CAS NO: | 1334294-76-6 |
包装 | 价格(元) |
10 mM * 1 mL in DMSO | 电议 |
5mg | 电议 |
10mg | 电议 |
50mg | 电议 |
100mg | 电议 |
200mg | 电议 |
500mg | 电议 |
生物活性 | GSK682753A is a selective and highly potent inverse agonist of the epstein-barr virus-induced receptor 2 (EBI2) with anIC50of 53.6 nM. | ||||||||||||||||
IC50& Target | IC50: 53.6 nM (EBI2)[1] | ||||||||||||||||
体外研究 (In Vitro) | GSK682753 is a selective and highly potent inverse agonist for murine as well as human EBI2 with inhibition of G protein-dependent signals as well as signals that are probably G protein-independent. In cAMP-response element-binding protein-based reporter and guanosine5'-3-O-(thio)-triphosphate (GTPγS) binding assays, the potency of this compound is 2.6-53.6 nM, and its inhibitory efficacy is 75%. GSK682753A dose-dependently inhibits EBI2 with an IC50of 53.6 nM. GSK682753A inhibits ERK phosphorylation, GTPγS binding, and cAMP-response element-binding protein activation with similar potency[1]. | ||||||||||||||||
分子量 | 479.78 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C23H21Cl3N2O3 | ||||||||||||||||
CAS 号 | 1334294-76-6 | ||||||||||||||||
运输条件 | Room temperature in continental US; may vary elsewhere. | ||||||||||||||||
储存方式 | 4°C, protect from light *In solvent : -80°C, 6 months; -20°C, 1 month (protect from light) | ||||||||||||||||
溶解性数据 | In Vitro: DMSO : ≥ 100 mg/mL(208.43 mM) *"≥" means soluble, but saturation unknown. 配制储备液
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