| Structure | Cat No. | Product Name | CAS No. | Product Description |
|---|---|---|---|---|
|
V122036 | (Rac)-Regaloside D | 1935714-45-6 | (Rac)-Regaloside D is a phenylpropanoid compound. |
|
V87379 | DPP-4-IN-10 | 1123219-12-4 | DPP-4-IN-10 (compound 1) is a DPP-4 inhibitor. |
|
V136159 | Fluostatin A | 160219-74-9 | The ability of flustatin A to inhibit DPP-III, using arginyl-arginine-2-naphthylcarboxamide as a substrate, has an IC50 of 0.44 μg/mL. |
|
V73070 | Gemigliptin tartrate (LC15-0444 tartrate) | 1374639-74-3 | Gemigliptin tartrate (LC15-0444 tartrate) is a selective, reversible, competitive dipeptidyl peptidase 4 (DPP-4) inhibitor (antagonist) with IC50 of 10.3 nM for human recombinant DPP-4. |
|
V137131 | HBK001 | 1942922-78-2 | HBK001 is an orally effective selective dual GPR119 agonist and DPP-IV inhibitor. |
|
V102981 | N-Boc-Sitagliptin | 486460-23-5 | N-Boc-sitagliptin is a synthetic intermediate of the dipeptidyl peptidase 4 (DPP-4) inhibitor sitagliptin. |
|
V87375 | NZ-97 | NZ-97 is an inhibitor of dipeptidyl peptidase 4 (DPP4) with an IC50 of 18 nM. | |
|
V143184 | Procizumab | Procizumab is a humanized IgG1 antibody that targets dipeptidyl peptidase 3 (DPP3). | |
|
V2857 | Prusogliptin (DBPR-108) | 1186426-66-3 | DBPR108 is a novel, potent, selective, and orally bioavailable dipeptide-derived inhibitor of DPP4 with IC50 of 15 nM; It shows no inhibition on DDP8 and DPP9. |
|
V143947 | RBx-0597 | 929105-33-9 | RBx-0597 is a highly potent and selective DPP-IV inhibitor with IC50 values of 32, 31, and 39 nM for human, mouse, and rat plasma DPP-IV, respectively. |
|
V144649 | Saxagliptin-15N,d2 Hydrochloride | Saxagliptin-15N,d2 Hydrochloride is the 15N and deuterium-labeled isotope of saxagliptin. | |
|
V73073 | Sheng Gelieting (CGT-8012) | 1152810-23-5 | Sheng Gelieting (CGT-8012) is a dipeptidyl peptidase-IV enzyme (DP-IV) inhibitor. |
|
V145449 | Sulphostin | 307345-51-3 | Sulphostin is a covalent inhibitor of dipeptidyl peptidase 4 (DPP4), dipeptidyl peptidase 9 (DPP9), and dipeptidyl peptidase 8 (DPP8), with IC50 values of 79 nM, 1392 nM, and 6930 nM, respectively. |
|
V146849 | Val-Pyrrolidide hydrochloride | 115201-28-0 | Val-Pyrrolidide hydrochloride is a DPIV inhibitor. |
|
V146943 | Verducatib | 1887236-33-0 | Verducatib is an orally effective inhibitor of cathepsin C (also known as DPP1). |
|
V73068 | γ-Glu-Tyr | 7432-23-7 | γ-Glu-Tyr is a competitive inhibitor (IC50=6.77 mM) of dipeptidyl peptidase-IV (DPP-IV) and a potential functional ingredient in type 2 diabetes diets. |
|
V32582 | Teneligliptin hydrobromide hydrate | 1572583-29-9 | Teneligliptin HBr hydrate (formerly MP513; MP-513; trade name Tenelia in Japan), the hydrobromide salt and hydrated form ofTeneligliptin, is an orally bioavailable and long-lasting dipeptidyl peptidase-4 (DPP-4) inhibitor approved for the treatment of type 2 diabetes mellitus in Japan. |
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