LTbetaR-IN-1
LTbetaR-IN-1
Résumé du produit
Aperçu rapide
- Famille de produits
- PROTAC, E3 Ligands & Proximity-Inducing Building Blocks
- Nom chimique
- LTbetaR-IN-1
- FM
- C18H16N4O2
- PM
- 320.35
LTbetaR-IN-1 is a small organic compound identified by CAS 2189366-77-4.
PubChem CID 51819448 and ChemicalBook support molecular formula C18H16N4O2 and molecular weight 320.35.
The verified IUPAC name describes a benzimidazole-linked isoindolinone propanamide structure.
Identité et spécifications
| Catalog No. | CH57006 |
| CAS No. | 2189366-77-4 |
| Product Name | LTbetaR-IN-1 |
| Synonyms | LT-beta-R-IN-1; Compound 919278 |
| Molecular Formula | C18H16N4O2 |
| Molecular Weight | 320.35 |
| PubChem CID | 51819448 |
| InChIKey | PWSSISUOJZBZFT-LLVKDONJSA-N |
| IUPAC Name | (2R)-N-(1H-benzimidazol-2-yl)-2-(3-oxo-1H-isoindol-2-yl)propanamide |
Contexte d’application
- Identity matching: connects LTbetaR-IN-1, LT-beta-R-IN-1, Compound 919278, and CAS 2189366-77-4.
- Structure reference: provides formula, molecular weight, IUPAC name, and InChIKey for compound comparison.
- Name cross-reference: supports consistent lookup between Greek-beta display text and the ASCII LTbetaR-IN-1 form.
Informations complémentaires sur le matériau
Utilisations
LTbetaR-IN-1 can be identified by CAS number, formula, molecular weight, PubChem CID, InChIKey, and the verified IUPAC name. These fields provide the clearest public basis for comparing the compound with related small-molecule records.
Caractéristiques
- Small organic compound with formula C18H16N4O2.
- PubChem and ChemicalBook agree on identity, formula, and molecular weight.
- Verified structure name includes benzimidazole, isoindolinone, and propanamide features.
Ressources techniques associées
Sources publiques
- LTbetaR-IN-1 | PubChem CID 51819448
- 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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