LTbetaR-IN-1
LTbetaR-IN-1

製品概要
クイックビュー
- 製品ファミリー
- PROTAC, E3 Ligands & Proximity-Inducing Building Blocks
- 化学名
- LTbetaR-IN-1
- 分子式
- C18H16N4O2
- 分子量
- 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.
同定情報と仕様
| 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 |
用途情報
- 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.
補足材料情報
用途
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.
特性
- 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.
関連技術資料
公開情報源
- 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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