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Results for "

cis-4-Hydroxy-L-proline

" in MedChemExpress (MCE) Product Catalog:

11

Inhibitors & Agonists

5

Peptides

2

Natural
Products

1

Isotope-Labeled Compounds

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Cat. No. Product Name Target Research Areas Chemical Structure
  • HY-40136

    Endogenous Metabolite Metabolic Disease Cancer
    cis-4-Hydroxy-L-proline, a proline analogue, is an inhibitor of collagen production. cis-4-Hydroxy-L-proline could inhibit fibroblast growth by preventing the deposition of triple-helical collagen on the cell layer. cis-4-Hydroxy-L-proline also depresses the growth of primary N-nitrosomethylurea-induced rat mammary tumors [4].
    <em>cis-4</em>-<em>Hydroxy</em>-L-<em>proline</em>
  • HY-W019213

    ADC Linker PROTAC Linkers Cancer
    cis-4-Hydroxy-L-proline hydrochloride is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs). cis-4-Hydroxy-L-proline hydrochloride is also a PEG-based PROTAC linker that can be used in the synthesis of PROTACs.
    <em>cis-4</em>-<em>Hydroxy</em>-L-<em>proline</em> hydrochloride
  • HY-W002886

    ADC Linker PROTAC Linkers Cancer
    N-Boc-cis-4-hydroxy-L-proline is a non-cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs). N-Boc-cis-4-hydroxy-L-proline is also a alkyl chain-based PROTAC linker that can be used in the synthesis of PROTACs[2
    N-Boc-<em>cis-4</em>-<em>hydroxy</em>-L-<em>proline</em>
  • HY-W008129

    Endogenous Metabolite Metabolic Disease
    cis-4-Hydroxy-D-proline is a precursor of conformationally restricted PNA adenine monomer. cis-4-Hydroxy-D-proline can be used to study the specificity and kinetics of D-alanine dehydrogenase .
    H-D-cis-Hyp-OH
  • HY-40136S

    Isotope-Labeled Compounds Endogenous Metabolite
    cis-4-Hydroxy-L-proline-d3 is the deuterium labeled cis-4-Hydroxy-L-proline. cis-4-Hydroxy-L-proline, a proline analogue, is an inhibitor of collagen production. cis-4-Hydroxy-L-proline could inhibit fibroblast growth by preventing the deposition of triple-helical collagen on the cell layer. cis-4-Hydroxy-L-proline also depresses the growth of primary N-nitrosomethylurea-induced rat mammary tumors[1][2][3][4].
    <em>cis-4</em>-<em>Hydroxy</em>-L-<em>proline</em>-d3
  • HY-76104

    ADC Linker PROTAC Linkers Cancer
    cis-4-Hydroxy-D-proline hydrochloride is a non-cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs). cis-4-Hydroxy-D-proline hydrochloride is also a alkyl chain-based PROTAC linker that can be used in the synthesis of PROTACs.
    (2R,<em>4</em>R)-<em>4</em>-Hydroxypyrrolidine-2-carboxylic acid hydrochloride
  • HY-W002887

    ADC Linker PROTAC Linkers Cancer
    N-Boc-cis-4-Hydroxy-D-proline is a non-cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs). N-Boc-cis-4-Hydroxy-D-proline is also a alkyl chain-based PROTAC linker that can be used in the Synthesis of ADCs or PROTACs.
    N-Boc-<em>cis-4</em>-<em>Hydroxy</em>-D-<em>proline</em>
  • HY-Y0755

    ADC Linker PROTAC Linkers Cancer
    N-Boc-cis-4-hydroxy-L-proline methyl ester is a non-cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs). N-Boc-cis-4-hydroxy-L-proline methyl ester is also a alkyl chain-based PROTAC linker that can be used in the synthesis of PROTACs[2
    N-Boc-<em>4</em>-<em>hydroxy</em>-L-<em>proline</em> methyl ester
  • HY-W002680

    ADC Linker PROTAC Linkers Cancer
    N-Boc-cis-4-hydroxy-D-proline methyl ester is a non-cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs). N-Boc-cis-4-hydroxy-D-proline methyl ester is also a alkyl chain-based PROTAC linker that can be used in the synthesis of PROTACs[1
    (2R,<em>4</em>R)-1-tert-Butyl 2-methyl <em>4</em>-hydroxypyrrolidine-1,2-dicarboxylate
  • HY-P3100

    Liposome Cancer
    Orfamide A is a liposome to simulate biological phospholipid membrane. Liposomes are the main component of vesicles with concentric phospholipid bilayer membranes, which can be used to construct drug delivery systems for anti-cancer and anti-infection fields. Highly polar water-soluble payloads can be trapped in the internal aqueous space of liposomes, while lipophilic payloads can partition into and become part of the lipid bilayer. Especially for delivering antisense oligonucleotides, it can overcome problems such as inefficient cellular uptake and rapid loss in the body .
    Orfamide A
  • HY-P10447

    Fengycin IX; SNA-60-367-3

    Liposome Cancer
    Plipastatin A1 is a liposome to simulate biological phospholipid membrane. Liposomes are the main component of vesicles with concentric phospholipid bilayer membranes, which can be used to construct drug delivery systems for anti-cancer and anti-infection fields. Highly polar water-soluble payloads can be trapped in the internal aqueous space of liposomes, while lipophilic payloads can partition into and become part of the lipid bilayer. Especially for delivering antisense oligonucleotides, it can overcome problems such as inefficient cellular uptake and rapid loss in the body .
    Plipastatin A1

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