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INCB059872

Catalog No. T39226   CAS 1802909-49-4
Synonyms: INCB059872

INCB059872 is a highly potent, orally active, selective, and irreversible inhibitor of Lysine-Specific Demethylase 1 (LSD1). Its chemical properties make it suitable for use in researching myeloid leukemia.

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INCB059872 Chemical Structure
INCB059872, CAS 1802909-49-4
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Biological Description
Chemical Properties
Storage & Solubility Information
Description INCB059872 is a highly potent, orally active, selective, and irreversible inhibitor of Lysine-Specific Demethylase 1 (LSD1). Its chemical properties make it suitable for use in researching myeloid leukemia.
In vitro INCB059872 (25 nM; 48 hours; 293T cells) increases enhancer activity and gene expression[1]. INCB059872 (25 nM; 24 hours; THP-1 cells) makes THP-1 show a growth defect within one cell doubling time or approximately 3 days. INCB059872 (100 nM; 24 hours; MV-4–11 cells) treated MV-4–11 cells continues to grow as DMSO-treated cells for multiple cell divisions. INCB059872 (THP-1 cells) regulates PRO-seq analysis identifies genes and enhancers[1]. Western Blot Analysis[1]Cell Line: 293T cells Concentration: 250 nM Incubation Time: 48 hours Result: Increased enhancer activity and gene expression.
In vivo INCB059872 (10 mg/kg; p.o.; 0, 4, or 6 days) administration in mice resulted in alterations in bone marrow progenitor populations, as identified by single-cell RNA sequencing[1].
Synonyms INCB059872
Molecular Weight 386.536
Formula C23H34N2O3
CAS No. 1802909-49-4

Storage

Powder: -20°C for 3 years | In solvent: -80°C for 1 year

TargetMolReferences and Literature

1. Johnston G, et al. Nascent transcript and single-cell RNA-seq analysis defines the mechanism of action of the LSD1 inhibitor INCB059872 in myeloid leukemia. Gene. 2020;752:144758.

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Keywords

INCB059872 1802909-49-4 INCB 059872 INCB-059872 inhibitor inhibit

 

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