中文名 | CYM 5541 |
英文名 | CYM 5541 |
别名 | CYM5541游离态 化合物CYM 5541 |
英文别名 | ML249 ML 249 ML-249 CYM5541 CYM-5541 CYM 5541 CYM 5541(ML-249) N,N-Dicyclohexyl-5-cyclopropyl-3-isoxazolecarboxamide N,N-dicyclohexyl-5-cyclopropyl-1,2-oxazole-3-carboxamide N,N-Dicyclohexyl(5-cyclopropylisoxazol-3-yl)-carboxamide |
CAS | 945128-26-7 |
化学式 | C19H28N2O2 |
分子量 | 316.44 |
密度 | 1.14±0.1 g/cm3(Predicted) |
沸点 | 503.1±38.0 °C(Predicted) |
溶解度 | DMSO: 可溶5mg/mL,澄清 (温热) |
酸度系数 | -2.57±0.20(Predicted) |
存储条件 | 2-8°C |
稳定性 | 从提供的购买之日起稳定1年。在DMSO或乙醇中的溶液可以在-20 ° 储存长达1个月。 |
外观 | 粉末 |
颜色 | white to beige |
体外研究 | CYM-5541 is a full agonist, able to reach the maximum level of ERK phosphorylation that is observed with S1P. CYM-5541 has an EC 50 of between 72 and 132 nM and exhibits exquisite selectivity over other S1P receptor subtypes: S1P1 EC 50 >10 μM, S1P2 EC 50 >50 μM, S1P4 EC 50 >50 μM, and S1P5 EC 50 >25 μM. CYM-5541 also shows selectivity over a large panel of protein targets, with no significant activities, in the Ricerca profiling panel of 55 GPCRs, ion channels, and transporters. CYM-5541 allowed us to identify an allosteric site where F263 is a key gate-keeper residue for its affinity and efficacy. The novel allosteric hydrophobic pocket may account for the S1P3 selectivity of CYM-5541. |
危险品标志 | Xn - 有害物品 |
风险术语 | 22 - 吞食有害。 |
WGK Germany | 3 |
1mg | 5mg | 10mg | |
---|---|---|---|
1 mM | 3.16 ml | 15.801 ml | 31.602 ml |
5 mM | 0.632 ml | 3.16 ml | 6.32 ml |
10 mM | 0.316 ml | 1.58 ml | 3.16 ml |
5 mM | 0.063 ml | 0.316 ml | 0.632 ml |
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