Strategies in the Design of Antiviral Drugs - Wikidata - awgldk - TriplyDB

Strategies in the Design of Antiviral Drugs

Strategies in the Design of Antiviral Drugs

http://www.wikidata.org/entity/Q56786281

about

Strategies in the Design of Antiviral Drugs

http://www.wikidata.org/entity/Q56786281

description

наукова стаття, опублікована в березні 2010

@uk

name

Strategies in the Design of Antiviral Drugs

@en

type

label

Strategies in the Design of Antiviral Drugs

@en

prefLabel

Strategies in the Design of Antiviral Drugs

@en

P1476

Q56786281-5C8BE10F-AD8F-4E2B-A095-E935C6458E9E

P2093

Q56786281-67223038-C3EF-4F60-A063-4FF6DA97924E

P2860

Q56786281-03A5E64A-C6D9-4659-8A3B-C790FE3794D9

Q56786281-07A0250B-D9BF-4F1F-9887-45A7C5E85FD6

Q56786281-0BFBD61C-2802-4AB6-9806-602FF8681A7B

Q56786281-0C8F7D03-A13B-4967-86F6-0C3D43DFBF7A

Q56786281-107F09AF-3994-42D9-A125-C589EB2F659C

Q56786281-13661296-FFB8-498A-A1EC-8E29DBC0F246

Q56786281-180B26A5-1802-42D7-807A-C176F5A991B5

Q56786281-189B1E5A-9D15-459F-80F6-A74A7ED8213B

Q56786281-18DB40AF-F6F6-4C93-97D3-2EB9A7027A5B

Q56786281-1C56C664-E293-4754-84D8-73DB488412BF

P31

Q56786281-72BA0124-D974-473D-BE97-C19C99E7D945

P356

Q56786281-A047A689-07D8-4386-8135-8515F10D609F

P50

Q56786281-FACF5AF1-1ABA-4C3B-A05F-F5947BCF013D

P577

Q56786281-53C699C0-5A14-49E9-807E-74D8B1BB3BD9

P356

9780470571224.PSE026

P1476

Strategies in the Design of Antiviral Drugs

@en

P2093

Piet Herdewijn

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

P2860

RNA virus error catastrophe: direct molecular test by using ribavirin

Structure-assisted design of mechanism-based irreversible inhibitors of human rhinovirus 3C protease with potent antiviral activity against multiple rhinovirus serotypes

Inhibiting HIV-1 entry: discovery of D-peptide inhibitors that target the gp41 coiled-coil pocket

Binding of the second generation non-nucleoside inhibitor S-1153 to HIV-1 reverse transcriptase involves extensive main chain hydrogen bonding

Crystal structure of rhodopsin: A G protein-coupled receptor

Structure and mechanism of inosine monophosphate dehydrogenase in complex with the immunosuppressant mycophenolic acid

Improved cyclic urea inhibitors of the HIV-1 protease: synthesis, potency, resistance profile, human pharmacokinetics and X-ray crystal structure of DMP 450

Hepatitis C virus NS3 RNA helicase domain with a bound oligonucleotide: the crystal structure provides insights into the mode of unwinding

Exploring the active site of herpes simplex virus type-1 thymidine kinase by X-ray crystallography of complexes with aciclovir and other ligands

A novel role for 3-O-sulfated heparan sulfate in herpes simplex virus 1 entry

P31

scholarly article

P356

10.1002/9780470571224.PSE026

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

P50

P577

2010-03-15T00:00:00Z

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