T-025

T-025 Suppliers list
Company Name: TargetMol Chemicals Inc.
Tel: +1-781-999-5354 +1-00000000000
Email: marketing@targetmol.com
Products Intro: Product Name:T025
CAS:2407433-00-3
Purity:98.00% Package:1 mL * 10mM (in DMSO);10 mg;100 mg;5 mg;50 mg;500 mg Remarks:REAGENT;FOR LABORATORY USE ONLY
Company Name: Shanghai Lollane Biological Technology Co.,Ltd.  
Tel: 021-52996696,15000506266 15000506266
Email:
Products Intro: Product Name:T025
CAS:2407433-00-3
Purity:98% HPLC Package:5mg,10mg,50mg,100mg,1g,5g
Company Name: Tianjin Kailiqi Biotechnology Co., Ltd.  
Tel: 15076683720
Email: klq@cw-bio.com
Products Intro: Product Name:T025
CAS:2407433-00-3
Purity:大于98% Package:1g,5g,10g,25g根据客户需要分装 Remarks:Not For Human Use, Lab Use Only.
Company Name: Shanghai hongqu biomedical technology co. LTD  
Tel: 88888888888
Email: hongquchem@qq.com
Products Intro: Product Name:T025
CAS:2407433-00-3
Purity:98% Package:100mg;1g;10g;100g;1kg
Company Name: Chunchuang (Wuhan) Technology Co., Ltd  
Tel: 15342225168
Email: yutianchun2007@126.com
Products Intro: Product Name:T-025
CAS:2407433-00-3
Purity:99.5+ Package:1g/RMB 100
T-025 Basic information
Product Name:T-025
Synonyms:T-025;T025,T-025;7H-Pyrrolo[2,3-d]pyrimidine-2,4-diamine, N2-methyl-N4-(2-pyrimidinylmethyl)-5-(6-quinolinyl)-;N2-Methyl-N4-(pyrimidin-2-ylmethyl)-5-(quinolin-6-yl)-7H-pyrrolo[2,3-d]pyrimidine-2,4-diamine
CAS:2407433-00-3
MF:C21H18N8
MW:382.42
EINECS:
Product Categories:
Mol File:2407433-00-3.mol
T-025 Structure
T-025 Chemical Properties
density 1.432±0.06 g/cm3(Predicted)
storage temp. Store at -20°C
solubility DMSO : 8.25 mg/mL (21.57 mM; Need ultrasonic)
pka13.45±0.50(Predicted)
Safety Information
MSDS Information
T-025 Usage And Synthesis
Biological ActivityT025 is an orally active and highly potent inhibitor of Cdc2-like kinase (CLKs), with Kd values of 4.8, 0.096, 6.5, 0.61, 0.074, 1.5 and 32 nM for CLK1, CLK2, CLK3, CLK4, DYRK1A, DYRK1B and DYRK2, respectively. T025 induces caspase-3/7-mediated cell apoptosis. T025 reduces CLK-dependent phosphorylation. T025 exerts anti-proliferative activities in both hematological and solid cancer cell lines (IC50 values: 30-300 nM). T025 has an anti-tumor efficiency, mainly for MYC-driven disease research[1]. T025 (0-1000 nM; 72 hours) significantly suppresses the growth of MDA-MB-468 cells in a dose-dependent manner[1].T025 (0-1000 nM; 6 hours) reduces phosphorylation levels in MDA-MB-468 cells[1]. T025 (50 mg/kg; p.o.; 2, 4, 8 hours, Balb/c nude mice (7 to 8 week-old females).) suppress the CLK-dependent phosphorylation and induce skipping exon in various genes[1]. T025 (50 mg/kg; p.o.; twice daily on 2 days per week, for 3 weeks, Balb/c nude mice (7 to 8 week-old females).) inhibits MDA-MB-468 xenograft mice tumor growth and without affect body weight [1].
References[1]. Iwai K, et al. Anti-tumor efficacy of a novel CLK inhibitor via targeting RNA splicing and MYC-dependent vulnerability. EMBO Mol Med. 2018 Jun;10(6):e8289.
T-025 Preparation Products And Raw materials
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