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1990504-72-7

1990504-72-7 Structure

1990504-72-7 Structure
IdentificationBack Directory
[Name]

Bomedemstat
[CAS]

1990504-72-7
[Synonyms]

Bomedemstat
IMG-7289 ditosylate
[Molecular Formula]

C35H42FN7O5S
[MDL Number]

MFCD32710081
[MOL File]

1990504-72-7.mol
[Molecular Weight]

691.82
Chemical PropertiesBack Directory
[storage temp. ]

4°C, away from moisture
[solubility ]

DMSO : 100 mg/mL (115.74 mM; Need ultrasonic)
[form ]

Solid
[color ]

White to off-white
Hazard InformationBack Directory
[Uses]

Bomedemstat (IMG-7289) ditosylate is an orally active and irreversible lysine-specific demethylase 1 (LSD1) inhibitor. Bomedemstat ditosylate can increase H3K4 and H3K9 methylation, and then alter gene expression. Bomedemstat ditosylate shows anti-cancer activities, inhibits cancer cell proliferation and induces apoptosis[1][2].
[in vivo]

Bomedemstat treatment (oral gavage; 45 mg/kg; once daily; 56 d) normalizes or improves blood cell counts, reduces spleen volumes, restores normal splenic architecture, and reduces bone marrow fibrosis[1].

Animal Model:Mx-Jak2V617F mice[1]
Dosage:45?mg/kg
Administration:Oral gavage; 45?mg/kg; once daily; 56 days
Result:Reduced splenomegaly significantly with a few treated mice normalizing their spleen weight, the 56-day course led to partial restoration of lymph follicles and spleen architecture by histological examination.
[IC 50]

KDM1/LSD1
[storage]

4°C, away from moisture
[References]

[1] Jonas S Jutzi,et al. LSD1 Inhibition Prolongs Survival in Mouse Models of MPN by Selectively Targeting the Disease Clone. Hemasphere.2018 Jun 8;2(3):e54. DOI:10.1097/HS9.0000000000000054
[2] Yuan Fang, et al. LSD1/KDM1A inhibitors in clinical trials: advances and prospects. J Hematol Oncol. 2019 Dec 4;12(1):129. DOI:10.1186/s13045-019-0811-9
Spectrum DetailBack Directory
[Spectrum Detail]

Bomedemstat(1990504-72-7)1HNMR
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