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6505-99-3

6505-99-3 Structure

6505-99-3 Structure
IdentificationBack Directory
[Name]

2H-Purin-2-one,1,3,6,9-tetrahydro-1,3-dimethyl-8-[[2-(4-morpholinyl)ethyl]thio]-6-thioxo-
[CAS]

6505-99-3
[Synonyms]

JA2131
1,3-dimethyl-8-(2-morpholin-4-ylethylsulfanyl)-6-sulfanylidene-7H-purin-2-one
2H-Purin-2-one,1,3,6,9-tetrahydro-1,3-dimethyl-8-[[2-(4-morpholinyl)ethyl]thio]-6-thioxo-
[Molecular Formula]

C13H19N5O2S2
[MDL Number]

MFCD34184555
[MOL File]

6505-99-3.mol
[Molecular Weight]

341.452
Chemical PropertiesBack Directory
[storage temp. ]

2-8°C
[solubility ]

DMSO: 2mg/mL, clear
[form ]

Solid
[color ]

White to off-white
Hazard InformationBack Directory
[Uses]

JA2131 is a small molecular inhibitor of Poly(ADP-ribose) Glycohydrolase (PARG) (IC50=0.4 μM). JA2131 regulate DNA damage responses, causes replication fork stalling and cancer cell death[1][2].
[Biological Activity]

JA2131 is a cell penetrantpotent and selective poly(ADP-ribose) glycohydrolase (PARG) inhibitor th at selectively kills cancer cells. JA2131 induces PARP1 hyper-PARylation and sensitizes cancer cells to radiation-induced DNA damage. JA2131 induces replication fork defects.
[References]

[1] Houl JH, et al. Selective small molecule PARG inhibitor causes replication fork stalling and cancer cell death. Nat Commun. 2019 Dec 11;10(1):5654. DOI:10.1038/s41467-019-13508-4
[2] Brosey CA, et al. Targeting SARS-CoV-2 Nsp3 macrodomain structure with insights from human poly(ADP-ribose) glycohydrolase (PARG) structures with inhibitors. Prog Biophys Mol Biol. 2021 Aug;163:171-186. DOI:10.1016/j.pbiomolbio.2021.02.002
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