B. Castro

发表

Oxybenzotriazole free peptide coupling reagents for N-methylated amino acids

E. Frérot, P. Jouin, J. Coste, 1991 .

Urate Oxidase Purification by Salting-in Crystallization: Towards an Alternative to Chromatography

N. Ferté, F. Bonneté, B. Castro, 2011, PloS one.

Brop: A new reagent for coupling N-methylated amino acids

J. Coste, B. Castro, M. Dufour, 1990 .

Synthesis of the cyclodepsipeptide nordidemnin B, a cytotoxic minor product isolated from the sea tunicate Trididemnum cyanophorum

J. Poncet, P. Jouin, B. Castro, 1989 .

Synthesis and biological activities of some pseudo-peptide analogues of tetragastrin: the importance of the peptide backbone.

J. Bali, R. Magous, B. Castro, 1985, Journal of medicinal chemistry.

PyBOP®: A new peptide coupling reagent devoid of toxic by-product

D. Le-Nguyen, J. Coste, B. Castro, 1990 .

PyBOP(R) (I): A New Peptide Coupling Reagent Devoid of Toxic By-Product.

D. Le-Nguyen, J. Coste, B. Castro, 1990 .

Synthesis of LH-RH using a new phenolic polymer as solid support and “BOP” reagent for fragment coupling

P. Rivaille, G. Milhaud, B. Castro, 1980 .

Solid‐phase peptide synthesis of human(Nle‐27)‐oxyntomodulin

D. Bataille, A. Kervran, B. Castro, 1986, FEBS letters.

Solution conformation of a synthetic bis-headed inhibitor of trypsin and carboxypeptidase A: new structural alignment between the squash inhibitors and the potato carboxypeptidase inhibitor.

A. Padilla, L. Chiche, A. Heitz, 1993, Protein engineering.

An efficient synthesis of optically active α-(t-butoxycarbonylamino)-aldehydes from α-amino acids

J. Fehrentz, B. Castro, 1983 .

Peptide Coupling Reagents; VIII. A High Yield Preparation of Phenyl Esters of Amino Acids using Benzotriazolyloxytris[dimethylamino]phosphonium Hexafluorophosphate (BOP Reagent)

G. Evin, R. Seyer, B. Castro, 1977 .

Tert-butyl esters of N-protected amino acids with tert-butyl fluorocarbonate (Boc-F)

N. Galéotti, P. Jouin, B. Castro, 1989 .

Isopropenyl chlorocarbonate (IPCC)1 in amino acid and peptide chemistry: Esterification of N-protected amino acids; Application to the synthesis of the depsipeptide valinomycin

J. Poncet, P. Jouin, B. Castro, 1989 .

Convenient one-pot esterification of N-protected aminoacids via isopropenyl chloroformate activation.

J. Senet, P. Jouin, B. Castro, 1987 .

Evidence for dopaminomimetic effect of intrastriatally injected cholecystokinin octapeptide in mice.

P. Worms, K. Bizière, B. Castro, 1986, European journal of pharmacology.

Peptide Coupling Reagents VI1. A Novel, Cheaper Preparation of Benzotriazolyloxytris[dimethylamino]phosphonium Hexafluorophosphate (BOP Reagent)

G. Evin, B. Castro, J. Dormoy, 1976 .

Stereospecific synthesis of N-protected statine and its analogues via chiral tetramic acid

D. Nisato, P. Jouin, B. Castro, 1987 .

An Efficient Synthesis of Optically Active α-(t-Butoxycarbonylamino)-aldehydes from α-Amino Acids

J. Fehrentz, B. Castro, 1983 .

An improved synthesis of β-keto ester units in didemnins, using 2,2'-carbonyl-bis(3,5-dioxo-4-methyl-1,2,4-oxadiazolidine)

J. Poncet, P. Jouin, B. Castro, 1988 .

Benzotriazol‐1‐yloxytris(dimethylamino)phosphonium Hexafluorophosphate

E. Giralt, F. Rabanal, B. Castro, 2004 .

Renin substrates. Part 2. Rapid solid phase synthesis of the ratine sequence tetradecapeptide using BOP reagent

A. Heitz, D. Le-Nguyen, B. Castro, 1987 .

The reaction of hexamethyl phosphoric triamide (HMPT) with phosphoryl chloride : A reexamination. Application to a novel preparation of BOP reagent for peptide coupling

B. Castro, J. Dormoy, 1979 .

Synthesis of aldehydic peptides inhibiting renin.

A. Heitz, J. Fehrentz, B. Castro, 2009, International journal of peptide and protein research.

Replacement of Alcoholic Hydroxyl Groups by Halogens and Other Nucleophiles via Oxyphosphonium Intermediates

B. Castro, 1984 .

Cationic π-allylic complexes: II. Cationic π-allylic complexes of nickel(II) from allyloxytris(dimethylamino)phosphonium salts

D. Neibecker, B. Castro, 1977 .

Cationic η3 allylic complexes. III6 The reaction of S-allyl iso tetramethyl thioUronium salts with nickel tetracarbonyl*

D. Neibecker, B. Castro, 1977 .

Nonclassical CH-π supramolecular interactions in artemisinic acid favor a single conformation, yielding high diastereoselectivity in the reduction with diazene.

K. Rossen, R. Chaudret, M. Kurz, 2014, The Journal of organic chemistry.

A Convenient Synthesis of C-Glycofuranosylmalonates and Related Derivatives

Y. Chapleur, B. Castro, F. Germain, 1983 .

Stereospecific Synthesis of N‐Protected Statine and Its Analogues via Chiral Tetramic Acid.

D. Nisato, P. Jouin, B. Castro, 1987 .

Tetramic acid chemistry. Part 1. Reinvestigation of racemisation during the synthesis of tetramic acids via Dieckmann cyclisation

J. Poncet, P. Jouin, A. Gaudemer, 1990 .

Synthesis and reduction of α-amino ketones derived from leucine

J. Poncet, P. Jouin, B. Castro, 1986 .

Sels d'alkyloxyphosphonium—XV: Activation de l'hydroxyle anomere des 2,3,4,6-tetra-o-acyl-d-glucopyranoses—II. Preparation d'orthoesters et de thioglucosides

Y. Chapleur, B. Gross, B. Castro, 1977 .

N-methyl N-carboxyanhydride: an unexpected by-product when coupling boc-n-methyl amino acids

E. Frérot, J. Poncet, P. Jouin, 1992 .

On the use of carboxamidomethyl esters (cam esters) in the synthesis of model peptides. scope and limitations

Jean Martínez, B. Castro, J. Laur, 1985 .

Synthesis of homogeneous polyoxyethylene perfluorcalkyl surfactants

G. Mathis, J. Delpuech, B. Castro, 1983 .

Polymorphism in Xaliproden (SR57746A): An X-ray Diffraction, Calorimetric, and Solid-State NMR Investigation

F. Taulelle, G. Althoff, P. Ochsenbein, 2013 .

Low molecular weight serine protease inhibitors from insects are proteins with highly conserved sequences.

M. Brehélin, M. Pugnière, R. Boigegrain, 2000, Insect biochemistry and molecular biology.

Active site chemical mutagenesis of Ecballium elaterium trypsin inhibitor II: new microproteins inhibiting elastase and chymotrypsin.

A. Favel, D. Le-Nguyen, M. Coletti-previero, 1989, Biochemical and biophysical research communications.

X‐ray, ESR, and quantum mechanics studies unravel a spin well in the cofactor‐less urate oxidase

T. Prangé, G. Monard, M. Chiadmi, 2011, Proteins.

Protease inhibitors from Ecballium elaterium seeds.

A. Favel, E. Robinson, R. Zwilling, 2009, International journal of peptide and protein research.

Pronase in amino acid technology: Optical resolution of nonproteinogenic α‐amino acids

M. Pugnière, B. Castro, N. Domergue, 1994 .

Optical resolution of two isomeric naphthylalanines by immobilized enyzmes

M. Pugnière, A. Previero, B. Castro, 1991 .

Sels d'alkyloxyphosphonium—XVI: Activation de l'hydroxyle anomere des 2,3,4,6 tetra-o-acyl-d-mannopyranoses

Y. Chapleur, B. Gross, B. Castro, 1977 .

Design and chemical synthesis of a 32 residues chimeric microprotein inhibiting both trypsin and carboxypeptidase A.

D. Le-Nguyen, M. Coletti-previero, B. Castro, 1989, Biochemical and biophysical research communications.

Novel preparation of N-protected amino acid active esters using 1,2,2,2-tetrachloroethyl carbonates

Jean Martínez, J. Senet, B. Castro, 1987 .

Renin substrates. Part 1. Liquid-phase synthesis of the equine sequence with benzotriazolyloxytris(dimethylamino)phosphonium hexafluorophosphate (BOP)

R. Seyer, A. Heitz, D. L. Nguyen, 1985 .

Sels d'alkyloxyphosphonium.

Y. Chapleur, B. Gross, B. Castro, 1974 .

Structure-activity relationships of C-terminal tri- and tetrapeptide fragments that inhibit gastrin activity.

D. Nisato, J. Bali, R. Magous, 1985, Journal of medicinal chemistry.

Crystal Structure of the protein drug urate oxidase-inhibitor complex at 2.05 Å resolution

T. Prangé, J. Mornon, G. L'hermite, 1997, Nature Structural Biology.

ATDP Salts; 22. A Novel and Efficient Method for the Preparation of Glycosyl Azides via Alkoxytris[dimethylamino]-phosphonium Salts

F. Chrétien, B. Gross, B. Castro, 1979 .

2‐Carboxyethyltriphenylphosphonium Perbromide

B. Castro, J. Dormoy, 2001 .

Salting-In Effects on Urate Oxidase Crystal Design†

N. Ferté, F. Bonneté, B. Castro, 2008 .

Racemization of α-amino acid esters by aliphatic ketones in the presence of carboxylic acids

M. Pugnière, A. Previero, L. Barry, 2009 .

1H 2D NMR and distance geometry study of the folding of Ecballium elaterium trypsin inhibitor, a member of the squash inhibitors family.

L. Chiche, A. Heitz, D. Le-Nguyen, 1989, Biochemistry.

Intrinsic reactivity of uric acid with dioxygen: Towards the elucidation of the catalytic mechanism of urate oxidase.

G. Monard, Muhannad Altarsha, B. Castro, 2009, Bioorganic chemistry.

Oxygen pressurized X-ray crystallography: probing the dioxygen binding site in cofactorless urate oxidase and implications for its catalytic mechanism.

T. Prangé, G. Monard, M. Chiadmi, 2008, Biophysical journal.

Complexed and ligand-free high-resolution structures of urate oxidase (Uox) from Aspergillus flavus: a reassignment of the active-site binding mode.

T. Prangé, G. Monard, J. Mornon, 2004, Acta crystallographica. Section D, Biological crystallography.

Quantum computations of the UV–visible spectra of uric acid and its anions

G. Monard, Muhannad Altarsha, B. Castro, 2006 .

Characterization and 2D NMR study of the stable [9–21, 15–27] 2 disulfide intermediate in the folding of the 3 disulfide trypsin inhibitor EETI II

L. Chiche, A. Heitz, D. Le-Nguyen, 1993, Protein science : a publication of the Protein Society.

Molecular recognition between serine proteases and new bioactive microproteins with a knotted structure.

L. Chiche, A. Favel, A. Heitz, 1990, Biochimie.

Synthesis of the C‐Terminal Octapeptide of Pig Oxyntomodulin. Lys‐Arg‐Asn‐ Lys‐Asn‐Asn‐Ile‐Ala: A Potent Inhibitor of Pentagastrin‐Induced Acid Secretion.

D. Bataille, Jean Martinez, A. Aumelas, 1986 .

Folding of the squash trypsin inhibitor EETI II. Evidence of native and non-native local structural preferences in a linear analogue.

L. Chiche, A. Heitz, D. Le-Nguyen, 1995, European journal of biochemistry.

Structural analysis of urate oxidase in complex with its natural substrate inhibited by cyanide: Mechanistic implications

T. Prangé, M. Chiadmi, B. Castro, 2008, BMC Structural Biology.

Use of restrained molecular dynamics in water to determine three‐dimensional protein structure: Prediction of the three‐dimensional structure of Ecballium elaterium trypsin inhibitor II

Christine Gaboriaud, Annie Heitz, Laurent Chiche, 1989, Proteins.

The Iodothyronine Selenodeiodinases Are Thioredoxin-fold Family Proteins Containing a Glycoside Hydrolase Clan GH-A-like Structure*

J. Harney, P. Larsen, J. Mornon, 2003, Journal of Biological Chemistry.

Carboxamidomethyl esters (CAM esters) as carboxyl protecting groups.

Jean Martínez, B. Castro, J. Laur, 1983 .

The disulfide folding pathway of Ecballium elaterium trypsin inhibitor II (EETI II)

E. Mahé, A. Heitz, D. L. Nguyen, 1995 .

Abilities of some tryptophan and phenylalanine derivatives to inhibit gastric acid secretion.

D. Nisato, J. Bali, R. Magous, 1985, Biochimica et biophysica acta.

Synthetic porphyrins bearing a lateral peptide chain—V

J. Goulon, B. Castro, C. Selve, 1981 .

Conformational study of a native monodisulfide bridge analogue of EETI II

L. Chiche, A. Heitz, D. Le-Nguyen, 1997, Letters in Peptide Science.

Solid phase synthesis of a trypsin inhibitor isolated from the Cucurbitaceae Ecballium elaterium.

D. Le-Nguyen, B. Castro, D. Nalis, 2009, International journal of peptide and protein research.

Crystallization and preliminary X-ray study of porcine trypsin, free and complexed with Ecballium elaterium trypsin inhibitor, a member of the squash inhibitors family.

M. Vaney, J. Mornon, D. Le-Nguyen, 1989, Journal of molecular biology.

Urate oxidase from Aspergillus flavus: new crystal-packing contacts in relation to the content of the active site.

T. Prangé, P. Retailleau, F. Bonneté, 2005, Acta crystallographica. Section D, Biological crystallography.

Synthesis of pseudo-peptide analogues of the C-terminal tetrapeptide of gastrin and evaluation of their biological activity on acid secretion.

J. Bali, R. Magous, B. Castro, 2009, International journal of peptide and protein research.

N-terminal domain of pepsin as a model for retroviral dimeric aspartyl protease.

R. Boigegrain, M. Coletti-previero, B. Castro, 1990, Biochemical and biophysical research communications.

Synthesis of the C-terminal octapeptide of pig oxyntomodulin. Lys-Arg-Asn-Lys-Asn-Asn-Ile-Ala: a potent inhibitor of pentagastrin-induced acid secretion.

D. Bataille, A. Aumelas, M. Dubrasquet, 1985, Journal of Medicinal Chemistry.

PEPTIDE COUPLING REAGENTS. VI. A NOVEL, CHEAPER PREPARATION OF BENZOTRIAZOLYLOXYTRIS(DIMETHYLAMINO)PHOSPHONIUM HEXAFLUOROPHOSPHATE (BOP REAGENT)

G. Evin, B. Castro, J. Dormoy, 1977 .

Recapture of [S]‐allantoin, the product of the two‐step degradation of uric acid, by urate oxidase

T. Prangé, M. Chiadmi, B. Castro, 2006, FEBS letters.

Synthia: Assisted Design of Peptide Synthesis Plans

Philippe Jégou, P. Janssen, B. Nouguier, 1991 .

Surfactant Poloxamer 188 as a New Crystallizing Agent for Urate Oxidase

G. Sciara, C. Cambillau, V. Delfosse, 2009 .

Structural analysis of urate oxidase in complex with its natural substrate inhibited by cyanide: Mechanistic implications

T. Prangé, M. Chiadmi, B. Castro, 2008, BMC Structural Biology.

X‐ray, ESR, and quantum mechanics studies unravel a spin well in the cofactor‐less urate oxidase

T. Prangé, G. Monard, M. Chiadmi, 2011, Proteins.

47 – EETI II (Ecballium elaterium Trypsin Inhibitor II) as a Vehicle for New Functions

D. Le-Nguyen, B. Castro, 1990 .