New indolo- and pyrrolo-pyrimidines of type 1-4 were studied for their ability to form stable complexes with DNA fragments. The calculated free energies of binding were found in the range -8.39 ÷ -16.72 Kcal/mol. The docking studies revealed a common binding mode with the chromophore intercalated between GC base pairs whereas the side chain lies along the minor groove.

LAURIA A, DIANA P, BARRAJA P, MONTALBANO A, DATTOLO G, CIRRINCIONE G, et al. (2004). Docking of indolo- and pyrrolo-pyrimidines to DNA. New DNA-interactive polycycles from amino-indoles/pyrroles and BMMA. ARKIVOC(v), 263-271.

Docking of indolo- and pyrrolo-pyrimidines to DNA. New DNA-interactive polycycles from amino-indoles/pyrroles and BMMA.

LAURIA, Antonino;DIANA, Patrizia;BARRAJA, Paola;MONTALBANO, Alessandra;DATTOLO, Gaetano;CIRRINCIONE, Girolamo;ALMERICO, Anna Maria
2004-01-01

Abstract

New indolo- and pyrrolo-pyrimidines of type 1-4 were studied for their ability to form stable complexes with DNA fragments. The calculated free energies of binding were found in the range -8.39 ÷ -16.72 Kcal/mol. The docking studies revealed a common binding mode with the chromophore intercalated between GC base pairs whereas the side chain lies along the minor groove.
2004
Settore CHIM/08 - Chimica Farmaceutica
LAURIA A, DIANA P, BARRAJA P, MONTALBANO A, DATTOLO G, CIRRINCIONE G, et al. (2004). Docking of indolo- and pyrrolo-pyrimidines to DNA. New DNA-interactive polycycles from amino-indoles/pyrroles and BMMA. ARKIVOC(v), 263-271.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/10447/20441
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