Blonanserin
CAS No. 132810-10-7
Blonanserin ( AD5423 | Lonasen )
产品货号. M11308 CAS No. 132810-10-7
Blonanserin 是一种新型非典型抗精神病药,具有有效的多巴胺 D2 和血清素 5-HT2 受体拮抗剂特性。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 5MG | ¥253 | 有现货 |
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| 10MG | ¥412 | 有现货 |
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| 25MG | ¥671 | 有现货 |
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| 50MG | ¥1014 | 有现货 |
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| 100MG | ¥1593 | 有现货 |
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| 500MG | 获取报价 | 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 | ¥454 | 有现货 |
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生物学信息
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产品名称Blonanserin
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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Blonanserin 是一种新型非典型抗精神病药,具有有效的多巴胺 D2 和血清素 5-HT2 受体拮抗剂特性。
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产品描述Blonanserin is a novel atypical antipsychotic agent with potent dopamine D2 and serotonin 5-HT2 receptors antagonist properties.(In Vitro):Blonanserin exerts some blockade of α1-adrenergic receptors (Ki=26.7 nM) and also shows significant affinity for the D3?receptor (Ki=0.494 nM). Blonanserin possesses low affinity for the sigma receptor (IC50=286 nM), but lacks significant affinity for numerous other sites including the 5-HT1A, 5-HT3, D1, α2-adrenergic, β-adrenergic, H1, and mACh receptors and the monoamine transporters.(In Vivo):Blonanserin (oral gavage; 1 mg/kg; 14 days) significantly ameliorates the social deficit observed in PCP-administered mice and inhibits the decrease in the levels of Ser897-phosphorylation, but preatment with blonanserin does not affect the social behaviors in saline-administered mice.
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体外实验Blonanserin exerts some blockade of?α1-adrenergic receptors?(Ki=26.7?nM) and also shows significant affinity for the?D3?receptor?(Ki=0.494 nM). Blonanserin possesses low affinity for the?sigma receptor?(IC50=286 nM), but lacks significant?affinity?for numerous other sites including the?5-HT1A,?5-HT3,?D1,?α2-adrenergic,?β-adrenergic,?H1, and?mACh receptors?and the?monoamine transporters.
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体内实验Blonanserin (oral gavage; 1 mg/kg; 14 days) significantly ameliorates the social deficit observed in PCP-administered mice and inhibits the decrease in the levels of Ser897-phosphorylation, but preatment with blonanserin does not affect the social behaviors in saline-administered mice. Animal Model:Mice received saline or phencyclidine once a day for 14 consecutive days Dosage:1 mg/kg Administration:Oral gavage; 1 mg/kg; 14 days Result:Had an effect on the social deficit in mice that received repeated PCP administration.
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同义词AD5423 | Lonasen
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通路Endocrinology/Hormones
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靶点5-HT Receptor
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受体5-HT2| D2
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研究领域Neurological Disease
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适应症——
化学信息
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CAS Number132810-10-7
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分子量367.5
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分子式C23H30FN3
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纯度>98% (HPLC)
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溶解度Ethanol: <1 mg/mL (<1 mM); Water: <1 mg/mL (<1 mM); DMSO: <1 mg/mL (<1 mM)
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SMILESCCN1CCN(CC1)C1=NC2=C(CCCCCC2)C(=C1)C1=CC=C(F)C=C1
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化学全称——
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.Kawabe K, et al. Clin Neuropharmacol. 2013, Nov-Dec; 36(6):239-4
产品手册
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