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Teneligliptin (hydrobromide)

CAT: 0804-HY-14806A-01Size: 5 mgDry Ice: NoHazardous: No
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CAT#:0804-HY-14806A-01Size:5 mg
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Description
Teneligliptin (MP-513) hydrobromide is an orally active and selective dipeptidyl peptidase 4 (DPP-4) inhibitor (IC50s: 0.37 and 0.29 nM for the human and rat DPP-4, respectively) . Teneligliptin hydrobromide improves blood glucose levels and can be used in researches related to type 2 diabetes mellitus[1][2][3][4][5][6][7][8].
CAS Number
906093-29-6
Product Name Alternative
MP-513 (hydrobromide)
UNSPSC
12352211
Hazard Statement
H302, H315, H319, H335
Target
AMPK; Apoptosis; Dipeptidyl Peptidase; Interleukin Related; JNK; NF-κB; NOD-like Receptor (NLR) ; p38 MAPK; Reactive Oxygen Species (ROS)
Type
Reference compound
Related Pathways
Apoptosis; Epigenetics; Immunology/Inflammation; MAPK/ERK Pathway; Metabolic Enzyme/Protease; NF-κB; PI3K/Akt/mTOR
Applications
Metabolism-sugar/lipid metabolism
Field of Research
Metabolic Disease; Neurological Disease; Cardiovascular Disease
Assay Protocol
https://www.medchemexpress.com/Teneligliptin-hydrobromide.html
Purity
99.99
Solubility
DMSO : ≥ 100 mg/mL|H2O : ≥ 200 mg/mL
Smiles
O=C(N1CSCC1)[C@H]2NC[C@@H](N3CCN(C4=CC(C)=NN4C5=CC=CC=C5)CC3)C2.[2.5HBr]
Molecular Formula
C22H30N6OS.5/2HBr
Molecular Weight
628.86
Precautions
H302, H315, H319, H335
References & Citations
[1]Yoshida T, et al. Discovery and preclinical profile of teneligliptin (3-[ (2S,4S) -4-[4- (3-methyl-1-phenyl-1H-pyrazol-5-yl) piperazin-1-yl]pyrrolidin-2-ylcarbonyl]thiazolidine) : a highly potent, selective, long-lasting and orally active dipeptidyl peptidase IV inhibitor for the treatment of type 2 diabetes. Bioorg Med Chem. 2012 Oct 1;20 (19) :5705-19.|[2]Guo D, et al. Beneficial effects of combination therapy of canagliflozin and teneligliptin on diabetic polyneuropathy and β-cell volume density in spontaneously type 2 diabetic Goto-Kakizaki rats. Metabolism. 2020 Jun;107:154232.|[3]Zhang GL, et al. Teneligliptin mitigates diabetic cardiomyopathy by inhibiting activation of the NLRP3 inflammasome. World J Diabetes. 2024 Apr 15;15 (4) :724-734.|[4]Fukuda-Tsuru S, et al. The novel dipeptidyl peptidase-4 inhibitor teneligliptin prevents high-fat diet-induced obesity accompanied with increased energy expenditure in mice. Eur J Pharmacol. 2014 Jan 15;723:207-15.|[5]Zhang Z, et al. Teneligliptin protects against hypoxia/reoxygenation-induced endothelial cell injury. Biomed Pharmacother. 2019 Jan;109:468-474.|[6]Peng W, et al. Teneligliptin prevents doxorubicin-induced inflammation and apoptosis in H9c2 cells. Arch Biochem Biophys. 2020 Apr 15;683:108238.|[7]Liu X, et al. Teneligliptin inhibits lipopolysaccharide-induced cytotoxicity and inflammation in dental pulp cells. Int Immunopharmacol. 2019 Aug;73:57-63.|[8]Elumalai S, et al. High glucose-induced PRDX3 acetylation contributes to glucotoxicity in pancreatic β-cells: Prevention by Teneligliptin. Free Radic Biol Med. 2020 Nov 20;160:618-629.
Shipping Conditions
Room Temperature
Storage Conditions
4°C (Powder, sealed storage, away from moisture)
Scientific Category
Reference compound1
Clinical Information
Launched
Isoform
DPP-4; p38 MAPK
Citation 01
Cosmetics. 2024 Mar 1, 11 (2), 35.|Antioxidants (Basel) . 2021 Sep 9;10 (9) :1438.|Antioxidants (Basel) . 2023 Jul 24;12 (7) :1478.|Chem Res Toxicol. 2020 Aug 17;33 (8) :2164-2171.|Eur J Med Chem. 2021 Feb 15;212:113030.|Nephrol Dial Transplant. 2019 Oct 1;34 (10) :1669-1680.

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