价键。

其他說明

JNK-IN-8 已由化学探针门户网站进行了专家审查和推荐。有关更多信息，请访问化学探针门户网站上的 JNK-IN-8 探针摘要。

儲存類別代碼

11 - Combustible Solids

水污染物質分類（WGK）

WGK 3

閃點（°F）

Not applicable

閃點（°C）

Not applicable

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