Fragment-based approaches to anti-HIV drug discovery: state of the art and future opportunities.

about

Novel diaryltriazines with a picolinonitrile moiety as potent HIV-1 RT inhibitors: a patent evaluation of WO2016059647(A2).

P2860

Q40447961-8E5743A0-F0F4-4369-AB0A-80250EE8419A

P2860

Fragment-based approaches to anti-HIV drug discovery: state of the art and future opportunities.

Item

http://www.wikidata.org/entity/Q38587368

description

2015 nî lūn-bûn

@nan

2015年の論文

@ja

2015年論文

@yue

2015年論文

@zh-hant

2015年論文

@zh-hk

2015年論文

@zh-mo

2015年論文

@zh-tw

2015年论文

@wuu

2015年论文

@zh

2015年论文

@zh-cn

name

Fragment-based approaches to a ...... art and future opportunities.

@en

type

Item

label

Fragment-based approaches to a ...... art and future opportunities.

@en

prefLabel

Fragment-based approaches to a ...... art and future opportunities.

@en

P1476

Fragment-based approaches to a ...... art and future opportunities.

@en

P2093

Boshi Huang

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

Dongwei Kang

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

Peng Zhan

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

P2860

Fragment screening and HIV therapeutics

Novel indazole non-nucleoside reverse transcriptase inhibitors using molecular hybridization based on crystallographic overlays

Structural basis for a new mechanism of inhibition of HIV-1 integrase identified by fragment screening and structure-based design

Small Molecule Inhibitors of the LEDGF Site of Human Immunodeficiency Virus Integrase Identified by Fragment Screening and Structure Based Design

Detecting Allosteric Sites of HIV-1 Reverse Transcriptase by X-ray Crystallographic Fragment Screening

Small Molecule Regulation of Protein Conformation by Binding in the Flap of HIV Protease

Crystallographic Fragment-Based Drug Discovery: Use of a Brominated Fragment Library Targeting HIV Protease

Identification of fragments targeting an alternative pocket on HIV-1 gp41 by NMR screening and similarity searching.

Rapid diversity-oriented synthesis in microtiter plates for in situ screening of HIV protease inhibitors.

A quick diversity-oriented amide-forming reaction to optimize P-subsite residues of HIV protease inhibitors.

P304

1271-1281

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

P31

scholarly article

P356

10.1517/17460441.2015.1083007

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

P407

English

P433

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

P478

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

P50

Xinyong Liu

P577

2015-09-15T00:00:00Z

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

P5875

281823466

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

P698

26372893

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

Fragment-based approaches to anti-HIV drug discovery: state of the art and future opportunities.

about

P2860

P2860

Fragment-based approaches to anti-HIV drug discovery: state of the art and future opportunities.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P50

P577

P5875

P698

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P50

P577

P5875

P698