ChemicalBook--->CAS DataBase List--->117089-08-4

117089-08-4

117089-08-4 Structure

117089-08-4 Structure
IdentificationBack Directory
[Name]

FW1256
[CAS]

117089-08-4
[Synonyms]

FW1256
1,3,2-Benzoxazaphosphole, 2,3-dihydro-2-phenyl-, 2-sulfide
[Molecular Formula]

C12H10NOPS
[MDL Number]

MFCD32690094
[MOL File]

117089-08-4.mol
[Molecular Weight]

247.25
Chemical PropertiesBack Directory
[Melting point ]

139-142 °C
[Boiling point ]

376.3±25.0 °C(Predicted)
[density ]

1.37±0.1 g/cm3(Predicted)
[storage temp. ]

Store at -20°C
[solubility ]

DMSO: ≥ 250 mg/mL (1011.12 mM)
[form ]

Solid
[pka]

-0.88±0.20(Predicted)
[color ]

White to off-white
Hazard InformationBack Directory
[Uses]

FW1256 is a phenyl analogue and a slow-releasing hydrogen sulfide (H2S) donor. FW1256 inhibits NF-κB activity and induces cell apoptosis. FW1256 exerts potent anti-inflammatory effects and has the potential for cancer and cardiovascular disease treatment[1][2].
[in vivo]

FW1256 (100 mg/kg; intraperitoneal injection; male C57BL/6 mice) treatment reduces IL-1β, TNFα, nitrate/nitrite and PGE2 levels in LPS-treated mice[1].

Animal Model:Male C57BL/6 mice (20-25 g, 6-10 weeks) injected with E. coli lipopolysaccharide (LPS)[1]
Dosage:100 mg/kg
Administration:Intraperitoneal injection
Result:Reduced IL-1β, TNFα, nitrate/nitrite and PGE2 levels in LPS-treated mice.
[storage]

Store at -20°C
[References]

[1] Huang CW, et al. A novel slow-releasing hydrogen sulfide donor, FW1256, exerts anti-inflammatory effects in mouse macrophages and in vivo. Pharmacol Res. 2016 Nov;113(Pt A):533-546. DOI:10.1016/j.phrs.2016.09.032
[2] Feng W, et al. Discovery of New H2S Releasing Phosphordithioates and 2,3-Dihydro-2-phenyl-2-sulfanylenebenzo[d][1,3,2]oxazaphospholes with Improved Antiproliferative Activity. J Med Chem. 2015 Aug 27;58(16):6456-80. DOI:10.1021/acs.jmedchem.5b00848
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