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APS6-45
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
APS6-45图片
规格:98%
分子量:548.39
包装与价格:
包装价格(元)
5mg电议
10mg电议
25mg电议
50mg电议
100mg电议

产品介绍
APS6-45是一种口服活性的肿瘤校准抑制剂(TCI)。APS6-45抑制RAS/MAPK信号传导并表现出抗肿瘤活性。
货号:ajcx30178
CAS:2188236-41-9
分子式:C23H16F8N4O3
分子量:548.39
溶解度:DMSO: 250 mg/mL (455.88 mM)
纯度:98%
存储:Store at -20°C
库存:现货

Background:

APS6-45 is an orally active tumor-calibrated inhibitor (TCI). APS6-45 inhibits RAS/MAPK signaling and exhibits antitumor activity[1].

APS6-45 (3-30 nM; 3 weeks) strongly suppresses TT human Medullary Thyroid Carcinoma (MTC) cells colony formation in a soft agar assay[1].APS6-45 (1 μM; 1 h) strongly inhibits RAS pathway activity signaling in human MTC cell lines TT and MZ-CRC-1[1].

APS6-45 (10 mg/kg; p.o. daily for 30 d) inhibits growth of TT tumors in mice and does not affect body weight[1].APS6-45 (0.1-160 mg/kg; a single p.o.) does not cause detectable toxic effects in mice[1].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[1]. Animal Model: Female nude mice (6 weeks) are implanted with TT cells[1]

[1]. Sonoshita M, et, al. A whole-animal platform to advance a clinical kinase inhibitor into new disease space. Nat Chem Biol. 2018 Mar;14(3):291-298.