Evidence map›Paper›PMID 25301950›Full record

ArticleThe Journal of biological chemistry2014

Mechanism of inhibition for BMS-791325, a novel non-nucleoside inhibitor of hepatitis C virus NS5B polymerase.

Karen L Rigat, Hao Lu, Ying-Kai Wang, Argyrides Argyrou, Caroline Fanslau, Brett Beno, Yi Wang, Jovita Marcinkeviciene, Min Ding, Robert G Gentles and 3 more

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
2.0field-weighted citation impact, top 13% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors at 4 institutions in 4 countries.

Karen L RigatFrom the Departments of Virology.
Hao Luthe Department of Mechanistic Biochemistry, Research and Development, Bristol Myers Squibb Co., Pennington, New Jersey 08534.
Ying-Kai WangFrom the Departments of Virology.
Argyrides Argyrouthe Department of Mechanistic Biochemistry, Research and Development, Bristol Myers Squibb Co., Pennington, New Jersey 08534.
Caroline Fanslauthe Department of Mechanistic Biochemistry, Research and Development, Bristol Myers Squibb Co., Pennington, New Jersey 08534.
Brett BenoComputer Assisted Drug Design, and.
Yi WangFrom the Departments of Virology.
Jovita Marcinkevicienethe Department of Mechanistic Biochemistry, Research and Development, Bristol Myers Squibb Co., Pennington, New Jersey 08534.
Min DingEarly Discovery Chemistry, Research and Development, Bristol Myers Squibb Co., Wallingford, Connecticut 06492 and.
Robert G GentlesEarly Discovery Chemistry, Research and Development, Bristol Myers Squibb Co., Wallingford, Connecticut 06492 and.
Min GaoFrom the Departments of Virology.
Lynn M Abellthe Department of Mechanistic Biochemistry, Research and Development, Bristol Myers Squibb Co., Pennington, New Jersey 08534.
Susan B RobertsFrom the Departments of Virology, susan.roberts@bms.com.
Bristol-Myers Squibb (Germany) · DEBristol-Myers Squibb (United States) · USDepartment of Virology · FRFeed Control (Norway) · NO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

HCV infection is an urgent global health problem that has triggered a drive to discover therapies that specifically target the virus. BMS-791325 is a novel direct antiviral agent specifically targeting HCV NS5B, an RNA-dependent RNA polymerase. Robust viral clearance of HCV was observed in infected patients treated with BMS-791325 in combination with other anti-HCV agents in Phase 2 clinical studies. Biochemical and biophysical studies revealed that BMS-791325 is a time-dependent, non-competitive inhibitor of the polymerase. Binding studies with NS5B genetic variants (WT, L30S, and P495L) exposed a two-step, slow binding mechanism, but details of the binding mechanism differed for each of the polymerase variants. For the clinically relevant resistance variant (P495L), the rate of initial complex formation and dissociation is similar to WT, but the kinetics of the second step is significantly faster, showing that this variant impacts the final tight complex. The resulting shortened residence time translates into the observed decrease in inhibitor potency. The L30S variant has a significantly different profile. The rate of initial complex formation and dissociation is 7-10 times faster for the L30S variant compared with WT; however, the forward and reverse rates to form the final complex are not significantly different. The impact of the L30S variant on the inhibition profile and binding kinetics of BMS-791325 provides experimental evidence for the dynamic interaction of fingers and thumb domains in an environment that supports the formation of active replication complexes and the initiation of RNA synthesis.

Indexed as

Amino Acid SubstitutionAntiviral AgentsBenzazepinesHepacivirusHepatitis CHumansIndolesMutation, MissenseProtein BindingRNA-Dependent RNA PolymeraseRNA, ViralViral Nonstructural Proteins8-cyclohexyl-N-((dimethylamino)sulfonyl)-1,1a,2,12b-tetrahydro-11-methoxy-1a-((3-methyl-3,8-diazabicyclo(3.2.1)oct-8-yl)carbonyl)cycloprop(d)indolo(2,1-a)(2)benzazepine-5-carboxamideAntiviral AgentsBenzazepinesIndolesNS-5 protein, hepatitis C virusRNA-Dependent RNA PolymeraseRNA, ViralViral Nonstructural ProteinsBMS-791325Drug DiscoveryHepatitis C Virus (HCV)Inhibition MechanismKineticsProtein-Drug InteractionRNA-dependent RNA Polymerase (NS5B)Viral Replication

Identifiers

PMID25301950
PMCPMC4246100
OpenAlexW2044903920

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.