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6(5H)-Phenanthridinone,3,8-dinitro

更新时间:2025-09-27 19:11:56

6(5H)-Phenanthridinone,3,8-dinitro结构式
6(5H)-Phenanthridinone,3,8-dinitro结构式
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常用名 6(5H)-Phenanthridinone,3,8-dinitro 英文名 6(5H)-Phenanthridinone,3,8-dinitro
CAS号 23818-38-4 分子量 285.21200
密度 1.564g/cm3 沸点 420.1ºC at 760mmHg
分子式 C13H7N3O5 熔点 N/A
MSDS N/A 闪点 207.9ºC

 6(5H)-Phenanthridinone,3,8-dinitro名称

英文名 3,8-dinitro-5H-phenanthridin-6-one

 6(5H)-Phenanthridinone,3,8-dinitro物理化学性质

密度 1.564g/cm3
沸点 420.1ºC at 760mmHg
分子式 C13H7N3O5
分子量 285.21200
闪点 207.9ºC
精确质量 285.03900
PSA 124.50000
LogP 3.54410
InChIKey NFQCBMOTZZLRCE-UHFFFAOYSA-N
SMILES O=c1[nH]c2cc([N+](=O)[O-])ccc2c2ccc([N+](=O)[O-])cc12
蒸汽压 2.88E-07mmHg at 25°C
折射率 1.698

 6(5H)-Phenanthridinone,3,8-dinitro上下游产品

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6(5H)-Phenanthridinone,3,8-dinitro下游产品  0

 6(5H)-Phenanthridinone,3,8-dinitro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:qHTS for Inhibitors of AMA1-RON; Towards Development of Antimalarial Drug Lead: Prima...
来源:NCGC
靶标:apical membrane antigen 1, AMA1 [Plasmodium falciparum 3D7]
External Id:AMA1100
实验名称:Fluorescence polarization-based biochemical high throughput primary assay to identify...
来源:The Scripps Research Institute Molecular Screening Center
靶标:abhydrolase domain-containing protein 4 isoform 1 [Mus musculus]
External Id:ABHD4_INH_FP_1536_1X%INH PRUN
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