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| Cat. No. | Product Name | Field of Application | Chemical Structure |
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| DC7289 | Imiloxan |
A moderately potent, but highly selective α2-adrenoceptor antagonist, the only reported selective antagonist at the α2B-adrenoceptor not having potent α1-adrenoceptor antagonist activity.
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| DCZ-156 | UR-144 |
>98%,Standard References
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| DC11364 | Levocetirizine；(R)-Cetirizine (hydrochloride) |
(R)-Cetirizine is the (R)-enantiomer of the histamine H1 receptor antagonist and second generation antihistamine cetirizine.
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| DC8964 | Phenylephrine hydrochloride |
(R)-(-)-Phenylephrine hydrochloride is a phenylephrine (PE) and an α1-adrenoceptor agonist
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| DC10160 | (1R,2S)-VU0155041 |
(1R,2S)-VU0155041, Cis regioisomer of VU0155041, is a partial mGluR4 agonist with an EC50 of 2.35 μM.
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| DC5060 | (+)PD 128907 |
(+)PD 128907 is a potent D3 dopamine receptor agonist (Ki = 2.3 nM). Displays 18 - 200-fold selectivity over other dopamine receptor subtypes.
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