909 resultados para Keys to Database Searching
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Key studies defining the DNA alkylation properties and selectivity of a new class of exceptionally potent, naturally occurring antitumor antibiotics including CC-1065, duocarmycin A, and duocarmycin SA are reviewed. Recent studies conducted with synthetic agents containing deep-seated structural changes and the unnatural enantiomers of the natural products and related analogs have defined the structural basis for the sequence-selective alkylation of duplex DNA and fundamental relationships between chemical structure, functional reactivity, and biological properties. The agents undergo a reversible, stereoelectronically controlled adenine-N3 addition to the least substituted carbon of the activated cyclopropane within selected AT-rich sites. The preferential AT-rich non-covalent binding selectivity of the agents within the narrower, deeper AT-rich minor groove and the steric accessibility to the alkylation site that accompanies deep AT-rich minor groove penetration control the sequence-selective DNA alkylation reaction and stabilize the resulting adduct. For the agents that possess sufficient reactivity to alkylate DNA, a direct relationship between chemical or functional stability and biological potency has been defined.
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Mode of access: Internet.
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Bibliographical footnotes.
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"For the identification of the Pteridophyta, Gymnospermae and the commoner species of early-flowering Angiospermae found in the vicinity of Ithaca, New York."
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Bibliography: p. 187-192.
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Vol. IV has title: Literature to the orders, families, genera, and species of insects and medical entomology.
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Leaves variously numbered.
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Bibliography: p. 83-88.
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Typewritten.
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University of Kansas, Department of Entomology contribution no. 1047.
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Mode of access: Internet.
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Includes index.
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"Previously issued under the same title by the Centers of Disease Control and PRevention of the U. S. Public Health Service, Atlanta, Georgia"--t.p. verso.