Yongnian Sun

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Maturation Inhibitor with Improved Potency, Anti-viral Spectrum and Gag Polymorphic

N. Meanwell, Zeyu Lin, M. Krystal, 2016 .

Identification and Characterization of BMS-955176, a Second-Generation HIV-1 Maturation Inhibitor with Improved Potency, Antiviral Spectrum, and Gag Polymorphic Coverage

N. Meanwell, Zeyu Lin, M. Krystal, 2016, Antimicrobial Agents and Chemotherapy.

Increased sensitivity of HIV variants selected by attachment inhibitors to broadly neutralizing antibodies.

L. Alexander, M. Krystal, R. Colonno, 2010, Virology.

Inhibitors of human immunodeficiency virus type 1 (HIV-1) attachment. 12. Structure-activity relationships associated with 4-fluoro-6-azaindole derivatives leading to the identification of 1-(4-benzoylpiperazin-1-yl)-2-(4-fluoro-7-[1,2,3]triazol-1-yl-1h-pyrrolo[2,3-c]pyridin-3-yl)ethane-1,2-dione (B

N. Meanwell, D. Langley, R. Colonno, 2013, Journal of medicinal chemistry.

Hepatitis C Virus (HCV) NS5B Nonnucleoside Inhibitors Specifically Block Single-Stranded Viral RNA Synthesis Catalyzed by HCV Replication Complexes In Vitro

Wen-gang Yang, M. Deshpande, A. Phadke, 2006, Antimicrobial Agents and Chemotherapy.

Pharmacodynamics‐based approach for efficacious human dose projection of BMS‐986260, a small molecule transforming growth factor beta receptor 1 inhibitor

Y. Shu, R. Borzilleri, M. Cvijic, 2020, Biopharmaceutics & drug disposition.

Activity of the HIV-1 Attachment Inhibitor BMS-626529, the Active Component of the Prodrug BMS-663068, against CD4-Independent Viruses and HIV-1 Envelopes Resistant to Other Entry Inhibitors

M. Krystal, N. Ray, G. Hanna, 2013, Antimicrobial Agents and Chemotherapy.

InhibitorsResistant to Other Entry CD4-Independent Viruses and HIV-1 Prodrug BMS-663068, against BMS-626529, the Active Component of the Activity of the HIV-1 Attachment Inhibitor

N. Ray, G. Hanna, M. Lataillade, 2013 .

Discovery and Characterization of a Novel CD4-Binding Adnectin with Potent Anti-HIV Activity

D. Fabrizio, M. Krystal, M. Cockett, 2017, Antimicrobial Agents and Chemotherapy.

Distinct Biology of Kaposi’s Sarcoma-Associated Herpesvirus from Primary Lesions and Body Cavity Lymphomas

G. Nabel, W. Kong, B. Nickoloff, 1998, Journal of Virology.

Pyrazolo-Piperidines Exhibit Dual Inhibition of CCR5/CXCR4 HIV Entry and Reverse Transcriptase.

J. Snyder, V. Bond, D. Liotta, 2015, ACS medicinal chemistry letters.

Antiviral inhibition of the HIV-1 capsid protein.

Eric Barklis, Chun Tang, M. Summers, 2003, Journal of molecular biology.

Regulation of β-catenin transformation by the p300 transcriptional coactivator

E. Fearon, G. Nabel, F. Kolligs, 2000 .

The assembly of Ebola virus nucleocapsid requires virion-associated proteins 35 and 24 and posttranslational modification of nucleoprotein.

G. Nabel, Ling Xu, Yue Huang, 2002, Molecular cell.

International Congress of Drug Therapy in HIV Infection 23-26 October 2016, Glasgow, UK

Raúl Tabarés Gutiérrez, Samit R. Joshi, H. Jessen, 2016, Journal of the International AIDS Society.

GSK3732394: a Multi-specific Inhibitor of HIV Entry

D. Langley, P. Nef, M. Krystal, 2019, Journal of Virology.

A Novel gp41-Binding Adnectin with Potent Anti-HIV Activity Is Highly Synergistic when Linked to a CD4-Binding Adnectin

D. Fabrizio, M. Krystal, M. Cockett, 2018, Journal of Virology.

The N17 region of gp41 in HIV-1 is the most conserved region in gp160. mRNA selection

D. Fabrizio, M. Krystal, M. Cockett, 2018 .

Resistance Mutations (NRTI) BMS-986001 against Known NRTI Nucleoside Reverse Transcriptase Inhibitor Cross-Resistance Profile of In Vitro

M. Krystal, G. Hanna, Tricia L. Protack, 2014 .

In Vitro Cross-Resistance Profile of Nucleoside Reverse Transcriptase Inhibitor (NRTI) BMS-986001 against Known NRTI Resistance Mutations

M. Krystal, G. Hanna, Tricia L. Protack, 2013, Antimicrobial Agents and Chemotherapy.

Comprehensive characterization and optimization of Caco-2 cells enabled the development of a miniaturized 96-well permeability assay

Shivani Patel, W. Shou, H. Weller, 2022, Xenobiotica; the fate of foreign compounds in biological systems.

On Ternary Complex Stability in Protein Degradation: In Silico Molecular Glue Binding Affinity Calculations

Dahlia R. Weiss, A. Bortolato, V. Shanmugasundaram, 2023, J. Chem. Inf. Model..

ACH-806, an NS4A Antagonist, Inhibits Hepatitis C Virus Replication by Altering the Composition of Viral Replication Complexes

A. Agarwal, Wen-gang Yang, M. Deshpande, 2013, Antimicrobial Agents and Chemotherapy.

Regulation of the proinflammatory effects of Fas ligand (CD95L).

G. Nabel, Y. Sun, Yongnian Sun, 1998, Science.

Active domains of human papillomavirus type 11 E1 protein for origin replication.

D. McCance, Y. Sun, Yongnian Sun, 1998, The Journal of general virology.

[583] ACH-806: A POTENT INHIBITOR OF HCV REPLICATION WITH A NOVEL MECHANISM OF ACTION

Amy Sanchez, Xingtie Nie, M. Deshpande, 2007 .