36
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Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T25487 |
Haloperidol decanoate
KD 16,KD-136,KD 136,Neoperidole,Haldol |
Others | Others |
Haloperidol decanoate (KD 16) 是一种典型的抗精神病药物,用作精神分裂症和情绪障碍的维持治疗,配制成用于肌肉注射的酯。 | |||
T5858 |
Sertindole
Lu 23-174,舍吲哚 |
Dopamine Receptor; 5-HT Receptor; Adrenergic Receptor; Autophagy | Autophagy; GPCR/G Protein; Neuroscience |
Sertindole (Lu 23-174) 是一种非典型抗精神病药,可与多巴胺 D2 受体和血清素受体亚型 5-HT1D、5-HT2A 和 5-HT2C 结合,Kd 值分别为 2.7、20、0.14 和 6 nM。 | |||
T28231 |
Olanzapine N-Oxide
|
Others | Others |
Olanzapine N-Oxide 是 Olanzapine 的代谢产物,Olanzapine 具有抗精神病活性。 | |||
T13620 |
Clothixamide
Clotixamide |
Others | Others |
Clothixamide(Clotixamide) 是一种噻吨类衍生物,具有抗精神失常活性。 | |||
T10989 |
Dehydroaripiprazole
OPC-14857,DM-14857 |
5-HT Receptor | GPCR/G Protein; Neuroscience |
Dehydroaripiprazole (DM-14857) 是 Aripiprazole 的活性代谢产物,具有抗精神病活性。Aripiprazole 是也一种抗精神病药。 | |||
T1740 |
BD-1047 dihydrobromide
BD1047.2HBr |
Sigma receptor | GPCR/G Protein |
BD-1047 dihydrobromide (BD1047.2HBr) 是一种选择性的 sigma-1 receptor 受体拮抗剂,在预测精神分裂症疗效的动物模型中具有抗精神病活性。 | |||
T28267 |
ORM-10921
ORM10921,ORM 10921 |
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
ORM-10921 是一种 α2C-肾上腺素受体拮抗剂,在动物实验中显示出抗精神病和抗抑郁活性。 | |||
T0031 |
Ziprasidone hydrochloride monohydrate
齐拉西酮盐酸盐一水合物,盐酸齐拉西酮水合物,CP 88059 |
Dopamine Receptor; 5-HT Receptor; Adrenergic Receptor; Norepinephrine; Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Ziprasidone hydrochloride monohydrate (CP 88059) 是一种联合 5-HT(5-羟色胺)和多巴胺受体拮抗剂,具有抗精神病活性的强效作用。它也是去甲肾上腺素再摄取抑制剂。 | |||
T20797 |
NE-100 hydrochloride
NE100 Hydrochloride,NE 100 HCl,NE 100 Hydrochloride,NE-100 Hydrochloride,NE-100 HCl |
Sigma receptor | GPCR/G Protein |
NE-100 hydrochloride (NE-100 HCl) 是选择性sigma-1 受体拮抗剂,IC50为 4.16 nM。它在体内具有抗精神病活性。它也能抑制内质网应激诱导的海马细胞死亡。 | |||
T0031L |
Ziprasidone hydrochloride
盐酸齐拉西酮,齐拉西酮盐酸盐,CP-88059 hydrochloride,CP-88059,Ziprasidone HCl |
Dopamine Receptor; 5-HT Receptor; Adrenergic Receptor; Norepinephrine; Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Ziprasidone hydrochloride (CP-88059 hydrochloride) 是一种联合 5-HT(5-羟色胺)和多巴胺受体拮抗剂,具有抗精神病活性的强效作用。它也是去甲肾上腺素再摄取抑制剂。 | |||
T68047 |
Clopipazan
|
Others | Others |
Clopipazan 是一种抗精神病和抗抑郁病化合物。Clopipazan 具有镇静和抗焦虑活性,可能由于选择性阻断某些中间神经元的GABergic发挥作用。 | |||
T23854 |
Carbidine
Carbidine dihydrochloride,Karbidin,Carbidin,Karbidine |
Others | Others |
Carbidine (Carbidin) 是γ-carboline 的衍生物,一种非典型的抗精神病药物。它可以在体内和体外降低DA 对伏隔核突触体释放3H-DA 和酪氨酸羟化酶活性的抑制作用。 | |||
T24885L |
Tiaspirone hydrochloride
BMY-13859 hydrochloride,Tiaspirone hydrochloride(87691-91-6 Free base) |
Dopamine Receptor; 5-HT Receptor | GPCR/G Protein; Neuroscience |
Tiaspirone hydrochloride (BMY-13859 hydrochloride) 具有抗精神病活性。 Tiaspirone hydrochloride 影响大鼠大脑黑质致密带(A9 DA 细胞)和腹侧被盖区(A10 DA 细胞)多巴胺能神经元的电生理活性。 | |||
T39211 | PD 144418 oxalate | Sigma receptor | GPCR/G Protein |
PD 144418 oxalate is a highly potent and selective sigma 1 (σ1) receptor ligand, displaying a Ki value of 0.08 nM for σ1 and 1377 nM for σ2. It exhibits negligible affinity for other receptors, ion channels, and enzymes. Additionally, PD 144418 oxalate demonstrates potential antipsychotic activity. | |||
T0766 |
Promazine hydrochloride
Romtiazin hydrochloride,Sinophenin hydrochloride,盐酸丙嗪 |
Dopamine Receptor; 5-HT Receptor; Adrenergic Receptor; AChR | GPCR/G Protein; Neuroscience |
Promazine hydrochloride (Romtiazin hydrochloride) 是一种抗精神病药,也是一种多巴胺受体 (D2) 拮抗剂,能够抑制多巴胺能神经传递。 | |||
T0031L2 |
Ziprasidone
齐拉西酮,Geodon,Zeldox,CP-88059 |
Dopamine Receptor; 5-HT Receptor; Adrenergic Receptor; Norepinephrine; Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Ziprasidone (Geodon) 是一种联合的 5-HT(5-羟色胺)和多巴胺受体拮抗剂,具有强大的抗精神病活性。它是去甲肾上腺素再摄取抑制剂,对大鼠和人的5-HT1A,5-HT2A 和多巴胺 D2 受体有很高的亲和力。 | |||
T23318L |
SB 258585
|
5-HT Receptor | GPCR/G Protein; Neuroscience |
SB 258585 是一种选择性 5-HT6受体拮抗剂。SB 258585 对人重组5-HT6受体的细胞系中的单个受体群体亲和力很高。SB 258585 可用于标记重组和天然5-HT6受体,可用于检测认知增强和抗精神病活性。 | |||
T0455 |
Clozapine
氯氮平,HF 1854,LX 100-129 |
Dopamine Receptor; Adrenergic Receptor; AChR | GPCR/G Protein; Neuroscience |
Clozapine (HF 1854) 是一种三环二苯二氮卓类药物,属于非典型抗精神病药物。它结合几种类型的中枢神经系统受体,并显示出独特的药理学特征。 它是一种血清素拮抗剂,与 5-HT 2A/2C 受体亚型具有强结合力。它还对几种多巴胺能受体表现出很强的亲和力,但对多巴胺 D2 受体仅表现出较弱的拮抗作用,这种受体通常被认为可调节精神抑制活性。 | |||
T11435 | GlyT1 Inhibitor 1 | Others | Others |
GlyT1 Inhibitor 1 is a potent and selective GlyT1 inhibitor (IC50: 38 nM for rGlyT1) with antipsychotic activity. | |||
T21368 |
Thioproperazine
Megeptil,Sulfenazin,Cephalmin,Majeptyl,Vontil,Mazeptyl |
||
Thioproperazine is a drug with the activity of antipsychotic. | |||
T29009 |
Trifluoperazine N-Glucuronide
|
||
Trifluoperazine N-Glucuronide is a metabolite of Trifluoperazine with antidepressant and antipsychotic activity. | |||
T26909 |
Bromerguride
|
||
Bromerguride is a dopamine antagonist with the activity of antipsychotic. | |||
T35307 |
Zicronapine
Lu-31130,Lu31-130,Lu 31130,Lu 31-130,Lu31130,Lu-31-130 |
||
Zicronapine( LU 31-130) is an atypical antipsychotic. Zicronapine has monoaminergic activity and multi-receptor properties. It has shown effective antagonism against dopamine D1, D2, and serotonin 5HT2A receptors in vitro and in vivo. | |||
T16445 | PD 144418 | Sigma receptor | GPCR/G Protein |
PD 144418 displays potential antipsychotic activity. PD 144418 is a high affinity, potent and selective sigma 1 (σ1) receptor ligand (Ki: 0.08 nM and 1377 nM for σ1 and σ2 respectively). It shows devoid of any significant affinity for other receptors, ion channels, and enzymes. | |||
T13400 |
Ziprasidone D8
CP-88059 D8 |
Others | Others |
Ziprasidone D8 is deuterium labeled Ziprasidone, which is a antagonist of combined 5-HT (serotonin) and dopamine receptor and exhibits potent effects of antipsychotic activity. | |||
T39010 |
Xanomeline tartrate
LY 246708 tartrate,Xanomeline tartrate |
||
Xanomeline (LY 246708), a potent agonist of muscarinic M1/M4 receptors, exhibits antipsychotic-like activity and enhances neuronal excitability. It is a valuable compound for studying schizophrenia. | |||
T15026 |
Cyamemazine
|
5-HT Receptor | GPCR/G Protein; Neuroscience |
Cyamemazine, contains the phenothiazine chromophore, is a neuroleptic agent used as an anxiolytic. Cyamemazine is a potent 5-HT3 (Ki: 12 nM), 5-HT2A (Ki: 1.5 nM) and 5-HT2C (Ki: 75 nM) receptors antagonist with antipsychotic activity. | |||
T78514 |
Timiperone
|
Dopamine Receptor | GPCR/G Protein; Neuroscience |
Timiperone对大脑多巴胺D2受体显示出高亲和力,具备抗精神病效果,能有效抑制刻板行为。该化合物在精神分裂症研究中可被广泛应用。 | |||
T73961 | Ziprasidone amino acid | ||
Ziprasidone amino acid (Ziprasidone Impurity C) 是 Ziprasidone 的杂质。Ziprasidone 是5-HT 和多巴胺 (dopamine receptor) 受体拮抗剂,具有抗精神病活性。 | |||
T81336 |
PZ-1190
|
Dopamine Receptor | GPCR/G Protein; Neuroscience |
PZ-1190是一种多靶点配体,针对啮齿动物的serotonin和dopamine受体,展现出潜在的抗精神病活性。 | |||
T62082 |
FPPQ
|
||
FPPQ 是一种 5-HT3 和 5-HT6 受体的双重拮抗剂,他们的 Ki 值分别为 0.9 nM 和 3 nM,表现出抗精神病和促认知活性。 | |||
T79802 |
5-HT2C agonist-3
|
5-HT Receptor | GPCR/G Protein; Neuroscience |
5-HT2C agonist-3 ((+)-19)为高选择性5-HT2C激动剂,其EC50为24 nM,Ki值为78 nM。该化合物表现出抗精神病药物样的活性,并能有效抑制安非他明诱导的多动症。 | |||
T38221 |
N,N-Dipropyldopamine (hydrobromide)
|
||
N,N-Dipropyldopamine is a dopamine receptor agonist.1,2,3 It decreases dihydrophenylalanine (DOPA) levels in the limbic forebrain and striatum of reserpinized rats (ED50s = 25 and 20 μmol/kg, respectively), as well as reduces homovanillic acid levels in rat striatum when administered at a dose of 80 μmol/kg.1 N,N-Dipropyldopamine (0.5-16 mg/kg) reduces spontaneous locomotor activity in mice, an effect that can be reversed by the antipsychotic spiroperidol.2,3 | |||
T69129 |
Clozapine HCl
|
||
Clozapine HCl is a tricylic dibenzodiazepine, classified as an atypical antipsychotic agent. It binds several types of central nervous system receptors, and displays a unique pharmacological profile. Clozapine is a serotonin antagonist, with strong binding to 5-HT 2A/2C receptor subtype. It also displays strong affinity to several dopaminergic receptors, but shows only weak antagonism at the dopamine D2 receptor, a receptor commonly thought to modulate neuroleptic activity. Agranulocytosis is a ... | |||
T79803 |
5-HT2C agonist-3 free base
|
5-HT Receptor | GPCR/G Protein; Neuroscience |
5-HT2C agonist-3 ((+)-19) free base 是选择性的5-HT2C激动剂,具EC50: 24 nM及Ki: 78 nM值。该化合物展现出抗精神病药物样活性,并能阻断安非他明引起的多动症。 | |||
T61915 |
Thiethylperazine
|
||
Thiethylperazine 是一种吩噻嗪衍生物。Thiethylperazine 是具有口服活性的组胺H1受体和多巴胺D2受体拮抗剂。Thiethylperazine 也是选择性的ABCC1激活剂,可减少小鼠中的淀粉样 β (Aβ) 负荷。Thiethylperazine 具有抗精神病,止吐和抗菌作用。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T21855 |
AMI-193
Espiramida,螺拉米特,Spiramide |
Dopamine Receptor; 5-HT Receptor | GPCR/G Protein; Neuroscience |
AMI-193 (Spiramide) 是一种有效和选择性的 5-HT2 和 D2 受体,对 5-HT2、D2 受体、5-HT1A、D1 受体和 5-HT1C 受体的 Kis 分别为 2、3、50、2530 和 4300 nM。 AMI-193 显示出抗精神病活性。 | |||
TN2267 |
Tetrahydroalstonine
|
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Tetrahydroalstonine 是从 Rhazya stricta 的果实中提取出来的吲哚类生物碱,是一种具有选择性的 α2-肾上腺素受体拮抗剂。Tetrahydroalstonine 在Rauwolfia tetraphylla 中表现出抗精神病活性。 |