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Adrenergic Receptor Isoform Specific Products
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Adrenergic Receptor Related Products (1628)
Related Products (1628)
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Antibodies (4)
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Adrenergic Receptor Isoform Comparison
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Bornaprolol
0 ImagesCat. No.: HY-106468CAS No.: 66451-06-7Synonyms: FM-24Bornaprolol (FM-24) is a β-adrenoceptor antagonist. Bornaprolol significantly depresses plasma levels of luteinizing hormone (LH) in orchidectomized rat models. Bornaprolol can be used for cardiovascular diseases like hypertension and angina pectoris research. -
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Acebutolol-d7
0 ImagesCat. No.: HY-17497SCAS No.: 2701782-36-5Acebutolol-d7 is a deuterium labeled Acebutolol. Acebutolol is a selective β1 adrenergic receptor antagonist used in the treatment of hypertension, angina pectoris and cardiac arrhythmias. -
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Talsupram
0 ImagesCat. No.: HY-150192CAS No.: 21489-20-3Talsupram is a selective noradrenaline inhibitor that has a high affinity for the noradrenaline transporter. Talsupram exhibits anti-hyperalgesic effects. Talsupram can decrease ethanol intake to the levels prior to REM-induced deprivation in rat model. -
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Picumeterol
0 ImagesCat. No.: HY-124950CAS No.: 130641-36-0Synonyms: GR114297APicumeterol (GR114297A) is a potent and selective β2-adrenoceptor agonist with bronchodilator and anti-bronchoconstrictor effects. Picumeterol produces long-lasting relaxation of airways smooth muscle both in vitro and in vivo. Picumeterol is cleared from plasma through a rapid and extensive hepatic metabolism. Picumeterol is proming for rasearch of asthma and related diseases. -
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Ciclazindol
0 ImagesCat. No.: HY-105975CAS No.: 37751-39-6Synonyms: WY-23409Ciclazindol (WY-23409) is an orally active antidepressant. Ciclazindol can inhibit the reuptake of norepinephrine. Ciclazindol also exhibits effects of lowering blood glucose, suppressing appetite and reducing weight. Ciclazindol can be used in the research of diseases such as depression and obesity. -
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SL-89.0591
0 ImagesCat. No.: HY-17019CAS No.: 194674-19-6SL-89.0591 is a uroselective α1-adrenoceptor antagonist. SL-89.0591 exhibits a more potent blocking effect on urethral receptors than on vascular receptors in anesthetized rabbits, with a lower risk of orthostatic hypotension. SL-89.0591 can be used in research related to benign prostatic hyperplasia. -
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Isamoltane hemifumarate
0 ImagesCat. No.: HY-19578BCAS No.: 874882-92-5Synonyms: (±)-Isamoltane hemifumarateIsamoltane hemifumarate is a selective antagonist of 5-HT1B receptor, with an IC50 of 39 nM for inhibits the binding of [125I]ICYP to 5-HT1B recognition sites in rat brain membranes. Isamoltane hemifumarate is also a β-adrenoceptor ligand, with an IC50 of 8.4 nM. Isamoltane hemifumarate shows anxiolytic activity. -
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Quinazosin dihydrochloride
0 ImagesCat. No.: HY-111984ACAS No.: 7262-00-2Quinazosin dihydrochloride is an antihypertensive α1-adrenergic receptor antagonist whose activity is associated with inhibition of granulopoiesis, resulting in neutropenia and leukopenia. Quinazosin dihydrochloride exhibits dose-related myelosuppression that is correlated with the duration of suppression. -
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ST91 free base
0 ImagesCat. No.: HY-103203ACAS No.: 4751-48-8ST91 free base is a α2-adrenoceptor (α2AR) agonist. ST91 free base activates both α2AAR and non-α2AAR subtypes to produce spinal antinociception. -
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Lidamidine
0 ImagesCat. No.: HY-107358CAS No.: 66871-56-5Synonyms: WHR-1142A free baseLidamidine (WHR-1142A free base) is an α2-adrenergic receptor agonist and antidiarrheal agent. -
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- Isoprenaline hemisulfate
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L-Mabuterol hydrochloride
0 ImagesCat. No.: HY-113749CAS No.: 95656-55-6L-Mabuterol hydrochloride is a selective β2-adrenergic receptor agonist with bronchodilator activity. L-Mabuterol hydrochloride can improve respiratory function and relieve asthma symptoms. L-Mabuterol hydrochloride also shows potential efficacy in the management of chronic obstructive pulmonary disease (COPD). -
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ZD-7114
0 ImagesCat. No.: HY-101320CAS No.: 129689-30-1Synonyms: ICI-D 7114ZD-7114 is a potent and selective agonist of β3-adrenergic. ZD-7114 is a selective thermogenic agent in vivo. ZD-7114 can be used in study obesity and diabetes. -
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Pimozide-d4-1
0 ImagesCat. No.: HY-12987S2Synonyms: R6238-d4-1Pimozide-d4-1 is the deuterium labeled Pimozide. Pimozide is a dopamine receptor antagonist, with Kis of 1.4 nM, 2.5 nM and 588 nM for dopamine D2, D3 and D1 receptors, respectively, and also has affinity at α1-adrenoceptor, with a Ki of 39 nM; Pimozide also inhibits STAT3 and STAT5. -
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S(-)-Bisoprolol fumarate
0 ImagesCat. No.: HY-139727ACAS No.: 1426853-23-7S(-)-Bisoprolol fumarate is a S(-)-enantiomer of Bisoprolol fumarate. Bisoprolol fumarate is a potent, selective and orally active β1-adrenergic receptor blocker. Bisoprolol has little activity on β2-receptor and has the potential for hypertension, coronary artery disease and stable ventricular dysfunction research. -
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O-Desmethyl Mebeverine alcohol
0 ImagesCat. No.: HY-G0008CAS No.: 155172-67-1Synonyms: Mebeverine metabolite O-desmethyl Mebeverine alcoholO-Desmethyl Mebeverine alcohol is a metabolite of Mebeverine, which is a potent α1 repector inhibitor, causing relaxation of the gastrointestinal tract. -
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Mafoprazine
0 ImagesCat. No.: HY-126635CAS No.: 80428-29-1Mafoprazine is a phenylpiperazine derivative with variable affinities for neuronal receptors. It may exert its antipsychotic effects primarily through D2 receptor blockade and α-adrenergic activity, and may increase the activity of dopamine metabolites. -
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Ibopamine hydrochloride
0 ImagesCat. No.: HY-112072CAS No.: 75011-65-3Synonyms: SB 7505 hydrochloride; SKF 100168 hydrochlorideIbopamine (SB 7505) hydrochloride is an orally active dopamine derivative. Ibopamine hydrochloride exerts agonistic effects on α, β adrenergic receptors and dopaminergic receptors. Ibopamine hydrochloride can be hydrolyzed to produce the active metabolite Epinine. Ibopamine hydrochloride possesses positive inotropic and vasodilatory effects, which can improve hemodynamics and renal function in heart failure models. Ibopamine hydrochloride has good safety profile and can be used in the research of diseases such as congestive heart failure. -
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TAK-259 hydrochloride
0 ImagesCat. No.: HY-120473ACAS No.: 1192347-42-4TAK-259 hydrochloride is an orally active α1D-adrenergic receptor antagonist with a Ki value of 1.1 nM for human α1D-adrenergic receptors. TAK-259 hydrochloride can inhibit the contraction of isolated bladder strips in rats with bladder outlet obstruction, reduce non-voiding bladder contractions, and improve urinary frequency symptoms. TAK-259 hydrochloride can be used in research related to overactive bladder. -
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Ractopamine-d6 hydrochloride
0 ImagesCat. No.: HY-B1421SCAS No.: 1276197-17-1Synonyms: LY031537-d6Ractopamine-d6 (LY031537-d6) hydrochloride is the deuterium labeled Ractopamine hydrochloride (HY-B1421). Ractopamine (LY031537) hydrochloride is a potent β-adrenergic receptor (βAR) agonist with Kd values of ~25 nM for pig β1AR and β2AR. Ractopamine hydrochloride is linked to protein metabolism. Ractopamine hydrochloride can be used for researching to increase lean tissue growth and improve production efficiency in pigs. -
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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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