ONC206 是 ONC201 的类似物。ONC206 是一种选择性拮抗剂，对多巴胺 D2 类受体 (DRD2/3/4) 具有纳摩尔效力。ONC206 表现出广谱抗肿瘤活性。

BP 897 hydrochloride是一种有效的部分多巴胺D3受体激动剂和弱D2受体拮抗剂。BP 897盐酸盐对多巴胺D3受体具有高亲和力（Ki=0.92 nM），对D2受体的亲和力是其的70倍（Ki=61 nM）。

Tavapadon (PF-06649751) 是一种口服活性、高选择性的多巴胺 D1/D5 受体部分激动剂。Tavapadon 有效促进运动和减少残疾，显示出治疗帕金森病的潜力。

Rotigotine 是一种有效的多巴胺受体激动剂，其对多巴胺D3受体的Ki值为0.71 nM，对D2、D5、D4受体的Ki值为4-15 nM，对多巴胺D1受体的Ki值为83 nM。Rotigotine 是5-HT1A受体的部分激动剂和α2B-肾上腺素受体的拮抗剂。Rotigotine 可用于帕金森病（PD）的研究。

Tetramethylrhodamine Methyl Ester Perchlorate是膜可渗透的阳离子荧光探针，特异性识别线粒体膜电位，附着在线粒体上并产生明亮的荧光。在某些浓度下，罗丹明染料对细胞的毒性低，使其成为检测动物细胞、植物细胞和微生物线粒体的理想选择。

Y3154207 is a novel, potent, and subtype selective human D1 positive allosteric modulator (PAM) with minimal allosteric agonist activity (EC50 = 3 nM). In contrast to orthosteric agonists, LY3154207 showed a distinct pharmacological profile without a bell-shaped dose-response relationship or tachyphylaxis in preclinical models. Identification of a crystalline form of free LY3154207 from the discovery lots was not successful. Instead, a novel cocrystal form with superior solubility was discovered and determined to be suitable for development. LY3154207 is now in clinical development as a potential first-in-class D1 PAM for Lewy body dementia.

GR 103691 is an effective and selective receptor antagonist of the dopamine D3 receptor (D3DR).

Ro 10-5824 2HCl is an agonist of dopamine D4 receptor with Ki of 5.2 nM.

Bromopride is a dopamine antagonist with prokinetic properties, widely used as an antiemetic.

PD 168077 maleate is an agonist of D4 dopamine receptor with Ki of 8.7 nM. It can induce synaptic translocation of CaMK II to postsynaptic sites in cultured prefrontal cortical neurons.

Dexpramipexole is a neuroprotective agent and weak non-ergoline dopamine agonist.

(+)-PD 128,907 HCl is an agonist of D3 dopamine receptor with Ki of 2.3 nM.

Pardoprunox HCl is a partial dopamine D2 and D3 receptor agonist and serotonin 5-HT1A receptor agonist, D2 (pKi = 8.1) and D3 receptor (pKi = 8.6) partial agonist and 5-HT1A receptor (pKi = 8.5) full agonist.

ABT-724 3HCl is a potent and highly selective dopamine D4 receptor agonist with EC50s of 12.4 nM, 14.3 nM and 23.2 nM for human dopamine D4 receptor, rat D4 receptor and ferret D4 receptor.