ChemicalBook--->CAS DataBase List--->19983-28-9

19983-28-9

19983-28-9 Structure

19983-28-9 Structure
IdentificationBack Directory
[Name]

Morpholine, 4-(4-phenyl-2-thiazolyl)-
[CAS]

19983-28-9
[Synonyms]

VPC-14228
VPC-14228 >=98% (HPLC)
Morpholine, 4-(4-phenyl-2-thiazolyl)-
[Molecular Formula]

C13H14N2OS
[MDL Number]

MFCD00628805
[MOL File]

19983-28-9.mol
[Molecular Weight]

246.33
Chemical PropertiesBack Directory
[Melting point ]

76.0-78.5 °C(Solv: hexane (110-54-3); benzene (71-43-2))
[Boiling point ]

422.0±55.0 °C(Predicted)
[density ]

1.227±0.06 g/cm3(Predicted)
[storage temp. ]

2-8°C
[solubility ]

DMSO: 20mg/mL, clear
[form ]

Solid
[pka]

4.47±0.50(Predicted)
[color ]

White to light yellow
Hazard InformationBack Directory
[Description]

VPC-14228 is a specific inhibitor of AR-DBD. It acts by inhibiting both Y594A and Q592A mutants, blocking the interaction of the AR with androgen response elements in the nucleus..
[Uses]

VPC-14228 is an inhibitor that selectively targets androgen receptor DNA binding domain (AR-DBD). VPC-14228 inhibits the interaction between AR and DNA, thereby blocking AR-mediated transcriptional activation. VPC-14228 does not rely on nuclear localization inhibition, but rather inhibits the activity of full-length AR and splice variant AR-V7 by interfering with AR binding to chromatin. And VPC-14228 has high selectivity for other nuclear receptors such as ER and PR. VPC-14228 can be used in the study of prostate cancer[1][2].
[References]

[1] Kush Dalal, et al. Selectively targeting the DNA-binding domain of the androgen receptor as a prospective therapy for prostate cancer. J Biol Chem. 2014 Sep 19;289(38):26417-26429. DOI:10.1074/jbc.M114.553818
[2] Bhumireddy A, et al. Design, synthesis, and biological evaluation of phenyl thiazole-based AR-V7 degraders. Bioorg Med Chem Lett. 2022 Jan 1;55:128448. DOI:10.1016/j.bmcl.2021.128448
Spectrum DetailBack Directory
[Spectrum Detail]

Morpholine, 4-(4-phenyl-2-thiazolyl)-(19983-28-9)1HNMR
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