4'-(Trifluoromethyl)flavone结构式
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常用名 | 4'-(Trifluoromethyl)flavone | 英文名 | 4'-(Trifluoromethyl)flavone |
|---|---|---|---|---|
| CAS号 | 128814-90-4 | 分子量 | 290.24 | |
| 密度 | N/A | 沸点 | N/A | |
| 分子式 | C16H9F3O2 | 熔点 | N/A | |
| MSDS | N/A | 闪点 | N/A |
| 英文名 | 4'-(Trifluoromethyl)flavone |
|---|
| 分子式 | C16H9F3O2 |
|---|---|
| 分子量 | 290.24 |
| InChIKey | XISMXQJXDBDZSJ-UHFFFAOYSA-N |
| SMILES | O=c1cc(-c2ccc(C(F)(F)F)cc2)oc2ccccc12 |
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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:Drug recovery in human liver microsomes assessed as NADPH-fortified oxidative metabol...
来源:ChEMBL
靶标:N/A
External Id:CHEMBL5115446
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实验名称:Drug recovery in human liver microsomes assessed as UDPGA-fortified conjugation recov...
来源:ChEMBL
靶标:N/A
External Id:CHEMBL5115447
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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:uHTS identification of small molecule activators of the adaptive arm of the Unfolded ...
来源:Burnham Center for Chemical Genomics
靶标:N/A
External Id:BCCG-A405-UPR-XBP1-PrimaryAgonist-Assay
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实验名称:Apparent permeability of the compound by PAMPA assay
来源:ChEMBL
靶标:N/A
External Id:CHEMBL5115442
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实验名称:Apparent permeability of the compound in human Caco-2 cells
来源:ChEMBL
靶标:N/A
External Id:CHEMBL5115443
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实验名称:Drug recovery in human HCT-116 cells incubated for 24 hrs
来源:ChEMBL
靶标:N/A
External Id:CHEMBL5115445
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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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