T7044

Norepinephrine is an alkaloid neurotransmitter and an effective adrenergic receptor (AR) agonist that activates α1, α2, and β1 receptors. It is commonly used as a vasoactive agent for the treatment of shock and can also be used to induce cardiomyopathy models.

DL-Norepinephrine-d6 HCl is a deuterated compound of DL-NorepinephrineHCl. DL-NorepinephrineHCl has a CAS number of 55-27-6. DL-Norepinephrine hydrochloride is a high-affinity basic amino acid substrate of amino acid transporter b0 + with a Km value in the range of 100-400 μM.

Norepinephrine (Standard) is a reference standard for research and analysis in studies involving Norepinephrine. Norepinephrine is an alkaloid neurotransmitter and an effective adrenergic receptor (AR) agonist that activates α1, α2, and β1 receptors. It is commonly used as a vasoactive agent for the treatment of shock and can also be used to induce cardiomyopathy models.

DL-Norepinephrine hydrochloride (Standard) is a reference standard for research and analysis in studies involving DL-Norepinephrine hydrochloride. DL-Norepinephrine hydrochloride (DL-lysine) is a high-affinity basic amino acid substrate of amino acid transporter b0 + with a Km value in the range of 100-400 μM.

Norepinephrine bitartrate monohydrate is an effective adrenergic receptor (AR) agonist that directly activates α1, α2, and β1 receptors, and is commonly used to induce cardiomyopathy models.

DL-Norepinephrine hydrochloride (DL-lysine) is a high-affinity basic amino acid substrate of amino acid transporter b0 + with a Km value in the range of 100-400 μM.

Norepinephrine hydrochloride is a β1-selective adrenergic receptor agonist with an EC₅₀ of 5.37 μM and can be used to induce cardiomyopathy models.

DL-Norepinephrine-d6 is a deuterated compound of DL-Norepinephrine. DL-Norepinephrine has a CAS number of 138-65-8.

Norepinephrine bitartrate salt is an adrenergic neurotransmitter.

(Rac)-Norepinephrine-d3 (formate) is the deuterated form of Norepinephrine. Norepinephrine (Levarterenol; L-Noradrenaline) functions as a potent agonist for adrenergic receptors (AR). It can activate α1, α2, and β1 receptors.