epinephrine

Dibenamine hydrochloride is a competitive and irreversible blocker of the β-adrenergic receptor.

AZD-1656 is a glucokinase activator (GKA) that can cause dose-limiting hypoglycemia in normal animals used in embryofetal development studies and type 2 diabetes.

L-Epinephrine is a hormone and neurotransmitter primarily secreted by the adrenal medulla, acting as an agonist for α-adrenergic and β-adrenergic receptors, causing systemic vasoconstriction and cardiac stimulation. It is used to treat glaucoma, allergies, and asthma.

D-Epinephrine can be used as a hormone, neurotransmitter, and medication. Epinephrine can be normally obtained from the adrenal glands and certain neurons. It involves in the fight-or-flight response by increasing blood flow to muscles, output of the hear

Epinephrine HCl, a compound functioning as a hormone, neurotransmitter, and medication, is synthesized by adrenal glands and some neurons. It is essential in the fight-or-flight response, enhancing blood flow to muscles, heart output, pupil dilation, and blood sugar levels through its interaction with alpha and beta receptors. Epinephrine HCl is present in various animals and some unicellular organisms.

DL-Epinephrine-d3 is a deuterated compound of DL-Epinephrine. DL-Epinephrine has a CAS number of 329-65-7. DL-Epinephrine(DL-Adrenaline) is a hormone and a neurotransmitter.

DL-Epinephrine-d6 is a deuterated compound of DL-Epinephrine. DL-Epinephrine has a CAS number of 329-65-7. DL-Epinephrine(DL-Adrenaline) is a hormone and a neurotransmitter.

L-Epinephrine Bitartrate is alpha- and beta-adrenergic receptor stimulator.

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 bitartrate salt is an adrenergic neurotransmitter.

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.

Ethylnorepinephrine hydrochloride is a unique bronchodilator.

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

Aminomenthylnorepinephrine is a partial agonist of the beta-adrenoreceptor that causes irreversible inactivation.

Dibutylephrine is a sympathomimetic agent.

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.

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

Dopamine hydrochloride (ASL279) is a natural catecholamine neurotransmitter that mainly acts on dopamine receptors (D1-5 receptors) (EC50=2.7 nM). Dopamine hydrochloride induces VEGFR2 endocytosis through D2 dopamine receptor and has pro-angiogenic activity.

Methyldopa hydrate (MK-351 hydrate) is a DOPA decarboxylase inhibitor and indirect α2-adrenergic receptor agonist used to treat hypertension. It inhibits the sympathetic nervous system, decreases production of dopamine, norepinephrine, and epinephrine, and exhibits NO-dependent sedative activity.

Dipivefrin hydrochloride (Dipivefrin HCl) that is available as an ophthalmic solution is a prodrug of adrenaline, which is used to treat glaucoma.

Dipivefrin is a prodrug of epinephrine, and is used to treat open-angle glaucoma.

Vanillylmandelic acid, the end product of the metabolism of catecholamines, epinephrine, and norepinephrine, has antioxidant activity and is commonly used to help diagnose pheochromocytoma, as well as its elevation in association with depressive symptoms.

Nadolol is a non-selective beta-adrenergic antagonist with antihypertensive and antiarrhythmic activities. Nadolol competitively blocks beta-1 adrenergic receptors located in the heart and vascular smooth muscle, inhibiting the activities of the catechola