ChemicalBook--->CAS DataBase List--->2271358-64-4

2271358-64-4

2271358-64-4 Structure

2271358-64-4 Structure
IdentificationBack Directory
[Name]

UAMC-3203
[CAS]

2271358-64-4
[Synonyms]

UAMC-3203
UAMC3203;UAMC 3203
[Molecular Formula]

C25H37N5O2S
[MDL Number]

MFCD31813707
[MOL File]

2271358-64-4.mol
[Molecular Weight]

471.66
Chemical PropertiesBack Directory
[Boiling point ]

668.3±65.0 °C(Predicted)
[density ]

1.214±0.06 g/cm3(Predicted)
[storage temp. ]

Store at -20°C
[solubility ]

Ethanol: Soluble
[form ]

A crystalline solid
[pka]

12.27±0.50(Predicted)
[color ]

White to off-white
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)Environment (GHS09)
GHS07,GHS09
[Signal word ]

Warning
[Hazard statements ]

H302-H400-H410
[Precautionary statements ]

P264-P270-P273-P301+P312-P330-P391-P501
Hazard InformationBack Directory
[Uses]

UAMC-3203 is a potent and selective Ferroptosis inhibitor with an IC50 of 12 nM.
[Biological Activity]

UAMC-3203 is a ferroptosis inhibitor with IC50 of 10 nM in IMR-32 neuroblastoma cells.
[in vitro]

UAMC-3203 was incubated with human microsomes or rat microsomes, and the T 1/2 were 20.5 h and 16.5 h, respectively. When co-incubated with mouse microsomes, UAMC-3203 showed relatively poor stability, with a T 1/2 of 3.46 h.

[in vivo]

In mice, UAMC-3203 can significantly reduce the plasma concentration of lactate dehydrogenase. After administration, it is rapidly removed from the blood and enters various tissues. Significant levels of UAMC-3203 were detected in the tissues tested, such as liver, kidney and lung.

[target]

< td style="border-bottom: 1px dotted #ccc;padding: 5px;"> 10 nM
TargetValue
Ferroptosis
(IMR-32 neuroblastoma cells)
[References]

[1] Devisscher L, et al. Discovery of Novel, Drug-Like Ferroptosis Inhibitors with in Vivo Efficacy. J Med Chem. 2018 Nov 21;61(22):10126-10140. DOI:10.1021/acs.jmedchem.8b01299
Spectrum DetailBack Directory
[Spectrum Detail]

UAMC-3203(2271358-64-4)1HNMR
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