GLPBio

DPP-4

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Dipeptidyl peptidase-4 (DPP-4), originally identified in 1966 as a dipeptide naphthylamidase hydrolyzing glycyl-prolyl-beta-naphthylamide, is a membrane-associated peptidase that selectively cleaves the N-terminal penultimate proline or alanine amino acids. The most common substrates of DPP-4 include glucagon-like peptide-1 (GLP-1), glucagon-like peptide-2 (GLP-2), peptide YY, neuropeptide, chemokine ligand 12/stromal-derived factor-1 (CXCL12/SDF-1) and substance P. DPP-4, as a type II cell surface protein and a soluble form, has been found to be widely distributed in organs (such as the bone marrow, the lung, spleen, liver, pancreas, kidney and intestines) and body fluids (such as serum/plasma, cerebrospinal fluid, synovial fluid and semen). Besides its peptidase activity, DPP-4 has been found to be associated with immune stimulation, extracellular matrix degradation, lipid accumulation and resistance to anticancer agents.

Products Related to DPP-4(18)

  • GC12895 structure
    GC12895Saxagliptin
    CAS: 361442-04-8
    Purity: >99.50%

    Saxagliptin est un inhibiteur très puissant de la dipeptidyl peptidase-4 (DPP-4) qui régule la glycémie en inhibant sélectivement l'enzyme DPP-4, ce qui augmentant ainsi le niveau du peptide 1 de glucagon-type (GLP-1) endogène et du polypeptide insulinotrope glucose-dépendant (GIP).

  • GC10104 structure
    GC10104Glimepiride
    CAS: 93479-97-1
    Purity: >98.00%

    Glimepiride est un sulfonylurée de deuxième génération qui stimule les cellules β gastriques à libérer de l'insuline. Glimepiride est utilisé pour le traitement du diabète de type 2 en monothérapie ainsi que en combinaison avec la métformine ou l'insuline.

  • GC10298 structure
    GC10298Sitagliptin phosphate monohydrate
    CAS: 654671-77-9
    Purity: >99.50%
  • GC10802 structure
    GC10802K 579
    CAS: 440100-64-1
    Purity: >98%
  • GC12235 structure
    GC12235Sitagliptin (phosphate)
    CAS: 654671-78-0
    Purity: >98.00%

    La sitagliptine (phosphate) (MK-0431 phosphate) est un puissant inhibiteur de DPP4 avec une IC50 de 19 nM dans les extraits de cellules Caco-2.

  • GC12603 structure
    GC12603DPPI 1c hydrochloride
    CAS: 866396-34-1
    Purity: >98%

    A DPP-4 inhibitor

  • GC13949 structure
    GC13949Alogliptin Benzoate
    CAS: 850649-62-6
    Purity: >99.50%

    A DPP-4 inhibitor

  • GC14126 structure
    GC14126NVP DPP 728 dihydrochloride
    CAS: 247016-69-9
    Purity: >98%
  • GC14201 structure
    GC14201PK 44 phosphate
    CAS: 1017682-65-3
    Purity: >98%

    DPP-IV inhibitor

  • GC14786 structure
    GC14786P32/98 (hemifumarate)
    CAS: 251572-86-8
    Purity: >98%

    P32/98 (hémifumarate) est un puissant inhibiteur de la dipeptidyl peptidase IV avec une valeur Ki de 130 nM.

  • GC14827 structure
    GC14827Linagliptin (BI-1356)
    CAS: 668270-12-0
    Purity: >99.50%

    A potent DPP-4 inhibitor

  • GC15130 structure
    GC15130Alogliptin (SYR-322)
    CAS: 850649-61-5
    Purity: >99.00%
  • GC15576 structure
    GC15576Teneligliptin hydrobromide
    CAS: 906093-29-6
    Purity: >99.50%

    A DPP-4 inhibitor

  • GC16613 structure
    GC16613Trelagliptin
    CAS: 865759-25-7
    Purity: >99.50%

    A DDP-4 inhibitor

  • GC16733 structure
    GC16733Vildagliptin (LAF-237)
    CAS: 274901-16-5
    Purity: >98.00%

    A DPP-4 inhibitor

  • GC17012 structure
    GC17012MK3102
    CAS: 1226781-44-7
    Purity: >99.00%

    Le MK3102 (Omarigliptine) est un nouvel inhibiteur de la dipeptidyl peptidase-4 (DPP-4) à prise hebdomadaire (IC50 : 2,2 nM) développé pour le traitement du diabète de type 2.

  • GC17479 structure
    GC17479Trelagliptin succinate
    CAS: 1029877-94-8
    Purity: >99.50%

    A DDP-4 inhibitor

  • GC10018 structure
    GC10018Talabostat mesylate
    CAS: 150080-09-4
    Purity: >99.00%

    Talabostat mesylate est un inhibiteur oralement actif et non s&eacute;lectif de la dipeptidyl peptidase IV (DPP-IV) (IC 50 < 4 nM; K i = 0.18 nM) , ainsi que le premier inhibiteur clinique de la fibroblast activation protein (FAP)(IC 50 = 560 nM). Il inhibe &eacute;galement les DPP 8/9 (IC 50 = 4/11 nM; K i = 1.5/0.76 nM), la prolyl endopeptidase (QPP) (IC50= 310 nM), DPP2 et d'autres enzymes de la famille DASH.