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906093-29-6

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  • 3-[[(2S,4S)-4-[4-(3-Methyl-1-phenyl-1H-pyrazol-5-yl)-1-piperazinyl]-2-pyrrolidinyl]carbonyl]-thiazolidine hydrobromide (2:5)

    Cas No: 906093-29-6

  • USD $ 10.0-10.0 / Gram

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906093-29-6 Usage

Description

Teneligliptin is a dipeptidyl peptidase-4 (DPP-4) inhibitor, a class of drugs used to treat type 2 diabetes. It works by inhibiting the DPP-4 enzyme, which in turn prolongs the action of incretin hormones, leading to improved glycemic control. Teneligliptin is characterized by its elimination via excretion and a half-life of 24.2 hours in the human body.

Uses

Used in Pharmaceutical Industry:
Teneligliptin is used as an oral antihyperglycemic agent for the treatment of type 2 diabetes. It helps to improve glycemic control by inhibiting the DPP-4 enzyme, which allows incretin hormones to stimulate insulin secretion and reduce glucagon release, thereby lowering blood glucose levels.

Biological Activity

teneligliptin hydrobromide is a novel, potent, and long-lasting dipeptidyl peptidase-4 (dpp-4) inhibitor with antioxidant properties; competitively inhibited human plasma, rat plasma, and human recombinant dpp-4 in vitro, with ic50 values of about 1 nm[1].dpp4 is also known as adenosine deaminase complexing protein 2 or cd26. dpp4 is an antigenic enzyme expressed on the membrane of most cell types and is associated with immune regulation, signal transduction and apoptosis [2].

Clinical Use

Teneligliptin is a DPP-4 inhibitor which was approved in Japan in 2012 for the treatment of type II diabetes. It was discovered and developed by Mitsubishi Tanabe Pharma under the trade name Tenelia?. Similar to other marketed DPP-4 inhibitors, teneligliptin was well tolerated in all studies and QD dosing produced a long-lasting inhibitory action against DPP-4 and an increase in active GLP-1 levels, with very low rates of renal excretion.

Synthesis

The only reported synthesis of teneligliptin is described in the scheme below. Reaction of commercially available N-Boc-piperazine (158) with diketene (159) in DMF at room temperature gave acetoacetamide 160 in 86% yield, and this material was immediately condensed with phenylhydrazine in methanesulfonic acid followed by a cyclodehydration with phosphorus oxychloride to give pyrazole 161 in 12% yield. The t-butyl carbamate was then removed with TFA in dichloromethane to give amine 162 in 88% yield. This amine was then subjected to butyrolactam 165 (which was prepared from N-Boctrans- 4-hydroxy-L-proline (163) coupled with thiazolidine (164) under conventional amide-forming conditions using EDC) in the presence of sodium triacetoxy borohydride (STAB-H) in acetic acid. This reductive amination reaction afforded the cis-aminopyrrolidine 166 exclusively in 50% yield. Removal of the t-butyl carbamate group with TFA afforded the teneligliptin free amine in 93% yield, and this freebase was then subsequently treated with 48% hydrobromic acid in refluxing ethanol to give teleligliptin hydrobromide hydrate (XXV) in 90% yield.

in vitro

in human umbilical vein endothelial cells, teneligliptin promoted the antioxidant response, reduced ros levels and induced nrf2-target genes messenger ribonucleic acid expression. teneligliptin improved proliferation rates in huvecs exposed to high glucose, regulating the expression of cell-cycle inhibitors markers (p21, p53 and p27), and reducing proapoptotic genes (bax and casp3), while promoteed bcl2 expression. teneligliptin ameliorated high glucose-induced endoplasmic reticulum stress. teneligliptin exihibited antioxidant properties and overcome the metabolic memory effect induced by chronic exposure to high glucose in huvecs[3].

in vivo

in teneligliptin-treated mice, serum alanine aminotransferase and intrahepatic triglyceride levels were significantly decreased (p < 0.05). teneligliptin also significantly downregulated hepatic mrna levels of the genes involved in de novo lipogenesis (p < 0.05). moreover, the hepatic expression levels of phosphorylated amp-activated protein kinase (ampk) protein were upregulated by teneligliptin[4]. orally administration of teneligliptin at a dosage of 20 mg once daily in adults in the ovariectomized (ovx) mice maintained on a high-fat diet, teneligliptin effectively ameliorated the characteristics of metabolic abnormalities associated with postmenopausal obesity. teneligliptin ameliorated the decreased energy consumption in the dark and light phases, reduced locomotor activity in the dark phase, and lowered core body temperature in ovx-hf[5].

references

[1] kishimoto m. teneligliptin: a dpp-4 inhibitor for the treatment of type 2 diabetes[j]. diabetes, metabolic syndrome and obesity: targets and therapy, 2013, 6: 187.[2] kameoka j, tanaka t, nojima y, et al. direct association of adenosine deaminase with a t cell activation antigen, cd26[j]. science, 1993, 261(5120): 466-469.[3] pujadas g, de nigris v, prattichizzo f, et al. the dipeptidyl peptidase-4 (dpp-4) inhibitor teneligliptin functions as antioxidant on human endothelial cells exposed to chronic hyperglycemia and metabolic high-glucose memory[j]. endocrine, 2016: 1-12.[4] ideta t, shirakami y, miyazaki t, et al. the dipeptidyl peptidase-4 inhibitor teneligliptin attenuates hepatic lipogenesis via ampk activation in non-alcoholic fatty liver disease model mice[j]. international journal of molecular sciences, 2015, 16(12): 29207-29218.[5] sameshima a, wada t, ito t, et al. teneligliptin improves metabolic abnormalities in a mouse model of postmenopausal obesity[j]. journal of endocrinology, 2015, 227(1): 25-36.

Check Digit Verification of cas no

The CAS Registry Mumber 906093-29-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,0,6,0,9 and 3 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 906093-29:
(8*9)+(7*0)+(6*6)+(5*0)+(4*9)+(3*3)+(2*2)+(1*9)=166
166 % 10 = 6
So 906093-29-6 is a valid CAS Registry Number.

906093-29-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name [(2S,4S)-4-[4-(5-methyl-2-phenylpyrazol-3-yl)piperazin-1-yl]pyrrolidin-2-yl]-(1,3-thiazolidin-3-yl)methanone,pentahydrobromide

1.2 Other means of identification

Product number -
Other names Teneligliptin hydrobromide

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:906093-29-6 SDS

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