DCLK1-IN-1

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DCLK1-IN-1

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。

CAS NO:

2222635-15-4

包装与价格：

包装	价格(元)
5mg	电议
10mg	电议
50mg	电议
100mg	电议

产品介绍

DCLK1-IN-1 是一种选择性的、体内相容的双皮质素样激酶1 DCLK1 激酶结构域化学探针。DCLK1-IN-1抑制 DCLK1 和 DCLK2 激酶 (结合和激酶测定 IC50 分别为: DCLK1=9.5/57.2 nM 和 DCLK2=31/103 nM)。DCLK1-IN-1 具有低毒性，可以研究 DCLK1 的生物学特性，确定其在肿瘤中的作用，如 DCLK1+ 胰腺导管腺癌 (PDAC)。

Cas No.	2222635-15-4
Canonical SMILES	O=C1N(CC(F)(F)F)C2=CN=C(NC3=CC=C(N4CCN(C)CC4)C=C3OC)N=C2N(C)C5=CC=CC=C15
分子式	C₂₆H₂₈F₃N₇O₂
分子量	527.54
溶解度	DMSO: 35.71 mg/mL (67.69 mM)
储存条件	Store at -20°C
General tips	For obtaining a higher solubility , please warm the tube at 37 ℃ and shake it in the ultrasonic bath for a while.
Shipping Condition	Evaluation sample solution : ship with blue ice All other available size: ship with RT , or blue ice upon request
产品描述	DCLK1-IN-1 is a selective, oral bioavailability in vivo-compatible chemical probe of the doublecortin like kinase 1 (DCLK1 kinase) domain. DCLK1-IN-1 inhibits DCLK1 and DCLK2 kinases (IC50: DCLK1=9.5/57.2 nM and DCLK2=31/103 nM in binding and kinase assay, respectively). DCLK1-IN-1 shows low toxicity, and can investigate DCLK1 biology and establish its role in cancer, like DCLK1+ pancreatic ductal adenocarcinoma (PDAC)[1]. [1]. Ferguson FM, et al. Discovery of a selective inhibitor of doublecortin like kinase 1. Nat Chem Biol. 2020 Apr 6.