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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
61 Results for "
peptide coupling
" in MedChemExpress (MCE) Product Catalog:
Products (61)
61 Results for "peptide coupling" in MCE Product Catalog:
Cat. No.: HY-158199
CAS No.: 2126749-95-7
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BCN-HS-PEG2-bis(PNP) is a p-nitrophenyl ADC linker that can be used for further coupling of ADC toxins with peptide linkers. BCN-HS-PEG2-bis(PNP) can be combined with vc-PABC-MMAE (HY-15162) to form drug-linker conjugates for ADCs.
Cat. No.: HY-P2398
CAS No.: 878797-01-4
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Fmoc-Phe-Ser(psi(Me,Me)pro)-OH is a pseudo-proline dipeptide building block corresponding to positions 27-28 of the teduglutide sequence. Fmoc-Phe-Ser(psi(Me,Me)pro)-OH is applied in solid-phase peptide synthesis. Fmoc-Phe-Ser(psi(Me,Me)pro)-OH can be used for the research of teduglutide synthesis .
Cat. No.: HY-151782
CAS No.: 2250437-45-5
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The azide function is widely used for coupling to alkyne-containing fragments via the renowned Click reaction. Polyglycine fragments containing up to 7 glycines are reported to bind to surfaces and have potential application in nanotechnology constructs: constructs of Gly7-NHCH2-fragment containing peptides bind on mica surface in aqueous solution . It contains an azide group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing alkyne groups. It can also undergo ring strain-promoted alkyne-azide cycloaddition (SPAAC) with molecules containing DBCO or BCN groups.
Cat. No.: HY-P11023
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Cat. No.: HY-P11428
CAS No.: 2425606-55-7
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Cat. No.: HY-W441014A
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DSPE-PEG10000-NHS ammonium is one of the most commonly used reactive phospholipids for coupling antibodies, proteins, peptides or other substrates to the surface of liposomes and other lipid PEG nanoparticles .
Cat. No.: HY-W283556
CAS No.: 162148-48-3
Cat. No.: HY-174358D
CAS No.: 39927-08-7
Cat. No.: HY-P2392
CAS No.: 252554-79-3
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N,N'-Carbonyldiimidazole (Standard) (1,1'-Carbonyldiimidazole (Standard)) is the analytical standard of N,N'-Carbonyldiimidazole (HY-79880). This product is intended for research and analytical applications. N,N'-Carbonyldiimidazole (1,1'-Carbonyldiimidazole) is a highly reactive carboxylating reagent that can activate hydroxyl groups to form reactive carbonyl groups. N,N'-Carbonyldiimidazole can be used as a coupling agent and a peptide synthesis reagent .
Cat. No.: HY-118112
CAS No.: 64191-06-6
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4-N-Maleimidobenzoicacid-NHS is a PEG linker that finds utility in bioconjugation endeavors and protein labeling ventures. Specifically designed for selective reaction with thiol groups, the maleimide group establishes covalent linkages, thereby facilitating the coupling of proteins, peptides, or diverse molecules to thiol-bearing biomolecules. The NHS ester is able to react specifically and efficiently with primary amines (e.g. the side chain of lysine residues or aminosilane-coated surfaces) at neutral or slightly basic conditions to form a covalent bond.
Cat. No.: HY-148031
CAS No.: 1638970-45-2
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Cat. No.: HY-120286
CAS No.: 108890-90-0
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Cat. No.: HY-78824
CAS No.: 128421-85-2
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Cat. No.: HY-174358A
CAS No.: 39927-08-7
Cat. No.: HY-174358E
CAS No.: 39927-08-7
Cat. No.: HY-149117
CAS No.: 467233-94-9
Cat. No.: HY-130282
CAS No.: 1643593-30-9
Ianthelliformisamine C ditrifluoroacetate is an antibiotic enhancer with activity against resistant Gram-negative bacteria. Ianthelliformisamine C ditrifluoroacetate has been shown to improve the efficacy of doxycycline against Pseudomonas aeruginosa. Ianthelliformisamine C ditrifluoroacetate was prepared using peptide coupling, resulting in high chemical yields of 27 to 91%. Ianthelliformisamine C ditrifluoroacetate exhibits its mechanism of action by inducing ATP efflux and causing membrane depolarization in bacterial cells.
Cat. No.: HY-P10306
Cat. No.: HY-174961
Synonyms: Fmoc-NH-PEG1000-Mal
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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
