Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T8452 |
Dantrolene
|
Others | Others |
Dantrolene 是一种肌肉松弛剂,是人红细胞谷胱甘肽还原酶的非竞争性抑制剂,其Ki 和IC50值分别为 111.6 μM 和 52.3 μM。它是兰尼碱受体拮抗剂及Ca2+信号稳定剂。它可用于研究恶性高热、亨廷顿病、肌肉痉挛和其他神经阻滞剂恶性综合征。 | |||
T3086 |
Mesoridazine Besylate
Mesoridazine benzenesulfonate,Serentil,苯磺酸美索达嗪 |
Dopamine Receptor; 5-HT Receptor | GPCR/G Protein; Neuroscience |
Mesoridazine Besylate (Serentil) 是一种哌啶类精神安定药,属于称为吩噻嗪类的药物,用于治疗精神分裂症。它是硫利达嗪的代谢物。 | |||
T7943 |
Fluphenazine decanoate
|
Dopamine Receptor | GPCR/G Protein; Neuroscience |
Fluphenazine decanoate 是一种高度连续的多巴胺 D2受体阻滞剂,是一种长效吩噻嗪抗精神病药,用于精神分裂症的研究。 | |||
T1478 |
Ondansetron hydrochloride dihydrate
盐酸昂丹司琼,SN 307,NSC 665799,GR 38032,Ondansetron hydrochloride |
5-HT Receptor | GPCR/G Protein; Neuroscience |
Ondansetron hydrochloride dihydrate (GR 38032) 是5- HT3受体拮抗剂,可治疗化疗后的恶心和呕吐,有抗焦虑和抗精神病作用。 | |||
T83648 |
Tenilapine
|
Others | Others |
Tenilapine 是一种神经安定化合物,可用于研究非典型抗精神病。 | |||
T11121 |
Duoperone
|
Others | Others |
Duoperone 是一种抗精神病药。Duoperone 在动物模型中显示出止吐活性。 | |||
T7561 |
Benzetimide hydrochloride
盐酸苄替米特,R4929 |
AChR | Neuroscience |
Benzetimide hydrochloride (R4929) 是毒蕈碱乙酰胆碱受体的拮抗剂,用于治疗神经安定药引起的帕金森症。 | |||
T6398 |
Azaperone
R-1929,Fluoperidol,阿扎哌隆,Stresnil,NSC 170976,Suicalm |
Others; Dopamine Receptor | GPCR/G Protein; Neuroscience; Others |
Azaperone (Fluoperidol) 是多巴胺拮抗剂,具有一些抗组胺和抗胆碱特性,具有止吐活性。 | |||
T14830 |
Bromperidol
溴哌利多,R-11333 |
5-HT Receptor | GPCR/G Protein; Neuroscience |
Bromperidol (R-11333) 是一种苯丁酮衍生物,是一种强效长效精神安定药。它被用作治疗精神分裂症的抗精神病药。 | |||
T0025 |
Haloperidol
Aloperidin,氟哌啶醇,Serenace,Haldol |
Dopamine Receptor; 5-HT Receptor | GPCR/G Protein; Neuroscience |
Haloperidol (Serenace) 是一种安定药,是一种dopamine D2 receptor 拮抗剂。 | |||
T67811 |
Tefludazine
|
||
Tefludazine 一种具有苯茚酮结构的新型神经抑制剂, 是一种具有良好口服活性且与多巴胺和5-羟色胺受体有拮抗作用的化合物。Tefludazine 在小鼠、大鼠和狗的体外和体内测试模型中表现出强大的多巴胺(DA)拮抗活性。Tefludazine 是一种用来治疗精神类疾病的潜在化合物。 | |||
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。 | |||
T35315 |
Zoloperone
Zoloperonum,LR511,LR 511,LR-511 |
||
Zoloperone is a neuroleptic. | |||
T34169 | Prothipendyl | ||
Prothipendyl is a neuroleptic azaphenothiazine. | |||
T34731 |
SU 23397
SU-23397,SU23397 |
||
SU 23397 is a structurally unique neuroleptic agent. | |||
T26360L |
Benperidol Hydrochloride
|
||
Benperidol Hydrochloride is a potent D2/D4 dopamine receptor antagonist, used as antipsychotic and neuroleptic. | |||
T0445L1 |
Promethazine hibenzate
D-08768,D08768,D 08768 |
||
Promethazine is a neuroleptic medication and first-generation antihistamine of the phenothiazine family. | |||
T71926 |
Melperone hydrochloride
|
||
Melperone hydrochloride is a butyrophenone neuroleptic and an inhibitor of the CYP2D6 catalyzed O-demethylation of venlafaxine. | |||
T15104 |
Dexetimide
(+)-Benzetimide,Dexbenzetimide,(S)-(+)-Dexetimide |
Others | Others |
Dexetimide ((+)-Benzetimide) is a high-affinity antagonist of the muscarinic receptor. It is a persistent anticholinergic agent and can be used to treat neuroleptic-induced parkinsonism. | |||
T34061 |
Picobenzide
M 14012-4,MA 14012 |
||
Picobenzide, also known as M-14012-4, is a neuroleptic agent, | |||
T15743 |
Levomepromazine
Methotrimeprazine |
Others | Others |
Methotrimeprazine is an orally available neuroleptic agent. It is commonly used to relieve nausea and vomiting in palliative care settings. Levomepromazine has antagonist actions at multiple neurotransmitter receptor sites, including cholinergic, dopamine | |||
T26472 |
A23887
A-23887,A 23887 |
||
A23887 is a potentially neuroleptic tetracyclic spiro amine that has affinity for dopamine D-2 receptors. | |||
T69825 |
Dexetimide HCl
|
||
Dexetimide HCl is a muscarinic antagonist that has been used to treat neuroleptic-induced parkinsonism. Benzetimide is the (-)-enantimorph of dexetimide. | |||
T70425 | Amiperone | ||
Amiperone is a neuroleptic drug. It prolonged the latency and reduced the frequency of the noise escape response rate in rats. It also inhibited lever-press response and reduced the shock-avoidance rate at very low dose levels in rats. | |||
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. | |||
T78535 |
trans-Clopenthixol dihydrochloride
(E)-Clopenthixol dihydrochloride |
Parasite | Microbiology/Virology |
trans-Clopenthixol ((E)-Clopenthixol) diHCl为一种抗生素,具备抗菌性质但不具有镇静效果。该化合物能够用于抑制体外铜绿假单胞菌与恶性疟原虫。 | |||
T61006 | Tropatepine | ||
Tropatepine 是具有口服活性的抗胆碱能毒蕈碱拮抗剂。Tropatepine 是一种抗帕金森病的药物,可用于研究由抗精神病药物所引起的锥体外系综合征。 | |||
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 ... | |||
T60943 |
Tiapride
|
||
Tiapride 是一种非典型的抗精神病剂,不会引起强直性昏厥和镇静。Tiapride 是多巴胺 D2受体的选择性拮抗剂,其对 D1;D2;D3;D4 受体的 IC50值分别为 1440、45.8、>100 和 11.7 μM。 |