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2319722-53-5

2319722-53-5 Structure

2319722-53-5 Structure
IdentificationBack Directory
[Name]

Benzoic acid, 5-chloro-2-[[2-[2-[[3-(3-furanyl)phenyl]amino]-2-oxoethoxy]acetyl]amino]-, sodium salt (1:1)
[CAS]

2319722-53-5
[Synonyms]

Benzoic acid, 5-chloro-2-[[2-[2-[[3-(3-furanyl)phenyl]amino]-2-oxoethoxy]acetyl]amino]-, sodium salt (1:1)
[Molecular Formula]

C21H18ClN2NaO6
[MOL File]

2319722-53-5.mol
[Molecular Weight]

452.82
Chemical PropertiesBack Directory
[solubility ]

Soluble to 100 mM in DMSO
Hazard InformationBack Directory
[Uses]

TM5441 is an orally bioavailable inhibitor of plasminogen activator inhibitor-1 (PAI-1), has IC50 values between 13.9 and 51.1 μM. TM5441 induces intrinsic apoptosis in several human cancer cell lines. TM5441 attenuates Nω-nitro-l-arginine methyl ester-induced cardiac hypertension and vascular senescence[1][2].
[Biological Activity]

TM 5441 is a plasminogen activator inhibitor-1 (PAI-1) inhibitor (IC50 = 3.58 - 60.3 μM). Increases apoptosis in human cancer cell lines. Reduces senescence and increases lifespan in mouse models of ageing (kl/kl). Inhibits L-NAME induced systolic blood pressure increases, telomere length reduction and cardiac hypertrophy in mice. Renoprotective. Orally bioavailable.
[storage]

Store at +4°C
[References]

[1] Placencio VR, et al. Small Molecule Inhibitors of Plasminogen Activator Inhibitor-1 Elicit Anti-Tumorigenic and Anti-Angiogenic Activity. PLoS One. 2015 Jul 24;10(7):e0133786. DOI:10.1371/journal.pone.0133786
[2] Jeong BY, et al. Novel Plasminogen Activator Inhibitor-1 Inhibitors Prevent Diabetic Kidney Injury in a Mouse Model. PLoS One. 2016 Jun 3;11(6):e0157012. DOI:10.1371/journal.pone.0157012
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