• 咨询热线
    客服服务热线 13671568941/15317326293
  • 在线咨询
  • 微信客服
    微信客服
  • 公众号
    扫码关注公众号

Quetiapine Fumarate

CAS No. 111974-72-2

Quetiapine Fumarate ( ICI 204636 )

产品货号. M10430 CAS No. 111974-72-2

Quetiapine hemifumarate 是一种 5-HT 受体激动剂,对人 5-HT1A 的 pEC50 值为 4.77。Quetiapine hemifumarate 是多巴胺受体 (dopamine receptor) 拮抗剂,对人 D2 的 pIC50 值为 6.33。Quetiapine hemifumarate 对人 D2,HT1A,5-HT2A,5-HT2C 受体具有中高等亲和力,pKi 值为 7.25,5.74,7.54,5.55。具有抗抑郁和抗焦虑作用。

纯度: >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
规格 价格/人民币 库存 数量
200MG ¥243 有现货
500MG ¥373 有现货
1G ¥389 有现货

生物学信息

  • 产品名称
    Quetiapine Fumarate
  • 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
  • 产品简述
    Quetiapine hemifumarate 是一种 5-HT 受体激动剂,对人 5-HT1A 的 pEC50 值为 4.77。Quetiapine hemifumarate 是多巴胺受体 (dopamine receptor) 拮抗剂,对人 D2 的 pIC50 值为 6.33。Quetiapine hemifumarate 对人 D2,HT1A,5-HT2A,5-HT2C 受体具有中高等亲和力,pKi 值为 7.25,5.74,7.54,5.55。具有抗抑郁和抗焦虑作用。
  • 产品描述
    Quetiapine Fumarate is an atypical antipsychotic used in the treatment of schizophrenia, bipolar I mania, bipolar II depression, bipolar I depression.(In Vitro):Quetiapine (<100?μM; 24?hours) has no significant effect on cell viabilities.Quetiapine (10?μM) inhibits NO release, which increased by LPS (0.1-100 ng/mL) in concentration-dependent manner.Quetiapine (10?μM) also inhibits TNF-α synthesis.(In Vivo):Quetiapine (10?mg/kg/day; ingested) can alleviate the recruitment and activation of microglia and promote myelin repair in Cuprizone (CPZ)-induced chronic mouse model of demyelination.
  • 体外实验
    Quetiapine (<100?μM; 24?hours) has no significant effect on cell viabilities.Quetiapine (10?μM) inhibits NO release, which increased by LPS (0.1-100 ng/mL) in concentration-dependent manner. Quetiapine (10?μM) also inhibits TNF-α synthesis. Cell Viability Assay Cell Line:N9 microglial cells Concentration:0, 0.1, 1, 10, 50, and 100?μM Incubation Time:24?hours Result:Had no significant effect on cell viabilities at various concentrations under 100?μM, in which significant toxicity could be observed. RT-PCR Cell Line:N9 microglial cells Concentration:10?μM Incubation Time:24?hours Result:Dramatically inhibited TNF-α synthesis.
  • 体内实验
    Quetiapine (10?mg/kg/day; ingested) can alleviate the recruitment and activation of microglia and promote myelin repair in Cuprizone (CPZ)-induced chronic mouse model of demyelination. Animal Model:C57BL/6 mice Dosage:10?mg/kg/day Administration:Ingested Result:Significantly increased in optical density of myelin basic protein (MBP) staining compared to Veh group.
  • 同义词
    ICI 204636
  • 通路
    Endocrinology/Hormones
  • 靶点
    5-HT Receptor
  • 受体
    HT| Adrenergic Receptor| Dopamine
  • 研究领域
    Neurological Disease
  • 适应症
    ——

化学信息

  • CAS Number
    111974-72-2
  • 分子量
    883.09
  • 分子式
    C46H54N6O8S2
  • 纯度
    >98% (HPLC)
  • 溶解度
    DMSO: 36 mg/mL (40.76 mM)
  • SMILES
    C1CN(CCN1CCOCCO)C2=NC3=CC=CC=C3SC4=CC=CC=C42.C1CN(CCN1CCOCCO)C2=NC3=CC=CC=C3SC4=CC=CC=C42.C(=C/C(=O)O)\C(=O)O
  • 化学全称
    ——

运输与储存

  • 储存条件
    (-20℃)
  • 运输条件
    With Ice Pack
  • 稳定性
    ≥ 2 years

参考文献

1.Nemeroff CB, et al. J Clin Psychiatry, 2002, 63 Suppl 13, 5-1
产品手册
关联产品
  • N-Desmethylclozapine

    N-Desmethylclozapine 是血清素 (5-HT) 受体亚型 5-HT2C 的拮抗剂 (IC50: 7.1 nM)。它也是多巴胺 D4 受体的拮抗剂、δ-阿片受体的激动剂。

  • Perospirone hydrochl...

    Perospirone (SM-9018 free base) 是具有口服活性的 5-HT2A 受体 (Ki=0.6 nM) 和多巴胺 D2 受体 (Ki=1.4 nM) 的拮抗剂,也是 5-HT1A 受体 (Ki=2.9 nM) 的部分激动剂。

  • RS 127445

    RS 127445 是一种选择性、高亲和力、口服生物可利用的 5-HT2B 受体拮抗剂 (pKi : 9.5)。