Benzenamine,3-nitro-N-(phenylmethylene)

• 常用名: Benzenamine,3-nitro-N-(phenylmethylene)
• 英文名: Benzenamine,3-nitro-N-(phenylmethylene)
• CAS号: 5341-44-6
• 分子量: 226.23100
• 密度: 1.16g/cm3
• 沸点: 386.7ºC at 760mmHg
• 分子式: C₁₃H₁₀N₂O₂
• 熔点: N/A
• 闪点: 187.7ºC

Benzenamine,3-nitro-N-(phenylmethylene)名称

• 英文名: N-(3-nitrophenyl)-1-phenylmethanimine

Benzenamine,3-nitro-N-(phenylmethylene)物理化学性质

• 密度: 1.16g/cm3
• 沸点: 386.7ºC at 760mmHg
• 分子式: C₁₃H₁₀N₂O₂
• 分子量: 226.23100
• 闪点: 187.7ºC
• 精确质量: 226.07400
• PSA: 58.18000
• LogP: 3.86860
• InChIKey: HFGFPUPROHHWFT-UHFFFAOYSA-N
• SMILES: O=[N+]([O-])c1cccc(N=Cc2ccccc2)c1
• 折射率: 1.651

Benzenamine,3-nitro-N-(phenylmethylene)毒性和生态

Benzenamine,3-nitro-N-(phenylmethylene)靶点实验

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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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Benzenamine,3-nitro-N-(phenylmethylene)英文别名

• PhCH=NC6H4-NO2-m
• ANILINE,N-BENZYLIDENE-m-NITRO
• Benzaldehyd-(3-nitro-phenylimin)
• Benzal-m-nitroaniline
• Benzenamine,3-nitro-N-(phenylmethylene)
• N-(3-nitrobenzylidene)aniline
• N-Benzyliden-3-nitro-anilin
• Benzal-3-nitroaniline
• Benzaldehyd-(3-nitro-anil)
• WLN: WNR CNU1R
• N-BENZYLIDENE-m-NITRO ANILINE
• N-benzylidene-3-nitro-aniline