MAPK Signaling
MAPK Signaling(MAPK信号通路)
MAPK Signaling 相关产品(575)
- GC17963CHPG Sodium saltCAS: 1303993-73-8纯度: >99.00%
CHPG 钠盐是一种选择性 mGluR5 激动剂，可通过 BV2 小胶质细胞中的 TSG-6/NF-κB 通路减弱 SO2 诱导的氧化应激和炎症。
- GC18241LysophosphatidylcholinesCAS: 9008-30-4纯度: >98.00% / >99.00%
Lysophosphatidylcholines是一类重要的磷脂分子，是磷脂酶A2水解磷脂酰胆碱的产物。
- GC18273SB 202190 (hydrochloride)CAS: 350228-36-3纯度: >99.50%
A potent and selective p38 MAP kinase inhibitor
| 货号 | 产品名称 | CAS号 | 纯度 | 结构 |
|---|---|---|---|---|
| GC17693 | Enniatin B | 917-13-5 | - | |
A natural inhibitor of Pdr5p in yeast | ||||
| GC17702 | K-Ras(G12C) inhibitor 9 | 1469337-91-4 | - | |
An allosteric inhibitor of oncogenic K-Ras(G12C) | ||||
| GC17712 | AT13148 | 1056901-62-2 | >99.50% | |
A multi-AGC kinase inhibitor | ||||
| GC17725 | SKF 86002 dihydrochloride | 116339-68-5 | - | |
An anti-inflammatory agent | ||||
| GC17818 | Vacquinol-1 | 5428-80-8 | >98.00% | |
An activator of cell death in glioblastoma cells | ||||
| GC17828 | BI-847325 | 1207293-36-4 | >99.00% | |
A selective dual MEK/Aurora kinase inhibitor | ||||
| GC17860 | CEP-32496 hydrochloride | 1227678-26-3 | - | |
A potent inhibitor of B-Raf | ||||
| GC17957 | SX 011 | 309913-42-6 | - | |
p38α inhibitor | ||||
| GC17963 | CHPG Sodium salt | 1303993-73-8 | >99.00% | |
CHPG 钠盐是一种选择性 mGluR5 激动剂，可通过 BV2 小胶质细胞中的 TSG-6/NF-κB 通路减弱 SO2 诱导的氧化应激和炎症。 | ||||
| GC17964 | PD 198306 | 212631-61-3 | - | |
A potent inhibitor of MEK1/2 | ||||
| GC18178 | BI-882370 | 1392429-79-6 | >99.00% | |
A RAF inhibitor | ||||
| GC18241 | Lysophosphatidylcholines | 9008-30-4 | >98.00% / >99.00% | |
Lysophosphatidylcholines是一类重要的磷脂分子，是磷脂酶A2水解磷脂酰胆碱的产物。 | ||||
| GC18257 | GNE-495 | 1449277-10-4 | >99.50% | |
An orally bioavailable, potent, and selective MAP4K4 inhibitor | ||||
| GC18273 | SB 202190 (hydrochloride) | 350228-36-3 | >99.50% | |
A potent and selective p38 MAP kinase inhibitor | ||||
| GC18532 | Skyrin | 602-06-2 | - | |
A fungal metabolite that blocks glucagon signaling | ||||
| GC18602 | p38 MAPK Inhibitor IV | 1638-41-1 | >98.00% | |
An inhibitor of p38 MAP kinases | ||||
| GC18666 | Debromohymenialdisine | 75593-17-8 | - | |
An inhibitor of Chk1 and Chk2 | ||||
| GC18751 | Reticulol | 26246-41-3 | - | |
A cAMP phosphodiesterase and DNA topoisomerase I inhibitor | ||||
| GC18951 | Obscurolide A1 | 144397-99-9 | - | |
A phosphodiesterase inhibitor | ||||
| GC19019 | Acumapimod | 836683-15-9 | >99.00% | |
An inhibitor of p38α MAPK | ||||
| GC19041 | ASK1-IN-1 | 1262041-49-5 | >99.50% | |
ASK1-IN-1 是一种有效的、口服的、选择性的 ATP 竞争性凋亡信号调节激酶 1 (ASK1) 抑制剂，IC50 为 2.87 nM。 | ||||
| GC19048 | AZD-0364 | 2097416-76-5 | >99.50% | |
An inhibitor of ERK1/2 | ||||
| GC19066 | BGB-283 | 1446090-77-2 | - | |
BGB-283 is a novel and potent Raf Kinase and EGFR inhibitor with IC50 values of 23 and 29 nM for recombinant BRafV600E and EGFR, respectively. | ||||
| GC19090 | CCG215022 | 1813527-81-9 | >98.00% | |
A GRK inhibitor | ||||