Coordination of {RuII(NO+)}3+ and {RuII(H2O)}2+ to bleomycin: Most favored [RuII(L)(BLM-A2)] structure according to 1H NMR and molecular mechanics methods

Inorganica Chimica Acta

Volumn 343, Issue , 2003, Pages 231-243

  Ward, Matthew S ^a   Lin, Fu Tyan ^a   Shepherd, Rex E ^a  

^a UNIVERSITY OF PITTSBURGH   (United States)

Author keywords

Antibiotics; Bleomycins; Crystal structures; MMFF94 molecular mechanics; Ruthenium nitrosyl

Indexed keywords

AMIDES; AMINES; AMINO ACIDS; ANTIBIOTICS; BINDING ENERGY; CHIRALITY; CHLORINE COMPOUNDS; CHROMOPHORES; CRYSTAL STRUCTURE; HYDROGEN BONDS; ISOMERS; LIGANDS; MECHANICS; METALS; MOLECULAR MECHANICS; MONTE CARLO METHODS; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; PEPTIDES; PLANTS (BOTANY); SCREWS; SPECTROSCOPIC ANALYSIS; STABILITY; STEREOCHEMISTRY;

ANTI-TUMOR AGENTS; BLEOMYCINS; DIFFERENT STRUCTURE; ENERGY MINIMIZED STRUCTURES; METAL BINDING DOMAIN; MOLECULAR MECHANICS CALCULATIONS; MOLECULAR MECHANICS METHOD; STRUCTURAL STABILITIES;

RUTHENIUM COMPOUNDS;

ALANINE DERIVATIVE; AMINE; ANTINEOPLASTIC AGENT; BLEOMYCIN A2; BLEOMYCIN B2; BLEOMYCIN SULFATE; COBALT DERIVATIVE; COPPER; HISTIDINE DERIVATIVE; IRON; MANNOSE; NITRIC OXIDE; PYRIMIDINE DERIVATIVE; RUTHENIUM DERIVATIVE; THIAZOLE; WATER;

ARTICLE; BINDING AFFINITY; CALCULATION; CARBON NUCLEAR MAGNETIC RESONANCE; CHEMICAL STRUCTURE; CHIRALITY; CHROMATOPHORE; DRUG SYNTHESIS; ENERGY; HYDROGEN BOND; ISOMER; MOLECULAR DYNAMICS; MOLECULAR INTERACTION; MONTE CARLO METHOD; PROTON NUCLEAR MAGNETIC RESONANCE; STEREOCHEMISTRY;

EID: 0037472413     PISSN: 00201693     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0020-1693(02)01174-X     Document Type: Article

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