Search Results - "McDonald, Edith"
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Synthesis and activity of N-acyl azacyclic urea HIV-1 protease inhibitors with high potency against multiple drug resistant viral strains
Published in Bioorganic & medicinal chemistry letters (15-12-2005)“…As part of our efforts to identify potent HIV-1 protease inhibitors that are active against resistant viral strains, structural modification of the azacyclic…”
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Synthesis and SAR studies of potent HIV protease inhibitors containing novel dimethylphenoxyl acetates as P 2 ligands
Published in Bioorganic & medicinal chemistry letters (01-11-2003)Get full text
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3
Synthesis and antitumor activity of structural analogs of the epipodophyllotoxins
Published in Journal of medicinal chemistry (01-03-1991)“…Several ring-contracted analogues of the antitumor agent etoposide have been prepared. The synthesis of the simple indanyl system 3 is described along with two…”
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ABT-378, a Highly Potent Inhibitor of the Human Immunodeficiency Virus Protease
Published in Antimicrobial Agents and Chemotherapy (01-12-1998)“…Classifications Services AAC Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley Reddit…”
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5
Pharmacokinetic enhancement of inhibitors of the human immunodeficiency virus protease by coadministration with ritonavir
Published in Antimicrobial Agents and Chemotherapy (01-03-1997)“…Services AAC Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley Reddit StumbleUpon…”
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6
ABT-538 is a Potent Inhibitor of Human Immunodeficiency Virus Protease and has High Oral Bioavailability in Humans
Published in Proceedings of the National Academy of Sciences - PNAS (28-03-1995)“…Examination of the structural basis for antiviral activity, oral pharmacokinetics, and hepatic metabolism among a series of symmetry-based inhibitors of the…”
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Discovery of Ritonavir, a Potent Inhibitor of HIV Protease with High Oral Bioavailability and Clinical Efficacy
Published in Journal of medicinal chemistry (12-02-1998)“…The structure−activity studies leading to the potent and clinically efficacious HIV protease inhibitor ritonavir are described. Beginning with the moderately…”
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Synthesis and SAR studies of potent HIV protease inhibitors containing novel dimethylphenoxyl acetates as P2 ligands
Published in Bioorganic & medicinal chemistry letters (03-11-2003)“…Isopropyl substituted 4-thioazolyl valine side chains are highly optimized P(2)-P(3) ligands for C2 symmetry-based HIV protease inhibitors, as exemplified by…”
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A Novel, Picomolar Inhibitor of Human Immunodeficiency Virus Type 1 Protease
Published in Journal of medicinal chemistry (19-01-1996)“…The design, synthesis, and molecular modeling studies of a novel series of azacyclic ureas, which are inhibitors of human immunodeficiency virus type 1 (HIV-1)…”
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Evaluation of furofuran as a P2 ligand for symmetry-based HIV protease inhibitors
Published in Bioorganic & medicinal chemistry letters (03-12-1996)Get full text
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Potent piperazine hydroxyethylamine HIV protease inhibitors containing novel P 3 ligands
Published in Bioorganic & medicinal chemistry letters (15-12-1998)“…The 2-isopropyl thiazolyl group is a highly optimized P 3 ligand for C 2 symmetry-based HIV protease inhibitors, as exemplified in the drug ritonavir. Here we…”
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Potent piperazine hydroxyethylamine HIV protease inhibitors containing novel p3 ligands
Published in Bioorganic & medicinal chemistry letters (15-12-1998)“…The 2-isopropyl thiazolyl group is a highly optimized P3 ligand for C2 symmetry-based HIV protease inhibitors, as exemplified in the drug ritonavir. Here we…”
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13
Evaluation of furofuran as a P 2 ligand for symmetry-based HIV protease inhibitors
Published in Bioorganic & medicinal chemistry letters (03-12-1996)“…The hexahydrofurofuranyloxy group was evaluated as a conformationally constrained P 2 ligand for symmetry-based HIV protease inhibitors. A number of compounds…”
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14
Novel Azacyclic Ureas That Are Potent Inhibitors of HIV-1 Protease
Published in Biochemical and biophysical research communications (14-08-1996)“…A series of novel, azacyclic ureas which are highly potent inhibitors of the HIV-1 protease (IC50= 4.1 to <0.5 nM) were synthesized. Aqueous solubilities of…”
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15
Potent Inhibitors of the HIV-1 Protease with Good Oral Bioavailabilities
Published in Biochemical and biophysical research communications (06-06-1995)“…A series of novel pseudo-symmetrical and unsymmetrical inhibitors based on the backbone modification of a peptidomimetic were synthesized and found to be…”
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16
Lack of stereospecificity in the binding of the P2 amino acid of ritonavir to HIV protease
Published in Bioorganic & medicinal chemistry letters (18-03-1997)“…The biological and pharmacokinetic properties of the HIV protease inhibitor ritonavir and its D-valinyl diastereomer, A-117673, were found to be…”
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Determination of ritonavir, a new HIV protease inhibitor, in biological samples using reversed-phase high-performance liquid chromatography
Published in Journal of chromatography. B, Biomedical sciences and applications (19-12-1997)“…A simple, accurate and precise high-performance liquid chromatographic method has been developed for measurement of ritonavir concentrations in human plasma…”
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ASSOCIATE DEGREE NURSE EDUCATORS' PERCEPTION OF NEED FOR TRANSCULTURAL CONCEPTS IN NURSING EDUCATION
Published 01-01-1985“…Statement of the Problem. This study addresses the problem of identifying the perceptions of Associate Degree nurse educators toward the need for transcultural…”
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