Biologically Active Small Molecules

A natural steroid sapogenin that has antioxidant and anti-inflammatory activities, is protective against metabolic and cardiovascular diseases, and can have immunomodulatory and estrogenic effects.

A natural steroid sapogenin that has antioxidant and anti-inflammatory activities, is protective against metabolic and cardiovascular diseases, and can have immunomodulatory and estrogenic effects.

A natural steroid sapogenin that has antioxidant and anti-inflammatory activities, is protective against metabolic and cardiovascular diseases, and can have immunomodulatory and estrogenic effects.

A natural O-methylated flavone that reversibly inhibits CYP1A1 and CYP1B1 in human liver microsomes with Ki values of 89 and 16 nM, respectively.

A natural O-methylated flavone that reversibly inhibits CYP1A1 and CYP1B1 in human liver microsomes with Ki values of 89 and 16 nM, respectively.

A natural O-methylated flavone that reversibly inhibits CYP1A1 and CYP1B1 in human liver microsomes with Ki values of 89 and 16 nM, respectively.

A natural O-methylated flavone that reversibly inhibits CYP1A1 and CYP1B1 in human liver microsomes with Ki values of 89 and 16 nM, respectively.

A first generation antihistamine which is a potent antagonist of the human H1 receptor (Ki = 11.7 nM) readily crosses the blood-brain barrier and produces diverse cognitive and psychomotor effects also antagonizes muscarinic cholinergic receptors

A first generation antihistamine which is a potent antagonist of the human H1 receptor (Ki = 11.7 nM) readily crosses the blood-brain barrier and produces diverse cognitive and psychomotor effects also antagonizes muscarinic cholinergic receptors

A non-selective mACh receptor antagonist and non-specific inhibitor of voltage-gated ion channels in neurons used to study animal models of vertigo and emesis.

A non-selective mACh receptor antagonist and non-specific inhibitor of voltage-gated ion channels in neurons used to study animal models of vertigo and emesis.

A non-selective mACh receptor antagonist and non-specific inhibitor of voltage-gated ion channels in neurons used to study animal models of vertigo and emesis.