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| Catalog | name | Description | price |
|---|---|---|---|
| R-C-7311 | 24:0 Lyso PC CAS:325171-59-3 | 24:0 Lyso PC(CAS: 325171-59-3)is a lysophosphatid (LyP),chemically named (R)-2-Hydroxy-3-(tetracosanoyloxy)propyl (2-(trimethylammonio)ethyl) phosphate , with a molecular weight of 607.84 and a molecular formula of C32H66NO7P. | price> |
| R-C-5732 | FFNPs | nanoscale zerovalent iron (Fe0-NPs) has gained prominence for environmental remediation,especially for the remediation of contaminants that are susceptible to reductive transformation such as azo dyes, especially,Agglomeration of magnetic metal nanoparticles takes place primarily through direct interparticle interactions. | price> |
| R-M2-9750 | DSP-PEG4-TK-COOH | DSP-PEG4-TK-COOH is a ROS-responsive linker molecule designed for: Anchoring to hydrophobic surfaces (e.g., liposomes, nanoparticles) via DSP or DSPE. Controlled release via thioketal cleavage in oxidative environments. Conjugation to amine-containing drugs, peptides, or targeting ligands through the carboxylic acid end. DSP-PEG4-TK-COOH was incorporated into the liposomal membrane to enable ROS-sensitive release of surface-bound cargo via thioketal cleavage. The terminal carboxyl group was used to conjugate targeting ligands through EDC/NHS chemistry. | price> |
| R-C-7312 | DMPC-d67 CAS:326495-32-3 | 1,2-Dimyristoyl-sn-glycero-3-phosphocholine(DMPC)is a synthetic phospholipid used in liposomes.14:0 PC-d67 is a deuterated phosphocholine(PC)wherein 67 protons of dimyristoyl are replaced by deuterium. | 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> |

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