Levomefolic acid

作者: 莫小枫 | 来源:发表于2017-11-17 13:32 被阅读0次

"目录号: HY-14782

GPCR/G ProteinNeuronal Signaling-

Adoprazine是5-HT1A受体的完全激动剂和D2/3受体的拮抗剂。

5-HT ReceptorDopamine Receptor

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Clozapine N-oxide-Chlorpromazine hydrochloride-Pimavanserin-Brexpiprazole-Lorcaserin Hydrochloride-Haloperidol-Cabergoline-Scopolamine hydrobromide-Cariprazine hydrochloride-Harmine-Lu AE58054 Hydrochloride-TG6-10-1-L-DOPA-Perphenazine-Aripiprazole-

生物活性

Description

Adoprazine, a potential atypical antipsychotic bearing potent D2 receptor antagonist and 5-HT1A receptor agonist properties.IC50 Value: N/ATarget: Dopamine Receptor; 5-HT ReceptorAdoprazine is a full 5-HT1A receptor agonist and full D2/3 receptor antagonist possessing characteristics of an atypical antipsychotic, representing a potential novel treatment for schizophrenia.

Clinical Trial

NCT00581243

Wyeth is now a wholly owned subsidiary of Pfizer-Solvay Pharmaceuticals

Healthy

January 2008

Phase 1

NCT00620568

Wyeth is now a wholly owned subsidiary of Pfizer-Solvay Pharmaceuticals

Healthy

February 2008

Phase 1

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References

[1].Auclair AL, Kleven MS, Barret-Grévoz C, Barreto M, Newman-Tancredi A, Depoortère R.  Differences among conventional, atypical and novel putative D(2)/5-HT(1A) antipsychotics on catalepsy-associated behaviour in cynomolgus monkeys.  Behav Brain Res. 2009 N

[2].Lange JH, Reinders JH, Tolboom JT, Glennon JC, Coolen HK, Kruse CG.Principal component analysis differentiates the receptor binding profiles of three antipsychotic drug candidates from current antipsychotic drugs.  J Med Chem. 2007 Oct 18;50(21):5103-8.

[3].McCreary AC, Glennon JC, Ashby CR Jr, Meltzer HY, Li Z, Reinders JH, Hesselink MB, Long SK, Herremans AH, van Stuivenberg H, Feenstra RW, Kruse CG.  SLV313 (1-(2,3-dihydro-benzo[1,4]dioxin-5-yl)-4- [5-(4-fluoro-phenyl)-pyridin-3-ylmethyl]-piperazine monoh

[4].Feenstra RW, van den Hoogenband A, Stroomer CN, van Stuivenberg HH, Tulp MT, Long SK, van der Heyden JA, Kruse CG.  SAR study of 1-aryl-4-(phenylarylmethyl)piperazines as ligands for both dopamine D2 and serotonin 5-HT1A receptors showing varying degrees

[5].Cosi C, Carilla-Durand E, Assié MB, Ormiere AM, Maraval M, Leduc N, Newman-Tancredi A.  Partial agonist properties of the antipsychotics SSR181507, aripiprazole and bifeprunox at dopamine D2 receptors: G protein activation and prolactin release.  Eur J Ph

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