Catalog |
name |
Description |
price |
R-C-6351 |
DSPE-GPLGIAGQ-PEG5000 |
DSPE-GPLGIAGQ-PEG,Distearoylphosphatidylethanolamine(DSPE)is a phospholipid derivative often used for the preparation of liposomes or nanoparticle systems in drug delivery due to its amphiphilic nature.GPLGIAGQ are short chains of amino acids. |
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R-C-6423 |
DSPE-PEG2000-CEPLQLKM-K-FITC |
DSPE-PEG-CEPLQLKM-K-FITC,1,2-Distearoyl-sn-glycero-3-phosphoethanolamine, a phospholipid commonly used in the creation of liposomes or as part of the lipid bilayer in nanoparticle formulations for drug delivery.Polyethylene glycol is a hydrophilic polymer .DSPE-PEG-CEPLQLKM-K-FITC is a construct where a fluorescent dye(FITC)is attached to a peptide(CEPLQLKM) that is further linked to a PEGylated phospholipid(DSPE-PEG).The entire conjugate can self-assemble into structures such as micelles or be used to modify the surface of liposomes or nanoparticles to achieve specific biological targeting with a fluorescent tag for visualization. |
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R-C-6424 |
DSPE-PEG5000-CBT |
DSPE-PEG-CBT,The DSPE domain allows for easy incorporation into liposomal formulations.The PEG helps to improve the pharmacokinetics of the formulation.Finally,the CBT moiety can be used for the site-specific attachment of targeting ligands or therapeutic agents that contain the complementary reactive group. |
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R-C-6425 |
DSPE-PEG2K-PSMA |
DSPE-PEG-PSMA,DSPE imparts stability and biocompatibility to liposomes and other lipid-based drug delivery systems.PEG is often used in drug delivery systems to increase circulation time in the bloodstream and reduce clearance by the immune system.PSMA (Prostate-Specific Membrane Antigen) is a protein target often found on the surface of prostate cancer cells.PSMA is likely serving as a targeting ligand.By conjugating PSMA to the DSPE-PEG2K compound, the resulting bioconjugate may be intended for the targeted delivery of drugs or imaging agents to prostate cancer cells bearing the PSMA receptor. |
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R-C-6426 |
DSPE-PEG2000-ANTPCGPYTHDCPVKR |
DSPE-PEG-ANTPCGPYTHDCPVKR,DSPE(1,2-distearoyl-sn-glycero-3-phosphoethanolamine)is a phospholipid that is often employed as a component in the formulation of liposomes and other lipid-based drug delivery systems.PEG is often used in drug delivery to enhance drug circulation time and reduce nonspecific interactions,thereby potentially improving the bioavailability of the delivered drug.This DSPE-PEG can couple peptides and other functional groups,such as ANTPCGPYTHDCPVKR,etc. |
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R-C-6428 |
DPPS-PEG2000-NH2 |
DPPS-PEG-NH2,DPPS-PEG-Amine,DPPS-PEG-NH2 is a molecular construct used in the field of nanomedicine and drug delivery.DPPS (1,2-dipalmitoyl-sn-glycero-3-phospho-L-serine) is a phospholipid that can form lipid bilayers and is often used in the design of liposomes and lipid-based drug delivery systems.PEG is a hydrophilic polymer commonly used in drug delivery systems to improve circulation time and reduce immunogenicity.DPPS-PEG-NH2 forms a complex designed for the targeted delivery of drugs, imaging agents, or other compounds to specific tissues or cells,potentially enhancing their pharmacokinetics and therapeutic effects. |
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R-C-6432 |
DSPE-PEG2000-TK-PEI1800 |
DSPE-PEG-TK-PEI,DSPE is the lipophilic part that anchors the molecule into liposomal or other lipid-based carriers,PEG serves as a hydrophilic linker,and PEI is the terminal part that may be used for binding and condensing nucleic acids for gene delivery.This kind of molecule could have potential applications in the delivery of genetic material to cells. |
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R-C-6436 |
DSPE-PEG2000-YTIWMPENPRPGTPCDIFTNSRGKRASNGC-FITC |
Such a molecular construct would be used in biomedical applications,potentially for the targeted delivery of drugs where the DSPE embeds the complex into liposome nanoparticles,the PEG2000 provides aqueous stability and stealth,the peptide mediates targeting,and the FITC allows for imaging and tracking of the delivery system.This setup would allow for the therapeutic payload to be delivered to a specific site while minimizing side effects and maximizing treatment efficacy. |
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R-C-6440 |
DSPE-TK-PEG2K-LSALTPSPSWLKYKAL |
DSPE-TK-PEG-LSALTPSPSWLKYKAL,DSPE would anchor the construct within a lipid bilayer of a liposome,the PEG would extend out from the surface,providing water solubility and biocompatibility,and the peptide sequence would be presented on the exterior for interaction with specific cellular targets.The thioketal(TK) component would be part of the linker that holds these units together. |
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R-C-6441 |
DSPE-PEG2000-CSTSMLK(Ac)AC |
DSPE-PEG-CSTSMLK(Ac)AC,The DSPE moiety serves as the lipid-soluble part that can be used to integrate this molecule into a liposomal or micelle structure.The PEG segment confers hydrophilicity and stealth properties to improve the pharmacokinetic profile of the liposome or drug delivery system.The peptide CSTSMLK(Ac)AC is likely to have a specific biological function or targeting capability.The modification of lysine with an acetyl group could be crucial for the peptides activity or its stability. |
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