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TL13-112
TL13-112 是一种有效的选择性 ALK-PROTAC 降解物,可抑制 ALK 活性,IC50 值 0.14 nM,并促进包括 Aurora A、FER、PTK2 和 RPS6KA1 在内的其他激酶的降解,IC50 值分别 8550 nM、42.4 nM、25.4 nM 和 677 nM。TL13-112 由 Ceritinib (HY-15656) 和 Cereblon 配体 Pomalidomide (HY-10984) 结合而成。
TL13-112 Chemical Structure
CAS No. : 2229037-19-6
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生物活性 |
TL13-112 is a potent and selective ALK-PROTAC degrader and inhibits ALK activity with an IC50 value of 0.14 nM. TL13-112 also prompts the degradation of additional kinases including Aurora A, FER, PTK2 and RPS6KA1 with IC50 values of 8550 nM, 42.4 nM, 25.4 nM, and 677 nM, respectively. TL13-112 is comprised of the conjugation of Ceritinib (HY-15656) and the Cereblon ligand of Pomalidomide (HY-10984)[1]. |
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IC50 & Target[1] |
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体外研究 (In Vitro) |
TL13-112 binds to cereblon with an IC50 value of 2.4 uM[1]. TL13-112 (0.01 μM-1 μM; 16 hours) is selective for degradation of ALK with the DC50s of 10 nM and 40 nM in H3122 cell and Karpas 299, respectively. ALK degradation acts at 4 hours of treatment in H3122 cells and at 8 hours of treatment in Karpas 299 cells. The maximum degradation achieves at 16 hours in both cell lines. [1].TL13-112 (0.01 μM-1 μM; 16 hours) inhibits PTK2, ALK, FER, RPS6KA1 and Aurora A expression as a dose-dependent manner in H3122, Karpas 299, and Kelly cells[1]. Shanghai Jinpan Biotech Co Ltd has not independently confirmed the accuracy of these methods. They are for reference only. Western Blot Analysis[1]
Western Blot Analysis[1]
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分子量 |
1002.57 |
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Formula |
C49H60ClN9O10S |
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CAS 号 |
2229037-19-6 |
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运输条件 |
Room temperature in continental US; may vary elsewhere. |
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储存方式 |
Please store the product under the recommended conditions in the Certificate of Analysis. |
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参考文献 |
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