Biologically Active Small Molecules

A mitochondrial protonophore uncoupler that does not depolarize the plasma membrane and protects mice from acute renal ischemic-reperfusion injury.

A mitochondrial protonophore uncoupler that does not depolarize the plasma membrane and protects mice from acute renal ischemic-reperfusion injury.

A mitochondrial protonophore uncoupler that does not depolarize the plasma membrane and protects mice from acute renal ischemic-reperfusion injury.

A mitochondrial protonophore uncoupler that does not depolarize the plasma membrane and protects mice from acute renal ischemic-reperfusion injury.

A prodrug for terbutaline, a long-acting &beta-adrenoceptor agonist (Ki = 15.4 &microM for human &beta2-adrenergic receptor) converted to terbutaline by butyrylcholinesterases in the liver and plasma.

A prodrug for terbutaline, a long-acting &beta-adrenoceptor agonist (Ki = 15.4 &microM for human &beta2-adrenergic receptor) converted to terbutaline by butyrylcholinesterases in the liver and plasma.

A prodrug for terbutaline, a long-acting &beta-adrenoceptor agonist (Ki = 15.4 &microM for human &beta2-adrenergic receptor) converted to terbutaline by butyrylcholinesterases in the liver and plasma.

A cell permeable analog of BAPTA that binds calcium only after the AM group is removed by cytoplasmic esterases commonly used at 10-100 &muM to evaluate the role of intracellular calcium in cell signaling also inhibits Kv channels, including

A cell permeable analog of BAPTA that binds calcium only after the AM group is removed by cytoplasmic esterases commonly used at 10-100 &muM to evaluate the role of intracellular calcium in cell signaling also inhibits Kv channels, including

A cell permeable analog of BAPTA that binds calcium only after the AM group is removed by cytoplasmic esterases commonly used at 10-100 &muM to evaluate the role of intracellular calcium in cell signaling also inhibits Kv channels, including

A cell permeable analog of BAPTA that binds calcium only after the AM group is removed by cytoplasmic esterases commonly used at 10-100 &muM to evaluate the role of intracellular calcium in cell signaling also inhibits Kv channels, including

A membrane-impermeable calcium chelator that binds extracellular calcium ions.