Iloperidone
CAS No. 133454-47-4
Iloperidone ( HP-873 )
产品货号. M11335 CAS No. 133454-47-4
一种非典型抗精神病药,对血清素 5HT2A (Ki = 5.6 nM)、多巴胺 D2 (Ki = 6.3 nM) 和 D3 (Ki = 7.1 nM) 以及去甲肾上腺素 α1 受体 (Ki = 0.36 nM) 具有高亲和力。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 5MG | ¥145 | 有现货 |
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| 10MG | ¥188 | 有现货 |
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| 25MG | ¥296 | 有现货 |
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| 50MG | ¥421 | 有现货 |
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| 100MG | ¥590 | 有现货 |
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| 500MG | ¥1422 | 有现货 |
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| 1G | 获取报价 | 有现货 |
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| 1 mL x 10 mM in DMSO | ¥163 | 有现货 |
|
生物学信息
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产品名称Iloperidone
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注意事项本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
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产品简述一种非典型抗精神病药,对血清素 5HT2A (Ki = 5.6 nM)、多巴胺 D2 (Ki = 6.3 nM) 和 D3 (Ki = 7.1 nM) 以及去甲肾上腺素 α1 受体 (Ki = 0.36 nM) 具有高亲和力。
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产品描述An atypical antipsychotic that exhibits high affinity to serotonin 5HT2A (Ki =5.6 nM), dopamine D2 (Ki=6.3 nM) and D3 (Ki=7.1 nM) and noradrenaline α1 receptors (Ki=0.36 nM), moderate affinity for D4 (25 nM), 5HT6 (43 nM), 5HT7 (22 nM), and low affinity for 5HT1A (168 nM), D1 and histamine H1 receptors; is used for the treatment of schizophrenia.Schizophrenia Approved(In Vitro):Iloperidone displays higher affinity for the dopamine D3 receptor (Ki=7.1 nM) than for the dopamine D4 receptor (Ki=25 nM). Iloperidone displays high affinity for the 5-HT6 and 5-HT7 receptors (Ki=42.7 and 21.6 nM, respectively), and is found to have higher affinity for the 5-HT2A (Ki=5.6 nM) than for the 5-HT2C receptor (Ki=42.8 nM).(In Vivo):Iloperidone is eliminated slowly, with a mean t1/2 of 13.5 to 14.0 hours. Coadministration with food did not significantly affect AUC, tmax, or Cmax. These results indicate that the rate of iloperidone's absorption is decreased, but the overall bioavailability is unchanged, when the drug is taken with food. Orthostatic hypotension, dizziness, and somnolence were the most commonly reported adverse events.
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体外实验Iloperidone displays higher affinity for the dopamine D3 receptor (Ki=7.1 nM) than for the dopamine D4 receptor (Ki=25 nM). Iloperidone displays high affinity for the 5-HT6 and 5-HT7 receptors (Ki=42.7 and 21.6 nM, respectively), and is found to have higher affinity for the 5-HT2A (Ki=5.6 nM) than for the 5-HT2C receptor (Ki=42.8 nM).
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体内实验Iloperidone is eliminated slowly, with a mean t1/2 of 13.5 to 14.0 hours. Coadministration with food did not significantly affect AUC, tmax, or Cmax. These results indicate that the rate of iloperidone's absorption is decreased, but the overall bioavailability is unchanged, when the drug is taken with food. Orthostatic hypotension, dizziness, and somnolence were the most commonly reported adverse events.
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同义词HP-873
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通路GPCR/G Protein
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靶点5-HT Receptor
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受体Dopamine|α-adrenergicreceptor
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研究领域Neurological Disease
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适应症Schizophrenia
化学信息
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CAS Number133454-47-4
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分子量426.4806
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分子式C24H27FN2O4
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纯度>98% (HPLC)
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溶解度10 mM in DMSO
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SMILESCC(C1=CC=C(OCCCN2CCC(C3=NOC4=CC(F)=CC=C34)CC2)C(OC)=C1)=O
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化学全称Ethanone, 1-[4-[3-[4-(6-fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]propoxy]-3-methoxyphenyl]-
运输与储存
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储存条件(-20℃)
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运输条件With Ice Pack
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稳定性≥ 2 years
参考文献
1. Barr AM, et al. Neuropharmacology. 2006 Sep;51(3):457-65.
2. Szewczak MR, et al. J Pharmacol Exp Ther. 1995 Sep;274(3):1404-13.
3. Sainati SM, et al. J Clin Pharmacol. 1995 Jul;35(7):713-20.
产品手册
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