1-(2,3,4-trimethoxyphenyl)cycloheptene结构式
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常用名 | 1-(2,3,4-trimethoxyphenyl)cycloheptene | 英文名 | 1-(2,3,4-trimethoxyphenyl)cycloheptene |
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| CAS号 | 189832-04-0 | 分子量 | 262.34400 | |
| 密度 | N/A | 沸点 | N/A | |
| 分子式 | C16H22O3 | 熔点 | N/A | |
| MSDS | N/A | 闪点 | N/A |
| 英文名 | 1-(2,3,4-trimethoxyphenyl)cycloheptene |
|---|---|
| 英文别名 | 更多 |
| 分子式 | C16H22O3 |
|---|---|
| 分子量 | 262.34400 |
| 精确质量 | 262.15700 |
| PSA | 27.69000 |
| LogP | 4.05990 |
| InChIKey | GJJCDBAVAYEJSG-UHFFFAOYSA-N |
| SMILES | COc1ccc(C2=CCCCCC2)c(OC)c1OC |
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~39%
1-(2,3,4-trimet... 189832-04-0 |
| 文献:Rohm and Haas Company Patent: US5866513 A1, 1999 ; |
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~%
1-(2,3,4-trimet... 189832-04-0 |
| 文献:Lotspeich,F.J.; Core,S. Journal of Heterocyclic Chemistry, 1969 , vol. 6, p. 423 - 427 |
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~%
1-(2,3,4-trimet... 189832-04-0 |
| 文献:Gutsche; Fleming Journal of the American Chemical Society, 1954 , vol. 76, p. 1771,1774 |
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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
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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
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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
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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
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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
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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
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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
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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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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
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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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| HMS3085J06 |
| 1-cyclohept-1-enyl-2,3,4-trimethoxy-benzene |
| 1-Cyclohept-1-enyl-2,3,4-trimethoxy-benzol |
| 1-<2',3',4'-Trimethoxy-phenyl>-cyclohepten |