New artificial siderophores based on a monosaccharide scaffold

[1]  M. Schnabelrauch,et al.  Novel catecholate-type siderophore analogs based on a myo-inositol scaffold , 1998, Biometals.

[2]  W. Rabsch,et al.  Growth promotion of synthetic catecholate derivatives on Gram-negative bacteria , 1993, Biometals.

[3]  U. Möllmann,et al.  8-Acyloxy-1,3-benzoxazine-2,4-diones as Siderophore Components for Antibiotics , 2000, Arzneimittelforschung.

[4]  G. Brittenham,et al.  HBED: the continuing development of a potential alternative to deferoxamine for iron-chelating therapy. , 1999, Blood.

[5]  J. Libman,et al.  Biomimetic siderophores: from structural probes to diagnostic tools. , 1998, Metal ions in biological systems.

[6]  J. Le bras,et al.  In vitro activities of novel catecholate siderophores against Plasmodium falciparum , 1996, Antimicrobial agents and chemotherapy.

[7]  G. Descotes,et al.  HYDROLYSIS OF CYANOETHYLATED CARBOHYDRATES : SYNTHESIS OF NEW CARBOXYLIC DERIVATIVES OF SUCROSE, D-GLUCOSE AND D-FRUCTOSE , 1995 .

[8]  T. Ikeda,et al.  Design and Synthesis of Artificial Siderophores: Lysine-based Triscatecholate Ligands as a Model for Enterobactin. , 1995 .

[9]  L. Navailles,et al.  CHIRAL LIQUID CRYSTALLINE COMPOUNDS FROM D-(+)-GLUCOSE , 1995 .

[10]  Z. Cabantchik Iron Chelators as antimalarials: the biochemical basis of selective cytotoxicity , 1995 .

[11]  F. Malouin,et al.  Microbial Iron Chelators as Drug Delivery Agents: The Rational Design and Synthesis of Siderophore‐Drug Conjugates , 1993 .

[12]  Y. Kishi,et al.  Chiral analogs of enterobactin with hydrophilic or lipophilic properties , 1993 .

[13]  Anthony W. Coleman,et al.  Synthese und Komplexierungsverhalten eines auf Cyclodextrin beruhenden Siderophors , 1992 .

[14]  U. Möllmann,et al.  [Synthesis and antibacterial activity of benzoylaminoacyl-penicillins and related compounds with and without acylated catechol substituents]. , 1992, Arzneimittel-Forschung.

[15]  J. Neilands,et al.  Universal chemical assay for the detection and determination of siderophores. , 1987, Analytical biochemistry.

[16]  D. Horton,et al.  Preparative acetonation of pyranoid, vicinal trans-glycols under kinetic control: methyl 2,3:4,6-di-O-isopropylidene-α- and -β-d-glucopyranoside , 1984 .

[17]  P. Tyler,et al.  Total synthesis of the C-3 – C-17 segment of boromycin , 1983 .

[18]  M. Venuti,et al.  Synthesis of iron chelators. Enterobactin, enantioenterobactin, and a chiral analog , 1981 .

[19]  K. Raymond,et al.  Ferric ion sequestering agents. 1. Hexadentate O-bonding N,N',N"-tris(2,3-dihydroxybenzoyl) derivatives of 1,5,9-triazacyclotridecane and 1,3,5-triaminomethylbenzene , 1979 .

[20]  H. Weidmann,et al.  Eine einfache Enttritylierungsmethode , 1978 .

[21]  E. Corey,et al.  Synthesis of the carbocyclic analog of enterobactin , 1978 .

[22]  F. Gibson,et al.  The structure of enterochelin and related 2,3-dihydroxy-N-benzoylserine conjugates from Escherichia coli. , 1970, Biochimica et biophysica acta.

[23]  J. Neilands,et al.  Enterobactin, an iron transport compound from Salmonella typhimurium. , 1970, Biochemical and biophysical research communications.

[24]  W. A. Bulen,et al.  The isolation and identification of 2,3-dihydroxybenzoic acid and 2-N,6-N-di-92,3-dihydroxybenzoyl)-L-lysine formed by iron-deficient Azotobacter vinelandii. , 1969, Biochemistry.