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GSK2982772

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    GSK2982772 是可口服的、有效的 ATP 竞争型的 RIP1 酶抑制剂,对人和猴子 RIP1 的 IC50 值分别为 16 nM 和 20 nM。


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更新时间:2026/10/7 8:42:29关注度:2482

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GSK2982772

CAS No. : 1622848-92-3

MCE 国际站:GSK2982772

产品活性:GSK2982772 是可口服的、有效的 ATP 竞争型的 RIP1 酶抑制剂,对人和猴子 RIP1 的 IC50 值分别为 16 nM 和 20 nM。

研究领域:Apoptosis

作用靶点:RIP kinase

In Vitro: GSK2982772 shows more than 1,000-fold selectivity for ERK5 over a panel of over 339 kinases at 10 µM. In stimulated cellular systems,GSK2982772 is also able to reduce spontaneous production of cytokines (IL-1β and IL-6) in a concentration-dependent fashion from ulcerative colitis explant tissue in overnight incubations. GSK2982772 produces a weak concentration dependent inhibition of hERG in human embryonic kidney (HEK-293) cells, with an estimated IC50 of 195 µM, and also shows a weak activation of the human Pregnane X receptor (hPXR) with an EC50 of 13 µM.

In Vivo: GSK2982772 is dosed orally 15 min prior to TNF and shows 68, 80, and 87% protection from temperature loss over 6 h, at doses of 3, 10, and 50 mg/kg, respectively. In the corresponding TNF/zVAD model, GSK2982772 shows 13, 63, and 93% protection from temperature loss over 3 h. GSK2982772 displays a good free fraction in blood in rats (4.2%), dogs (11%), cynomolgus monkeys (11%), and humans (7.4%). The inhibitor has a good pharmacokinetic profile across both rats and monkeys. GSK2982772 distributes into a range of tissues including the colon, liver, kidney, and heart at concentrations comparable to those of blood. However, GSK2982772 has low brain penetration in rat (4%) despite possessing good cell permeability (21×10-6 cm/s).

相关产品:Drug Repurposing Compound Library Plus | Clinical Compound Library Plus | Bioactive Compound Library Plus | Apoptosis Compound Library | Immunology/Inflammation Compound Library | Kinase Inhibitor Library | NF-κB Signaling Compound Library | Clinical Compound Library | CNS-Penetrant Compound Library | Drug Repurposing Compound Library | Anti-COVID-19 Compound Library | Pyroptosis Compound Library | Orally Active Compound Library | Necrostatin-1 | GSK-872 | GSK583 | GSK840 | GSK-843 | HS-1371 | RIP2 kinase inhibitor 2 | PROTAC RIPK degrader-2 | RIPK-IN-4 | RIPK1-IN-4 | RIPK1-IN⁻⁷ | PROTAC RIPK degrader-6 | Kongensin A | GNE684 | cRIPGBM

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