V. Ilyin

发表

Cysteine racemization during the Fmoc solid phase peptide synthesis of the Nav1.7‐selective peptide – protoxin II

K. Carlin, Gang Wu, D. Kyle, 2012, Journal of peptide science : an official publication of the European Peptide Society.

Components of the GABAergic signaling in the peripheral cholinergic synapses of vertebrates: a review

E. Nikolsky, V. Ilyin, A. Malomouzh, 2019, Amino Acids.

1-Hydroxy-1,4-dihydroquinoxaline-2,3-diones: Novel antagonists at NMDA receptor glycine sites

J. Hawkinson, S. Espitia, J. Keana, 1996 .

Subtype-selective inhibition of N-methyl-D-aspartate receptors by haloperidol.

E. R. Whittemore, J. Guastella, E. Weber, 1996, Molecular pharmacology.

New evidence for dual binding site inhibitors of acetylcholinesterase as improved drugs for treatment of Alzheimer's disease

N. Petrova, P. Masson, T. Pashirova, 2019, Neuropharmacology.

Pharmacology of ACEA-1416: a potent systemically active NMDA receptor glycine site antagonist.

E. R. Whittemore, S. Cai, M. Tran, 1996, European journal of pharmacology.

Intracellular ATP modifies the voltage dependence of the fast transient outward K+ current in Lymnaea stagnalis neurones.

N. Lozovaya, V. Ilyin, C. Vulfius, 1993, The Journal of physiology.

Effects of alcohols on responses evoked by inositol trisphosphate in Xenopus oocytes.

I. Parker, V. Ilyin, Ian Parker, 1992, Journal of Physiology.

Phenoxyphenyl pyridines as novel state-dependent, high-potency sodium channel inhibitors.

R. B. Carter, G. Sakellaropoulos, Qun Sun, 2004, Journal of medicinal chemistry.

3-(4-phenoxyphenyl)pyrazoles: a novel class of sodium channel blockers.

R. B. Carter, P. Gharagozloo, D. Hogenkamp, 2004, Journal of medicinal chemistry.

Structure-activity relationships of alkyl- and alkoxy-substituted 1,4-dihydroquinoxaline-2,3-diones: potent and systemically active antagonists for the glycine site of the NMDA receptor.

J. Hawkinson, S. Espitia, S. Cai, 1997, Journal of medicinal chemistry.

5-(N-oxyaza)-7-substituted-1,4-dihydroquinoxaline-2,3-diones: novel, systemically active and broad spectrum antagonists for NMDA/glycine, AMPA, and kainate receptors.

J. Hawkinson, S. Espitia, S. Cai, 1997, Journal of medicinal chemistry.

Specific inhibition of acetylcholinesterase as an approach to decrease muscarinic side effects during myasthenia gravis treatment

E. Nikolsky, I. Zueva, K. Petrov, 2018, Scientific Reports.

Generation of twitch tension in frog atrial fibers by Na/Ca exchange.

A. Filippov, V. Ilyin, V. Porotikov, 1988, General physiology and biophysics.

Validation of a Fluorescent Imaging Plate Reader Membrane Potential Assay for High-Throughput Screening of Glycine Transporter Modulators

K. Valenzano, E. Benjamin, V. Ilyin, 2005, Journal of biomolecular screening.

V102862 (Co 102862): a potent, broad‐spectrum state‐dependent blocker of mammalian voltage‐gated sodium channels

R. B. Carter, E. R. Whittemore, S. Cai, 2005, British journal of pharmacology.

Synthesis and structure-activity relationships of substituted 1,4-dihydroquinoxaline-2,3-diones: antagonists of N-methyl-D-aspartate (NMDA) receptor glycine sites and non-NMDA glutamate receptors.

S. Cai, S. Kher, J. Guastella, 1995, Journal of medicinal chemistry.

Synthesis and Structure‐Activity Relationships of Substituted 1,4‐ Dihydroquinoxaline‐2,3‐diones: Antagonists of N‐Methyl‐D‐aspartate ( NMDA) Receptor Glycine Sites and Non‐NMDA Glutamate Receptors.

S. Cai, S. Kher, J. Guastella, 1996 .

Roleofcytosolic Ca2" ininhibition ofInsP3-evoked Ca2" release inXenopus oocytes

V. Ilyin, 2011 .

Role of cytosolic Ca2+ in inhibition of InsP3‐evoked Ca2+ release in Xenopus oocytes.

I. Parker, V. Ilyin, 1994, The Journal of physiology.

A-317491, a selective P2X3/P2X2/3 receptor antagonist, reverses inflammatory mechanical hyperalgesia through action at peripheral receptors in rats.

Gary Lee, M. Niosi, Gang Wu, 2004, European journal of pharmacology.

Fast kinetics of calcium liberation induced in Xenopus oocytes by photoreleased inositol trisphosphate.

I. Parker, Y. Yao, I Parker, 1996, Biophysical journal.

State-Dependent Compound Inhibition of Nav1.2 Sodium Channels Using the FLIPR Vm Dye: On-Target and Off-Target Effects of Diverse Pharmacological Agents

K. Valenzano, E. Benjamin, V. Ilyin, 2006, Journal of biomolecular screening.

Antagonism of N-methyl-D-aspartate receptors by sigma site ligands: potency, subtype-selectivity and mechanisms of inhibition.

E. R. Whittemore, V. Ilyin, R. Woodward, 1997, The Journal of pharmacology and experimental therapeutics.

Shear stress regulates the endothelial Kir2.1 ion channel

A. Hoger, V. Ilyin, S. Forsyth, 2002, Proceedings of the National Academy of Sciences of the United States of America.

and Off-Target Effects of Diverse Pharmacological Agents Dye: On-Target m 1.2 Sodium Channels Using the FLIPR V v State-Dependent Compound Inhibition of Na

K. Valenzano, E. Benjamin, V. Ilyin, 2013 .

The cole-moore effect in nodal membrane of the frogRana ridibunda: Evidence for fast and slow potassium channels

A. V. Lonskii, V. Ilyin, V. Makovsky, 1980, The Journal of Membrane Biology.

Pharmacological characterization of recombinant N-type calcium channel (Cav2.2) mediated calcium mobilization using FLIPR.

K. Valenzano, E. Benjamin, V. Ilyin, 2006, Biochemical pharmacology.

Synthesis of 7,8-(methylenedioxy)-1-phenyl-3,5-dihydro-4H-2, 3-benzodiazepin-4-ones as novel and potent noncompetitive AMPA receptor antagonists.

R. B. Carter, S. Cai, Y. Wang, 1998, Journal of Medicinal Chemistry.

Subtype-selective antagonism of NMDA receptors by nylidrin.

E. R. Whittemore, V. Ilyin, R. Woodward, 1997, European journal of pharmacology.

Intracellular ATP modulates desensitization of acetylcholine receptors controlling chloride current in Lymnaea neurons

N. Lozovaya, V. Ilyin, C. Vulfius, 1993, Pflügers Archiv.

The Higgs Working Group: Summary report

A. Bocci, R. Pittau, D. Cavalli, 1999, 0803.1154.

Pharmacology of 2-[4-(4-Chloro-2-fluorophenoxy)phenyl]-pyrimidine-4-carboxamide: A Potent, Broad-Spectrum State-Dependent Sodium Channel Blocker for Treating Pain States

R. B. Carter, J. Pomonis, D. Hogenkamp, 2006, Journal of Pharmacology and Experimental Therapeutics.

Studies examining the relationship between the chemical structure of protoxin II and its activity on voltage gated sodium channels.

K. Carlin, P. Blake, Gang Wu, 2014, Journal of medicinal chemistry.

Intracellular Mg2+ modulates the A-current and its blockage by catechol in isolated Lymnaea neurons

N. Lozovaya, V. Ilyin, L. Erdélyi, 1990, Neuroscience Letters.