2H-Benzimidazol-2-one,1,3-dihydro-1-[1-(2-phenoxyethyl)-4-piperidinyl] structure
|
Common Name | 2H-Benzimidazol-2-one,1,3-dihydro-1-[1-(2-phenoxyethyl)-4-piperidinyl] | ||
|---|---|---|---|---|
| CAS Number | 5322-53-2 | Molecular Weight | 337.41600 | |
| Density | 1.208g/cm3 | Boiling Point | N/A | |
| Molecular Formula | C20H23N3O2 | Melting Point | N/A | |
| MSDS | N/A | Flash Point | N/A | |
Use of 2H-Benzimidazol-2-one,1,3-dihydro-1-[1-(2-phenoxyethyl)-4-piperidinyl]Oxiperomide is an orally active dopamine-blocking agent[1]. |
| Name | 3-[1-(2-phenoxyethyl)piperidin-4-yl]-1H-benzimidazol-2-one |
|---|---|
| Synonym | More Synonyms |
| Description | Oxiperomide is an orally active dopamine-blocking agent[1]. |
|---|---|
| Related Catalog | |
| References |
| Density | 1.208g/cm3 |
|---|---|
| Molecular Formula | C20H23N3O2 |
| Molecular Weight | 337.41600 |
| Exact Mass | 337.17900 |
| PSA | 50.26000 |
| LogP | 2.98340 |
| Index of Refraction | 1.607 |
| InChIKey | NVDBBGBUTKLRSN-UHFFFAOYSA-N |
| SMILES | O=c1[nH]c2ccccc2n1C1CCN(CCOc2ccccc2)CC1 |
| HS Code | 2933990090 |
|---|
| HS Code | 2933990090 |
|---|---|
| Summary | 2933990090. heterocyclic compounds with nitrogen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0% |
|
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
|
|
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
|
|
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
|
|
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
|
|
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
|
|
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
|
|
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
|
|
Name: Primary Screen Inhibitors of CD40 Signaling in BL2 Cells Measured in Cell-Based Syste...
Source: Broad Institute
Target: N/A
External Id: 7124-01_Inhibitor_SinglePoint_HTS_Activity
|
|
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
|
|
Name: Fluorescence polarization-based biochemical high throughput primary assay to identify...
Source: The Scripps Research Institute Molecular Screening Center
Target: abhydrolase domain-containing protein 4 isoform 1 [Mus musculus]
External Id: ABHD4_INH_FP_1536_1X%INH PRUN
|
| Peromide |
| Oxiperomida |
| 1-[1-(2-phenoxyethyl)piperidin-4-yl]-1,3-dihydro-2h-benzimidazol-2-one |
| Oxiperomide |
| R-4714 |
| 1-[1-(2-phenoxy-ethyl)-piperidin-4-yl]-1,3-dihydro-benzoimidazol-2-one |
| Oxiperomidum |
| 1-(1-(2-phenoxyethyl)piperidin-4-yl)-1H-benzo[d]imidazol-2(3H)-one |
| Oxiperomide (USAN/INN) |