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1.
Chemistry ; 24(21): 5444-5449, 2018 Apr 11.
Article in English | MEDLINE | ID: mdl-29338097

ABSTRACT

The synthesis of multifunctional spirocycles was achieved from common cyclic carboxylic acids (cyclobutane carboxylate, cyclopentane carboxylate, l-proline, etc.). The whole sequence included only two chemical steps-synthesis of azetidinones, and reduction into azetidines. The obtained spirocyclic amino acids were incorporated into a structure of the known anesthetic drug Bupivacaine. The obtained analogues were more active and less toxic than the original drug. We believe that this discovery will lead to a wide use of spirocyclic building blocks in drug discovery in the near future.


Subject(s)
Azetidines/chemical synthesis , Azetidines/pharmacology , Drug Discovery , Spiro Compounds/chemical synthesis , Spiro Compounds/pharmacology , Anesthetics/chemistry , Azetidines/chemistry , Bupivacaine/chemistry , Carboxylic Acids/chemistry , Cyclopentanes/chemistry , Proline/chemistry , Spiro Compounds/chemistry
2.
Biochim Biophys Acta ; 1834(10): 2170-5, 2013 Oct.
Article in English | MEDLINE | ID: mdl-23220417

ABSTRACT

Recent studies of insulin receptor-related receptor (IRR) revealed its unusual property to activate upon extracellular application of mildly alkaline media, pH>7.9. The activation of IRR with hydroxyl anion has typical features of ligand-receptor interaction; it is specific, dose-dependent, involves the IRR extracellular domain and is accompanied by a major conformational change. IRR is a member of the insulin receptor minifamily and has been long viewed as an orphan receptor tyrosine kinase since no peptide or protein agonist of IRR was found. In the evolution, IRR is highly conserved since its divergence from the insulin and insulin-like growth factor receptors in amphibia. The latter two cannot be activated by alkali. Another major difference between them is that unlike ubiquitously expressed insulin and insulin-like growth factor receptors, IRR is found in specific sets of cells of only some tissues, most of them being exposed to extracorporeal liquids of extreme pH. In particular, largest concentrations of IRR are in beta-intercalated cells of the kidneys. The primary physiological function of these cells is to excrete excessive alkali as bicarbonate into urine. When IRR is removed genetically, animals loose the property to excrete bicarbonate upon experimentally induced alkalosis. In this review, we will discuss the available in vitro and in vivo data that support the hypothesis of IRR role as a physiological alkali sensor that regulates acid-base balance. This article is part of a Special Issue entitled: Emerging recognition and activation mechanisms of receptor tyrosine kinases.


Subject(s)
Acid-Base Equilibrium/physiology , Hydroxides/metabolism , Kidney/physiology , Receptor, Insulin/chemistry , Animals , Bicarbonates/metabolism , Biological Evolution , Extracellular Space/metabolism , Humans , Hydrogen-Ion Concentration , Insulin/chemistry , Insulin/physiology , Models, Molecular , Organ Specificity , Protein Structure, Tertiary , Receptor, Insulin/physiology , Signal Transduction
3.
Cell Metab ; 13(6): 679-89, 2011 Jun 08.
Article in English | MEDLINE | ID: mdl-21641549

ABSTRACT

The insulin receptor-related receptor (IRR), an orphan receptor tyrosine kinase of the insulin receptor family, can be activated by alkaline media both in vitro and in vivo at pH >7.9. The alkali-sensing property of IRR is conserved in frog, mouse, and human. IRR activation is specific, dose-dependent and quickly reversible and demonstrates positive cooperativity. It also triggers receptor conformational changes and elicits intracellular signaling. The pH sensitivity of IRR is primarily defined by its L1F extracellular domains. IRR is predominantly expressed in organs that come in contact with mildly alkaline media. In particular, IRR is expressed in the cell subsets of the kidney that secrete bicarbonate into urine. Disruption of IRR in mice impairs the renal response to alkali loading attested by development of metabolic alkalosis and decreased urinary bicarbonate excretion in response to this challenge. We therefore postulate that IRR is an alkali sensor that functions in the kidney to manage metabolic bicarbonate excess.


Subject(s)
Receptor, Insulin/metabolism , Recombinant Fusion Proteins/metabolism , Animals , Cell Line , Culture Media , Humans , Hydrogen-Ion Concentration , Kidney/drug effects , Kidney/metabolism , Mice , Mice, Inbred C57BL , Mice, Knockout , Mutagenesis, Site-Directed , Phosphorylation , Protein Processing, Post-Translational , Protein Structure, Tertiary , Rats , Receptor, Insulin/genetics , Recombinant Fusion Proteins/genetics , Signal Transduction , Sodium Bicarbonate/pharmacology , Sodium Bicarbonate/urine , Xenopus laevis
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