Search Results - "DOOSEOP KIM"
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Discovery of a peripheral 5HT2A antagonist as a clinical candidate for metabolic dysfunction-associated steatohepatitis
Published in Nature communications (20-01-2024)“…Metabolic Dysfunction-Associated Steatotic Liver Disease (MASLD) is currently the leading cause of chronic liver disease worldwide. Metabolic…”
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2
Potent, orally absorbed glucagon receptor antagonists
Published in Bioorganic & medicinal chemistry letters (08-03-1999)“…The SAR of 2-pyridyl-3,5-diaryl pyrroles, ligands of the human glucagon receptor and inhibitors of p38 kinase, were investigated. This effort resulted in the…”
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3
Characterization of Two Cyclic Metabolites of Sitagliptin
Published in Drug metabolism and disposition (01-04-2007)“…Two novel metabolites of the dipeptidyl peptidase inhibitor sitagliptin (MK-0431, (2 R )-4-oxo-4-[3-(trifluoromethyl)-5,6-dihydro[1,2,4]triazolo[4,3- a…”
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4
Translocation of radical sites by intramolecular 1,5-hydrogen atom transfer
Published in Journal of the American Chemical Society (01-08-1988)Get full text
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5
Dipeptidyl Peptidase IV Inhibition for the Treatment of Type 2 Diabetes
Published in Diabetes (New York, N.Y.) (01-10-2005)“…Dipeptidyl Peptidase IV Inhibition for the Treatment of Type 2 Diabetes Potential Importance of Selectivity Over Dipeptidyl Peptidases 8 and 9 George R. Lankas…”
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6
Atom transfer cyclization reactions of hex-5-ynyl iodides: synthetic and mechanistic studies
Published in Journal of the American Chemical Society (01-08-1989)Get full text
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7
Design, Synthesis, and Biological Evaluation of New Peripheral 5HT2A Antagonists for Nonalcoholic Fatty Liver Disease
Published in Journal of medicinal chemistry (23-04-2020)“…Nonalcoholic fatty liver disease (NAFLD) is increasingly prevalent worldwide, causing serious liver complications, including nonalcoholic steatohepatitis…”
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8
Atom-transfer cyclization. A novel isomerization of hex-5-ynyl iodides to (iodomethylene)cyclopentanes
Published in Journal of the American Chemical Society (30-04-1986)Get full text
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9
Design, Synthesis, and Biological Evaluation of New Peripheral 5HT 2A Antagonists for Nonalcoholic Fatty Liver Disease
Published in Journal of medicinal chemistry (23-04-2020)“…Nonalcoholic fatty liver disease (NAFLD) is increasingly prevalent worldwide, causing serious liver complications, including nonalcoholic steatohepatitis…”
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10
NMR uncovers direct interaction between human NEDD4-1 and p34SEI−1
Published in Biochemical and biophysical research communications (26-08-2017)“…PTEN, an important tumor suppressor and a key regulator of the PI3K/AKT signaling pathway, is often deleted/mutated in different types of cancer. The E3…”
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11
Dipeptidyl peptidase IV inhibition for the treatment of type 2 diabetes : Potential importance of selectivity over dipeptidyl peptidases 8 and 9
Published in Diabetes (New York, N.Y.) (01-10-2005)“…Dipeptidyl peptidase (DPP)-IV inhibitors are a new approach to the treatment of type 2 diabetes. DPP-IV is a member of a family of serine peptidases that…”
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12
Discovery of a peripheral 5HT 2A antagonist as a clinical candidate for metabolic dysfunction-associated steatohepatitis
Published in Nature communications (20-01-2024)“…Metabolic Dysfunction-Associated Steatotic Liver Disease (MASLD) is currently the leading cause of chronic liver disease worldwide. Metabolic…”
Get full text
Journal Article -
13
Discovery and optimization of adamantane carboxylic acid derivatives as potent diacylglycerol acyltransferase 1 inhibitors for the potential treatment of obesity and diabetes
Published in European journal of medicinal chemistry (28-08-2015)“…We have developed a series of adamantane carboxylic acid derivatives exhibiting potent diacylglycerol acyltransferase 1 (DGAT1) inhibitory activities…”
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14
Discovery of Potent and Selective Dipeptidyl Peptidase IV Inhibitors Derived from β-Aminoamides Bearing Subsituted Triazolopiperazines
Published in Journal of medicinal chemistry (14-02-2008)“…A series of β-aminoamides bearing triazolopiperazines have been discovered as potent, selective, and orally active dipeptidyl peptidase IV (DPP-4) inhibitors…”
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15
Potent 1,3,4-trisubstituted pyrrolidine CCR5 receptor antagonists: effects of fused heterocycles on antiviral activity and pharmacokinetic properties
Published in Bioorganic & medicinal chemistry letters (15-04-2005)“…[Display omitted] A series of 1,3,4-trisubstituted pyrrolidine CCR5 receptor antagonists containing a variety of fused heterocycles at the 4-position of the…”
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16
(2R)-4-Oxo-4-[3-(Trifluoromethyl)-5,6-dihydro[1,2,4]triazolo[4,3-a]pyrazin- 7(8H)-yl]-1-(2,4,5-trifluorophenyl)butan-2-amine: A Potent, Orally Active Dipeptidyl Peptidase IV Inhibitor for the Treatment of Type 2 Diabetes
Published in Journal of medicinal chemistry (13-01-2005)“…A novel series of β-amino amides incorporating fused heterocycles, i.e., triazolopiperazines, were synthesized and evaluated as inhibitors of dipeptidyl…”
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17
NMR uncovers direct interaction between human NEDD4-1 and p34 SEI-1
Published in Biochemical and biophysical research communications (26-08-2017)“…PTEN, an important tumor suppressor and a key regulator of the PI3K/AKT signaling pathway, is often deleted/mutated in different types of cancer. The E3…”
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18
2-Arylbenzoxazoles as CETP inhibitors: Raising HDL-C in cynoCETP transgenic mice
Published in Bioorganic & medicinal chemistry letters (01-01-2011)“…Compound 4 was found to be a potent inhibitor of CETP (CE IC50=16nM, TG IC50=18nM) with good pharmacokinetic properties and in vivo efficacy (ΔHDL-C=24mg/dL)…”
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19
Triazolopiperazine-amides as dipeptidyl peptidase IV inhibitors: Close analogs of JANUVIA™ (sitagliptin phosphate)
Published in Bioorganic & medicinal chemistry letters (15-06-2007)“…A series of β-aminoamides bearing triazolopiperazines has been prepared and evaluated as potent, selective, orally active dipeptidyl peptidase IV (DPP-4)…”
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20
AT1/AT2-BALANCED ANGIOTENSIN II ANTAGONISTS
Published in European journal of medicinal chemistry (1995)“…Three heterocyclic series of nonpeptide angiotensin II receptor antagonists (quinazolinones, imidazo[4,5-b]pyridines, and triazolinones) have been transformed…”
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