Home Metabolism DPP inhibitor Sitagliptin phosphate monohydrate For research use only.

Sitagliptin phosphate monohydrate

Synonyms: MK-0431

Sitagliptin phosphate monohydrate (MK-0431) is a potent inhibitor of DPP-IV with IC50 of 19 nM in Caco-2 cell extracts.

Sitagliptin phosphate monohydrate Chemical Structure

Sitagliptin phosphate monohydrate Chemical Structure

CAS: 654671-77-9

Selleck's Sitagliptin phosphate monohydrate has been cited by 6 Publications

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Purity & Quality Control

Batch: Purity: 99.88%
99.88

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Biological Activity

Description Sitagliptin phosphate monohydrate (MK-0431) is a potent inhibitor of DPP-IV with IC50 of 19 nM in Caco-2 cell extracts.
Features A potent, orally active inhibitor of DPP-4.
Targets
DPP-4 [1]
(Cell-free assay)
19 nM
In vitro
In vitro As an orally active agent, Sitagliptin phosphate exhibits a potent inhibitory effect on DPP-4 with IC50 of 19 nM from Caco-2 cell extracts. [1] MK0431 reduces in vitro migration of isolated splenic CD4 T-cells through a pathway involving cAMP/PKA/Rac1 activation. [2] A recent study demonstrates that sitagliptin exerts a novel, direct action in order to stimulate GLP-1 secretion by the intestinal L cell through a DPP-4-independent, protein kinase A- and MEK-ERK1/2-dependent pathway. It therefore reduces the effect of autoimmunity on graft survival. [3]
Kinase Assay Plasma DPP-4 Activity[2]
DPP-4 is extracted from confluent Caco-2 cells. After 5 minutes of incubation at room temperature with lysis buffer (10 mM Tris-HCl, 150 mM NaCl, 0.04 U/mL aprotinin, 0.5% Nonidet P40, pH 8.0), cells are centrifuged at 35,000 g at 4 °C for 30 minutes, and the supernatant is stored at -80°C. Assays are performed by mixing 20 μL of appropriate compound dilutions with 50 μL of the substrate for the DPP-4 enzyme, H-Ala-Pro-7-amido-4-trifluoromethylcoumarin (final concentration in the assay, 100 μM) and 30 μL of the Caco-2 cell extract (diluted 1000-fold with 100 mM Tris-HCl, 100 mM NaCl, pH 7.8). Plates are incubated at room temperature for 1 hour, and fluorescence is measured at excitation/emission wavelengths of 405/535 nm using a SpectraMax GeminiXS. Dissociation kinetics of inhibitors from the DPP-4 enzyme is determined after a 1-hour preincubation of Caco-2 cell extracts with high inhibitor concentrations (30 nM for BI 1356, 3 μM for vildagliptin). The enzymatic reaction is started by adding the substrate H-Ala-Pro-7-amido-4-trifluoromethylcoumarin after a 3000-fold dilution of the preincubation mixture with assay buffer. Under these conditions, the difference in DPP-4 activity at a certain time point in the presence or absence of an inhibitor reflects the amount of this inhibitor still bound to the DPP-4 enzyme. Maximal reaction rates (fluorescence units/seconds × 1000) at 10-minute intervals are calculated using the SoftMax software of the SpectraMax and corrected for the rate of an uninhibited reaction [(vcontrol-vinhibitor)/vcontrol].
Cell Research Cell lines CD4 T-cells
Concentrations 100 μM
Incubation Time 1 hour
Method CD4T-cells are plated on membrane inserts in serum-free RPMI 1640, and cell migration is assayed using Transwell chambers (Corning), in the presence or absence of purified porcine kidney DPP-4 (32.1 units/mg; 100 mU/mL final concentration) and DPP-4 inhibitor (100 μM). After 1 hour, cells on the upper surface are removed mechanically, and cells that have migrated into the lower compartment are counted. The extent of migration is expressed relative to the control sample.
In Vivo
In vivo In vivo, the ED50 value of Sitagliptin phosphate for inhibition of plasma DPP-4 activity is calculated to be 2.3 mg/kg 7 hour postdose and 30 mg/kg 24 hour postdose in freely fed Han-Wistar rats. [1] The streptozotocin-induced type 1 diabetes mouse model exhibits elevated DPP-4 levels in the plasma that can be substantially inhibited in mice on an Sitagliptin phosphate diet. This is achieved by a positive effect on the regulation of hyperglycemia, potentially through prolongation of islet graft survival. [4] The plasma clearance and volume of distribution of Sitagliptin phosphate are higher in rats (40-48 mL/min/kg, 7-9 L/kg) than in dogs (9 mL/min/kg, 3 L/kg); and its half-life is shorter in rats,2 hours compared with 4 hours in dogs. [5]
Animal Research Animal Models Freely fed Han-Wistar rats
Dosages ≤10 mg/kg
Administration Administered via p.o.
NCT Number Recruitment Conditions Sponsor/Collaborators Start Date Phases
NCT05219409 Not yet recruiting Type 1 Diabetes University of Milan July 2023 Phase 2|Phase 3
NCT05403281 Completed Healthy Subjects Dong Wha Pharmaceutical Co. Ltd. November 5 2021 Phase 1
NCT03790839 Completed Patients Hua Medicine Limited January 31 2019 Phase 1
NCT03359590 Completed Pharmacological Action Profil Institut für Stoffwechselforschung GmbH|Merck Sharp & Dohme LLC March 21 2018 Phase 2
NCT03659461 Completed Type 2 Diabetes Mellitus|PreDiabetes National University of Malaysia October 1 2017 Not Applicable

Chemical lnformation & Solubility

Molecular Weight 523.32 Formula

C16H15F6N5O.H3PO4.H2O
CAS No. 654671-77-9 SDF Download Sitagliptin phosphate monohydrate SDF Download Sitagliptin phosphate monohydrate SDF
Smiles C1CN2C(=NN=C2C(F)(F)F)CN1C(=O)CC(CC3=CC(=C(C=C3F)F)F)N.O.OP(=O)(O)O
Storage (From the date of receipt)

In vitro
Batch:

DMSO : 100 mg/mL ( (191.08 mM)； Moisture-absorbing DMSO reduces solubility. Please use fresh DMSO.)

Water : 41 mg/mL

Ethanol : Insoluble


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