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False positives in the early stages of drug discovery

Current medicinal chemistry, 2010-12, Vol.17 (34), p.4231-4255

2010

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Inhibitors of cathepsin B

Current medicinal chemistry, 2006-08, Vol.13 (19), p.2309-2327

2006

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Antifungal activity of cinnamic acid derivatives involves inhibition of benzoate 4‐hydroxylase (CYP53)

Journal of applied microbiology, 2014-04, Vol.116 (4), p.955-966

2014

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Inhibitors of 17β-Hydroxysteroid Dehydrogenase Type 1

Current medicinal chemistry, 2008-01, Vol.15 (2), p.137-150

2008

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Inhibitors of aldo-keto reductases AKR1C1-AKR1C4

Current medicinal chemistry, 2011-06, Vol.18 (17), p.2554-2565

2011

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Progestins as inhibitors of the human 20-ketosteroid reductases, AKR1C1 and AKR1C3

Chemico-biological interactions, 2011-05, Vol.191 (1), p.227-233

2011

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Biochemical and biological evaluation of novel potent coumarin inhibitor of 17β-HSD type 1

Chemico-biological interactions, 2011-05, Vol.191 (1), p.60-65

2011

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Derivatives of pyrimidine, phthalimide and anthranilic acid as inhibitors of human hydroxysteroid dehydrogenase AKR1C1

Chemico-biological interactions, 2009-03, Vol.178 (1), p.158-164

2009

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Trihydroxynaphthalene reductase of Curvularia lunata—A target for flavonoid action?

Chemico-biological interactions, 2009-03, Vol.178 (1), p.259-267

2009

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A road map for prioritizing warheads for cysteine targeting covalent inhibitors

European journal of medicinal chemistry, 2018-12, Vol.160, p.94-107

2018

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Preventing cystatin F proteolytic activation by cathepsin V increases cytotoxicity of effector immune cells

European journal of cancer (1990), 2022-10, Vol.174, p.S124-S124

2022

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Synthesis and biochemical evaluation of some novel N-acyl phosphono-and phosphinoalanine derivatives as potential inhibitors of the D-glutamic acid-adding enzyme

Pharmazie, 2001-04, Vol.56 (4), p.295-297

2001

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P09.04 Cathepsin V inhibition prevents the activation of cystatin F and increases immune cell cytotoxicity

Journal for immunotherapy of cancer, 2022-09, Vol.10 (Suppl 1), p.A33-A34

2022

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Intercomparison of dosimetry systems based on CaF2:Mn TL detectors

Radiation protection dosimetry, 2006-09, Vol.119 (1-4), p.300-305

2006

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Synthesis of N-phthalimido β-aminoethanesulfonyl chlorides: the use of thionyl chloride for a simple and efficient synthesis of new peptidosulfonamide building blocks

Tetrahedron letters, 2005-06, Vol.46 (23), p.4069-4072

2005

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Synthesis and modulation of cytokine production by two new adamantane substituted acyclic desmuramyldipeptide analogs

Pharmazie, 2001-07, Vol.56 (7), p.523-526

2001

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Design, synthesis and structure–activity relationships of new phosphinate inhibitors of MurD

Bioorganic & medicinal chemistry letters, 2006-01, Vol.16 (2), p.343-348

2006

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Structural and Functional Characterization of Enantiomeric Glutamic Acid Derivatives as Potential Transition State Analogue Inhibitors of MurD Ligase

Journal of molecular biology, 2007-06, Vol.370 (1), p.107-115

2007

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SARS-CoV-2 molecular epidemiology in Slovenia, January to September 2021

Euro surveillance : bulletin européen sur les maladies transmissibles, 2023-02, Vol.28 (8), p.1

2023

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Modulation of tumour necrosis factor production with desmuramyldipeptide analogues

Pflügers Archiv, 2000, Vol.440 (5 Suppl), p.R64

2000

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Determination of cytotoxic activity of adamantyl-desmuramyl dipeptides

Pharmazie, 2003-06, Vol.58 (6), p.442-443

2003

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Recent advances in design, synthesis and biological activity of aminoalkylsulfonates and sulfonamidopeptides

Current medicinal chemistry, 2004-12, Vol.11 (24), p.3263-3278

2004

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Nonsteroidal anti-inflammatory drugs and their analogues as inhibitors of aldo-keto reductase AKR1C3: New lead compounds for the development of anticancer agents

Bioorganic & medicinal chemistry letters, 2005-12, Vol.15 (23), p.5170-5175

2005

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Inhibitors of 17beta-hydroxysteroid dehydrogenase type 1

Current medicinal chemistry, 2008, Vol.15 (2), p.137

2008

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Epoxide opening with amino acids: improved synthesis of hydroxyethylamine dipeptide isosteres

Tetrahedron letters, 2006-03, Vol.47 (11), p.1733-1735

2006

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False positives in the early stages of drug discovery

Inhibitors of cathepsin B

Antifungal activity of cinnamic acid derivatives involves inhibition of benzoate 4‐hydroxylase (CYP53)

Inhibitors of 17β-Hydroxysteroid Dehydrogenase Type 1

Inhibitors of aldo-keto reductases AKR1C1-AKR1C4

Progestins as inhibitors of the human 20-ketosteroid reductases, AKR1C1 and AKR1C3

Biochemical and biological evaluation of novel potent coumarin inhibitor of 17β-HSD type 1

Derivatives of pyrimidine, phthalimide and anthranilic acid as inhibitors of human hydroxysteroid dehydrogenase AKR1C1

Trihydroxynaphthalene reductase of Curvularia lunata—A target for flavonoid action?

A road map for prioritizing warheads for cysteine targeting covalent inhibitors

Preventing cystatin F proteolytic activation by cathepsin V increases cytotoxicity of effector immune cells

Synthesis and biochemical evaluation of some novel N-acyl phosphono-and phosphinoalanine derivatives as potential inhibitors of the D-glutamic acid-adding enzyme

P09.04 Cathepsin V inhibition prevents the activation of cystatin F and increases immune cell cytotoxicity

Intercomparison of dosimetry systems based on CaF2:Mn TL detectors

Synthesis of N-phthalimido β-aminoethanesulfonyl chlorides: the use of thionyl chloride for a simple and efficient synthesis of new peptidosulfonamide building blocks

Synthesis and modulation of cytokine production by two new adamantane substituted acyclic desmuramyldipeptide analogs

Design, synthesis and structure–activity relationships of new phosphinate inhibitors of MurD

Structural and Functional Characterization of Enantiomeric Glutamic Acid Derivatives as Potential Transition State Analogue Inhibitors of MurD Ligase

SARS-CoV-2 molecular epidemiology in Slovenia, January to September 2021

Modulation of tumour necrosis factor production with desmuramyldipeptide analogues

Determination of cytotoxic activity of adamantyl-desmuramyl dipeptides

Recent advances in design, synthesis and biological activity of aminoalkylsulfonates and sulfonamidopeptides

Nonsteroidal anti-inflammatory drugs and their analogues as inhibitors of aldo-keto reductase AKR1C3: New lead compounds for the development of anticancer agents

Inhibitors of 17beta-hydroxysteroid dehydrogenase type 1

Epoxide opening with amino acids: improved synthesis of hydroxyethylamine dipeptide isosteres

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