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Adrenergic Receptor Related Products (1649)
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Antibodies (4)
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Adrenergic Receptor Isoform Comparison
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BMS-201620
0 ImagesCat. No.: HY-19294CAS No.: 197643-49-5BMS-201620 is a selective β3 full agonist, with a Ki of 93 nM. BMS-201620 can be used in the research of obesity and non-insulin-dependent diabetes. -
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(Rac)-Rotigotine-d7 (hydrochloride)
0 ImagesCat. No.: HY-15394SCAS No.: 3026226-88-7Synonyms: N-0437-d7 (hydrochloride)(Rac)-Rotigotine-d7 (hydrochloride) is deuterium labeled (Rac)-Rotigotine (hydrochloride). (Rac)-Rotigotine hydrochloride is a racemate of Rotigotine. Rotigotine is a full agonist of dopamine receptor, a partial agonist of the 5-HT1A receptor, and an antagonist of the α2B-adrenergic receptor, with Kis of 0.71 nM, 4-15 nM, and 83 nM for the dopamine D3 receptor and D2, D5, D4 receptors, and dopamine D1 receptor. -
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rac-Levonordefrin
0 ImagesSynonyms: rac-Cobefrin; rac-α-Methylnoradrenaline; rac-NordefrinRac-Levonordefrin (rac-Cobefrin; rac-α-Methylnoradrenaline; rac-Nordefrin) is the racemic form of Levonordefrin (HY-107915). Levonordefrin is an α-adrenergic receptor agonist with blood pressure regulating properties. -
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IMTPPE
0 ImagesCat. No.: HY-121588CAS No.: 851688-13-6IMTPPE is an inhibitor of the androgen receptor (AR) in C4-2 prostate cancer cells, inhibiting its transcriptional activity and protein levels. IMTPPE inhibited the proliferation of AR-positive prostate cancer cells but had no effect on AR-negative prostate cancer cells. IMTPPE also inhibited the growth of enzalutamide-resistant 22Rv1 xenograft tumors. -
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Oxaprotiline hydrochloride
0 ImagesCat. No.: HY-122300CCAS No.: 39022-39-4Synonyms: (Rac)-Levoprotiline hydrochlorideOxaprotiline hydrochloride is a potent norepinephrine (NA) uptake inhibitor. Oxaprotiline hydrochloride has antidepressant activity. -
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- β2AR agonist 4
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- Dibenamine
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- AH 11110A
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2-(1-Piperazinyl)pyrimidine-d8
0 ImagesCat. No.: HY-W004464SCAS No.: 1309283-31-52-(1-Piperazinyl)pyrimidine-d8 is the deuterated-labeled 2-(1-Piperazinyl)pyrimidine (HY-W004464). 2-(1-Piperazinyl)pyrimidine is an orally effective α2-adrenoceptor antagonist and 5-HT1A receptor agonist. 2-(1-Piperazinyl)pyrimidine is an in vivo metabolite related to buspirone. 2-(1-Piperazinyl)pyrimidine modulates excitatory synaptic transmission in the hippocampus and the release of monoamine transmitters such as norepinephrine and 5-HT by blocking α2-adrenoceptor and activating 5-HT1A Receptor. 2-(1-Piperazinyl)pyrimidine is used in research on psychiatric disorders such as anxiety and depression. -
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Clozapine-d3
0 ImagesCat. No.: HY-14539S3CAS No.: 1215691-72-7Synonyms: HF 1854-d3Clozapine-d3 (HF 1854-d3) is deuterium labeled Clozapine. Clozapine (HF 1854) is an antipsychotic used for the research of schizophrenia. Clozapine has high affinity for a number of neuroreceptors. Clozapine is a potent antagonist of dopamine D2 with a Ki of 75 nM. Clozapine inhibits the muscarinic M1 receptor and serotonin 5HT2A receptor with Kis of 9.5 nM and 4 nM, respectively. Clozapine is also a potent and selective agonist at the muscarinic M4 receptor (EC50=11 nM). -
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Bisoprolol-d7
0 ImagesCat. No.: HY-W707407CAS No.: 1310012-16-8Bisoprolol-d7 is deuterium labeled Bisoprolol. Bisoprolol is a potent, selective and orally active β1-adrenergic receptor blocker with little activity on β2-receptor. Bisoprolol has the potential for hypertension, coronary artery disease and stable ventricular dysfunction research. -
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Platelet aggregation-IN-3
0 ImagesCat. No.: HY-176060CAS No.: 1029802-21-8Platelet aggregation-IN-3 (Compound 5) is a ligand for H2 histamine receptors, α2(A,C)-adrenergic receptors (α2-AR), and 5-HT2(B,C) serotonin receptors. Platelet aggregation-IN-3 can inhibit platelet aggregation induced by ADP and collagen and can also modulate tumour cell-induced platelet aggregation (TCIPA). Platelet aggregation-IN-3 is promising for research of antiplatelet therapy in cardiovascular diseases and the prevention of cancer-related thrombosis and tumour metastasis. -
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Dilevalol
0 ImagesCat. No.: HY-119485CAS No.: 75659-07-3Synonyms: (+)-LabetalolDilevalol ((+)-Labetalol) is a novel agonist of ß2-receptor that can be used to suppress hypertension during pregnancy. -
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GYKI 12743
0 ImagesCat. No.: HY-106390ACAS No.: 110714-10-8GYKI 12743 is a vasoselective, postsynaptic α-adrenoceptor blocker. GYKI 12743 inhibits but does not completely eliminate the cutaneous microcirculatory blood flow reduction evoked by electrical stimulation of the peripheral stump of the cut saphenous nerve in rats. GYKI 12743 can be used for the study of neurological diseases. -
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Salmeterol-d5
0 ImagesCat. No.: HY-14302S1CAS No.: 1093433-84-1Synonyms: GR33343X-d5Salmeterol-d5 is a deuterated labeled Salmeterol. Salmeterol (GR33343X) is a potent and selective human β2 adrenoceptor agonist. Salmeterol shows potent stimulation of cAMP accumulation in CHO cells expressing human β2, β1 and β3 adrenoceptors with pEC50s of 9.6, 6.1, and 5.9, respectively. -
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Prenalterol hydrochloride
0 ImagesCat. No.: HY-112071ACAS No.: 61260-05-7Prenalterol hydrochloride is a partial adrenal agonist with functional β1-receptor specificity and positive inotropic effects. Prenalterol hydrochloride is effective in suppressing acute heart failure, low output syndrome after myocardial infarction, shock, and reducing orthostatic hypotension in Shy-Drager syndrome. -
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Ractopamine
0 ImagesCat. No.: HY-113781CAS No.: 97825-25-7Synonyms: LY031537 free baseRactopamine (LY031537 free base) is a potent and orally active β-adrenergic receptor (βAR) agonist with Kd value of ~25 nM for pig β1AR and β2AR. Ractopamine also is a mTAAR1 agonist with an EC50 of 16 μM. Ractopamine promotes muscle mass development, limits fat deposition, reduces feed consumption, increases total cellular protein synthesis, and improves growth rate and feed efficiency in finishing swine. Ractopamine can be used for researching to increase lean tissue growth and improve production efficiency in pigs. -
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Timolol (Standard)
0 ImagesCat. No.: HY-17494RCAS No.: 26839-75-8Synonyms: (S)-L-714,465 (Standard); MK 950 free base (Standard)Timolol (Standard) is the analytical standard of Timolol. This product is intended for research and analytical applications. Timolol is a β-blocker available for both topical and systemic administration. Topical Timolol is primarily used to reduce intraocular pressure with open-angle glaucoma and ocular hypertension. Timolol can also be used for the research of infantile hemangiomas, hypertension, myocardial infarction, migraine prophylaxis, and atrial fibrillation.Timolol also has cardioprotective effect. -
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Guanadrel sulfate
0 ImagesCat. No.: HY-B1660CAS No.: 22195-34-2Guanadrel sulfate is an orally active, potent and postganglionic sympathetic inhibitor. Guanadrel sulfate lowers blood pressure by reducing systemic vascular resistance with little effect on cardiac output. Guanadrel sulfate is promising for research of hypertension. -
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Esprolol
0 ImagesCat. No.: HY-107010CAS No.: 396654-09-4Esprolol is an orally active and potent β-adrenergic receptor antagonist. Esprolol is rapidly metabolized by blood and tissue esterases to form the active metabolite amoxolol. Esprolol holds potential for research in exercise-induced angina. -
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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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