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Adrenergic Receptor Isoform Specific Products
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Adrenergic Receptor Inhibitors
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Adrenergic Receptor Ligands
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Adrenergic Receptor Related Products (1649)
Related Products (1649)
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Antibodies (4)
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Adrenergic Receptor Isoform Comparison
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α1A-AR ligand-1
0 ImagesCat. No.: HY-185003CAS No.: 1571081-31-6α1A-AR ligand-1 (Compound 3) is an α1A-AR ligand that can be used to synthesize PROTACs, such as α1A-AR Degrader 9c (HY-147100). -
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CP-331684
0 ImagesCat. No.: HY-120057CAS No.: 207922-70-1CP-331684 is an orally active agonist of β3-Adrenergic receptor. CP-331684 can be studied in research on obesity. -
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Levomoprolol
0 ImagesCat. No.: HY-129231CAS No.: 77164-20-6Synonyms: (-)-MoprololLevomoprolol ((-)-Moprolol), the (S)-enantiomer of moprolol, serves as a beta adrenergic antagonist. -
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Celiprolol hydrochloride (Standard)
0 ImagesCat. No.: HY-B1264RCAS No.: 57470-78-7Celiprolol (hydrochloride) (Standard) is the analytical standard of Celiprolol (hydrochloride). This product is intended for research and analytical applications. Celiprolol (REV 5320) is a potent, cardioselective and orally active β1-andrenoceptor r antagonist with partial β2 agonist activity, with Ki values of 0.14-8.3 μM. Celiprolol has antihypertensive and antianginal activity, and can be used for the research of cardiovascular disease such as high blood pressure. -
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DSP 4 free base
0 ImagesCat. No.: HY-121602CAS No.: 62078-98-2DSP 4 Free base is a selective neurotoxin that targets noradrenergic neurons in the locus coeruleus noradrenergic system. DSP 4 Free base possesses the unique ability to cross the blood–brain barrier. DSP 4 Free base cyclizes to form a reactive aziridinium derivative that accumulates in noradrenergic neurons. -
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N-1518
0 ImagesCat. No.: HY-19012CAS No.: 93750-14-2N-1518 is an α and β adrenergic receptor blocker that has competitive antagonism against β1 and α1 receptors, but does not show selectivity for β1 receptors, but shows about 20-fold selectivity for α1 receptors. N-1518 has vasodilatory effects and can be used in the research field of hypertension treatment. -
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Agroclavine
0 ImagesAgroclavine acts as an agonist of the D1-dopamine receptor and α1-adrenergic receptor. Agroclavine enhances the sensitivity of the brain to magnetic fields; it impairs spatial memory without affecting hippocampal long-term potentiation (LTP). Agroclavine exerts bidirectional regulatory effects on immune activity: it enhances NK cell activity with low toxicity under normal conditions, while it inhibits NK cell activity and exhibits significant cardiac and hepatic toxicity under stress conditions. Agroclavine can be used for research on neuroelectrophysiology, learning and memory, and immunoregulation. -
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Metoprolol tartrate (Standard)
0 ImagesMetoprolol (tartrate) (Standard) is the analytical standard of Metoprolol (tartrate). This product is intended for research and analytical applications. Metoprolol tartrate is an orally active, selective β1-adrenoceptor antagonist. Metoprolol tartrate shows anti-inflammation, antitumor and anti-angiogenic properties. -
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Landiolol
0 ImagesCat. No.: HY-100607CAS No.: 133242-30-5Synonyms: ONO1101Landiolol (ONO1101) is a highly selective, ultra-short-acting competitive inhibitor of β1 adrenergic receptors. Landiolol specifically blocks cardiac β1 receptors, reducing heart rate and myocardial oxygen consumption. Landiolol inhibits TNF-α-induced excessive mitochondrial oxygen consumption and reactive oxygen species production in a sepsis model, alleviating renal injury. Landiolol has little effect on cardiac ion channels (such as L-type calcium current and inward rectifier potassium current) and has a weak negative inotropic effect. Landiolol can be used for perioperative tachycardia control and protection studies of sepsis-related acute kidney injury. -
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β2AR agonist 5
0 ImagesCat. No.: HY-179274CAS No.: 2759727-47-2β2AR agonist 5 (Compound alpha-β2-008) is a β2AR agonist, with an EC50 value of 0.19 nM. β2AR agonist 5 induces the BRET signal. β2AR agonist 5 can be used in the research of asthma and chronic obstructive pulmonary disease. -
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Desglymidodrine (Standard)
0 ImagesCat. No.: HY-114794RCAS No.: 3600-87-1Synonyms: ST 1059 (Standard)Desglymidodrine (Standard) is the analytical standard of Desglymidodrine. This product is intended for research and analytical applications. Desglymidodrine (ST 1059), the active metabolite of Midodrine(HY-12749), is a selective α1-adrenoceptor agonist. Desglymidodrine is an effective arterial and venous vasoconstrictor and can be used to regulate blood pressure. -
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BRL-44408
0 ImagesCat. No.: HY-12716CAS No.: 118343-19-4BRL-44408 is a selective, blood-brain barrier-permeable α2A-adrenergic receptor antagonist with a Ki value of 8.56 nM against human targets. BRL-44408 exhibits activities such as antidepressant, analgesic effects and attenuation of sepsis-induced acute lung injury by regulating the release of neurotransmitters such as norepinephrine and dopamine, or inhibiting signaling pathways including ERK1/2, p38MAPK and p65. BRL-44408 can be used in studies related to acute respiratory distress syndrome, depression and visceral pain. -
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Etafenone
0 ImagesEtafenone is an antiarrhythmic agent and vasodilator. Etafenone exerts β-adrenergic agonistic effects. Etafenone inhibits the automaticity of sinoatrial nodes, atrioventricular junctions and Purkinje fibers, prolongs action potential duration and refractory period, slows the rising rate of action potentials, and prolongs conduction time. Etafenone enhances collateral circulation after coronary occlusion and suppresses ventricular premature beats. Etafenone delays ischemic myocardial energy imbalance, improves the recovery of high-energy phosphates after ischemia, and reduces myocardial oxygen consumption. Etafenone can be used in research related to ischemic heart disease, arrhythmia and angina pectoris. -
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(S)-Bucindolol
0 ImagesCat. No.: HY-129436CAS No.: 91548-61-7(S)-Bucindolol is the (S)-isomer of Bucindolol (HY-103214), a β1-adrenergic receptor blocker. (S)-Bucindolol can be utilized in research on cardiac failure. -
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S(-)-Cyanopindolol hemifumarate
0 ImagesCat. No.: HY-125973CAS No.: 874882-72-1S(−)-Cyanopindolol hemifumarate is an isomer of Cyanopindolol (HY-W795507). S(-)-Cyanopindolol hemifumarate is a 5-HT1A/1B serotonin receptor antagonist and a β3-adrenoceptor antagonist. -
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Jingsongling
0 ImagesCat. No.: HY-118390CAS No.: 25332-05-2Jingsongling is a Xylazine analog and anesthetic agent. Jingsongling causes bradycardia and hypertension by mediating α2-adrenoceptors. Jingsongling inhibits canine gastric motility through mediation of α1 and α2 adrenergic receptors. -
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Oberadilol
0 ImagesCat. No.: HY-19088CAS No.: 114856-44-9Synonyms: CID-3047798Oberadilol (CID-3047798) is a Phosphodiesterase III inhibitor, non-selective β-adrenergic receptor blocker, vasodilator and positive inotropic agent. Oberadilol reduces left ventricular end-diastolic volume. Oberadilol is used in research related to chronic congestive heart failure and SARS-CoV-2 infection. -
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DOV-102,677
0 ImagesCat. No.: HY-18332BCAS No.: 410074-75-8DOV-102,677 is an orally sctive triple monoamine neurotransmitter reuptake inhibitor that simultaneously inhibits the dopamine (DAT) (IC50 = 129 nM; Ki = 222 nM), norepinephrine (NET) (IC50 = 103 nM; Ki = 1030 nM), and serotonin (SERT) (IC50 = 133 nM; Ki = 740 nM) transporters. DOV-102,677 demonstrated significant antidepressant-like activity and sensory-motor gating regulatory effects in mouse experiments. DOV-102,677 can be used for research on depression. -
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Yohimbic acid (Standard)
0 ImagesCat. No.: HY-121936RCAS No.: 522-87-2Yohimbic acid (Standard) is the analytical standard of Yohimbic acid (HY-121936). This product is intended for research and analytical applications. Yohimbic acid is a derivative of Yohimbine Hydrochloride (HY-N0127). Yohimbic acid exhibits vasodilatory and anticancer activities. Yohimbic acid can be used for the research of cancer, inflammation and cardiovascular disease. -
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XEN-2174
0 ImagesCat. No.: HY-16525CAS No.: 701909-57-1XEN-2174 is a noradrenaline transporter (NET) inhibitor. XEN-2174 inhibits the reuptake of noradrenaline through non-competitive inhibition, increasing the concentration of noradrenaline in the synaptic cleft, thereby activating α2-adrenergic receptor at the spinal level and exerting analgesic effects. XEN-2174 exhibits long-lasting analgesic effects in models of neuropathic pain and postoperative pain in rats. XEN-2174 can be used in pain research. -
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Sorry. There is currently no product that acts on isoform Bcl-2, Bcl-W and Bim together.Please
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