目錄:MedChemExpress LLC>>生化試劑>> ACT-777991 | MCE
CAS | 1967811-46-6 | 分子量 | 550.48 |
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分子式 | C??H??F?N?O?S | 供貨周期 | 現(xiàn)貨 |
貨號 | HY-149055 | 應(yīng)用領(lǐng)域 | 醫(yī)療衛(wèi)生,化工,生物產(chǎn)業(yè),制藥 |
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CAS No. : 1967811-46-6
產(chǎn)品活性:ACT-777991 is an orally active and selective CXCR3 antagonist. ACT-777991 has microsomes and hepatocytes stability across animal models. ACT-777991 inhibits the migration of activated T cells toward CXCL11.
研究領(lǐng)域:GPCR/G Protein | Immunology/Inflammation
作用靶點(diǎn):CXCR
In Vitro: ACT-777991 inhibits hEGR with an IC50 value of 26 μM in CHO cells.
ACT-777991 (1 μM; 45 min) is stable in microsomes and hepatocytes across humans, rats, and dogs.
ACT-777991 (0.01-1 μM; ) inhibits the migration of both human and mouse-activated T cells toward CXCL11 with IC50s range of 3.2-64 nM and 4.9-21 nM, respectively.
ACT-777991 (1 nM, 5 nM, 20 nM, and 50 nM) inhibits CXCR3-mediated chemotaxis of human and mouse T cells.
In Vivo: ACT-777991 (0.5 mg/kg, 1 mg/kg; i.v.; single dose) has low in vivo plasma clearance in male Wistar rats (14/156) or Beagle dogs (5/15).
ACT-777991 (0.006-2 mg/g food; po; started 3 days before and 72 h post LPS challenge) dose-dependently inhibits chemotaxis of CXCR3+ T cells in vivo in mouse model.
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