Name | 2-pyridin-2-yl-1,3-benzothiazin-4-one |
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Synonyms |
BTZO-1
2-pyridin-2-yl-4H-1,3-benzothiazin-4-one |
Description | BTZO-1 binds to Macrophage migration inhibitory factor (MIF) with a Kd value of 68.6 nM, and its binding requires the N-terminal Pro1. BTZO-1 can activate antioxidant response element (ARE)-mediated gene expression and suppress oxidative stress-induced cardiomyocyte apoptosis in vitro[1]. |
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Related Catalog | |
Target |
Kd:68.6 nM (Macrophage migration inhibitory factor)[1] |
In Vitro | BTZO-1 (0-330 nM; 24 hours) dose-dependently suppressed serum deprivation-induced cardiomyocyte death; the minimum effective concentration (MEC1.5), the concentration of a sample necessary to give a 50% increase in cell viability, is 16 nM[1]. BTZO-1 (0.37 μM; 21 hours) upregulates mRNA protein levels of GST Ya and HO-1 in cardiomyocytes[1]. Cell Viability Assay[1] Cell Line: Primary Neonatal Rat Cardiomyocytes Concentration: 0-330 nM Incubation Time: 24 hours Result: Suppressed serum deprivation or DOX-induced cell death. |
References |
Molecular Formula | C13H8N2OS |
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Molecular Weight | 240.28000 |
Exact Mass | 240.03600 |
PSA | 71.09000 |
LogP | 2.71850 |
~44% 99420-15-2 |
Literature: Takeda Pharmaceutical Company Limited Patent: EP1500402 A1, 2005 ; Location in patent: Page 12 ; |
~% 99420-15-2 |
Literature: Conti; Leandri Bollettino Scientifico della Facolta di Chimica Industriale di Bologna, 1957 , vol. 15, p. 37 |
~43% 99420-15-2 |
Literature: Kimura, Harihide; Tanida, Seiichi; Kaneko, Tatsuhiko Patent: US2003/186971 A1, 2003 ; |