Una solución en etanol for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Conservar a -20°C Ships Hielera + almohadillas de hielo Check lot-specific COA for exact specifications.
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
El EDHF (factor hiperpolarizante derivado del endotelio) es un mediador no identificado liberado por las células endoteliales vasculares en respuesta a la acetilcolina y la bradicinina, distinto de los vasodilatadores derivados de la NOS (óxido nítrico) y la COX (prostaciclina). El metabolismo del citocromo P450 (CYP450) de los ácidos grasos poliinsaturados produce epóxidos como 14(15)-EpETrE, que son los principales candidatos a mediador activo real. Sin embargo, los metabolitos CYP450 del ácido eicosapentaenoico (EPA) y del ácido docosahexaenoico (DHA) se han estudiado poco en comparación con los metabolitos de la araquidonato epoxigenasa. el 19(20)-EpDPE es un metabolito de la epoxigenasa del DHA, que se deriva a través de la epoxidación del doble enlace ω-3 del DHA. No se ha determinado la actividad EDHF del 19(20)-EpDPE. Los metabolitos epoxigenasa del DHA también se han detectado en un modelo de inflamación murino.
| Sonrisas canónicas | CC(C)N1C=NC=C1C=O |
|---|---|
| IUPAC Name | 3-propan-2-ylimidazole-4-carbaldehyde |
| InChIKey | VGIWEUWQSDSUIF-UHFFFAOYSA-N |
| INCHI | 1S/C7H10N2O/c1-6(2)9-5-8-3-7(9)4-10/h3-6H,1-2H3 |
| Isómeros SMILES | CC(C)N1C=NC=C1C=O |
| Peso molecular | 344.5 |
| Reaxy-Rn | 116343 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=116343&ln= |
Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS →Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA →Full quality attributes and acceptance criteria for this grade.
View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organoheterocyclic compounds |
| Clase | Azoles |
| Subclass | Imidazoles |
| Intermediate Tree Nodes | Substituted imidazoles |
| Direct Parent | Carbonylimidazoles |
| Alternative Parents | Aryl-aldehydes N-substituted imidazoles Heteroaromatic compounds Azacyclic compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives |
| Molecular Framework | Aromatic heteromonocyclic compounds |
| Substituents | Aryl-aldehyde - Imidazole-4-carbonyl group - N-substituted imidazole - Heteroaromatic compound - Azacycle - Organic nitrogen compound - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Aldehyde - Aromatic heteromonocyclic compound |
| Descripción | This compound belongs to the class of organic compounds known as carbonylimidazoles. These are substituted imidazoles in which the imidazole ring bears a carbonyl group. |
| External Descriptors | Not available |
| Peso molecular | 138.170 g/mol |
|---|---|
| XLogP3 | 0.500 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 2 |
| Exact Mass | 138.079 Da |
| Monoisotopic Mass | 138.079 Da |
| Topological Polar Surface Area | 34.900 Ų |
| Heavy Atom Count | 10 |
| Formal Charge | 0 |
| Complexity | 125.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 0 |
| Covalently-Bonded Unit Count | 1 |
