7H-Pyrrolo[3,2-e]benzothiazol-7-one,4,6,8,8a-tetrahydro-6,8a-dimethyl

• 常用名: 7H-Pyrrolo[3,2-e]benzothiazol-7-one,4,6,8,8a-tetrahydro-6,8a-dimethyl
• 英文名: 7H-Pyrrolo[3,2-e]benzothiazol-7-one,4,6,8,8a-tetrahydro-6,8a-dimethyl
• CAS号: 79123-76-5
• 分子量: 220.29100
• 密度: 1.34g/cm3
• 沸点: 418.6ºC at 760mmHg
• 分子式: C₁₁H₁₂N₂OS
• 熔点: N/A
• 闪点: 207ºC

名称

• 英文名: 6,8a-dimethyl-4,8-dihydropyrrolo[3,2-e][1,3]benzothiazol-7-one

物理化学性质

• 密度: 1.34g/cm3
• 沸点: 418.6ºC at 760mmHg
• 分子式: C₁₁H₁₂N₂OS
• 分子量: 220.29100
• 闪点: 207ºC
• 精确质量: 220.06700
• PSA: 61.44000
• LogP: 1.64080
• InChIKey: FGXSQKVEJXRMMM-UHFFFAOYSA-N
• SMILES: CN1C(=O)CC2(C)C1=CCc1scnc12
• 折射率: 1.645

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：Antibacterial activity against Klebsiella pneumoniae MDR ATCC 70063 (CO-ADD:GN_003); ... 来源：ChEMBL 靶标：Klebsiella pneumoniae External Id：CHEMBL4296186

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：Identifying Sarm1 TIR NADase inhibitors through high throughput HPLC assay 来源：24386 靶标：N/A External Id：Sarm1 TIR NADase inhibitors

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

• 6,8a-Dimethyl-4,6,8,8a-tetrahydro-7H-(1,3)thiazolo(4,5-e)indol-7-one
• 4,6,7,8a-tetrahydro-6,8a-dimethyl-7-oxo-8H-thiazolo<4,5e>indole