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Merck
CN

SML1246

Sigma-Aldrich

JNK-IN-8

≥96% (HPLC), JNK inhibitor, powder

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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关于此项目

经验公式(希尔记法):
C29H29N7O2
化学文摘社编号:
分子量:
507.59
MDL编号:
UNSPSC代码:
12352200
PubChem化学物质编号:
NACRES:
NA.77
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产品名称

JNK-IN-8, ≥96% (HPLC)

质量水平

方案

≥96% (HPLC)

表单

powder

颜色

white to beige

溶解性

DMSO: 20 mg/mL, clear

储存温度

2-8°C

SMILES字符串

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 key

GJFCSAPFHAXMSF-UHFFFAOYSA-N

应用

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。
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。

其他说明

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

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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A c-Jun N-terminal kinase inhibitor, JNK-IN-8, sensitizes triple negative breast cancer cells to lapatinib.
Ebelt ND, et al.
Oncotarget, 8(62), 104894-104894 (2017)
Oxidative stress-induced JNK/AP-1 signaling is a major pathway involved in selective apoptosis of myelodysplastic syndrome cells by Withaferin-A
Oben KZ, et al.
Oncotarget, 8(44), 77436?77452-77436?77452 (2017)
Yi Huang et al.
Antioxidants (Basel, Switzerland), 11(7) (2022-07-28)
Puerarin was shown to exert anti-oxidative and anti-ferroptosis effects in multiple diseases. The goal of this study was to explore the neuroprotective effect of puerarin on early brain injury (EBI) after subarachnoid hemorrhage (SAH) in rats. A total of 177
Mei-Chou Lai et al.
Nutrients, 15(3) (2023-02-12)
Degenerative diseases of the brain include Parkinson's disease (PD), which is associated with moveable signs and is still incurable. Hispidin belongs to polyphenol and originates primarily from the medicinal fungi Inonotus and Phellinus, with distinct biological effects. In the study
Eugene Y Kim et al.
FASEB journal : official publication of the Federation of American Societies for Experimental Biology, fj201800425R-fj201800425R (2018-05-26)
Rheumatoid arthritis (RA) is characterized by hyperplastic pannus formation mediated by activated synovial fibroblasts (RASFs) that cause joint destruction. We have shown earlier that RASFs exhibit resistance to apoptosis, primarily as a result of enhanced expression of myeloid cell leukemia-1

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