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94164-88-2

中文名稱 COMPOUND 3K
英文名稱 PKM2 inhibitor
CAS 94164-88-2
分子式 C18H19NO2S2
分子量 345.48
MOL 文件 94164-88-2.mol
94164-88-2 結構式 94164-88-2 結構式

基本信息

中文別名
PKM2抑制劑(化合物3K)
PKM2抑制劑(PKM2-IN-1)
英文別名
PKM2-IN-1
compound 3k
PKM2 inhibitor
PKM2 inhibitor 1
PKM2-IN-1
COMPOUND 3K
PKM2 inhibitor(compound 3k)
piperidine-1-carbodithioic acid 3-methyl-1,4-dioxo-1,4-dihydronaphthalen-2-ylmethyl ester
1-Piperidinecarbodithioic acid, (1,4-dihydro-3-methyl-1,4-dioxo-2-naphthalenyl)methyl ester

物理化學性質

沸點496.5±55.0 °C(Predicted)
密度1.302±0.06 g/cm3(Predicted)
儲存條件Sealed in dry,Store in freezer, under -20°C
溶解度DMF: 1 mg/ml; DMSO: insol; Ethanol: insol; PBS (pH 7.2): insol
酸度系數(shù)(pKa)0.81±0.20(Predicted)
形態(tài)固體
顏色Light yellow to yellow

安全數(shù)據(jù)

危險性符號(GHS)GHS hazard pictograms
GHS07
警示詞警告
危險性描述H302-H315-H319-H335

常見問題列表

生物活性
PKM2-IN-1 是一種丙酮酸激酶 M2 (PKM2) 抑制劑,其 IC50 值為 2.95 μM。
靶點

IC50: 2.95 μM (PKM2)

體外研究

PKM2-IN-1 is a pyruvate kinase M2 (PKM2) inhibitor with an IC 50 of 2.95±0.53 μM. Results show that most of the tested compounds exhibit some degree of PKM2 inhibition and some compounds, such as PKM2-IN-1 (compound 3k) and 6d, display more potent activity than the positive control shikonin. The representative compounds PKM2-IN-1, 6d display dose-dependent inhibition of PKM2 with less inhibition of PKM1 and PKL like shikonin. Among all tested compounds, the most potent compounds are 3a, PKM2-IN-1 and 3r, which exhibit IC 50 values against HCT116 and Hela cells ranging from 0.39 to 0.41 μM, 0.18 to 0.29 μM and 0.18 to 0.38 μM, respectively.

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