ChemicalBook--->CAS DataBase List--->1630086-20-2

1630086-20-2

1630086-20-2 Structure

1630086-20-2 Structure
IdentificationBack Directory
[Name]

Amgen IRE1α Inhibitor
[CAS]

1630086-20-2
[Synonyms]

Kira8
KIRA8 (AMG-18)
IRE-1 INHIBITOR
Amgen IRE1α Inhibitor
Benzenesulfonamide, 2-chloro-N-[6-methyl-5-[[3-[2-[(3S)-3-piperidinylamino]-4-pyrimidinyl]-2-pyridinyl]oxy]-1-naphthalenyl]-
[Molecular Formula]

C31H29ClN6O3S
[MDL Number]

MFCD28404657
[MOL File]

1630086-20-2.mol
[Molecular Weight]

601.12
Chemical PropertiesBack Directory
[Boiling point ]

812.6±75.0 °C(Predicted)
[density ]

1.383±0.06 g/cm3(Predicted)
[storage temp. ]

Store at -20°C
[solubility ]

Water:30.0(Max Conc. mg/mL);49.91(Max Conc. mM)
[form ]

Solid
[pka]

7.66±0.30(Predicted)
[color ]

Light yellow to yellow
[InChIKey]

XMWUCMFVDXDRDE-NRFANRHFSA-N
[SMILES]

[S](=O)(=O)(Nc2c3c(c(c(cc3)C)Oc4ncccc4c5nc(ncc5)N[C@@H]6CNCCC6)ccc2)c1c(cccc1)Cl
Safety DataBack Directory
[WGK Germany ]

WGK 3
[Storage Class]

11 - Combustible Solids
Hazard InformationBack Directory
[Uses]

Amgen IRE1α Inhibitor is an inhibitor of IRE1α. IRE1α is a sensor of unfolded protein accumulation that triggers the unfolded protein response.
[Biological Activity]

KIRA8 is an ATP-competitivepotent and selective IRE1α kinase inhibitor (IRE1α/β Ki = 2/120 nM) th at attenuates IRE1α endonuclease activity (IRE1α/β IC50 = 5/55 nM) with good kinome selectivity. KIRA8 inhibits thapsigargin-induced UPR (IC50 = 99 nM; HT1080 XBP1-Luc cells) and shows therapeutic efficacy in murine models of type 1 diabetes (T1D)pulmonary fibrosismultiple myeloma (MM)and pancreatic neuroendocrine tumors (PanNET) in vivo (30-50 mg/kg/day i.p.).
[in vivo]

Male Ins2+/Akita mice are injected i.p. with KIRA8 (50 mg/kg; daily; for 35 days), significant reduction of hyperglycemia become apparent over several weeks[1].
? One week treatment of pre-diabetic NODs mice with Kira8 (50 mg/kg; i.p.; once a day) leads to significant reductions in islet XBP1 splicing and TXNIP mRNAs, and preserves Ins1/Ins2, BiP and MANF mRNAs[1].

Animal Model:Male Ins2+/Akita mice[1]
Dosage:50 mg/kg
Administration:Injected i.p.; daily; for 35 days
Result:Significant reduction of hyperglycemia became apparent over several weeks.
Spectrum DetailBack Directory
[Spectrum Detail]

Amgen IRE1α Inhibitor(1630086-20-2)1HNMR
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