GSK-626616

GSK-626616 Suppliers list
Company Name: ATK CHEMICAL COMPANY LIMITED
Tel: +undefined-21-51877795
Email: ivan@atkchemical.com
Products Intro: Product Name:GSK 626616
CAS:1025821-33-3
Purity:98% Package:10MG;50MG;100MG,1G,5G,10G.100G
Company Name: TargetMol Chemicals Inc.
Tel: +1-781-999-5354 +1-00000000000
Email: marketing@targetmol.com
Products Intro: Product Name:GSK-626616
CAS:1025821-33-3
Purity:98.00% Package:1 mL * 10mM (in DMSO);10 mg;100 mg;2 mg;25 mg;5 mg;50 mg Remarks:REAGENT;FOR LABORATORY USE ONLY
Company Name: InvivoChem
Tel: +1-708-310-1919 +1-13798911105
Email: sales@invivochem.cn
Products Intro: Product Name:GSK-626616
CAS:1025821-33-3
Purity:98% Package:5mg Remarks:V21894
Company Name: Hangzhou MolCore BioPharmatech Co.,Ltd.
Tel: +86-057181025280; +8617767106207
Email: sales@molcore.com
Products Intro: Product Name:GSK-626616
CAS:1025821-33-3
Purity:NLT 98% Remarks:MC502795
Company Name: LEAPCHEM CO., LTD.
Tel: +86-852-30606658
Email: market18@leapchem.com
Products Intro: Product Name:GSK-626616
CAS:1025821-33-3
Purity:0 Package:1g; 5g; 25g; 1kg; 5kg; 25kg Remarks:0
GSK-626616 Basic information
Product Name:GSK-626616
Synonyms:GSK-626616;(5Z)-2-[(2,6-Dichlorophenyl)amino]-5-(6-quinoxalinylmethylene)-4(5H)-thiazolone;4(5H)-Thiazolone, 2-[(2,6-dichlorophenyl)amino]-5-(6-quinoxalinylmethylene)-, (5Z)-;GSK 626616,DYRK,Inhibitor,Dual specificity tyrosine regulated kinase,GSK-626616,GSK626616,inhibit,Dual specificity tyrosine phosphorylation regulated kinase
CAS:1025821-33-3
MF:C18H10Cl2N4OS
MW:401.27
EINECS:
Product Categories:
Mol File:1025821-33-3.mol
GSK-626616 Structure
GSK-626616 Chemical Properties
Melting point 281 - 282oC
Boiling point 574.8±60.0 °C(Predicted)
density 1.55±0.1 g/cm3(Predicted)
storage temp. Refrigerator, under inert atmosphere
solubility Chloroform (Slightly, Heated), Methanol (Slightly)
pka-0.94±0.20(Predicted)
form Solid
color Pale Yellow to Light Yellow
Safety Information
MSDS Information
GSK-626616 Usage And Synthesis
UsesGSK-626616 is a potent and selective DYRK inhibitor (IC50 = 0.7 nM for DYRK3, similar potency for DYRK1 and 2). Exhibits ~20-fold selectivity over casein kinase 2 and negligible activity against a panel of 451 kinases screened. Enhances number of CFU-E stimulated by Epo from human marrow. Increases hemoglobin levels in anemic mice. Orally bioavailable.
storageStore at +4°C
GSK-626616 Preparation Products And Raw materials
Tag:GSK-626616(1025821-33-3) Related Product Information
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