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| Catalog | name | Description | price |
|---|---|---|---|
| R-C-7577 | DSPE-PEG-TPP-CY5 | DSPE-PEG2K-TPP-CY5,PEG chains are connected to DSPE through esterification or amidation reactions, forming a hydration layer to reduce non-specific adsorption and prolong the circulation time of the material in biological media.As a mitochondrial targeting group TPP(Triphenyl phosphate)structure interacts with the mitochondrial membrane potential through positive charges,achieving precise subcellular localization,Cyanine5 is a commonly used indocyanine near-infrared fluorescent dye,widely used for fluorescence labeling in the field of biomedical research.This product is only for scientific research and cannot be used on the human body. | price> |
| R-C-7578 | DSPE-PEG-HFBA | HFBA-PEG-DSPE,DSPE-PEG-HFBA exhibits good uniformity and dispersion stability in buffer solution.The hydration of PEG segments prolongs the cycle time,while the Heptafluorobutyric Anhydride group enhances thermodynamic stability through its fluorine repellent properties.Its self-assembly behavior is influenced by environmental parameters such as H or ionic strength,and can form controllable micelles or liposomes,providing a foundation for functional applications.This product is only for scientific research and cannot be used on the human body. | price> |
| R-C-7579 | DSPE-PEG-CRLTRKRGLK | CRLTRKRGLK-PEG-DSPE,A lipid polyethylene glycol peptide conjugate composed of DSPE phospholipids,PEG chains,and functional CRLTRKRGK peptides is used for surface modification of nanocarriers to enhance targeting,cellular uptake, and delivery efficiency.CRLTRKRGLK is a cell targeted transmembrane peptide sequence,belonging to alkaline peptides,generally responsible for guiding the entire delivery carrier to specifically target tumor cells or penetrate cell membranes,improving the intracellular delivery efficiency of drugs.This product is only for scientific research and cannot be used on the human body. | price> |
| R-C-7585 | DSPE-PEG-CHRHTKQRHTALH | DSPE-PEG2k-CHRHTKQRHTALH,CHRHTKQRHTALH-PEG-DSPE,DSPE-PEG-HRH,The hydrophobic DSPE tail can be embedded in a lipid bilayer,and the hydrophilic PEG chain can extend outward, spontaneously forming nanostructures such as liposomes and micelles in aqueous phase. The CHRHTKQRHTALH peptide specifically recognizes high metastatic potential tumor cells,mediates carrier targeted binding and penetration into tumor cells,and achieves precise delivery of anti-tumor drugs to metastatic lesions.This product is only for scientific research and cannot be used on the human body. | price> |
| R-C-7586 | DSPE-PEG-PPRRGLIKLKTSGPAC(MAL-SH) | DSPE-PEG2K-PPRRGLIKLKTSGPAC(MAL-SH),PPRRGLIKLKTSGPAC-PEG-DSPE,DSPE is responsible for hydrophobic anchoring embedded in nanocarrier lipid membranes,while PEG is responsible for providing long-term cycling stability and reducing non-specific clearance.PPRRGLIKLKTSGPAC is an ovarian cancer specific targeted transmembrane peptide responsible for mediating nanocarrier targeted binding and penetration of ovarian cancer cells,enhancing drug lesion enrichment efficiency.This product is only for scientific research and cannot be used on the human body. | price> |
| R-C-7590 | DSPE-PEG-CDCA | DSPE-PEG2K-CDCA,CDCA-PEG-DSPE,DSPE-PEG-Chenodeoxycholic acid,DSPE is responsible for hydrophobic anchoring embedded in nanocarrier lipid membranes,while PEG is responsible for providing long-term cycling stability and reducing non-specific clearance.CDCA (Deoxycholic Acid)is a natural bile acid that not only enhances overall hydrophobicity but also improves self-assembly stability;It can also specifically bind to bile acid receptors(ASBT,NTCP,etc.)on the surface of intestinal and liver cells,mediate targeted delivery of liver cells/hepatobiliary system,and activate FXR receptors,which can be used for research on bile acid related metabolic diseases.This product is only for scientific research and cannot be used on the human body. | price> |
| R-C-7591 | DSPE-PEG-DCA | DSPE-PEG-Deoxycholic Acid,DCA-PEG-DSPE,DSPE-PEG-DCA can be used as a component of lipid membranes to improve the stability, flexibility, and fluidity of liposome membranes. At the same time, the DCA at the PEG end further enhances the interaction between the membrane and cells, increasing cell uptake rate.This product is only for scientific research and cannot be used on the human body. | price> |
| R-C-7592 | DSPE-PEG-Benzenesulfonamide | Benzenesulfonamide-PEG-DSPE,DSPE(hydrophobic lipid anchor,embedded membrane bilayer), PEG (flexible hydrophilic spacer arm,enhances stability and long circulation),Benzenesulfonamide (targeting ligand,recognizes tumor associated carbonic anhydrase).Mainly used for tumor targeted drug delivery,molecular imaging probes,and liposome surface functionalization; Benzene sulfonamide can inhibit carbonic anhydrase activity,with dual effects of targeting and potential therapy.This product is only for scientific research and cannot be used on the human body. | price> |
| R-C-7593 | DSPE-PEG-GluNAC | DSPE-PEG2k-GluNAC,GluNAC-PEG-DSPE,DSPE PEG GluNAC is an amphiphilic phospholipid complex composed of phospholipids(DSPE),polyethylene glycol(PEG),and N-acetylglucosamine (GluNAc).Among them,DSPE provides a hydrophobic core and self-assembly ability,PEG chains enhance hydrophilicity and stability,and the terminal GluNAc endows the material with good interfacial functional properties and biometric potential.This product is only for scientific research and cannot be used on the human body. | price> |
| R-C-7594 | DSPE-PEOz-Galactose | Galactose-PEOz-DSPE,DSPE-PEOz-Galactose is a multifunctional lipid nanomaterial that targets liver cells with galactose and utilizes PEOz pH responsiveness for precise drug release.It combines biocompatibility and stability and is suitable for liver cancer treatment,immunotherapy, and gene delivery.This product is only for scientific research and cannot be used on the human body. | price> |
| R-C-7595 | DSPE-PEOz-GluNAC | DSPE is a hydrophobic phospholipid component that can be embedded in phospholipid bilayers of delivery carriers such as liposomes, nanomicelles,and LNP,stabilizing the carrier structure and preventing drug leakage.PEOz is a novel hydrophilic spacer arm with low immunogenicity and long in vivo circulation stability.N-acetylglucosamine derivatives are ligands that target the asialoglycoprotein receptor(ASGPR)in liver cells.This product is only for scientific research and cannot be used on the human body. | price> |
| R-C-7596 | DSPE-PEG-Creatine Phosphate | DSPE-PEG-Phosphocreatine,DSPE-PEG2K-Creatine Phosphate,Creatine Phosphate-PEG-DSPE,The hydrophobic tail of DSPE forms an amphiphilic structure with the hydrophilic chain of PEG,which can self assemble to form nanomicelles.Creatine phosphate is covalently connected to the PEG end,exposed on the surface of the micelles or embedded in the hydrophilic layer,ensuring the activity of creatine phosphate and avoiding its degradation during storage. | price> |
| R-C-7597 | DSPE-PEG-Palmitic Acid | DSPE-PEG-PA,Palmitic Acid-PEG-DSPE,DSPE itself is a phospholipid with good biocompatibility and amphiphilicity,capable of forming stable liposome structures in aqueous solutions.The introduction of PEG(polyethylene glycol)endows the compound with better water solubility and stability,prolonging its circulation time in vivo.Palmitic acid as a long-chain fatty acid,further enhances the hydrophobicity of compounds,enabling them to function better in specific biological environments. | price> |
| R-C-7598 | DSPE-PEG-TD139 | TD139-PEG-DSPE,DSPE-PEG-TD139 is a functionalized lipid derivative. DSPE provides a stable hydrophobic lipid anchoring skeleton that can be embedded in lipid bilayers or nano self-assembly systems.PEG serves as a hydrophilic flexible spacer segment to regulate spatial conformation,improve water phase dispersion,and reduce non-specific interfacial interactions. TD139 acts as the end functional unit,introducing specific molecular recognition features to endow the material with targeted binding ability and interface regulation function. | price> |
| R-C-7599 | DSPE-PEOz-TD139 | TD139-PEOz-DSPE,The molecular structure of DSPE-PEOz-TD139 consists of a hydrophobic distearoyl phosphatidylethanolamine (DSPE)anchored end,a hydrophilic poly(2-ethyl-2-oxazoline) (PEOz)chain segment,and a functionalized ligand TD139.Compared to traditional PEG chains, PEoz segments exhibit unique advantages in anti protein adsorption and prolonging in vivo circulation time,while TD139,as a high affinity ligand for galectin-3,endows the molecule with targeted recognition ability. | price> |
| R-C-7600 | DSPE-PEOz-TCPP | TCPP-PEOz-DSPE,DSPE-PEOz-TCPP is a highly customized amphiphilic block copolymer.Its molecular skeleton combines hydrophobic distearoyl phosphatidylethanolamine(DSPE), hydrophilic and stain resistant poly(2-ethyl-2-oxazoline)(PEOz)segments,and photosensitive Tetrakis (4-carboxyphenyl) porphyrin(TCPP)functional units.This composite structure endows the material with unique self-assembly ability,allowing it to form stable micelles or vesicles in aqueous environments while retaining the photophysical activity of TCPP. | price> |
| R-C-7601 | DSPE-PEG-Ambroxol | Ambroxol-PEG-DSPE,DSPE-PEG-Ambroxol typically refers to an amphiphilic lipid drug conjugate (DSPE-PEG-AMB)formed by covalently linking Ambroxol to the end of DSPE-PEG molecules. DSPE-PEG itself is a widely used PEGylated phospholipid material in the field of drug delivery, which can improve the stability of nanocarriers,prolong circulation time, and reduce the clearance of the reticuloendothelial system. | price> |
| R-C-7605 | DSPE-PEG-Idebenone | Idebenone-PEG-DSPE,DSPE-PEG2K-Idebenone achieves effective encapsulation of hydrophobic drugs through phospholipid self-assembly design;Improved water solubility and stability through PEG modification;By constructing nanocarriers, potential targeted delivery capabilities have been provided.This product is only for scientific research and cannot be used on the human body. | price> |
| R-C-7606 | DSPE-PEG-TK-Paeoniflorin | Paeoniflorin-TK-PEG-DSPE,DSPE-PEG-TK is an amphiphilic block material composed of distearoyl phosphatidylethanolamine(DSPE,hydrophobic anchor),thioketal(TK,reactive oxygen species/ROS responsive linker),and polyethylene glycol(PEG,hydrophilic stealth layer),used to construct tumor microenvironment responsive liposomes or nanomicelles that can break and release drug carriers under high ROS (such as tumor site)triggering.Paeoniflorin:It is an active pharmacological ingredient connected to the end of the material.Paeoniflorin itself has anti-inflammatory, anti-tumor,and antioxidant pharmacological activities.After coupling,it can achieve multiple effects of material modification,targeted drug delivery,and synergistic drug efficacy.This product is only for scientific research and cannot be used on the human body. | price> |
| R-C-7607 | DSPE-PEG-Paeoniflorin | Paeoniflorin-PEG-DSPE,DSPE-PEG is an amphiphilic lipid polymer block copolymer (1,2-distearoyl-sn-glycerin-3-phosphate ethanolamine polyethylene glycol)commonly used to construct PEGylated liposomes or nanomicelles,which can prolong in vivo circulation time and enhance stability.Paeoniflorin itself has anti-inflammatory,anti-tumor,and antioxidant pharmacological activities.After coupling,it can achieve multiple effects of material modification,targeted drug delivery,and synergistic drug efficacy.This product is only for scientific research and cannot be used on the human body. | price> |

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