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0.5‑Gy X‑ray irradiation induces reorganization of cytoskeleton and differentiation of osteoblasts

Molecular medicine reports, 2021-05, Vol.23 (5), Article 379

2021

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(09) Comparison of the potency of newly developed and currently available oximes to reactivate nerve agent-inhibited acetylcholinesterase in vitro and in vivo

Chemico-biological interactions, 2005-12, Vol.157, p.367-368

2005

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1,1,1-Trichloropropene-2,3-oxide: an alternate mechanism for its inhibition of cytochrome P-450

Research communications in chemical pathology and pharmacology, 1982-01, Vol.35 (1), p.111

1982

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1,1,2-Tris-organoselenide alkene derivatives, but not 1,2-bis-organoselenide alkene derivatives, inhibited δ-aminolevulinate dehydratase activity from human erythrocytic cells in vitro

Toxicology in vitro, 2007-04, Vol.21 (3), p.387-391

2007

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1-(1,3-Benzodioxol-5-ylmethyl)-3-[4-(1 H-imidazol-1-yl)phenoxy]-piperidine analogs as potent and selective inhibitors of nitric oxide formation

Bioorganic & medicinal chemistry letters, 2007-05, Vol.17 (9), p.2499-2504

2007

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1-(1-Acetyl-piperidin-4-yl)-3-adamantan-1-yl-urea (AR9281) as a potent, selective, and orally available soluble epoxide hydrolase inhibitor with efficacy in rodent models of hypertension and dysglycemia

Bioorganic & medicinal chemistry letters, 2011-02, Vol.21 (3), p.983-988

2011

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1-(1-Arylethylidene)thiosemicarbazide derivatives: A new class of tyrosinase inhibitors

Bioorganic & medicinal chemistry, 2008-02, Vol.16 (3), p.1096-1102

2008

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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′-Bis(anilino)-4-,4′-bis(naphtalene)-8,8′-disulfonate Acts as an Inhibitor of Lipoprotein Lipase and Competes for Binding with Apolipoprotein CII

The Journal of biological chemistry, 2003-09, Vol.278 (39), p.37183-37194

2003

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1,1-Bisphosphonate Squalene Synthase Inhibitors: Interplay Between the Isoprenoid Subunit and the Diphosphate Surrogate

Journal of medicinal chemistry, 1995-07, Vol.38 (14), p.2596-2605

1995

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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-diphenyl-2-picrylhydrazyl radical scavenging activity and tyrosinase inhibitory effects of constituents of sugarcane molasses

Bioscience, biotechnology, and biochemistry, 2007-01, Vol.71 (1), p.183-191

2007

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1,10-Phenanthroline phosphorylates (activates) MAP kinase in Xenopus oocytes

Cellular signalling, 2003-12, Vol.15 (12), p.1139-1147

2003

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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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1,2,3,4,6 Penta-O-galloyl-β-d-glucose, a bioactivity guided isolated compound from Mangifera indica inhibits 11β-HSD-1 and ameliorates high fat diet-induced diabetes in C57BL/6 mice

Phytomedicine (Stuttgart), 2013-03, Vol.20 (5), p.417-426

2013

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1,2,3,4-Tetrahydrobenzo[h][1,6]naphthyridines as a new family of potent peripheral-to-midgorge-site inhibitors of acetylcholinesterase: Synthesis, pharmacological evaluation and mechanistic studies

European journal of medicinal chemistry, 2014-02, Vol.73, p.141-152

2014

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1,2,3,4-Tetrahydroisoquinolinyl sulfamic acids as phosphatase PTP1B inhibitors

Bioorganic & medicinal chemistry letters, 2006-03, Vol.16 (6), p.1574-1578

2006

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1,2,3-Benzoxathiazine-2,2-dioxides - effective inhibitors of human carbonic anhydrases

Journal of enzyme inhibition and medicinal chemistry, 2023-01, Vol.38 (1), p.225-238

2023

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1, 2, 3-current ways to fight HIV

Positively aware, 1998-11, Vol.9 (6), p.31

Vazquez, E

1998

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1,2,3-Thiadiazole substituted pyrazolones as potent KDR/VEGFR-2 kinase inhibitors

Bioorganic & medicinal chemistry letters, 2007-03, Vol.17 (6), p.1793-1798

2007

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1,2,3-Triazole-Containing Uracil Derivatives with Excellent Pharmacokinetics as a Novel Class of Potent Human Deoxyuridine Triphosphatase Inhibitors

Journal of medicinal chemistry, 2012-07, Vol.55 (14), p.6427-6437

2012

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1,2,3-Triazole-Dithiocarbamate Hybrids, a Group of Novel Cell Active SIRT1 Inhibitors

Cellular physiology and biochemistry, 2016-01, Vol.38 (1), p.185-193

2016

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1,2,3-triazole tethered Indole-3-glyoxamide derivatives as multiple inhibitors of 5-LOX, COX-2 & tubulin: Their anti-proliferative & anti-inflammatory activity

Bioorganic chemistry, 2018-12, Vol.81, p.1-20

2018

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1,2,3-Triazoles as inhibitors of indoleamine 2,3-dioxygenase 2 (IDO2)

Bioorganic & medicinal chemistry letters, 2016-09, Vol.26 (17), p.4330-4333

2016

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[1,2,3]Triazolo[4,5-d]pyrimidine derivatives incorporating (thio)urea moiety as a novel scaffold for LSD1 inhibitors

European journal of medicinal chemistry, 2020-02, Vol.187, p.111989-111989, Article 111989

2020

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0.5‑Gy X‑ray irradiation induces reorganization of cytoskeleton and differentiation of osteoblasts

(09) Comparison of the potency of newly developed and currently available oximes to reactivate nerve agent-inhibited acetylcholinesterase in vitro and in vivo

1,1,1-Trichloropropene-2,3-oxide: an alternate mechanism for its inhibition of cytochrome P-450

1,1,2-Tris-organoselenide alkene derivatives, but not 1,2-bis-organoselenide alkene derivatives, inhibited δ-aminolevulinate dehydratase activity from human erythrocytic cells in vitro

1-(1,3-Benzodioxol-5-ylmethyl)-3-[4-(1 H-imidazol-1-yl)phenoxy]-piperidine analogs as potent and selective inhibitors of nitric oxide formation

1-(1-Acetyl-piperidin-4-yl)-3-adamantan-1-yl-urea (AR9281) as a potent, selective, and orally available soluble epoxide hydrolase inhibitor with efficacy in rodent models of hypertension and dysglycemia

1-(1-Arylethylidene)thiosemicarbazide derivatives: A new class of tyrosinase inhibitors

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

1,1′-Bis(anilino)-4-,4′-bis(naphtalene)-8,8′-disulfonate Acts as an Inhibitor of Lipoprotein Lipase and Competes for Binding with Apolipoprotein CII

1,1-Bisphosphonate Squalene Synthase Inhibitors: Interplay Between the Isoprenoid Subunit and the Diphosphate Surrogate

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

1,1-diphenyl-2-picrylhydrazyl radical scavenging activity and tyrosinase inhibitory effects of constituents of sugarcane molasses

1,10-Phenanthroline phosphorylates (activates) MAP kinase in Xenopus oocytes

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

1,2,3,4,6 Penta-O-galloyl-β-d-glucose, a bioactivity guided isolated compound from Mangifera indica inhibits 11β-HSD-1 and ameliorates high fat diet-induced diabetes in C57BL/6 mice

1,2,3,4-Tetrahydrobenzo[h][1,6]naphthyridines as a new family of potent peripheral-to-midgorge-site inhibitors of acetylcholinesterase: Synthesis, pharmacological evaluation and mechanistic studies

1,2,3,4-Tetrahydroisoquinolinyl sulfamic acids as phosphatase PTP1B inhibitors

1,2,3-Benzoxathiazine-2,2-dioxides - effective inhibitors of human carbonic anhydrases

1, 2, 3-current ways to fight HIV

1,2,3-Thiadiazole substituted pyrazolones as potent KDR/VEGFR-2 kinase inhibitors

1,2,3-Triazole-Containing Uracil Derivatives with Excellent Pharmacokinetics as a Novel Class of Potent Human Deoxyuridine Triphosphatase Inhibitors

1,2,3-Triazole-Dithiocarbamate Hybrids, a Group of Novel Cell Active SIRT1 Inhibitors

1,2,3-triazole tethered Indole-3-glyoxamide derivatives as multiple inhibitors of 5-LOX, COX-2 & tubulin: Their anti-proliferative & anti-inflammatory activity

1,2,3-Triazoles as inhibitors of indoleamine 2,3-dioxygenase 2 (IDO2)

[1,2,3]Triazolo[4,5-d]pyrimidine derivatives incorporating (thio)urea moiety as a novel scaffold for LSD1 inhibitors

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