Skip to search form
Skip to main content
Skip to account menu
Semantic Scholar
Semantic Scholar's Logo
Search 218,268,568 papers from all fields of science
Search
Sign In
Create Free Account
styrylquinoline
National Institutes of Health
Create Alert
Alert
Related topics
Related topics
1 relation
Broader (1)
Quinolines
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2013
2013
A Fluorescent Styrylquinoline with Combined Therapeutic and Diagnostic Activities against Alzheimer's and Prion Diseases.
Matteo Staderini
,
Suzana Aulic
,
+10 authors
M. Bolognesi
ACS Medicinal Chemistry Letters
2013
Corpus ID: 32568310
(E)-6-Methyl-4'-amino-2-styrylquinoline (3) is a small molecule with the proper features to potentially diagnose, deliver therapy…
Expand
Review
2010
Review
2010
Chemistry and Structure-Activity Relationship of the Styrylquinoline-Type HIV Integrase Inhibitors
J. Mouscadet
,
D. Desmaële
Molecules
2010
Corpus ID: 12359538
In spite of significant progress in anti-HIV-1 therapy, current antiviral chemo-therapy still suffers from deleterious side…
Expand
Highly Cited
2005
Highly Cited
2005
New HIV-1 replication inhibitors of the styryquinoline class bearing aroyl/acyl groups at the C-7 position: synthesis and biological activity.
Marie Normand-Bayle
,
C. Bénard
,
+6 authors
J. D'angelo
Bioorganic & Medicinal Chemistry Letters
2005
Corpus ID: 37572776
Highly Cited
2004
Highly Cited
2004
Mechanism of HIV-1 integrase inhibition by styrylquinoline derivatives in vitro.
E. Deprez
,
S. Barbe
,
+6 authors
J. Mouscadet
Molecular Pharmacology
2004
Corpus ID: 29052691
Styrylquinoline derivatives (SQ) efficiently inhibit the 3'-processing activity of integrase (IN) with IC50 values of between 0.5…
Expand
Highly Cited
2004
Highly Cited
2004
Nuclear Import of HIV-1 Integrase Is Inhibited in Vitro by Styrylquinoline Derivatives
A. Mousnier
,
H. Leh
,
J. Mouscadet
,
C. Dargemont
Molecular Pharmacology
2004
Corpus ID: 2362568
Nuclear import of HIV-1 preintegration complexes (PICs) allows the virus to infect nondividing cells. Integrase (IN), the PIC…
Expand
2004
2004
Exploring binding mode for styrylquinoline HIV-1 integrase inhibitors using comparative molecular field analysis and docking studies.
Xiao-hui Ma
,
Xiaoyi Zhang
,
J. Tan
,
Wei-zu Chen
,
Cunxin Wang
Acta Pharmacologica Sinica
2004
Corpus ID: 13564272
AIM To understand pharmacophore properties of styrylquinoline derivatives and to design inhibitors of HIV-1 integrase. METHODS…
Expand
Highly Cited
2002
Highly Cited
2002
Use of the Kohonen neural network for rapid screening of ex vivo anti-HIV activity of styrylquinolines.
J. Polanski
,
F. Zouhiri
,
+6 authors
M. Le Bret
Journal of Medicinal Chemistry
2002
Corpus ID: 28777389
Using the Kohonen neural network, the electrostatic potentials on the molecular surfaces of 14 styrylquinoline derivatives were…
Expand
Highly Cited
2000
Highly Cited
2000
Structure-activity relationships and binding mode of styrylquinolines as potent inhibitors of HIV-1 integrase and replication of HIV-1 in cell culture.
F. Zouhiri
,
J. Mouscadet
,
+7 authors
J. D'angelo
Journal of Medicinal Chemistry
2000
Corpus ID: 46258318
Our prior studies showed that polyhydroxylated styrylquinolines are potent HIV-1 integrase (IN) inhibitors that block the…
Expand
Highly Cited
2000
Highly Cited
2000
Modeling of the inhibition of retroviral integrases by styrylquinoline derivatives.
M. Ouali
,
C. Laboulais
,
+8 authors
M. Le Bret
Journal of Medicinal Chemistry
2000
Corpus ID: 12279690
Styrylquinoline derivatives, known to be potent inhibitors of HIV-1 integrase, have been experimentally tested for their…
Expand
Highly Cited
1948
Highly Cited
1948
The fermentation of cellulose in vitro by organisms from the rumen of sheep.
H. Marston
Biochemical Journal
1948
Corpus ID: 13635179
The suggestion that micro-organisms are responsible for the decomposition of cellulose in the alimentary canal (Wildt, 1874…
Expand
By clicking accept or continuing to use the site, you agree to the terms outlined in our
Privacy Policy
(opens in a new tab)
,
Terms of Service
(opens in a new tab)
, and
Dataset License
(opens in a new tab)
ACCEPT & CONTINUE
or Only Accept Required