3-morpholin-4-ylphenalen-1-one
Modify Date: 2025-08-26 09:32:29
3-morpholin-4-ylphenalen-1-one structure
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Common Name | 3-morpholin-4-ylphenalen-1-one | ||
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| CAS Number | 3357-17-3 | Molecular Weight | 265.30600 | |
| Density | 1.309g/cm3 | Boiling Point | 470.8ºC at 760 mmHg | |
| Molecular Formula | C17H15NO2 | Melting Point | N/A | |
| MSDS | N/A | Flash Point | 238.6ºC | |
| Name | 4-(1-ethyl-propenyl)-morpholine |
|---|---|
| Synonym | More Synonyms |
| Density | 1.309g/cm3 |
|---|---|
| Boiling Point | 470.8ºC at 760 mmHg |
| Molecular Formula | C17H15NO2 |
| Molecular Weight | 265.30600 |
| Flash Point | 238.6ºC |
| Exact Mass | 265.11000 |
| PSA | 29.54000 |
| LogP | 2.64710 |
| Index of Refraction | 1.692 |
| InChIKey | BOZSJCIQKDQGPW-UHFFFAOYSA-N |
| SMILES | O=C1C=C(N2CCOCC2)c2cccc3cccc1c23 |
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3-morpholin-4-y... CAS#:3357-17-3 |
| Literature: Cromwell et al. Journal of the American Chemical Society, 1951 , vol. 73, p. 1230 |
| Precursor 1 | |
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| DownStream 1 | |
CAS#:5472-84-4|
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: Antileishmanial activity against Leishmania amazonensis MHOM/BR/77/LTB0016 promastigo...
Source: ChEMBL
Target: Leishmania amazonensis
External Id: CHEMBL4141691
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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: Antileishmanial activity against Leishmania donovani MHOM/IN/90/GE1F8R promastigotes ...
Source: ChEMBL
Target: Leishmania donovani
External Id: CHEMBL4141690
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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: S100A4: HTS Measured in Biochemical System Using Plate Reader - 7045-01_Inhibitor_Dos...
Source: Broad Institute
Target: S100A4 (Hs)
External Id: 7045-01_Inhibitor_Dose_CherryPick_Activity
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| 4-(1-ethylprop-1-en-1-yl)morpholine |
| 3-morpholino-phenalen-1-one |
| Morpholine,4-[(1E)-1-ethyl-1-propenyl] |
| 3-morpholinopent-2-ene |
| 3-morpholin-4-yl-phenalen-1-one |
| 3-morpholino-2-pentene |
| 3-Morpholino-phenalen-1-on |