Literature DB >> 31630858

One-pot synthesis of novel tert-butyl-4-substituted phenyl-1H-1,2,3-triazolo piperazine/piperidine carboxylates, potential GPR119 agonists.

Nagaraju Bashetti1, J V Shanmukha Kumar1, Naresh Varma Seelam1, B Prasanna1, Akiva Mintz2, Naresh Damuka3, Sriram Devanathan4, Kiran Kumar Solingapuram Sai5.   

Abstract

We have synthesized a new series of 1,2,3-triazolo piperazine and piperidine carboxylate derivatives using a simple and one-pot click chemistry with significantly reduced reaction times (~5 min) and enhanced reaction yields (~95-98%). The fourteen novel compounds thus synthesized were tested for ability to target GPR119, a G-protein coupled target receptor that plays critical role in regulation of type-2 diabetes mellitus. Four analogs (3e, 3g, 5e and 5g) demonstrated similar or better EC50 values over previously reported AR231453 activity towards GPR119.
Copyright © 2019 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Agonist; Click chemistry; GPR119; PET

Mesh:

Substances:

Year:  2019        PMID: 31630858      PMCID: PMC9214832          DOI: 10.1016/j.bmcl.2019.126707

Source DB:  PubMed          Journal:  Bioorg Med Chem Lett        ISSN: 0960-894X            Impact factor:   2.940


  17 in total

Review 1.  GPR119 agonists for the potential treatment of type 2 diabetes and related metabolic disorders.

Authors:  Unmesh Shah; Timothy J Kowalski
Journal:  Vitam Horm       Date:  2010       Impact factor: 3.421

2.  Discovery and characterization of novel small molecule agonists of G protein-coupled receptor 119.

Authors:  Shu-yong Zhang; Jing Li; Xin Xie
Journal:  Acta Pharmacol Sin       Date:  2014-03-31       Impact factor: 6.150

3.  The inhibition of receptor-mediated and voltage-dependent calcium entry by the antiproliferative L-651,582.

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4.  First triazole-bridged unsymmetrical porphyrin dyad via click chemistry.

Authors:  Sokkalingam Punidha; Jasmine Sinha; Anil Kumar; Mangalampalli Ravikanth
Journal:  J Org Chem       Date:  2007-12-11       Impact factor: 4.354

5.  Synthesis and pharmacological evaluation of CNS activities of [1,2,3]triazolo[4,5-b][1,5]-, imidazolo[4,5-b][1,5]-, and pyrido[2,3-b][1,5]benzodiazepines. 10-Piperazinyl-4H-1,2,3-triazolo[4,5-b][1,5]benzodiazepines with neuroleptic activity.

Authors:  J K Chakrabarti; T M Hotten; I A Pullar; D J Steggles
Journal:  J Med Chem       Date:  1989-10       Impact factor: 7.446

6.  GABA receptors on the somatic muscle cells of the parasitic nematode, Ascaris suum: stereoselectivity indicates similarity to a GABAA-type agonist recognition site.

Authors:  L Holden-Dye; P Krogsgaard-Larsen; L Nielsen; R J Walker
Journal:  Br J Pharmacol       Date:  1989-11       Impact factor: 8.739

7.  Biased signaling of lipids and allosteric actions of synthetic molecules for GPR119.

Authors:  Helle A Hassing; Suzan Fares; Olav Larsen; Hamideh Pad; Maria Hauge; Robert M Jones; Thue W Schwartz; Harald S Hansen; Mette M Rosenkilde
Journal:  Biochem Pharmacol       Date:  2016-08-26       Impact factor: 5.858

8.  Evaluation of N-phenyl homopiperazine analogs as potential dopamine D3 receptor selective ligands.

Authors:  Aixiao Li; Yogesh Mishra; Maninder Malik; Qi Wang; Shihong Li; Michelle Taylor; David E Reichert; Robert R Luedtke; Robert H Mach
Journal:  Bioorg Med Chem       Date:  2013-04-06       Impact factor: 3.641

9.  Bioisosteres of arecoline: 1,2,3,6-tetrahydro-5-pyridyl-substituted and 3-piperidyl-substituted derivatives of tetrazoles and 1,2,3-triazoles. Synthesis and muscarinic activity.

Authors:  E K Moltzen; H Pedersen; K P Bøgesø; E Meier; K Frederiksen; C Sánchez; H Løve Lembøl
Journal:  J Med Chem       Date:  1994-11-25       Impact factor: 7.446

10.  1,2,3-Triazole-[2',5'-bis-O-(tert-butyldimethylsilyl)-beta-D- ribofuranosyl]-3'-spiro-5"-(4"-amino-1",2"-oxathiole 2",2"-dioxide) (TSAO) analogues: synthesis and anti-HIV-1 activity.

Authors:  R Alvarez; S Velázquez; A San-Félix; S Aquaro; E De Clercq; C F Perno; A Karlsson; J Balzarini; M J Camarasa
Journal:  J Med Chem       Date:  1994-11-25       Impact factor: 7.446

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