2H-Pyran-2,4(3H)-dione,3-[1-[(3-chlorophenyl)imino]ethyl]-6-methyl structure
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Common Name | 2H-Pyran-2,4(3H)-dione,3-[1-[(3-chlorophenyl)imino]ethyl]-6-methyl | ||
|---|---|---|---|---|
| CAS Number | 33757-23-2 | Molecular Weight | 277.70300 | |
| Density | 1.29g/cm3 | Boiling Point | 443.5ºC at 760mmHg | |
| Molecular Formula | C14H12ClNO3 | Melting Point | N/A | |
| MSDS | N/A | Flash Point | 222ºC | |
| Name | 2H-Pyran-2,4(3H)-dione,3-[1-[(3-chlorophenyl)imino]ethyl]-6-methyl |
|---|
| Density | 1.29g/cm3 |
|---|---|
| Boiling Point | 443.5ºC at 760mmHg |
| Molecular Formula | C14H12ClNO3 |
| Molecular Weight | 277.70300 |
| Flash Point | 222ºC |
| Exact Mass | 277.05100 |
| PSA | 55.73000 |
| LogP | 3.07830 |
| Index of Refraction | 1.59 |
| InChIKey | IYZVOUCJWLJXEN-UHFFFAOYSA-N |
| SMILES | CC1=CC(=O)C(C(C)=Nc2cccc(Cl)c2)C(=O)O1 |
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2H-Pyran-2,4(3H... CAS#:33757-23-2 |
| Literature: Mane; Patange; Arbad Journal of the Indian Chemical Society, 2007 , vol. 84, # 11 p. 1086 - 1091 |
| Precursor 2 | |
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| DownStream 0 | |
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Name: Luminescence-based cell-based primary high throughput screening assay to identify ago...
Source: The Scripps Research Institute Molecular Screening Center
Target: mu-type opioid receptor isoform MOR-1 [Homo sapiens]
External Id: OPRM1-OPRD1_AG_LUMI_1536_1X%ACT PRUN
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Name: QFRET-based biochemical primary high throughput screening assay to identify exosite i...
Source: The Scripps Research Institute Molecular Screening Center
Target: disintegrin and metalloproteinase domain-containing protein 17 preproprotein [Homo sapiens]
External Id: ADAM17_INH_QFRET_1536_1X%INH PRUN
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Name: Fluorescence-based cell-based primary high throughput screening assay to identify ago...
Source: The Scripps Research Institute Molecular Screening Center
Target: muscarinic acetylcholine receptor M1 [Homo sapiens]
External Id: CHRM1_AG_FLUO8_1536_1X%ACT PRUN
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Name: qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in...
Source: NCGC
Target: TDP1 protein [Homo sapiens]
External Id: TDP1100
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Name: qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in...
Source: NCGC
Target: TDP1 protein [Homo sapiens]
External Id: TDP1101
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Name: Schnurri-3 Inhibitors: specific inducers of adult bone formation Measured in Cell-Bas...
Source: Broad Institute
Target: N/A
External Id: 2134-01_Inhibitor_SinglePoint_HTS_Activity_Set2
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Name: Fluorescence polarization to screen for inhibitor that competite the binding of FadD2...
Source: Broad Institute
Target: FATTY-ACID-CoA LIGASE FADD28 (FATTY-ACID-CoA SYNTHETASE)
External Id: 2147-01_Inhibitor_SinglePoint_HTS_Activity
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Name: Bursicon-induced LGR2 mediated cAMP production in LGR-2/CRE6x-Luciferase co-transfect...
Source: Broad Institute
Target: 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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Name: High throughput screen for small molecule inhibitors of a hypoxia-regulated fluoresce...
Source: ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
Target: N/A
External Id: HMS1149-MLP
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Name: qHTS for Inhibitors of AMA1-RON; Towards Development of Antimalarial Drug Lead: Prima...
Source: NCGC
Target: apical membrane antigen 1, AMA1 [Plasmodium falciparum 3D7]
External Id: AMA1100
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