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)
- GC12895SaxagliptinCAS: 361442-04-8Purity: >99.50%
Saxagliptin (BMS-477118) ist ein potenter, selektiver, reversibler, kompetitiver und oral aktiver Inhibitor der Dipeptidylpeptidase-4 (DPP-4) (Ki = 0,6-1,3 nM).
- GC10104GlimepirideCAS: 93479-97-1Purity: >98.00%
Glimepiride is a second-generation sulfonylurea that stimulates pancreatic β cells to release insulin. Glimepiride is used for the treatment of type 2 diabetes mellitu as monotherapy as well as in combination with metformin or insulin.
- GC12235Sitagliptin (phosphate)CAS: 654671-78-0Purity: >98.00%
Sitagliptin (Phosphat) (MK-0431-Phosphat) ist ein potenter Inhibitor von DPP4 mit einem IC50 von 19 nM in Caco-2-Zellextrakten.
- GC14786P32/98 (hemifumarate)CAS: 251572-86-8Purity: >98%
P32/98 (Hemifumarat) ist ein potenter Inhibitor der Dipeptidylpeptidase IV mit einem Ki-Wert von 130 nM.
- GC10018Talabostat mesylateCAS: 150080-09-4Purity: >99.00%
Talabostat mesylate(PT100) ist ein oral wirksamer, nicht-selektiver Inhibitor der Dipeptidylpeptidase IV(DPP-IV)(IC 50 i = 0.18 nM) und der erste klinisch eingesetzte Inhibitor der Fibroblasten-Aktivierungsproteins(FAP)(IC 50 = 560 nM). Es hemmt auch DPP 8/9 (IC 50 = 4/11 nM; K i = 1.5/0.76 nM), Prolylendopeptidase(QPP) (IC50= 310 nM), DPP2 und weitere Enzyme der DASH-Familie.
| Catalog No. | Product Name | CAS No. | Purity | Structure |
|---|---|---|---|---|
| GC12895 | Saxagliptin | 361442-04-8 | >99.50% | |
Saxagliptin (BMS-477118) ist ein potenter, selektiver, reversibler, kompetitiver und oral aktiver Inhibitor der Dipeptidylpeptidase-4 (DPP-4) (Ki = 0,6-1,3 nM). | ||||
| GC10104 | Glimepiride | 93479-97-1 | >98.00% | |
Glimepiride is a second-generation sulfonylurea that stimulates pancreatic β cells to release insulin. Glimepiride is used for the treatment of type 2 diabetes mellitu as monotherapy as well as in combination with metformin or insulin. | ||||
| GC10298 | Sitagliptin phosphate monohydrate | 654671-77-9 | >99.50% | |
| GC10802 | K 579 | 440100-64-1 | >98% | |
| GC12235 | Sitagliptin (phosphate) | 654671-78-0 | >98.00% | |
Sitagliptin (Phosphat) (MK-0431-Phosphat) ist ein potenter Inhibitor von DPP4 mit einem IC50 von 19 nM in Caco-2-Zellextrakten. | ||||
| GC12603 | DPPI 1c hydrochloride | 866396-34-1 | >98% | |
A DPP-4 inhibitor | ||||
| GC13949 | Alogliptin Benzoate | 850649-62-6 | >99.50% | |
A DPP-4 inhibitor | ||||
| GC14126 | NVP DPP 728 dihydrochloride | 247016-69-9 | >98% | |
| GC14201 | PK 44 phosphate | 1017682-65-3 | >98% | |
DPP-IV inhibitor | ||||
| GC14786 | P32/98 (hemifumarate) | 251572-86-8 | >98% | |
P32/98 (Hemifumarat) ist ein potenter Inhibitor der Dipeptidylpeptidase IV mit einem Ki-Wert von 130 nM. | ||||
| GC14827 | Linagliptin (BI-1356) | 668270-12-0 | >99.50% | |
A potent DPP-4 inhibitor | ||||
| GC15130 | Alogliptin (SYR-322) | 850649-61-5 | >99.00% | |
| GC15576 | Teneligliptin hydrobromide | 906093-29-6 | >99.50% | |
A DPP-4 inhibitor | ||||
| GC16613 | Trelagliptin | 865759-25-7 | >99.50% | |
A DDP-4 inhibitor | ||||
| GC16733 | Vildagliptin (LAF-237) | 274901-16-5 | >98.00% | |
A DPP-4 inhibitor | ||||
| GC17012 | MK3102 | 1226781-44-7 | >99.00% | |
MK3102(Omarigliptin) ist ein neuartiger, einmal wöchentlich zu verabreichender Dipeptidylpeptidase-4(DPP-4)-Inhibitor(IC50-Wert: 2.2 nM), der zur Behandlung von Typ-2-Diabetes entwickelt wurde. | ||||
| GC17479 | Trelagliptin succinate | 1029877-94-8 | >99.50% | |
A DDP-4 inhibitor | ||||
| GC10018 | Talabostat mesylate | 150080-09-4 | >99.00% | |
Talabostat mesylate(PT100) ist ein oral wirksamer, nicht-selektiver Inhibitor der Dipeptidylpeptidase IV(DPP-IV)(IC 50 i = 0.18 nM) und der erste klinisch eingesetzte Inhibitor der Fibroblasten-Aktivierungsproteins(FAP)(IC 50 = 560 nM). Es hemmt auch DPP 8/9 (IC 50 = 4/11 nM; K i = 1.5/0.76 nM), Prolylendopeptidase(QPP) (IC50= 310 nM), DPP2 und weitere Enzyme der DASH-Familie. | ||||
