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Methylmercury Alters Intrasynaptosomal Concentrations of Endogenous Polyvalent Cations

Toxicology and applied pharmacology, 1993-10, Vol.122 (2), p.222-232

1993

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Synthesis and biological evaluation of solubilized sulfonamide analogues of the phosphatidylinositol 3-kinase inhibitor ZSTK474

Bioorganic & medicinal chemistry, 2019-04, Vol.27 (8), p.1529-1545

2019

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Inhibition of the Cytolytic Protein Perforin Prevents Rejection of Transplanted Bone Marrow Stem Cells in Vivo

Journal of medicinal chemistry, 2020-03, Vol.63 (5), p.2229-2239

2020

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Morpholylureas are a new class of potent and selective inhibitors of the type 5 17-β-hydroxysteroid dehydrogenase (AKR1C3)

Bioorganic & medicinal chemistry, 2014-02, Vol.22 (3), p.967-977

2014

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Biological characterization of SN32976, a selective inhibitor of PI3K and mTOR with preferential activity to PI3Kα, in comparison to established pan PI3K inhibitors

Oncotarget, 2017-07, Vol.8 (29), p.47725-47740

2017

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Synthesis and biological evaluation of sulfonamide analogues of the phosphatidylinositol 3-kinase inhibitor ZSTK474

Bioorganic & medicinal chemistry, 2017-10, Vol.25 (20), p.5859-5874

2017

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Synthesis and Biological Evaluation of Novel Analogues of the Pan Class I Phosphatidylinositol 3-Kinase (PI3K) Inhibitor 2-(Difluoromethyl)-1-[4,6-di(4-morpholinyl)-1,3,5-triazin-2-yl]-1 H -benzimidazole (ZSTK474)

Journal of medicinal chemistry, 2011-10, Vol.54 (20), p.7105-7126

2011

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General cognitive abilities in orangutans (Pongo abelii and Pongo pygmaeus)

Intelligence (Norwood), 2019-05, Vol.74, p.3-11

2019

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Discovery of pyrazolo[1,5-a]pyridines as p110α-selective PI3 kinase inhibitors

Bioorganic & medicinal chemistry, 2012-01, Vol.20 (1), p.69-85

2012

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Novel pyrazolo[1,5-a]pyridines with improved aqueous solubility as p110α-selective PI3 kinase inhibitors

Bioorganic & medicinal chemistry letters, 2017-01, Vol.27 (2), p.187-190

2017

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Synthesis and structure-activity relationships for 1-(4-(piperidin-1-ylsulfonyl)phenyl)pyrrolidin-2-ones as novel non-carboxylate inhibitors of the aldo-keto reductase enzyme AKR1C3

European journal of medicinal chemistry, 2013-04, Vol.62, p.738-744

2013

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Exploration of a Series of 5‑Arylidene-2-thioxoimidazolidin-4-ones as Inhibitors of the Cytolytic Protein Perforin

Journal of medicinal chemistry, 2013-12, Vol.56 (23), p.9542-9555

2013

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3‑(3,4-Dihydroisoquinolin-2(1H)‑ylsulfonyl)benzoic Acids: Highly Potent and Selective Inhibitors of the Type 5 17-β-Hydroxysteroid Dehydrogenase AKR1C3

Journal of medicinal chemistry, 2012-09, Vol.55 (17), p.7746-7758

2012

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The Activity of SN33638, an Inhibitor of AKR1C3, on Testosterone and 17β-Estradiol Production and Function in Castration-Resistant Prostate Cancer and ER-Positive Breast Cancer

Frontiers in oncology, 2014-01, Vol.4, p.159-159

2014

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Spatial Patterns of Public Facility Services based on Grid/Cell Supply Approach (Case Study: Elementary School in Malang, Surakarta & Banjarmasin City)

MATEC Web of Conferences, 2017, Vol.97, p.1063

2017

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A Heuristic Framework for Process Safety Assessment during Research and Development Design Stage

Chemical engineering transactions, 2017-03, Vol.56

2017

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Novel pyrazolo[1,5-a]pyridines as p110α-selective PI3 kinase inhibitors: Exploring the benzenesulfonohydrazide SAR

Bioorganic & medicinal chemistry, 2012-01, Vol.20 (1), p.58-68

2012

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Synthesis and biological evaluation of novel phosphatidylinositol 3-kinase inhibitors: Solubilized 4-substituted benzimidazole analogs of 2-(difluoromethyl)-1-[4,6-di(4-morpholinyl)-1,3,5-triazin-2-yl]-1H-benzimidazole (ZSTK474)

European journal of medicinal chemistry, 2013-06, Vol.64, p.137-147

2013

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Waste Recovery and Regeneration (REGEN) System for Palm Oil Industry

Chemical engineering transactions, 2015-10, Vol.45

2015

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Combined neutron and X-ray diffraction studies of DNA in crystals and solutions

Acta crystallographica. Section D, Biological crystallography., 2010-11, Vol.66 (11), p.1244-1248

2010

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REPORT OF AN ILLNESS OUTBREAK AT THE HARRY S TRUMAN STATE OFFICE BUILDING

American journal of epidemiology, 1989-03, Vol.129 (3), p.550-558

1989

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Some effects of varying the duration, frequency and intensity of grazing on the growth of steers on veld

Proceedings - Grassland Society of Southern Africa, 1974-01, Vol.9 (1), p.133-137

1974

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Methylmercury Alters Intrasynaptosomal Concentrations of Endogenous Polyvalent Cations

Synthesis and biological evaluation of solubilized sulfonamide analogues of the phosphatidylinositol 3-kinase inhibitor ZSTK474

Inhibition of the Cytolytic Protein Perforin Prevents Rejection of Transplanted Bone Marrow Stem Cells in Vivo

Morpholylureas are a new class of potent and selective inhibitors of the type 5 17-β-hydroxysteroid dehydrogenase (AKR1C3)

Biological characterization of SN32976, a selective inhibitor of PI3K and mTOR with preferential activity to PI3Kα, in comparison to established pan PI3K inhibitors

Synthesis and biological evaluation of sulfonamide analogues of the phosphatidylinositol 3-kinase inhibitor ZSTK474

Synthesis and Biological Evaluation of Novel Analogues of the Pan Class I Phosphatidylinositol 3-Kinase (PI3K) Inhibitor 2-(Difluoromethyl)-1-[4,6-di(4-morpholinyl)-1,3,5-triazin-2-yl]-1 H -benzimidazole (ZSTK474)

General cognitive abilities in orangutans (Pongo abelii and Pongo pygmaeus)

Discovery of pyrazolo[1,5-a]pyridines as p110α-selective PI3 kinase inhibitors

Novel pyrazolo[1,5-a]pyridines with improved aqueous solubility as p110α-selective PI3 kinase inhibitors

Synthesis and structure-activity relationships for 1-(4-(piperidin-1-ylsulfonyl)phenyl)pyrrolidin-2-ones as novel non-carboxylate inhibitors of the aldo-keto reductase enzyme AKR1C3

Exploration of a Series of 5‑Arylidene-2-thioxoimidazolidin-4-ones as Inhibitors of the Cytolytic Protein Perforin

3‑(3,4-Dihydroisoquinolin-2(1H)‑ylsulfonyl)benzoic Acids: Highly Potent and Selective Inhibitors of the Type 5 17-β-Hydroxysteroid Dehydrogenase AKR1C3

The Activity of SN33638, an Inhibitor of AKR1C3, on Testosterone and 17β-Estradiol Production and Function in Castration-Resistant Prostate Cancer and ER-Positive Breast Cancer

Spatial Patterns of Public Facility Services based on Grid/Cell Supply Approach (Case Study: Elementary School in Malang, Surakarta & Banjarmasin City)

A Heuristic Framework for Process Safety Assessment during Research and Development Design Stage

Novel pyrazolo[1,5-a]pyridines as p110α-selective PI3 kinase inhibitors: Exploring the benzenesulfonohydrazide SAR

Synthesis and biological evaluation of novel phosphatidylinositol 3-kinase inhibitors: Solubilized 4-substituted benzimidazole analogs of 2-(difluoromethyl)-1-[4,6-di(4-morpholinyl)-1,3,5-triazin-2-yl]-1H-benzimidazole (ZSTK474)

Waste Recovery and Regeneration (REGEN) System for Palm Oil Industry

Combined neutron and X-ray diffraction studies of DNA in crystals and solutions

REPORT OF AN ILLNESS OUTBREAK AT THE HARRY S TRUMAN STATE OFFICE BUILDING

Some effects of varying the duration, frequency and intensity of grazing on the growth of steers on veld

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