Nalorphine hydrochloride

A dual orexin 1 and 2 receptor antagonist (Kds = 1.3 and 0.17 nM, respectively) 100 mg/kg promotes nonrapid eye movement sleep and exacerbates cataplexy in a mouse model of narcolepsy.

A dual orexin 1 and 2 receptor antagonist (Kds = 1.3 and 0.17 nM, respectively) 100 mg/kg promotes nonrapid eye movement sleep and exacerbates cataplexy in a mouse model of narcolepsy.

A dual orexin 1 and 2 receptor antagonist (Kds = 1.3 and 0.17 nM, respectively) 100 mg/kg promotes nonrapid eye movement sleep and exacerbates cataplexy in a mouse model of narcolepsy.

Anagyrine ((-)-Anagyrine) is a quinolizidine alkaloid that has been found in Lupinus albus. Anagyrine binds to muscarinic and nicotinic acetylcholine receptors with IC 50 values of 132 and 2096 µM respectively. Anagyrine is a potent and effective

Anagyrine ((-)-Anagyrine) is a quinolizidine alkaloid that has been found in Lupinus albus. Anagyrine binds to muscarinic and nicotinic acetylcholine receptors with IC 50 values of 132 and 2096 µM respectively. Anagyrine is a potent and effective

Application Butyrophenone has been used to study the relationship between the electrolyte counter-ion concentration and the critical micelle concentration for several surfactants . It has been used to generate PhCO + ions by 70 eV electron

Application Butyrophenone has been used to study the relationship between the electrolyte counter-ion concentration and the critical micelle concentration for several surfactants . It has been used to generate PhCO + ions by 70 eV electron

This product is provided as delivered and specified by the issuing Pharmacopoeia. All information provided in support of this product, including SDS and any product information leaflets have been developed and issued under the Authority of the

Tipepidine hydrochloride reversibly inhibits dopamine (DA) D 2 receptor-mediated GIRK currents (I DA(GIRK) ) with an IC 50 of 7.0 μM. Tipepidine hydrochloride subsequently activates VTA dopamine neuron Tipepidine hydrochloride, a non-narcotic

Tipepidine hydrochloride reversibly inhibits dopamine (DA) D 2 receptor-mediated GIRK currents (I DA(GIRK) ) with an IC 50 of 7.0 μM. Tipepidine hydrochloride subsequently activates VTA dopamine neuron Tipepidine hydrochloride, a non-narcotic

Tipepidine hydrochloride reversibly inhibits dopamine (DA) D 2 receptor-mediated GIRK currents (I DA(GIRK) ) with an IC 50 of 7.0 μM. Tipepidine hydrochloride subsequently activates VTA dopamine neuron Tipepidine hydrochloride, a non-narcotic

Tipepidine hydrochloride reversibly inhibits dopamine (DA) D 2 receptor-mediated GIRK currents (I DA(GIRK) ) with an IC 50 of 7.0 μM. Tipepidine hydrochloride subsequently activates VTA dopamine neuron Tipepidine hydrochloride, a non-narcotic