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Catalog	name	Description	price
R-C-5733	FA-PEG37-PDMAEMA40	PDMAEMA-PEG-FA,FA-PEG-PDMAEMA,PDMAEMA possesses pH-responsive properties, as it becomes protonated and water-soluble under acidic conditions. It has been widely used in drug delivery systems and as a gene delivery vector due to its ability to encapsulate and release therapeutic molecules.The PDMAEMA-PEG-Folate conjugate can be used for targeted drug delivery, where the PDMAEMA segment can encapsulate therapeutic molecules and respond to the acidic environment in the tumor, leading to drug release.	price>
R-M2-9751	DMG-peg-CGEAIPMSIPPEVK	DMG-PEG-CGEAIPMSIPPEVK is a lipid–PEG–peptide conjugate designed for surface presentation of a bioactive or targeting peptide on lipid-based systems (e.g., liposomes, micelles). The DMG anchors the molecule into lipid bilayers, while PEG spaces the peptide outward, allowing biological interaction with targets such as receptors or enzymes.	price>
R-C-7313	14:0 PC-d13 CAS:326495-28-7	1,2-Dimyristoyl-sn-glycero-3-phosphocholine-d13,It is a stable isotope labeled synthetic phospholipid with important application value in metabolomics,membrane biology,and drug delivery research.	price>
R-C-5734	Galactosylated chitosan(GC)	Galactosylated chitosan is a modified form of chitosan, a polysaccharide derived from the deacetylation of chitin, a natural polymer found in the shells of crustaceans.Galactosylation imparts Galactose receptors targeting properties to chitosan, which can selectively bind to the asialoglycoprotein receptor (ASGPR) found on the surface of hepatocytes in the liver.	price>
R-M2-9752	Chol-peg-CGEAIPMSIPPEVK	Chol-PEG-CGEAIPMSIPPEVK/Cholesterol-peg-CGEAIPMSIPPEVK is a surface-functionalized amphiphilic conjugate, designed for incorporation into lipid membranes. The cholesterol moiety anchors into lipid bilayers, the PEG linker provides spatial separation and mobility, and the peptide is displayed on the membrane surface for biological recognition, targeting, or signaling.Chol-PEG-CGEAIPMSIPPEVK was inserted into preformed liposomes to present the peptide sequence on the outer surface, facilitating targeted interaction with specific cellular receptors.	price>
R-C-7314	DMPC (rac) CAS:18656-38-7	DL-α-Dimyristoyl-phosphatidylcholine,DMPC (rac),14:0 PC (rac)1,2-Dimyristoyl-rac-glycor-3-phosphocholine(CAS:18656-38-7)is a synthetic phospholipid belonging to the phosphatidylcholine(PC)class of compounds.The glycerol skeleton is connected to a nutmeg chain(C14:0,tetradecanoic acid) at the sn-1 and sn-2 positions, with a head group of phosphatidylcholine.Rac indicates that the glycerol skeleton is a racemic form(sn-1 and sn-2 positions have no stereoselectivity),which is different from the naturally occurring sn-3 configuration.	price>
R-C-5735	DSPE-PEG2K-N-acetyl-L-cysteine	DSPE-PEG-N-acetyl-L-cysteine,N-acetyl-L-cysteine(NAC) is a mucolytic agent with antibacterial and antibiofilm properties against several bacterial strains. it shows potential in inhibiting biofilm formation and even disrupting mature biofilms,that NAC acts on reducing the production of exopolysaccharides and leads to disruption and degradation of EPS matrix components.	price>
R-M2-9753	DMG-TK-PEG2K-CGEAIPMSIPPEVK	DMG-TK-PEG2K-CGEAIPMSIPPEVK is a lipid–ROS-cleavable–PEG–peptide conjugate, engineered for surface display of a bioactive peptide on lipid-based systems with ROS-triggered release capability.	price>
R-C-7315	16:0-5 Doxyl PC CAS:188004-24-2	16: 0-5 Doxyl PC (CAS: 188004-24-2) is a nitroxyl labeled phosphatidylcholine compound commonly used in the study of biofilm fluidity, electron spin resonance(ESR)experiments, and dynamic analysis of liposome structure.	price>
R-C-5736	MTX-PEI25k (Branched chain)	PEI-MTX,MTX-PEI,Polyethyleneimine(PEI)is a cationic polymer,it widely used as a gene delivery vector.PEI can complex with nucleic acids,protect them from degradation,and facilitate their intracellular delivery.Additionally,PEI possesses protonatable amino groups that enable endosomal escape, enhancing gene expression.MTX refers to methotrexate, a chemotherapy drug that inhibits the synthesis of nucleotides,leading to the suppression of DNA replication and cell proliferation.PEI-MTX conjugate combines the beneficial properties of both PEI and MTX for targeted drug delivery.The MTX moiety in the conjugate acts as a targeting ligand that can specifically bind to folate receptors,which are frequently overexpressed on the surface of cancer cells.	price>
R-M2-9754	N3-PEG1000-TK-NHS ester	N3-PEG1000-TK-NHS ester,Azido-PEG1000-TK-NHS ester is a bifunctional, ROS-cleavable linker.N3-PEG1000-TK-NHS ester,Azido-PEG1000-TK-NHS ester was used to conjugate a targeting peptide to DBCO-functionalized liposomes.The TK linker allowed ROS-sensitive release of the conjugated ligand in tumor-like oxidative conditions.	price>
R-C-7316	16:0-16 Doxyl PC CAS:216491-65-5	16: 0-16 Doxyl PC(CAS: 216491-65-5)is a phospholipid compound labeled with nitroxyl radicals.It belongs to the PC phospholipid derivatives and has good lipid solubility.It can be embedded in lipid bilayers and used to detect fluidity and polarity changes in deep membrane regions.	price>
R-C-5737	PEG2K-Se-Se-PEI20K	PEG-Se-Se-PEI,PEI-Se-Se-PEG,The disulfide bonds linking the PEI and Se atoms in the conjugate are sensitive to the intracellular environment,specifically the high levels of reductive agents such as glutathione.This sensitivity allows for the controlled release of the payload (e.g,genes or drugs) in the target cells.The reduction of the disulfide bonds leads to the detachment of the payload from the delivery system,facilitating its release and subsequent biological activity.	price>
R-M2-9755	COOH-CeO2 nanoparticles 3-5nm	Carboxyl-modified ceria nanoparticles(CeO2-COOH) were conjugated to amine-functionalized peptides via EDC/NHS coupling for targeted antioxidant delivery in oxidative stress models.	price>
R-C-7317	LNP Lipid-7 CAS:1190203-55-4	LNP Lipid-7 is a cationic lipid As an ionizable or auxiliary lipid component,it enhances the encapsulation efficiency and cellular uptake ability of nucleic acid drugs.Including mRNA vaccine delivery(such as new coronal vaccine technology path),siRNA silencing therapy, liver targeted gene therapy,etc.	price>
R-C-5738	PCL5000-PEG2000-TTBZ	PCL-PEG-TTBZ,The carrier(PEG-PCL)has low cytotoxicity and forms micelles with a hydrophobic core and hydrophilic outer layer due to the amphiphilic block of PEG-PCL.This structure increases the water solubility of levodopa,improves its stability in circulation,provides targeted drug delivery,increases the local accumulation concentration of levodopa in dopamine neurons,thereby improving the bioavailability of the drug,enhancing its protective effect on neurological diseases such as Parkinsons disease,and reducing its peripheral toxic side effects.	price>
R-M2-9756	NH2-PEG2k-Se-Se-COOH	NH2-PEG2k-Se-Se-COOH/Amine-PEG2k-Se-Se-COOH could serve as a PEG-based linker for PROTAC (PErotein Degradation Tag) molecules.The structure could be used to modify nanoparticles, enhancing their stability, solubility, and surface properties.	price>
R-C-7318	CCD Lipid01 CAS:1799316-64-5	CCD Lipid01(CAS:1799316-64-5)is a cationic lipid widely used for cell and tissue delivery of bioactive agents,particularly playing a critical role in RNA and DNA based drug delivery systems.This compound is also known as LP-01,with a molecular formula of C50H93NO9 and a molecular weight of 852.27.	price>
R-C-5739	DMSNs coated CdTe Quantum Dots (50-60nm)	Dendritic mesoporous silica nanoparticles (DMSNs) not only have a three-dimensional dendritic skeleton and a large central radial emission mesoporous structure, but also have a variable pore surface structure, larger specific surface area, and higher loading capacity. As carriers, they can effectively load large molecule proteins, small molecule drugs, and luminescent compounds. The special multi-level structure and co loading capacity of this material demonstrate potential application prospects in collaborative therapy applications.	price>
R-M2-9757	DMG-PEG2K-Chitosan	DMG-PEG2K-Chitosan,1,2-Dimyristoyl-sn-glycerol-PEG2000-Chitosan was incorporated into lipid nanoparticles to provide a chitosan-coated surface for improved cellular uptake and nucleic acid binding, while maintaining colloidal stability through PEG shielding. It is typically designed for nanoparticle surface modification, mucoadhesion, or biocompatible delivery systems.	price>

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