ONO-4059 hydrochloride
CAS No. 1439901-97-9
ONO-4059 hydrochloride ( ONO4059 hydrochloride | Tirabrutinib hydrochloride | GS4059 hydrochloride )
产品货号. M11864 CAS No. 1439901-97-9
一种有效的、选择性的、第三代不可逆突变 EGFR 抑制剂。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 2MG | ¥269 | 有现货 |
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| 5MG | ¥455 | 有现货 |
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| 10MG | ¥787 | 有现货 |
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| 25MG | ¥1535 | 有现货 |
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| 50MG | ¥2306 | 有现货 |
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| 100MG | ¥3357 | 有现货 |
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| 500MG | 获取报价 | 有现货 |
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| 1G | 获取报价 | 有现货 |
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| 1 mL x 10 mM in DMSO | ¥519 | 有现货 |
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生物学信息
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产品名称ONO-4059 hydrochloride
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注意事项本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
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产品简述一种有效的、选择性的、第三代不可逆突变 EGFR 抑制剂。
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产品描述A potent, selective, third-generation irreversible inhibitor of mutant EGFR with IC50s of 1/12/5 nM for L858R-T790M/L858R/L861Q respectively; weak activity against wt EGFR (IC50=184 nM); inhibits signaling pathways and cellular growth in both EGFRm(+) and EGFRm(+)/T790M(+) mutant cell lines in vitro; exhibits tumor regression in EGFR-mutant tumor xenograft and transgenic models; orally active.Blood Cancer Phase 3 Clinical.
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体外实验Tirabrutinib hydrochloride (0.1-1000 nM or 0.001-100 nM; 72 h) inhibits the proliferation of OCI-L Y10 and SU-DHL-6 cells with IC50s of 9.127 nM, and 17.10 nM, respectively.Tirabrutinib hydrochloride (0.5, 5, 50 μM; 24, 48 h) induces SU-DHL-6 cells apoptosis needs high dosage and prolonged administration (concentration up to 50 μM and incubates for 48 h).Tirabrutinib hydrochloride (300 nM, 72 h) induces caspase-3 and PARP cleavage in TMD8 cells. Cell Proliferation Assay Cell Line:SU-DHL-6 and OCI-L Y10 cells Concentration:0.1-1000 nM; 0.001 nM-100 nM.Incubation Time:72 h Result:Showed good anti-proliferative activity with IC50s of 9.127 nM, and 17.10 nM for OCI-L Y10 and SU-DHL-6 cells, respectively.Apoptosis AnalysisCell Line:SU-DHL-6 cellsConcentration:0.5, 5, 50 μM Incubation Time:24, 48 h Result:Induced cell apoptosis when concentration up to 50 μM and incubated for 48 h.Western Blot AnalysisCell Line:TMD8 cells Concentration:300 nM Incubation Time:72 h Result:Induced caspase-3 and PARP cleavage.
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体内实验Tirabrutinib hydrochloride (10 mg/kg; p.o.; single) is rapidly absorbed into plasma and brain, and reaches Cmax (blood Cmax =339.53 ng/mL; brain Cmax =28.9 ng/mL) 2 hours post administration.Tirabrutinib hydrochloride (6, 20 mg/kg; p.o.; single daily for 3 weeks) shows inhibition of tumour growth in vivo. Animal Model:Male SD rats (219.0–260.5g).Animal Model:Immunodeficiency (SCID) mice (mouse xenograft model).Dosage:6, 20 mg/kg Administration:Oral administration; single daily for 3 weeks.Result:Inhibited tumour growth, and when dosage up to 20 mg/kg, a complete tumor suppression at day 14.
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同义词ONO4059 hydrochloride | Tirabrutinib hydrochloride | GS4059 hydrochloride
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通路Tyrosine Kinase
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靶点BTK
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受体BTK
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研究领域Cancer
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适应症Blood cancer
化学信息
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CAS Number1439901-97-9
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分子量490.9415
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分子式C25H23ClN6O3
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纯度>98% (HPLC)
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溶解度10 mM in DMSO
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SMILESCC#CC(=O)N1CCC(C1)N2C3=NC=NC(=C3N(C2=O)C4=CC=C(C=C4)OC5=CC=CC=C5)N.Cl
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化学全称8H-Purin-8-one, 6-amino-7,9-dihydro-9-[(3R)-1-(1-oxo-2-butyn-1-yl)-3-pyrrolidinyl]-7-(4-phenoxyphenyl)-, hydrochloride (1:1)
运输与储存
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储存条件(-20℃)
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运输条件With Ice Pack
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稳定性≥ 2 years
参考文献
1. Walter HS, et al. Blood. 2016 Jan 28;127(4):411-9.
2. Yahiaoui A, et al. PLoS One. 2017 Feb 8;12(2):e0171221.
3. Yasuhiro T, et al. Leuk Lymphoma. 2017 Mar;58(3):699-707.
产品手册
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