KIRA6

CAS No. 1589527-65-0

KIRA6( —— )

Catalog No. M22059 CAS No. 1589527-65-0

KIRA6 is an effective inhibitor of IRE1α RNase kinase (IC50: 0.6 μM). It can trigger an apoptotic response.KIRA6 (10-1000 nM, 72 hours) strongly compromises the viability of the KIT-dependent cell line HMC-1.1 at the low nM concentration, in a manner that coincided with KIT blockade.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
1 mL x 10 mM in DMSO 93 In Stock
2MG 51 In Stock
5MG 86 In Stock
10MG 133 In Stock
25MG 272 In Stock
50MG 384 In Stock
100MG 572 In Stock
200MG Get Quote In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    KIRA6
  • Note
    Research use only, not for human use.
  • Brief Description
    KIRA6 is an effective inhibitor of IRE1α RNase kinase (IC50: 0.6 μM). It can trigger an apoptotic response.KIRA6 (10-1000 nM, 72 hours) strongly compromises the viability of the KIT-dependent cell line HMC-1.1 at the low nM concentration, in a manner that coincided with KIT blockade.
  • Description
    KIRA6 is an effective inhibitor of IRE1α RNase kinase (IC50: 0.6 μM). It can trigger an apoptotic response.KIRA6 (10-1000 nM, 72 hours) strongly compromises the viability of the KIT-dependent cell line HMC-1.1 at the low nM concentration, in a manner that coincided with KIT blockade. KIRA6 (1nM-100μM) bounds to the cytoplasmic domain of KIT with a Kd value of 10.8 μM. KIRA6 (10-1000 nM, 1 hour) reduces signaling output of KIT, including the phosphorylation of KIT as well as its downstream signaling modules, PSTAT5 and phosphorylated ERK1/2.KIRA6 (1 μM, 0-48 hours) inhibits Ins1 mRNA decay from IRE1α hyperactivation in a dose-dependent manner. KIRA6 (0.1-10μM, 72 hours) dose-dependently reduces 1NM-PP1 potentiation of Ins1 apoptosis during ER stress in a dose-dependent manner [2].KIRA6 (intraperitoneal injection; 5 mg/kg; 37 days) shows significant amelioration of random glucose levels over several weeks compared to the vehicle, both fed ad lib. KIRA6 (i.p, 5 mg/kg, 21 or 18 days post injections) increases both plasma insulin and C-peptide levels, remains insulin-positive islet areas at a high level after stopping injections in the Akita Mouse.
  • In Vitro
    Cell Viability Assay Cell Line:HMC-1.1 cellsConcentration:10 nM, 30 nM, 100 nM, 300 nM, 1000 nM Incubation Time:72 hours Result:Inhibited cell viability from 30 nM.Western Blot Analysis Cell Line:HMC-1.1 cells Concentration:10 nM, 30 nM, 100 nM, 300 nM, 1000 nM Incubation Time:1 hours Result:Reduced expression of phosphorylated KIT, STAT5 and ERK1/2.RT-PCRCell Line:INS-1 IRE1α (WT) cells Concentration:1 μM Incubation Time: 0 hour, 12 hours, 24 hours, 48 hours Result:Inhibited Ins1 mRNA expression.Apoptosis Analysis Cell Line:INS-1 IRE1α (WT) cells Concentration:1-10 μM Incubation Time:72 hours Result:Reduced 1NM-PP1 potentiation of Ins1 apoptosis during ER stress.
  • In Vivo
    Animal Model:Male Ins2+/Akita miceDosage:5 mg/kg Administration:Intraperitoneal injection; 5 mg/kg; 21 or 18 days postinjections Result:Attenuates b cell functional loss, increased insulin levels.
  • Synonyms
    ——
  • Pathway
    Others
  • Target
    Other Targets
  • Recptor
    IRE1α
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    1589527-65-0
  • Formula Weight
    518.53
  • Molecular Formula
    C28H25F3N6O
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO:5 mg/mL (9.64 mM);Ethanol:2 mg/mL (3.86 mM; Need ultrasonic)
  • SMILES
    CC(C)(C)C1=NC(=C2N1C=CN=C2N)C1=CC=C(NC(=O)NC2=CC=CC(=C2)C(F)(F)F)C2=CC=CC=C12
  • Chemical Name
    ——

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • Stability
    ≥ 2 years

Reference

1. Mahameed M,et al. The unfolded protein response modulators GSK2606414 and KIRA6 are potent KIT inhibitors. Cell Death Dis. 2019 Apr 1;10(4):300.
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