JNK Inhibitor VIII
TCS JNK 6o · JNK Inhibitor VIII · TCS JNK 6o(JNK Inhibitor VIII) · JNK INHIBITOR VIII (TCS JNK 6O) · JNK Inhibitor VIII, 10 mM in DMSO · JNK,inhibit,Inhibitor,JNK Inhibitor VIII · JNK inhibitor VIII - JNK inhibitor compound 6o · N-(4-Amino-5-cyano-6-ethoxy-2-pyridinyl)-2,5-dimethoxybenzeneacetamide
식별자 및 물리적 특성
| CAS No. | 894804-07-0 |
|---|---|
| 분자식 | C18H20N4O4 |
| 평균 분자량 | 356.4 g/mol |
| 단동위원소 질량 | 356.14845513 g/mol |
| SMILES | CCOc1nc(NC(=O)Cc2cc(OC)ccc2OC)cc(N)c1C#N |
| InChIKey | KQMPRSZTUSSXND-UHFFFAOYSA-N |
| PubChem CID | 11624601 |
| ChEMBL | CHEMBL210618 |
| DTXSID | DTXSID20469650 |
화학 및 물리적 성질
| XLogP | 2.2 |
|---|---|
| 극성 표면적 | 119 |
| 수소 결합 공여자 수 | 2 |
| 수소 결합 수용자 수 | 7 |
| 회전 가능 결합 수 | 7 |
| 무거운 원자 수 | 26 |
| 형식 전하 | 0 |
| 복잡도 | 509 |
| 저장 조건 | Store at -20°C |
| 용해도 | DMSO에 용해됨 |
| 물리적 상태 | 결정질 고체 |
| 색상 | White to off-white |
| InChI | 1S/C18H20N4O4/c1-4-26-18-13(10-19)14(20)9-16(22-18)21-17(23)8-11-7-12(24-2)5-6-15(11)25-3/h5-7,9H,4,8H2,1-3H3,(H3,20,21,22,23) |
| InChIKey | KQMPRSZTUSSXND-UHFFFAOYSA-N |
| SMILES | N(c2nc(c(c(c2)N)C#N)OCC)C(=O)Cc1c(ccc(c1)OC)OC |
안전 및 규제
| 수질 위해 등급(WGK) | WGK 2 |
|---|---|
| 저장 분류 | 11 - Combustible Solids |
용도
개요
c-Jun amino terminal kinases (JNKs) are MAP kinase family members that become highly activated after cells are exposed to stress conditions and are poorly activated by exposure to growth factors or mitogens. They have been implicated in neurodegeneration, rheumatoid arthritis, inflammation, cancer, and diabetes. JNK1 and JNK2 are widely expressed throughout the body whereas JNK3 is predominantly distributed in the brain. JNK Inhibitor VIII is an aminopyridine compound that inhibits JNK1, JNK2, and JNK3 with Ki values of 2, 4, and 52 nM, respectively. It has been reported to inhibit the phosphorylation of the JNK substrate c-Jun in HepG2 cells (EC50 = 920 nM) without affecting the expression of IL-6, IL-8, or COX-2.
용도
JNK Inhibitor VIII is an inhibitor shown to suppress apoptosis, caspase cleavage, and cytochrome C release.