Search Results - "Liang, Sidney"
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Design of a Janus Kinase 3 (JAK3) Specific Inhibitor 1‑((2S,5R)‑5-((7H‑Pyrrolo[2,3‑d]pyrimidin-4-yl)amino)-2-methylpiperidin-1-yl)prop-2-en-1-one (PF-06651600) Allowing for the Interrogation of JAK3 Signaling in Humans
Published in Journal of medicinal chemistry (09-03-2017)“…Significant work has been dedicated to the discovery of JAK kinase inhibitors resulting in several compounds entering clinical development and two FDA approved…”
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2
Identification of Cyanamide-Based Janus Kinase 3 (JAK3) Covalent Inhibitors
Published in Journal of medicinal chemistry (13-12-2018)“…Ongoing interest in the discovery of selective JAK3 inhibitors led us to design novel covalent inhibitors that engage the JAK3 residue Cys909 by cyanamide, a…”
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3
Long-Term Refugee Health: Health Behaviors and Outcomes of Cambodian Refugee and Immigrant Women
Published in Health education & behavior (01-12-2015)“…Refugees in the United States have high rates of chronic disease. Both long-term effects of the refugee experience and adjustment to the U.S. health…”
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4
Portal vein tumor thrombus from gastric cancer
Published in Journal of ultrasonography (01-01-2018)“…A 53-year-old woman presented with left-sided abdominal pain, nausea and vomiting for the past 3 months with associated loss of appetite and weight. On…”
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Decreases in Smoking Prevalence in Asian Communities Served by the Racial and Ethnic Approaches to Community Health (REACH) Project
Published in American journal of public health (1971) (01-05-2010)“…We examined trends in smoking prevalence from 2002 through 2006 in 4 Asian communities served by the Racial and Ethnic Approaches to Community Health (REACH)…”
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6
Oxidative C−C Bond-Forming Reaction of Electron-Rich Alkylbenzyl Ether with Trimethylvinyloxysilane
Published in Organic letters (13-05-2004)“…Treatment of an electron-rich benzyl ether with DDQ at ambient temperature followed by addition of a silyl enol ether undergoes a C−C bond-forming reaction to…”
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Tertiary Pentyl Groups Enhance Salen Titanium Catalyst for Highly Enantioselective Trimethylsilylcyanation of Aldehydes
Published in Journal of organic chemistry (19-04-2002)“…tert-Pentyl groups are recognized to be highly effective steric groups that can enhance enantioselectivity of salen titanium complexes when they are used in…”
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8
PDE-10A inhibitors as insulin secretagogues
Published in Bioorganic & medicinal chemistry letters (15-05-2007)“…A series of quinoline-based PDE-10A inhibitors was determined to cause insulin secretion in vitro. Optimized compounds were evaluated in vivo where…”
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Unsymmetric chiral salen Schiff bases: A new chiral ligand pool from bis-schiff bases containing two different salicylaldehyde units
Published in Tetrahedron letters (11-06-1998)“…An efficient and facile synthesis of a new class of novel chiral Salen Schiff base ligands has been developed via a stepwise approach. An important feature of…”
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10
Self-reported health among Cambodians in Lowell, Massachusetts
Published in Journal of health care for the poor and underserved (01-05-2006)“…National health data reported for Asians in the aggregate present a picture of good health, but significant health disparities exist between Southeast Asian…”
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11
Imaging features of toxic megacolon
Published in BMJ case reports (30-09-2018)“…In earlier reviews, mortality rates vary from 19% to 27% with up to fivefold increase in mortality rate in case of perforation.1 2 In 2018, however, Doshi et…”
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Stereoselective, Oxidative C−C Bond Coupling of Naphthopyran Induced by DDQ: Stereocontrolled Total Synthesis of Deoxyfrenolicin
Published in Organic letters (18-11-1999)“…A formal total synthesis of pyranonaphthoquinone natural product deoxyfrenolicin 1 is described. The key step in the synthesis involves the use of…”
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13
Incidental discovery of Amyand's hernia
Published in BMJ case reports (01-11-2018)“…A 58-year-old woman was referred to Hospital Tuanku Ja’afar (Seremban, Malaysia) for contrast-enhanced CT abdomen and pelvis following discovery of a solid…”
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The readily available tert-pentyl group as a most effective simple directing group for asymmetric synthesis: a case study on Salen–Mn(III)-catalyzed epoxidation
Published in Tetrahedron: asymmetry (04-10-2002)“…The tert-pentyl group has been found to produce a pronounced stereodirecting effect, which is manifested in a study on Salen–Mn(III) complexes bearing such…”
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15
Design, synthesis and evaluation of bicyclic benzamides as novel 5-HT1F receptor agonists
Published in Bioorganic & medicinal chemistry letters (20-12-2004)“…Several fused bicyclic systems have been investigated to serve as the core structure of potent and selective 5-HT1F receptor agonists. Replacement of the…”
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Discovery of a JAK3-Selective Inhibitor: Functional Differentiation of JAK3-Selective Inhibition over pan-JAK or JAK1-Selective Inhibition
Published in ACS chemical biology (16-12-2016)“…PF-06651600, a newly discovered potent JAK3-selective inhibitor, is highly efficacious at inhibiting γc cytokine signaling, which is dependent on both JAK1 and…”
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17
Discovery and Lead Optimization of Atropisomer D1 Agonists with Reduced Desensitization
Published in Journal of medicinal chemistry (27-12-2018)“…The discovery of D1 subtype-selective agonists with drug-like properties has been an enduring challenge for the greater part of 40 years. All known…”
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Improved Synthesis of a Macrocyclic Peptide-Like C5aR Antagonist for Intravenous Applications
Published in Organic process research & development (17-11-2023)“…A multigram scale synthetic procedure for the preparation of a complex and polar macrocyclic peptidic C5aR antagonist is described. The route was developed…”
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Cyclic Peptide C5aR1 Antagonist Design Using Solution Conformational Analysis Derived from Residual Dipolar Couplings
Published in ACS medicinal chemistry letters (14-11-2024)“…To gain further insight into the conformational properties of small cyclic peptides that bind to the G-protein coupled receptor C5aR1, we report here for the…”
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N-Methyl-5-tert-butyltryptamine: A Novel, Highly Potent 5-HT1D Receptor Agonist
Published in Journal of medicinal chemistry (11-02-1999)“…It has been observed that reported 5-HT1D receptor agonists have at least one heteroatom (N, O, or S) on the 5-substituent of the indole. This has led to the…”
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