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ChemicalBook--->CAS DataBase List--->459420-09-8

459420-09-8

459420-09-8 Structure

459420-09-8 Structure
IdentificationBack Directory
[Name]

4(3H)-Pyrimidinone, 6-methyl-2-[[2-(1-naphthalenyl)-2-oxoethyl]thio]-
[CAS]

459420-09-8
[Synonyms]

I3MT-3
13MT-3
4(3H)-Pyrimidinone, 6-methyl-2-[[2-(1-naphthalenyl)-2-oxoethyl]thio]-
[Molecular Formula]

C17H14N2O2S
[MDL Number]

MFCD33023210
[MOL File]

459420-09-8.mol
[Molecular Weight]

310.37
Chemical PropertiesBack Directory
[Boiling point ]

514.9±52.0 °C(Predicted)
[density ]

1.30±0.1 g/cm3(Predicted)
[storage temp. ]

Store at -20°C
[solubility ]

DMSO: 125 mg/mL (402.75 mM)
[form ]

Solid
[pka]

7.72±0.50(Predicted)
[color ]

Off-white to light brown
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P280-P301+P312-P302+P352-P305+P351+P338
Hazard InformationBack Directory
[Uses]

I3MT-3 (HMPSNE) is a potent, selective, and cell-membrane permeable inhibitor of 3-Mercaptopyruvate sulfurtransferase (3MST) (IC50=2.7 μM). I3MT-3 is inactive for other H2S/sulfane sulfur-producing enzymes.?I3MT-3 targets a persulfurated cysteine residue located in the active site of 3MST[1].
[Biological Activity]

I3MT-3 (HMPSNE) is a potent, selective and cell membrane permeable inhibitor of 3-mercaptopyruvate sulfurtransferase (3MST) (IC50=2.7 μM), inactive against other hydrogen sulfide/sulfanilamide sulfur enzymes. I3MT-3 targets a perthiocysteine residue located in the active site of 3MST.
[target]

IC50: 2.7 μM (3-Mercaptopyruvate sulfurtransferase (3MST))

[storage]

Store at -20°C
[References]

[1] Kenjiro Hanaoka, et al. Discovery and Mechanistic Characterization of Selective Inhibitors of H 2 S-producing Enzyme: 3-Mercaptopyruvate Sulfurtransferase (3MST) Targeting Active-site Cysteine Persulfide. Sci Rep. 2017 Jan 12;7:40227 DOI:10.1038/srep40227
[2] Fiona Augsburger, et al. Role of 3-Mercaptopyruvate Sulfurtransferase in the Regulation of Proliferation, Migration, and Bioenergetics in Murine Colon Cancer Cells. Biomolecules. 2020 Mar 13;10(3):447. DOI:10.3390/biom10030447
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