Product phospholipids -phospholipid-peg-customization

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Catalog	name	Description	price
R-C-7110	DSPE-PEG-L-DOPA	DSPE-PEG-levodopa,L-DOPA-PEG-DSPE,The biofilm fusion ability is provided by distearoyl phosphatidylethanolamine(DSPE),the hydrophilicity and stability are enhanced by polyethylene glycol(PEG),and levodopa(L-DOPA)is used as the active ingredient to bind to dopamine receptors.	price>
R-C-7111	DSPE-PEG-JPH203	JPH203-PEG-DSPE,DSPE-PEG is a commonly used nanocarrier material that is widely used in drug delivery, gene transfection, and other fields by prolonging blood circulation time,improving drug stability,and encapsulation efficiency.JPH203(KYT-0353)is an inhibitor of L-type amino acid transporter 1(LAT-1)with effectiveness and specificity.	price>
R-C-7112	DSPE-PEG-PP1(LSLERFLRCWSDAPAK)	DSPE-PEG-PP1(LSLERFLRCWSDAPAK)is a biomaterial composed of phospholipids (DSPE),polyethylene glycol(PEG),and targeting peptides(PP1),which has the function of targeting specific cells or tissues.It is commonly used in drug delivery systems and plaque imaging research.Its core targeting peptide is LSLERFLRCWSDAPAK,which can guide molecular targeting to specific targets such as atherosclerotic plaque.	price>
R-C-7127	DSPE-TK-PEG-CREKA(Cys-Arg-Glu-Lys-Ala)	DSPE-PEG is a multifunctional nanomaterial composed of phospholipids(DSPE)and polyethylene glycol(PEG),widely used in drug delivery, biological imaging,and targeted therapy fields.The TK linker breaks in the reducing tumor microenvironment,triggering the release of loaded drugs such as chemotherapy drugs and photosensitizers.The CREKA peptide(pentapeptide sequence Cys-Arg-Glu-Lys-Ala)can specifically recognize fibrin in tumor blood vessels,achieving precise targeting.	price>
R-C-7128	DSPE-PEG-DTBP-3(GGYTFHWHRLNP(Amino acid D configuration))	DTBP-3-PEG-DSPE,DSPE-PEG-DTBP-3(GGYTFHWHRLNP)is composed of lipid DSPE,flexible PEG chain,and terminal D-type peptide DTBP-3.DTBP-3 is a high affinity TIGIT blocking peptide obtained through mirror phage screening,composed of all D-amino acids,with excellent protease resistance and prolonged in vivo half-life.	price>
R-C-7129	DSPE-PEG-PS(Phosphatidylserine)	PS-PEG-DSPE,DSPE-PEG-PS(phosphatidylserine polyethylene glycol distearoyl phosphatidylethanolamine)is a functionalized phospholipid derivative that combines the membrane anchoring ability of DSPE,the hydrophilic modification effect of PEG,and the biological activity of phosphatidylserine(PS).It is mainly used in targeted drug delivery systems and biomedical research.	price>
R-C-7134	DSPE-PEG-TCPP	TCPP-PEG-DSPE,DSPE-PEG-TCPP is a composite material formed by chemical bonding between di stearoyl phosphatidylethanolamine(DSPE)and polyethylene glycol (PEG),with a core structure of tetrakis(4-carboxyphenyl) porphyrin(TCPP).This compound combines the hydrophobicity of phospholipids and the hydrophilicity of PEG,and is commonly used for surface modification of nanoparticles and biomedical applications.	price>
R-C-7135	DSPE-PEG-TCPP-Mn	TCPP-Mn-PEG-DSPE,DSPE-PEG-TCPP is a composite material formed by chemical bonding between di stearoyl phosphatidylethanolamine(DSPE)and polyethylene glycol (PEG),with a core structure of tetrakis(4-carboxyphenyl)porphyrin(TCPP).The doping of metallic manganese may endow it with magnetic or catalytic properties.Commonly used for surface modification of nanoparticles and biomedical applications.	price>
R-C-7137	DSPE-PEG-lys-RVG29-FITC	FITC-Lys-RVG29-PEG-DSPE,DSPE-PEG-Lys-RVG29-FITC is a molecular compound used for targeted drug delivery systems and biomedical imaging.RVG29 is derived from the peptide sequence of rabies virus glycoprotein and can specifically bind to neuronal surface acetylcholine receptors(nAChRs)to achieve blood-brain barrier penetration.	price>
R-C-7138	DSPE-PEG-curcumin	Curcumin-PEG-DSPE,PEG is connected to DSPE through amide or ester bonds,forming a hydrophilic hydrophobic active three-stage structure.This design enables the complex to form a stable core-shell structure in water,hydrophobic segments encapsulate curcumin, hydrophilic PEG chains extend outward,significantly reducing non-specific binding between the complex and plasma proteins and prolonging in vivo circulation time.	price>

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