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PF-06840003(EOS200271)
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
PF-06840003(EOS200271)图片
CAS NO:198474-05-4
包装与价格:
包装价格(元)
10mM (in 1mL DMSO)电议
1mg电议
5mg电议
10mg电议
50mg电议
100mg电议

产品介绍
PF-06840003 (EOS200271) (EOS200271) 是一种高选择性的口服生物利用度 IDO-1 抑制剂,IC50 为 0.41 μM, 0.59 μM 和 1.5 μM 和 hIDO-1, md-DO-1 , 分别。
Cas No.198474-05-4
别名3-(5-氟-1H-吲哚-3-基)-2,5-吡咯烷二酮,EOS200271
Canonical SMILESO=C(C(C1=CNC2=C1C=C(F)C=C2)C3)NC3=O
分子式C12H9FN2O2
分子量232.21
溶解度DMSO : ≥ 28 mg/mL (120.58 mM)
储存条件Store at -20°C
General tipsFor obtaining a higher solubility , please warm the tube at 37 ℃ and shake it in the ultrasonic bath for a while.
Shipping ConditionEvaluation sample solution : ship with blue ice
All other available size: ship with RT , or blue ice upon request
产品描述

PF-06840003 is a highly selective orally bioavailable IDO-1 inhibitor.

PF-06840003 reverses IDO-1-induced T-cell anergy in vitro[1].

PF-06840003 reduces intratumoral kynurenine levels in mice by >80% and inhibits tumor growth in multiple preclinical syngeneic models in mice, in combination with immune checkpoint inhibitors. PF-0684003 has favorable predicted human pharmacokinetic properties, including a predicted t1/2 of 16-19 hours[1].

[1]. Tumang J, et al. PF-06840003: a highly selective IDO-1 inhibitor that shows good in vivo efficacy in combination with immune checkpoint inhibitors. [abstract]. In: Proceedings of the 107th Annual Meeting of the American Association for Cancer Research; 2016 Apr 16-20; New Orleans, LA. Philadelphia (PA): AACR; Cancer Res 2016;76(14 Suppl):Abstract nr4863.