PPIase-Parvulin Inhibitor - CAS 64005-90-9 - Calbiochem

A cell-permeable napthalenetetracarboxylic-bisimide compound that displays anti-proliferative properties (IC₅₀<5 µM against a panel of human cancer cell lines). Causes cell cycle arrest and acts as a potent, selective, reversible, competitive, active site binding inhibitor of Pin1/Par14 PPIase (peptidyl prolyl cis-trans isomerase) activity (IC₅₀ = ~ 1.5 µM). Does not bind to DNA or functions as a topoisomerase I inhibitor.

A cell-permeable, napthalenetetracarboxylic-bismide compound that displays anti-proliferative properties (IC₅₀<5 µM against a panel of human cancer cell lines). Causes cell cycle arrest and acts as a potent, selective, reversible, competitive, active site-binding inhibitor of Pin1/Par14 peptidylprolyl cis-trans isomerase (PPIase) activity (IC₅₀ ~ 1.5 µM). Does not bind to DNA or function as a topoisomerase I inhibitor.

Cell permeable: yes

Primary Target
Pin1/Par14 PPIase (peptidyl prolyl cis-trans isomerase) activity

Product competes with ATP.

Reversible: yes

Target IC₅₀: <5 µM for anti-proliferative properties against a panel of human cancer cell lines; ~ 1.5 µM inhibiting Pin1/Par14 PPIase (peptidyl prolyl cis-trans isomerase) activity

Packaged under inert gas

Following reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 3 months at -20°C.

Uchida, T., et al. 2003. Chem. Biol.10, 15.

CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany

Toxicity: Standard Handling (A)