Name | Methanesulfonamide, N-[[1-[6-(trifluoromethyl)-4-quinazolinyl]-3-piperidinyl]methyl]- |
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Description | SRI-37330 is an orally active TXNIP inhibitor. SRI-37330 decreases glucagon secretion and action and blocks hepatic glucose output. SRI-37330 can be used in the research of obesity and diabetes[1]. |
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Related Catalog | |
Target |
TXNIP[1] |
In Vitro | SRI-37330 (1 μM, 24 h) inhibits the activity of the human TXNIP promoter in INS-1 cells[1]. SRI-37330 (1 μM, 24 h) inhibits Mrna and protein levels of TXNIP in INS-1 cells[1]. SRI-37330 (5 μM, 24 h) inhibits polymerase II (Pol II) binding to the E-box motif region of the TXNIP promoter[1]. SRI-37330 (5 μM, 24 h) lowers glucagon secretion in TC1-6 cells[1]. SRI-37330 (0-5 μM, 24 h) inhibits glucagon-induced glucose output from primary hepatocytes[1]. RT-PCR[1] Cell Line: INS-1 cells Concentration: 1 μM Incubation Time: 24 h Result: Inhibited endogenous TXNIP mRNA expression with an IC50 of 0.64 μM. |
In Vivo | SRI-37330 (100 mg/kg, p.o., in drinking water, 3 weeks) decreases glucagon secretion and action and blocks hepatic glucose output[1]. SRI-37330 (100 mg/kg, p.o., in drinking water, 3 weeks) is well tolerated in male C57BL/6J mice[1]. SRI-37330 (100 mg/kg, p.o., in drinking water, 3 weeks) reverses obesity- and STZ-induced diabetes and hepatic steatosis in mice[1]. Animal Model: C57BL/6J mice[1] Dosage: 100 mg/kg Administration: Oral administration (p.o.), in drinking water, 3 weeks. Result: Lowered serum glucagon levels, inhibited hepatic glucose production and improved glucose homeostasis in mice. |
Molecular Formula | C16H19F3N4O2S |
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Molecular Weight | 388.41 |