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A 0.82 μW CIS-Based Action Recognition SoC With Self-Adjustable Frame Resolution for Always-on IoT Devices

IEEE transactions on circuits and systems. II, Express briefs, 2021-05, Vol.68 (5), p.1700-1704

2021

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1-(1-Arylethylpiperidin-4-yl)thymine Analogs as Antimycobacterial TMPK Inhibitors

Molecules (Basel, Switzerland), 2020-06, Vol.25 (12), p.2805

2020

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1,1-Difluoroethyl-substituted triazolothienopyrimidines as inhibitors of a human urea transport protein (UT-B): New analogs and binding model

Bioorganic & medicinal chemistry letters, 2013-06, Vol.23 (11), p.3338-3341

2013

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1,1-Diheterocyclic Ethylenes Derived from Quinaldine and Carbazole as New Tubulin-Polymerization Inhibitors: Synthesis, Metabolism, and Biological Evaluation

Journal of medicinal chemistry, 2019-02, Vol.62 (4), p.1902-1916

2019

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1,1-Dioxo-5,6-dihydro-[4,1,2]oxathiazines, a novel class of 11ß-HSD1 inhibitors for the treatment of diabetes

Bioorganic & medicinal chemistry letters, 2013-08, Vol.23 (16), p.4685-4691

2013

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1,1′-Disubstituted Ferrocenes as Molecular Hinges in Mono- and Bivalent Dopamine Receptor Ligands

Journal of medicinal chemistry, 2009-11, Vol.52 (21), p.6860-6870

2009

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1-[(1-Methyl-1H-imidazol-2-yl)methyl]-4-phenylpiperidines as mGluR2 Positive Allosteric Modulators for the Treatment of Psychosis

Journal of medicinal chemistry, 2011-03, Vol.54 (6), p.1724-1739

2011

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1,10-Seco-Eudesmane sesquiterpenoids as a new type of anti-neuroinflammatory agents by suppressing TLR4/NF-κB/MAPK pathways

European journal of medicinal chemistry, 2021-11, Vol.224, p.113713-113713, Article 113713

2021

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L-[1- 13C] phenylalanine oxidation as a measure of hepatocyte functional capacity in end-stage liver disease

The American journal of surgery, 1997-04, Vol.173 (4), p.270-273

1997

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1-(1H-Indol-3-yl)ethanamine Derivatives as Potent Staphylococcus aureus NorA Efflux Pump Inhibitors

ChemMedChem, 2014-07, Vol.9 (7), p.1534-1545

2014

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1-(2-(2,2,2-trifluoroethoxy)ethyl-1H-pyrazolo[4,3-d]pyrimidines as potent phosphodiesterase 5 (PDE5) inhibitors

Bioorganic & medicinal chemistry letters, 2010-05, Vol.20 (10), p.3125-3128

2010

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1-[2-(2-Benzoyl- and 2-benzylphenoxy)ethyl]uracils as potent anti-HIV-1 agents

Bioorganic & medicinal chemistry, 2011-10, Vol.19 (19), p.5794-5802

2011

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1,2,3,4,6-Penta-O-galloyl-β-d-glucose suppresses colon cancer through induction of tumor suppressor

Bioorganic & medicinal chemistry letters, 2018-07, Vol.28 (12), p.2117-2123

2018

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1,2,3,4,6-Pentakis[-O-(3,4,5-trihydroxybenzoyl)]-α,β-D-glucopyranose (PGG) analogs: design, synthesis, anti-tumor and anti-oxidant activities

Carbohydrate research, 2016-07, Vol.430, p.72-81

2016

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1,2,3,4-Tetrahydroisoquinoline (THIQ) as privileged scaffold for anticancer de novo drug design

Expert opinion on drug discovery, 2021-10, Vol.16 (10), p.1119-1147

2021

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1,2,3,4-Tetrahydroquinoline-Based Selective Human Neuronal Nitric Oxide Synthase (nNOS) Inhibitors: Lead Optimization Studies Resulting in the Identification of N-(1-(2-(Methylamino)ethyl)-1,2,3,4-tetrahydroquinolin-6-yl)thiophene-2-carboximidamide as a Preclinical Development Candidate

Journal of medicinal chemistry, 2012-03, Vol.55 (6), p.2882-2893

2012

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1,2,3-thiadiazole thioacetanilides. Part 2: Synthesis and biological evaluation of a new series of 2-{[4-(3,4-dichlorophenyl)-1,2,3-thiadiazol-5-yl]sulfanyl}acetanilides as HIV-1 inhibitors

Chemistry & biodiversity, 2010-07, Vol.7 (7), p.1717-1727

2010

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1,2,3-Triazine scaffold as a potent biologically active moiety: a mini review

Mini reviews in medicinal chemistry, 2014-01, Vol.14 (1), p.72-83

2014

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1,2,3-Triazole- and Quinoline-based Hybrids with Potent Antiplasmodial Activity

Medicinal chemistry (Shp-sariqah, United Arab Emirates), 2022-01, Vol.18 (5), p.521-535

2022

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1,2,3-Triazole-, arylamino- and thio-substituted 1,4-naphthoquinones: Potent antitumor activity, electrochemical aspects, and bioisosteric replacement of C-ring-modified lapachones

Bioorganic & medicinal chemistry, 2014-03, Vol.22 (5), p.1608-1619

2014

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1,2,3-Triazole as a Peptide Surrogate in the Rapid Synthesis of HIV-1 Protease Inhibitors

Chembiochem : a European journal of chemical biology, 2005-07, Vol.6 (7), p.1167-1169

2005

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1,2,3‐Triazole‐based esters and carboxylic acids as nonclassical carbonic anhydrase inhibitors capable of cathepsin B inhibition

Archiv der Pharmazie (Weinheim), 2024-03, Vol.357 (3), p.e2300372-n/a

2024

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1,2,3-Triazole-containing hybrids as potential anticancer agents: Current developments, action mechanisms and structure-activity relationships

European journal of medicinal chemistry, 2019-12, Vol.183, p.111700-111700, Article 111700

2019

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1,2,3‐Triazole Derivatives as an Emerging Scaffold for Antifungal Drug Development against Candida albicans: A Comprehensive Review

Chemistry & biodiversity, 2023-05, Vol.20 (5), p.e202300024-n/a

2023

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A 0.82 μW CIS-Based Action Recognition SoC With Self-Adjustable Frame Resolution for Always-on IoT Devices

1-(1-Arylethylpiperidin-4-yl)thymine Analogs as Antimycobacterial TMPK Inhibitors

1,1-Difluoroethyl-substituted triazolothienopyrimidines as inhibitors of a human urea transport protein (UT-B): New analogs and binding model

1,1-Diheterocyclic Ethylenes Derived from Quinaldine and Carbazole as New Tubulin-Polymerization Inhibitors: Synthesis, Metabolism, and Biological Evaluation

1,1-Dioxo-5,6-dihydro-[4,1,2]oxathiazines, a novel class of 11ß-HSD1 inhibitors for the treatment of diabetes

1,1′-Disubstituted Ferrocenes as Molecular Hinges in Mono- and Bivalent Dopamine Receptor Ligands

1-[(1-Methyl-1H-imidazol-2-yl)methyl]-4-phenylpiperidines as mGluR2 Positive Allosteric Modulators for the Treatment of Psychosis

1,10-Seco-Eudesmane sesquiterpenoids as a new type of anti-neuroinflammatory agents by suppressing TLR4/NF-κB/MAPK pathways

L-[1- 13C] phenylalanine oxidation as a measure of hepatocyte functional capacity in end-stage liver disease

1-(1H-Indol-3-yl)ethanamine Derivatives as Potent Staphylococcus aureus NorA Efflux Pump Inhibitors

1-[2-(1-Cyclobutylpiperidin-4-yloxy)-6,7-dihydro-4H-thiazolo[5,4-c]pyridin-5-yl]propan-1-one: a Histamine H 3 Receptor Inverse Agonist with Efficacy in Animal Models of Cognition

1-(2-(2,2,2-trifluoroethoxy)ethyl-1H-pyrazolo[4,3-d]pyrimidines as potent phosphodiesterase 5 (PDE5) inhibitors

1-[2-(2-Benzoyl- and 2-benzylphenoxy)ethyl]uracils as potent anti-HIV-1 agents

1,2,3,4,6-Penta-O-galloyl-β-d-glucose suppresses colon cancer through induction of tumor suppressor

1,2,3,4,6-Pentakis[-O-(3,4,5-trihydroxybenzoyl)]-α,β-D-glucopyranose (PGG) analogs: design, synthesis, anti-tumor and anti-oxidant activities

1,2,3,4-Tetrahydroisoquinoline (THIQ) as privileged scaffold for anticancer de novo drug design

1,2,3,4-Tetrahydroquinoline-Based Selective Human Neuronal Nitric Oxide Synthase (nNOS) Inhibitors: Lead Optimization Studies Resulting in the Identification of N-(1-(2-(Methylamino)ethyl)-1,2,3,4-tetrahydroquinolin-6-yl)thiophene-2-carboximidamide as a Preclinical Development Candidate

1,2,3-thiadiazole thioacetanilides. Part 2: Synthesis and biological evaluation of a new series of 2-{[4-(3,4-dichlorophenyl)-1,2,3-thiadiazol-5-yl]sulfanyl}acetanilides as HIV-1 inhibitors

1,2,3-Triazine scaffold as a potent biologically active moiety: a mini review

1,2,3-Triazole- and Quinoline-based Hybrids with Potent Antiplasmodial Activity

1,2,3-Triazole-, arylamino- and thio-substituted 1,4-naphthoquinones: Potent antitumor activity, electrochemical aspects, and bioisosteric replacement of C-ring-modified lapachones

1,2,3-Triazole as a Peptide Surrogate in the Rapid Synthesis of HIV-1 Protease Inhibitors

1,2,3‐Triazole‐based esters and carboxylic acids as nonclassical carbonic anhydrase inhibitors capable of cathepsin B inhibition

1,2,3-Triazole-containing hybrids as potential anticancer agents: Current developments, action mechanisms and structure-activity relationships

1,2,3‐Triazole Derivatives as an Emerging Scaffold for Antifungal Drug Development against Candida albicans: A Comprehensive Review

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