TG100-115
目录号: PL09797 纯度: ≥99%
CAS No. :677297-51-7
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中文名称
TG100-115
中文别名
3,3'-(2,4-二氨基-6,7-蝶啶二基)二苯酚;3,3-(2,4-二氨基-6,7-蝶啶二基)二苯酚;TG100-115 抑制剂;银杏苦内酯B
英文名称
TG100-115
英文别名
3,3'-(2,4-Diamino-6,7-pteridinediyl)bisphenol;TG100-115;3-[2,4-diamino-7-(3-hydroxyphenyl)pteridin-6-yl]phenol;TG-100115;3,3'-(2,4-diaminopteridine-6,7-diyl)diphenol;3-[2,4-diamino-6-(3-hydroxyphenyl)pteridin-7-yl]phenol;6,7-bis-(3-hydroxyphenyl)-pteridine-2,4-diamine;TG100115;TG-100-115;TG 100115;6,7-Bis(3-hydroxyphenyl)pteridine-2,4-diamine;7ACH1U1E2M;3-(2,4-diamino-6-(3-hydroxyphenyl)pteridin-7-yl)phenol;MLS006010976;JMC504279 Compound 6;Phenol, 3,3'-(2,4-diamino-6,7-pteridi
Cas No.
677297-51-7
分子式
C18H14N6O2
分子量
346.34
包装储存
Powder -20°C 3 years;4°C 2 years
产品详情
TG100-115 是一种选择性的 PI3Kγ/PI3Kδ 抑制剂,IC50 分别为 83 和 235 nM。
生物活性
TG100-115 is a selective PI3Kγ/PI3Kδ inhibitor with IC 50 s of 83 and 235 nM, respectively.
性状
Solid
IC50 & Target[1][2]
PI3Kδ 235 nM (IC50) PI3Kγ 83 nM (IC50
体外研究(In Vitro)
TG100-115 inhibits PI3Kγ and PI3Kδ with IC50s of 83 and 235 nM, respectively, whereas both PI3Kα and PI3Kβ are relatively unaffected (IC50 values >1 μM). As a gauge of general specificity, TG100-115 is also assayed against a 133 protein kinase panel, none of which are inhibited at IC50 values <1 μM. TG100-115 potently inhibits edema and inflammation in response to multiple mediators known to participate in myocardial infarction, including vascular endothelial growth factor and platelet-activating factor; by contrast, endothelial cell mitogenesis, a repair process important to tissue survival after ischemic damage. has not independently confirmed the accuracy of these methods. They are for reference only.
体内研究(In Vivo)
To correlate these in vivo responses with the molecular target of interest, PI3K pathway signaling is monitored through western blot analyses of Akt phosphorylation (a PI3K-mediated event). VEGF injection i.v. in mice induces a rapid Akt phosphorylation readily detectable in lung lysates, pretreatment with TG100-115 blocks this response. Blockade is seen with TG100-115 doses as low as 0.5 mg/kg and persists over a period of several hours. In initial dose-ranging studies, generally equivalent responses are observed using TG100-115 doses of 0.5-10 mg/kg, and we therefore elected to conduct a statistically powered test at the lowest dose. Animals dosed with TG100-115 as a single 0.5 mg/kg i.v. bolus 30 min after reperfusion developed smaller infarcts vs. vehicle-treated controls. Measuring infarct area as percent of total LV ischemic area, infarct size is reduced by 35% (P=0.04).
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
ClinicalTrial
参考文献
[1]. Doukas J, et al. Phosphoinositide 3-kinase gamma/delta inhibition limits infarct size after myocardial ischemia/reperfusion injury. Proc Natl Acad Sci U S A. 2006 Dec 26;103(52):19866-71.
溶解度数据
In Vitro: DMSO : 33.33 mg/mL (96.23 mM; ultrasonic and warming and adjust pH to 2 with HCl and heat to 60°C)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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