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Targeted therapy! The Capetin Prize winning "Click Chemistry" can be used like this!Targeted therapy! The Nobel Prize winning "Click Chemistry" can be used like this!2025-02-06
24 Results for "
Tumor Homing Peptide
" in MedChemExpress (MCE) Product Catalog:
Products (24)
24 Results for "Tumor Homing Peptide" in MCE Product Catalog:
2
2 Cited Publications
Cat. No.: HY-P2526
CAS No.: 454487-07-1
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2 Cited Publications
Cat. No.: HY-P2526A
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Cat. No.: HY-P4089
CAS No.: 945245-82-9
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Cat. No.: HY-P10894
CAS No.: 2283322-63-2
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Cat. No.: HY-172271
DSPE-PEG1000-Mal-Cys-CGNKRTRGC (Disulfide bridge: Cys2-Cys10) is a PEG compound which composed of DSPE and a nine residue peptide (LyP-1) (HY-P2526). LyP-1 is a cyclic 9-amino-acids tumor homing peptide and selectively bind to p32 receptors overexpressed in various tumor-associated cells .
Cat. No.: HY-P10997
CAS No.: 536971-53-6
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F3 peptide is a nucleolin-binding tumor-homing peptide that mediates selective uptake and internalization by tumor cells. F3 peptide is a 31-amino acid fragment of human high mobility group nucleosomal protein 2 (HMGN2). F3 peptide inhibits protein synthesis through ribosome inactivation. F3 peptide targets the tumor vasculature. F3 peptide can serve as an effective ligand to improve the druggability of macromolecular drugs or nanoparticles. F3 peptide is used in research on cancers such as glioblastoma and breast cancer .
Cat. No.: HY-172271A
DSPE-PEG2000-LyP-1 is a PEG compound which composed of DSPE and a nine residue peptide (LyP-1) (HY-P2526). LyP-1 is a cyclic 9-amino-acids tumor homing peptide and selectively bind to p32 receptors overexpressed in various tumor-associated cells .
Cat. No.: HY-172271B
DSPE-PEG3000-LyP-1 is a PEG compound which composed of DSPE and a nine residue peptide (LyP-1) (HY-P2526). LyP-1 is a cyclic 9-amino-acids tumor homing peptide and selectively bind to p32 receptors overexpressed in various tumor-associated cells .
Cat. No.: HY-P11415
CAS No.: 1189359-89-4
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Cat. No.: HY-P10997A
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F3 peptide acetate is a nucleolin-binding tumor-homing peptide that mediates selective uptake and internalization by tumor cells. F3 peptide acetate is a 31-amino acid fragment of human high mobility group nucleosomal protein 2 (HMGN2). F3 peptide acetate inhibits protein synthesis through ribosome inactivation. F3 peptide acetate targets the tumor vasculature. F3 peptide acetate can serve as an effective ligand to improve the druggability of macromolecular drugs or nanoparticles. F3 peptide acetate is used in research on cancers such as glioblastoma and breast cancer .
Cat. No.: HY-187402A
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DOPE-PEG2000-CSTSMLKAC is an amphiphilic lipid-PEG-peptide conjugate composed of DOPE (1,2-dioleoyl-sn-glycero-3-phosphoethanolamine), PEG2000, and the CSTSMLKAC peptide, a cyclic tumor-homing peptide with a disulfide bond formed by flanking cysteine residues. DOPE-PEG2000-CSTSMLKAC is used for tumor-targeted drug delivery through liposome and nanoparticle surface modification.
Cat. No.: HY-187410A
Synonyms: DOPE-PEG2000-Mal-Cys-APRPG
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DOPE-PEG2000-APRPG (DOPE-PEG2000-Mal-Cys-APRPG) is an amphiphilic lipid-PEG-peptide conjugate consisting of DOPE (1,2-dioleoyl-sn-glycero-3-phosphoethanolamine), PEG2000, and the APRPG peptide (Ala-Pro-Arg-Gly), a tumor-homing peptide. DOPE-PEG2000-APRPG is used for tumor vasculature-targeted drug delivery.
Cat. No.: HY-187416A
Synonyms: DOPE-PEG2000-Mal-Cys-CGKRK
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DOPE-PEG2000-CGKRK (DOPE-PEG2000-Mal-Cys-CGKRK) is an amphiphilic lipid-PEG-peptide conjugate consisting of DOPE (1,2-dioleoyl-sn-glycero-3-phosphoethanolamine), PEG2000, and the CGKRK peptide, a tumor-homing peptide identified by in vivo phage display. DOPE-PEG2000-CGKRK is used for tumor-targeted drug delivery through liposome and nanoparticle surface modification.
Cat. No.: HY-187490A
Synonyms: DOPE-PEG2000-Mal-Cys-CREKA
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DOPE-PEG2000-CREKA (DOPE-PEG2000-Mal-Cys-CREKA) is an amphiphilic lipid-PEG-peptide conjugate consisting of DOPE (1,2-dioleoyl-sn-glycero-3-phosphoethanolamine), PEG2000, and the CREKA peptide (Cys-Arg-Glu-Lys-Ala), a tumor-homing peptide identified by in vivo phage display. DOPE-PEG2000-CREKA is used for tumor stroma-targeted drug delivery.
Cat. No.: HY-187474A
Synonyms: DOPE-PEG2000-Mal-Cys-HTMYYHHYQHHL
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DOPE-PEG2000-K237 (DOPE-PEG2000-Mal-Cys-HTMYYHHYQHHL) is an amphiphilic lipid-PEG-peptide conjugate composed of DOPE (1,2-dioleoyl-sn-glycero-3-phosphoethanolamine), PEG2000, and the K237 peptide (sequence: HTMYYHHYQHHL). K237 peptide is a tumor-homing peptide identified by phage display that specifically binds to vasculature in tumor tissues. DOPE-PEG2000-K237 is used for tumor-targeted drug delivery via functionalization of liposomes and nanoparticles.
Cat. No.: HY-P10989
CAS No.: 241478-23-9
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Cat. No.: HY-187399A
Synonyms: DOPE-PEG2000-Mal-Cys-NGR
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DOPE-PEG2000-NGR (DOPE-PEG2000-Mal-Cys-NGR) is an amphiphilic lipid-PEG-peptide conjugate composed of DOPE (1,2-dioleoyl-sn-glycero-3-phosphoethanolamine), PEG2000, and the NGR (Asn-Gly-Arg) peptide, a tumor-homing tripeptide motif. NGR peptide specifically binds to aminopeptidase N (CD13) that is overexpressed on angiogenic tumor vasculature. DOPE-PEG2000-NGR is used for tumor vasculature-targeted drug delivery and anti-angiogenic research.
Cat. No.: HY-P11815
CAS No.: 1227627-77-1
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Cat. No.: HY-181742
ULK1/2-IN-1 is a tissue-targeted ULK1/2 inhibitor conjugated to the RGR (CRGRRST) tumor neovasculature-homing peptide. ULK1/2-IN-1 mediates autophagy inhibition and induces cytotoxicity in endothelial cells. ULK1/2-IN-1 can be used for the research of tumor-targeted autophagy inhibitors .
Cat. No.: HY-187401A
Synonyms: DOPE-PEG2000-Mal-Cys-KDEPQRRSARLSAKPAPPKPEPKPKKAPAKK
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DOPE-PEG2000-F3 (DOPE-PEG2000-Mal-Cys-KDEPQRRSARLSAKPAPPKPEPKPKKAPAKK) is an amphiphilic lipid-PEG-peptide conjugate composed of DOPE (1,2-dioleoyl-sn-glycero-3-phosphoethanolamine), PEG2000, and the F3 peptide, a tumor-homing peptide derived from the high-mobility group protein N2 (HMGN2). DOPE-PEG2000-F3 is used for tumor-targeted drug delivery.
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Protocols
Targeted therapy! The Capetin Prize winning "Click Chemistry" can be used like this!Targeted therapy! The Nobel Prize winning "Click Chemistry" can be used like this!A suitable model is crucial in drug screening experiments. Organs can mimic the three-dimensional functional structure of internal organs, have similar spatial organization to corresponding organs, maintain some key characteristics, and reproduce some physiological functions. They are widely used for modeling and personalized drug screening physiological functions.2025-02-06
