Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T74798 | Antipsychotic agent-2 | ||
Antipsychotic agent-2 (Compound 11) 是一种有效的抗精神病剂。Antipsychotic agent-2 对5-HT1A、5-HT2A、5-HT2C、D2和 H1受体具有亲和力,Ki 分别为 56.6、66.7、552、596 和 1140 nM。Antipsychotic agent-2 可以透过血脑屏障。 | |||
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。 | |||
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。 | |||
T10232 |
Acetophenazine dimaleate
|
Dopamine Receptor | GPCR/G Protein; Neuroscience |
Acetophenazine dimaleate 是抗精神病试剂,能够有效治疗焦虑抑郁。 | |||
T19680 |
Zotepine
|
Dopamine Receptor; 5-HT Receptor; Adrenergic Receptor; Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Zotepine 是一种抗精神病剂,是有效的5-HT2A、5-HT2C、组胺H1、α1-肾上腺素能和多巴胺D2受体拮抗剂,Kd 值分别为 2.6、3.2、3.3、7.3 和 8 nM。它在体内表现出抗抑郁和抗焦虑作用。 | |||
T1539 |
Iloperidone
伊潘立酮,HP 873 |
Dopamine Receptor; 5-HT Receptor; Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Iloperidone (HP 873) 是一种D2/5-HT2受体拮抗剂,是非典型抗精神病药,可治疗精神分裂症。 | |||
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。 | |||
T8136 |
Perospirone hydrochloride
Perospirone HCl,盐酸哌罗匹隆,SM-9018 hydrochloride |
Dopamine Receptor; 5-HT Receptor | GPCR/G Protein; Neuroscience |
Perospirone hydrochloride (Perospirone HCl) 是非典型的抗精神病剂,可用于精神分裂症的研究。它是可口服的5-HT2A 受体和多巴胺 D2受体的拮抗剂,也是5-HT1A 受体的部分激动剂。 | |||
T12899L |
SEP-363856 hydrochloride
SEP-856 hydrochloride |
Others; 5-HT Receptor | GPCR/G Protein; Neuroscience; Others |
SEP-363856 hydrochloride (SEP-856 hydrochloride) 是一种口服活性和 CNS 活性的精神药物,具有独特的非 D2/5-HT2A 作用机制,发挥其抗精神病样作用,具有治疗精神分裂症的潜力。 | |||
T1566 |
Aripiprazole
阿立哌唑,OPC-14597 |
5-HT Receptor | GPCR/G Protein; Neuroscience |
Aripiprazole (OPC-14597) 是血清素受体 5-HT1A 和多巴胺 D2 受体的部分激动剂,还用作突触后拮抗剂和血清素受体 5-HT2A 的拮抗剂。 | |||
T0351 |
Risperidone
Risperidal,R 64 766,利培酮 |
Dopamine Receptor; 5-HT Receptor; Adrenergic Receptor; P-gp | GPCR/G Protein; Membrane transporter/Ion channel; Neuroscience |
Risperidone (R 64 766) 是5-HT2受体阻断剂、P-糖蛋白抑制剂和多巴胺 D2受体的拮抗剂,对 5-HT2A 和多巴胺 D2受体的 Ki 值分别为 4.8 和 5.9 nM。 | |||
T23733 |
Amperozide
FG 5606,安哌齐持,Amperozida,Amperozidum |
5-HT Receptor | GPCR/G Protein; Neuroscience |
Amperozide (FG 5606) 是一种非典型抗精神病药,可拮抗5-HT2A 受体。它抑制多巴胺的释放并改变多巴胺能神经元的放电。关于该药物使用的调查主要围绕其治疗人类精神分裂症的能力展开。 | |||
T1951 |
Asenapine Maleate
Org 5222 maleate,Org 5222,马来酸阿塞那平,阿塞那平马来酸盐 |
5-HT Receptor | GPCR/G Protein; Neuroscience |
Asenapine Maleate (Org 5222 maleate) 是5-HT 和D2的拮抗剂,Ki 值分别为 0.03-4.0 nM, 1.3 nM。它也是抗精神病药物,用于治疗与双相 1 型障碍相关的精神分裂症和躁狂或混合发作。 | |||
T1735 |
Lurasidone hydrochloride
Lurasidone HCl,SM-13496 (Hydrochloride),盐酸鲁拉西酮,SM-13496 |
Dopamine Receptor; 5-HT Receptor; Norepinephrine | GPCR/G Protein; Neuroscience |
Lurasidone hydrochloride (Lurasidone HCl) 是多巴胺 D2和5-HT7的拮抗剂,IC50值分别为 1.68 和 0.495 nM,用于治疗精神分裂症和双相情感障碍。它也是5-HT1A 受体的部分激动剂,IC50值为 6.75 nM。 | |||
T2546 |
Pimozide
R6238,匹莫奇特,匹莫齐特 |
Potassium Channel; Dopamine Receptor; Adrenergic Receptor; STAT | GPCR/G Protein; JAK/STAT signaling; Membrane transporter/Ion channel; Neuroscience; Stem Cells |
Pimozide (R6238) 是多巴胺受体拮抗剂,对多巴胺 D1、D2 和 D3 受体的 Ki 值分别为 588、1.4 和 2.5 nM。它也是STAT3和STAT5的抑制剂,对 α1 肾上腺素受体也有较高亲和性,Ki 值为 39 nM。 | |||
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。 | |||
T24399 |
Lenperone HCl
|
||
Lenperone HCl is a dopamine antagonist and an antipsychotic agent. | |||
T25432 |
Fluspiperone
NSC 354855,NSC354855,NSC-354855,R-28930,R 28930 |
||
Fluspiperone is an antipsychotic agent. | |||
T31830 |
Flutroline
CP-36,584,Flutrolinum,CP36,584,Flutrolino |
||
Flutroline is a gamma-carboline antipsychotic agent. | |||
T29004 | Trebenzomine | ||
Trebenzomine is apsychotropic agent with potential as an antidepressant and an antipsychotic. | |||
T10290 |
Alpertine
Win 31665 |
Others | Others |
Alpertine is an antipsychotic agent. | |||
T28719 |
Sch 40853
Sch-40853,Sch40853 |
||
Sch 40853 is an active metabolite of a benzonaphthazepine antipsychotic agent. | |||
T28514 |
Remoxipride
|
||
Remoxipride is an antipsychotic agent. Remoxipride is specific for dopamine D2 receptors. | |||
T11753 |
Keto Ziprasidone
|
Potassium Channel | Membrane transporter/Ion channel |
Ziprasidone, an antipsychotic agent, functions as a dual antagonist of 5-HT (serotonin) and dopamine receptors. Keto Ziprasidone represents an impurity found within Ziprasidone. | |||
T70263 | U 101958 | ||
U 101958 is a putative antipsychotic agent It is also a highly selective dopamine D4 receptor antagonist. | |||
T30753 |
Carphenazine Dimaleate
Procethazine dimaleate,Proketazine maleate,Proketazine,carphenazine maleate,Proketazine dimaleate |
||
Carphenazine is used for the treatment of chronic schizophrenia, which is an antipsychotic agent. | |||
T25181 |
Bromperidol decanoate
R46541,R-46541,R 46541 |
||
Bromperidol decanoate is an antipsychotic agent that is utilized for long-term maintenance treatment for schizophrenia. | |||
T0068L |
Fluphenazine Decanoate Dihydrochloride
|
||
Fluphenazine Decanoate Dihydrochloride is an antipsychotic agent, it could block postsynaptic dopamine D2 receptors in the limbic, cortical system and basal ganglia. | |||
T60944 |
(±)-Levomepromazine
|
||
(±)-Levomepromazine 是 Levomepromazine 的外消旋体, Levomepromazine 是具有口服活性的典型抗精神病剂。 | |||
T21669 | Haloperidol hydrochloride | ||
Haloperidol hydrochloride 是一种有效的 dopamine D2 receptor 拮抗剂,广泛用作抗精神病药 | |||
T63592 |
Thiothixene hydrochloride
|
||
Thiothixene hydrochloride 是抗精神病剂,能够用于研究精神分裂症和双相性躁狂症。 | |||
T28845 |
SR142948A HCl
SR142948A,SR 142948A,SR-142948A,SR142948A hydrochloride |
||
SR 142948A is a non-peptide antagonist of neurotensin receptor. SR 142948A affects the expression of c-Fos and has properties of antipsychotic agent. SR 142948A blocks hypothermia and analgesia induced by neurotensin. It blocks the increase in the concent | |||
T11586 |
Hydroxy ziprasidone
|
Others | Others |
Hydroxy ziprasidone is an impurity of Ziprasidone. Ziprasidone, an antipsychotic agent, is a 5-HT and dopamine receptor antagonist. | |||
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. | |||
T12899 |
SEP-363856
SEP-856 |
Others | Others |
SEP-363856 是一种口服活性和 CNS 活性的精神药物,具有独特的非 D2/5-HT2A 作用机制,发挥其抗精神病样作用,具有治疗精神分裂症的潜力。 | |||
T62840 |
Bromperidol hydrochloride
|
||
Bromperidol hydrochloride (R-11333 hydrochloride) 具有抗精神病作用,能够较好的亲和中枢多巴胺受体 D2 (dopamine receptors D2)。Bromperidol hydrochloride 与 Spectinomycin 能够协同杀灭分枝杆菌 (mycobacteria)。 | |||
T10681 |
Cariprazine D6
RGH-188 D6 |
Dopamine Receptor | GPCR/G Protein; Neuroscience |
Cariprazine D6 (RGH-188 D6) is a deuterium-labeled Cariprazine. Cariprazine is an antipsychotic agent (D3 receptors, Ki: 0.085 nM; D2 receptors, Ki: 0.49 nM). | |||
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 ... | |||
T22044 |
BGC 20-761
|
||
BGC20-761 是一种选择性的5-HT6和多巴胺受体 (dopamine receptor) 拮抗剂,对人 5-HT6,5-HT2A,D2 受体的Ki 值分别为 20,69,和 140 nM。BGC20-761 可增强长期记忆。BGC20-761 具有作为抗精神病药物的潜在效用。 |