
RO1138452
CAS No. 221529-58-4
RO1138452 ( CAY10441 )
产品货号. M17442 CAS No. 221529-58-4
RO1138452 是一种选择性、口服生物可利用的前列环素受体拮抗剂 (pKi: 8.3)。
纯度: >98% (HPLC)






规格 | 价格/人民币 | 库存 | 数量 |
2MG | ¥510 | 有现货 |
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5MG | ¥786 | 有现货 |
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10MG | ¥1256 | 有现货 |
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25MG | ¥2811 | 有现货 |
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50MG | ¥4836 | 有现货 |
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100MG | ¥6901 | 有现货 |
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200MG | 获取报价 | 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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生物学信息
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产品名称RO1138452
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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RO1138452 是一种选择性、口服生物可利用的前列环素受体拮抗剂 (pKi: 8.3)。
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产品描述RO1138452 is a selective and orally bioavailable antagonist of prostacyclin receptor (pKi: 8.3). It antagonizes the carbaprostacyclin-induced activation of human neuroblastoma adenylate cyclase, blocking cyclic AMP accumulation in a dose-dependent manner. Likewise, it inhibits the binding of tritiated iloprost to rodent neuroblastoma cells with a Ki of about 1.5 nM. At levels between 2-20 mg/kg in rats, CAY10441 shows significant analgesic activity in standard antinociceptive assays.
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体外实验RO1138452 is IP receptor antagonist. The pIC50 values of RO1138452 in attenuating cAMP accumulation is 7.0±0.07. Functional antagonism of RO1138452 is studied by measuring inhibition of carbaprostacyclin-induced cAMP accumulation in CHO-K1 cells stably expressing the human IP receptor. The antagonist affinity (pKi) of RO1138452 is 9.0±0.06. Selectivity profiles for RO1138452 are determined via a panel of receptor binding and enzyme assays. RO1138452 displays affinity at imidazoline2 (I2) (8.3) and platelet activating factor (PAF) (7.9) receptors. RO1138452 (10 pM-10 μM) added to cells concurrently with a fixed concentration of Taprostene (1 μM) prevents, in a concentration-dependent manner, the inhibition of CXCL9 and CXCL10 release, with p[A]50 (molar) values of -8.73±0.11 and -8.47±0.16 (p>0.05), respectively.
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体内实验RO1138452 is a potent and selective antagonist for both human and rat IP receptors and that is possesses analgesic and anti-inflammatory potential. RO1138452 (1-10?mg/kg, i.v.) significantly reduces acetic acid-induced abdominal constrictions. RO1138452 (3-100?mg/kg, p.o.) significantly reduces carrageenan-induced mechanical hyperalgesia and edema formation. One?hour after administration of RO1138452 (5?mg/kg, i.v.) to rats, the total plasma concentration is 0.189 ?μg/mL, whereas the free plasma concentrations is calculated to be 0.009?μg/mL (28 nM).
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同义词CAY10441
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通路Chromatin/Epigenetic
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靶点COX
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受体prostacyclin receptor
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研究领域Inflammation/Immunology
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适应症——
化学信息
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CAS Number221529-58-4
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分子量309.41
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分子式C19H23N3O
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纯度>98% (HPLC)
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溶解度DMSO : 33.33 mg/mL. 107.72 mM; H2O : < 0.1 mg/mL
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SMILESCC(C)Oc1ccc(Cc2ccc(NC3=NCCN3)cc2)cc1
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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.Clark R D, Jahangir A, Severance D, et al. Bioorganic & medicinal chemistry letters, 2004, 14(4): 1053-1056.
产品手册




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