Dopamine Receptor

信号通路图

研究领域

抑制剂选择性比较
溶解性比较

目录号	产品目录	溶解度(25°C)
目录号	产品目录	水	DMSO	酒精
S3163	Benztropine mesylate	81 mg/mL	50 mg/mL	81 mg/mL
S2456	Chlorpromazine HCl	71 mg/mL	71 mg/mL	71 mg/mL
S5796	Vanoxerine dihydrochloride	5 mg/mL	17 mg/mL	2 mg/mL
S2452	Amfebutamone (Bupropion) HCl	<1 mg/mL	8 mg/mL	<1 mg/mL
S3201	Trifluoperazine 2HCl	96 mg/mL	88 mg/mL	96 mg/mL
S2461	Domperidone	<1 mg/mL	48 mg/mL	1 mg/mL
S4569	Fluphenazine dihydrochloride	100 mg/mL	100 mg/mL	30 mg/mL
S1642	Methyldopa	<1 mg/mL	2 mg/mL	<1 mg/mL
S3189	Ropinirole HCl	60 mg/mL	10 mg/mL	<1 mg/mL
S2493	Olanzapine	<1 mg/mL	62 mg/mL	9 mg/mL
S1763	Quetiapine Fumarate	<1 mg/mL	36 mg/mL	<1 mg/mL
S1444	Ziprasidone HCl	<1 mg/mL	90 mg/mL	<1 mg/mL
S5862	Metoclopramide	<1 mg/mL	60 mg/mL	<1 mg/mL
S5565	Triflupromazine hydrochloride	-1 mg/mL	78 mg/mL	-1 mg/mL
S9509	Tiapride Hydrochloride	-1 mg/mL	35 mg/mL	-1 mg/mL
S5399	Chlorprothixene hydrochloride	-1 mg/mL	70 mg/mL	-1 mg/mL
S5714	lurasidone	<1 mg/mL	7 mg/mL	<1 mg/mL
S5624	Paliperidone Palmitate	<1 mg/mL	1 mg/mL	3 mg/mL
S5559	Tetrahydropalmatine	<1 mg/mL	16 mg/mL	<1 mg/mL
S5153	Tetrahydroberberine	-1 mg/mL	6 mg/mL	-1 mg/mL
S5428	Promazine hydrochloride	-1 mg/mL	64 mg/mL	-1 mg/mL
S5481	Molindone hydrochloride	-1 mg/mL	9 mg/mL	-1 mg/mL
S5324	Oxidopamine (hydrobromide)	50 mg/mL	50 mg/mL	50 mg/mL
S4889	Perospirone hydrochloride	-1 mg/mL	92 mg/mL	-1 mg/mL
S5034	Melitracen hydrochloride	65 mg/mL	65 mg/mL	65 mg/mL
S1280	Amisulpride	<1 mg/mL	73 mg/mL	73 mg/mL
S1724	Paliperidone	<1 mg/mL	4 mg/mL	<1 mg/mL
S1920	Haloperidol	<1 mg/mL	75 mg/mL	8 mg/mL
S1771	Chlorprothixene	<1 mg/mL	6 mg/mL	28 mg/mL
S4251	Phenothiazine	<1 mg/mL	40 mg/mL	<1 mg/mL
S4096	Droperidol	<1 mg/mL	76 mg/mL	<1 mg/mL
S3044	Lurasidone HCl	<1 mg/mL	1 mg/mL	<1 mg/mL
S2104	Levosulpiride	<1 mg/mL	69 mg/mL	<1 mg/mL
S4086	Loxapine Succinate	<1 mg/mL	89 mg/mL	2 mg/mL
S4731	Perphenazine	<1 mg/mL	74 mg/mL	74 mg/mL
S4151	Penfluridol	<1 mg/mL	100 mg/mL	100 mg/mL
S2437	Rotundine	<1 mg/mL	8 mg/mL	<1 mg/mL
S4631	Prochlorperazine dimaleate salt	<1 mg/mL	74 mg/mL	2 mg/mL
S4257	Alizapride HCl	70 mg/mL	42 mg/mL	<1 mg/mL
S4655	Sulpiride	<1 mg/mL	68 mg/mL	<1 mg/mL
S1789	Tetrabenazine (Xenazine)	<1 mg/mL	58 mg/mL	32 mg/mL
S4219	Azaperone	<1 mg/mL	65 mg/mL	34 mg/mL
S4289	Metoclopramide HCl	67 mg/mL	67 mg/mL	67 mg/mL
S5849	Cariprazine HCl	3 mg/mL	5 mg/mL	4 mg/mL
S5842	Cabergoline	<1 mg/mL	90 mg/mL	90 mg/mL
S5066	Pramipexole dihydrochloride	-1 mg/mL	56 mg/mL	-1 mg/mL
S1726	Levodopa	<1 mg/mL	<1 mg/mL	<1 mg/mL
S2451	Amantadine HCl	38 mg/mL	38 mg/mL	38 mg/mL
S2011	Pramipexole 2HCl Monohydrate	60 mg/mL	41 mg/mL	<1 mg/mL
S2460	Pramipexole	<1 mg/mL	42 mg/mL	42 mg/mL
S2529	Dopamine HCl	38 mg/mL	38 mg/mL	<1 mg/mL
S4000	Pergolide Mesylate	82 mg/mL	10 mg/mL	<1 mg/mL
S3664	Flupenthixol dihydrochloride	100 mg/mL	100 mg/mL	30 mg/mL
S4618	Fenoldopam mesylate	<1 mg/mL	80 mg/mL	<1 mg/mL
S7993	SKF38393 HCl	<1 mg/mL	58 mg/mL	6 mg/mL
S4639	Brexpiprazole	<1 mg/mL	24 mg/mL	<1 mg/mL
S3656	Piribedil	<1 mg/mL	59 mg/mL	59 mg/mL
S2168	PD128907 HCl	50 mg/mL	12 mg/mL	<1 mg/mL
S4274	Rotigotine	<1 mg/mL	63 mg/mL	63 mg/mL
S4732	MPTP hydrochloride	41 mg/mL	20 mg/mL	41 mg/mL
S8097	C-DIM12	<1 mg/mL	71 mg/mL	71 mg/mL
S3188	(+,-)-Octopamine HCl	38 mg/mL	38 mg/mL	11 mg/mL

特异性亚型抑制剂

Dopamine Receptor产品

所有产品 Dopamine Receptor抑制剂(10) Dopamine Receptor拮抗剂(34) Dopamine Receptor激动剂(16) Dopamine Receptor化学产品(3) 新Dopamine Receptor产品

产品目录	产品描述	文献引用	实验数据
S3163	Benztropine mesylate Benztropine mesylate是一种多巴胺转运蛋白抑制剂，IC50为118 nM。
S2456	Chlorpromazine HCl Chlorpromazine HCl是一种多巴胺和钾离子通道抑制剂，对内向整流钾电流和与时间无关的外向电流IC50分别为6.1和16 μM。	Antimicrob Agents Chemother, 2014, 58(8):4875-84 Virol J, 2016, 13:25 Fish Shellfish Immunol, 2018, 84:138-147	Low-micromolar amounts of chlorpromazine inhibit SARS-CoV-induced cytopathology. Vero E6 cells in 96-well plates were infected with SARS-CoV isolate Frankfurt-1 (MOI, 0.005) in the presence of 0 to 16 μM CPZ (B), given at t of +1 h p.i. Cells were incubated for 3 days, and viability was monitored using an MTS assay. In parallel, potential compound cytotoxicity was monitored in mock-infected Vero E6 cells. Graphs show the results (averages and SD) of a representative experiment that was performed in quadruplicate. All experiments were repeated at least twice. For each compound, the EC50, CC50, and SI values are given.
S5856^New	Trifluoperazine Trifluoperazine是FDA认证的抗精神病药，用于治疗精神分裂症。它是calmodulin (CaM)和Dopamine D2 receptor抑制剂，对D2受体的IC50值为1.2 nM。
S5796^New	Vanoxerine dihydrochloride Vanoxerine是一种有效的、选择性的多巴胺摄取（dopamine uptake）抑制剂。
S2452	Amfebutamone (Bupropion) HCl Amfebutamone (Bupropion) HCl是一种选择性去甲肾上腺素-多巴胺再摄取的抑制剂，IC50分别为6.5和3.4μM。	G3 (Bethesda), 2014, 4(6):1081-9 Georgia State University, 2014, Chaquettea Felton G3 (Bethesda), 2014, 10.1534/g3.114.010819
S3201	Trifluoperazine 2HCl Trifluoperazine 2HCl是一种多巴胺D2受体抑制剂，IC50为1.1 nM。
S2461	Domperidone Domperidone 是一种多巴胺受体抑制剂，是一种抗多巴胺试剂。
S4569	Fluphenazine dihydrochloride Fluphenazine dihydrochloride是吩噻嗪类的D1DR和D2DR抑制剂。它能够抑制组胺H1受体。	Methods Mol Biol, 2017, 1513:119-140
S1642	Methyldopa Methyldopa 是DOPA 脱羧酶竞争性抑制剂，ED50为21.8 mg/kg。
S3189	Ropinirole HCl Ropinirole HCl是一种选择性的D2受体抑制剂，IC50为29 nM。
S2493	Olanzapine Olanzapine是一种高亲和力的5-HT2 5-羟色胺和多巴胺D2受体拮抗剂。	J Psychiatr Res, 2017, 88:18-27 J Psychiatr Res, 2018, 105:95-102 Sci Rep, 2018, 8(1):11260	Olanzapine and aripiprazole differentially regulate cellular glucose uptake of PBMC. Bar graphs depict cellular glucose uptake assessed by 18F-FDG in PBMC after 72 h of stimulation with the indicated concentrations of olanzapine (Olan, A) or aripiprazole (Arip, B) relative to corresponding DMSO controls (Ctrl) and normalized to protein content. Data are depicted as mean ± SD. P-values were computed by one-way ANOVA followed by Dunnett's Multiple Comparison Test. *P < 0.001, P < 0.01, *P < 0.05 versus control; results were obtained from n ¼ 4e6 independent cell isolations measured in duplicate.
S1763	Quetiapine Fumarate Quetiapine Fumarate是一种非典型抗精神病药物，用于治疗精神分裂症，双相I型躁狂，双相II型抑郁症，双相I型抑郁症。对多种神经递质受体如serotonin, dopamine, histamine和adrenergic receptors有亲和力。
S1444	Ziprasidone HCl Ziprasidone HCl 是一类有效的dopamine 和 serotonin (5-HT) receptor的拮抗剂，用于精神分裂症以及双向性障碍的治疗。	Nature, 2018, 560(7718):372-376 Sci Rep, 2017, 7(1):8491	a, Quantification of sterol levels in OPCs (oligodendrocyte progenitor cells) treated with the indicated molecules at 2 μM.
S5862^New	Metoclopramide Metoclopramide是一种多巴胺拮抗剂，用于治疗恶心呕吐。
S5565^New	Triflupromazine hydrochloride Triflupromazine hydrochloride is an antipsychotic medication of the phenothiazine class.
S9509^New	Tiapride Hydrochloride Tiapride is a drug that selectively blocks D2 and D3 dopamine receptors in the brain and is used to treat a variety of neurological and psychiatric disorders.
S5399^New	Chlorprothixene hydrochloride Chlorprothixene HCl is the hydrochloride salt form of chlorprothixene, a typical antipsychotic drug of the thioxanthene (tricyclic) class. It exerts strong blocking effects by blocking the 5-HT2 D1, D2, D3, histamine H1, muscarinic and alpha1 adrenergic receptors.
S5714^New	lurasidone Lurasidone is a second-generation antipsychotic agent that exhibits full antagonism at dopamine D2 and serotonin 5-HT2A receptors with binding affinities Ki = 1 nM and Ki = 0.5 nM, respectively. It also has high affinity for serotonin 5-HT7 receptors (Ki = 0.5 nM), partial agonist activity at 5-HT1A receptors (Ki = 6.4 nM) and lacks affinity for histamine H1 and muscarinic M1 receptors.
S5624^New	Paliperidone Palmitate Paliperidone Palmitate is a palmitate ester of paliperidone, which is a dopamine antagonist and 5-HT2A antagonist of the atypical antipsychotic class.
S5559^New	Tetrahydropalmatine Tetrahydropalmatine, a plant alkaloid used as an ingredient in dietary supplement products, is a potent and selective D1 receptor antagonist.
S5153^New	Tetrahydroberberine Tetrahydroberberine is an isoquinoline alkaloid with micromolar affinity for dopamine D2 (antagonist, pKi = 6.08) and 5-HT1A (agonist, pKi = 5.38) receptors but moderate to no affinity for other relevant serotonin receptors.
S5428^New	Promazine hydrochloride Promazine is an antagonist at types 1, 2, and 4 dopamine receptors, 5-HT receptor types 2A and 2C, muscarinic receptors 1 through 5, alpha(1)-receptors, and histamine H1-receptors with antipsychotic effects.
S5481^New	Molindone hydrochloride Molindone hydrochloride is the hydrochloride salt form of molindone, a conventional antipsychotic used in the therapy of schizophrenia. It is a dopamine D2/D5 receptor antagonist.
S5324^New	Oxidopamine (hydrobromide) Oxidopamine is a neurotoxic synthetic organic compound that acts as an antagonist of the neurotransmitter dopamine with potential antineoplastic activity.
S4889^New	Perospirone hydrochloride Perospirone is an atypical or second-generation antipsychotic of the azapirone family that antagonizes serotonin 5HT2A receptors and dopamine D2 receptors. It also displays affinity towards 5HT1A receptors as a partial agonist.
S5034^New	Melitracen hydrochloride Melitracen hydrochloride是一种潜在的dopamine D1/2 receptor拮抗剂，具有抗抑郁作用。
S1280	Amisulpride Amisulpride是一种非典型的抗精神病药物，用于治疗精神病的精神分裂症和双相情感障碍的躁狂发作。
S1724	Paliperidone Paliperidone，作为 Risperidone主要的活性代谢物，是一种高效的serotonin-2A 和dopamine-2 receptor 拮抗剂，用于治疗精神分裂症。
S1920	Haloperidol Haloperidol 是一种丁酰苯类的抗精神病药。
S1771	Chlorprothixene Chlorprothixene与多巴胺和组织胺受体（如D1， D2， D3， D5， H1， 5-HT2， 5-HT6和5-HT7）具有强结合力， K_i值分别为18nM， 2.96 nM， 4.56 nM， 9 nM， 3.75 nM， 9.4 nM， 3 nM和5.6 nM。
S4251	Phenothiazine Phenothiazine是多巴胺-2(D2)受体拮抗剂，因此能够降低多巴胺在大脑中的作用。
S4096	Droperidol Droperidol在边缘系统中有效拮抗多巴胺受体亚型2(D2DR)。
S3044	Lurasidone HCl Lurasidone HCl是一种非典型的抗精神病药物，抑制D2， 5-HT2A， 5-HT7， 5-HT1A和去甲肾上腺素α2C，IC50分别为1.68 nM， 2.03 nM， 0.495 nM， 6.75 nM和10.8 nM。
S2104	Levosulpiride Levosulpiride是一种选择性D2多巴胺受体拮抗剂，用作抗精神病药和促动力剂。
S4086	Loxapine Succinate Loxapine Succinate是D2DR和D4DR抑制剂,5-羟色胺受体拮抗剂，也是Dibenzoxazepine类的抗精神病试剂。
S4731	Perphenazine Perphenazine是一种吩噻嗪衍生物，它是多巴胺受体阻滞剂，具有止吐和治疗精神疾病的特性。
S4151	Penfluridol Penfluridol是一种高效的，第一代二苯丁哌啶类抗精神病药物。
S2437	Rotundine Rotundine是一种选择性多巴胺D1受体拮抗剂， IC50为166 nM。
S4631	Prochlorperazine dimaleate salt Prochlorperazine是抗精神病药物中属于吩噻嗪类的多巴胺受体D2拮抗剂。
S4257	Alizapride HCl Alizapride在以外消旋混合物服用时，作为多巴胺拮抗剂促肠胃运动和止吐治疗癌症化疗引起的恶心和呕吐。
S4655	Sulpiride Sulpiride是一种多巴胺D2受体拮抗剂。在临床治疗中，它被用作抗抑郁剂、安定药和助消化药。
S1789	Tetrabenazine (Xenazine) Tetrabenazine(Nitoman, Xenazine)主要是一种可逆的、高亲和力的突触前神经元的颗粒小泡吸收单胺的抑制剂，选择性与VMAT-2结合。也能阻止dopamine D2 receptors，但亲和力相对于对VMAT-2的亲和力弱1000倍。
S4219	Azaperone Azaperone 是一种吡啶哌嗪和丁酰苯类抗精神病药，具有镇静和止吐的效果，主要是在兽医上用作镇静剂。它是Dopamine receptors的拮抗剂，能够透过血脑屏障，结合D1和D2受体。
S4289	Metoclopramide HCl Metoclopramide HCl是一种选择性的 dopamine D2 receptor 拮抗剂，用于治疗恶心和呕吐。
S5849^New	Cariprazine HCl Cariprazine是一种新型二代抗精神病药物，是偏好于D3受体的dopamine D2/D3 receptor部分激动剂。
S5842^New	Cabergoline Cabergoline是一种长效多巴胺（dopamine）激动剂和催乳激素（prolactin）抑制剂。
S5066^New	Pramipexole dihydrochloride Pramipexole dihydrochloride是非麦角灵类的dopamine激动剂，用于治疗帕金森氏病和多动腿综合征，对D2S受体、D2L受体、D3和D4受体的Ki值分别为3.9 nM, 2.2 nM, 0.5 nM 和5.1 nM。
S1726	Levodopa Levodopa 是多巴胺,，肾上腺素以及去甲肾上腺素的前体，具有抗帕金森病的特性。	PLoS One, 2017, 12(3):e0173240	(A) A focused screening of Aβ generation in response to levodopa, piribedil, bromocriptine or carbidopa at indicated concentrations in SK-N-SH cells. Data are mean ± s.e.m., n = 3-4. p < 0.05; **p < 0.001 versus the control of each group.
S2451	Amantadine HCl Amantadine HCl用于治疗或预防某些病毒引起的呼吸道感染。
S2011	Pramipexole 2HCl Monohydrate Pramipexole 2HCl Monohydrate 是一种部分/全部D2S， D2L， D3， D4受体激动剂，K_i为3.9， 2.2， 0.5， 5.1 nM。
S2460	Pramipexole Pramipexole是部分/全部D2S， D2L， D3， D4受体激动剂，作用于D2S， D2L， D3， D4受体，K_i分别为3.9， 2.2， 0.5和5.1 nM。
S2529	Dopamine HCl Dopamine HCl 是一种广泛存在于各种动物的儿茶酚胺类神经递质，是多巴胺D1-5受体激动剂。
S4000	Pergolide Mesylate Pergolide Mesylate是一种抗震颤麻痹剂，作为dopaminergic（多巴胺能）激动剂。	Sci Rep, 2018, 8(1):11554 Pharm Res, 2011, 28(2):337-63 J Pharm Biomed Anal, 2011, 56(2):173-82
S3664	Flupenthixol dihydrochloride Flupentixol是一种抗精神病安定药物，是D1 and D2多巴胺受体的强效拮抗剂，也是α肾上腺素能受体的拮抗剂。
S4618	Fenoldopam mesylate Fenoldopam是一种选择性的多巴胺受体（dopamine-1 receptor）激动剂，具有利尿特性。它可以通过小动脉的血管舒张降低血压。
S7993	SKF38393 HCl SKF38393 HCl是一种选择性dopamine D1/D5 receptor激动剂。
S4639	Brexpiprazole Brexpiprazole是一种新型的多巴胺受体D2和5-羟色胺1A受体的部分激动剂，同时也是5-羟色胺2A受体和去甲肾上腺素alpha1B、alpha2C受体的拮抗剂。其对D_2L, 5-HT_1A, 5-HT_2A, α_1B受体和 α_2C受体的Ki值分别为 0.3, 0.12, 0.47, 0.17 和 0.59 nM。
S3656	Piribedil Piribedil is a relatively selective dopamine (D2/D3) agonist with moderate antidepressant activity. It also has α2-adrenergic (α2A/α2C) antagonist properties.
S2168	PD128907 HCl PD128907 HCl是一种有效的，选择性的多巴胺D3受体激动剂，EC50为0.64 nM，比作用于多巴胺D2受体的选择性高53倍。
S4274	Rotigotine Rotigotine是一种dopamine receptor的激动剂，用于帕金森氏症和不宁腿综合征的治疗。
S4732	MPTP hydrochloride MPTP HCl是一种多巴胺能的神经毒素，能在帕金森动物模型中选择性破坏多巴胺能神经元。
S8097	C-DIM12 C-DIM12是Nurr1的激活剂，刺激膀胱癌细胞和肿瘤中Nurr1所介导的细胞凋亡、抑制胶质细胞中对NF-κB依赖的基因表达。
S3188	(+,-)-Octopamine HCl (+,-)-Octopamine HCl,是一种生命必需的一元胺，结构上与去甲肾上腺素相关, 在无脊椎动物中作为一种神经激素，神经调节物质以及神经递质。

产品目录	产品描述	文献引用	实验数据
S3163	Benztropine mesylate Benztropine mesylate是一种多巴胺转运蛋白抑制剂，IC50为118 nM。
S2456	Chlorpromazine HCl Chlorpromazine HCl是一种多巴胺和钾离子通道抑制剂，对内向整流钾电流和与时间无关的外向电流IC50分别为6.1和16 μM。	Antimicrob Agents Chemother, 2014, 58(8):4875-84 Virol J, 2016, 13:25 Fish Shellfish Immunol, 2018, 84:138-147	Low-micromolar amounts of chlorpromazine inhibit SARS-CoV-induced cytopathology. Vero E6 cells in 96-well plates were infected with SARS-CoV isolate Frankfurt-1 (MOI, 0.005) in the presence of 0 to 16 μM CPZ (B), given at t of +1 h p.i. Cells were incubated for 3 days, and viability was monitored using an MTS assay. In parallel, potential compound cytotoxicity was monitored in mock-infected Vero E6 cells. Graphs show the results (averages and SD) of a representative experiment that was performed in quadruplicate. All experiments were repeated at least twice. For each compound, the EC50, CC50, and SI values are given.
S5856^New	Trifluoperazine Trifluoperazine是FDA认证的抗精神病药，用于治疗精神分裂症。它是calmodulin (CaM)和Dopamine D2 receptor抑制剂，对D2受体的IC50值为1.2 nM。
S5796^New	Vanoxerine dihydrochloride Vanoxerine是一种有效的、选择性的多巴胺摄取（dopamine uptake）抑制剂。
S2452	Amfebutamone (Bupropion) HCl Amfebutamone (Bupropion) HCl是一种选择性去甲肾上腺素-多巴胺再摄取的抑制剂，IC50分别为6.5和3.4μM。	G3 (Bethesda), 2014, 4(6):1081-9 Georgia State University, 2014, Chaquettea Felton G3 (Bethesda), 2014, 10.1534/g3.114.010819
S3201	Trifluoperazine 2HCl Trifluoperazine 2HCl是一种多巴胺D2受体抑制剂，IC50为1.1 nM。
S2461	Domperidone Domperidone 是一种多巴胺受体抑制剂，是一种抗多巴胺试剂。
S4569	Fluphenazine dihydrochloride Fluphenazine dihydrochloride是吩噻嗪类的D1DR和D2DR抑制剂。它能够抑制组胺H1受体。	Methods Mol Biol, 2017, 1513:119-140
S1642	Methyldopa Methyldopa 是DOPA 脱羧酶竞争性抑制剂，ED50为21.8 mg/kg。
S3189	Ropinirole HCl Ropinirole HCl是一种选择性的D2受体抑制剂，IC50为29 nM。

产品目录	产品描述	文献引用	实验数据
S2493	Olanzapine Olanzapine是一种高亲和力的5-HT2 5-羟色胺和多巴胺D2受体拮抗剂。	J Psychiatr Res, 2017, 88:18-27 J Psychiatr Res, 2018, 105:95-102 Sci Rep, 2018, 8(1):11260	Olanzapine and aripiprazole differentially regulate cellular glucose uptake of PBMC. Bar graphs depict cellular glucose uptake assessed by 18F-FDG in PBMC after 72 h of stimulation with the indicated concentrations of olanzapine (Olan, A) or aripiprazole (Arip, B) relative to corresponding DMSO controls (Ctrl) and normalized to protein content. Data are depicted as mean ± SD. P-values were computed by one-way ANOVA followed by Dunnett's Multiple Comparison Test. *P < 0.001, P < 0.01, *P < 0.05 versus control; results were obtained from n ¼ 4e6 independent cell isolations measured in duplicate.
S1763	Quetiapine Fumarate Quetiapine Fumarate是一种非典型抗精神病药物，用于治疗精神分裂症，双相I型躁狂，双相II型抑郁症，双相I型抑郁症。对多种神经递质受体如serotonin, dopamine, histamine和adrenergic receptors有亲和力。
S1444	Ziprasidone HCl Ziprasidone HCl 是一类有效的dopamine 和 serotonin (5-HT) receptor的拮抗剂，用于精神分裂症以及双向性障碍的治疗。	Nature, 2018, 560(7718):372-376 Sci Rep, 2017, 7(1):8491	a, Quantification of sterol levels in OPCs (oligodendrocyte progenitor cells) treated with the indicated molecules at 2 μM.
S5862^New	Metoclopramide Metoclopramide是一种多巴胺拮抗剂，用于治疗恶心呕吐。
S5565^New	Triflupromazine hydrochloride Triflupromazine hydrochloride is an antipsychotic medication of the phenothiazine class.
S9509^New	Tiapride Hydrochloride Tiapride is a drug that selectively blocks D2 and D3 dopamine receptors in the brain and is used to treat a variety of neurological and psychiatric disorders.
S5399^New	Chlorprothixene hydrochloride Chlorprothixene HCl is the hydrochloride salt form of chlorprothixene, a typical antipsychotic drug of the thioxanthene (tricyclic) class. It exerts strong blocking effects by blocking the 5-HT2 D1, D2, D3, histamine H1, muscarinic and alpha1 adrenergic receptors.
S5714^New	lurasidone Lurasidone is a second-generation antipsychotic agent that exhibits full antagonism at dopamine D2 and serotonin 5-HT2A receptors with binding affinities Ki = 1 nM and Ki = 0.5 nM, respectively. It also has high affinity for serotonin 5-HT7 receptors (Ki = 0.5 nM), partial agonist activity at 5-HT1A receptors (Ki = 6.4 nM) and lacks affinity for histamine H1 and muscarinic M1 receptors.
S5624^New	Paliperidone Palmitate Paliperidone Palmitate is a palmitate ester of paliperidone, which is a dopamine antagonist and 5-HT2A antagonist of the atypical antipsychotic class.
S5559^New	Tetrahydropalmatine Tetrahydropalmatine, a plant alkaloid used as an ingredient in dietary supplement products, is a potent and selective D1 receptor antagonist.
S5153^New	Tetrahydroberberine Tetrahydroberberine is an isoquinoline alkaloid with micromolar affinity for dopamine D2 (antagonist, pKi = 6.08) and 5-HT1A (agonist, pKi = 5.38) receptors but moderate to no affinity for other relevant serotonin receptors.
S5428^New	Promazine hydrochloride Promazine is an antagonist at types 1, 2, and 4 dopamine receptors, 5-HT receptor types 2A and 2C, muscarinic receptors 1 through 5, alpha(1)-receptors, and histamine H1-receptors with antipsychotic effects.
S5481^New	Molindone hydrochloride Molindone hydrochloride is the hydrochloride salt form of molindone, a conventional antipsychotic used in the therapy of schizophrenia. It is a dopamine D2/D5 receptor antagonist.
S5324^New	Oxidopamine (hydrobromide) Oxidopamine is a neurotoxic synthetic organic compound that acts as an antagonist of the neurotransmitter dopamine with potential antineoplastic activity.
S4889^New	Perospirone hydrochloride Perospirone is an atypical or second-generation antipsychotic of the azapirone family that antagonizes serotonin 5HT2A receptors and dopamine D2 receptors. It also displays affinity towards 5HT1A receptors as a partial agonist.
S5034^New	Melitracen hydrochloride Melitracen hydrochloride是一种潜在的dopamine D1/2 receptor拮抗剂，具有抗抑郁作用。
S1280	Amisulpride Amisulpride是一种非典型的抗精神病药物，用于治疗精神病的精神分裂症和双相情感障碍的躁狂发作。
S1724	Paliperidone Paliperidone，作为 Risperidone主要的活性代谢物，是一种高效的serotonin-2A 和dopamine-2 receptor 拮抗剂，用于治疗精神分裂症。
S1920	Haloperidol Haloperidol 是一种丁酰苯类的抗精神病药。
S1771	Chlorprothixene Chlorprothixene与多巴胺和组织胺受体（如D1， D2， D3， D5， H1， 5-HT2， 5-HT6和5-HT7）具有强结合力， K_i值分别为18nM， 2.96 nM， 4.56 nM， 9 nM， 3.75 nM， 9.4 nM， 3 nM和5.6 nM。
S4251	Phenothiazine Phenothiazine是多巴胺-2(D2)受体拮抗剂，因此能够降低多巴胺在大脑中的作用。
S4096	Droperidol Droperidol在边缘系统中有效拮抗多巴胺受体亚型2(D2DR)。
S3044	Lurasidone HCl Lurasidone HCl是一种非典型的抗精神病药物，抑制D2， 5-HT2A， 5-HT7， 5-HT1A和去甲肾上腺素α2C，IC50分别为1.68 nM， 2.03 nM， 0.495 nM， 6.75 nM和10.8 nM。
S2104	Levosulpiride Levosulpiride是一种选择性D2多巴胺受体拮抗剂，用作抗精神病药和促动力剂。
S4086	Loxapine Succinate Loxapine Succinate是D2DR和D4DR抑制剂,5-羟色胺受体拮抗剂，也是Dibenzoxazepine类的抗精神病试剂。
S4731	Perphenazine Perphenazine是一种吩噻嗪衍生物，它是多巴胺受体阻滞剂，具有止吐和治疗精神疾病的特性。
S4151	Penfluridol Penfluridol是一种高效的，第一代二苯丁哌啶类抗精神病药物。
S2437	Rotundine Rotundine是一种选择性多巴胺D1受体拮抗剂， IC50为166 nM。
S4631	Prochlorperazine dimaleate salt Prochlorperazine是抗精神病药物中属于吩噻嗪类的多巴胺受体D2拮抗剂。
S4257	Alizapride HCl Alizapride在以外消旋混合物服用时，作为多巴胺拮抗剂促肠胃运动和止吐治疗癌症化疗引起的恶心和呕吐。
S4655	Sulpiride Sulpiride是一种多巴胺D2受体拮抗剂。在临床治疗中，它被用作抗抑郁剂、安定药和助消化药。
S1789	Tetrabenazine (Xenazine) Tetrabenazine(Nitoman, Xenazine)主要是一种可逆的、高亲和力的突触前神经元的颗粒小泡吸收单胺的抑制剂，选择性与VMAT-2结合。也能阻止dopamine D2 receptors，但亲和力相对于对VMAT-2的亲和力弱1000倍。
S4219	Azaperone Azaperone 是一种吡啶哌嗪和丁酰苯类抗精神病药，具有镇静和止吐的效果，主要是在兽医上用作镇静剂。它是Dopamine receptors的拮抗剂，能够透过血脑屏障，结合D1和D2受体。
S4289	Metoclopramide HCl Metoclopramide HCl是一种选择性的 dopamine D2 receptor 拮抗剂，用于治疗恶心和呕吐。

产品目录	产品描述	文献引用	实验数据
S5849^New	Cariprazine HCl Cariprazine是一种新型二代抗精神病药物，是偏好于D3受体的dopamine D2/D3 receptor部分激动剂。
S5842^New	Cabergoline Cabergoline是一种长效多巴胺（dopamine）激动剂和催乳激素（prolactin）抑制剂。
S5066^New	Pramipexole dihydrochloride Pramipexole dihydrochloride是非麦角灵类的dopamine激动剂，用于治疗帕金森氏病和多动腿综合征，对D2S受体、D2L受体、D3和D4受体的Ki值分别为3.9 nM, 2.2 nM, 0.5 nM 和5.1 nM。
S1726	Levodopa Levodopa 是多巴胺,，肾上腺素以及去甲肾上腺素的前体，具有抗帕金森病的特性。	PLoS One, 2017, 12(3):e0173240	(A) A focused screening of Aβ generation in response to levodopa, piribedil, bromocriptine or carbidopa at indicated concentrations in SK-N-SH cells. Data are mean ± s.e.m., n = 3-4. p < 0.05; **p < 0.001 versus the control of each group.
S2451	Amantadine HCl Amantadine HCl用于治疗或预防某些病毒引起的呼吸道感染。
S2011	Pramipexole 2HCl Monohydrate Pramipexole 2HCl Monohydrate 是一种部分/全部D2S， D2L， D3， D4受体激动剂，K_i为3.9， 2.2， 0.5， 5.1 nM。
S2460	Pramipexole Pramipexole是部分/全部D2S， D2L， D3， D4受体激动剂，作用于D2S， D2L， D3， D4受体，K_i分别为3.9， 2.2， 0.5和5.1 nM。
S2529	Dopamine HCl Dopamine HCl 是一种广泛存在于各种动物的儿茶酚胺类神经递质，是多巴胺D1-5受体激动剂。
S4000	Pergolide Mesylate Pergolide Mesylate是一种抗震颤麻痹剂，作为dopaminergic（多巴胺能）激动剂。	Sci Rep, 2018, 8(1):11554 Pharm Res, 2011, 28(2):337-63 J Pharm Biomed Anal, 2011, 56(2):173-82
S3664	Flupenthixol dihydrochloride Flupentixol是一种抗精神病安定药物，是D1 and D2多巴胺受体的强效拮抗剂，也是α肾上腺素能受体的拮抗剂。
S4618	Fenoldopam mesylate Fenoldopam是一种选择性的多巴胺受体（dopamine-1 receptor）激动剂，具有利尿特性。它可以通过小动脉的血管舒张降低血压。
S7993	SKF38393 HCl SKF38393 HCl是一种选择性dopamine D1/D5 receptor激动剂。
S4639	Brexpiprazole Brexpiprazole是一种新型的多巴胺受体D2和5-羟色胺1A受体的部分激动剂，同时也是5-羟色胺2A受体和去甲肾上腺素alpha1B、alpha2C受体的拮抗剂。其对D_2L, 5-HT_1A, 5-HT_2A, α_1B受体和 α_2C受体的Ki值分别为 0.3, 0.12, 0.47, 0.17 和 0.59 nM。
S3656	Piribedil Piribedil is a relatively selective dopamine (D2/D3) agonist with moderate antidepressant activity. It also has α2-adrenergic (α2A/α2C) antagonist properties.
S2168	PD128907 HCl PD128907 HCl是一种有效的，选择性的多巴胺D3受体激动剂，EC50为0.64 nM，比作用于多巴胺D2受体的选择性高53倍。
S4274	Rotigotine Rotigotine是一种dopamine receptor的激动剂，用于帕金森氏症和不宁腿综合征的治疗。

产品目录	产品描述	文献引用	实验数据
S4732	MPTP hydrochloride MPTP HCl是一种多巴胺能的神经毒素，能在帕金森动物模型中选择性破坏多巴胺能神经元。
S8097	C-DIM12 C-DIM12是Nurr1的激活剂，刺激膀胱癌细胞和肿瘤中Nurr1所介导的细胞凋亡、抑制胶质细胞中对NF-κB依赖的基因表达。
S3188	(+,-)-Octopamine HCl (+,-)-Octopamine HCl,是一种生命必需的一元胺，结构上与去甲肾上腺素相关, 在无脊椎动物中作为一种神经激素，神经调节物质以及神经递质。

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