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GSK-872

  Cat. No.:  DC10471   Featured
Chemical Structure
1346546-69-7
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More than 5000 active chemicals with high quality for research!
Field of application
GSK-872 is a potent and selective RIPK3 (receptor-interacting protein kinase-3) inhibitor.
Cas No.: 1346546-69-7
Chemical Name: Benzothiazol-5-yl-[6-(propane-2-sulfonyl)-quinolin-4-yl]-amine
Synonyms: GSK-872,GSK 872,GSK872
SMILES: CC(C)S(=O)(=O)C1=CC2=C(C=CN=C2C=C1)NC3=CC4=C(C=C3)SC=N4
Formula: C19H17N3O2S2
M.Wt: 383.49
Sotrage: 2 years -20°C Powder, 2 weeks 4°C in DMSO, 6 months -80°C in DMSO
Description: GSK'872 is a RIPK3 inhibitor, which binds RIP3 kinase domain with an IC50 of 1.8 nM, and inhibits kinase activity with an IC50 of 1.3 nM.
In Vitro: GSK'872 blocks necroptosis in mouse cells. RIP3i GSK'872 inhibits TLR3- or DAI-induced death, two RIP1-independent pathways of necroptosis[1]. Pretreatment with GSK'872 (GSK-872) confers significant protection to primary hepatocytes. However, RIPK1 inhibition (by Nec1) does not impart any protection to primary hepatocytes[2].
MSDS
COA
LOT NO. DOWNLOAD
2018-0101
2018-0101
Cat. No. Product name Field of application
DC10373 WEHI-345 WEHI-345 is a potent and selective inhibitor of RIPK2, with IC50 of 0.13 μM.
DC12045 HS-1371 HS-1371 is a novel kinase inhibitor of RIP3-mediated necroptosis.
DC10471 GSK-872 GSK-872 is a potent and selective RIPK3 (receptor-interacting protein kinase-3) inhibitor.
DC9733 GSK583 GSK583 is a Highly Potent and Selective Inhibitor of RIP2 Kinase (RIP2K bing IC50=5 nM; rat in vivo PD IC50 = 50 nM).
DC10787 GSK2982772 GSK2982772 is a potent and ATP competitive RIP1 inhibitor with an IC50 of 16 nM.
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