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 |
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| 10MG | ¥4803 | 有现货 |
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| 25MG | ¥7679 | 有现货 |
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| 50MG | ¥10449 | 有现货 |
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| 100MG | 获取报价 | 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ONO-8130
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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ONO-8130 是一种口服 EP1 受体拮抗剂。
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产品描述ONO-8130 is an orally available antagonist of EP1 receptor.
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体外实验——
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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.
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同义词——
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通路GPCR/G Protein
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靶点Prostaglandin Receptor
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受体EP1
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研究领域——
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适应症——
化学信息
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CAS Number459841-96-4
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分子量500.63
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分子式C25H28N2O5S2
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纯度>98% (HPLC)
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溶解度DMSO:10 mM
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SMILESCC1=CSC(=N1)S(=O)(=O)N(CC(C)C)C2=C(C=C3CCCC3=C2)OCC4=CC=C(C=C4)C(=O)O
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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.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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