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Results for "

FmocNH-PEG3-CH2CH2NH2

" in MedChemExpress (MCE) Product Catalog:

4

Inhibitors & Agonists

7

Peptides

Cat. No. Product Name Target Research Areas Chemical Structure
  • HY-W190961
    FmocNH-PEG3-CH2CH2NH2 hydrochloride

    		PROTAC Linkers Cancer
    FmocNH-PEG3-CH2CH2NH2 (hydrochloride) is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
    <em>FmocNH-PEG3-CH2CH2NH2</em> hydrochloride
  • HY-41189
    Fmoc-Val-Cit-PAB-PNP

    		ADC Linker Cancer
    Fmoc-Val-Cit-PAB-PNP is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs). Fmoc-Val-Cit-PAB-PNP has superior plasma stability comparable to that of non-cleavable linkers .
    <em>Fmoc</em>-Val-Cit-PAB-PNP
  • HY-P4543
    HIV-IN petide

    		HIV HIV Protease Infection
    HIV-IN petide is a competitive inhibitor of HIV-1 protease (Ki=50 nM) .
    HIV-IN petide
  • HY-P10319
    RI-STAD-2

    		PKA Cardiovascular Disease Cancer
    RI-STAD-2 is a high-affinity interfering peptide that regulates the subunit RI of protein kinase A (PKA). RI-STAD-2 interferes with the binding of AKAPs and PKA-RI by simulating the interaction between AKAPs' α-helix domain and PKA-RI's dimerization/anchoration (D/D) domain, thereby affecting PKA activity and intracellular localization. RI-STAD-2 can be used to study the role of AKAPs interaction with PKA-RI in pathological processes such as cardiovascular disease and cancer .
    RI-STAD-2

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