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Quinolines, antirheumatic drugs
Known as:
Quinolines
National Institutes of Health
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Quinolines
Papers overview
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Highly Cited
2014
Highly Cited
2014
Modular o-Quinone Catalyst System for Dehydrogenation of Tetrahydroquinolines under Ambient Conditions
Alison E. Wendlandt
,
S. Stahl
Journal of the American Chemical Society
2014
Corpus ID: 38049968
Quinolines are common pharmacophores present in numerous FDA-approved pharmaceuticals and other bioactive compounds. Here, we…
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Highly Cited
2011
Highly Cited
2011
Iridium-catalyzed hydrogenation of N-heterocyclic compounds under mild conditions by an outer-sphere pathway.
Graham E. Dobereiner
,
A. Nova
,
+4 authors
R. Crabtree
Journal of the American Chemical Society
2011
Corpus ID: 31830748
A new homogeneous iridium catalyst gives hydrogenation of quinolines under unprecedentedly mild conditions-as low as 1 atm of H(2…
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Highly Cited
2006
Highly Cited
2006
Asymmetric hydrogenation of quinolines and isoquinolines activated by chloroformates.
Shenglin Lu
,
You-Qing Wang
,
Xiuwen Han
,
Yong‐Gui Zhou
Angewandte Chemie
2006
Corpus ID: 30379584
Despite significant progress in the area of asymmetric hydrogenation, the enantioselective hydrogenation of aromatic and…
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Highly Cited
2004
Highly Cited
2004
Entrapment and release of quinoline derivatives using a hydrogel of a low molecular weight gelator.
A. Friggeri
,
B. Feringa
,
J. V. van Esch
Journal of Controlled Release
2004
Corpus ID: 18644349
Highly Cited
2002
Highly Cited
2002
Discovery of novel targets of quinoline drugs in the human purine binding proteome.
P. Graves
,
J. Kwiek
,
+5 authors
T. Haystead
Molecular Pharmacology
2002
Corpus ID: 2703196
The quinolines have been used in the treatment of malaria, arthritis, and lupus for many years, yet the precise mechanism of…
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Highly Cited
2000
Highly Cited
2000
Antiplasmodial activity of Cryptolepis sanguinolenta alkaloids from leaves and roots.
A. Paulo
,
E. Gomes
,
J. Steele
,
D. C. Warhurst
,
P. Houghton
Planta Medica
2000
Corpus ID: 36893765
The roots of Cryptolepis sanguinolenta have been investigated for their chemical composition since 1931 but so far no studies on…
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Highly Cited
1998
Highly Cited
1998
A Common Mechanism for Blockade of Heme Polymerization by Antimalarial Quinolines*
D. J. Sullivan
,
H. Matile
,
R. Ridley
,
D. Goldberg
Journal of Biological Chemistry
1998
Corpus ID: 3477241
The antimalarial quinolines are believed to work by blocking the polymerization of toxic heme released during hemoglobin…
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Highly Cited
1996
Highly Cited
1996
In vivo efficacy of oral and intralesional administration of 2-substituted quinolines in experimental treatment of new world cutaneous leishmaniasis caused by Leishmania amazonensis
A. Fournet
,
M. Ferreira
,
+5 authors
R. Hocquemiller
Antimicrobial Agents and Chemotherapy
1996
Corpus ID: 7218148
The antileishmanial efficacies of 2-n-propylquinoline, chimanines B and D, 2-n-pentylquinoline, 2-phenylquinoline, 2-(3,4…
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Highly Cited
1995
Highly Cited
1995
Interactions of atovaquone with other antimalarial drugs against Plasmodium falciparum in vitro.
C. Canfield
,
M. Pudney
,
W. Gutteridge
Experimental parasitology
1995
Corpus ID: 37189247
A series of Plasmodium falciparum in vitro drug sensitivity studies were conducted in order to evaluate atovaquone in combination…
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Highly Cited
1988
Highly Cited
1988
Physical-chemical properties shared by compounds that modulate multidrug resistance in human leukemic cells.
J. Zamora
,
H. Pearce
,
W. T. Beck
Molecular Pharmacology
1988
Corpus ID: 23614241
Multidrug resistance (MDR), typified by resistance to Vinca alkaloids and anthracyclines, is a well characterized experimental…
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