Product phospholipids -phosphadylethanolamine-pe

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Catalog	name	Description	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>
R-C-7679	DOPE-4-(Hydroxymethyl)phenylboronic acid pinacol ester	4-(Hydroxymethyl)phenylboronic acid pinacol ester-DOPE,DOPE is a commonly used cationic liposome formulation component in the field of biomedicine,mainly used for liposome transfection and construction of nanocarriers for drug delivery;4-(hydroxymethyl)phenylboronic acid pinal ester is a commercially mature boronic acid ester intermediate,which is generally functionalized by covalently modifying DOPE into a molecular skeleton with phenylboronic acid active groups during material synthesis.	price>

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