Biologically Active Small Molecules

A fluorescent probe that reacts stoichiometrically and rapidly with ONOO- (rate constant (k) = 1.1 &muM/s) excitation of 332 nm and emission &gt 400 nm.

A fluorescent probe that reacts stoichiometrically and rapidly with ONOO- (rate constant (k) = 1.1 &muM/s) excitation of 332 nm and emission &gt 400 nm.

A fluorescent probe that reacts stoichiometrically and rapidly with ONOO- (rate constant (k) = 1.1 &muM/s) excitation of 332 nm and emission &gt 400 nm.

An aromatic hydrazine-containing fluorophore that reacts with aldehydes or ketones for fluorescent labeling.

An aromatic hydrazine-containing fluorophore that reacts with aldehydes or ketones for fluorescent labeling.

An aromatic hydrazine-containing fluorophore that reacts with aldehydes or ketones for fluorescent labeling.

An aromatic hydrazine-containing fluorophore that reacts with aldehydes or ketones for fluorescent labeling.

A fluorescent probe that competitively binds HDAC demonstrates fluorescence excitation and emission maxima of 325 and 400 nm, respectively, which is quenched by 50% when bound to HDAC.

A fluorescent probe that competitively binds HDAC demonstrates fluorescence excitation and emission maxima of 325 and 400 nm, respectively, which is quenched by 50% when bound to HDAC.

A fluorescent probe that competitively binds HDAC demonstrates fluorescence excitation and emission maxima of 325 and 400 nm, respectively, which is quenched by 50% when bound to HDAC.

A fluorescent probe that competitively binds HDAC demonstrates fluorescence excitation and emission maxima of 325 and 400 nm, respectively, which is quenched by 50% when bound to HDAC.

A phytoestrogen that competitively (vs. 17&beta-estradiol) binds the estrogen receptors ER&alpha (IC50 = 11 nM) and ER&beta (IC50 = 2 nM) and can induce ER-dependent gene expression in isolated cells a weak antagonist of pregnane X receptor