ホーム 計算ツール
代理店ログイン

検索結果

Search Results for " Fluphenazine "

ターゲット

9

阻害剤

カタログ番号 製品名 別名 ターゲット
T0068 Fluphenazine dihydrochloride Prolixin,Fluphenazine hydrochloride Dopamine Receptor
Fluphenazine dihydrochloride (Prolixin) is an inhibitor of phenothiazine-class D1DR and D2DR; In studies, Fluphenazine can be used to probe the effects and metabolic process of this commonly used dopamine antagonist.
T7943 Fluphenazine decanoate Dopamine Receptor
Fluphenazine decanoate is dopamine D2 receptor blocke,and is a long-acting phenothiazine neuroleptic that used to treat schizophrenia.
T0068L2 Fluphenazine free base Siqualine,Fluphenazine,Fluorophenazine,Fluorphenazine,Triflumethazine,Fluorfenazine
Flufenazine is an antipsychotic drug. It is used to treat chronic mental illnesses such as schizophrenia. Flufenazine works by blocking postsynaptic dopamine D2 receptors in the limbic system, cortical system, and basal ...
T11304 Fluphenazine enanthate Others
Fluphenazine enanthate is a novel long-acting injectable (LAI) antipsychotic compound specifically designed for the treatment of 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.
T36820 Fluphenazine-N-2-chloroethane (hydrochloride)
Fluphenazine is a traditional antipsychotic compound that tightly binds the dopamine D2 receptor (Ki = 0.55 nM) and also reversibly inhibits calmodulin at micromolar concentrations. Fluphenazine-N-2-chloroethane is a der...
TMIH-0241 Fluphenazine-d8 Dihydrochloride
Fluphenazine-d8 Dihydrochloride is a deuterated compound of Fluphenazine Dihydrochloride. Fluphenazine Dihydrochloride has a CAS number of 146-56-5. Fluphenazine dihydrochloride is an inhibitor of phenothiazine-class D1D...
T37150 ADTN hydrobromide
ADTN hydrobromide (6,7-ADTN) is a dopamine receptor agonist (EC50s = 3.5 and 0.65 μM in rat striatal and nucleus accumbens homogenates, respectively). ADTN hydrobromide stimulates production of cAMP in rat striatal homog...
T36805 TPC2-A1-N TPC2-A1-N
TPC2-A1-N is a novel, lipophilic, membrane permeable isoform-selective small molecule agonist of two-pore channel 2 (TPC2). TPC2-A1-N plays its role by mimicking the physiological actions of NAADP and PI(3,5)P2 through i...