IDO-IN-7 (Synonyms: NLG-919 analogue; GDC-0919 analogue)
目录号: PL03879 纯度: ≥99%
CAS No. :1402836-58-1
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中文名称
IDO-IN-7
中文别名
1-环己基-2-(5H-咪唑并[5,1-a]异吲哚-5-基)乙醇;NLG919 抑制剂;alpha-环己基-5H-咪唑并[5,1-a]异吲哚-5-乙醇;1-CYCLOHEXYL-2-(5H-IMIDAZO[5,1-A]ISOINDOL-5-YL)ETHANOL
英文名称
IDO-IN-7
英文别名
1-CYCLOHEXYL-2-(5H-IMIDAZO[5,1-A]ISOINDOL-5-YL)ETHANOL;NLG919;1-Cyclohexyl-2-(5H-imidazo-[5,1-a]isoindol-5-yl)ethanol;1-CYCLOHEXYL-2-(5H-IMIDAZO[5,1-A]ISOINDOL-5-YL)ETHANOL;NLG-919;AK166956;alpha-Cyclohexyl-5H-imidazo[5,1-a]isoindole-5-ethanol;1-Cyclohexyl-2-(5H-imidazo[5,1-a]isoindol-5-yl)ethan-1-ol;YTRRAUACYORZLX-UHFFFAOYSA-N;GTPL9019;NLG 919;GDC0919;HMS3653M05;AOB87373;GDC 0919;RG6078;BDBM50126144;2588AH;s7111;SB16495;IDO-IN-7
Cas No.
1402836-58-1
分子式
C18H22N2O
分子量
282.38
包装储存
Powder -20°C 3 years;4°C 2 years
产品详情
IDO-IN-7 (NLG-919 analogue) 是一种有效的 IDO1 抑制剂, IC50为 38 nM。
生物活性
IDO-IN-7 (NLG-919 analogue) is a a potent IDO1 inhibitor with an IC 50 of 38 nM.
性状
Solid
IC50 & Target[1][2]
IDO1 38 nM (IC50)
体外研究(In Vitro)
IDO-IN-7 (NLG-919 analogue) is a potent IDO1 inhibitor (IC50=38 nM). The binding mode of IDO-IN-7 to IDO1 is experimentally available and shows a direct coordinative interaction to the sixth coordination site of ferric heme. IDO-IN-7 has been used as reference compound in other studies to validate high-throughput screening assay for IDO1 inhibition and develop immunostimulatory nanomicellar carrier. has not independently confirmed the accuracy of these methods. They are for reference only.
运输条件
Room temperature in continental US; may vary elsewhere.
储存方式
Powder -20°C 3 years;4°C 2 years
参考文献
[1]. Coletti A, et al. Fragment-based approach to identify IDO1 inhibitor building blocks. Eur J Med Chem. 2017 Dec 1;141:169-177.
溶解度数据
In Vitro: DMSO : 50 mg/mL (177.07 mM; Need ultrasonic)Ethanol : 25 mg/mL (88.53 mM; Need ultrasonic)配制储备液
搜索质检报告(COA)

1:一般建议:溶解度为Medlife测试数据,可能与文献描述存在差异。这是由于生产工艺和批次不同产生的正常现象。为了使其更好的溶解,请用37℃加热试管并在超声波水浴中震动片刻。不同批次产品溶解度各有差异,仅做参考,具体以实验方案为准。

2:储存条件:粉末-20°C一般情况可以保存3年,溶于溶剂-80°C一般情况可以保存1年。不同产品及不同批次产品可能存在差异,请细致阅读产品信息,并辅助参考相关文献描述。

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