2,4-Pyrimidinediamine, 5-(4-chlorophenoxy)-6-methyl- (9CI)

• 常用名: 2,4-Pyrimidinediamine, 5-(4-chlorophenoxy)-6-methyl- (9CI)
• 英文名: 2,4-Pyrimidinediamine, 5-(4-chlorophenoxy)-6-methyl- (9CI)
• CAS号: 7331-19-3
• 分子量: 250.68400
• 密度: 1.398g/cm3
• 沸点: 447.7ºC at 760 mmHg
• 分子式: C₁₁H₁₁ClN₄O
• 熔点: N/A
• 闪点: 224.5ºC

名称

• 英文名: 5-(4-chlorophenoxy)-6-methylpyrimidine-2,4-diamine

物理化学性质

• 密度: 1.398g/cm3
• 沸点: 447.7ºC at 760 mmHg
• 分子式: C₁₁H₁₁ClN₄O
• 分子量: 250.68400
• 闪点: 224.5ºC
• 精确质量: 250.06200
• PSA: 87.05000
• LogP: 3.55750
• InChIKey: SRAYHJGJNAQSTI-UHFFFAOYSA-N
• SMILES: Cc1nc(N)nc(N)c1Oc1ccc(Cl)cc1
• 折射率: 1.671

毒性和生态

靶点实验

查看更多实验

实验名称：Luminescence-based cell-based primary high throughput screening assay to identify ago... 来源：The Scripps Research Institute Molecular Screening Center 靶标：mu-type opioid receptor isoform MOR-1 [Homo sapiens] External Id：OPRM1-OPRD1_AG_LUMI_1536_1X%ACT PRUN

实验名称：QFRET-based biochemical primary high throughput screening assay to identify exosite i... 来源：The Scripps Research Institute Molecular Screening Center 靶标：disintegrin and metalloproteinase domain-containing protein 17 preproprotein [Homo sapiens] External Id：ADAM17_INH_QFRET_1536_1X%INH PRUN

实验名称：Fluorescence-based cell-based primary high throughput screening assay to identify ago... 来源：The Scripps Research Institute Molecular Screening Center 靶标：muscarinic acetylcholine receptor M1 [Homo sapiens] External Id：CHRM1_AG_FLUO8_1536_1X%ACT PRUN

实验名称：qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in... 来源：NCGC 靶标：TDP1 protein [Homo sapiens] External Id：TDP1100

实验名称：qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in... 来源：NCGC 靶标：TDP1 protein [Homo sapiens] External Id：TDP1101

实验名称：Schnurri-3 Inhibitors: specific inducers of adult bone formation Measured in Cell-Bas... 来源：Broad Institute 靶标：N/A External Id：2134-01_Inhibitor_SinglePoint_HTS_Activity_Set2

实验名称：Fluorescence polarization to screen for inhibitor that competite the binding of FadD2... 来源：Broad Institute 靶标：FATTY-ACID-CoA LIGASE FADD28 (FATTY-ACID-CoA SYNTHETASE) External Id：2147-01_Inhibitor_SinglePoint_HTS_Activity

实验名称：Bursicon-induced LGR2 mediated cAMP production in LGR-2/CRE6x-Luciferase co-transfect... 来源：Broad Institute 靶标：N/A External Id：Bursicon-induced LGR2 mediated cAMP production in LGR-2/CRE6x-Luciferase co-transfected HEK293 cells Inhibition - 7011-01_Antagonist_SinglePoint_HTS_Activity

实验名称：High throughput screen for small molecule inhibitors of a hypoxia-regulated fluoresce... 来源：ICCB-Longwood/NSRB Screening Facility, Harvard Medical School 靶标：N/A External Id：HMS1149-MLP

实验名称：Primary Screen Inhibitors of CD40 Signaling in BL2 Cells Measured in Cell-Based Syste... 来源：Broad Institute 靶标：N/A External Id：7124-01_Inhibitor_SinglePoint_HTS_Activity

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英文别名

• BW 48-210
• 5-(4-chloro-phenoxy)-6-methyl-pyrimidine-2,4-diyldiamine
• 5-(4-Chlorophenoxy)-6-methyl-2,4-pyrimidinediamine
• 5-(4-Chlor-phenoxy)-6-methyl-pyrimidin-2,4-diyldiamin
• 5-(p-Chlorophenoxy)-2,4-diamino-6-methylpyrimidine
• 2,4-Diamino-5-(4'-chlorophenoxy)-6-methylpyrimidine
• 2,4-Diamino-5-(p-chlorophenoxy)-6-methylpyrimidine