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4-(2,6-Diethylphenyl)thiomorpholine-3,5-dione

更新时间:2026-06-20 12:22:39

4-(2,6-Diethylphenyl)thiomorpholine-3,5-dione结构式
4-(2,6-Diethylphenyl)thiomorpholine-3,5-dione结构式
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常用名 4-(2,6-Diethylphenyl)thiomorpholine-3,5-dione 英文名 4-(2,6-Diethylphenyl)thiomorpholine-3,5-dione
CAS号 338953-60-9 分子量 263.36
密度 N/A 沸点 N/A
分子式 C14H17NO2S 熔点 N/A
MSDS N/A 闪点 N/A

 名称

本表展示该化学物质的中文名称、英文系统名、各类中文与英文别名信息。

英文名 4-(2,6-Diethylphenyl)thiomorpholine-3,5-dione

 物理化学性质

本表包含该物质理化参数,如熔点、沸点、密度、溶解度、旋光性等理化指标,无数据项标记为N/A。

分子式 C14H17NO2S
分子量 263.36
InChIKey LBWIYTPSBIWZRS-UHFFFAOYSA-N
SMILES CCC1=C(C(=CC=C1)CC)N2C(=O)CSCC2=O

 靶点实验

查看更多实验

本表记录该化合物靶点、体外体内实验、生物测定实验相关实验数据。

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: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
实验名称:High Throughput Screen to Identify Inhibitors Targeting HIV-1 Vif-dependent Degradati...
来源:Southern Research Institute
靶标:HIV-1 Vif
External Id:HIV1-VIF_MS
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 常见问题

本部分为该化合物相关常见问答,包含基础参数、性状、储存条件等高频咨询问题与对应答案。

Q: 338953-60-9的分子量是多少?
A: 338953-60-9分子量为263.36。
Q: 338953-60-9的英文名称是什么?
A: 338953-60-9英文名称为4-(2,6-Diethylphenyl)thiomorpholine-3,5-dione。
Q: 338953-60-9的CAS号是多少?
A: 338953-60-9CAS号为338953-60-9。
Q: 338953-60-9的分子式是什么?
A: 338953-60-9分子式为C14H17NO2S。
Q: 338953-60-9的SMILES表达式是什么?
A: 338953-60-9SMILES表达式为CCC1=C(C(=CC=C1)CC)N2C(=O)CSCC2=O。
Q: 338953-60-9的中文名称是什么?
A: 338953-60-9的中文名称为338953-60-9。
Q: 338953-60-9的InChIKey是什么?
A: 338953-60-9InChIKey为LBWIYTPSBIWZRS-UHFFFAOYSA-N。
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