Catalog name Description price
R-C-5523 C8 PEG Ceramide CAS:212116-76-2 C8 PEG Ceramide CAS: 212116-76-2 is a product of sphingolipid metabolism, and its acyl chain length is different. For the research preparation of liposomes and preparation of PEGylated lipoplexes. price>
R-C-5525 DSPE-PEG2000-SS-RGD DSPE stands for 1,2-distearoyl-sn-glycero-3-phosphoethanolamine,which is a phospholipid derivative commonly used in drug delivery systems.PEG2000 refers to polyethylene glycol 2000,a polymer that provides stability and solubility to the compound. SS can be cleaved in response to specific stimuli such as the presence of reducing agents. RGD is the abbreviation for the amino acid sequence Arg-Gly-Asp,which is a recognition motif for integrin receptors commonly found on cells. price>
R-C-5527 DSPE-Se-Se-PEG-ADA The presence of diselenide bonds in DSPE-Se-Se-PEG-ADA allows for its redox-responsive behavior. Under specific conditions,such as the presence of high levels of reducing agents,the diselenide bonds can be cleaved, leading to the release of the ADA enzyme from the liposomes.This property can be exploited to trigger the controlled release or activation of ADA in the targeted cells or tissues. price>
R-C-5529 18:1 PDP PE CAS:474944-13-3 DOPE-SPDP DOPE stands for 1,2-dioleoyl-sn-glycero-3-phosphoethanolamine. It is a phospholipid commonly found in liposomes or lipid nanoparticles used for drug delivery. DOPE provides stability and fluidity to the lipid bilayer, facilitating the encapsulation and delivery of therapeutic agents.SPDP stands for N-succinimidyl 3-(2-pyridyldithio) propionate. It is a bifunctional cross-linking reagent used to link molecules together in bioconjugation reactions. price>
R-C-5531 DOPE-HA DOPE-HA is a conjugation system that combines DOPE with HA to create targeted drug delivery systems. By leveraging the properties of DOPE for lipid-based delivery and HA for specific receptor targeting,it offers potential benefits in cancer therapy and other applications where specific targeting and efficient drug delivery are desired. price>
R-C-5542 DPPE-PEG400-dibenzylcyclooctyne The hydrophobic properties of the DSPE allow for the encapsulation and congregation of other hydrophobic drugs. The hydrophilic PEG linker increases the water solubility of the overall compound allowing for the delivery of the drug. The DBCO group can be used for copper-free Click Chemistry reactions. price>
R-C-5551 DSPE-PEG45-NH-Mal DSPE-PEG45-NH-Mal is a compound used in the field of drug delivery and molecular conjugation. It combines a phospholipid derivative(DSPE),a hydrophilic polymer with an average molecular weight of 45 units(PEG45),an amino group(NH)for further modifications,and a maleimide group(Mal)for specific conjugation to thiol-containing molecules.This structure enables the conjugation of drugs,targeting ligands,or other molecules to DSPE-PEG45-NH-Mal for targeted drug delivery or other biomedical applications. price>
R-C-5553 Amino-Gly-Gly-DSPE Amino-Gly-Gly-DSPE is a lipid molecule that consists of a glycerol backbone linked to a long hydrophobic acyl chain and an amino acid dipeptide, glycine-glycine, attached to the glycerol through an amide bond.The long acyl chains of DSPE provide hydrophobic properties, making it suitable for the self-assembly of lipids into lipid bilayers. price>
R-C-7142 DSPE-PEG-TK-NHS NHS-TK-PEG-DSPE,DSPE provides hydrophobicity and cell membrane penetration ability,PEG enhances biocompatibility and stability,TK(thioketal)functional group is sensitive to reactive oxygen species for drug controlled release,and NHS functional group can undergo coupling reactions with molecules containing amino groups (such as proteins, antibodies,etc.). price>
R-C-7143 DSPE-HYD-PEG-RVG29 The core structure of DSPE-HYD-PEG consists of three parts DSPE,Hyd bond,and PEG. This molecule combines amphiphilicity,environmental responsiveness,and targeting ability, and is widely used in nanomedicine delivery systems.RVG29(rabies virus glycoprotein derived peptide)is a peptide that targets nerve cells and achieves blood-brain barrier penetration by binding to acetylcholine receptors. price>