911739
C5 Lenalidomide-PEG1-NH2 hydrochloride
≥95%
别名:
2-(2-Aminoethoxy)-N-(2-(2,6-dioxopiperidin-3-yl)-1-oxoisoindolin-5-yl)acetamide hydrochloride, C5 Lenalidomide conjugate, Crosslinker−E3 Ligase ligand conjugate, Protein degrader building block for PROTAC® research, Template for synthesis of targeted protein degrader
About This Item
推荐产品
ligand
C5 Lenalidomide
品質等級
化驗
≥95%
形狀
powder
反應適用性
reactivity: carboxyl reactive
reagent type: ligand-linker conjugate
官能基
amine
儲存溫度
2-8°C
SMILES 字串
O=C1N(C2CCC(NC2=O)=O)CC3=CC(NC(COCCN)=O)=CC=C31.Cl
1 of 4
此商品 | 911755 | 911720 | 917303 |
---|---|---|---|
≥95% | - | ≥95% | ≥95% |
reactivity: carboxyl reactive, reagent type: ligand-linker conjugate | reactivity: carboxyl reactive, reagent type: ligand-linker conjugate | reactivity: carboxyl reactive, reagent type: ligand-linker conjugate | reactivity: carboxyl reactive, reagent type: ligand-linker conjugate |
100 | 100 | 100 | 100 |
2-8°C | 2-8°C | 2-8°C | 2-8°C |
powder | powder or crystals | powder | powder or crystals |
應用
Automate your CRBN-PEG based PROTACs with Synple Automated Synthesis Platform (SYNPLE-SC002)
其他說明
Portal: Building PROTAC® Degraders for Targeted Protein Degradation
Targeted Protein Degradation by Small Molecules
Small-Molecule PROTACS: New Approaches to Protein Degradation
Targeted Protein Degradation: from Chemical Biology to Drug Discovery
法律資訊
相關產品
訊號詞
Warning
危險聲明
危險分類
Repr. 2 - STOT RE 2
標靶器官
Blood
儲存類別代碼
11 - Combustible Solids
水污染物質分類(WGK)
WGK 1
閃點(°F)
Not applicable
閃點(°C)
Not applicable
商品
Partial PROTACs are a collection of crosslinker-E3 ligand conjugates with a pendant functional group for covalent linkage to a target ligand.
Partial PROTACs are a collection of crosslinker-E3 ligand conjugates with a pendant functional group for covalent linkage to a target ligand.
Partial PROTACs are a collection of crosslinker-E3 ligand conjugates with a pendant functional group for covalent linkage to a target ligand.
Partial PROTACs are a collection of crosslinker-E3 ligand conjugates with a pendant functional group for covalent linkage to a target ligand.
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