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ChemicalBook--->CAS DataBase List--->646530-37-2

646530-37-2

646530-37-2 Structure

646530-37-2 Structure
IdentificationBack Directory
[Name]

3-Isoxazolecarboxamide, N-(2,4-dichlorophenyl)-5-methyl-
[CAS]

646530-37-2
[Synonyms]

UTL-5g
UGL-5g
3-Isoxazolecarboxamide, N-(2,4-dichlorophenyl)-5-methyl-
[Molecular Formula]

C11H8Cl2N2O2
[MDL Number]

MFCD08724989
[MOL File]

646530-37-2.mol
[Molecular Weight]

271.1
Chemical PropertiesBack Directory
[Boiling point ]

336.2±42.0 °C(Predicted)
[density ]

1.469±0.06 g/cm3(Predicted)
[storage temp. ]

Store at -20°C
[form ]

Solid
[pka]

9.45±0.70(Predicted)
[color ]

White to off-white
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
Spectrum DetailBack Directory
[Spectrum Detail]

3-Isoxazolecarboxamide, N-(2,4-dichlorophenyl)-5-methyl-(646530-37-2)1HNMR
Hazard InformationBack Directory
[Biological Activity]

UTL-5g (GBL-5g) is an anti-inflammatory TNF-α inhibitor with chemoprotective and hepatic radioprotective effects. It reduces cisplatin-induced hepatotoxicity, nephrotoxicity and bone marrow toxicity by inhibiting factors such as TNF-α.
[in vitro]

RAW 264.7 macrophages are transfected with the respective reporter assay plasmids, pretreated with UTL-5g at 1, 10 or 50 μM for 60 min and then challenged with 100 ng/ml LPS. After a 16 h incubation, transcription factor activity is measured. Transcription factors that shows a UTL-5g dose-dependent decrease in activity in two experiments are categorized as being disrupted by UTL-5g.

[in vivo]

UTL-5g (GBL-5g) lowers levels of TGF-β and TNF-α elevated by lung irradiation.
UTL-5g (60 mg/kg; po; daily for 4 days) shows positive effects in increasing the survival rates and extending the survival times.

< /tr>
Animal Model: C57BL/6, male mice (8-10 weeks)
Dosage: 15, 30, and 60 mg/kg
Administration: Ip; before irradiation, daily x 5
Result: Blood levels of TGF-β were lowered.
Animal Model: BDF1 female mice
Dosage: Po; daily for 4 days
Administration: 60 mg/kg (30 min before ip injection of Cisplatin at 10, 15, and 20 mg/kg respectively on Day 0)
Result: Increased the survival rate and delayed the time to death for mice treated with 150% of the maximum tolerated dose (MTD) of Cisplatin (15 mg/kg). At 200% of the MTD of Cisplatin (20 mg/kg), treatment of UTL-5g increased the survival rate and delayed the time to death.
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