Substituted tetrahydroquinolines as potent allosteric inhibitors of reverse transcriptase and its key mutants
about
Exploiting protein flexibility to predict the location of allosteric sitesHalogen-enriched fragment libraries as chemical probes for harnessing halogen bonding in fragment-based lead discovery.Recent syntheses of 1,2,3,4-tetrahydroquinolines, 2,3-dihydro-4(1H)-quinolinones and 4(1H)-quinolinones using domino reactions.Conformational restriction: an effective tactic in 'follow-on'-based drug discovery.HIV Reverse Transcriptase Inhibitors
P2860
Substituted tetrahydroquinolines as potent allosteric inhibitors of reverse transcriptase and its key mutants
description
2009 nî lūn-bûn
@nan
2009 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
2009 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
2009年の論文
@ja
2009年論文
@yue
2009年論文
@zh-hant
2009年論文
@zh-hk
2009年論文
@zh-mo
2009年論文
@zh-tw
2009年论文
@wuu
name
Substituted tetrahydroquinolin ...... nscriptase and its key mutants
@ast
Substituted tetrahydroquinolin ...... nscriptase and its key mutants
@en
Substituted tetrahydroquinolin ...... nscriptase and its key mutants
@nl
type
label
Substituted tetrahydroquinolin ...... nscriptase and its key mutants
@ast
Substituted tetrahydroquinolin ...... nscriptase and its key mutants
@en
Substituted tetrahydroquinolin ...... nscriptase and its key mutants
@nl
prefLabel
Substituted tetrahydroquinolin ...... nscriptase and its key mutants
@ast
Substituted tetrahydroquinolin ...... nscriptase and its key mutants
@en
Substituted tetrahydroquinolin ...... nscriptase and its key mutants
@nl
P2093
P1476
Substituted tetrahydroquinolin ...... nscriptase and its key mutants
@en
P2093
Bang-Lin Wan
Carolyn Bahnck
Dai-Shi Su
Daniel J Distefano
Deanne Rudd
Elizabeth Tinney
Gregory Moyer
Jessica A Flynn
Joe P Vacca
John J Lim
P304
P356
10.1016/J.BMCL.2009.07.031
P407
P577
2009-09-01T00:00:00Z