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Results for "

APN

" in MedChemExpress (MCE) Product Catalog:

21

Inhibitors & Agonists

2

Peptides

1

Inhibitory Antibodies

6

Natural
Products

3

Recombinant Proteins

1

Isotope-Labeled Compounds

1

Antibodies

6

Click Chemistry

Cat. No. Product Name Target Research Areas Chemical Structure
  • HY-139859

    ADC Linker Cancer
    APN-PEG36-tetrazine is an analogue of APN-PEG4-tetrazine. APN-PEG4-tetrazine is a cleavable 4 unit PEG ADC linker used in the synthesis of antibody-drug conjugates (ADCs) . APN-PEG36-tetrazine is a click chemistry reagent, it contains a Tetrazine group that can undergo an inverse electron demand Diels-Alder reaction (iEDDA) with molecules containing TCO groups.
    APN-PEG36-tetrazine
  • HY-145244

    Akt Cancer
    APN/AKT-IN-1 is a potent and dual inhibitor of APN and AKT with IC50s of 0.21 and 0.27 μM, respectively. APN/AKT-IN-1 can effectively inhibit the phosphorylation of GSK3β, the intracellular substrate of AKT .
    APN/AKT-IN-1
  • HY-140348

    PROTAC Linkers Cancer
    APN- NH2 is an alkyl chain-based PROTAC linker that can be used in the synthesis of PROTACs . APN- NH2 is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
    APN-​NH2
  • HY-136030

    PROTAC Linkers Cancer
    APN-PEG4-PFP is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs . APN-PEG4-PFP is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
    APN-PEG4-PFP
  • HY-136049

    ADC Linker Cancer
    APN-PEG4-DBCO is a cleavable 4 unit PEG ADC linker used in the synthesis of antibody-drug conjugates (ADCs) . APN-PEG4-DBCO is a click chemistry reagent, it contains a DBCO group that can undergo strain-promoted alkyne-azide cycloaddition (SPAAC) with molecules containing Azide groups.
    APN-PEG4-DBCO
  • HY-136044

    ADC Linker Cancer
    APN-PEG4-BCN is a cleavable 4 unit PEG ADC linker used in the synthesis of antibody-drug conjugates (ADCs) . APN-PEG4-BCN is a click chemistry reagent, it contains a BCN group that can undergo strain-promoted alkyne-azide cycloaddition (SPAAC) with molecules containing Azide groups.
    APN-PEG4-BCN
  • HY-130939

    ADC Linker Cancer
    APN-PEG4-Amine (hydrochloride) is a cleavable 4 unit PEG ADC linker used in the synthesis of antibody-drug conjugates (ADCs) . APN-PEG4-Amine (hydrochloride) is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
    APN-PEG4-Amine hydrochloride
  • HY-136045

    ADC Linker Cancer
    APN-PEG4-tetrazine is a cleavable 4 unit PEG ADC linker used in the synthesis of antibody-drug conjugates (ADCs) . APN-PEG4-tetrazine is a click chemistry reagent, it contains a Tetrazine group that can undergo an inverse electron demand Diels-Alder reaction (iEDDA) with molecules containing TCO groups.
    APN-PEG4-tetrazine
  • HY-116025

    PROTAC Linkers Cancer
    APN-C3-PEG4-alkyne is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs . APN-C3-PEG4-alkyne is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
    APN-C3-PEG4-alkyne
  • HY-E70199

    APN/CD13

    Others Others
    A Aminopeptidase N (rat) (APN/CD13) is a Zn 2+ dependent membrane-bound ectopeptidase that degrades preferentially proteins and peptides with a N-terminal neutral amino acid .
    Aminopeptidase N (rat)
  • HY-163549

    Drug-Linker Conjugates for ADC Cancer
    APN-PEG5-VC-PAB-MMAE is a drug-linker conjugate part of INA03 (a transferrin-competitive antibody-drug conjugate against CD71) .
    APN-PEG5-VC-PAB-MMAE
  • HY-140841

    PROTAC Linkers Cancer
    APN-C3-PEG4-azide is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs . APN-C3-PEG4-azide is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. It can also undergo strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with molecules containing DBCO or BCN groups.
    APN-C3-PEG4-azide
  • HY-140347

    tert-Butyl 3-(4-(2-cyanoethynyl)phenylcarbamoyl)propylcarbamate

    PROTAC Linkers Cancer
    APN-C3-NH-Boc is an alkyl/ether-based PROTAC linker that can be used in the synthesis of PROTACs . APN-C3-NH-Boc is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
    APN-C3-NH-Boc
  • HY-116306

    Aminopeptidase Others
    Probestin is a potent aminopeptidase N (APN) inhibitor produced by Streptomyces cyanogens MH663-2F6 .
    Probestin
  • HY-B0134A
    Bestatin hydrochloride
    Maximum Cited Publications
    7 Publications Verification

    Ubenimex hydrochloride

    Aminopeptidase Bacterial Antibiotic Infection Cancer
    Bestatin hydrochloride is an inhibitor of CD13 (Aminopeptidase N)/APN and leukotriene A4 hydrolase, used for cancer research.
    Bestatin hydrochloride
  • HY-B0134B

    Ubenimex trifluoroacetate

    Aminopeptidase Bacterial Antibiotic Infection Cancer
    Bestatin trifluoroacetate is an inhibitor of CD13 (Aminopeptidase N)/APN and leukotriene A4 hydrolase, used for cancer research.
    Bestatin trifluoroacetate
  • HY-B0134
    Bestatin
    Maximum Cited Publications
    7 Publications Verification

    Ubenimex

    Aminopeptidase Bacterial Antibiotic Infection Cancer
    Bestatin is a natural, broad-spectrum, and competitive CD13 (Aminopeptidase N)/APN and leukotriene A4 hydrolase inhibitor. Bestatin has anticancer effects .
    Bestatin
  • HY-B0134AS

    Ubenimex-d7 hydrochloride

    Isotope-Labeled Compounds Aminopeptidase Bacterial Antibiotic Infection Cancer
    Bestatin-d7 (hydrochloride) is deuterium labeled Bestatin (hydrochloride). Bestatin hydrochloride is an inhibitor of CD13 (Aminopeptidase N)/APN and leukotriene A4 hydrolase, used for cancer research.
    Bestatin-d7 hydrochloride
  • HY-P1043A
    NGR peptide Trifluoroacetate
    1 Publications Verification

    Aminopeptidase Cancer
    NGR peptide Trifluoroacetatecontaining the Asn-Gly-Arg (NGR) motif. NGR peptide Trifluoroacetate binds to APN/CD13. NGR peptide Trifluoroacetate is directly conjugated to imaging agents that can be used for tumor imaging .
    NGR peptide Trifluoroacetate
  • HY-P1043

    Aminopeptidase Cancer
    NGR peptide containing the Asn-Gly-Arg (NGR) motif. NGR peptide binds to APN/CD13. NGR peptide is directly conjugated to imaging agents that can be used for tumor imaging .
    NGR peptide
  • HY-B0134R

    Aminopeptidase Bacterial Antibiotic Infection Cancer
    Bestatin (Standard) is the analytical standard of Bestatin. This product is intended for research and analytical applications. Bestatin is a natural, broad-spectrum, and competitive CD13 (Aminopeptidase N)/APN and leukotriene A4 hydrolase inhibitor. Bestatin has anticancer effects .
    Bestatin (Standard)

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