Azido-PEG6-NHS ester
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Category | Azido-PEGn-NHS ester |
Catalog NO. | BPG-2224 |
Product Name | Azido-PEG6-NHS ester |
CAS | 2055014-64-5 |
Molecular Formula | C19H32N4O10 |
Molecular Weight | 476.48 |
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Description | Azido-PEG6-NHS ester is a cleavable 6 unit PEG ADC linker used in the synthesis of antibody-drug conjugates (ADCs). Azido-PEG6-NHS ester is also a PEG- and Alkyl/ether based PROTAC linker that can be used in the synthesis of PROTACs. |
Synonyms | Azido-PEG6-NHS;Azido-PEG6-CH2CO2-NHS; N3-PEG6-C2-NHS ester; N3-PEG6-CH2CH2COONHS Ester; 1-[(1-Azido-21-oxo-3,6,9,12,15,18-hexaoxahenicosan-21-yl)oxy]-2,5-pyrrolidinedione; 2,5-Pyrrolidinedione, 1-[(21-azido-1-oxo-4,7,10,13,16,19-hexaoxaheneicos-1-yl)oxy]-; 2,5-Dioxopyrrolidin-1-yl 1-azido-3,6,9,12,15,18-hexaoxahenicosan-21-oate |
IUPAC Name | (2,5-dioxopyrrolidin-1-yl) 3-[2-[2-[2-[2-[2-(2-azidoethoxy)ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]propanoate |
Canonical SMILES | C1CC(=O)N(C1=O)OC(=O)CCOCCOCCOCCOCCOCCOCCN=[N+]=[N-] |
InChI | InChI=1S/C19H32N4O10/c20-22-21-4-6-28-8-10-30-12-14-32-16-15-31-13-11-29-9-7-27-5-3-19(26)33-23-17(24)1-2-18(23)25/h1-16H2 |
InChIKey | WXKOAPGNZNSYPW-UHFFFAOYSA-N |
Purity | ≥95% |
Solubility | Soluble in DCM, DMF, DMSO, Water |
Related CAS | 1108750-59-9 (polymer) |
Appearance | Pale Yellow or Colorless Oily Liquid |
Shelf Life | 0-4°C for short term (days to weeks), or -20°C for long term (months). |
Storage | Store at -20°C, keep in dry and avoid sunlight |
Azido-PEG6-NHS ester, a versatile chemical reagent in the realms of bioconjugation and molecular biology, finds diverse applications. Here are four key applications portrayed with high perplexity and burstiness: Protein Labeling: Widely embraced in protein research, Azido-PEG6-NHS ester plays a pivotal role in labeling proteins with azide groups, setting the stage for subsequent bioorthogonal reactions. By engaging with primary amines on proteins, it facilitates the attachment of PEGylated azide groups that can be conjugated with various probes or tags using click chemistry. This methodology is indispensable for exploring protein interactions, cellular localization, and dynamics with unparalleled depth and precision. Drug Delivery: In the sphere of drug delivery, Azido-PEG6-NHS ester emerges as a key player in modifying therapeutic molecules or carrier systems like nanoparticles or liposomes. The ensuing azide-functionalized compounds can be further tethered to targeting ligands or drug molecules, enhancing selective delivery to specific tissues or cells. This strategic approach not only boosts the efficacy of therapeutic agents but also mitigates unwanted side effects, heralding a new era of targeted and efficient drug delivery mechanisms. Surface Functionalization: Harnessing the power of Azido-PEG6-NHS ester, researchers unlock the potential to functionalize surfaces of diverse materials, from microarray chips to biomaterials and sensors. By introducing azide groups onto surfaces, it creates docking sites for covalent attachment of an array of molecules through click chemistry, paving the way for the development of bioactive surfaces with a myriad of applications. This innovation serves as a cornerstone for the advancement of biosensors, tissue engineering scaffolds, and diagnostic tools, driving progress in biotechnological research and applications. Crosslinking Studies: Delving into the intricate realm of biomolecular interactions, Azido-PEG6-NHS ester stands as a valuable tool in crosslinking experiments aimed at studying and stabilizing complexes. Through its interaction with various proteins or nucleic acids, it forms bridges through a flexible PEG linker, maintaining the native conformation of molecules while allowing controlled distance modulation. This methodology proves particularly invaluable in structural biology and biophysical studies, shedding light on the spatial arrangement of molecules and unlocking key insights into molecular interactions and structures. |
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Resources
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Technical Information
- Aqueous Two-Phase System (ATPS) Technique
- Capillary Electrophoresis (CE) Technique
- Enzyme-linked immunosorbent assay (ELISA) Technique
- High performance liquid chromatography (HPLC) Technique
- How to Perform Polyethylene Glycol (PEG) Modification?
- Hydrophobic Interaction Chromatography (HIC) Technique
- Introduction of Polyethylene Glycol (PEG)
- Ion Exchange Chromatography (IEX) Technique
- PEG for Chemical Synthesis
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- PEG Purification Techniques of Plasmid DNA
- PEGylated Protein Purification Techniques
- Polyethylene Glycol (PEG) Modifier Selection Guide
- Radiolabeling Technique
- SDS-PAGE Technique
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Industry News
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- FDA-Approved Antibody-Drug Conjugates up to 2024
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- Lipid Classification and Drug Delivery Systems
- Lipid Formulations: Key Absorption-Enhancing Technologies in New Drug Development
- Lipid-Drug Conjugates (LDCs) for Nanoparticle Drug Delivery
- Liposome in Drug Delivery
- Overview of Liposome Preparation Process
- PEG in Pharmaceutical Preparations (I): Solvents, Lubricants, Adhesives and More
- PEG in Pharmaceutical Preparations (II): Stabilizers, Plasticizers and Modification Materials
- PEG Linkers in Antibody Drug Conjugates and PROTACs
- PEG-DSPE Block Copolymers and Their Derivatives
- PEGylated Drugs: Definition, Structure, Classification and Benefits
- PEGylated RGD Peptides: A Promising Tool for Targeted Drug Delivery
- Pharmacokinetics and Bioanalysis of PEGylated Drugs
- Polyethylene Glycol (PEG) Modified Targeting Nanomaterials
- Preparation Method of PEG Hydrogel
- The PROTAC Technology in Drug Development
- Vaccines: Definition, History, Ingredients, Types and Mechanism of Action
- What are Lipid Excipients and Their Applications?
- What are Lipid Nanoparticles and Their Applications?
- What are Lipid-Drug Conjugates (LDCs)?
- What are Lipids?
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- What are PEG Lipids?
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