Fenpiverinium

Increases cellular pools of free radical scavenger Prevents apoptotic death of neuronal cells Induces apoptosis in human and rat smooth muscle cells Pyrogen free

Biochem/physiol Actions Potent, non-selective A 3 adenosine receptor agonist. Features and Benefits This compound is featured on the Adenosine Receptors page of the Handbook of Receptor Classification and Signal Transduction.

Biochem/physiol Actions &#945:-Adrenergic receptor antagonist: peripheral vasodilator. Features and Benefits This compound was developed by Novartis .

Biochem/physiol Actions &#945:-Adrenergic receptor antagonist: peripheral vasodilator. Features and Benefits This compound was developed by Novartis .

Biochem/physiol Actions Ramelteon is a cell penetrant, potent and selective agonist at MT1/MT2 melatonin receptor that exhibits sleep-promoting properties. It is not binding to GABA receptor complex.

Biochem/physiol Actions Ramelteon is a cell penetrant, potent and selective agonist at MT1/MT2 melatonin receptor that exhibits sleep-promoting properties. It is not binding to GABA receptor complex.

InformationSongorine, a ubiquitous alkaloid in the genus Aconitum, is a novel antagonist of the GABAA receptor in rat brain and has antiarrhythmic, antinociceptive, anti-inflammatory, regenerative and CNS-modulating properties.

Biochem/physiol Actions Sparsentan (BMS346567) is an orally available and highly potent dual antagonist of angiotensin II AT1 receptor and endothelin A ETA receptor. It is an analog of BMS-248360 that is orally available in rats and higher

Biochem/physiol Actions Sparsentan (BMS346567) is an orally available and highly potent dual antagonist of angiotensin II AT1 receptor and endothelin A ETA receptor. It is an analog of BMS-248360 that is orally available in rats and higher

Biochem/physiol Actions SR58894A is a potent and selective antagonist of &#946:3-adrenergic receptor. SR&nbsp:58894A&nbsp:is also known as (3-(2-allylphenoxy)-1-[(1 S)-1,2,3,4-tetrahydronaphth-1-ylamino]-(2 S)-2-propanol hydrochloride, Kissei).

Biochem/physiol Actions SR58894A is a potent and selective antagonist of &#946:3-adrenergic receptor. SR&nbsp:58894A&nbsp:is also known as (3-(2-allylphenoxy)-1-[(1 S)-1,2,3,4-tetrahydronaphth-1-ylamino]-(2 S)-2-propanol hydrochloride, Kissei).

Biochem/physiol Actions SR-95531 is a specific GABA A receptor antagonist that does not affect GABA-transaminase or glutamate-decarboxylase activities. Features and Benefits This compound is a featured product for Neuroscience research.