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19 articles for thisTarget


The following articles (labelled with PubMed ID or TBD) are for your review

PMID
Data
Article Title
Organization
Control of hepatitis C: a medicinal chemistry perspective.EBI
University of Wollongong
SAR and pharmacokinetic studies on phenethylamide inhibitors of the hepatitis C virus NS3/NS4A serine protease.EBI
Merck Research Laboratories
Peptide-based inhibitors of the hepatitis C virus serine protease.EBI
Boehringer Ingelheim (Canada)
Inhibitors of hepatitis C virus NS3.4A protease. Part 3: P2 proline variants.EBI
Vertex Pharmaceuticals
Inhibitors of hepatitis C virus NS3.4A protease 2. Warhead SAR and optimization.EBI
Vertex Pharmaceuticals
Discovery of Quinoxaline-Based P1-P3 Macrocyclic NS3/4A Protease Inhibitors with Potent Activity against Drug-Resistant Hepatitis C Virus Variants.EBI
University of Massachusetts Medical School
Inhibitors of hepatitis C virus NS3.4A protease 1. Non-charged tetrapeptide variants.EBI
Vertex Pharmaceuticals
Phenethyl amides as novel noncovalent inhibitors of hepatitis C virus NS3/4A protease: discovery, initial SAR, and molecular modeling.EBI
Mrl Rome
Design and synthesis of ethyl pyrrolidine-5,5-trans-lactams as inhibitors of hepatitis C virus NS3/4A protease.EBI
Glaxosmithkline
Capped dipeptide alpha-ketoacid inhibitors of the HCV NS3 protease.EBI
Irbm, Mrl Rome
Highly potent non-peptidic inhibitors of the HCV NS3/NS4A serine protease.EBI
Celera
Evolution, synthesis and SAR of tripeptide alpha-ketoacid inhibitors of the hepatitis C virus NS3/NS4A serine protease.EBI
Irbm, Mrl Rome
A designed P1 cysteine mimetic for covalent and non-covalent inhibitors of HCV NS3 protease.EBI
Irbm, Mrl Rome
The identification of alpha-ketoamides as potent inhibitors of hepatitis C virus NS3-4A proteinase.EBI
Roche Discover Welwyn
Studies on the C-terminal of hexapeptide inhibitors of the hepatitis C virus serine protease.EBI
Boehringer Ingelheim (Canada)
A review on HCV inhibitors: Significance of non-structural polyproteins.EBI
Institute of Pharmaceutical Education and Research
P3-P4 ureas and reverse carbamates as potent HCV NS3 protease inhibitors: Effective transposition of the P4 hydrogen bond donor.EBI
Bristol-Myers Squibb Research and Development
Quinoxaline-Based Linear HCV NS3/4A Protease Inhibitors Exhibit Potent Activity against Drug Resistant Variants.EBI
University of Massachusetts Medical School
Potent Inhibitors of Hepatitis C Virus NS3 Protease: Employment of a Difluoromethyl Group as a Hydrogen-Bond Donor.EBI
Bristol-Myers Squibb