NRX-103094
NRX-103094
Résumé du produit
Aperçu rapide
- Famille de produits
- PROTAC, E3 Ligands & Proximity-Inducing Building Blocks
- Nom chimique
- NRX-103094
- FM
- C20H11Cl2F3N2O4S
- PM
- 503.3
NRX-103094 is a halogenated pyridone-benzoic acid compound identified by CAS 2763260-36-0.
The verified record matches molecular formula C20H11Cl2F3N2O4S, molecular weight about 503.3, PubChem CID 137628320, and InChIKey HFBGFWJURBVNFD-UHFFFAOYSA-N.
The identifiers support comparison of the dichlorophenyl sulfanyl, trifluoromethyl pyridone, and benzoic acid features across catalog records.
Identité et spécifications
| Catalog No. | CH57008 |
| CAS No. | 2763260-36-0 |
| Chemical Name | NRX-103094 |
| Molecular Formula | C20H11Cl2F3N2O4S |
| Molecular Weight | 503.3 |
| PubChem CID | 137628320 |
| IUPAC Name | 3-[[4-(2,6-dichlorophenyl)sulfanyl-2-oxo-6-(trifluoromethyl)-1H-pyridine-3-carbonyl]amino]benzoic acid |
| InChIKey | HFBGFWJURBVNFD-UHFFFAOYSA-N |
Contexte d’application
- Chemical identity reference: supports matching NRX-103094 with CAS 2763260-36-0 and PubChem CID 137628320.
- Halogenated pyridone context: provides a record for a dichlorophenyl sulfanyl, trifluoromethyl pyridone, and benzoic acid structure.
- Catalog data alignment: helps keep formula C20H11Cl2F3N2O4S, molecular weight, CAS number, and InChIKey consistent across records.
Informations complémentaires sur le matériau
Utilisations
NRX-103094 can be matched by CAS 2763260-36-0, formula C20H11Cl2F3N2O4S, molecular weight about 503.3, PubChem CID 137628320, and InChIKey HFBGFWJURBVNFD-UHFFFAOYSA-N.
Caractéristiques
- Pyridone-benzoic acid structure containing dichlorophenyl sulfanyl and trifluoromethyl substituents.
- Halogenated sulfur-containing compound with formula C20H11Cl2F3N2O4S.
- CAS and name lookups both resolve to PubChem CID 137628320.
Ressources techniques associées
Sources publiques
- 3-{4-[(2,6-Dichlorophenyl)sulfanyl]-2-oxo-6-(trifluoromethyl)-1,2-dihydropyridine-3-amido}benzoic acid | PubChem CID 137628320
- Catalytic in vivo protein knockdown by small-molecule PROTACs
Nature Chemical Biology, 2015
Product-family technical context
- Structural basis of PROTAC cooperative recognition for selective protein degradation
Nature Chemical Biology, 2017
Product-family technical context
- Structural Basis of PROTAC Cooperative Recognition for Selective Protein Degradation
Nature Chemical Biology, 2017
Product-family technical context
- 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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