6-(1,3-benzodioxol-5-yl)-7,8-dihydro-6H-benzo[f][1,3]benzodioxol-5-one

• 常用名: 6-(1,3-benzodioxol-5-yl)-7,8-dihydro-6H-benzo[f][1,3]benzodioxol-5-one
• 英文名: 6-(1,3-benzodioxol-5-yl)-7,8-dihydro-6H-benzo[f][1,3]benzodioxol-5-one
• CAS号: 88775-69-3
• 分子量: 310.30100
• 密度: N/A
• 沸点: N/A
• 分子式: C₁₈H₁₄O₅
• 熔点: N/A
• 闪点: N/A

名称

• 英文名: 6-(1,3-benzodioxol-5-yl)-7,8-dihydro-6H-benzo[f][1,3]benzodioxol-5-one

物理化学性质

• 分子式: C₁₈H₁₄O₅
• 分子量: 310.30100
• 精确质量: 310.08400
• PSA: 53.99000
• LogP: 3.05670
• InChIKey: WDSBEFNHNUOXFU-UHFFFAOYSA-N
• SMILES: O=C1c2cc3c(cc2CCC1c1ccc2c(c1)OCO2)OCO3

靶点实验

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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：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

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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英文别名

• 1,2,3,4-Tetrahydro-6,7-methylendioxy-2-<3,4-methylendioxy-phenyl>-1-oxo-napthalin
• 6,7-methylenedioxy-2-(3,4-methylenedioxyphenyl)-3,4-dihydronaphthalen-1(2H)-one
• 6-benzo[1,3]dioxol-5-yl-7,8-dihydro-6H-naphtho[2,3-d][1,3]dioxol-5-one
• 6-(1,3-benzodioxol-5-yl)-7,8-dihydronaphtho[2,3-d][1,3]dioxol-5(6H)-one
• 1,2,3,4-Tetrahydro-6,7-methylendioxy-2-<3,4-methylendioxy-phenyl>-1-oxo-naphthalin