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

CAS No.
646530-37-2
Chemical Name:
3-Isoxazolecarboxamide, N-(2,4-dichlorophenyl)-5-methyl-
Synonyms
GBL-5g;UGL-5g;UTL-5g;N-(2,4-Dichlorophenyl)-5-methylisoxazole-3-carboxamide;3-Isoxazolecarboxamide, N-(2,4-dichlorophenyl)-5-methyl-;liver,inhibit,Inhibitor,chemoprotective,Tumor Necrosis Factor Receptor,radioprotective,acute,toxicity,hepatotoxicity,anti-inflammatory,TNF Receptor,UTL 5g,UTL5g,TNFR,UTL-5g
CBNumber:
CB58146679
Molecular Formula:
C11H8Cl2N2O2
Molecular Weight:
271.1
MDL Number:
MFCD08724989
MOL File:
646530-37-2.mol
MSDS File:
SDS
Last updated:2024-07-02 08:55:11

3-Isoxazolecarboxamide, N-(2,4-dichlorophenyl)-5-methyl- Properties

Boiling point 336.2±42.0 °C(Predicted)
Density 1.469±0.06 g/cm3(Predicted)
storage temp. Store at -20°C
pka 9.45±0.70(Predicted)
form Solid
color White to off-white
FDA UNII BL421NQ9XM

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H302-H315-H319-H335
Precautionary statements  P261-P280-P301+P312-P302+P352-P305+P351+P338

3-Isoxazolecarboxamide, N-(2,4-dichlorophenyl)-5-methyl- Chemical Properties,Uses,Production

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.

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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.

3-Isoxazolecarboxamide, N-(2,4-dichlorophenyl)-5-methyl- Preparation Products And Raw materials

Raw materials

Preparation Products

3-Isoxazolecarboxamide, N-(2,4-dichlorophenyl)-5-methyl- Suppliers

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3-Isoxazolecarboxamide, N-(2,4-dichlorophenyl)-5-methyl- Spectrum

3-Isoxazolecarboxamide, N-(2,4-dichlorophenyl)-5-methyl- UTL-5g UGL-5g GBL-5g liver,inhibit,Inhibitor,chemoprotective,Tumor Necrosis Factor Receptor,radioprotective,acute,toxicity,hepatotoxicity,anti-inflammatory,TNF Receptor,UTL 5g,UTL5g,TNFR,UTL-5g N-(2,4-Dichlorophenyl)-5-methylisoxazole-3-carboxamide 646530-37-2