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ChemicalBook--->CAS DataBase List--->618913-30-7

618913-30-7

618913-30-7 Structure

618913-30-7 Structure
IdentificationBack Directory
[Name]

AZD-5904
[CAS]

618913-30-7
[Synonyms]

AZD-5904
AZ1;TX4;AZD5904
AZD5904 (AZD 5904
AZD5904,AZD-5904,Inhibitor,AZD 5904,Glutathione Peroxidase,inhibit
(R)-3-((Tetrahydrofuran-2-yl)methyl)-2-thioxo-1,2,3,9-tetrahydro-6H-purin-6-one
6H-Purin-6-one, 1,2,3,9-tetrahydro-3-[[(2R)-tetrahydro-2-furanyl]methyl]-2-thioxo-
[EINECS(EC#)]

642-433-3
[Molecular Formula]

C10H12N4O2S
[MDL Number]

MFCD31619279
[MOL File]

618913-30-7.mol
[Molecular Weight]

252.29
Chemical PropertiesBack Directory
[density ]

1.54±0.1 g/cm3(Predicted)
[storage temp. ]

Store at -20°C
[solubility ]

dmso:22.73(Max Conc. mg/mL);90.09(Max Conc. mM)
[form ]

A solid
[pka]

8.53±0.20(Predicted)
[color ]

White to yellow
Safety DataBack Directory
[Symbol(GHS) ]


GHS08
[Signal word ]

Warning
[Hazard statements ]

H361
[Precautionary statements ]

P201-P202-P281-P308+P313-P405-P501
Hazard InformationBack Directory
[Uses]

(S)-3-((Tetrahydrofuran-2-yl)methyl)-2-thioxo-1,2,3,7-tetrahydro-6H-purin-6-one is used as an internal standard and also as an analytical standard.
[Biological Activity]

AZD5904 (TX4) is an orally active 2-thioxanthine class suicide substrate th at targets myeloperoxidase (MPO) for mechanism-based inactivationcovalently modifying MPO heme group without converting the enzyme to compound II. AZD5904 effectively inhibits peroxide-induced human MPO chlorination activity (IC50 = 0.2 μM) and extracellular MPO activity in PMA-stimulated human neutrophil cultures (by 68% at 1 μM). Oral administration (20-180 μmol/kg) of the racemate (TX3) is efficacious in reducing inflammation site MPO activity in mice in vivo with 10- to 19-fold selectivity over lactoperoxidase (LPO)thyroid peroxidase (TPO)and >70-fold selectivity over a panel of other enzymesion channelsand receptors.
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