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Volumn 100, Issue 9, 2006, Pages 1449-1461
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Theoretical investigations of the reactivity of verdoheme analogues: Opening of the planar macrocycle by amide, dimethyl amide, and hydroxide nucleophiles to form helical biliverdin type complexes
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Author keywords
B3LYP; NBO analysis; Nucleophilic addition; Zinc(II) verdoheme complex
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Indexed keywords
AMIDE;
BILIVERDIN;
CARBON;
DIMETHYLAMIDE;
HEME DERIVATIVE;
HYDROXIDE;
MACROCYCLIC COMPOUND;
OXYGEN;
UNCLASSIFIED DRUG;
ZINC COMPLEX;
ZINC ION;
ADDITION REACTION;
ARTICLE;
ATOM;
COMPLEX FORMATION;
REACTION ANALYSIS;
RING OPENING;
THEORETICAL STUDY;
AMIDES;
BILIVERDINE;
BINDING SITES;
HEME;
HYDROXIDES;
MODELS, MOLECULAR;
MOLECULAR CONFORMATION;
MOLECULAR STRUCTURE;
PROTEIN STRUCTURE, TERTIARY;
ZINC COMPOUNDS;
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EID: 33746864900
PISSN: 01620134
EISSN: None
Source Type: Journal
DOI: 10.1016/j.jinorgbio.2006.04.010 Document Type: Article |
Times cited : (15)
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References (26)
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