TL13-12

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

TL13-12 是一种新型间变性淋巴瘤激酶 (ALK)-PROTAC，通过 TAE684 和 cereblon 配体泊马度胺缀合而开发。

TL13-12 is a novel Anaplastic Lymphoma Kinase (ALK)-PROTAC developed through conjugation of TAE684 and the cereblon ligand pomalidomide; also promotes the degradation of additional kinases including PTK2 (FAK), Aurora A, FER, and RPS6KA1 (RSK1).

TL13-12 (0-200 nM; 16 hours) ?is selective for degradation of ALK with the DC50s of 10 nM and 180 nM in H3122 cell and Karpas 299, respectively.TL13-12 (0-160 nM; 16 hours) degrades ALK and aurora A protein expression as a dose-dependent manner in Kelly and CHLA20 cells.TL13-12 (100 nM; 16 hours) significantly inhibits Tariqudan-induced ALK and Aurora A protein expression in CHLA20 cells. Western Blot Analysis Cell Line:Kelly and CHLA20 cells Concentration:0 nM; 20 nM; 40 nM; 60 nM; 80 nM; 100 nM; 140 nM; 160 nM Incubation Time:16 hours Result:Exhibited degrader behavior in cells.Western Blot Analysis Cell Line:CHLA20 cells Concentration:100 nM Incubation Time:16 hoursResult:Decreased ALK and Aurora A protein expression.

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PROTACs

PROTAC

PROTAC

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2229037-04-9

961.489

C45H53ClN10O10S

>98% (HPLC)

In Vitro:?DMSO : ≥ 100 mg/mL (104.01 mM)

CC(C)S(=O)(=O)C1=CC=CC=C1NC2=NC(=NC=C2Cl)NC3=C(C=C(C=C3)N4CCN(CC4)CCOCCOCCNC(=O)CNC5=CC=CC6=C5C(=O)N(C6=O)C7CCC(=O)NC7=O)OC

N-(2-(2-(2-(4-(4-((5-Chloro-4-((2-(isopropylsulfonyl)phenyl)-amino)pyrimidin-2-yl)amino)-3-methoxyphenyl)piperazin-1-yl)ethoxy)ethoxy)ethyl)-2-((2-(2,6-dioxopiperidin-3-yl)-1,3-dioxoisoindolin-4-yl)amino)acetamide

(-20℃)

With Ice Pack

≥ 2 years