SML1528

伊潘立酮(Iloperidone)

≥98% (HPLC)

• 别名: 1-[4-[3-[4-(6-Fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]propoxy]-3-methoxyphenyl]ethanone, Zomaril
• 经验公式（希尔记法）: C₂₄H₂₇FN₂O₄
• CAS号: 133454-47-4
• 分子量: 426.48
• MDL號碼: MFCD00866688
• 分類程式碼代碼: 12352200
• PubChem物質ID: 329825945
• NACRES: NA.77

属性

• 品質等級: 100
• 化驗: ≥98% (HPLC)
• 形狀: powder
• 顏色: white to beige
• 溶解度: DMSO: 5 mg/mL, clear
• 儲存溫度: −20°C
• InChI: 1S/C24H27FN2O4/c1-16(28)18-4-7-21(23(14-18)29-2)30-13-3-10-27-11-8-17(9-12-27)24-20-6-5-19(25)15-22(20)31-26-24/h4-7,14-15,17H,3,8-13H2,1-2H3
• InChI 密鑰: XMXHEBAFVSFQEX-UHFFFAOYSA-N
• 基因資訊: human ... DRD2(1813) , HTR2A(3356)

说明

生化／生理作用

Iloperidone is an atypical antipsychotic, a combined dopamine (D2) and serotonin (5HT2) receptor antagonist. Iloperidone targets a selective set of dopamine, serotonin and also norepinephrine receptor subtypes. Like similar atypical antipsychotics, Iloperidone has higher affinity for the 5-HT2A receptor (Ki < 10 nM) than for the D2 receptor (Ki = 10–100) nM). Iloperidone has high affinity for dopamine D3 (Ki < 10 nM) and lower affinity for other serotonin or dopamine subtypes. Unlike most atypical antipsychotics, Iloperidone also has high affinity for norepinephrine alpha1 receptors (Ki < 10 nM) which may contribute to the drug′s efficacy on mood and cognition.

安全信息

• 象形圖: GHS06
• 訊號詞: Danger
• 危險聲明: H301,H413
• 防範說明: P264 - P270 - P273 - P301 + P310 - P405 - P501
• 危險分類: Acute Tox. 3 Oral - Aquatic Chronic 4
• 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