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Adrenergic Receptor

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Adrenergic Receptor

Chemical Structure Cat. No. Product Name CAS No.
Centhaquine Chemical Structure
BCP31600 Centhaquine 57961-90-7
Centhaquine is an adrenergic receptor potentially for the treatment of postoperative pain and for the resuscitation of hypovolemic shock.
(S)-(+)-Norepinephrine L-bitartrate Chemical Structure
BCP31352 (S)-(+)-Norepinephrine L-bitartrate 636-88-4
Norepinephrine is a β1-selective adrenergic receptor agonist with EC50 of 5.37 μM.
Propanolol Chemical Structure
BCP31343 Propanolol 525-66-6
Propranolol is a nonselective β-adrenergic receptor (βAR) antagonist, has high affinity for the β1AR and β2AR with Ki values of 1.8 nM and 0.8 nM, respectively. Propranolol inhibits [3H]-DHA binding to rat brain membrane preparation with an IC50 of 12 nM. Propranolol is used to control hypertension, pheochromocytoma, myocardial infarction, cardiac arrhythmias, angina pectoris, and hypertrophic cardiomyopathy.
Levalbuterol tartrate Chemical Structure
BCP21346 Levalbuterol tartrate 661464-94-4
Levosalbutamol tartrate(levalbuterol) is the R-enantiomer of the short-acting β2-adrenergic receptor agonist salbutamol.
Labetalol Chemical Structure
BCP31095 Labetalol 36894-69-6
Labetalol is a competitive antagonist of both α- and β-adrenoreceptors that is used to treat high blood pressure.
Solabegron Chemical Structure
BCP31054 Solabegron 252920-94-8
Solabegron (GW 427353) is a selective β3-adrenergic receptor agonist, stimulating cAMP accumulation in Chinese hamster ovary cells expressing the human β3-AR, with an EC50 value of 22 nM. Solabegron (GW 427353) is being developed for the treatment of overactive bladder and irritable bowel syndrome.
L-796568 dihydrochloride Chemical Structure
BCP30793 L-796568 dihydrochloride 211031-81-1
L-796568 is an β3 adrenergic receptor agonist that was progressed into clinical studies for the treatment of obesity in the early 2000s but discontinued due to unacceptable toxicity.
Urapidil HCl Chemical Structure
BCP23389 Urapidil HCl 64887-14-5
Urapidil HCl is an α1-adrenoceptor antagonist and 5-HT1A receptor agonist.
Guanabenz Chemical Structure
BCP30851 Guanabenz 5051-62-7
Guanabenz is an alpha agonist of the alpha-2 adrenergic receptor that is used as an antihypertensive drug.
Detomidine Chemical Structure
BCP29001 Detomidine 76631-46-4
Detomidine produce dose-dependent sedative and analgesic effects, is a nonnarcotic, synthetic α2-adrenergic agonist
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