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ONO-8130

CAS No. 459841-96-4

ONO-8130 ( —— )

产品货号. M24411 CAS No. 459841-96-4

ONO-8130 是一种口服 EP1 受体拮抗剂。

纯度: >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
规格 价格/人民币 库存 数量
5MG ¥2916 有现货
10MG ¥4803 有现货
25MG ¥7679 有现货
50MG ¥10449 有现货
100MG 获取报价 有现货
200MG 获取报价 有现货
500MG 获取报价 有现货
1G 获取报价 有现货

生物学信息

  • 产品名称
    ONO-8130
  • 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
    ONO-8130 是一种口服 EP1 受体拮抗剂。
  • 产品描述
    ONO-8130 is an orally available antagonist of EP1 receptor.
  • 体外实验
    ——
  • 体内实验
    ONO-8130 (0.3-30 mg/kg; Oral preadministration, once) strongly prevents both the bladder pain-like behavior and referred hyperalgesia in a dose-dependent manner.ONO-8130 (30 mg/kg; Orally, once) reverses the established cystitis-related bladder pain.ONO-8130 (30 mg/kg; Orally, once) strongly inhibits phosphorylation of ERK in MDH, DCM, and SPN of the L6 spinal cord caused by intravesical administration of PGE2. Animal Model:Female ddY mice (18-22 g, 4-5 weeks old)Dosage:0.3, 3, 10, and 30 mg/kg Administration: Orally, once Result:Strongly prevented both the bladder pain-like behavior and referred hyperalgesia in a dose-dependent manner, but had slight effect on the increased bladder weight and vascular permeability.Animal Model:Female ddY mice (18-22 g, 4-5 weeks old, established bladder pain caused by IP cyclophosphamide)Dosage:10, 30 mg/kgAdministration:Orally, once (administered 2.75 hours after i.p. cyclophosphamide) Result:Markedly attenuated the bladder pain-like nociceptive behavior and referred hyperalgesia in the acute phase (3.5-4 h after cyclophosphamide).Animal Model:Female ddY mice (18-22 g, 4-5 weeks old, established bladder pain caused by IP cyclophosphamide)Dosage:30 mg/kgAdministration:Orally, once (administered 4.75 hours after i.p. cyclophosphamide)Result:Significantly suppressed the bladder pain-like nociceptive behavior and tended to reduce the referred hyperalgesia in the persistent phase, 5.5-6 hours after cyclophosphamide.Animal Model:Female ddY mice (18-22 g, 4-5 weeks old, intravesical administration of PGE2 at 5 nmol/mouse)Dosage:30 mg/kg Administration:Orally, once Result:Strongly inhibited phosphorylation of ERK in MDH, DCM, and SPN of the L6 spinal cord caused by intravesical administration of PGE2 at 5 nmol/mouse, exerted complete blockade in DCM, while its inhibitory effects in MDH and SPN were partial.
  • 同义词
    ——
  • 通路
    GPCR/G Protein
  • 靶点
    Prostaglandin Receptor
  • 受体
    EP1
  • 研究领域
    ——
  • 适应症
    ——

化学信息

  • CAS Number
    459841-96-4
  • 分子量
    500.63
  • 分子式
    C25H28N2O5S2
  • 纯度
    >98% (HPLC)
  • 溶解度
    DMSO:10 mM
  • SMILES
    CC1=CSC(=N1)S(=O)(=O)N(CC(C)C)C2=C(C=C3CCCC3=C2)OCC4=CC=C(C=C4)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.Miki T , Matsunami M , Nakamura S , et al. ONO-8130, a selective prostanoid EP1 receptor antagonist, relieves bladder pain in mice with cyclophosphamide-induced cystitis.[J]. Pain, 2011, 152(6):1373-1381.
产品手册
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