Hepatitis C Virus NS3/4A Protease Inhibitors Incorporating Flexible P2 Quinoxalines Target Drug Resistant Viral Variants.

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Hepatitis C Virus NS3/4A Protease Inhibitors Incorporating Flexible P2 Quinoxalines Target Drug Resistant Viral Variants.

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2017 nî lūn-bûn

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2017年の論文

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2017年論文

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2017年論文

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2017年論文

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2017年論文

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name

Hepatitis C Virus NS3/4A Prote ...... Drug Resistant Viral Variants.

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label

Hepatitis C Virus NS3/4A Prote ...... Drug Resistant Viral Variants.

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prefLabel

Hepatitis C Virus NS3/4A Prote ...... Drug Resistant Viral Variants.

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P1476

Hepatitis C Virus NS3/4A Prote ...... Drug Resistant Viral Variants

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P2093

Alicia Newton

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Ashley N Matthew

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Caitlin J Hill

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Christos J Petropoulos

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Jacqueto Zephyr

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Muhammad Jahangir

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Nese Kurt-Yilmaz

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Wei Huang

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P2860

PHENIX: a comprehensive Python-based system for macromolecular structure solution

MolProbity: all-atom contacts and structure validation for proteins and nucleic acids

Processing of X-ray diffraction data collected in oscillation mode

Global epidemiology and genotype distribution of the hepatitis C virus infection

Drug resistance against HCV NS3/4A inhibitors is defined by the balance of substrate recognition versus inhibitor binding

The Molecular Basis of Drug Resistance against Hepatitis C Virus NS3/4A Protease Inhibitors

Molecular Mechanism by Which a Potent Hepatitis C Virus NS3-NS4A Protease Inhibitor Overcomes Emergence of Resistance

Ligand bioactive conformation plays a critical role in the design of drugs that target the hepatitis C virus NS3 protease

Structural and Thermodynamic Effects of Macrocyclization in HCV NS3/4A Inhibitor MK-5172

Coot: model-building tools for molecular graphics

P304

5699-5716

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P31

scholarly article

P356

10.1021/ACS.JMEDCHEM.7B00426

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P407

English

P433

http://www.w3.org/2001/XMLSchema#string

P478

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P50

Celia A Schiffer

Akbar Ali

P577

2017-06-19T00:00:00Z

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P698

28594175

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P932

5748155

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