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493028-20-9

493028-20-9 Structure

493028-20-9 Structure
IdentificationBack Directory
[Name]

5-ETHYL-4-(4-METHOXY-PHENYL)-THIAZOL-2-YLAMINE
[CAS]

493028-20-9
[Synonyms]

CBFβInhibitor
CBFβ Inhibitor
TIMTEC-BB SBB011699
Runx1-CBFβ interaction inhibitor 1
2-Thiazolamine, 5-ethyl-4-(4-methoxyphenyl)-
CBFβ Inhibitor - CAS 493028-20-9 - Calbiochem
5-ETHYL-4-(4-METHOXY-PHENYL)-THIAZOL-2-YLAMINE
5-ethyl-4-(4-methoxyphenyl)-1,3-thiazol-2-amine
[Molecular Formula]

C12H14N2OS
[MDL Number]

MFCD02232182
[MOL File]

493028-20-9.mol
[Molecular Weight]

234.32
Chemical PropertiesBack Directory
[Boiling point ]

421.6±40.0 °C(Predicted)
[density ]

1.192±0.06 g/cm3(Predicted)
[storage temp. ]

+2C to +8C
[solubility ]

DMF: 50 mg/ml; DMF:PBS(pH 7.2)(1:1): 0.5 mg/ml; DMSO: 30 mg/ml; Ethanol: 25 mg/ml
[form ]

Tan solid
[pka]

5.00±0.10(Predicted)
Safety DataBack Directory
[Hazard Codes ]

Xi
[HazardClass ]

IRRITANT
Hazard InformationBack Directory
[Description]

Core binding factors (CBFs) are heterodimeric transcription factors consisting of a DNA-binding CBFα component (a RUNX protein) and an enhancer of binding, CBFβ. CBF dimers have central roles in hematopoiesis and, when dysfunctional, in leukemias. CBFβ inhibitor is a small molecule that binds to CBFβ and inhibits its association with Runx1 (IC50 = 3.2 μM). It blocks CBFβ-Runx1 interactions in ME-1 cells, acute myeloid leukemia cells harboring dysfunctional CBF, reducing proliferation without toxicity.
[Uses]

Core binding factors (CBFs) are heterodimeric transcription factors consisting of a DNA-binding CBFα component (a RUNX protein) and an enhancer of binding, CBFβ. CBF dimers have central roles in hematopoiesis and, when dysfunctional, in leukemias. CBFβ inhibitor is a small molecule that binds to CBFβ and inhibits its association with Runx1 (IC50 = 3.2 μM). It blocks CBFβ-Runx1 interactions in ME-1 cells, acute myeloid leukemia cells harboring dysfunctional CBF, reducing proliferation without toxicity.
[References]

[1] KEVIN A. LINK  James C M  Fu Sheng Chou. Core binding factor at the crossroads: Determining the fate of the HSC?[J]. Journal of Cellular Physiology, 2009, 222 1: 50-56. DOI: 10.1002/jcp.21950
[2] GEMMA SWIERS  Nancy A S  Marella de Bruijn. Hematopoietic stem cell emergence in the conceptus and the role of Runx1.[J]. International Journal of Developmental Biology, 2010, 54 6-7: 1151-1163. DOI: 10.1387/ijdb.103106gs
[3] MICHAEL J GORCZYNSKI. Allosteric inhibition of the protein-protein interaction between the leukemia-associated proteins Runx1 and CBFbeta.[J]. Chemistry & biology, 2007, 14 10: 1186-1197. DOI: 10.1016/j.chembiol.2007.09.006
Spectrum DetailBack Directory
[Spectrum Detail]

5-ETHYL-4-(4-METHOXY-PHENYL)-THIAZOL-2-YLAMINE(493028-20-9)1HNMR
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