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P0099

Sigma-Aldrich

帕潘立酮

≥98% (HPLC)

同義詞:

3-[2-[4-（6-氟-1,2-苯并异恶唑-3-基）-1-哌啶基] 乙基]-6,7,8,9-四氢-9-羟基-2-甲基-4H-吡啶并 [1,2-a] 嘧啶-4-酮, 9-羟基利培酮

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About This Item

經驗公式（希爾表示法）:
C23H27FN4O3
CAS號碼:
144598-75-4
分子量：:
426.48
MDL號碼:
MFCD00871802
分類程式碼代碼:
12352200
PubChem物質ID:
329820012
NACRES:
NA.77

品質等級

100

化驗

≥98% (HPLC)

形狀

powder

顏色

white to brown

溶解度

DMSO: 2 mg/mL, clear (warmed)

起源

Johnson & Johnson

儲存溫度

room temp

SMILES 字串

CC1=C(CCN2CCC(CC2)c3noc4cc(F)ccc34)C(=O)N5CCCC(O)C5=N1

InChI

1S/C23H27FN4O3/c1-14-17(23(30)28-9-2-3-19(29)22(28)25-14)8-12-27-10-6-15(7-11-27)21-18-5-4-16(24)13-20(18)31-26-21/h4-5,13,15,19,29H,2-3,6-12H2,1H3

InChI 密鑰

PMXMIIMHBWHSKN-UHFFFAOYSA-N

基因資訊

human ... DRD2(1813) , HTR2A(3356)

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應用

帕潘立酮已被用作非典型抗精神病药（AAPD），用于研究其预防脂多糖（LPS）激发的产前免疫小鼠精神疾病的功效。它还被用作非典型抗精神病药（AAPD），用于诠释以细菌内毒素脂多糖（LPS）处理的雌性产前小鼠中下丘脑-垂体-肾上腺（HPA）轴的调节。

生化／生理作用

帕利哌酮属于非典型抗精神病药；利培酮的活性代谢产物。

特點和優勢

《受体分类和信号转导》手册的多巴胺受体页有该化合物的介绍。想要浏览手册的其他页面， 请单击此处。
该化合物由 强生开发。如需浏览其他制药公司开发的化合物和批准的药物/候选药物列表，请点击此处。

象形圖

Skull and crossbones
GHS06

訊號詞

Danger

危險聲明

H301

危險分類

Acute Tox. 3 Oral

儲存類別代碼

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

水污染物質分類（WGK）

WGK 3

閃點（°F）

Not applicable

閃點（°C）

Not applicable

個人防護裝備

Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges

分析證明 (COA)

輸入產品批次/批號來搜索 分析證明 (COA)。在產品’s標籤上找到批次和批號，寫有 ‘Lot’或‘Batch’.。

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您可以在文件庫中找到最近購買的產品相關文件。

存取文件庫

Mehrul Hasnain et al.
CNS drugs, 28(10), 887-920 (2014-08-30)
We comprehensively reviewed published literature to determine whether it supported the link between corrected QT (QTc) interval prolongation and torsade de pointes (TdP) for the 11 second-generation antipsychotics and seven second-generation antidepressants commonly implicated in these complications. Using PubMed and
Umesh Kumar et al.
European journal of pharmacology, 747, 181-189 (2014-09-23)
Studies on animal models provide enough evidences that old age appearance of psychosis on exposures to various insults during critical period of brain development could be prevented by antipsychotic drug treatment. Presently, gestational intervention of the atypical antipsychotic paliperidone (PAL)
Eliyahu Dremencov et al.
Psychopharmacology, 194(1), 63-72 (2007-05-29)
Paliperidone (9-OH-risperidone) is the main metabolite of the atypical antipsychotic risperidone. While both drugs are potent dopamine (D)2 antagonists, they have quantitative differential affinities for serotonin (5-HT) and norepinephrine (NE) receptor binding sites. The present study aimed to determine if
Richard Newton et al.
Current medical research and opinion, 28(4), 559-567 (2012-02-11)
Paliperidone palmitate is an atypical long-acting injectable (LAI) antipsychotic that has been approved for use in the US, EU, Australia and numerous other countries for acute and maintenance therapy of schizophrenia. LAI antipsychotics are often viewed as a 'last-resort' treatment
Saeko Ikai et al.
The Journal of clinical psychiatry, 73(8), 1147-1152 (2012-09-13)
While 65%-80% occupancy of dopamine D2 receptors with antipsychotics has been proposed to achieve optimal therapeutic response during acute treatment of schizophrenia, it remains unclear as to whether it is also necessary to maintain D2 receptor occupancy within this "safe"
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