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ChemicalBook--->CAS DataBase List--->168021-79-2

168021-79-2

168021-79-2 Structure

168021-79-2 Structure
IdentificationBack Directory
[Name]

1,3-BENZENEDISULFONIC ACID, 4-[[(1,1-DIMETHYLETHYL)OXIDOIMINO]METHYL]-,DISODIUM SALT
[CAS]

168021-79-2
[Synonyms]

CPI22
CPI-22
CPI 22
CXY059
OKN007
D03875
HPN-07
CS-791
OKN-007
CXY-059
CXY 059
OKN 007
ARL16556
Cerovive
ARL-16556
ARL 16556
Disufenton
NXY059/NXY-059
disufenton sodium
Cerovive(NXY-059)
NXY-059(Cerovive)
NXY-059(Disufentonsodium)
NXY 059 (CEROVIVE);NXY059
Disufenton sodium (NXY-059)
Disufenton sodium (usan/inn)
Disufenton sodiuM (NXY 059,Cerovive)
4-[[(1,1-Dimethylethyl)oxoimino]methyl]-1,3-benzenedisulfonicaciddisodiumsalt
Disodium,4-[(Z)-[tert-butyl(oxido)azaniumylidene]methyl]benzene-1,3-disulfonate
1,3-BENZENEDISULFONIC ACID, 4-[[(1,1-DIMETHYLETHYL)OXIDOIMINO]METHYL]-,DISODIUM SALT
1,3-Benzenedisulfonic acid, 4-[[(1,1-dimethylethyl)imino]methyl]-, N-oxide, disodium salt
NXY059; NXY 059; NXY-059; CXY 059; CXY059; CXY-059; OKN007; OKN-007; OKN 007; ARL 16556; ARL16556; ARL-16556; CPI-22; CPI22; CPI 22; CEROVIVE; DISUFENTON SODIUM
[Molecular Formula]

C11H14NNa2O7S2
[MDL Number]

MFCD09833648
[MOL File]

168021-79-2.mol
[Molecular Weight]

382.341
Chemical PropertiesBack Directory
[Melting point ]

>300 °C
[storage temp. ]

-20°C
[solubility ]

Soluble in DMSO
[form ]

powder
[color ]

white to beige
[Water Solubility ]

H2O: 2mg/mL, clear
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302
[Precautionary statements ]

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

A free radical trapping compound
[Uses]

Cerovive (NXY-059) is a novel nitrone, shows efficacious neuroprotective effects that prevents ischemic damage by trapping free radicals. Neuroprotectant.
[Biological Activity]

Free radical trapping agent. Reduces infarct size and preserves brain function in several animal models of acute ischemic stroke. Neuroprotectant.
[Biochem/physiol Actions]

Originally characterized for its NO-mimicking activity in preventing peroxynitrite formation and in vivo neuroprotective efficacy in animal models of cerebral ischemia (100 mg/kg i.v. in rabbits; 30-60 mg/kg plus 30-60 mg/kg/h i.v. or 50 mg/kg plus 8.8 mg/kg/h s.c. in rats; 28 mg/kg plus 16 mg/kg/h i.v. in monkeys), OKN-007 (HPN-07, NXY-059) is an orally available α-phenyl-tert-butylnitrone (PBN) derivative that is also shown to exhibit sulfatase 2 (SULF2) inhibitory activity and anticancer efficacy both in cultures (effective conc. 170-200 μM in Huh7 heptoma cultures) and in several rodent glioma models in vivo (C6, RG2, and GL261; 75 mg/kg/day for rats and 168 mg/kg/day for mice via drinking water).
[storage]

Store at -20°C
[References]

[1] kuroda s1, tsuchidate r, smith ml, maples kr, siesj? bk.
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