Sigma-Aldrich
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Agonists



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E4250(−)-Epinephrine Adrenoceptor agonist.
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E1016(−)-Epinephrine (+)-bitartrate salt Sigma Reference Standard Adrenergic receptor agonist.
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E4375(−)-Epinephrine (+)-bitartrate salt solid Adrenergic receptor agonist.
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I2760(−)-Isoproterenol (+)-bitartrate salt powder β-Adrenoceptor agonist; increases cytosolic cAMP.
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I6504(−)-Isoproterenol hydrochloride β-adrenoceptor agonist; increases cytosolic cAMP.
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A7257(−)-Norepinephrine ≥98%, crystalline Adrenergic neurotransmitter
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C125(±)-CGP-12177A ≥98% (HPLC), solid β-adrenoceptor nonconventional partial agonist.
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E4642(±)-Epinephrine hydrochloride Adrenergic receptor agonist.
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E1635(±)-Epinephrine ≥95% Adrenoceptor agonist.
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A0937(±)-Norepinephrine (+)-bitartrate salt Adrenergic neurotransmitter
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O0250(±)-Octopamine hydrochloride ≥95%, solid α-adrenoceptor agonist; invertebrate neurotransmitter.
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S0752(±)-Synephrine ≥98% α-adrenoceptor agonist, vasoconstrictor.
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P8155(R)-(−)-Phenylephrine hydrochloride Sigma Reference Standard α-Adrenergic agonist
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P6126(R)-(−)-Phenylephrine hydrochloride powder α1-adrenoceptor agonist.
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B0126-Fluoronorepinephrine hydrochloride solid α-adrenoceptor agonist.
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A9512L-(−)-Norepinephrine (+)-bitartrate salt monohydrate ≥98%, solid Adrenergic neurotransmitter, vasoconstrictor.
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N3146L-(−)-Norepinephrine (+)-bitartrate salt monohydrate Sigma Reference Standard pricing
A5861A-61603 hydrate ≥98% (HPLC) New A-61603 is an α1A agonist. In radioligand binding assays, A-61603 was at least 35-fold more potent at α1A receptors than at α1b or α1d sites. In fibroblast cells transfected with α1a receptors, A-61603 more potently stimulated phosphoinositide hydrolysis than norepinephrine, and was antagonized by prazosin. A-61603 is less potent in cells transfected with α1b or α1d receptors. It is a potent agonist at α1A receptors in rat vas deferens (200- to 300-fold more potent than norepinephrine or phenylephrine, respectively) and in isolated canine prostate strips (130- to 165-fold more potent than norepinephrine or phenylephrine, respectively). In contrast, it is only 40-fold more potent than phenylephrine at α1B sites in rat spleen and 35-fold less potent at rat aortic, α1D sites. A-61603 induces a pressor response in conscious rats at doses 50- to 100-fold lower than phenylephrine.
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B162B-HT 920 dihydrochloride solid, ≥98% (HPLC) α2-adrenoceptor agonist; D2 dopamine receptor agonist.
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B161B-HT 933 dihydrochloride ≥98% (HPLC), solid Selective α2-adrenoceptor agonist.
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B0185BRL 35135A >96% (HPLC), solid β3-adrenoceptor agonist.
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B169BRL 37344 sodium salt hydrate solid BRL 37344 is a selective β3-adrenoceptor agonist. Studies support the hypothesis that there are peripheral β3 adrenergic receptors that can reduce food intake and that central β2 or β3 adrenergic receptors mediate the peripheral effects of the β3 agonist.
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B8684Bambuterol hydrochloride >98% (HPLC), powder β-adrenoceptor agonist; bronchodilator; anti-asthmatic; terbutaline prodrug
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C5976CL 316,243 ≥98%, solid CL 316,243 is a β3 adrenoceptor agonist; anti-obesity agent.
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C5423Clenbuterol hydrochloride ≥95% β2-adrenoceptor agonist, bronchodilator.
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D0676Dobutamine hydrochloride ≥98% β1-Adrenoceptor receptor agonist.
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F1016Fenoterol hydrobromide β2-adrenoceptor agonist; bronchodilator.
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F9552Formoterol fumarate dihydrate >98% (HPLC) β2-Adrenoreceptor agonist.
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G110Guanabenz acetate salt solid Centrally acting α2 adrenoceptor agonist; I2 imidazoline binding site ligand; antihypertensive.
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G1043Guanfacine hydrochloride >98% (TLC) α-2 noradrenergic receptor agonist.
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I3639Isoetharine mesylate salt β-Adrenergic receptor agonist; bronchodilator.
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I5627Isoprenaline hydrochloride β-adrenoceptor agonist; increases cytosolic cAMP.
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M3656Mephentermine hemisulfate salt α-adrenoceptor agonist.
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M2398Metaproterenol hemisulfate salt β2-adrenoceptor agonist
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M4773Metaraminol (+)-bitartrate salt α-adrenoceptor agonist.
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M6524Methoxamine hydrochloride α1-adrenoceptor agonist.
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M1559Moxonidine hydrochloride ≥98% α2-adrenoceptor agonist and I1 imidazoline binding site agonist that, in many applications, demonstrates selectivity for the high-affinity I1 imidazoline binding site over the α2-adrenoceptor; antihypertensive. Its analgesic effects appear to be due to its agonist activity at spinal α2C-adrenoceptors.
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N5504Naphazoline hydrochloride α-adrenoceptor agonist; imidazoline receptor agonist; vasoconstrictor.
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O2378Oxymetazoline hydrochloride ≥99%, solid Oxymetazoline hydrochloride is a partial α2A-adrenoceptor agonist; agonist at 5-HT1A, 5-HT1B, and 5-HT1D serotonin receptors. It is a mixed agonist-antagonist at 5-HT1C serotonin receptors.
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P9180Procaterol hydrochloride β2-adrenoceptor agonist; bronchodilator.
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D7815R(−)-Denopamine ≥98% (HPLC), powder β1-adrenoceptor agonist.
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R0758Ritodrine hydrochloride β2-adrenoceptor agonist; relaxes uterine muscle contraction.
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S8260Salbutamol β2-adrenoceptor agonist
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S5013Salbutamol hemisulfate salt ≥98% β2-Adrenergic receptor agonist.
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S5068Salmeterol xinafoate ≥98% (HPLC), solid β2-adrenoceptor agonist.
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T2528Terbutaline hemisulfate salt β-adrenoceptor agonist; bronchodilator.
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T4264Tetrahydrozoline hydrochloride ≥98% α-adrenoceptor agonist; imidazoline binding site ligand; vasoconstrictor.
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T6950Tizanidine hydrochloride ≥98% (HPLC), solid α2-adrenoceptor agonist.
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U104UK 14,304 UK 14,304 is an α2-adrenoceptor agonist.
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X3253Xamoterol hemifumarate salt >98% (HPLC), solid Specific β1-adrenoceptor partial agonist.
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X1251Xylazine hydrochloride ≥99% α2-Adrenergic receptor agonist, sedative, muscle relaxant.
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X1126Xylazine ≥99% α2-adrenoceptor agonist, sedative, muscle relaxant.
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X6000Xylometazoline hydrochloride α-adrenoceptor agonist; imidazoline binding site ligand.
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A0779p-Aminoclonidine hydrochloride solid α2-adrenoceptor agonist.
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