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688347-51-5

688347-51-5 Structure

688347-51-5 Structure
IdentificationBack Directory
[Name]

4-[[2-[[(2-Cyanophenyl)methyl]thio]-4-oxothieno[3,2-d]pyrimidin-3(4H)-yl]methyl]benzoic acid
[CAS]

688347-51-5
[Synonyms]

SPL 334
SPL-334 >=98% (HPLC)
4-[[2-[[(2-Cyanophenyl)methyl]thio]-4-oxothieno[3,2-d]pyrimidin-3(4H)-yl]methyl]benzoic acid
Benzoic acid, 4-[[2-[[(2-cyanophenyl)methyl]thio]-4-oxothieno[3,2-d]pyrimidin-3(4H)-yl]methyl]-
[Molecular Formula]

C22H15N3O3S2
[MOL File]

688347-51-5.mol
[Molecular Weight]

433.5
Chemical PropertiesBack Directory
[Boiling point ]

694.0±65.0 °C(Predicted)
[density ]

1.41±0.1 g/cm3(Predicted)
[storage temp. ]

2-8°C
[solubility ]

DMSO: 20mg/mL, clear
[form ]

powder
[pka]

4.21±0.10(Predicted)
[color ]

white to beige
[InChIKey]

UWWSCLNCHCROLL-UHFFFAOYSA-N
[SMILES]

OC(C1=CC=C(CN2C(SCC3=CC=CC=C3C#N)=NC(C=CS4)=C4C2=O)C=C1)=O
Safety DataBack Directory
[WGK Germany ]

WGK 3
[Storage Class]

11 - Combustible Solids
[Hazard Classifications]

Aquatic Chronic 4
Hazard InformationBack Directory
[Uses]

SPL 334 is an S-Nitrosoglutathione Reductase inhibitor.
[Biological Activity]

SPL-334 is an inhibitor of S-Nitrosoglutathione reductase (GSNOR)the enzyme responsible for regulating cellular concentrations of S-Nitrosoglutathione (GSNO)which plays a critical role in nitric oxide signaling in the respiratory tract. In a mouse model of allergic airway inflammationSPL-334 reduced airway hyperreactivityand in a bleomycin injury model of interstitial lung diseaseSPL-334 reduced lung inflammation and fibrosis. Studies for treatment of asthmaidiopathic pulmonary fibrosis (IPF)and inflammation are ongoing.
[in vivo]

SPL-334 (0.1-1 mg/kg; Intranasal administration; daily, for 7 d; BALB/c recipient mice with DO11.10 CD4+ Th2 xenograft) causes a reduction in allergic airway inflammation[1].

Animal Model:BALB/c recipient mice with DO11.10 CD4+ Th2 xenograft[1]
Dosage:0.1 or 1 mg/kg
Administration:Intranasal administration; daily, for 7 days
Result:Caused a significant reduction in the influx of lymphocytes and eosinophils into the airways and the level of EPO in the BALF.
Reduced the number of OVA-specific T cells and eosinophils during allergic airway inflammation.
Reduced in peribronchial inflammation and mucus secretion during airway inflammation.
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