SML3575
TY-51469
≥98% (HPLC)
Synonym(s):
2-[4-[[(5-Fluoro-3-methylbenzo[b]thien-2-yl)sulfonyl]amino]-3-(methylsulfonyl)phenyl]-4-thiazolecarboxylic acid, TY 51469
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About This Item
Empirical Formula (Hill Notation):
C20H15FN2O6S4
CAS Number:
Molecular Weight:
526.60
UNSPSC Code:
12352200
NACRES:
NA.21
MDL number:
Product Name
TY-51469, ≥98% (HPLC)
InChI key
CBRCULCCRGSSLB-UHFFFAOYSA-N
SMILES string
FC1=CC2=C(C=C1)SC(S(NC3=CC=C(C=C3S(C)(=O)=O)C4=NC(C(O)=O)=CS4)(=O)=O)=C2C
assay
≥98% (HPLC)
form
powder
color
white to beige
solubility
DMSO: 2 mg/mL, clear
storage temp.
2-8°C
Quality Level
Related Categories
Biochem/physiol Actions
Potent and selective chymase inhibitor that prevents development and progression of non-alcoholic steatohepatitis in rats
TY-51469 is a potent and selective chymase inhibitor that prevents development and progression of non-alcoholic steatohepatitis in rats. TY-51469 inhibits activation of intestinal MMP-9 and prevents intestinal damage in indomethacin-induced small intestinal damage in rats. Also TY-51469 might protect against pancreatic islet disorganization.
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
Regulatory Information
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Chymase inhibition reduces infarction and matrix metalloproteinase-9 activation and attenuates inflammation and fibrosis after acute myocardial ischemia/reperfusion
Oyamada S, Bianchi C, Takai S, Chu LM, Sellke FW
Journal of Pharmacology and Experimental Therapeutics, 339, 143-151 (2011)
Chymase inhibitor prevents the development and progression of non-alcoholic steatohepatitis in rats fed a high-fat and high-cholesterol diet
Miyaoka Y, Jin D, Tashiro K, Komeda K, Masubuchi S, Hirokawa F, Hayashi M, Takai S, Uchiyama K
Journal of Pharmacological Sciences, 134, 139-146 (2017)
Significance of chymase-dependent matrix metalloproteinase-9 activation on indomethacin-induced small intestinal damages in rats
Kakimoto K, Takai S, Murano M, Ishida K, Yoda Y, Inoue T, Jin D, Umegaki E, Higuchi K
Journal of Pharmacology and Experimental Therapeutics, 332, 684-689 (2010)
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