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GSK143 dihydrochloride

目录号 : GC68447

GSK143 dihydrochloride 是一种具有口服活性,高选择性的脾酪氨酸激酶 (Syk) 抑制剂,pIC50 为 7.5。GSK143 dihydrochloride 抑制 Erk 磷酸化 (pErk: pIC50=7.1)。GSK143 dihydrochloride 可以减轻炎症,并防止小鼠肠道肌层中免疫细胞的募集。

GSK143 dihydrochloride Chemical Structure

Cas No.:2341796-81-2

规格 价格 库存 购买数量
5mg
¥1,350.00
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10mg
¥2,250.00
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25mg
¥4,860.00
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50mg
¥8,280.00
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Sample solution is provided at 25 µL, 10mM.

产品文档

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产品描述

GSK143 dihydrochloride is an orally active and highly selective spleen tyrosine kinase (SYK) inhibitor with a pIC50 of 7.5. GSK143 dihydrochloride inhibits phosphorylated Erk (pErk: pIC50=7.1)[1]. GSK143 dihydrochloride reduces inflammation and prevents recruitment of immune cells in the intestinal muscularis in mice[2][3].

GSK143 dihydrochloride (compound 20) inhibits ZAP-70 (pIC50=4.7), LCK (pIC50=5.3), LYN (pIC50=5.4), JAK1/2/3 (pIC50=5.8/5.8/5.7), Aurora B (pIC50=4.8), hWB (pIC50=6.6), hERG (pIC50=4.7)[1].
GSK143 dihydrochloride (10-10000 nM; every 24 hours for 3 days) has an IC50 of 323 nM in CLL cells. GSK 143 dihydrochloride (1 μM; 30 mins) abrogates early signalling events including SYK phosphorylation and calcium flux[2].
GSK143 dihydrochloride (0.1-10 μM; for 30 min) reduces cytokine expression in bone marrow derived macrophages in a concentration-dependent manner[3].

Cell Viability Assay[2]

Cell Line: Chronic lymphocytic leukaemia (CLL) cells
Concentration: 10, 100, 1000, 10000 nM
Incubation Time: Every 24 hours for 3 days
Result: Had an IC50 of 323 nM.

GSK143 (0.1-10 mg/kg; orally; 1.5 hours) reduces inflammation and prevents recruitment of immune cells in the intestinal muscularis of 1 mg/kg[3].
GSK143 (3, 10, 30, 100 mg/kg; oral; 1 hour before ovalbumin challenge) reduces the cutaneous reverse passive Arthus reaction in a dose dependent manner by approximately 50% and 70% at 10 mg/kg and 30 mg/kg, respectively[2].
GSK143 (iv of 1 mg/kg; po of 3 mg/kg) has a T1/2 of 4.2 hours, low clearance (16 mL/min/kg), moderate bioavailability of 30% and a Vss of 4.1 L/kg in rats[1].

Animal Model: Wild type C57NL/BL6 mice, 10-12 weeks old[3]
Dosage: 0.1, 1, 3, 10 mg/kg
Administration: Orally; 1.5 hours before intestinal manipulation (IM)
Result: Reduced inflammation and prevented recruitment of immune cells in the intestinal muscularis.
Animal Model: Male CD rats (175-200 g)[1]
Dosage: 1 mg/kg of iv; 3 mg/kg of po (Pharmacokinetic Analysis)
Administration: IV or PO
Result: Had a T1/2 of 4.2 hours, low clearance (16 mL/min/kg), moderate bioavailability of 30% and a Vss of 4.1 L/kg.

[1]. John Liddle, et al. Discovery of GSK143, a Highly Potent, Selective and Orally Efficacious Spleen Tyrosine Kinase Inhibitor. Bioorg Med Chem Lett. 2011 Oct 15;21(20):6188-94.
[2]. Abraham M Varghese, et al. Highly Selective SYK Inhibitor, GSK143, Abrogates Survival Signals in Chronic Lymphocytic Leukaemia. Br J Haematol. 2018 Sep;182(6):927-930.
[3]. Sjoerd H W van Bree, et al. Inhibition of Spleen Tyrosine Kinase as Treatment of Postoperative Ileus. Gut. 2013 Nov;62(11):1581-90.

Chemical Properties

Cas No. 2341796-81-2 SDF Download SDF
分子式 C17H24Cl2N6O2 分子量 415.32
溶解度 储存条件 4°C, away from moisture and light
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1 mg 5 mg 10 mg
1 mM 2.4078 mL 12.0389 mL 24.0778 mL
5 mM 0.4816 mL 2.4078 mL 4.8156 mL
10 mM 0.2408 mL 1.2039 mL 2.4078 mL
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