Catalog |
name |
Description |
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. |
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R-M2-9760 |
DMG-TK-PEG2K-Mal CHHSSSARC |
DMG-TK-PEG2K-Mal CHHSSARC is a coupling molecule with lipid anchoring, PEG protection, ROS responsive release, and targeting/transmembrane peptide function. It can be used for targeted delivery systems such as nanoparticles or liposomes. |
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R-M2-9761 |
DMG-TK-PEG2K-LTHVVWL |
DMG-TK-PEG2k-LTHVVWL is a lipid–polymer–peptide conjugate composed of a lipophilic DMG anchor, a ROS-sensitive thioketal linker, a polyethylene glycol spacer (2 kDa), and a C-terminal hydrophobic peptide (LTHVVWL). This multifunctional molecule is designed for insertion into lipid bilayers or nanoparticles, enabling prolonged circulation, ROS-triggered peptide exposure or drug release, and potential targeting or bio-interactivity mediated by the LTHVVWL peptide segment. |
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R-M2-9762 |
Bisdemethoxycurcumin-PEG2000-TK-CKLVFF |
Bisdemethoxycurcumin-PEG2000-TK-CKLVFF is a composite nanocarrier or therapeutic conjugate. Bisdemethoxycurcumin (BDMC): A potent curcuminoid derivative with antioxidant, anti-inflammatory, and anticancer properties.PEG2000-TK (Thioether Ketone linker): A redox-sensitive cleavable linker often used in prodrug or nanocarrier design.CKLVFF peptide: A β-sheet breaker sequence derived from amyloid-β used to inhibit aggregation—often explored in Alzheimer therapy. |
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R-M2-9778 |
Chol-PEG-GNYTCEVTELTREGETIIELK |
Cholesterol-PEG-GNYTCEVTELTREGETIIELK for use in targeted drug delivery, cell penetration, or nanoparticle functionalization. |
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R-M2-9779 |
GNYTCEVTELTREGETIIELK-PEG-DMG |
GNYTCEVTELTREGETIELK-PEG-DMG is a peptide conjugate. Allows the peptide-PEG to integrate into lipid bilayers or micelles.
Probable Applications:
mRNA or siRNA delivery (LNPs):Enables targeted delivery of nucleic acids to specific cells (e.g., tumor, immune cells).
Cancer therapy:Peptide may target tumor-specific markers; PEG-DMG ensures carrier stability.
Drug delivery across barriers (BBB, mucosa) :Peptides can promote penetration or receptor-mediated uptake.
Theranostics:Combines therapy with imaging or tracking in a single nanoparticle system. |
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R-M2-9792 |
Propargyl-PEG2k-WLSEAGPVVTVRALRGTGSW |
Propargyl-PEG2k-WLSEAGPVVTVRALRGTGSW is a synthetic peptide–polymer conjugate engineered for targeted drug delivery, imaging, or biosensing, using click chemistry. |
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R-M2-9793 |
Propargyl-PEG2k-CSTSMLKAC |
Propargyl-PEG2k-CSTSMLKAC is a molecule composed of a propargyl group, a PEG2000 linker, and the peptide CSTSMLKAC. The propargyl group can be used for copper-catalyzed azide-alkyne cycloaddition (CuAAC) click chemistry. The peptide CSTSMLKAC has been identified as a targeting sequence for ischemic heart tissue. PEGylation with PEG2000 enhances water solubility and biocompatibility. |
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R-M2-9797 |
DMG-PEG3.4K-HHLGGAKQAGDV |
DMG-PEG3.4K-HHLGGAKQAGDV is a stealthy, lipid-anchored, integrin-targeting peptide conjugate, well-suited for applications in Cardiovascular drug delivery,Inflammation-targeted nanocarriers,Liposome surface functionalization,Thrombus imaging or therapy. |
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R-M2-9798 |
Chol-PEG3.4K-HHLGGAKQAGDV |
Cholesterol-PEG3.4K-HHLGGAKQAGDV is a rationally engineered molecule designed to:
Embed into lipid-based nanoparticles;
Present an integrin-targeting peptide (especially for platelet or vascular targeting);
Enable fluorescence imaging, drug delivery, or antithrombotic treatment. |
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