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Adrenergic Receptor Related Products (1649)
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Antibodies (4)
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Adrenergic Receptor Isoform Comparison
- Trimethaphan camsylate
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GG-818
0 ImagesCat. No.: HY-19268CAS No.: 179535-60-5Synonyms: GW 1818GG-818 (GW 1818) is a potent and selective α1 adrenoceptor antagonist, with pKi values of 9.7 for α1a, 7.8 for α1b, and 7.6 for α1d. GG-818 (GW 1818) can be used for benign prostatic hyperplasia research. -
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Garomefrine (hydrochlorid)
0 ImagesCat. No.: HY-123459CAS No.: 137431-04-0Synonyms: ABT-232; NS-49; PNO-49BGaromefrine hydrochlorid (ABT-232) is an α1A-adrenergic agonist with the potential to inhibit urinary incontinence. Garomefrine hydrochlorid showed the greatest contractility in pig nasal mucosal vessels. The biological activity of Garomefrine hydrochlorid has been shown to give it a competitive advantage compared to other drugs. The potency of Garomefrine hydrochlorid makes it a valuable research object in related research. -
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A 131701
0 ImagesCat. No.: HY-135488CAS No.: 181490-18-6A 131701 is a selective α1a- (Ki: 0.22 nM for human α1a) and α1d-adrenoceptor antagonist. A 131701 antagonizes epinephrine-induced increases in intraurethral pressure (IUP). A 131701 causes transient decreases in mean arterial blood pressure (MABP) and transient tachycardia. A 131701 can be used in the research of spontaneous hypertension. -
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Tamsolusin hydrochloride
0 ImagesCat. No.: HY-B0661CCAS No.: 80223-99-0Synonyms: YM12617 hydrochloride; LY253351 hydrochlorideTamsolusin hydrochloride (YM12617 hydrochloride; LY253351 hydrochloride) is an isomer of Tamsulosin (HY-B0661). Tamsolusin hydrochloride is a sulfonamide phenethylamine derivative and a competitive antagonist of selective post-synaptic α1-adrenoceptors. Tamsolusin hydrochloride inhibits CYP3A4 activity in a non-competitive, enantiomer-specific manner, with an IC50 and Ki of 6.75 μM. Tamsolusin hydrochloride produces dose-dependent hypotension, preferentially antagonizing α1-adrenoceptor-mediated pressor responses, and inhibits α2-adrenoceptor-mediated pressor responses at high doses. Tamsolusin hydrochloride can be used in research related to various diseases such as metabolism. -
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PF-4348235
0 ImagesCat. No.: HY-148525CAS No.: 1017857-38-3Synonyms: β2AR/M-receptor agonist-2β2AR/M-receptor agonist-2 (compound 15) is a muscarinic antagonist and β2 adrenoceptor agonist (MABA). β2AR/M-receptor agonist-2 shows potency to β2 adrenoceptor with an EC50 value of 3.7 nM. β2AR/M-receptor agonist-2 also has potency to human cloned M3 receptor with a Ki value of 0.73 nM. β2AR/M-receptor agonist-2 is a potent bronchodilator, it can be used for the research of chronic obstructive pulmonary disease (COPD). -
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Reboxetine
0 ImagesCat. No.: HY-14560CAS No.: 71620-89-8Reboxetine is an orally active, potent and selective noradrenaline uptake blocker. Reboxetine can be used for antidepressant research. -
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ADRA1D receptor antagonist 1 free base
0 ImagesCat. No.: HY-148252CAS No.: 1191908-24-3ADRA1D receptor antagonist 1 (free base) (compound (R)-9s) is an orally active, potent and selective human α1D-adrenoceptor (α1D-AR) antagonist (Ki=1.6 nM). ADRA1D receptor antagonist 1 (free base) dose-dependently inhibits bladder contraction with an IC30 value of 15 nM. ADRA1D receptor antagonist 1 (free base) can be used in studies of overactive bladder disorders such as urinary urgency, frequency and incontinence. -
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KUL-7211 racemate
0 ImagesCat. No.: HY-19673ACAS No.: 911196-40-2KUL-7211 racemate is the racemate of KUL-7211. KUL-7211 is a selective β-adrenoceptor agonist. -
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(±)-Befunolol
0 ImagesCat. No.: HY-101752CAS No.: 39552-01-7(±)-Befunolol is a β-adrenoceptor blocking agent. -
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Naminterol
0 ImagesCat. No.: HY-101822CAS No.: 93047-40-6Naminterol is a phenethanolamine derivative, is a β2 adrenoceptor agonist with bronchodilatory properties. Naminterol is used for treatment of asthma. -
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(S)-Dabelotine
0 ImagesCat. No.: HY-114552CAS No.: 152985-35-8(S)-Dabelotine is the S-isomer of Dabelotine and serves as an adrenergic agonist in the investigation of dementia. -
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Daledalin tosylate
0 ImagesCat. No.: HY-125047CAS No.: 23226-37-1Synonyms: UK 3557 tosylateDaledalin tosylate is an orally active indoline antidepressant targeting noradrenaline and serotonin transporters in the brain. Daledalin tosylate enhances central monoaminergic neurotransmission to alleviate depressive symptoms. Daledalin tosylate is proming for rasearch of depression, including endogenous and neurotic depression. -
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SAR-150640
0 ImagesCat. No.: HY-169340CAS No.: 433212-21-6SAR-150640, a selective β3-adrenoceptor agonist, prevents the increase in MMP activity and production observed after LPS stimulation or in cases of chorioamnionitis. -
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Navafenterol
0 ImagesCat. No.: HY-120802CAS No.: 1435519-06-4Synonyms: AZD-8871; LAS191351Navafenterol (AZD-8871) is an inhaled dual-acting, potent, selective, and long-lasting M3-antagonist/β2-agonist (MABA) with long-lasting effects and favorable safety profile. The pIC50 is 9.5 for human M3 receptor, and the pEC50 is 9.5 for β2-adrenoceptor. Navafenterol can be used for the research of chronic obstructive pulmonary disease (COPD). Bronchoprotective and antisialagogue effects. Favorable cardiovascular profile. -
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LK 204-545
0 ImagesCat. No.: HY-129660CAS No.: 83068-69-3LK 204-545 is a potent and highly selective β1-adrenoceptor antagonist. LK 204-545 is promising for research of cardiovascular diseases. -
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Asenapine-13C,d3 maleate
0 ImagesCat. No.: HY-W769200Synonyms: Org 5222-13C,d3 maleateAsenapine-13C,d3 Maleate is the deuterium labeled and 13C-Asenapine Maleate (HY-11100). Asenapine (Org 5222) Maleate, an atypical antipsychotic, is an antagonist of serotonin receptors (pKi: 8.4-10.5), adrenoceptors (pKi: 8.9-9.5), dopamine receptors (pKi: 8.9-9.4) and histamine receptors (pKi: 8.2-9.0). Asenapine Maleate can be used in the research of schizophrenia and bipolar disorder. -
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Dronedarone-d6 hydrochloride
0 ImagesCat. No.: HY-A0016SCAS No.: 1329809-23-5Dronedarone-d6 (hydrochloride) is the deuterium labeled Dronedarone. Dronedarone hydrochloride, a derivative of Amiodarone (HY-14187), is a class III antiarrhythmic agent for the study of atrial fibrillation (AF) and atrial flutter. Dronedarone hydrochloride is a potent blocker of multiple ion currents, including potassium current, sodium current, and L-type calcium current, and exhibits antiadrenergic effects by noncompetitive binding to β-adrenergic receptors. Dronedarone hydrochloride is a substrate for and a moderate inhibitor of CYP3A4. -
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Atenolol hydrochloride
0 ImagesCat. No.: HY-17498BCAS No.: 51706-40-2Synonyms: (RS)-Atenolol hydrochloride; Tenormin hydrochloride; ICI 66082 hydrochlorideAtenolol hydrochloride is a cardioselective β1-adrenergic receptor blocker, with a Ki of 697 nM at β1-adrenoceptor in guine pig left ventricle membrane. Atenolol hydrochloride can be used for the research of hypertension and angina pectoris. -
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Bucumolol
0 ImagesCat. No.: HY-184751CAS No.: 58409-59-9Bucumolol is an orally active β-adrenergic receptor blocker. Bucumolol inhibits Renin release. Bucumolol exhibits activities including local anesthesia, antiarrhythmia, antihypertension, heart rate reduction, negative inotropy, cardiac action potential inhibition, and action potential duration shortening. Bucumolol does not increase cardiac electrical threshold, prolong atrial refractory period, or affect body weight in rodents. Bucumolol can be used in research related to arrhythmia and hypertension. -
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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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