A. Mitschler

发表

Ultrahigh resolution drug design I: Details of interactions in human aldose reductase–inhibitor complex at 0.66 Å

R E Cachau, B Chevrier, V. Lamour, 2004, Proteins.

Transmembrane Signaling across the Ligand-Gated FhuA Receptor Crystal Structures of Free and Ferrichrome-Bound States Reveal Allosteric Changes

Luc Moulinier, Bernard Rees, Dino Moras, 1998, Cell.

A 'specificity' pocket inferred from the crystal structures of the complexes of aldose reductase with the pharmaceutically important inhibitors tolrestat and sorbinil.

D. Moras, P. Barth, A. Urzhumtsev, 1997, Structure.

Linear and extended : a common polyglutamine conformation recognized by the three antibodies MW 1 , 1 C 2 and 3 B 5 H 10

J. Mandel, A. Mitschler, A. Podjarny, 2013 .

Linear and extended: a common polyglutamine conformation recognized by the three antibodies MW1, 1C2 and 3B5H10.

J. Mandel, A. Mitschler, A. Podjarny, 2013, Human molecular genetics.

Comparison of hydrogen determination with X-ray and neutron crystallography in a human aldose reductase–inhibitor complex

A. Mitschler, A. Podjarny, D. Myles, 2006, European Biophysics Journal.

Palladium(II) tert-butyl peroxide carboxylates. New reagents for the selective oxidation of terminal olefins to methyl ketones. The role of peroxymetalation in selective oxidative processes

A. Mitschler, J. Fischer, R. Weiss, 1980 .

Frataxin from Psychromonas ingrahamii as a model to study stability modulation within the CyaY protein family.

Javier Santos, A. Mitschler, A. Podjarny, 2013, Biochimica et biophysica acta.

Class II aminoacyl transfer RNA synthetases: crystal structure of yeast aspartyl-tRNA synthetase complexed with tRNA(Asp)

D. Moras, A. Mitschler, A. Podjarny, 1991, Science.

A high resolution diffracting crystal form of the complex between yeast tRNAAsp and aspartyl-tRNA synthetase.

B. Lorber, R. Giegé, D. Moras, 1988, Journal of molecular biology.

Structural analysis of sulindac as an inhibitor of aldose reductase and AKR1B10.

A. Mitschler, A. Podjarny, J. Farrés, 2015, Chemico-biological interactions.

Design, synthesis, structure-activity relationships and X-ray structural studies of novel 1-oxopyrimido[4,5-c]quinoline-2-acetic acid derivatives as selective and potent inhibitors of human aldose reductase.

D. Kletsas, H. Pratsinis, A. Mitschler, 2018, European journal of medicinal chemistry.

Neutron macromolecular crystallography with LADI-III.

E. Howard, A. Mitschler, A. Podjarny, 2010, Acta crystallographica. Section D, Biological crystallography.

X-ray-radiation-induced cooperative atomic movements in protein.

A. Joachimiak, V. Lunin, T. Petrova, 2009, Journal of molecular biology.

Ultrahigh-resolution study of protein atomic displacement parameters at cryotemperatures obtained with a helium cryostat.

A. Joachimiak, V. Lunin, T. Petrova, 2006, Acta crystallographica. Section D, Biological crystallography.

High-resolution neutron protein crystallography with radically small crystal volumes: application of perdeuteration to human aldose reductase.

A. van Dorsselaer, A. Mitschler, A. Podjarny, 2005, Acta crystallographica. Section D, Biological crystallography.

Production of crystals of human aldose reductase with very high resolution diffraction.

V. Lamour, D. Moras, P. Barth, 1999, Acta crystallographica. Section D, Biological crystallography.

Model of the catalytic mechanism of human aldose reductase based on quantum chemical calculations

V. Lamour, A. Joachimiak, D. Moras, 2000 .

X-ray crystallography at subatomic resolution

C. Lecomte, E. Howard, A. Mitschler, 2002 .

The crystal structure of the nuclear receptor for vitamin D bound to its natural ligand.

D. Moras, N. Rochel, J. Wurtz, 2000, Molecular cell.

Enantiomer discrimination illustrated by high-resolution crystal structures of the human nuclear receptor hRARgamma.

D. Moras, B. Klaholz, A. Mitschler, 2000, Proceedings of the National Academy of Sciences of the United States of America.

Structural basis for isotype selectivity of the human retinoic acid nuclear receptor.

D. Moras, B. Klaholz, A. Mitschler, 2000, Journal of molecular biology.

RARβ ligand‐binding domain bound to an SRC‐1 co‐activator peptide: purification, crystallization and preliminary X‐ray diffraction analysis

H. Gronemeyer, D. Moras, N. Rochel, 2004 .

A eucentric goniometer head sliding on an extended removable arc modified for use in cryocrystallography

D. Moras, B. Klaholz, A. Mitschler, 1998 .

X-ray-induced deterioration of disulfide bridges at atomic resolution.

A. Joachimiak, V. Lunin, Youngchang Kim, 2010, Acta crystallographica. Section D, Biological crystallography.

IDD388 Polyhalogenated Derivatives as Probes for an Improved Structure-Based Selectivity of AKR1B10 Inhibitors.

A. Mitschler, A. Podjarny, P. Hobza, 2016, ACS chemical biology.

Enhancing Binding Affinity of an Intrinsically Disordered Protein by α-Methylation of Key Amino Acid Residues

N. Rochel, Y. Nominé, G. Travé, 2019 .

High-Risk Mucosal Human Papillomavirus 16 (HPV16) E6 Protein and Cutaneous HPV5 and HPV8 E6 Proteins Employ Distinct Strategies To Interfere with Interferon Regulatory Factor 3-Mediated Beta Interferon Expression

P. Peixoto, D. Altschuh, Y. Chebaro, 2022, Journal of virology.

Structural Basis of Outstanding Multivalent Effects in Jack Bean α-Mannosidase Inhibition.

E. Howard, A. Mitschler, A. Podjarny, 2018, Angewandte Chemie.

Organometallic complexes with metal—metal bonds: XVI. Synthesis of new tri- and tetrametallic platinum-manganese complexes. Crystal structures of (OC)4Mn(μ2-PPh2)Pt(CO)(μ2-PPh2)Mn(CO)4, (OC)4Mn(μ2-PPh2)PtH(μ2-PPh2)2Mn(CO)4 and (OC)4Mn(μ2-PPh2)Pt(μ2-PPh2)2Pt(μ2-PPh2)Mn(CO)4

A. Mitschler, J. Fischer, P. Braunstein, 1981 .

Structural basis for the inhibition of AKR1B10 by the C3 brominated TTNPB derivative UVI2008.

A. Mitschler, A. Podjarny, A. D. de Lera, 2017, Chemico-biological interactions.

Structural variability of E. coli thioredoxin captured in the crystal structures of single-point mutants

Javier Santos, E. Howard, A. Mitschler, 2017, Scientific Reports.

Structural and functional studies of ReP1-NCXSQ, a protein regulating the squid nerve Na+/Ca2+ exchanger.

C. Schulze-Briese, R. Dipolo, V. Olieric, 2012, Acta crystallographica. Section D, Biological crystallography.

X-rays-Induced Cooperative Atomic Movement in a Protein Crystal

A. Joachimiak, V. Lunin, Youngchang Kim, 2013 .

Crystallization and preliminary X-ray analysis ofEscherichia coli methionyl–tRNAfMet formyltransferase

D. Moras, Y. Mechulam, E. Schmitt, 1996 .

Crystallization and preliminary X‐ray analysis of Escherichia coli methionyl–tRNA fMet formyltransferase

D. Moras, Y. Mechulam, E. Schmitt, 1996, Proteins.

Crystallization of threonyl‐tRNA synthetase from Thermus thermophilus and preliminary crystallographic data

D. Moras, D. Kern, A. Mitschler, 1995, FEBS letters.

2-Substituted-2-amino-6-boronohexanoic acids as arginase inhibitors.

A. Mazur, A. Mitschler, M. V. Van Zandt, 2013, Bioorganic & medicinal chemistry letters.

Factorizing selectivity determinants of inhibitor binding toward aldose and aldehyde reductases: structural and thermodynamic properties of the aldose reductase mutant Leu300Pro-fidarestat complex.

G. Klebe, O. El-Kabbani, A. Joachimiak, 2005, Journal of medicinal chemistry.

Bonding in a binuclear metal carbonyl: experimental charge density in Mn2(CO)10

A. Mitschler, B. Rees, M. Martin, 1982 .

MODELS FOR THE REDUCED STATES OF CYTOCHROME P-450 AND CHLOROPEROXIDASE. STRUCTURES OF A PENTACOORDINATE HIGH-SPIN IRON(II) MERCAPTIDE MESOPORPHYRIN DERIVATIVE AND ITS CARBONYL ADDUCT

A. Mitschler, R. Weiss, L. Ricard, 1979 .

Discovery of (R)-2-amino-6-borono-2-(2-(piperidin-1-yl)ethyl)hexanoic acid and congeners as highly potent inhibitors of human arginases I and II for treatment of myocardial reperfusion injury.

E. Howard, A. Mitschler, M. V. Van Zandt, 2013, Journal of medicinal chemistry.

Discovery of 3-[(4,5,7-trifluorobenzothiazol-2-yl)methyl]indole-N-acetic acid (lidorestat) and congeners as highly potent and selective inhibitors of aldose reductase for treatment of chronic diabetic complications.

T. Petrova, J. Sredy, D. Sawicki, 2005, Journal of medicinal chemistry.

Modulation of aldose reductase inhibition by halogen bond tuning.

Martin Lepšík, Jindřich Fanfrlík, Pavel Hobza, 2013, ACS chemical biology.

Complexes of functional phosphines. 4. Coordination properties of (diphenylphosphino)acetonitrile, ethyl (diphenylphosphino)acetate and corresponding carbanions. Characterization of a new facile reversible carbon dioxide insertion into palladium(II) complexes

A. Mitschler, J. Fischer, P. Braunstein, 1981 .

Synthesis of new heteropolymetallic compounds with carbonylmetallate anions as bridges between two palladium atoms: x-ray crystal structures of [{PdNMe2CH2C6H4}2.mu.-{Co(CO)4}.mu.Cl] and [{PdNMe2CH2C6H4}2.mu.-{Mo(CO)3(.eta.-C5H5)}.mu.Cl]

A. Mitschler, J. Fischer, L. Ricard, 1980 .

Structural adaptability in the ligand-binding pocket of the ecdysone hormone receptor

Dino Moras, Natacha Rochel, D. Moras, 2003, Nature.

THE CRYSTAL AND MOLECULAR STRUCTURE OF A SERIES OF OXO MOLYBDENUM DITHIOCARBAMATES

A. Mitschler, J. Estienne, J. Fischer, 1974 .

Reactivity of cyclopalladated compounds. 4. Crystal and molecular structures of tetra-n-butylammonium chlorobromo(N-(phenylamino)-.alpha.-methylbenzylidenimino-2-C,N)palladate(II) and trans-chloro(N-(phenylamino)-.alpha.-methylbenzylidenimino-2-(C,N)bis(triethylphosphine)palladium(II)

A. Mitschler, J. Fischer, M. Pfeffer, 1976 .

Phosphole [2 + 2] and [4 + 2] dimerizations around metal carbonyl moieties. Structure and chemistry of a new type of exo [4 + 2] dimers

C. Santini, A. Mitschler, J. Fischer, 1980 .

Etude structurale du dioxychlorure de phosphore-hexachlorodiétain(IV)-di-μ-dichlorophosphate. I. Structure cristalline

D. Moras, A. Mitschler, R. Weiss, 1969 .

Dicoordinated 2H-phospholes as transient intermediates in the reactions of tervalent phospholes at high temperature. One-step syntheses of 1-phosphanorbornadienes and phosphorins from phospholes

A. Mitschler, J. Fischer, F. Mercier, 1981 .

A new heteronuclear cluster compound: [P(C6H5)3]2Pt2Co2(CO)3. Synthesis and crystal structure

A. Mitschler, J. Fischer, R. Weiss, 1975 .

Synthetic, physicochemical, and structural study of phosphacymantrenes

A. Mitschler, R. Weiss, F. Mathey, 1978 .

Electronic structure of chromium hexacarbonyl at liquid nitrogen temperature. 2. Experimental study (x-ray and neutron diffraction) of .sigma. and .pi. bonding

A. Mitschler, B. Rees, 1976 .

4,5-Dimethyl-2-(2-pyridyl)phosphorin as a chelating ligand. Synthesis and X-ray crystal structure analysis of (4,5-dimethyl-2-(2-pyridyl)phosphorin)tetracarbonylchromium

C. Santini, A. Mitschler, J. Fischer, 1984 .

Thermal tetramerization of 1-phenyl-3,4-dimethylphosphole. An access to 2,2'-biphospholes and to 2,2'-diphosphafulvalene complexes

A. Mitschler, J. Fischer, F. Mercier, 1982 .

Generation and trapping of terminal phosphinidene complexes. Synthesis and x-ray crystal structure of stable phosphirene complexes

A. Mitschler, A. Marinetti, J. Fischer, 1982 .

Binding of aldose reductase inhibitors: correlation of crystallographic and mass spectrometric studies

D. Moras, P. Barth, H. Rogniaux, 1999, Journal of the American Society for Mass Spectrometry.

Electron density in bis(dicarbonyl-.pi.-cyclopentadienyliron) at liquid nitrogen temperature by x-ray and neutron diffraction

M. Lehmann, A. Mitschler, B. Rees, 1978 .

1,1'-Diphosphaferrocenes. Synthesis, basic chemistry, and structure

A. Mitschler, J. Fischer, F. Mathey, 1980 .

Synthesis of quaternary α-amino acid-based arginase inhibitors via the Ugi reaction.

A. Mitschler, M. V. Van Zandt, A. Podjarny, 2013, Bioorganic & medicinal chemistry letters.

Stabilization of 2H-phospholes by complexation. A phosphorus-carbon double bond acting as a four-electron donor

A. Mitschler, J. Fischer, F. Mathey, 1984 .

Preparation of 3,3',4,4'-tetramethyl-1,1'-biphospholyl and its reactions with iron and cobalt carbonyls. Synthesis and x-ray crystal structure of a phospholyl complex with a chain of four cobalt atoms

A. Mitschler, J. Fischer, F. Mathey, 1983 .

Reaction of 1-alkyl-1,1'-diphosphaferrocene monoanions with acyl chlorides. Synthesis and zwitterionic structure of stable .lambda.3,.lambda.5-diphosphaferrocenes

A. Mitschler, J. Fischer, L. Ricard, 1982 .

Reaction of lithium alkyls and aryls with 1,1'-diphosphaferrocenes. Synthesis and structure of a stable bis(diene)iron(-I) species

A. Mitschler, J. Fischer, F. Mathey, 1981 .

Stabilization of 7-phosphanorbornadienes by complexation; X-ray crystal structure of 2,3-bis(methoxycarbonyl)-5,6-dimethyl-7-phenyl-7-phosphanorbornadiene(pentacarbonyl)-chromium

A. Mitschler, A. Marinetti, J. Fischer, 1982 .

Direct synthesis, reactivity, fluxional behavior, and molecular structure of Cp2Mo2(CO)3[PhP(OCH2CH2)2NH] (Cp = .eta.5-C5H5), a compound with a dissymmetrically substituted Mo=Mo Bond. Synthesis and molecular structure of Cp2Mo2(CO)3P(OMe)3

A. Mitschler, J. Riess, J. Wachter, 1984 .

Synthesis and molecular structure of the dissymmetric molybdenum.cntdot.molybdenum compound [(.eta.5-C5H5)2Mo2(CO)3(C6H5P(OCH2CH2)NH)]: first example of direct carbonyl-substitution in bis[(.eta.5-cyclopentadienyl)dicarbonylmolybdenum]

A. Mitschler, J. Riess, J. Wachter, 1981 .

X-Ray crystal structure and Diels–Alder reactivity of the 3,4-dimethyl-2H-phosphole dimer

A. Mitschler, J. Fischer, F. Mathey, 1982 .

Peroxo and alkylperoxidic molybdenum(VI) complexes as intermediates in the epoxidation of olefins by alkyl hydroperoxides

A. Mitschler, J. Fischer, L. Saussine, 1983 .

Synthesis and X-ray crystal structure of 1,2,3-triphenylphosphirene

A. Mitschler, A. Marinetti, J. Fischer, 1984 .

X-ray absorption, refraction and resonant scattering tensors in selenated protein crystals: implications for data collection strategies in macromolecular crystallography

G. Bricogne, P. Roversi, G. Evans, 2005 .

Structural characterization of metal binding to a cold-adapted frataxin

Javier Santos, A. Mitschler, A. Podjarny, 2015, JBIC Journal of Biological Inorganic Chemistry.

Design and synthesis of highly potent and selective (2-arylcarbamoyl-phenoxy)-acetic acid inhibitors of aldose reductase for treatment of chronic diabetic complications.

J. Sredy, D. Sawicki, B. Flam, 2004, Bioorganic & medicinal chemistry.

Structures cristallines du di‐μ‐oxo‐tétraperoxo‐dioxo‐diaquo‐dimolybdate(VI) de pyridinium et du di‐μ‐hydroperoxo‐tétraperoxo‐dioxo‐dimolybdate(VI) de pyridinium

A. Mitschler, R. Weiss, Jenny Carpentier, 1972 .

Probing the roles of two tryptophans surrounding the unique zinc coordination site in lipase family I.5

A. Mitschler, A. Podjarny, O. U. Sezerman, 2015, Proteins.

Neutron structure of type‐III antifreeze protein allows the reconstruction of AFP–ice interface

Michael Haertlein, Alberto Podjarny, T. Petrova, 2011, Journal of molecular recognition : JMR.

Perdeuteration, purification, crystallization and preliminary neutron diffraction of an ocean pout type III antifreeze protein.

E. Howard, A. Mitschler, A. Podjarny, 2009, Acta crystallographica. Section F, Structural biology and crystallization communications.

High-resolution structures of human aldose reductase holoenzyme in complex with stereoisomers of the potent inhibitor Fidarestat: stereospecific interaction between the enzyme and a cyclic imide type inhibitor.

T. Tomizaki, O. El-Kabbani, A. Mitschler, 2004, Journal of medicinal chemistry.

Structure of the E6/E6AP/p53 complex required for HPV-mediated degradation of p53

M. Masson, J. Ramirez-Ramos, G. Travé, 2015, Nature.

The role of the C-terminal region on the oligomeric state and enzymatic activity of Trypanosoma cruzi hypoxanthine phosphoribosyl transferase.

Javier Santos, J. M. Delfino, A. Mitschler, 2016, Biochimica et biophysica acta.

Discovery of N-substituted 3-amino-4-(3-boronopropyl)pyrrolidine-3-carboxylic acids as highly potent third generation inhibitors of human arginase I and II.

A. Pyle, O. Potapova, E. Howard, 2019, Journal of medicinal chemistry.

Molecular recognition of agonist ligands by RXRs.

D. Moras, A. Mitschler, P. Egea, 2002, Molecular endocrinology.

X-Ray Crystal Structure of the Full Length Human Chitotriosidase (CHIT1) Reveals Features of Its Chitin Binding Domain

Firas Fadel, A. Mitschler, A. Podjarny, 2016, PloS one.

Dimerization of Escherichia coli DNA-gyrase B Provides a Structural Mechanism for Activating the ATPase Catalytic Center*

D. Moras, C. Bronner, A. Urzhumtsev, 2000, The Journal of Biological Chemistry.

New insights into the enzymatic mechanism of human chitotriosidase (CHIT1) catalytic domain by atomic resolution X-ray diffraction and hybrid QM/MM.

K. Harlos, Firas Fadel, R. Cachau, 2015, Acta crystallographica. Section D, Biological crystallography.

Targeting Acidic Mammalian chitinase Is Effective in Animal Model of Asthma.

J. Gołąb, Firas Fadel, A. Mitschler, 2018, Journal of medicinal chemistry.

Crystal structure of the human RXRα ligand‐binding domain bound to its natural ligand: 9‐cis retinoic acid

P. Chambon, D. Moras, N. Rochel, 2000 .

Identification of a novel polyfluorinated compound as a lead to inhibit the human enzymes aldose reductase and AKR1B10: structure determination of both ternary complexes and implications for drug design.

G. Klebe, A. Mitschler, A. Podjarny, 2014, Acta crystallographica. Section D, Biological crystallography.

Quantum model of catalysis based on a mobile proton revealed by subatomic x-ray and neutron diffraction studies of h-aldose reductase

Raul Cachau, Isabelle Hazemann, Oscar N Ventura, 2008, Proceedings of the National Academy of Sciences.

Perdeuteration: improved visualization of solvent structure in neutron macromolecular crystallography.

T. Petrova, E. Howard, A. Mitschler, 2014, Acta crystallographica. Section D, Biological crystallography.

Conformational editing of intrinsically disordered protein by α-methylation

N. Rochel, Y. Nominé, G. Travé, 2020, Chemical science.

Crystal structure of the human RXRalpha ligand-binding domain bound to its natural ligand: 9-cis retinoic acid.

P. Chambon, D. Moras, N. Rochel, 2000, The EMBO journal.

Conformational adaptation of agonists to the human nuclear receptor RARγ

P. Chambon, D. Moras, P. Chambon, 1998, Nature Structural Biology.

Crystal packing modifies ligand binding affinity: The case of aldose reductase

Alain Van Dorsselaer, Isabelle Hazemann, Alberto Podjarny, 2012, Proteins.

High-resolution neutron and X-ray diffraction room-temperature studies of an H-FABP–oleic acid complex: study of the internal water cluster and ligand binding by a transferred multipolar electron-density distribution

T. Tomizaki, T. Petrova, Firas Fadel, 2016, IUCrJ.

X-ray structure of the V301L aldo-keto reductase 1B10 complexed with NADP(+) and the potent aldose reductase inhibitor fidarestat: implications for inhibitor binding and selectivity.

A. Mitschler, A. Podjarny, J. Farrés, 2013, Chemico-biological interactions.

Structural Determinants of the Selectivity of 3‐Benzyluracil‐1‐acetic Acids toward Human Enzymes Aldose Reductase and AKR1B10

G. Klebe, A. Mitschler, A. Podjarny, 2015, ChemMedChem.

Electron deformation density for the "supershort" chromium-chromium quadruple bond: a joint experimental and theoretical study

R. Wiest, A. Mitschler, B. Rees, 1982 .

Crystal structures of the vitamin D receptor complexed to superagonist 20-epi ligands

D. Moras, N. Rochel, J. Wurtz, 2001, Proceedings of the National Academy of Sciences of the United States of America.

Structural investigation of the ligand binding domain of the zebrafish VDR in complexes with 1α,25(OH)2D3 and Gemini: purification, crystallization and preliminary X-ray diffraction analysis

D. Moras, N. Rochel, A. Mitschler, 2004, The Journal of Steroid Biochemistry and Molecular Biology.

Structure of High-Risk Papillomavirus 31 E6 Oncogenic Protein and Characterization of E6/E6AP/p53 Complex Formation

T. Iftner, F. Stubenrauch, M. Masson, 2020, Journal of virology.

Crystal structure of histidyl‐tRNA synthetase from Escherichia coli complexed with histidyl‐adenylate.

C. Francklyn, D. Moras, A. Mitschler, 1995, The EMBO journal.

Crystals of Thermus thermophilus tRNAAsp complexed with its cognate aspartyl-tRNA synthetase have a solvent content of 75%. Comparison with other aminoacylation systems.

D. Moras, C. Briand, M. Yusupov, 1998, Acta crystallographica. Section D, Biological crystallography.

Preparation and crystal structure of π-cyclopentadienyl-1,2-bis(diphenylphosphino)ethaneironmagnesium bromide tris(tetrahydrofuran), a transition–metal Grignard reagent

P. Knowles, A. Mitschler, B. Meunier, 1974 .

Preliminary X-ray investigation of 70 S ribosome crystals from Thermus thermophilus.

D. Moras, M. Yusupov, A. Mitschler, 1989, Journal of molecular biology.

Crystal Structure of a Subcomplex of Human Transcription Factor TFIID Formed by TATA Binding Protein-associated Factors hTAF4 (hTAFII135) and hTAF12 (hTAFII20)*

D. Moras, C. Romier, A. Mitschler, 2002, The Journal of Biological Chemistry.

Crystal Structure Of The Nuclear Receptor For Vitamin D Ligand Binding Domain Bound to KH1060

D. Moras, N. Rochel, J. Wurtz, 2001 .

CRYSTAL STRUCTURE OF THE NUCLEAR RECEPTOR FOR VITAMIN D COMPLEXED TO VITAMIN D

D. Moras, N. Rochel, J. Wurtz, 2000 .

The active site of yeast aspartyl‐tRNA synthetase: structural and functional aspects of the aminoacylation reaction.

G. Eriani, F. Martin, D. Moras, 1994 .

The Effect of Halogen-to-Hydrogen Bond Substitution on Human Aldose Reductase Inhibition.

Martin Lepšík, Jindřich Fanfrlík, Pavel Hobza, 2015, ACS chemical biology.

The active site of yeast aspartyl-tRNA synthetase: structural and functional aspects of the aminoacylation reaction.

G. Eriani, F. Martin, D. Moras, 1994, The EMBO journal.

Structure of aldehyde reductase holoenzyme in complex with the potent aldose reductase inhibitor fidarestat: implications for inhibitor binding and selectivity.

Connie Darmanin, Clemens Schulze-Briese, Mitsuru Oka, 2005, Journal of medicinal chemistry.

Ultrahigh resolution drug design. II. Atomic resolution structures of human aldose reductase holoenzyme complexed with fidarestat and minalrestat: Implications for the binding of cyclic imide inhibitors

T. Tomizaki, C. Schulze-Briese, O. El-Kabbani, 2004, Proteins.

Synthesis and inhibitory properties of α(chlorofluoromethyl)-α-amino acids, a novel class of irreversible inactivators of decarboxylases

A. Mitschler, D. Schirlin, A. Cian, 1992 .