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Home >> Signaling Pathways >> GPCR/G protein >> Adrenergic Receptor

Adrenergic Receptor

Adrenergic receptor is a class of G protein-coupled receptors that are targets of the catecholamines, especially norepinephrine and epinephrine.

Products for  Adrenergic Receptor

  1. Cat.No. Product Name Information
  2. GC11531 Salmeterol xinafoate A long-acting β2-adrenergic receptor agonist Salmeterol xinafoate Chemical Structure
  3. GC48067 Salmeterol-d3 An internal standard for the quantification of salmeterol Salmeterol-d3 Chemical Structure
  4. GC14220 Scopine α1-adrenergic receptor agonist Scopine Chemical Structure
  5. GC11373 Scopine HCl Scopine HCl (6,7-Epoxytropine hydrochloride) is the metabolite of anisodine, which is a α1-adrenergic receptor agonist and used in the treatment of acute circulatory shock. Scopine HCl Chemical Structure
  6. GC13623 SDZ 21009 β-adrenoceptor and 5-HT1A/1B receptor antagonist SDZ 21009 Chemical Structure
  7. GC13990 Setiptiline Setiptiline Chemical Structure
  8. GC13549 Setiptiline maleate Setiptiline maleate Chemical Structure
  9. GC15719 Silodosin α1-adrenoceptor antagonist Silodosin Chemical Structure
  10. GC12856 SKF 86466 hydrochloride α2-adrenoceptor antagonist SKF 86466 hydrochloride Chemical Structure
  11. GC15426 SNAP 5089 α1A-adrenoceptor antagonist SNAP 5089 Chemical Structure
  12. GC34808 Solabegron

    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 Chemical Structure
  13. GC13173 Sotalol

    Adrenergic receptor antagonist

     Sotalol Chemical Structure
  14. GC15631 Sotalol hydrochloride β-adrenergic receptor antagonist Sotalol hydrochloride Chemical Structure
  15. GC45893 Sotalol-d6 (hydrochloride) An internal standard for the quantification of sotalol Sotalol-d6 (hydrochloride) Chemical Structure
  16. GC31005 Spirendolol (Li 32-468) Spirendolol (Li 32-468) is a β adrenergic receptor antagonist. Spirendolol (Li 32-468) Chemical Structure
  17. GC13338 Spiroxatrine 5-HT1A antagonist and α2C adrenergic receptor antagonist Spiroxatrine Chemical Structure
  18. GC16091 SR 58611A hydrochloride SR 58611A hydrochloride is a selective β3-adrenoceptor agonist, with an EC50 of 3.5 nM for β-adrenoceptor in rat colon; SR 58611A hydrochloride has anxiolytic and antidepressant activity. SR 58611A hydrochloride Chemical Structure
  19. GC12227 SR 59230A hydrochloride β3 adrenoceptor antagonist SR 59230A hydrochloride Chemical Structure
  20. GC39725 SR59230A SR59230A is a potent, selective, and blood-brain barrier penetrating β3-adrenergic receptor antagonist with IC50s of 40, 408, and 648 nM for β3, β1, and β2 receptors, respectively. SR59230A Chemical Structure
  21. GC11913 ST 91 α2-adrenoceptor agonist ST 91 Chemical Structure
  22. GC38438 Synephrine Synephrine Chemical Structure
  23. GC12715 Synephrine HCl Synephrine (Oxedrine) hydrochloride, an alkaloid, is an α-adrenergic and β-adrenergic agonist derived from the Citrus aurantium. Synephrine HCl Chemical Structure
  24. GC39449 Tamsulosin Tamsulosin ((R)-(-)-YM12617 free base) is an inhibitor of α1-adrenergic receptor. Tamsulosin Chemical Structure
  25. GC50035 Tamsulosin hydrochloride Selective α1A antagonist Tamsulosin hydrochloride Chemical Structure
  26. GC65276 Tasipimidine sulfate Tasipimidine sulfate is an orally active and selective α2A-adrenoceptor agonist with a pEC50 of 7.57 against human α2A-adrenoceptor. Tasipimidine sulfate Chemical Structure
  27. GC16217 TC-G 1000 α2D-adrenoceptor agonist TC-G 1000 Chemical Structure
  28. GC31453 TD-5471 hydrochloride TD-5471 hydrochloride is a potent and selective full agonist of the human β2-adrenoceptor. TD-5471 hydrochloride Chemical Structure
  29. GC30273 Tedatioxetine hydrobromide (Lu AA 24530 hydrobromide) Tedatioxetine (Lu AA24530) hydrobromide acts as a serotonin and norepinephrine (NE)-preferring triple reuptake inhibitor (TRI) and 5-HT2A, 5-HT2C, 5-HT3 and α1A-adrenergic receptor antagonist. Tedatioxetine hydrobromide (Lu AA 24530 hydrobromide) Chemical Structure
  30. GC30458 Teoprolol Teoprolol is a β-adrenergic receptor blocker. Teoprolol Chemical Structure
  31. GC13085 Terazosin α1-adrenergic receptor antagonist Terazosin Chemical Structure
  32. GC61320 Terazosin dimer impurity dihydrochloride Terazosin dimer impurity dihydrochloride, a dimer of Terazosin, is an impurity of Terazosin. Terazosin dimer impurity dihydrochloride Chemical Structure
  33. GC13993 Terazosin HCl Terazosin HCl is a quinazoline derivative and a competitive and orally active α1-adrenoceptor antagonist. Terazosin HCl Chemical Structure
  34. GC50017 Terazosin hydrochloride α1 and α2B antagonist (α1 > α2B). Orally active Terazosin hydrochloride Chemical Structure
  35. GC11211 Terbutaline Sulfate Selective β2-adrenergic receptor agonist Terbutaline Sulfate Chemical Structure
  36. GC32637 Tertatolol ((±)-Tertatolol) Tertatolol ((±)-Tertatolol) is a potent antagonist of beta-adrenoceptor and 5-HT receptor, with unique renal vasodilatatory effects. Tertatolol ((±)-Tertatolol) Chemical Structure
  37. GC39016 Tetrahydroalstonine Tetrahydroalstonine, a indole alkaloid isolated from the fruits of Rhazya stricta, is a selective alpha 2-adrenoceptor antagonist. Tetrahydroalstonine Chemical Structure
  38. GC14962 Tetrahydrozoline HCl Tetrahydrozoline HCl (Tetryzoline hydrochloride), a derivative of imidazoline, is an α-adrenergic agonist that causes vasoconstriction. Tetrahydrozoline HCl Chemical Structure
  39. GC12468 Timolol Maleate Timolol Maleate (L-714,465 Maleate) is a non-cardioselective hydrophilic β-adrenoceptor blocker. Timolol Maleate Chemical Structure
  40. GC31150 Tiodazosin (BL-5111) Tiodazosin (BL-5111) is a potent competitive postsynaptic alpha adrenergic receptor antagonist. Tiodazosin (BL-5111) Chemical Structure
  41. GC15629 Tizanidine α2 adrenergic agonist Tizanidine Chemical Structure
  42. GC17891 Tizanidine HCl Tizanidine HCl is an α2-adrenergic receptor agonist and inhibits neurotransmitter release from CNS noradrenergic neurons. Tizanidine HCl Chemical Structure
  43. GC63310 Tizanidine-d4 Tizanidine-d4 Chemical Structure
  44. GC32574 Todralazine (Ecarazine) Todralazine (Ecarazine) (Ecarazine) is an anti-hypertensive agent, acts as a β2AR blocker, with antioxidant and free radical scavenging activity. Todralazine (Ecarazine) Chemical Structure
  45. GC18327 Todralazine (hydrochloride) Todralazine (hydrochloride) is a β2-adrenergic receptor antagonist with peripheral vasodilator activity. Todralazine (hydrochloride) Chemical Structure
  46. GC30405 Tolazoline (Imidaline) Tolazoline (Imidaline)(Imidaline) is a non-selective competitive α-adrenergic receptor antagonist. Tolazoline (Imidaline) Chemical Structure
  47. GC18092 Tolazoline HCl Tolazoline (hydrochloride)(Imidaline (hydrochloride)) Hcl is a non-selective competitive α-adrenergic receptor antagonist. Tolazoline HCl Chemical Structure
  48. GC13031 Trifluoperazine 2HCl Dopamine D2 receptor inhibitor Trifluoperazine 2HCl Chemical Structure
  49. GC63241 Trifluoperazine D8 Trifluoperazine D8 Chemical Structure
  50. GC32642 Tropodifene (Tropaphen) Tropodifene (Tropaphen) (Tropaphen) is an α-Adrenergic receptor inhibitor. Tropodifene (Tropaphen) Chemical Structure
  51. GC62650 Tulobuterol Tulobuterol (C-78 free base) is a long-acting β2-adrenoceptor agonist, which reduces the frequency of exacerbations of chronic obstructive pulmonary disease and bronchial asthma. Tulobuterol Chemical Structure
  52. GC31730 Tulobuterol hydrochloride Tulobuterol hydrochloride (C-78) is a long-acting β2-adrenoceptor agonist, which reduces the frequency of exacerbations of chronic obstructive pulmonary disease and bronchial asthma. Tulobuterol hydrochloride Chemical Structure
  53. GC63349 Tulobuterol-D9 hydrochloride Tulobuterol-D9 hydrochloride Chemical Structure
  54. GC13552 UK 14,304 UK 14,304 (UK 14304) is a full α2-adrenergic receptor (α2-AR) agonist. UK 14,304 Chemical Structure
  55. GC67715 Upidosin Upidosin Chemical Structure
  56. GC37861 Urapidil Urapidil is an α1 adrenoreceptor antagonist and a 5-HT1A receptor agonist. Urapidil Chemical Structure
  57. GC15829 Urapidil HCl Urapidil HCl is an orally active α1-adrenoceptor antagonist and 5-HT1A receptor agonist with a pIC50 of 6.13 and 4.38 against α1- and α2-adrenoceptor, respectively. Urapidil HCl Chemical Structure
  58. GC30994 Vanilpyruvic acid (Vanylpyruvic acid) Vanilpyruvic acid (Vanylpyruvic acid) is a catecholamine metabolite and precursor to vanillactic acid. Vanilpyruvic acid (Vanylpyruvic acid) Chemical Structure
  59. GC30938 Vatinoxan hydrochloride (MK-467 hydrochloride) Vatinoxan hydrochloride (MK-467 hydrochloride) (MK-467 hydrochloride;L-659066 hydrochloride) is a peripheral α2 adrenergic receptor antagonist. Vatinoxan hydrochloride (MK-467 hydrochloride) Chemical Structure
  60. GC63254 Vibegron Vibegron (MK-4618) is a potent, highly selective β3-adrenoceptor agonist (EC50=1.1 nM). Vibegron Chemical Structure
  61. GC13747 Vilanterol β2-AR agonist Vilanterol Chemical Structure
  62. GC14950 Vilanterol trifenatate β2-AR agonist Vilanterol trifenatate Chemical Structure
  63. GC17740 WB 4101 hydrochloride α1A-adrenergic antagonist WB 4101 hydrochloride Chemical Structure
  64. GC17666 Xamoterol hemifumarate β1-adrenoceptor partial agonist Xamoterol hemifumarate Chemical Structure
  65. GC12073 Xylazine α2-adrenoceptor agonist Xylazine Chemical Structure
  66. GC17296 Xylazine HCl α2 Adrenoceptor agonist Xylazine HCl Chemical Structure
  67. GC11479 Xylometazoline HCl Xylometazoline HCl is an α-adrenergic receptor agonist (Ki=0.05-1.7 μM). Xylometazoline HCl Chemical Structure
  68. GC37952 Yohimbine Yohimbine is a potent and relatively nonselective alpha 2-adrenergicreceptor (AR) antagonist, with IC50 of 0.6 μM. Yohimbine Chemical Structure
  69. GN10606 Yohimbine Hydrochloride

    An α2-adrenoceptor antagonist

     Yohimbine Hydrochloride Chemical Structure
  70. GC37954 YS-49 YS-49 is a PI3K/Akt (a downstream target of RhoA) activator, to reduce RhoA/PTEN activation in the 3-methylcholanthrene-treated cells. YS-49 Chemical Structure
  71. GC37955 YS-49 monohydrate YS-49 (monohydrate) is a PI3K/Akt (a downstream target of RhoA) activator, to reduce RhoA/PTEN activation in the 3-methylcholanthrene-treated cells. YS-49 monohydrate Chemical Structure
  72. GC11174 ZD 2079 ZD 2079 (ZD2079 hydrochloride) is a potent β3-adrenoceptor agonist with a pD2 of 3.72 on phenylephrine-preconstricted rat mesenteric artery. ZD 2079 Chemical Structure
  73. GC17543 ZD 7114 hydrochloride β3-adrenoceptor agonist ZD 7114 hydrochloride Chemical Structure
  74. GC13333 Zilpaterol β-adrenergic receptor agonist Zilpaterol Chemical Structure
  75. GC48269 Zilpaterol-d7 An internal standard for the quantification of zilpaterol Zilpaterol-d7 Chemical Structure
  76. GC16111 Zinterol hydrochloride Zinterol hydrochloride (MJ 9184) is a potent and selective β2-adrenoceptor agonist. Zinterol hydrochloride Chemical Structure
  77. GC32034 ZK-90055 hydrochloride ZK-90055 hydrochloride is a β2 adrenergic receptor agonist. ZK-90055 hydrochloride Chemical Structure

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