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249886-47-3

249886-47-3 Structure

249886-47-3 Structure
IdentificationBack Directory
[Name]

Benzeneacetic acid, α-[(3,5-dimethoxyphenyl)methylene]-4-[4-[(2,4-dioxo-5-thiazolidinyl)methyl]phenoxy]-, methyl ester
[CAS]

249886-47-3
[Synonyms]

CLX0921
THR0921
THR-0921
CLX-0921
THR 0921
CLX 0921
Benzeneacetic acid, α-[(3,5-dimethoxyphenyl)methylene]-4-[4-[(2,4-dioxo-5-thiazolidinyl)methyl]phenoxy]-, methyl ester
[Molecular Formula]

C28H25NO7S
[MOL File]

249886-47-3.mol
[Molecular Weight]

519.57
Chemical PropertiesBack Directory
[Boiling point ]

706.3±60.0 °C(Predicted)
[density ]

1.308±0.06 g/cm3(Predicted)
[pka]

6.32±0.50(Predicted)
Hazard InformationBack Directory
[Description]

CLX 0921 is a peroxisome proliferator-activated receptor(PPAR)gamma agonist potentially for the treatment of type 2 diabetes.
[Uses]

CLX-0921 is an orally active PPARγ agonist with an IC50 of 1.54 μM. CLX-0921 has a potent antihyperglycemic activity, and can be used for the study of type 2 diabetes[1].
[in vivo]

CLX-0921 (3.1-12.5 mg/kg; oral gavage; once daily; for 19 days) shows dose-dependent antihyperglycemic activity[1].

Animal Model:Male C57BL/KsJ-db/db and C57BL/6J-ob/ob mice (7-week-old)[1]
Dosage:3.1 mg/kg, 6.3 mg/kg, and 12.5 mg/kg
Administration:Oral gavage; once daily; for 19 days
Result: Showed dose-dependent antihyperglycemic activity.
[IC 50]

PPARγ: 1.54 μM (IC50)
[References]

[1] Debendranath Dey, et al. A novel peroxisome proliferator-activated gamma (PPAR gamma) agonist, CLX-0921, has potent antihyperglycemic activity with low adipogenic potential. Metabolism. 2003 Aug;52(8):1012-8. DOI:10.1016/s0026-0495(03)00152-5
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