
Sarpogrelate hydrochloride
CAS No. 135159-51-2
Sarpogrelate hydrochloride ( MCI 9042 | MCI9042 | MCI-9042 )
产品货号. M11420 CAS No. 135159-51-2
一种有效的、特异性的 5HT2 受体拮抗剂,对 5-HT2A 的 Ki 值为 8.39 nM;还显示出对 5-HT2B 的结合亲和力。
纯度: >98% (HPLC)






规格 | 价格/人民币 | 库存 | 数量 |
5MG | ¥332 | 有现货 |
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10MG | ¥535 | 有现货 |
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25MG | ¥988 | 有现货 |
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50MG | ¥1580 | 有现货 |
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100MG | ¥2333 | 有现货 |
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500MG | ¥5573 | 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Sarpogrelate hydrochloride
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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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产品简述一种有效的、特异性的 5HT2 受体拮抗剂,对 5-HT2A 的 Ki 值为 8.39 nM;还显示出对 5-HT2B 的结合亲和力。
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产品描述A potent, specific 5HT2 receptor antagonist with Ki of 8.39 nM for 5-HT2A; also shows binding affinity for 5-HT2B; displays selectivity over 5-HT1-like, 5-HT3, beta, H1, H2 and M3; blocks serotonin-induced platelet aggregation.Heart Failure Approved(In Vitro):Sarpogrelate is selective for 5-HT2 (pKi=7.54) over 5-HT1 (pKi=4.58), α1-, α2-, and β-adrenergic (pKi=3.17-6.19), and muscarinic receptors (pKi=4.39).Sarpogrelate (10 μM) significantly reduces the number of platelet-rich plasma (PRP)-induced THP-1 cell that adheres to human umbilical vein endothelial cells (HUVECs).Sarpogrelate (10 μM) significantly reduces the expression of PRP-induced E-selectin in HUVECs.(In Vivo):Sarpogrelate (5 mg/kg; i.p. daily for 4 weeks) inhibits HFFD-induced obesity and decreases leukocyte-endothelial interactions in mice.
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体外实验Sarpogrelate is selective for 5-HT2 (pKi=7.54) over 5-HT1 (pKi=4.58), α1-, α2-, and β-adrenergic (pKi=3.17-6.19), and muscarinic receptors (pKi=4.39).Sarpogrelate (10 μM) significantly reduces the number of platelet-rich plasma (PRP)-induced THP-1 cell that adheres to human umbilical vein endothelial cells (HUVECs).Sarpogrelate (10 μM) significantly reduces the expression of PRP-induced E-selectin in HUVECs.
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体内实验Sarpogrelate (5 mg/kg; i.p. daily for 4 weeks) inhibits HFFD-induced obesity and decreases leukocyte-endothelial interactions in mice. Animal Model:Male C57BL/6 mice (7 weeks old) are fed normal chow (NC) or a high-fat diet with 30% fructose in the drinking water (HFFD)Dosage:5 mg/kg Administration:I.p. daily for 4 weeks Result:Prevented the HFFD-induced increases of the body weight, visceral fat weight, and serum monocyte chemoattractant protein-1 levels.Decreased leukocyte-endothelial interactions and serum monocyte chemoattractant protein-1 (MCP-1) level.
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同义词MCI 9042 | MCI9042 | MCI-9042
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通路Endocrinology/Hormones
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靶点5-HT Receptor
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受体5-HT Receptor
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研究领域Cardiovascular Disease
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适应症——
化学信息
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CAS Number135159-51-2
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分子量465.967
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分子式C24H32ClNO6
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纯度>98% (HPLC)
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溶解度DMSO: ≥ 62 mg/mL
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SMILESCN(C)CC(COC1=CC=CC=C1CCC2=CC(=CC=C2)OC)OC(=O)CCC(=O)O.Cl
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化学全称Butanedioic acid, 1-[2-(dimethylamino)-1-[[2-[2-(3-methoxyphenyl)ethyl]phenoxy]methyl]ethyl] ester, hydrochloride (1:1)
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. Kikumoto R, et al. J Med Chem. 1990 Jun;33(6):1818-23.
2. Pertz H, et al. J Pharm Pharmacol. 1995 Apr;47(4):310-6.
3. Nishio H, et al. Arch Int Pharmacodyn Ther. 1996 Mar-Apr;331(2):189-202.