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Linagliptin

Catalog No. T0191   CAS 668270-12-0
Synonyms: BI 1356

Linagliptin (BI 1356) is a potent, orally bioavailable dihydropurinedione-based inhibitor of dipeptidyl peptidase 4 (DPP-4), with hypoglycemic activity.

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Linagliptin Chemical Structure
Linagliptin, CAS 668270-12-0
Pack Size Availability Price/USD Quantity
50 mg In stock $ 38.00
100 mg In stock $ 54.00
1 mL * 10 mM (in DMSO) In stock $ 50.00
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Purity: 99.95%
Purity: 99.66%
Purity: 99.15%
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Biological Description
Chemical Properties
Storage & Solubility Information
Description Linagliptin (BI 1356) is a potent, orally bioavailable dihydropurinedione-based inhibitor of dipeptidyl peptidase 4 (DPP-4), with hypoglycemic activity.
Targets&IC50 DPP4:1 nM
In vitro Linagliptin shows a potent inhibition effect against DPP-4 in vitro and a low affinity for hERG channel and M1 receptor (IC50 295 nM). [1] Linagliptin acts as a competitive inhibitor with a Ki of 1 nM, and also shows 10,000-fold more selectivity for DPP-4 than DPP-8, DPP-9, amino-peptidases N and P, prolyloligopeptidase, trypsin, plasmin, and thrombin, and 90-fold more selectivity than fibroblast activation protein in vitro. [2]
In vivo In male Wistar rats, Beagle dogs, and Rhesus monkeys, Linagliptin shows a highly efficacious, long-lasting, and potent inhibitory activity against DPP-4 by more than 70% inhibition for all three species after oral administration of 1 mg/kg. Oral administration of Linagliptin to db/db mice 45 min before an oral glucose tolerance test reduces plasma glucose excursion in a dose-dependent manner from 0.1 mg/kg (15% inhibition) to 1 mg/kg (66% inhibition). [1] By inhibiting DPP-4 activity, Linagliptin reduces the expression of the proinflammatory markers cyclooxygenase-2 and macrophage inflammatory protein-2, and enhances the formation of myofibroblasts in healing wounds from ob/ob mice. [3]
Kinase Assay EDTA plasma (20 μL) is diluted with 30 μL of DPP-4 assay buffer (100 mM Tris and 100 mM NaCl, adjusted to pH 7.8 with HCl) and mixed with 50 μL of H-Ala-Pro-7-amido-4-trifluoromethylcoumarin. The 200 mM stock solution in dimethylformamide is diluted 1:1000 with water to yield a final concentration of 100 μM. The plate is incubated at room temperature for 10 min, and fluorescence in the wells is determined by using a Victor 1420 Multilabel Counter at an excitation wavelength of 405 nm and an emission wavelength of 535 nm. For the detection of DPP-4 activity in wound lysates, 100 μg of protein from the respective wound lysates are used instead of 20 μL of plasma. Active GLP-1 is also detected from 100 μg of respective wound tissue samples and analyzed by using the Mouse/Rat Total Active GLP-1 Assay Kit.
Cell Research A total of 4.0×107 keratinocytes per well are seeded into 24-well plates. After reaching 50% confluence, cells are starved for 24 h with DMEM. Proliferation of cells is assessed by using 1 μCi/mL of [3H]methyl-thymidine in DMEM in the presence of 10% fetal bovine serum and increasing concentrations of linagliptin (3, 30, 300, or 600 nM) for 24 h. Cells are then washed twice with phosphate-buffered saline and incubated in 5% trichloroacetic acid at 4°C for 30 min, and the DNA is solubilized in 0.5mol/LNaOH for 30 min at 37°C. Finally, [3H]thymidine incorporation is determined.
Synonyms BI 1356
Molecular Weight 472.54
Formula C25H28N8O2
CAS No. 668270-12-0

Storage

keep away from direct sunlight,store under nitrogen

Powder: -20°C for 3 years | In solvent: -80°C for 1 year

Solubility Information

DMSO: 14 mg/mL (29.6 mM)

H2O: < 1 mg/mL (insoluble or slightly soluble)

Ethanol: 1 mg/mL (2.11 mM)

TargetMolReferences and Literature

1. Eckhardt M, et al. J Med Chem. 2007, 50(26), 6450-6453. 2. Thomas L, J Pharmacol Exp Ther. 2008, 325(1), 175-182. 3. Schürmann C, et al. J Pharmacol Exp Ther. 2012, 342(1), 71-8.

Related compound libraries

This product is contained In the following compound libraries:
Anti-Cancer Drug Library Anti-Cancer Clinical Compound Library Bioactive Compounds Library Max Clinical Compound Library Anti-Diabetic Compound Library Drug Repurposing Compound Library Inhibitor Library Anti-Cancer Approved Drug Library Highly Selective Inhibitor Library EMA Approved Drug Library

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Keywords

Linagliptin 668270-12-0 Apoptosis Autophagy Proteases/Proteasome Ubiquitination Ferroptosis Proteasome DPP-4 Dipeptidyl Peptidase BI 1356 BI-1356 Inhibitor BI1356 DPP inhibit inhibitor

 

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