Naratriptan hydrochloride

Biochem/physiol Actions Naratriptan hydrochloride is a triptan drug that is used to relieve acute migraine headaches. It has poor bioavailability, short half-life, and the incidence of migraine recurrence therefore, it is occasionally used.

Nitecapone (OR-462) is an orally active and short-acting catechol-O-methyltransferase (COMT) inhibitor with gastroprotective and antioxidant properties. Nitecapone (OR-462) scavenges reactive oxygen and nitric radicals and prevents lipid

Nitecapone (OR-462) is an orally active and short-acting catechol-O-methyltransferase (COMT) inhibitor with gastroprotective and antioxidant properties. Nitecapone (OR-462) scavenges reactive oxygen and nitric radicals and prevents lipid

General description Norharmane is an alkaloid widely present in living organisms and can also be chemically synthesized. It is a &#946:-carboline derivative composed of indole and pyridine.

General description Norharmane is an alkaloid widely present in living organisms and can also be chemically synthesized. It is a &#946:-carboline derivative composed of indole and pyridine.

Application NSC23766 trihydrochloride has been used as a ras-related C3 botulinum toxin substrate 1 (RAC1) inhibitor. Biochem/physiol Actions NSC23766 is an inhibitor of Rac1, a Rho-family GTPase.

Application NSC23766 trihydrochloride has been used as a ras-related C3 botulinum toxin substrate 1 (RAC1) inhibitor. Biochem/physiol Actions NSC23766 is an inhibitor of Rac1, a Rho-family GTPase.

A potent water-soluble agonist of CB1 and CB2 receptors with Ki values of 1.5 and 0.32 nM, respectively when dissolved in saline, is highly efficacious in mouse behavioral models when administered either intravenously or intracerebroventricularly.

A potent water-soluble agonist of CB1 and CB2 receptors with Ki values of 1.5 and 0.32 nM, respectively when dissolved in saline, is highly efficacious in mouse behavioral models when administered either intravenously or intracerebroventricularly.

A potent water-soluble agonist of CB1 and CB2 receptors with Ki values of 1.5 and 0.32 nM, respectively when dissolved in saline, is highly efficacious in mouse behavioral models when administered either intravenously or intracerebroventricularly.

A potent water-soluble agonist of CB1 and CB2 receptors with Ki values of 1.5 and 0.32 nM, respectively when dissolved in saline, is highly efficacious in mouse behavioral models when administered either intravenously or intracerebroventricularly.

Arundic acid (ONO-2506) is an astrocyte-modulating agent, which delays the expansion of cerebral infarcts by modulating the activation of astrocytes through inhibition of S-100β synthesis. Arundic acid has the potential for stroke and Alzheimer’s