| Catalog | name | Description | price |
|---|---|---|---|
| R-C-7647 | DSPE-PEG-Cyclohexanedione | Cyclohexanedione-PEG-DSPE,DSPE-PEG is a typical amphiphilic molecule,DSPE covalently linked to a hydrophilic polyethylene glycol chain(PEG).The DSPE part has a long-chain fatty acid structure that can be embedded in lipid bilayer systems,while the PEG chain exhibits a flexible linear structure that extends into the aqueous environment.Cyclohexanedione is an active functional group that can specifically bind to arginine residues in proteins through condensation reactions, achieving selective protein labeling and coupling for constructing targeted modified drug delivery systems.This product is only for scientific research and cannot be used on the human body. | price> |
| R-C-7648 | DSPE-PEG-Rhein | Rhein-PEG-DSPE,Rhein is a natural anthraquinone compound with various biological activities such as anti-inflammatory,antioxidant,anti-tumor,and antibacterial.Its hydrophobicity allows it to form a micelle core together with DSPE,while covalently modifying the PEG end to endow nanoparticles with pharmacological activity or targeted recognition function.This product is only for scientific research and cannot be used on the human body. | price> |
| R-C-7651 | DSPE-PEG-ConA | DSPE-PEG-Concanavalin A,Concanavalin A-PEG-DSPE,The DSPE part has a long-chain fatty acid structure that can be embedded in lipid bilayer systems,while the PEG chain exhibits a flexible linear structure that extends into the aqueous environment.Concanavalin A is a natural lectin that can specifically recognize and bind to α-D-mannose and α-D-glucose residues on the cell surface.This enables the modified nanocarrier to actively target specific cells,such as certain tumor cells or immune cells. | price> |
| R-C-6073 | N-Linoleoyl-DPPE cas:2148334-94-3 | 1,2-dipalmitoyl-sn-glycero-3-phosphoethanolamine-N-linoleoyl(N-linoleoyl-DPPE)is a specific non-endocannabinoid type of N-acylphosphatidylethanolamine (NAPE).NAPEs are the substrates of a specific phospholiase D(NAPE-PLD)which produces aqueous-soluble bioactive fatty acid amides or N-acylethanolamines. | price> |
| R-C-6074 | N-Oleoyl-DPPE CAS:113701-57-8 | 1,2-dipalmitoyl-sn-glycero-3-phosphoethanolamine-N-oleoyl(N-oleoyl-DPPE)is a type of N-acylphosphatidylethanolamine(NAPE)and an important intermediate in the endocannabinoid biosynthesis pathway.Fatty acid amides are synthesized by a specific phospholiase D(NAPE-PLD)and metabolized by fatty acid amide hydrolases(FAAH)and N-Acylethanolamine acid amidase (NAAA). | price> |
| R-C-7655 | DLPE-PEG-TCO | TCO-PEG-DLPE,DLPE as a phospholipid backbone,can effectively embed into the lipid bilayer.PEG provides steric hindrance,extending the circulation time and reducing non-specific adsorption.Meanwhile,TCO serves as a highly reactive tetrazine click reaction partner,enabling rapid and catalyst-free covalent coupling.This product is only for scientific research and cannot be used on the human body. | price> |
| R-C-7658 | DSPE-PEG-Pemafibrate | Pemafibrate-PEG-DSPE,The DSPE hydrophobic phospholipid anchoring segment can also be directly embedded into the phospholipid membrane of existing nanocarriers to maintain the stability of the nanostructure.The PEG hydrophilic spacer chain can reduce the phagocytosis of the carrier by the reticuloendothelial system,prolong the blood circulation time,and simultaneously reduce the immunogenicity of the conjugate,enhancing its stability in vivo. Pemafibrate is a conjugated functional drug and a novel selective peroxisome proliferator-activated receptor α(PPARα)modulator.This product is only for scientific research and cannot be used on the human body. | price> |
| R-C-7661 | DSPE-PEG-CMRRLRGC-NH2 | This product consists of a hydrophobic phospholipid anchoring unit DSPE,a hydrophilic linker PEG, and a CMRRLRGC targeting functional cyclic peptide sequence,with an active group NH₂ at the end. CMRRLRGC:targeting functional cyclic peptide sequence.The cysteine C at both ends can form a ring structure through disulfide bonds.RRLR is the core functional peptide segment,which usually possesses tumor vascular targeting or cell penetration capabilities.It can guide the specific enrichment of nanocarriers in tumor lesions,enhancing the efficiency of targeted delivery.This product is only for scientific research and cannot be used on the human body. | price> |
| R-C-7665 | DOPE-PEG-TAT(CYGRKKRRQRRR) | TAT-PEG-DOPE,DOPE-PEG-CYGRKKRRQRRR,DOPE-PEG-TAT integrates lipid anchoring,hydrophilic segments,and penetrating peptides to achieve synergistic delivery of environmental response and active penetration,providing efficient intracellular transport for large molecules such as nucleic acids and proteins. | price> |
| R-C-7669 | DOPE-Gly-Gly-Gly-Asp-Phe-Glu-Ile | Ile-Glu-Phe-Asp-Gly-Gly-Gly-DOPE,DOPE-Gly-Gly-Gly-Asp-Phe-Glu-Ile is a lipid peptide complex formed by coupling the lipid molecule DOPE with a specific amino acid sequence peptide chain. This structure is commonly used for surface modification of drug delivery systems,such as liposomes and nanoparticles,to achieve targeted delivery or enhance cellular uptake. | price> |

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