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Bicyclo[3.2.1]octane-2,4-dione,1,8,8-trimethyl

更新时间:2025-10-11 17:35:42

Bicyclo[3.2.1]octane-2,4-dione,1,8,8-trimethyl结构式
Bicyclo[3.2.1]octane-2,4-dione,1,8,8-trimethyl结构式
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常用名 Bicyclo[3.2.1]octane-2,4-dione,1,8,8-trimethyl 英文名 Bicyclo[3.2.1]octane-2,4-dione,1,8,8-trimethyl
CAS号 3278-94-2 分子量 180.24400
密度 1.065g/cm3 沸点 273.3ºC at 760 mmHg
分子式 C11H16O2 熔点 N/A
MSDS N/A 闪点 101.4ºC

 名称

英文名 5,8,8-trimethylbicyclo[3.2.1]octane-2,4-dione
英文别名 更多

 物理化学性质

密度 1.065g/cm3
沸点 273.3ºC at 760 mmHg
分子式 C11H16O2
分子量 180.24400
闪点 101.4ºC
精确质量 180.11500
PSA 34.14000
LogP 1.97080
InChIKey ZTIUZVPQAUZNLG-UHFFFAOYSA-N
SMILES CC12CCC(C(=O)CC1=O)C2(C)C
折射率 1.492

 合成线路

~%

Bicyclo[3.2.1]octane-2,4-dione,1,8,8-trimethyl结构式

Bicyclo[3.2.1]o...

3278-94-2

文献:Shitole, H.R.; Nayak, U.R. Indian Journal of Chemistry, Section B: Organic Chemistry Including Medicinal Chemistry, 1984 , vol. 23, # 5 p. 415 - 417

 靶点实验

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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
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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
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External Id:AMA1100
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External Id:ABHD4_INH_FP_1536_1X%INH PRUN
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 英文别名

3,3-Dimethyl-bicyclo<2.2.2>octan-2-on
Homocamphenilon
1,8,8-Trimethyl-bicyclo<3.2.1>octan-2,4-dion
homocamphorquinoline
Homocamphorquinone
3,3-dimethylbicyclo<2.2.2>octan-2-one
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