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4,7-Epoxy-1H-isoindole-1,3(2H)-dione,hexahydro-4,7-dimethyl-2-(2-thiazolyl)

更新时间:2025-09-23 19:01:45

4,7-Epoxy-1H-isoindole-1,3(2H)-dione,hexahydro-4,7-dimethyl-2-(2-thiazolyl)结构式
4,7-Epoxy-1H-isoindole-1,3(2H)-dione,hexahydro-4,7-dimethyl-2-(2-thiazolyl)结构式
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常用名 4,7-Epoxy-1H-isoindole-1,3(2H)-dione,hexahydro-4,7-dimethyl-2-(2-thiazolyl) 英文名 4,7-Epoxy-1H-isoindole-1,3(2H)-dione,hexahydro-4,7-dimethyl-2-(2-thiazolyl)
CAS号 19783-63-2 分子量 278.32700
密度 1.457g/cm3 沸点 410.4ºC at 760mmHg
分子式 C13H14N2O3S 熔点 N/A
MSDS N/A 闪点 202ºC

 名称

英文名 4,7-dimethyl-2-(1,3-thiazol-2-yl)-3a,5,6,7a-tetrahydro-octahydro-1H-4,7-epoxyisoindole-1,3-dione
英文别名 更多

 物理化学性质

密度 1.457g/cm3
沸点 410.4ºC at 760mmHg
分子式 C13H14N2O3S
分子量 278.32700
闪点 202ºC
精确质量 278.07300
PSA 87.74000
LogP 1.65510
InChIKey WESNUVHBKHZVAG-UHFFFAOYSA-N
SMILES CC12CCC(C)(O1)C1C(=O)N(c3nccs3)C(=O)C12
蒸汽压 6.02E-07mmHg at 25°C
折射率 1.637

 上下游产品

上游产品  2

下游产品  0

 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:High throughput screen for small molecule inhibitors of a hypoxia-regulated fluoresce...
来源:ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
靶标:N/A
External Id:HMS1149-MLP
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

4,7-dimethyl-2-thiazol-2-yl-hexahydro-4,7-epioxido-isoindole-1,3-dione
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