GSK2850163

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Company Name: Sigma-Aldrich  
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GSK2850163 manufacturers

  • GSK2850163
  • GSK2850163 pictures
  • $64.00
  • 2026-07-27
  • CAS:2121989-91-9
  • Purity: 99.04%
  • Supply Ability: 10g
  • GSK2850163
  • GSK2850163 pictures
  • $64.00
  • 2026-07-27
  • CAS:2121989-91-9
  • Purity: 99.04%
  • Supply Ability: 10g
GSK2850163 Basic information
Product Name:GSK2850163
Synonyms:GSK2850163;2,7-Diazaspiro[4.5]decane-7-carboxamide, 2-[(3,4-dichlorophenyl)methyl]-N-[(4-methylphenyl)methyl]-, (5R)-;inhibit,IRE1,GSK 2850163,Inhibitor,Inositol requiring enzyme 1,GSK2850163,GSK-2850163;GSK2850163, 10 mM in DMSO
CAS:2121989-91-9
MF:C24H29Cl2N3O
MW:446.41
EINECS:
Product Categories:
Mol File:2121989-91-9.mol
GSK2850163 Structure
GSK2850163 Chemical Properties
Boiling point 625.6±55.0 °C(Predicted)
density 1.28±0.1 g/cm3(Predicted)
storage temp. 2-8°C
solubility DMSO : 67.5 mg/mL (151.21 mM);Water : < 0.1 mg/mL (insoluble)
form oil
pka13.81±0.20(Predicted)
color colorless to light yellow
InChI1S/C24H29Cl2N3O/c1-18-3-5-19(6-4-18)14-27-23(30)29-11-2-9-24(17-29)10-12-28(16-24)15-20-7-8-21(25)22(26)13-20/h3-8,13H,2,9-12,14-17H2,1H3,(H,27,30)/t24-/m1/s1
InChIKeyYFDASBFQKMHSSJ-XMMPIXPASA-N
SMILESClC1=CC(CN(C2)CC[C@]32CN(C(NCC4=CC=C(C)C=C4)=O)CCC3)=CC=C1Cl
Safety Information
WGK Germany WGK 3
Storage Class11 - Combustible Solids
Hazard ClassificationsAquatic Chronic 4
MSDS Information
GSK2850163 Usage And Synthesis
UsesGSK2850163 is a novel inhibitor of inositol-requiring enzyme-1 alpha (IRE1α) which can inhibit IRE1α kinase activity and RNase activity with IC50s of 20 and 200 nM, respectively.
Biochem/physiol ActionsGSK2850163 is a highly selective inhibitor of inositol requiring enzyme-1 alpha (IRE1α) with dual activity: it inhibits IRE1α kinase activity with an IC50 value of 20 nM and RNase activity with an IC50 value of 200 nM. IRE1α is a dual serine/threonine-protein kinase/endoribonuclease with two enzymatic domains: a trans-autophosphorylation domain and and endoribonuclease (RNase) domain. When activated, usually in response to endoplasmic reticulum (ER) stress such as the unfolded protein response (UPR), IRE1α oligomerizes and activates mRNA splicing of adaptive XBP1 transcription factor, which upregulates ER chaperones and ER associated degradation (ERAD) genes that promote degradation of ER unfolded proteins and facilitate recovery from ER stress. However, if ER stress is too high or chronic, IRE1α is hyperactivated, increasing many ER mRNAs, resulting in apoptosis. GSK2850163 interacts with IRE1α catalytic residues Lys599 and Glu612, displacing the kinase activation loop to the inactive DFG-out conformation. The rearrangement of the kinase domain-dimer interface also results in the RNAse domains rotating away from each other, inhibiting the RNase activity.
References[1] Nestor O. Concha, et al. Long-Range Inhibitor-Induced Conformational Regulation of Human IRE1α Endoribonuclease Activity. Molecular Pharmacology December 2015, 88 (6) 1011-1023.
GSK2850163 Preparation Products And Raw materials
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