CAS NO: | 897016-82-9 |
包装 | 价格(元) |
10 mM * 1 mL in DMSO | 电议 |
5mg | 电议 |
10mg | 电议 |
50mg | 电议 |
100mg | 电议 |
200mg | 电议 |
500mg | 电议 |
生物活性 | Tirbanibulin (KX2-391) is an inhibitor ofSrcthat targets the peptide substrate site ofSrc, withGI50of 9-60 nM incancercell lines. | ||||||||||||||||
IC50& Target | GI50: 9 nM (Src, in HuH7 cells), 13 nM (Src, in PLC/PRF/5 cells), 26 nM (Src, in Hep3B cells), 60 nM (Src, in HepG2 cells)[1] | ||||||||||||||||
体外研究 (In Vitro) | Tirbanibulin (KX2-391) is a Src inhibitor that is directed to the Src substrate pocket. Tirbanibulin (KX2-391) shows steep dose-response curves against Huh7 (GI50=9 nM), PLC/PRF/5 (GI50=13 nM), Hep3B (GI50=26 nM), and HepG2 (GI50=60 nM), four hepatic cell cancer (HCC) cell lines[1]. Tirbanibulin (KX2-391) is found to inhibit certain leukemia cells that are resistant to current commercially available drugs, such as those derived from chronic leukemia cells with the T3151 mutation. Tirbanibulin (KX2-391) is evaluated in engineered Src driven cell growth assays inNIH3T3/c-Src527F and SYF/c-Src527F cells and exhibits GI50with 23 nM and 39 nM, respectively[2]. | ||||||||||||||||
体内研究 (In Vivo) | Orally administered Tirbanibulin (KX2-391) is shown to inhibit primary tumor growth and to suppress metastasis, in pre-clinical animal models of cancer[2]. | ||||||||||||||||
Clinical Trial | |||||||||||||||||
分子量 | 431.53 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C26H29N3O3 | ||||||||||||||||
CAS 号 | 897016-82-9 | ||||||||||||||||
运输条件 | Room temperature in continental US; may vary elsewhere. | ||||||||||||||||
储存方式 |
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溶解性数据 | In Vitro: DMSO : 41.67 mg/mL(96.56 mM;Need ultrasonic) 配制储备液
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