CLK inhibitor T3 (T3)

CLK inhibitor T3 (T3) Suppliers list
Company Name: Nanjing Chemlin Chemical Co., Ltd  
Tel: 025-83697070 13770331960
Email: info@chemlin.com.cn
Company Name: Shanghai EFE Biological Technology Co., Ltd.  
Tel: 021-65675885 18964387627
Email: info@efebio.com
Company Name: Shanghai YuanYe Biotechnology Co., Ltd.  
Tel: 15026964105
Email: 2881489226@qq.com
Company Name: ShangHai Biochempartner Co.,Ltd  
Tel: 177-54423994 17754423994
Email: 2853530910@QQ.com
Company Name: Shanghai Chaolan Chemical Technology Center  
Tel: QQ:65489617 13301690235
Email: Sales@ATKchemical.com

CLK inhibitor T3 (T3) manufacturers

  • CLK-IN-T3
  • CLK-IN-T3 pictures
  • $42.00
  • 2026-07-27
  • CAS:2109805-56-1
  • Purity: 99.61%
  • Supply Ability: 10g
CLK inhibitor T3 (T3) Basic information
Product Name:CLK inhibitor T3 (T3)
Synonyms:CLK inhibitor T3 (T3);CLK-IN-T3;Benzamide, 4-[1,1-dimethyl-2-(4-methyl-1-piperazinyl)-2-oxoethyl]-N-[6-(4-pyridinyl)imidazo[1,2-a]pyridin-2-yl]-;T3-CLK;CDC-like,Dual specificity tyrosine phosphorylation regulated kinase,inhibit,Dual specificity tyrosine regulated kinase,stable,anti-cancer,DYRK,CLK,kinase,CDK,CLK-IN-T-3,CLKINT3,DYRK1A,Inhibitor,activity,CLK IN T3,DYRK1B,Cyclin dependent kinase;T3 CLK New;CLK-IN-T3, 10 mM in DMSO;4-[1,1-Dimethyl-2-(4-methyl-1-piperazinyl)-2-oxoethyl]-N-[6-(4-pyridinyl)imidazo[1,2-a]pyridin-2-yl]benzamide
CAS:2109805-56-1
MF:C28H30N6O2
MW:482.58
EINECS:
Product Categories:
Mol File:2109805-56-1.mol
CLK inhibitor T3

(T3) Structure
CLK inhibitor T3 (T3) Chemical Properties
density 1.25±0.1 g/cm3(Predicted)
storage temp. room temp
solubility DMSO: 2mg/mL, clear (warmed)
form Solid
pka4.70±0.46(Predicted)
color Off-white to light yellow
InChIKeyIEFFSHLHNYVSEF-UHFFFAOYSA-N
SMILESC(NC1=CN2C(=N1)C=CC(C1C=CN=CC=1)=C2)(=O)C1=CC=C(C(C)(C)C(N2CCN(C)CC2)=O)C=C1
Safety Information
WGK Germany WGK 3
Storage Class11 - Combustible Solids
MSDS Information
CLK inhibitor T3 (T3) Usage And Synthesis
UsesCLK-IN-T3 is a high potent, selective, and stable CDC-like kinase (CLK) inhibitor with IC50s of 0.67 nM, 15 nM, and 110 nM for CLK1, CLK2, and CLK3 protein kinases, respectively. CLK-IN-T3 has anti-cancer activity[1].
Biological ActivityT3-CLK (T3) is a cell permeable, highly potent and selective cell-base stable inhibitor of CDC-like kinase (CLK) th at exhibits dose-dependent alternative splicing effects in HCT116 colorectal cancer cells. T3-CLK increases conjoined gene (CG) transcription.
IC 50CLK1: 0.67 nM (IC50); CLK2: 15 nM (IC50); CLK3: 110 nM (IC50); DYRK1A: 260 nM (IC50); DYRK1B: 230 nM (IC50)
References[1] Funnell T, et al. CLK-dependent exon recognition and conjoined gene formation revealed with a novel smallmolecule inhibitor. Nat Commun. 2017 Feb 23;8(1):7. DOI:10.1038/s41467-016-0008-7
CLK inhibitor T3 (T3) Preparation Products And Raw materials
Tag:CLK inhibitor T3 (T3)(2109805-56-1) Related Product Information
NA Benzamide, 4-(1,1-dimethylethyl)-N-imidazo[1,2-a]pyridin-2-yl- CLK inhibitor T3 (T3) Benzamide, N-[6-[3,5-bis(1,1-dimethylethyl)phenyl]imidazo[1,2-a]pyridin-2-yl]-4-[1,1-dimethyl-2-(4-methyl-1-piperazinyl)-2-oxoethyl]- SGC-CLK-1 GW806742X