
APS6-45
CAS No. 2188236-41-9
APS6-45 ( —— )
产品货号. M23989 CAS No. 2188236-41-9
APS6-45 抑制 RAS/MAPK 信号传导并表现出抗肿瘤活性。
纯度: >98% (HPLC)






规格 | 价格/人民币 | 库存 | 数量 |
5MG | ¥1442 | 有现货 |
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10MG | ¥2341 | 有现货 |
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25MG | ¥4277 | 有现货 |
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50MG | ¥6229 | 有现货 |
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100MG | ¥8748 | 有现货 |
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200MG | 获取报价 | 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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生物学信息
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产品名称APS6-45
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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APS6-45 抑制 RAS/MAPK 信号传导并表现出抗肿瘤活性。
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产品描述APS6-45 inhibits RAS/MAPK signaling and exhibits anti-tumor activity.
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体外实验APS6-45 (3-30 nM; 3 weeks) strongly suppresses TT human Medullary Thyroid Carcinoma (MTC) cells colony formation in a soft agar assay.APS6-45 (1 μM; 1 h) strongly inhibits RAS pathway activity signaling in human MTC cell lines TT and MZ-CRC-1.
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体内实验APS6-45 (10 mg/kg; p.o. daily for 30 d) inhibits growth of TT tumors in mice and does not affect body weight.APS6-45 (0.1-160 mg/kg; a single p.o.) does not cause detectable toxic effects in mice.APS6-45 (20 mg/kg; a single p.o.) exhibits long half-life (5.6 h), Cmax (9.7 μM) and AUC0-24 (123.7 μM?h) in mice. Animal Model:Female nude mice (6 weeks) are implanted with TT cellsDosage:10 mg/kgAdministration:P.o. daily for 30 days Result:Led to partial or complete responses in 75% and was well tolerated.Animal Model:Male ICR mice (6 weeks of age)Dosage:20 mg/kg (Pharmacokinetic Analysis)Administration:A single p.o.Result:T1/2=5.6 h, Cmax=9.7 μM,AUC0-24=123.7 μM?h.
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同义词——
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通路MAPK/ERK Signaling
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靶点p38 MAPK
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受体MAPK|Ras
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研究领域——
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适应症——
化学信息
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CAS Number2188236-41-9
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分子量548.4
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分子式C23H16F8N4O3
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纯度>98% (HPLC)
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溶解度DMSO:240mg/mL (437.67mM)
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SMILESO=C(NC)C1=NC=CC(OC2=CC=C(NC(NC3=CC(C(C(F)(F)F)(F)C(F)(F)F)=CC=C3F)=O)C=C2)=C1
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化学全称——
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.Sonoshita M, Scopton AP, Ung PMU, et al. A whole-animal platform to advance a clinical kinase inhibitor into new disease space. Nat Chem Biol. 2018;14(3):291-298. doi:10.1038/nchembio.2556