Preferential inhibition of the magnesium-dependent strand transfer reaction of HIV-1 integrase by alpha-hydroxytropolones.
about
Peptide HIV-1 integrase inhibitors from HIV-1 gene products.Peptidic HIV integrase inhibitors derived from HIV gene products: structure-activity relationship studies.HIV-1 IN inhibitors: 2010 update and perspectivesThe biology and synthesis of α-hydroxytropolones.Basic quinolinonyl diketo acid derivatives as inhibitors of HIV integrase and their activity against RNase H function of reverse transcriptase.3-Hydroxypyrimidine-2,4-diones as an inhibitor scaffold of HIV integraseHydroxylated tropolones inhibit hepatitis B virus replication by blocking viral ribonuclease H activity.Inhibition of the ANT(2")-Ia resistance enzyme and rescue of aminoglycoside antibiotic activity by synthetic α-hydroxytropolones.Synthesis and HIV-1 integrase inhibitory activity of spiroundecane(ene) derivativesAuthentic HIV-1 integrase inhibitors.Madurahydroxylactone derivatives as dual inhibitors of human immunodeficiency virus type 1 integrase and RNase H.An oxidopyrylium cyclization/ring-opening route to polysubstituted α-hydroxytropolonesSynthetic α-Hydroxytropolones Inhibit Replication of Wild-Type and Acyclovir-Resistant Herpes Simplex Viruses.Inhibition of Mg2+ binding and DNA religation by bacterial topoisomerase I via introduction of an additional positive charge into the active site region.Metabolism, excretion, and mass balance of the HIV-1 integrase inhibitor dolutegravir in humansA fresh look at natural tropolonoids.3-Hydroxypyrimidine-2,4-dione-5-N-benzylcarboxamides Potently Inhibit HIV-1 Integrase and RNase H.Diketoacid-genre HIV-1 integrase inhibitors containing enantiomeric arylamide functionality.Triflic acid-mediated rearrangements of 3-methoxy-8-oxabicyclo[3.2.1]octa-3,6-dien-2-ones: synthesis of methoxytropolones and furans.Active site and allosteric inhibitors of the ribonuclease H activity of HIV reverse transcriptase.Identification of spirocyclic or phosphate substituted quinolizine derivatives as novel HIV-1 integrase inhibitors: a patent evaluation of WO2016094197A1, WO2016094198A1 and WO2016154527A1.6-Cyclohexylmethyl-3-hydroxypyrimidine-2,4-dione as an inhibitor scaffold of HIV reverase transcriptase: Impacts of the 3-OH on inhibiting RNase H and polymerase.The exonuclease activity of HSV-1 UL12 is required for the production of viral DNA that can be packaged to produce infectious virus.A divalent metal ion-dependent N(1)-methyl transfer to G37-tRNA.TrmD: A Methyl Transferase for tRNA Methylation With m1G37.
P2860
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P2860
Preferential inhibition of the magnesium-dependent strand transfer reaction of HIV-1 integrase by alpha-hydroxytropolones.
description
2006 nî lūn-bûn
@nan
2006 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2006 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2006年の論文
@ja
2006年論文
@yue
2006年論文
@zh-hant
2006年論文
@zh-hk
2006年論文
@zh-mo
2006年論文
@zh-tw
2006年论文
@wuu
name
Preferential inhibition of the ...... se by alpha-hydroxytropolones.
@ast
Preferential inhibition of the ...... se by alpha-hydroxytropolones.
@en
type
label
Preferential inhibition of the ...... se by alpha-hydroxytropolones.
@ast
Preferential inhibition of the ...... se by alpha-hydroxytropolones.
@en
prefLabel
Preferential inhibition of the ...... se by alpha-hydroxytropolones.
@ast
Preferential inhibition of the ...... se by alpha-hydroxytropolones.
@en
P2093
P356
P1476
Preferential inhibition of the ...... se by alpha-hydroxytropolones.
@en
P2093
Allison A Johnson
Christophe Marchand
David A Davis
Elena A Semenova
Robert Yarchoan
P304
P356
10.1124/MOL.105.020321
P50
P577
2006-01-17T00:00:00Z