3-(1-cyano-1-methylethyl)-N-{4-methyl-3-[(3-methyl-4-oxo-3,4-dihydroquinazolin-6-yl)amino]phenyl}benzamide

• ChemBase编号: 73304
• 分子式: C27H25N5O2
• 平均质量: 451.5197
• 单一同位素质量: 451.20082507
• SMILES: c1(cccc(c1)C(=O)Nc1ccc(c(c1)Nc1cc2c(cc1)ncn(c2=O)C)C)C(C#N)(C)C
• Canonical SMILES: N#CC(c1cccc(c1)C(=O)Nc1ccc(c(c1)Nc1ccc2c(c1)c(=O)n(cn2)C)C)(C)C
• InChI: InChI=1S/C27H25N5O2/c1-17-8-9-21(31-25(33)18-6-5-7-19(12-18)27(2,3)15-28)14-24(17)30-20-10-11-23-22(13-20)26(34)32(4)16-29-23/h5-14,16,30H,1-4H3,(H,31,33)
• InChIKey: ZGBGPEDJXCYQPH-UHFFFAOYSA-N

名称和登记号

名称

• IUPAC标准名: 3-(1-cyano-1-methylethyl)-N-{4-methyl-3-[(3-methyl-4-oxo-3,4-dihydroquinazolin-6-yl)amino]phenyl}benzamide
• IUPAC传统名: 3-(1-cyano-1-methylethyl)-N-{4-methyl-3-[(3-methyl-4-oxoquinazolin-6-yl)amino]phenyl}benzamide
• 别名: AZ628

登记号

• CAS号: 878739-06-1
• PubChem SID: 162038224
• PubChem CID: 11676786

理论计算性质

• Acid pKa: 12.707882
• 质子受体: 5
• 质子供体: 2
• LogD (pH = 5.5): 4.694179
• LogD (pH = 7.4): 4.7870164
• Log P: 4.7883477
• 摩尔折射率: 136.2194 cm^3
• 极化性: 49.125027 Å^3
• 极化表面积: 97.59 Å^2
• 可自由旋转的化学键: 5
• 里宾斯基五规则: true

分子性质

安全信息

• 保存条件: -20°C

药理学性质

• 作用靶点: B-Raf

产品相关信息

• 成盐信息: Free Base

详细说明

Selleck Chemicals - S2746

Research Area

• Description: Cancer

Biological Activity

• Description: AZ628 is a potent inhibitor for wild-type CRAF and BRAF^V600E with IC50 of 29 nM and 34 nM, respectively.
• Targets: wild-type CRAF; BRAF^V600E; wild-type BRAF
• IC50: 29 nM; 34 nM; 100 nM ^[1]
• In Vitro: AZ628 prevents activation of number of tyrosine protein kinases including VEGFR2, DDR2, Lyn, Flt1, FMS and others. AZ628 suppresses anchorage-dependent and -independent growth, gives rise to cell cycle arrest, and induces apoptosis in colon and melanoma cell lines harboring B-RafV600E mutation. The profile of AZ628 cross-reactivity suggests that similar to sorafenib, AZ628 may be antiangiogenic based on prevention of VEGFR2. ^[1] AZ628-resistant clones are approximately 100-fold more resistant to AZ628 than the parental cell line, exhibiting IC50 of approximately 10 μM, compared with 0.1 μM for the parental cell line. Effective suppression of p-ERK1/2 levels is observed in the M14 parental cell line following treatment with increasing concentrations of AZ628. AZ628-resistant clones express elevated CRAF. Elevated CRAF expression is a potential mechanism of acquired resistance to continuous AZ628 exposure, resulting in sustained activation of ERK1/2. p-ERK1/2 activity is not significantly inhibited by exposure to AZ628 in one of these three AZ628-insensitive cell lines (Wm1552C). Unlike in the AZ628-resistant M14 cells in which AZ628 fails to suppress the activation of ERK, AZ628 treatment efficiently attenuates ERK activation in the NRAS mutant melanoma cells.^[2]

Protocol

• Protocol: Cell Assay ^[1]
• Cell Lines: M14 expressing the V600E BRAF mutation
• Concentrations: 0.01-10 μM
• Incubation Time: Overnight
• Methods: Approximately 0.5-2.5 × 10^5 M14 cells are seeded in 12 or 24 - well plates, respectively, in medium supplemented with 5% FBS. After overnight incubation, the cells are treated with various concentrations of AZ628. Fresh medium and drug is replaced every 2 days until the untreated control wells reached confluence. At this time-point, the media is removed and the cells are fixed in 4% formaldehyde in PBS for 20 minutes at room temperature. Cells are then washed twice with PBS and stained with a 1:5000 solution of the fluorescent nucleic acid stain Syto60. Quantitation of fluorescent signal intensity is carried out at 700 nm, using an Odyssey Infrared Imager. Each experiment is performed in quadruplicate and the results shown represent the average of the four values compared to untreated wells. Error bars represent standard deviation of the 4 values from the mean. High-throughput cell growth/viability assays are performed.

References

• References: [1] Khazak V, et al. Expert Opin Ther Targets. 2007, 11(12), 1587-1609.
• References: [2] Montagut C, et al. Cancer Res. 2008, 68(12), 4853-4861.

参考文献

• Khazak V, et al. Expert Opin Ther Targets. 2007, 11(12), 1587-1609.
• Montagut C, et al. Cancer Res. 2008, 68(12), 4853-4861.