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ChemicalBook--->CAS DataBase List--->1422535-52-1

1422535-52-1

1422535-52-1 Structure

1422535-52-1 Structure
IdentificationBack Directory
[Name]

T-3775440 hydrochloride
[CAS]

1422535-52-1
[Synonyms]

T-3775440HCl
T 3775440;T3775440
T-3775440 hydrochloride
[EINECS(EC#)]

604-604-1
[Molecular Formula]

C18H23ClN4O
[MDL Number]

MFCD31692337
[MOL File]

1422535-52-1.mol
[Molecular Weight]

346.86
Chemical PropertiesBack Directory
[storage temp. ]

Store at -20°C
[solubility ]

DMSO : ≥ 30.18 mg/mL (87.01 mM)
[form ]

Solid
[color ]

Light yellow to yellow
Hazard InformationBack Directory
[Biological Activity]

TargetValue
LSD1
()
2.1 nM
[Biological Activity]

T-3775440 hydrochloride is an irreversible LSD1 inhibitor. It is highly selective for LSD1 relative to other monoamine oxidases with IC50 of 2.1 nM.
[in vitro]

T-3775440 hydrochloride enhances the transdifferentiation of erythrocytes/megakaryocytes to granule-like monocytes. It disrupts the interaction of LSD1 and GFI1B. AEL (TF-1a, HEL92.1.7) cells and AMKL (CMK11-5, M07e) cells were treated with T-3775440 for 48 hours, which induced cell cycle arrest and apoptosis. In TF-1a and CMK11-5 cells, treatment with T-3775440 increased cells in G1 and sub-G1 phases.

[in vivo]

T-3775440 inhibits tumor growth in a mouse xenograft model of AML. In mice T-3775440 hydrochloride caused a transient decrease in platelets followed by a large rebound. After a single dose, it had no apparent effect on red blood cell counts. T-3775440 hydrochloride also exerted antitumor activity in AEL (HEL 92.1.7) model and AMKL (CMK11-5) model.

[storage]

Store at -20°C
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