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4(5H)-Thiazolone,2-amino-5,5-diphenyl

更新时间:2025-09-24 00:14:04

4(5H)-Thiazolone,2-amino-5,5-diphenyl结构式
4(5H)-Thiazolone,2-amino-5,5-diphenyl结构式
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常用名 4(5H)-Thiazolone,2-amino-5,5-diphenyl 英文名 4(5H)-Thiazolone,2-amino-5,5-diphenyl
CAS号 4694-95-5 分子量 268.33400
密度 1.29g/cm3 沸点 442.9ºC at 760mmHg
分子式 C15H12N2OS 熔点 N/A
MSDS N/A 闪点 221.7ºC

 4(5H)-Thiazolone,2-amino-5,5-diphenyl名称

英文名 2-amino-5,5-diphenyl-1,3-thiazol-4-one
英文别名 更多

 4(5H)-Thiazolone,2-amino-5,5-diphenyl物理化学性质

密度 1.29g/cm3
沸点 442.9ºC at 760mmHg
分子式 C15H12N2OS
分子量 268.33400
闪点 221.7ºC
精确质量 268.06700
PSA 80.75000
LogP 2.65420
InChIKey BDASUGIISLUZMZ-UHFFFAOYSA-N
SMILES NC1=NC(=O)C(c2ccccc2)(c2ccccc2)S1
折射率 1.678

 4(5H)-Thiazolone,2-amino-5,5-diphenyl靶点实验

查看更多实验

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: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
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 4(5H)-Thiazolone,2-amino-5,5-diphenyl英文别名

2-amino-5,5-diphenyl-thiazol-4-one
5,5-Diphenyl-pseudohydantoin
5,5-Diphenyl-thiohydantoin
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