Hexanedioic acid,1,6-bis[2-[(2-hydroxyphenyl)methylene]hydrazide]结构式
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常用名 | Hexanedioic acid,1,6-bis[2-[(2-hydroxyphenyl)methylene]hydrazide] | 英文名 | Hexanedioic acid,1,6-bis[2-[(2-hydroxyphenyl)methylene]hydrazide] |
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| CAS号 | 5287-26-3 | 分子量 | 382.41300 | |
| 密度 | 1.363g/cm3 | 沸点 | 558.7ºC at 760 mmHg | |
| 分子式 | C20H22N4O4 | 熔点 | N/A | |
| MSDS | N/A | 闪点 | 179.3ºC |
| 英文名 | 1-N',6-N'-bis[(E)-(6-oxocyclohexa-2,4-dien-1-ylidene)methyl]hexanedihydrazide |
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| 英文别名 | 更多 |
| 密度 | 1.363g/cm3 |
|---|---|
| 沸点 | 558.7ºC at 760 mmHg |
| 分子式 | C20H22N4O4 |
| 分子量 | 382.41300 |
| 闪点 | 179.3ºC |
| 精确质量 | 382.16400 |
| PSA | 123.38000 |
| LogP | 3.04040 |
| InChIKey | JLZRXDKIRXEOIZ-UHFFFAOYSA-N |
| SMILES | O=C(CCCCC(=O)NN=Cc1ccccc1O)NN=Cc1ccccc1O |
| 折射率 | 1.685 |
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Hexanedioic aci... 5287-26-3 |
| 文献:Curtius Journal fuer Praktische Chemie (Leipzig), 1915 , vol. <2> 91, p. 23 |
| 上游产品 2 | |
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| 下游产品 0 | |
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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:Counterscreen for inhibitors of the Steroid Receptor Coactivator 1 (SRC1; NCOA1): Lum...
来源:The Scripps Research Institute Molecular Screening Center
靶标:transactivating tegument protein VP16 [Human herpesvirus 1]
External Id:VP16_INH_LUMI_1536_3X%INH CSRUN for SRC1
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