Biologically Active Small Molecules

A bifunctional cross-linking reagent reactive toward primary amines is membrane-permable and commonly used to cross-link proteins in intact cell.

A bifunctional cross-linking reagent reactive toward primary amines is membrane-permable and commonly used to cross-link proteins in intact cell.

A bifunctional cross-linking reagent reactive toward primary amines is membrane-permable and commonly used to cross-link proteins in intact cell.

A bifunctional cross-linking reagent reactive toward primary amines is membrane-permable and commonly used to cross-link proteins in intact cell.

A copper and zinc chelator and an irreversible inhibitor of aldehyde dehydrogenase (IC₅₀ = 0.1 mM) that has been indicated for the treatment of alcohol dependence targets the ubiquitin-proteasome pathway, induces ROS, activates JNK and

A copper and zinc chelator and an irreversible inhibitor of aldehyde dehydrogenase (IC₅₀ = 0.1 mM) that has been indicated for the treatment of alcohol dependence targets the ubiquitin-proteasome pathway, induces ROS, activates JNK and

A copper and zinc chelator and an irreversible inhibitor of aldehyde dehydrogenase (IC₅₀ = 0.1 mM) that has been indicated for the treatment of alcohol dependence targets the ubiquitin-proteasome pathway, induces ROS, activates JNK and

Calcimycin is a pyrrole polyether antibiotic that exhibits antibacterial, antifungal, pro-inflammatory, and pro-allergic activities. Calcimycin is a divalent cation ionophore that increases intracellular Ca2+ levels, uncouples oxidative

Calcimycin is a pyrrole polyether antibiotic that exhibits antibacterial, antifungal, pro-inflammatory, and pro-allergic activities. Calcimycin is a divalent cation ionophore that increases intracellular Ca2+ levels, uncouples oxidative

Calcimycin is a pyrrole polyether antibiotic that exhibits antibacterial, antifungal, pro-inflammatory, and pro-allergic activities. Calcimycin is a divalent cation ionophore that increases intracellular Ca2+ levels, uncouples oxidative

An irreversible inhibitor of ornithine decarboxylase that suppresses polyamine biosynthesis displays antiangiogenic, cytostatic, and antiparasitic effects.

An irreversible inhibitor of ornithine decarboxylase that suppresses polyamine biosynthesis displays antiangiogenic, cytostatic, and antiparasitic effects.