CAS NO: | 353791-85-2 |
生物活性 | J-113863 is a potent and selectiveCCR1(CD18)antagonist withIC50values of 0.9 nM and 5.8 nM for human and mouseCCR1receptors, respectively. J-113863 is also a potent antagonist of the humanCCR3(IC50of 0.58 nM) , but a weak antagonist of the mouseCCR3(IC50of 460 nM). J-113863 is inactive againstCCR2,CCR4andCCR5, as well as the LTB4 or TNF-α receptors. Anti-inflammatory effect[1][2][3]. | ||||||||||||||||
IC50& Target[2][3] |
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体外研究 (In Vitro) | Modified Vaccinia virus Ankara (MVA) but not MVA and vaccinia virus (VACV) infected MH-S cells increase the expression of the CXCR2 acting chemokine CXCL2. MH-S cells constitutively produce CCL2 and CCR1 acting chemokines CCL3, CCL5 and CCL9. Consequently, supernatants of mock treated and virus infected MH-S cells induce chemotaxis of murine promyelocyte MPRO cells and human monocytic THP-1 cells at the same level. However, supernatants of MVA infected MH-S cells significantly increase chemotaxis of the CCR2 deficient human monocytic cell line U-937. Chemotaxis of all above cell types is inhibited by J-113863[1]. | ||||||||||||||||
体内研究 (In Vivo) | J-113863 (3-10 mg/kg; intraperitoneal injection; once daily; for 11 days; DBA-1 male mice) treatment improves paw inflammation and joint damage, and dramatically decreases cell infiltration into joints in arthritic mice[2].
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分子量 | 655.44 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C30H37Cl2IN2O2 | ||||||||||||||||
CAS 号 | 353791-85-2 | ||||||||||||||||
运输条件 | Room temperature in continental US; may vary elsewhere. | ||||||||||||||||
储存方式 | 4°C, sealed storage, away from moisture *In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture) | ||||||||||||||||
溶解性数据 | In Vitro: DMSO : 50 mg/mL(76.28 mM;Need ultrasonic) 配制储备液
* 请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效。 In Vivo: 请根据您的实验动物和给药方式选择适当的溶解方案。以下溶解方案都请先按照In Vitro方式配制澄清的储备液,再依次添加助溶剂: ——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议您现用现配,当天使用;
以下溶剂前显示的百
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