吩噻嗪-3-酮

• 常用名: 吩噻嗪-3-酮
• 英文名: 3-Phenothiazone
• CAS号: 581-30-6
• 分子量: 213.25500
• 密度: 1.36g/cm3
• 沸点: 349.3ºC at 760 mmHg
• 分子式: C₁₂H₇NOS
• 熔点: N/A
• 闪点: 165ºC

吩噻嗪-3-酮名称

• 中文名: 吩噻嗪-3-酮
• 英文名: phenothiazin-3-one

吩噻嗪-3-酮物理化学性质

• 密度: 1.36g/cm3
• 沸点: 349.3ºC at 760 mmHg
• 分子式: C₁₂H₇NOS
• 分子量: 213.25500
• 闪点: 165ºC
• 精确质量: 213.02500
• PSA: 58.20000
• LogP: 2.76130
• InChIKey: YKGCCFHSXQHWIG-UHFFFAOYSA-N
• SMILES: O=c1ccc2nc3ccccc3sc-2c1
• 折射率: 1.72
• 储存条件: 2-8°C

吩噻嗪-3-酮安全信息

• 海关编码: 2934300000

吩噻嗪-3-酮海关

• 海关编码: 2934300000
• 中文概述: 2934300000. 含一个吩噻嗪环系的化合物(吩噻嗪环系不论是否氢化,化合物未经进一步稠合的 ). 增值税率:17.0%. 退税率:13.0%. 监管条件:无. 最惠国关税:6.5%. 普通关税:20.0%
• 申报要素: 品名, 成分含量, 用途
• Summary: 2934300000. other compounds containing in the structure a phenothiazine ring-system (whether or not hydrogenated), not further fused. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

吩噻嗪-3-酮靶点实验

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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：Small Molecule Inhibitors of FGF22-Mediated Excitatory Synaptogenesis & Epilepsy Meas... 来源：Broad Institute 靶标：FGF22 human recombinant External Id：7012-04_Inhibitor_Dose_CherryPick_Activity

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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吩噻嗪-3-酮英文别名

• 3H-phenothiazine-3-one
• phenothiazone
• 3-Phenothiazone
• phenothiazine-3-one
• 3H-pheno-thiazinone
• 3-phenothiazinone