Bcr-Abl inhibitor AT9283, Purity ≥98%

Cat. No.: X23-10-ZQ354

Bcr-Abl inhibitor AT9283, Purity ≥98%

Synonym: AT9283; 896466-04-9; 1-Cyclopropyl-3-(3-(5-(morpholinomethyl)-1H-benzo[d]imidazol-2-yl)-1H-pyrazol-4-yl)urea; AT-9283; AT 9283; AT-9283 free base; Bcr-Abl inhibitor

  • MDL: MFCD12031513
  • CAS Number: 896466-04-9
  • Compound CID: 135398495
Product Size
5 mg; 10 mg; 25 mg; 50 mg; 100 mg
Price
Datasheet
MSDS
Properties
Description
AT9283, soluble in DMSO and ethanol and insoluble in water, specifically inhibits the activity of the Bcr-Abl tyrosine kinase. It targets Aurora A, JAK2, Abl (Q252H), Abl1 (T315I), AuroraB, DRAK1, FGFR1, FGFR1 (V561M), FGFR2, FGFR2 (N549H), and FGFR3.
Molecular Weight
381.4
Molecular Formula
C19H23N7O2
Targets
Aurora A: 3.0 nM; JAK2: 1.2 nM; Abl (Q252H): 10-30 nM; Abl1 (T315I): 4 nM; AuroraB: 3.0 nM; DRAK1: 10-30 nM; FGFR1: 10-30 nM; FGFR1 (V561M): 10-30 nM; FGFR2: 1-10 nM; FGFR2 (N549H): 10-30 nM; FGFR3: 10-30 nM
Form
Lyophilized powder
Purity
≥98%
Solubility
DMSO: 68 mg/mL (178.28 mM); Water: Insoluble; Ethanol: 34 mg/mL (89.13 mM)
Identity
Confirmed by NMR/HPLC/MS.
Stability
The product is stable for three years when stored at the recommended temperature in lyophilized powder.
Applications
AT9283 serves as a research compound to investigate inhibition of multiple kinases including JAK2, with applications in cancer therapy.
Storage
Store at -20ºC.

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