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Discovery and SAR of Novel 2,3-Dihydroimidazo[1,2-c]quinazoline PI3K Inhibitors: Identification of Copanlisib (BAY 80-6946)

ChemMedChem, 2016-07, Vol.11 (14), p.1517-1530

2016

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Enzymatic Characterization of Recombinant Food Vacuole Plasmepsin 4 from the Rodent Malaria Parasite Plasmodium berghei

PloS one, 2015-10, Vol.10 (10), p.e0141758-e0141758

2015

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Selective hydrophobic pocket binding observed within the carbonic anhydrase II active site accommodate different 4-substituted-ureido-benzenesulfonamides and correlate to inhibitor potency

Chemical communications (Cambridge, England), 2010-11, Vol.46 (44), p.8371-8373

2010

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Structure and catalysis by carbonic anhydrase II: Role of active-site tryptophan 5

Archives of biochemistry and biophysics, 2011-12, Vol.516 (2), p.97-102

2011

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Structural Insights into the Extracytoplasmic Thiamine-Binding Lipoprotein p37 of Mycoplasma hyorhinis

Journal of Bacteriology, 2009-04, Vol.191 (8), p.2585-2592

2009

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Anticonvulsant 4-Aminobenzenesulfonamide Derivatives with Branched-Alkylamide Moieties: X-ray Crystallography and Inhibition Studies of Human Carbonic Anhydrase Isoforms I, II, VII, and XIV

Journal of medicinal chemistry, 2011-06, Vol.54 (11), p.3977-3981

2011

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Sulfonamides incorporating 1,3,5-triazine moieties selectively and potently inhibit carbonic anhydrase transmembrane isoforms IX, XII and XIV over cytosolic isoforms I and II: Solution and X-ray crystallographic studies

Bioorganic & medicinal chemistry, 2011-05, Vol.19 (10), p.3105-3119

2011

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Recombinant Plasmepsin 1 from the Human Malaria Parasite Plasmodium falciparum: Enzymatic Characterization, Active Site Inhibitor Design, and Structural Analysis

Biochemistry (Easton), 2009-05, Vol.48 (19), p.4086-4099

2009

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Coumarinyl-substituted sulfonamides strongly inhibit several human carbonic anhydrase isoforms: solution and crystallographic investigations

Bioorganic & medicinal chemistry, 2010-07, Vol.18 (14), p.4873-4878

2010

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Carbonic anhydrase inhibitors. The X-ray crystal structure of human isoform II in adduct with an adamantyl analogue of acetazolamide resides in a less utilized binding pocket than most hydrophobic inhibitors

Bioorganic & medicinal chemistry letters, 2010-08, Vol.20 (15), p.4376-4381

2010

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Structural and Kinetic Effects on Changes in the CO2 Binding Pocket of Human Carbonic Anhydrase II

Biochemistry (Easton), 2012-11, Vol.51 (45), p.9156-9163

2012

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Characterization of Carbonic Anhydrase Isozyme Specific Inhibition by Sulfamated 2-Ethylestra Compounds

Letters in drug design & discovery, 2011-10, Vol.8 (8), p.678-684

2011

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The Escherichia coli Clamp Loader Can Actively Pry Open the β-Sliding Clamp

The Journal of biological chemistry, 2011-12, Vol.286 (49), p.42704-42714

2011

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Role of Trp19 and Tyr200 in catalysis by the γ-class carbonic anhydrase from Methanosarcina thermophila

Archives of biochemistry and biophysics, 2013-01, Vol.529 (1), p.11-17

2013

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High-resolution structure of human carbonic anhydrase II complexed with acetazolamide reveals insights into inhibitor drug design

Acta crystallographica. Section F, Structural biology and crystallization communications, 2009-10, Vol.65 (10), p.992-995

2009

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Structure of a monoclinic polymorph of human carbonic anhydrase II with a doubled a axis

Acta crystallographica. Section D, Biological crystallography., 2010-05, Vol.66 (5), p.628-634

2010

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Structure of the unbound form of HIV-1 subtype A protease: comparison with unbound forms of proteases from other HIV subtypes

Acta crystallographica. Section D, Biological crystallography., 2010-03, Vol.66 (3), p.233-242

2010

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The Contribution of Naturally Occurring Polymorphisms in Altering the Biochemical and Structural Characteristics of HIV-1 Subtype C Protease

Biochemistry (Easton), 2008-01, Vol.47 (2), p.731-743

2008

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Structure determination of the cancer-associated Mycoplasma hyorhinis protein Mh-p37

Acta crystallographica. Section D, Biological crystallography., 2008-11, Vol.64 (11), p.1172-1178

2008

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Crystallographic evidence for noncoplanar catalytic aspartic acids in plasmepsin II resides in the Protein Data Bank

Acta crystallographica. Section D, Biological crystallography., 2009-03, Vol.65 (3), p.294-296

2009

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Emerging from pseudo-symmetry: the redetermination of human carbonic anhydrase II in monoclinic P2(1) with a doubled a axis

Acta crystallographica. Section D, Biological crystallography., 2010-08, Vol.66 (Pt 8), p.950-952

2010

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Emerging from pseudo-symmetry: the redetermination of human carbonic anhydrase II in monoclinic P21 with a doubled a axis

Acta crystallographica. Section D, Biological crystallography., 2010-08, Vol.66 (8), p.950-952

2010

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High-resolution structure of unbound human immunodeficiency virus 1 subtype C protease: implications of flap dynamics and drug resistance

Acta crystallographica. Section D, Biological crystallography., 2008-07, Vol.64 (7), p.754-763

2008

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Structural and Kinetic Effects on Changes in the CO 2 Binding Pocket of Human Carbonic Anhydrase II

Biochemistry (Easton), 2012-11, Vol.51 (45), p.9156-9163

2012

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2.3 Å crystal structure of a drug resistant HIV C N88D/L90M protease complexed with Saquinavir

The FASEB journal, 2011-04, Vol.25, p.707.2-707.2

2011

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Discovery and SAR of Novel 2,3-Dihydroimidazo[1,2-c]quinazoline PI3K Inhibitors: Identification of Copanlisib (BAY 80-6946)

Enzymatic Characterization of Recombinant Food Vacuole Plasmepsin 4 from the Rodent Malaria Parasite Plasmodium berghei

Selective hydrophobic pocket binding observed within the carbonic anhydrase II active site accommodate different 4-substituted-ureido-benzenesulfonamides and correlate to inhibitor potency

Structure and catalysis by carbonic anhydrase II: Role of active-site tryptophan 5

Structural Insights into the Extracytoplasmic Thiamine-Binding Lipoprotein p37 of Mycoplasma hyorhinis

Anticonvulsant 4-Aminobenzenesulfonamide Derivatives with Branched-Alkylamide Moieties: X-ray Crystallography and Inhibition Studies of Human Carbonic Anhydrase Isoforms I, II, VII, and XIV

Sulfonamides incorporating 1,3,5-triazine moieties selectively and potently inhibit carbonic anhydrase transmembrane isoforms IX, XII and XIV over cytosolic isoforms I and II: Solution and X-ray crystallographic studies

Recombinant Plasmepsin 1 from the Human Malaria Parasite Plasmodium falciparum: Enzymatic Characterization, Active Site Inhibitor Design, and Structural Analysis

Coumarinyl-substituted sulfonamides strongly inhibit several human carbonic anhydrase isoforms: solution and crystallographic investigations

Carbonic anhydrase inhibitors. The X-ray crystal structure of human isoform II in adduct with an adamantyl analogue of acetazolamide resides in a less utilized binding pocket than most hydrophobic inhibitors

Structural and Kinetic Effects on Changes in the CO2 Binding Pocket of Human Carbonic Anhydrase II

Characterization of Carbonic Anhydrase Isozyme Specific Inhibition by Sulfamated 2-Ethylestra Compounds

The Escherichia coli Clamp Loader Can Actively Pry Open the β-Sliding Clamp

Role of Trp19 and Tyr200 in catalysis by the γ-class carbonic anhydrase from Methanosarcina thermophila

High-resolution structure of human carbonic anhydrase II complexed with acetazolamide reveals insights into inhibitor drug design

Structure of a monoclinic polymorph of human carbonic anhydrase II with a doubled a axis

Structure of the unbound form of HIV-1 subtype A protease: comparison with unbound forms of proteases from other HIV subtypes

The Contribution of Naturally Occurring Polymorphisms in Altering the Biochemical and Structural Characteristics of HIV-1 Subtype C Protease

Structure determination of the cancer-associated Mycoplasma hyorhinis protein Mh-p37

Crystallographic evidence for noncoplanar catalytic aspartic acids in plasmepsin II resides in the Protein Data Bank

Emerging from pseudo-symmetry: the redetermination of human carbonic anhydrase II in monoclinic P2(1) with a doubled a axis

Emerging from pseudo-symmetry: the redetermination of human carbonic anhydrase II in monoclinic P21 with a doubled a axis

High-resolution structure of unbound human immunodeficiency virus 1 subtype C protease: implications of flap dynamics and drug resistance

Structural and Kinetic Effects on Changes in the CO 2 Binding Pocket of Human Carbonic Anhydrase II

2.3 Å crystal structure of a drug resistant HIV C N88D/L90M protease complexed with Saquinavir

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