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Antiviral lectins from red and blue-green algae show potent in vitro and in vivo activity against hepatitis C virus

PloS one, 2013-05, Vol.8 (5), p.e64449

2013

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Broad-Spectrum In Vitro Activity and In Vivo Efficacy of the Antiviral Protein Griffithsin against Emerging Viruses of the Family Coronaviridae

Journal of Virology, 2010-03, Vol.84 (5), p.2511-2521

2010

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Identification of an Inhibitor of the EWS-FLI1 Oncogenic Transcription Factor by High-Throughput Screening

JNCI : Journal of the National Cancer Institute, 2011-06, Vol.103 (12), p.962-978

2011

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Scaleable manufacture of HIV-1 entry inhibitor griffithsin and validation of its safety and efficacy as a topical microbicide component

Proceedings of the National Academy of Sciences - PNAS, 2009-04, Vol.106 (15), p.6099-6104

2009

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Isolation and Characterization of Griffithsin, a Novel HIV-inactivating Protein, from the Red Alga Griffithsia sp.

The Journal of biological chemistry, 2005-03, Vol.280 (10), p.9345-9353

2005

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The cyanobacterial lectin scytovirin displays potent in vitro and in vivo activity against Zaire Ebola virus

Antiviral research, 2014-12, Vol.112, p.1-7

2014

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Stellettapeptins A and B, HIV-inhibitory cyclic depsipeptides from the marine sponge Stelletta sp

Tetrahedron letters, 2015-07, Vol.56 (28), p.4215-4219

2015

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Monomerization of Viral Entry Inhibitor Griffithsin Elucidates the Relationship between Multivalent Binding to Carbohydrates and anti-HIV Activity

Structure (London), 2010-09, Vol.18 (9), p.1104-1115

2010

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Isobutylhydroxyamides from the Pericarp of Nepalese Zanthoxylum armatum Inhibit NF1-Defective Tumor Cell Line Growth

Journal of natural products (Washington, D.C.), 2013-01, Vol.76 (1), p.59-63

2013

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Isolation, Structural Elucidation, and Absolute Stereochemistry of Enigmazole A, a Cytotoxic Phosphomacrolide from the Papua New Guinea Marine Sponge Cinachyrella enigmatica

Journal of the American Chemical Society, 2010-08, Vol.132 (30), p.10278-10285

2010

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Erioflorin stabilizes the tumor suppressor Pdcd4 by inhibiting its interaction with the E3-ligase β-TrCP1

PloS one, 2012-10, Vol.7 (10), p.e46567

2012

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Engineering soya bean seeds as a scalable platform to produce cyanovirin‐N, a non‐ARV microbicide against HIV

Plant biotechnology journal, 2015-09, Vol.13 (7), p.884-892

2015

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Domain-Swapped Structure of the Potent Antiviral Protein Griffithsin and Its Mode of Carbohydrate Binding

Structure (London), 2006-07, Vol.14 (7), p.1127-1135

2006

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Binding of the Mannose-Specific Lectin, Griffithsin, to HIV-1 gp120 Exposes the CD4-Binding Site

Journal of Virology, 2011-09, Vol.85 (17), p.9039-9050

2011

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Growth Inhibition of Human Colon Carcinoma Cells by Sesquiterpenoids and Tetralones of Zygogynum calothyrsum

Journal of natural products (Washington, D.C.), 2013-04, Vol.76 (4), p.710-714

2013

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Lack of a Functional VHL Gene Product Sensitizes Renal Cell Carcinoma Cells to the Apoptotic Effects of the Protein Synthesis Inhibitor Verrucarin A

Neoplasia (New York, N.Y.), 2012-08, Vol.14 (8), p.771-IN28

2012

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T7 lytic phage-displayed peptide libraries exhibit less sequence bias than M13 filamentous phage-displayed peptide libraries

Proteomics (Weinheim), 2006-08, Vol.6 (15), p.4210-4222

2006

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Tricyclic guanidine alkaloids from the marine sponge Acanthella cavernosa that stabilize the tumor suppressor PDCD4

Marine drugs, 2014-08, Vol.12 (8), p.4593-4601

2014

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New inhibitors of ABCG2 identified by high-throughput screening

Molecular cancer therapeutics, 2007-12, Vol.6 (12), p.3271-3278

2007

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Synthesis and Biological Evaluation of New Madecassic Acid Derivatives Targeting ERK Cascade Signaling

Frontiers in chemistry, 2018-09, Vol.6, p.434-434

2018

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Inhibition of ABCG2-mediated drug efflux by naphthopyrones from marine crinoids

Bioorganic & medicinal chemistry letters, 2010-07, Vol.20 (13), p.3848-3850

2010

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Neamphamide A, a New HIV-Inhibitory Depsipeptide from the Papua New Guinea Marine Sponge Neamphius huxleyi

Journal of natural products (Washington, D.C.), 2004-08, Vol.67 (8), p.1407-1411

2004

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A high-throughput cell-based assay for inhibitors of ABCG2 activity

Journal of biomolecular screening, 2006-03, Vol.11 (2), p.176-183

2006

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Crystallographic, thermodynamic, and molecular modeling studies of the mode of binding of oligosaccharides to the potent antiviral protein griffithsin

Proteins, structure, function, and bioinformatics, 2007-05, Vol.67 (3), p.661-670

2007

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Unequivocal determination of caulamidines A and B: application and validation of new tools in the structure elucidation tool box

Chemical science (Cambridge), 2018-01, Vol.9 (2), p.307-314

2018

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Antiviral lectins from red and blue-green algae show potent in vitro and in vivo activity against hepatitis C virus

Broad-Spectrum In Vitro Activity and In Vivo Efficacy of the Antiviral Protein Griffithsin against Emerging Viruses of the Family Coronaviridae

Identification of an Inhibitor of the EWS-FLI1 Oncogenic Transcription Factor by High-Throughput Screening

Scaleable manufacture of HIV-1 entry inhibitor griffithsin and validation of its safety and efficacy as a topical microbicide component

Isolation and Characterization of Griffithsin, a Novel HIV-inactivating Protein, from the Red Alga Griffithsia sp.

The cyanobacterial lectin scytovirin displays potent in vitro and in vivo activity against Zaire Ebola virus

Stellettapeptins A and B, HIV-inhibitory cyclic depsipeptides from the marine sponge Stelletta sp

Monomerization of Viral Entry Inhibitor Griffithsin Elucidates the Relationship between Multivalent Binding to Carbohydrates and anti-HIV Activity

Isobutylhydroxyamides from the Pericarp of Nepalese Zanthoxylum armatum Inhibit NF1-Defective Tumor Cell Line Growth

Isolation, Structural Elucidation, and Absolute Stereochemistry of Enigmazole A, a Cytotoxic Phosphomacrolide from the Papua New Guinea Marine Sponge Cinachyrella enigmatica

Erioflorin stabilizes the tumor suppressor Pdcd4 by inhibiting its interaction with the E3-ligase β-TrCP1

Engineering soya bean seeds as a scalable platform to produce cyanovirin‐N, a non‐ARV microbicide against HIV

Domain-Swapped Structure of the Potent Antiviral Protein Griffithsin and Its Mode of Carbohydrate Binding

Binding of the Mannose-Specific Lectin, Griffithsin, to HIV-1 gp120 Exposes the CD4-Binding Site

Growth Inhibition of Human Colon Carcinoma Cells by Sesquiterpenoids and Tetralones of Zygogynum calothyrsum

Lack of a Functional VHL Gene Product Sensitizes Renal Cell Carcinoma Cells to the Apoptotic Effects of the Protein Synthesis Inhibitor Verrucarin A

T7 lytic phage-displayed peptide libraries exhibit less sequence bias than M13 filamentous phage-displayed peptide libraries

Tricyclic guanidine alkaloids from the marine sponge Acanthella cavernosa that stabilize the tumor suppressor PDCD4

New inhibitors of ABCG2 identified by high-throughput screening

Synthesis and Biological Evaluation of New Madecassic Acid Derivatives Targeting ERK Cascade Signaling

Inhibition of ABCG2-mediated drug efflux by naphthopyrones from marine crinoids

Neamphamide A, a New HIV-Inhibitory Depsipeptide from the Papua New Guinea Marine Sponge Neamphius huxleyi

A high-throughput cell-based assay for inhibitors of ABCG2 activity

Crystallographic, thermodynamic, and molecular modeling studies of the mode of binding of oligosaccharides to the potent antiviral protein griffithsin

Unequivocal determination of caulamidines A and B: application and validation of new tools in the structure elucidation tool box

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