Literature DB >> 22052555

Development of a comprehensive set of P2 receptor pharmacological research compounds.

R A Felix1, S Martin, S Pinion, D J Crawford.   

Abstract

Pharmacological manipulation of P2X and P2Y receptors has been critical to the elucidation of the biological roles of these receptors within a multitude of physiological and pathological processes. Initial purinergic signalling research made use of compounds based on pyridoxal phosphate, suramin and nucleotide analogues; recently developed compounds are often derivatives of these early tools. Tocris Bioscience first entered the field of purinergic signalling reagents with the commercial release of the pyridoxal phosphate derivative, iso-PPADS. During the past two decades, Tocris has assembled a collection of over 50 compounds for P2 receptor modulation, including research tools commercialised from both academic and industrial laboratories. Recently, a number of P2X subtype-selective compounds have been generated by pharmaceutical company medicinal chemistry programmes, supplementing our range of P2Y-selective compounds. Here, we detail the current, commercially available agonists and antagonists of P2X(1,2/3,3,4,7) and P2Y(1,6,11,12) receptors; considered together, they form the foundations of a comprehensive P2 receptor pharmacological 'toolkit'.

Entities:  

Year:  2011        PMID: 22052555      PMCID: PMC3265712          DOI: 10.1007/s11302-011-9270-7

Source DB:  PubMed          Journal:  Purinergic Signal        ISSN: 1573-9538            Impact factor:   3.765


  54 in total

1.  The suramin analogue NF279 is a novel and potent antagonist selective for the P2X(1) receptor.

Authors:  J Rettinger; G Schmalzing; S Damer; G Müller; P Nickel; G Lambrecht
Journal:  Neuropharmacology       Date:  2000-08-23       Impact factor: 5.250

2.  The novel pyridoxal-5'-phosphate derivative PPNDS potently antagonizes activation of P2X(1) receptors.

Authors:  G Lambrecht; J Rettinger; H G Bäumert; S Czeche; S Damer; M Ganso; C Hildebrandt; B Niebel; G Spatz-Kümbel; G Schmalzing; E Mutschler
Journal:  Eur J Pharmacol       Date:  2000-01-17       Impact factor: 4.432

3.  Emerging structures and ligands for P2X(3) and P2X(4) receptors-towards novel treatments of neuropathic pain.

Authors:  Christa E Müller
Journal:  Purinergic Signal       Date:  2010-05-16       Impact factor: 3.765

4.  Profiling at recombinant homomeric and heteromeric rat P2X receptors identifies the suramin analogue NF449 as a highly potent P2X1 receptor antagonist.

Authors:  Jürgen Rettinger; Kirsten Braun; Henrike Hochmann; Matthias U Kassack; Heiko Ullmann; Peter Nickel; Günther Schmalzing; Günter Lambrecht
Journal:  Neuropharmacology       Date:  2005-03       Impact factor: 5.250

5.  A-740003 [N-(1-{[(cyanoimino)(5-quinolinylamino) methyl]amino}-2,2-dimethylpropyl)-2-(3,4-dimethoxyphenyl)acetamide], a novel and selective P2X7 receptor antagonist, dose-dependently reduces neuropathic pain in the rat.

Authors:  Prisca Honore; Diana Donnelly-Roberts; Marian T Namovic; Gin Hsieh; Chang Z Zhu; Joe P Mikusa; Gricelda Hernandez; Chengmin Zhong; Donna M Gauvin; Prasant Chandran; Richard Harris; Arturo Perez Medrano; William Carroll; Kennan Marsh; James P Sullivan; Connie R Faltynek; Michael F Jarvis
Journal:  J Pharmacol Exp Ther       Date:  2006-09-18       Impact factor: 4.030

6.  Identification of regions of the P2X(7) receptor that contribute to human and rat species differences in antagonist effects.

Authors:  A D Michel; W C Clay; S W Ng; S Roman; K Thompson; J P Condreay; M Hall; J Holbrook; D Livermore; S Senger
Journal:  Br J Pharmacol       Date:  2008-07-28       Impact factor: 8.739

7.  Structure-activity relationships of analogues of NF449 confirm NF449 as the most potent and selective known P2X1 receptor antagonist.

Authors:  Matthias U Kassack; Kirsten Braun; Matthias Ganso; Heiko Ullmann; Peter Nickel; Barbara Böing; Gregor Müller; Günter Lambrecht
Journal:  Eur J Med Chem       Date:  2004-04       Impact factor: 6.514

8.  NF546 [4,4'-(carbonylbis(imino-3,1-phenylene-carbonylimino-3,1-(4-methyl-phenylene)-carbonylimino))-bis(1,3-xylene-alpha,alpha'-diphosphonic acid) tetrasodium salt] is a non-nucleotide P2Y11 agonist and stimulates release of interleukin-8 from human monocyte-derived dendritic cells.

Authors:  Sabine Meis; Alexandra Hamacher; Darunee Hongwiset; Claudia Marzian; Michael Wiese; Niels Eckstein; Hans-Dieter Royer; Didier Communi; Jean-Marie Boeynaems; Ralf Hausmann; Günther Schmalzing; Matthias U Kassack
Journal:  J Pharmacol Exp Ther       Date:  2009-10-08       Impact factor: 4.030

9.  2-Substitution of adenine nucleotide analogues containing a bicyclo[3.1.0]hexane ring system locked in a northern conformation: enhanced potency as P2Y1 receptor antagonists.

Authors:  Hak Sung Kim; Michihiro Ohno; Bin Xu; Hea Ok Kim; Yongseok Choi; Xiao D Ji; Savitri Maddileti; Victor E Marquez; T Kendall Harden; Kenneth A Jacobson
Journal:  J Med Chem       Date:  2003-11-06       Impact factor: 7.446

10.  Mammalian P2X7 receptor pharmacology: comparison of recombinant mouse, rat and human P2X7 receptors.

Authors:  Diana L Donnelly-Roberts; Marian T Namovic; Ping Han; Michael F Jarvis
Journal:  Br J Pharmacol       Date:  2009-06-22       Impact factor: 8.739

View more
  6 in total

Review 1.  G protein-coupled adenosine (P1) and P2Y receptors: ligand design and receptor interactions.

Authors:  Kenneth A Jacobson; Ramachandran Balasubramanian; Francesca Deflorian; Zhan-Guo Gao
Journal:  Purinergic Signal       Date:  2012-02-29       Impact factor: 3.765

Review 2.  Supportive or detrimental roles of P2Y receptors in brain pathology?--The two faces of P2Y receptors in stroke and neurodegeneration detected in neural cell and in animal model studies.

Authors:  Daniel Förster; Georg Reiser
Journal:  Purinergic Signal       Date:  2015-09-25       Impact factor: 3.765

3.  [PSB0739 inhibits formation of semen-derived amyloid fibril].

Authors:  Yan Lan; Zichao Yang; Han Liu; Hongyan Cheng; Shuwen Liu; Suiyi Tan
Journal:  Nan Fang Yi Ke Da Xue Xue Bao       Date:  2018-11-30

Review 4.  Exploring the Therapeutic Potential of Targeting Purinergic and Orexinergic Receptors in Alcoholic Neuropathy.

Authors:  Piyush Madaan; Tapan Behl; Aayush Sehgal; Sukhbir Singh; Neelam Sharma; Shivam Yadav; Satvinder Kaur; Saurabh Bhatia; Ahmed Al-Harrasi; Ahmed A H Abdellatif; Ghulam Md Ashraf; Mohamed M Abdel-Daim; Hamad Ghaleb Dailah; Md Khalid Anwer; Simona Bungau
Journal:  Neurotox Res       Date:  2022-01-26       Impact factor: 3.911

5.  P2Y2R is a direct target of HIF-1α and mediates secretion-dependent cyst growth of renal cyst-forming epithelial cells.

Authors:  Andre Kraus; Steffen Grampp; Margarete Goppelt-Struebe; Rainer Schreiber; Karl Kunzelmann; Dorien J M Peters; Jens Leipziger; Gunnar Schley; Johannes Schödel; Kai-Uwe Eckardt; Bjoern Buchholz
Journal:  Purinergic Signal       Date:  2016-08-26       Impact factor: 3.765

6.  The role of purinergic receptors in cancer-induced bone pain.

Authors:  Sarah Falk; Maria Uldall; Anne-Marie Heegaard
Journal:  J Osteoporos       Date:  2012-10-03
  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.