Search Results - "Steven, Coats"
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1
Synthesis of Nucleoside Phosphate and Phosphonate Prodrugs
Published in Chemical reviews (24-09-2014)“…Pradere et al examine the synthesis of nucleoside phosphate and phosphonate prodrugs…”
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2
A database of North American double modals and self-repairs from YouTube
Published in Psychology of language and communication (01-01-2022)“…Sequences of two modal verbs in spoken English can represent use of a nonstandard syntactic feature (double modal) or a corrected utterance in which a speaker…”
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3
Antibody-Drug Conjugates: Future Directions in Clinical and Translational Strategies to Improve the Therapeutic Index
Published in Clinical cancer research (15-09-2019)“…Since the first approval of gemtuzumab ozogamicin (Mylotarg; Pfizer; CD33 targeted), two additional antibody-drug conjugates (ADC), brentuximab vedotin…”
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4
A Biparatopic HER2-Targeting Antibody-Drug Conjugate Induces Tumor Regression in Primary Models Refractory to or Ineligible for HER2-Targeted Therapy
Published in Cancer cell (11-01-2016)“…Antibody-drug conjugate (ADC) which delivers cytotoxic drugs specifically into targeted cells through internalization and lysosomal trafficking has emerged as…”
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5
HIV nucleoside reverse transcriptase inhibitors
Published in European journal of medicinal chemistry (05-10-2022)“…More than 40 years into the pandemic, HIV remains a global burden and as of now, there is no cure in sight. Fortunately, highly active antiretroviral therapy…”
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6
Synthesis of (2S)‑2-Chloro-2-fluororibolactone via Stereoselective Electrophilic Fluorination
Published in Journal of organic chemistry (15-12-2017)“…A novel and efficient route for the preparation of (2S)-2-chloro-2-fluorolactone 29 is described. This approach takes advantage of a highly efficient…”
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7
HER2-targeted antibody-drug conjugate induces host immunity against cancer stem cells
Published in Cell chemical biology (20-05-2021)“…We previously tested HER2-targeted antibody-drug conjugates (ADCs) in immunocompromised (SCID) mice, precluding evaluation of host immunity, impact on cancer…”
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8
A Biparatopic HER2-Targeting Antibody-Drug Conjugate Induces Tumor Regression in Primary Models Refractory to or Ineligible for HER2-Targeted Therapy
Published in Cancer cell (10-06-2019)Get full text
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9
Synthesis and antiviral evaluation of novel heteroarylpyrimidines analogs as HBV capsid effectors
Published in Bioorganic & medicinal chemistry letters (15-02-2017)“…[Display omitted] New modifications to the scaffold of previously reported HBV capsid assembly effectors such as BAY 41-4109, HAP-12 and GLS4 were explored…”
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10
Synthesis and anti-HCV activity of β-d-2′-deoxy-2′-α-chloro-2′-β-fluoro and β-d-2′-deoxy-2′-α-bromo-2′-β-fluoro nucleosides and their phosphoramidate prodrugs
Published in Bioorganic & medicinal chemistry (15-02-2019)“…[Display omitted] We report herein the synthesis and evaluation of a series of β-d-2′-deoxy-2′-α-chloro-2′-β-fluoro and β-d-2′-deoxy-2′-α-bromo-2′-β-fluoro…”
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11
2′-Chloro,2′-fluoro Ribonucleotide Prodrugs with Potent Pan-genotypic Activity against Hepatitis C Virus Replication in Culture
Published in Journal of medicinal chemistry (13-07-2017)“…Pan-genotypic nucleoside HCV inhibitors display a high genetic barrier to drug resistance and are the preferred direct-acting agents to achieve complete…”
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12
Synthesis of carbocyclic nucleoside analogs with five-membered heterocyclic nucleobases
Published in Tetrahedron letters (03-06-2015)“…[Display omitted] New carbocyclic nucleoside analogs with five-membered heterocyclic nucleobases were synthesized and evaluated as potential anti-HIV and…”
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13
Asymmetric Binding to NS5A by Daclatasvir (BMS-790052) and Analogs Suggests Two Novel Modes of HCV Inhibition
Published in Journal of medicinal chemistry (11-12-2014)“…Symmetric, dimeric daclatasvir (BMS-790052) is the clinical lead for a class of picomolar inhibitors of HCV replication. While specific, resistance-bearing…”
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14
Azetidines and spiro azetidines as novel P2 units in hepatitis C virus NS3 protease inhibitors
Published in Bioorganic & medicinal chemistry letters (01-12-2013)“…Herein, we report the synthesis and structure–activity relationship studies of new analogs of boceprevir 1 and telaprevir 2. Introduction of azetidine and…”
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15
Synthesis and anti-HCV activity of a series of β-d-2′-deoxy-2′-dibromo nucleosides and their corresponding phosphoramidate prodrugs
Published in Bioorganic & medicinal chemistry letters (01-12-2017)“…[Display omitted] Several β-d-2′-deoxy-2′-substituted nucleoside analogs have displayed potent and selective anti-HCV activities and some of them have reached…”
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16
Synthesis and antiviral evaluation of 2′,2′,3′,3′-tetrafluoro nucleoside analogs
Published in Tetrahedron letters (15-02-2017)“…[Display omitted] •The synthesis of novel 2′,2′,3′,3′-tetrafluoro nucleoside analogs is described.•Glycosylation reactions are achieved via Mitsunobu…”
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17
A Therapeutic Uricase with Reduced Immunogenicity Risk and Improved Development Properties
Published in PloS one (21-12-2016)“…Humans and higher primates are unique in that they lack uricase, the enzyme capable of oxidizing uric acid. As a consequence of this enzyme deficiency, humans…”
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18
Discovery of a Series of 2′-α-Fluoro,2′-β-bromo-ribonucleosides and Their Phosphoramidate Prodrugs as Potent Pan-Genotypic Inhibitors of Hepatitis C Virus
Published in Journal of medicinal chemistry (28-02-2019)“…Hepatitis C virus (HCV) nucleoside inhibitors display pan-genotypic activity, a high barrier to the selection of resistant virus, and are some of the most…”
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19
Dual IGF-I/II-Neutralizing Antibody MEDI-573 Potently Inhibits IGF Signaling and Tumor Growth
Published in Cancer research (Chicago, Ill.) (01-02-2011)“…Insulin-like growth factors (IGF), IGF-I and IGF-II, are small polypeptides involved in regulating cell proliferation, survival, differentiation, and…”
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20
Synthesis of 5′-Methylene-Phosphonate Furanonucleoside Prodrugs: Application to D‑2′-Deoxy-2′-α-fluoro-2′-β‑C‑methyl Nucleosides
Published in Organic letters (07-09-2012)“…A new and facile synthetic pathway to metabolically stable 5′-methylene-bis(pivaloyloxymethyl)(POM)phosphonate furanonucleoside prodrugs is reported. The key…”
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