N-[3-(benzenesulfonamido)-2,4,6-trimethyl-phenyl]benzenesulfonamide

• 常用名: N-[3-(benzenesulfonamido)-2,4,6-trimethyl-phenyl]benzenesulfonamide
• 英文名: N-[3-(benzenesulfonamido)-2,4,6-trimethyl-phenyl]benzenesulfonamide
• CAS号: 6324-61-4
• 分子量: 430.54000
• 密度: 1.36g/cm3
• 沸点: 574ºC at 760 mmHg
• 分子式: C₂₁H₂₂N₂O₄S₂
• 熔点: N/A
• 闪点: 300.9ºC

名称

• 英文名: N,N'-Dihydroxy-2,3-dimethyl-2,3-butanediamine

物理化学性质

• 密度: 1.36g/cm3
• 沸点: 574ºC at 760 mmHg
• 分子式: C₂₁H₂₂N₂O₄S₂
• 分子量: 430.54000
• 闪点: 300.9ºC
• 精确质量: 430.10200
• PSA: 109.10000
• LogP: 6.52100
• InChIKey: AYTAROZYGOMGFA-UHFFFAOYSA-N
• SMILES: Cc1cc(C)c(NS(=O)(=O)c2ccccc2)c(C)c1NS(=O)(=O)c1ccccc1
• 折射率: 1.646

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：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

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英文别名

• 2.4-Bis-benzolsulfamino-1.3.5-trimethyl-benzol
• N,N'-dihydroxy-2,3-diamino-2,3-dimethyl-butane
• 1,1,2,2-tetramethyl-1,2-dihydroxylaminoethane
• N.N'-Dibenzolsulfonyl-2.4.6-trimethyl-m-phenylendiamin