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1448723-60-1

1448723-60-1 Structure

1448723-60-1 Structure
IdentificationBack Directory
[Name]

UM729
[CAS]

1448723-60-1
[Synonyms]

C07
UM729
CS-1240
UM-729;UM 729
UM729 USP/EP/BP
methyl 4-(3-(piperidin-1-yl)propylamino)-9H-pyrimido[4,5-b]indole-7-carboxylate
4-[[3-(1-Piperidinyl)propyl]amino]-9H-pyrimido[4,5-b]indole-7-carboxylic acid methyl ester
9H-Pyrimido[4,5-b]indole-7-carboxylic acid, 4-[[3-(1-piperidinyl)propyl]amino]-, methyl ester
[Molecular Formula]

C20H25N5O2
[MDL Number]

MFCD28167784
[MOL File]

1448723-60-1.mol
[Molecular Weight]

367.44
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
Hazard InformationBack Directory
[Biological Activity]

UM729 is an enhancer of aryl hydrocarbon receptor (AhR) antagonists.
[in vitro]

um729 expands normal hematopoietic stem and progenitor cells (HSPC) in an AhR-independent manner, and UM729 inhibits AML cell differentiation. In 05H163 cells, the addition of UM729 increased CD34+CD15- Number of cells. It can inhibit the differentiation of most AML cells in combination with AhR antagonists.
[in vivo]

In NSG mice, UM729, alone or in combination with SR1, enhanced engraftment but not leukemia stem cell (LSC) frequency distribution.
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