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Results for "

fmoc-lys (biotin-peg4)-oh

" in TargetMol Product Catalog
  • Inhibitors & Agonists
    417
    TargetMol | Activity
  • Peptide Products
    258
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    18
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    39
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    TargetMol | Activity
Fmoc-Lys (biotin-PEG4)-OH
T153081334172-64-3
Fmoc-Lys (biotin-PEG4)-OH is a biotinylated and PEG-modified linker used for PROTAC synthesis [1].
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Fmoc-Lys-OH hydrochloride
T41312139262-23-0
Fmoc-Lys-OH hydrochloride is an alkyl-chain-based PROTAC linker and a non-cleavable ADC linker utilized in the synthesis of antibody-drug conjugates (ADCs).
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TargetMol | Inhibitor Sale
Fmoc-Gly-Gly-OH
T1795235665-38-4
Fmoc-Gly-Gly-OH, a cleavable ADC linker, can be used in the synthesis of antibody-drug conjugates (ADCs).
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TargetMol | Inhibitor Sale
Thalidomide-4-OH
Cereblon ligand 2,E3 ligase Ligand 2
T77635054-59-1
Thalidomide-4-OH (E3 ligase Ligand 2) (Cereblon ligand 2) is the Thalidomide-based Cereblon ligand used to recruit of CRBN protein. Thalidomide-4-OH (Cereblon ligand 2) is a linker to form PROTACs
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DSPE-PEG-OH (MW 2000)
T17854
DSPE-PEG-OH (MW 2000) is a PEG-based PROTAC linker for PROTAC synthesis.
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TargetMol | Inhibitor Sale
Fmoc-Ala-Ala-Asn(Trt)-OH
T179461951424-92-2
Fmoc-Ala-Ala-Asn(Trt)-OH, a cleavable linker essential in ADC (Antibody-Drug Conjugate) synthesis, facilitates the attachment of cytotoxic drugs to antibodies for precise delivery to targeted cells or proteins. Its cleavable properties ensure controlled drug release, thereby optimizing the efficacy of the ADC.
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TargetMol | Inhibitor Sale
Biotin-PEG3-OH
T175751263044-40-1
Biotin-PEG3-OH is a PEG-based PROTAC linker used in PROTAC synthesis.
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TargetMol | Inhibitor Sale
Biotin-PEG2-OH
T17567717119-80-7
Biotin-PEG2-OH is a PEG-based PROTAC linker utilized in PROTAC synthesis.
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TargetMol | Inhibitor Sale
FMOC-3VVD-OH
T22334863971-44-2
FMOC-3VVD-OH is an active chemical.
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TargetMol | Inhibitor Sale
Fmoc-Val-Ala-PAB-OH
Fmoc-Val-Ala-PAB
T42861394238-91-5
Fmoc-Val-Ala-PAB-OH (Fmoc-Val-Ala-PAB) is a useful linker for making Antibody-Drug-Conjugation (ADC) conjugate for targeting drug delivery. It is also utilized in the synthesis of RGD peptidomimetic-paclitaxel conjugates bearing lysosomally cleavable linkers.
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    TargetMol | Inhibitor Sale
    Fmoc-Hyp(Bom)-OH
    T66591187223-15-0
    Fmoc-Hyp(Bom)-OH is an amino acid derivative and has a wide range of applications in life science related research.
      7-10 days
      Inquiry
      m-PEG-Lys-NHS ester (MW 20000)
      T18090
      m-PEG-Lys-NHS ester (MW 20,000) is an alkyl ether-based PROTAC linker commonly used in PROTAC synthesis[1].
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      Biotin-PEG-triethoxysilane (MW 1000)
      T17553
      Biotin-PEG-triethoxysilane (MW 1000) is a PEG-based PROTAC linker used in the synthesis of PROTACs[1].
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      Aminooxy-PEG-OH (MW 2000)
      T17446
      Aminooxy-PEG-OH (MW 2000) is a PEG-based PROTAC linker utilized in the synthesis of PROTACs[1].
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      Acrylate-PEG-OH (MW 5000)
      T17362
      Acrylate-PEG-OH (MW 5000) is a Polyethylene Glycol (PEG)-based linker compound primarily utilized in PROTAC synthesis [1].
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      Fmoc-Lys(Pal-Glu-OtBu)-OH
      T667861491158-62-3
      Fmoc-Lys(Pal-Glu-OtBu)-OH, catalog number T66786 and CAS number 1491158-62-3, is a valuable organic compound for life sciences research.
        7-10 days
        Inquiry
        (+)-Biotin-PEG10-OH
        (+)-Biotin-PEG10-alcohol
        T18547
        (+)-Biotin-PEG10-OH is a PEG-based linker for PROTACs that joins two essential ligands, facilitating selective protein degradation via the ubiquitin-proteasome system in cells.
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        Acrylate-PEG-OH (MW 10000)
        T17360
        Acrylate-PEG-OH (MW 10000) is a Polyethylene Glycol (PEG)-derived PROTAC linker used in the synthesis of PROTACs[1].
        • Inquiry Price
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        (+)-Biotin-PEG12-OH
        T18548
        (+)-Biotin-PEG12-OH, a PEG-based linker for PROTACs, joins two essential ligands to form PROTAC molecules, facilitating selective protein degradation via the ubiquitin-proteasome system within cells.
        • Inquiry Price
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        Fmoc-N-PEG-CH2COOH (MW 5000)
        T17958
        Fmoc-N-amido-PEG-CH2COOH (MW 5000), a PEG-based PROTAC linker, is used in PROTAC synthesis [1].
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        Fmoc-Phe-Lys(Boc)-PAB-PNP
        T179811646299-50-4
        Fmoc-Phe-Lys(Boc)-PAB-PNP is a cleavable antibody-drug conjugate (ADC) linker utilized in ADC synthesis.
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        Fmoc-Phe-Lys(Trt)-PAB-PNP
        T179801116086-09-9
        Fmoc-Phe-Lys(Trt)-PAB-PNP is a cleavable linker designed specifically for antibody-drug conjugate (ADC) synthesis.
        • Inquiry Price
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        Biotin-PEG-triethoxysilane (MW 2000)
        T17554
        Biotin-PEG-triethoxysilane (MW 2000) is a polyethylene glycol (PEG) derivative functionalized with triethoxysilane and biotin moieties, serving as a PEG-based linker for PROTAC synthesis to facilitate the targeted degradation of proteins of interest.
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        Biotin-PEG-triethoxysilane (MW 5000)
        T17555
        Biotin-PEG-triethoxysilane (MW 5000) is a PEG-based PROTAC linker used in PROTAC synthesis[1].
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        Dioxoisoindolin-O-PEG-OH (MW 2000)
        (1,3-dioxoisoindolin-2-yl)-O-PEG-OH (MW 2000)
        T17830
        Dioxoisoindolin-O-PEG-OH (MW 2000) is a polyethylene glycol (PEG)-based linker used in the synthesis of PROTACs (proteolysis targeting chimeras)[1].
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        m-PEG-OH (MW 2000)
        T158329004-74-4
        m-PEG-OH (MW 2000) is a PEG-based linker for PROTACs, facilitating the connection of two essential ligands to form PROTAC molecules, thereby enabling selective protein degradation through the ubiquitin-proteasome system within cells.
        • Inquiry Price
        7-10 days
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        Phe-Lys(Fmoc)-PAB
        T185392149584-03-0
        Phe-Lys(Fmoc)-PAB is a cathepsin-cleavable linker used in the conjugation of antibody-drug conjugates (ADCs)[1].
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        Lenalidomide-4-OH
        T384571061604-41-8
        Lenalidomide-4-OH is a cereblon (CRBN) ligand derived from Lenalidomide, utilized in the recruitment of the CRBN protein. It can be conjugated to the protein ligand via a linker, facilitating the formation of PROTAC.
        • Inquiry Price
        7-10 days
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        m-PEG-OH (MW5000)
        T18106
        m-PEG-OH (MW5000) is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs[1].
        • Inquiry Price
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        DSPE-PEG-Biotin (MW 2000)
        T17850385437-57-0
        DSPE-PEG-Biotin (MW 2000) is a PEG-based PROTAC linker for PROTAC synthesis.
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        Fmoc-N-PEG-CH2COOH (MW 3400)
        T17957
        Fmoc-N-amido-PEG-CH2COOH (MW 3400) is a PEG-based PROTAC linker used in PROTAC synthesis[1].
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        TAMRA-Azide-PEG-biotin
        T169811797415-74-7
        TAMRA-Azide-PEG-biotin is a PEG-based linker for PROTACs, joining two essential ligands. This linker facilitates selective protein degradation by utilizing the ubiquitin-proteasome system within cells.
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        Acrylate-PEG-OH (MW 3400)
        T17361
        Acrylate-PEG-OH (MW 3400) is a polyethylene glycol (PEG)-derived PROTAC linker used in PROTAC synthesis[1].
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        m-PEG-Lys-NHS ester (MW 40000)
        T18091
        m-PEG-Lys-NHS ester (MW 40000) is an alkyl ether-based PROTAC linker used in the synthesis of PROTACs [1].
        • Inquiry Price
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        Biotin-PEG-Biotin (MW 1000)
        T17552
        Biotin-PEG-Biotin (MW 1000) is a PEG-derived PROTAC linker utilized in PROTAC synthesis [1].
        • Inquiry Price
        4-6 weeks
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        Biotin-PEG-amine (MW 3400)
        T17551
        Biotin-PEG-amine (MW 3400) is a polyethylene glycol (PEG)-based linker compound used in the synthesis of PROTACs [1].
        • Inquiry Price
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        Biotin-PEG-amine (MW 2000)
        T17550
        Biotin-PEG-amine (MW 2000) is a polyethylene glycol (PEG) derivative commonly used as a linker in the synthesis of proteolysis targeting chimeras (PROTACs)[1].
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        Fmoc-Lys (biotin-PEG12)-OH
        T17954
        Fmoc-Lys (biotin-PEG12)-OH is a PEGylation-based linker compound employed in PROTAC synthesis[1].
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        Biotin-PEG4-OH
        T146021217609-84-1
        Biotin-PEG4-OH, a PEG-based linker for PROTACs, joins two essential ligands crucial for forming PROTAC molecules, enabling selective protein degradation by leveraging the ubiquitin-proteasome system within cells.
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