Acetamide, N-(4,5-dihydronaphtho[1,2-d]thiazol-2-yl)

• 常用名: Acetamide, N-(4,5-dihydronaphtho[1,2-d]thiazol-2-yl)
• 英文名: Acetamide, N-(4,5-dihydronaphtho[1,2-d]thiazol-2-yl)
• CAS号: 7496-70-0
• 分子量: 244.31200
• 密度: 1.343g/cm3
• 沸点: N/A
• 分子式: C₁₃H₁₂N₂OS
• 熔点: N/A
• 闪点: N/A

名称

• 英文名: N-(4,5-dihydrobenzo[e][1,3]benzothiazol-2-yl)acetamide

物理化学性质

• 密度: 1.343g/cm3
• 分子式: C₁₃H₁₂N₂OS
• 分子量: 244.31200
• 精确质量: 244.06700
• PSA: 70.23000
• LogP: 2.94010
• InChIKey: QMHPCMDFILVHES-UHFFFAOYSA-N
• SMILES: CC(=O)Nc1nc2c(s1)CCc1ccccc1-2
• 折射率: 1.685

靶点实验

查看更多实验

实验名称：Primary cell-based high-throughput screening assay for identification of compounds th... 来源：Johns Hopkins Ion Channel Center 靶标：regulator of G-protein signaling 4 isoform 2 [Homo sapiens] External Id：JHICC_RGS_Act_HTS

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：USP8 deubiquitinase inhibition: Primary qHTS 来源：24642 靶标：ubiquitin specific peptidase 8 External Id：USP8 FAST DUB HTS Primary

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：USP17 deubiquitinase inhibition: Primary qHTS 来源：24642 靶标：ubiquitin specific peptidase 17 like family member 5 External Id：USP17 FAST DUB HTS Primary

实验名称：USP7 deubiquitinase inhibition: Primary qHTS 来源：24642 靶标：ubiquitin specific peptidase 7 External Id：USP7 FAST DUB HTS Primary

实验名称：uHTS identification of small molecule activators of the adaptive arm of the Unfolded ... 来源：Burnham Center for Chemical Genomics 靶标：N/A External Id：BCCG-A405-UPR-XBP1-PrimaryAgonist-Assay

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

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英文别名

• HMS1414G09
• N-(4,5-dihydro-naphtho[1,2-d]thiazol-2-yl)-acetamide
• HMS2954F13