Basic information Safety Supplier Related

GSK481

Basic information Safety Supplier Related

GSK481 Basic information

Product Name:
GSK481
Synonyms:
  • GSK481
  • CS-2186
  • GSK481 - GSK'481
  • 3-Isoxazolecarboxamide, 5-(phenylmethyl)-N-[(3S)-2,3,4,5-tetrahydro-5-methyl-4-oxo-1,5-benzoxazepin-3-yl]-
  • (S)-5-Benzyl-N-(5-methyl-4-oxo-2,3,4,5-tetrahydrobenzo[b][1,4]oxazepin-3-yl)isoxazole-3-carboxamide
  • GSK481,inhibit,Inhibitor,RIPK,GSK-481,RIP kinase,GSK 481,Receptor-interacting protein kinases
CAS:
1622849-58-4
MF:
C21H19N3O4
MW:
377.39
Mol File:
1622849-58-4.mol
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GSK481 Chemical Properties

Boiling point:
677.0±55.0 °C(Predicted)
Density 
1.35±0.1 g/cm3(Predicted)
storage temp. 
Store at -20°C
solubility 
Soluble in DMSO
form 
crystalline solid
pka
11.68±0.20(Predicted)
color 
Light brown to brown
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GSK481 Usage And Synthesis

Biological Activity

gsk481 is a receptor interacting protein kinase 1 (rip1) inhibitor.the role of rip1 kinase in tumor necrosis factor mediated inflammation has resulted in its emergence as a promising target for the treatment of multiple inflammatory diseases.

in vitro

previous study showed that gsk481 could not only trigger an increase in biochemical activity but also exhibit great translation in the u937 cellular assay with ic50 of 10 nm. moreover, gsk481 also showed complete specificity for rip1 kinase against all other tested kinases when profiled over both a p33 radiolabeled assay screen. in tight-binding adp-glo ic50 evaluation with increasing atp concentration, gsk481 exhibited a shift to lower potency, which was corresponding to a competitive model. in addition, gsk481 was also found to be a potent inhibitor of s166 phosphorylation in wild-type human rip1 but was ineffective at reducing s166 phosphorylation for wild-type mouse rip1. gsk481 was also able to more potently inhibit ser166 phosphorylation in all three tested mouse rip1 mutants than in wild-type mouse [1].

target

TargetValue
RIP1

IC 50

1.3 nm for rip1

References

[1] harris pa et al. dna-encoded library screening identifies benzo[b][1,4]oxazepin-4-ones as highly potent and monoselective receptor interacting protein 1 kinase inhibitors. j med chem, 2016 mar 10, 59(5):2163-78.

GSK481Supplier

HangZhou YuHao Chemical Technology Co., Ltd.
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AdooQ Bioscience CHINA
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Shanghai Lollane Biological Technology Co.,Ltd.
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