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产品价格：电议 采购度：1595 原产地：美洲
发布时间：2021/7/30 0:48:24 所属地区：上海 上海市
简要描述：
Ilginatinib hydrochloride (NS-018 hydrochloride) 是一种高度有效的，可口服的 JAK2 抑制剂，IC50 值为 nM，对其选择性是对 JAK1 的 46 倍 (IC50, 33 nM)，JAK3 的 54 倍 (IC50, 39 nM)，以及 Tyk2 的 22 倍 (IC50, 22 nM)。
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CAS No. : 1239358-85-0
MCE 站：Ilginatinib hydrochloride
产品活性：Ilginatinib hydrochloride (NS-018 hydrochloride) 是一种高度有效的，可口服的 JAK2 抑制剂，IC50 值为 0.72 nM，对其选择性是对 JAK1 的 46 倍 (IC50, 33 nM)，JAK3 的 54 倍 (IC50, 39 nM)，以及 Tyk2 的 22 倍 (IC50, 22 nM)。
研究领域：Epigenetics | Stem Cell/Wnt | JAK/STAT Signaling
作用靶点：JAK
In Vitro: Ilginatinib hydrochloride (NS-018 hydrochloride) is a highly active JAK2 inhibitor, with an IC50 of 0.72 nM, 46-, 54-, and 31-fold selectivity for JAK2 over JAK1 (IC50, 33 nM), JAK3 (IC50, 39 nM), and Tyk2 (IC50, 22 nM). Ilginatinib hydrochloride also inhibits Src-family kinases, especially SRC and FYN, and weakly inhibits ABL and FLT3 with 45- and 90-fold selectivity for JAK2, respectively. Ilginatinib hydrochloride shows potent inhibitory activity against cell lines JAK2V617F or MPLW515L mutations or the TEL-JAK2 fusion gene (expressing a constitutively activated JAK2) with IC50 of 11-120?nM, but has only minimal cytotoxicity against most other hematopoietic cell lines that have no constitutively activated JAK2.
Ilginatinib hydrochloride (0.5 μM) preferentially suppresses colony-forming unitgranulocyte/macrophage (CFU-GM) formation from myelodysplastic syndrome (MDS)-derived bone marrow mononuclear cells (BMMNCs). Ilginatinib hydrochloride (1 μM) suppresses the phosphorylation of STAT3 (the downstream kinase of JAK2) in CFU-GM-forming cells from MDS patients.
In Vivo: Ilginatinib hydrochloride (NS-018 hydrochloride) (12.5, 25, 50, 100 mg/kg, p.o.) potently prolongs the survival of mice and reduces splenomegaly in a mouse Ba/F3-JAK2V617F disease model.
Ilginatinib hydrochloride (25, 50 mg/kg, p.o.) significantly reduces leukocytosis, hepatosplenomegaly and extramedullary hematopoiesis, improves nutritional status, and prolongs survival in JAK2V617F transgenic mice.
相关产品：Drug Repurposing Compound Library Plus | Clinical Compound Library Plus | Bioactive Compound Library Plus | Epigenetics Compound Library | Immunology/Inflammation Compound Library | JAK/STAT Compound Library | Kinase Inhibitor Library | Stem Cell Signaling Compound Library | Anti-Cancer Compound Library | Clinical Compound Library | Anti-Aging Compound Library | Drug Repurposing Compound Library | Differentiation Inducing Compound Library | Reprogramming Compound Library | Anti-COVID-19 Compound Library | Orally Active Compound Library | Anti-Breast Cancer Compound Library | Anti-Pancreatic Cancer Compound Library | Anti-Blood Cancer Compound Library | AG490 | Upadacitinib | AT9283 | Gandotinib | Lestaurtinib | Cucurbitacin I | Oclacitinib maleate | JANEX-1 | XL019 | Atractylenolide I | FLLL32 | LFM-A13 | Brevilin A | ZM39923 hydrochloride | Ginsenoside Rk1 | WHI-P154 | Curculigoside | FM-381 | RO8191 | Reticuline | TCS 21311 | WHI-P97 | Coumermycin A1 | Delphinidin chloride | Ilginatinib maleate | Protosappanin A | Dehydrocrenatidine | FM-479 | NSC 33994
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更新时间：2024/1/2 10:17:17
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