2-{[4-amino-3-(3-hydroxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl]methyl}-5-methyl-3-(2-methylphenyl)-3,4-dihydroquinazolin-4-one

• ChemBase编号: 73087
• 分子式: C28H23N7O2
• 平均质量: 489.52792
• 单一同位素质量: 489.19132301
• SMILES: n1cnc2c(c1N)c(nn2Cc1n(c(=O)c2c(n1)cccc2C)c1c(cccc1)C)c1cc(ccc1)O
• Canonical SMILES: Oc1cccc(c1)c1nn(c2c1c(N)ncn2)Cc1nc2cccc(c2c(=O)n1c1ccccc1C)C
• InChI: InChI=1S/C28H23N7O2/c1-16-7-3-4-12-21(16)35-22(32-20-11-5-8-17(2)23(20)28(35)37)14-34-27-24(26(29)30-15-31-27)25(33-34)18-9-6-10-19(36)13-18/h3-13,15,36H,14H2,1-2H3,(H2,29,30,31)
• InChIKey: WFSLJOPRIJSOJR-UHFFFAOYSA-N

名称和登记号

名称

• IUPAC标准名: 2-{[4-amino-3-(3-hydroxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl]methyl}-5-methyl-3-(2-methylphenyl)-3,4-dihydroquinazolin-4-one
• IUPAC传统名: 2-{[4-amino-3-(3-hydroxyphenyl)pyrazolo[3,4-d]pyrimidin-1-yl]methyl}-5-methyl-3-(2-methylphenyl)quinazolin-4-one
• 别名: PIK294; PIK-294

登记号

• CAS号: 900185-02-6
• PubChem SID: 162038007
• PubChem CID: 24905149

理论计算性质

• 质子受体: 7
• 质子供体: 2
• LogD (pH = 5.5): 3.696448
• LogD (pH = 7.4): 4.6813197
• Log P: 4.742224
• 摩尔折射率: 155.2525 cm^3
• 极化性: 54.280655 Å^3
• 极化表面积: 122.52 Å^2
• 可自由旋转的化学键: 3
• 里宾斯基五规则: true
• Acid pKa: 9.536047

分子性质

安全信息

• 保存条件: -20°C

药理学性质

• 作用靶点: PI3K

产品相关信息

• 成盐信息: Free Base

详细说明

Selleck Chemicals - S2227

Research Area

• Description: Cancer

Biological Activity

• Description: PIK-294 is a highly potent and selective p110δ inhibitor with IC50 of 10 nM.
• Targets: p110δ; p110β; p110γ
• IC50: 10 nM; 490 nM; 160 nM ^[1]
• In Vitro: PIK-294 shows distinct patterns of isoform selectivity to inhibit different subsets of class I PI3K isoforms (p110β, p110δ, and p110γ) and exhibits low sensitivity to p110α with IC50 of 10 μM). The m-phenol moiety of PIK-294 is able to penetrate the deep-affinity pocket of the ATP binding site, and thus increases in vitro inhibitory activity. ^[1]
• Features: p110δ inhibitor

Combination Therapy

• Description: A recent study shows that activation of Akt in response to ER stress in NIH3T3 cells coadministered with 10 nM Wortmannin, 10 μM PIK-294, or 10 μM IC-87114 could inhibit endogenous PI3K activity. ^[2]

Protocol

• Protocol: Kinase Assay ^[1]
• Assay of p110α/p85α, p110β/p85α, p110δ/p85α, and p110γ: IC50 values are measured using either a standard TLC assay for lipid kinase activity or a high-throughput membrane capture assay. Kinase reactions are performed by preparing a reaction mixture containing kinase, inhibitor (2% DMSO final concentration), buffer (25 mM HEPES, pH 7.4, 10 mM MgCl₂), and freshly sonicated phosphatidylinositol (100 μg/mL). Reactions are initiated by the addition of ATP containing 10 μCi of γ-^32P-ATP to a final concentration 10 μM or 100 μM, and allowed to proceed for 20 minutes at room temperature. For TLC analysis, reactions are then terminated by the addition of 105 μL 1N HCl followed by 160 μL CHCl₃:MeOH (1:1). The biphasic mixture is vortexed, briefly centrifuged, and the organic phase transferred to a new tube using a gel loading pipette tip precoated with CHCl₃. This extract is spotted on TLC plates and developed for 3-4 hours in a 65:35 solution of n-propanol:1M acetic acid. The TLC plates are then dried, exposed to a phosphorimager screen, and quantitated. For each compound, kinase activity is typically measured at 10-12 inhibitor concentrations representing two-fold dilutions from the highest concentration tested (100 μM). For compounds showing significant activity, IC50 determinations are repeated two to four times, and the reported value is the average of these independent measurements.

References

• References: [1] Knight ZA, et al. Cell. 2006, 125(4), 733-747.
• References: [2] Bobrovnikova-Marjon E, et al. Mol Cell Biol. 2012, 32(12), 2268-2278.

参考文献

• Knight ZA, et al. Cell. 2006, 125(4), 733-747.
• Bobrovnikova-Marjon E, et al. Mol Cell Biol. 2012, 32(12), 2268-2278.