生物活性 体外研究 体内研究 靶点
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LY310762

LY310762,192927-92-7,结构式
LY310762
  • CAS号:192927-92-7
  • 英文名:LY310762
  • 中文名:LY310762
  • CBNumber:CB0488147
  • 分子式:C24H27O2N2FHCl
  • 分子量:0
  • MOL File:192927-92-7.mol
LY310762化学性质
  • 储存条件 :Sealed in dry,Room Temperature
  • 溶解度 :DMSO: 10 mg/mL with heating, soluble
  • 形态 :white powder
  • CAS 数据库 :192927-92-7
安全信息
  • 危险品标志 :Xi
  • 危险类别码 :36/37/38
  • 安全说明 :26-36
  • WGK Germany :3

LY310762性质、用途与生产工艺

  • 生物活性 LY310762是一种5-HT1D受体拮抗剂,Ki为249 nM,对5-HT1B受体具有较低的亲和力。
  • 体外研究 LY310762 has a higher affinity for the guinea pig 5-HT1D receptor than for the 5-HT1B receptor. LY310762 potentiates the potassium-induced [3H]5-HT outflow from guinea pig cortical slices with an EC50 of 30 nM. The maximum potentiation of the potassium-induced outflow which is obtained with LY310762 is about 40%. LY310762 blocks the decreased EPSC amplitude induced by Sumatriptan.
  • 体内研究 Systemic administration of LY310762 (10 mg/kg i.p.) produces a further significant enhancement in the 5-HT response to fluoxetine (20 mg/kg i.p.) when compared to animals receiving a control vehicle injection. In fluoxetine treated animals, levels of 5-HT increases from 312±43% to a maximum of 683% after LY310762. In control animals, levels of 5-HT remains unchanged (250%). LY310762 administered alone also significantly increases basal levels of 5-HT above vehicle controls, reaching a maximum of 258% compared to the pre-injection control.
  • 靶点

    5-HT 1D Receptor

    249 nM (Ki)

LY310762上下游产品信息
上游原料
下游产品
LY310762生产厂家
  • 公司名称:成都诺维生物科技有限公司
  • 联系电话:028-81458053
  • 电子邮件:novibiotech@163.com sales@novi-biotech.com
  • 国家:中国
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  • 公司名称:Wuhan NCE Biomedical Co.,Ltd.
  • 联系电话:4000-027-021 |24 +86-13986109188 | +86-15623472865 | +81-08033611988
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  • 国家:中国
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  • 公司名称:AdooQ BioScience, LLC
  • 联系电话:+1 (866) 930-6790
  • 电子邮件:info@adooq.com
  • 国家:美国
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