Timolol anhydrous

Cell-permeable, non-competitive adenylate cyclase inhibitor (IC 50 = 3 &#181M), that binds to the adenosine P1 binding site. Blocks positive inotropic and chronotropic effects of &#946-adrenergic agents.

A cell-permeable selective inhibitor of Ca 2+ -calmodulin-dependent phosphodiesterase (PDE I IC 50 = 4 &#181M). A cell-permeable, selective inhibitor of Ca 2+ -calmodulin-dependent phosphodiesterase (PDE I, IC 50 = 4 &#181M).

General description Racemic mixture of diastereomers. Biochem/physiol Actions Anisodamine is a muscarinic receptor antagonist.

General description Racemic mixture of diastereomers. Biochem/physiol Actions Anisodamine is a muscarinic receptor antagonist.

General description Anti-ADORA2A Antibody detects endogenous levels of total ADORA2A protein. Adenosinergic A2A receptor (ADORA2A) is a G-protein-coupled receptor and is expressed in the brain.

Anti-TIMM23 translocase of inner mitochondrial membrane 23 h

Anti-TIMM23 translocase of inner mitochondrial membrane 23 h

A dual acting antithrombogenic agent inhibitor of TXA2 synthase (IC50 = 12 nM) acts as an TP receptor antagonist (IC50 = 1.1 nM).

A dual acting antithrombogenic agent inhibitor of TXA2 synthase (IC50 = 12 nM) acts as an TP receptor antagonist (IC50 = 1.1 nM).

InformationCiforadenant (CPI-444) Ciforadenant (CPI-444, V81444) is a potent and selective Adenosine A2A receptor antagonist. It binds to A2A receptors with a Ki of 3.54 nmol/L and demonstrates a greater than 50-fold selectivity for the A2A receptor

Anisodamine is a tropane alkaloid originally found in plants in the Solanaceae family it exhibits anti-inflammatory activity and is clinically used to induce atropinization in organophosphate poisoning subjects and to improve acute lung injury

Anisodamine is a tropane alkaloid originally found in plants in the Solanaceae family it exhibits anti-inflammatory activity and is clinically used to induce atropinization in organophosphate poisoning subjects and to improve acute lung injury