NRX-1933
NRX-1933
Resumen del producto
Vista rápida
- Familia de productos
- PROTAC, E3 Ligands & Proximity-Inducing Building Blocks
- Nombre químico
- NRX-1933
- FM
- C14H9F3N6O2
- PM
- 350.26
NRX-1933 is a trifluoromethyl pyridone carboxamide compound identified by CAS 2763260-30-4.
The verified record matches molecular formula C14H9F3N6O2, molecular weight 350.26, PubChem CID 137628322, and InChIKey IAVMZDPIQIVLOG-UHFFFAOYSA-N.
The identifiers support comparison of the trifluoromethyl pyridone and tetrazolyl phenyl carboxamide features across catalog records.
Identidad y especificaciones
| Catalog No. | CH57012 |
| CAS No. | 2763260-30-4 |
| Chemical Name | NRX-1933 |
| Molecular Formula | C14H9F3N6O2 |
| Molecular Weight | 350.26 |
| PubChem CID | 137628322 |
| IUPAC Name | 2-oxo-N-[3-(2H-tetrazol-5-yl)phenyl]-6-(trifluoromethyl)-1H-pyridine-3-carboxamide |
| InChIKey | IAVMZDPIQIVLOG-UHFFFAOYSA-N |
Contexto de aplicación
- Chemical identity reference: supports matching NRX-1933 with CAS 2763260-30-4 and PubChem CID 137628322.
- Pyridone carboxamide context: provides a record for a trifluoromethyl pyridone and tetrazolyl phenyl carboxamide structure.
- Catalog data alignment: helps keep formula C14H9F3N6O2, molecular weight, CAS number, and InChIKey consistent across records.
Información adicional del material
Usos
NRX-1933 can be matched by CAS 2763260-30-4, formula C14H9F3N6O2, molecular weight 350.26, PubChem CID 137628322, and InChIKey IAVMZDPIQIVLOG-UHFFFAOYSA-N.
Características
- Trifluoromethyl pyridone carboxamide structure bearing a tetrazolyl phenyl group.
- Fluorinated nitrogen-rich compound with formula C14H9F3N6O2.
- CAS and name lookups both resolve to PubChem CID 137628322.
Recursos técnicos relacionados
Fuentes públicas
- 2-oxo-N-[3-(2H-tetrazol-5-yl)phenyl]-6-(trifluoromethyl)-1H-pyridine-3-carboxamide | PubChem CID 137628322
- Catalytic in vivo protein knockdown by small-molecule PROTACs
Nature Chemical Biology, 2015
Product-family technical context
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Nature Chemical Biology, 2017
Product-family technical context
- Structural Basis of PROTAC Cooperative Recognition for Selective Protein Degradation
Nature Chemical Biology, 2017
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- Direct-to-Biology Accelerates PROTAC Synthesis and the Evaluation of Linker Effects on Permeability and Degradation
ACS Medicinal Chemistry Letters, 2022
Product-family technical context
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