货号	规格	价格	上海	北京	珠海	武汉
S88133-5mg	≥97%	￥50.00 S88133-5mg ￥50.00 2-3天	0 货期：2-3天	-	-	-
S88133-10mg	97.60%	￥90.00 S88133-10mg ￥90.00 现货	5 5	-	-	-
S88133-25mg	97.60%	￥200.00 S88133-25mg ￥200.00 现货	3 3	-	-	-
S88133-50mg	97.60%	￥350.00 S88133-50mg ￥350.00 现货	4 4	-	-	-

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产品描述：

Ticlopidine (PCR 5332), an antithrombotic prodrug, acts as an allosteric, noncompetitive inhibitor of CD39 with the IC50 of 81.7 µM. Ticlopidine blocks several NTPDase isoenzymes with IC50s of 170 µM and 149 µM for NTPDase2 and NTPDase3, respectively. Ticlopidine is an inhibitor of CYP2C19 human liver cytochrome. Ticlopidine inhibits CYP2C9 and CYP3A4 with IC50s of 26.0 and 32.3 μM, respectively

靶点：

Cytochrome P450;ATPase; Adiponectinreceptor

体内研究：

Oral administration of Losartan with 10 mg/kg Ticlopidine significantly increases the AUC (by 65.0%), suggesting that Ticlopidine can effectively inhibit the metabolism of losartan in the intestine and/or liver. Animal Model: Male Sprague-Dawley rats (7-8 weeks old, weighing 270-300 g) Dosage: 4 or 10 mg/kg Administration: Orally administered 30 min before oral administration of losartan. Result: The AUC and Cmax of Losartan after oral administration with Losartan and 10 mg/kg Ticlopidine were significantly greater (by 65.0% and 49.4%, respectively) than those of control rats.

参考文献：

1. Laura Schäkel, et al. 2-Substituted thienotetrahydropyridine derivatives: Allosteric ectonucleotidase inhibitors. Arch Pharm (Weinheim). 2021 Dec;354(12):e2100300. 2. I.KRASLOVA1, et al. Ticlopidine-Induced Cholestatic Inflammatory Hepatitis: New Insights into Pathogenetic Mechanisms of Drug-Related Hepatotoxicity. 3. Si-hyung Yang, et al. Effects of ticlopidine on pharmacokinetics of losartan and its main metabolite EXP-3174 in rats. Acta Pharmacol Sin. 2011 Jul;32(7):967-72. 4. F Piovella, et al. The effect of Ticlopidine on human endothelial cells in culture. Thromb Res. 1984 Feb 1;33(3):323-32.

保存条件：

-20℃

配置溶液浓度参考：

	1mg	5mg	10mg
1 mM	3.791 ml	18.954 ml	37.909 ml
5 mM	0.758 ml	3.791 ml	7.582 ml
10 mM	0.379 ml	1.895 ml	3.791 ml
50 mM	0.076 ml	0.379 ml	0.758 ml

注意：

部分产品我司仅能提供部分信息，我司不保证所提供信息的权威性，仅供客户参考交流研究之用。

参考文献(2篇)

2. [IF=2.9] Jinqiu Rao et al."Inactivation of CYP2D6 by Berberrubine and the Chemical Mechanism."BIOCHEMISTRY.2024;XXXX(XXX):XXX-XXX 1. [IF=4.3] Peng Ting et al."Elucidation of the relationship between evodiamine-induced liver injury and CYP3A4-mediated metabolic activation by UPLC-MS/MS analysis."ANALYTICAL AND BIOANALYTICAL CHEMISTRY.2023 Jul;:1-17

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