6,7-二羟基苯并呋喃-3(2H)-酮结构式
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常用名 | 6,7-二羟基苯并呋喃-3(2H)-酮 | 英文名 | 3(2H)-Benzofuranone,6,7-dihydroxy |
|---|---|---|---|---|
| CAS号 | 6272-27-1 | 分子量 | 166.13100 | |
| 密度 | 1.614g/cm3 | 沸点 | 433.3ºC at 760 mmHg | |
| 分子式 | C8H6O4 | 熔点 | N/A | |
| MSDS | N/A | 闪点 | 189.1ºC |
| 中文名 | 6,7-二羟基氯杀鼠灵酮 |
|---|---|
| 英文名 | 6,7-dihydroxy-1-benzofuran-3-one |
| 英文别名 | 更多 |
| 密度 | 1.614g/cm3 |
|---|---|
| 沸点 | 433.3ºC at 760 mmHg |
| 分子式 | C8H6O4 |
| 分子量 | 166.13100 |
| 闪点 | 189.1ºC |
| 精确质量 | 166.02700 |
| PSA | 66.76000 |
| LogP | 0.67290 |
| InChIKey | ZDHCVQNIRWDINX-UHFFFAOYSA-N |
| SMILES | O=C1COc2c1ccc(O)c2O |
| 折射率 | 1.689 |
| 储存条件 | 室温 |
| 6,7-二羟基苯并呋喃-3(2H)-酮上游产品 2 | |
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| 6,7-二羟基苯并呋喃-3(2H)-酮下游产品 4 | |
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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...
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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:Antibacterial activity against Klebsiella pneumoniae MDR ATCC 70063 (CO-ADD:GN_003); ...
来源:ChEMBL
靶标:Klebsiella pneumoniae
External Id:CHEMBL4296186
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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:Identifying Sarm1 TIR NADase inhibitors through high throughput HPLC assay
来源:24386
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External Id:Sarm1 TIR NADase inhibitors
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实验名称:Primary Screen Inhibitors of CD40 Signaling in BL2 Cells Measured in Cell-Based Syste...
来源:Broad Institute
靶标:N/A
External Id:7124-01_Inhibitor_SinglePoint_HTS_Activity
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实验名称:Fluorescence-based cell-based primary high throughput screening assay to identify pos...
来源:The Scripps Research Institute Molecular Screening Center
靶标:muscarinic acetylcholine receptor M1 [Homo sapiens]
External Id:CHRM1_PAM_FLUO8_1536_1X%ACT PRUN
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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:RecName: Full=Sialate O-acetylesterase; AltName: Full=H-Lse; AltName: Full=Sialic acid-specific 9-O-acetylesterase; Flags: Precursor [Homo sapiens]
External Id:SIAE_INH_FP_1536_1X%INH PRUN
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| 6,7-dihydroxy-2-hydrobenzo[b]furan-3-one |
| 6,7-dihydroxy-benzofuran-3-one |
| 6,7-Dihydroxy-benzofuran-3-on |
| 6.7-Dioxy-cumaranon |
| 6,7-Dihydroxycoumeranone |
| 6,7-Dihydroxy-1-benzofuran-3(2H)-one |
| 3(2H)-Benzofuranone,6,7-dihydroxy |
| 6,7-Dihydroxy-3-coumaranone |
| 6,7-Dihydroxycoumaranon |
| 6,7-dihydroxybenzofuran-3(2H)-one |
| 6,7-dihydroxy-2H-benzofuran-3-one |