Catalog |
name |
Description |
price |
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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R-M2-9799 |
GGG-PEG3-N3 |
GGG-PEG3-N3/Gly-Gly-Gly-PEG3-Azide is a modular linker used in click chemistry, bioconjugation, and site-selective surface modifications and peptide-based materials, surface tagging, or nanoconjugate development. |
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