Search Results - "Trent, J O"
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A novel small molecule antagonist of choline kinase-α that simultaneously suppresses MAPK and PI3K AKT signaling
Published in Oncogene (28-07-2011)“…Choline kinase-α expression and activity are increased in multiple human neoplasms as a result of growth factor stimulation and activation of cancer-related…”
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Inhibition of Human Telomerase by a G-Quadruplex-Interactive Compound
Published in Journal of medicinal chemistry (04-07-1997)“…Our laboratories have initiated a structure-based approach to discovering non-nucleoside compounds that will selectively inhibit human telomerase by targeting…”
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Human Telomerase Inhibition by Regioisomeric Disubstituted Amidoanthracene-9,10-diones
Published in Journal of medicinal chemistry (19-11-1998)“…Telomerase is an attractive target for the design of new anticancer drugs. We have previously described a series of 1,4- and 2,6-difunctionalized…”
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Molecular modeling of drug-DNA complexes: an update
Published in Methods in enzymology (2001)Get more information
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5
Exploiting anthracycline scaffold for designing DNA-targeting agents
Published in Methods in enzymology (2001)Get more information
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6
Antiproliferative Activity of G-rich Oligonucleotides Correlates with Protein Binding
Published in The Journal of biological chemistry (10-09-1999)“…Oligonucleotides have been extensively studied as antisense or antigene agents that can potentially modulate the expression of specific genes. These strategies…”
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7
Cytotoxicity of bis(phenylamidinium)furan alkyl derivatives in human tumour cell lines: Relation to DNA minor groove binding
Published in Bioorganic & medicinal chemistry letters (03-06-1997)“…A series of alkyl derivatives of bis(phenylamidinium)furan are shown to have cytotoxic activity in several human tumour cell lines. Xray crystallographic…”
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8
Allosteric, Chiral-Selective Drug Binding to DNA
Published in Proceedings of the National Academy of Sciences - PNAS (24-10-2000)“…The binding interactions of (-)-daunorubicin (WP900), a newly synthesized enantiomer of the anticancer drug (+)-daunorubicin, with right- and left-handed DNA,…”
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Inhibition of DNA Replication and Induction of S Phase Cell Cycle Arrest by G-rich Oligonucleotides
Published in The Journal of biological chemistry (16-11-2001)“…The discovery of G-rich oligonucleotides (GROs) that have non-antisense antiproliferative activity against a number of cancer cell lines has been recently…”
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10
Rationally Designed Analogs of Tamoxifen with Improved Calmodulin Antagonism
Published in Journal of medicinal chemistry (01-01-1995)“…Computerized molecular modeling studies on the interactions of the antiestrogen tamoxifen (1) and its analogues bound to the calcium-binding protein calmodulin…”
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11
Mammary carcinogen-protein binding potentials: novel and biologically relevant structure-activity relationship model descriptors
Published in SAR and QSAR in environmental research (01-07-2010)“…Previously, SAR models for carcinogenesis used descriptors that are essentially chemical descriptors. Herein we report the development of models with the…”
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12
Targeting the Minor Groove of DNA: Crystal Structures of Two Complexes between Furan Derivatives of Berenil and the DNA Dodecamer d(CGCGAATTCGCG)2
Published in Journal of medicinal chemistry (08-11-1996)“…Crystal structures are reported of complexes of two novel furan derivatives of berenil with alkyl benzamidine groups bound to the DNA sequence…”
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13
Stability and kinetics of G-quadruplex structures
Published in Nucleic acids research (01-10-2008)“…In this review, we give an overview of recent literature on the structure and stability of unimolecular G-rich quadruplex structures that are relevant to drug…”
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14
Molecular anatomy of CCR5 engagement by physiologic and viral chemokines and HIV-1 envelope glycoproteins: differences in primary structural requirements for RANTES, MIP-1 alpha, and vMIP-II Binding
Published in Journal of molecular biology (09-11-2001)“…Molecular analysis of CCR5, the cardinal coreceptor for HIV-1 infection, has implicated the N-terminal extracellular domain (N-ter) and regions vicinal to the…”
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Identification of ENV determinants in V3 that influence the molecular anatomy of CCR5 utilization
Published in Journal of molecular biology (15-09-2000)“…The V3 loop of the ENV glycoprotein exerts a dominant influence on the interaction of gp120 with coreceptors. Primary env genes cloned from sequential isolates…”
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Triplex formation by morpholino oligodeoxyribonucleotides in the HER-2/neu promoter requires the pyrimidine motif
Published in Nucleic acids research (01-12-2001)“…Triplex-forming oligonucleotides (TFOs) are good candidates to be used as site-specific DNA-binding agents. Two obstacles encountered with TFOs are…”
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Understanding base-assisted desulfurization using a variety of disulfide-bridged peptides
Published in Biopolymers (2003)“…A recently rediscovered reaction of base‐assisted lanthionine formation has been applied to several systems of disulfide‐bridged peptides. In addition to…”
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Characterization of the active site of group B streptococcal hyaluronan lyase
Published in Proteins, structure, function, and bioinformatics (01-07-2000)“…Hyaluronan lyase is secreted by most strains of the human pathogen, group B streptococcus. Site‐directed mutagenesis of the enzyme identified three amino acid…”
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Recognition of GC Base Pairs by Triplex Forming Oligonucleotides Containing Nucleosides Derived from 2-Aminopyridine
Published in Nucleic acids research (15-12-1997)“…We have attempted to alleviate the pH dependency of triplex recognition of guanine by using intermolecular triplexes containing…”
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Sequence-dependent crossed helix packing in the crystal structure of a B-DNA decamer yields a detailed model for the Holliday junction
Published in Journal of molecular biology (27-06-1997)“…The structure of the B-DNA decamer d(CGCAATTGCG)2 has been determined by X-ray diffraction analysis to a resolution of 2.3 A and an R-factor of 17.7%. The…”
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