SML2649

T3-CLK-N

Name: T3-CLK-N
Brand: SIGMA
Price: 75.31 USD
Availability: InStock

≥98% (HPLC)

Synonym(s):

N-(6-(3,5-Di-tert-butylphenyl)imidazo[1,2-a]pyridin-2-yl)-4-(2-methyl-1-(4-methylpiperazin-1-yl)-1-oxopropan-2-yl)benzamide

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About This Item

Empirical Formula (Hill Notation):

C₃₇H₄₇N₅O₂

Molecular Weight:

593.80

UNSPSC Code:

12352200

NACRES:

NA.77

Key Documents

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Quality Level

100

assay

≥98% (HPLC)

form

powder

color

white to beige

solubility

DMSO: 2 mg/mL, clear

storage temp.

room temp

Related Categories

Bioactive Small Molecule Inhibitors

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This Item	SML2650	SML2644	SML0766
Sigma-Aldrich SML2649 T3-CLK-N	Sigma-Aldrich SML2650 T3-CLK	Sigma-Aldrich SML2644 NCGC00135472	Sigma-Aldrich SML0766 GSK343
assay ≥98% (HPLC)	assay ≥98% (HPLC)	assay ≥98% (HPLC)	assay ≥98% (HPLC)
form powder	form powder	form powder	form powder
Quality Level 100	Quality Level 100	Quality Level -	Quality Level 100
storage temp. room temp	storage temp. room temp	storage temp. room temp	storage temp. 2-8°C
solubility DMSO: 2 mg/mL, clear	solubility DMSO: 2 mg/mL, clear (warmed)	solubility DMSO: 2 mg/mL, clear	solubility DMSO: 15 mg/mL, clear
color white to beige	color white to beige	color white to beige	color , white to beige to brown

Biochem/physiol Actions

T3-CLK-N (T3N) is a negative control for CDC-like kinase (CLK) inhibitor T3-CLK.

negative control for CDC-like kinase (CLK) inhibitor T3-CLK

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

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CLK-dependent exon recognition and conjoined gene formation revealed with a novel small molecule inhibitor.

Tyler Funnell et al.

Nature communications, 8(1), 7-7 (2017-02-25)

CDC-like kinase phosphorylation of serine/arginine-rich proteins is central to RNA splicing reactions. Yet, the genomic network of CDC-like kinase-dependent RNA processing events remains poorly defined. Here, we explore the connectivity of genomic CDC-like kinase splicing functions by applying graduated, short-exposure

Donated chemical probes for open science.

Susanne Müller et al.

eLife, 7 (2018-04-21)

Potent, selective and broadly characterized small molecule modulators of protein function (chemical probes) are powerful research reagents. The pharmaceutical industry has generated many high-quality chemical probes and several of these have been made available to academia. However, probe-associated data and

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T3-CLK-N