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quinapyramine

Known as: 4-amino-6-((2-amino-1,6-dimethyl-4-pyrimidinyl)amino)-1-methylquinaldinium ion 
 
National Institutes of Health

Papers overview

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2016
2016
We synthesized quinapyramine sulfate loaded-sodium alginate nanoparticles (QS-NPs) to reduce undesirable toxic effects of QS… Expand
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2013
2013
Trypanosoma evansi infection typically produces wasting disease, but it can also develop into a neurological or… Expand
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Review
2010
Review
2010
In the present article, we summarize our studies of antrycide-resistance of Trypanosoma brucei evansi in four aspects in the last… Expand
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Highly Cited
1999
Highly Cited
1999
The drug sensitivities of 16 Trypanosoma evansi isolates from Sudan were examined using two different in vitro assays and rodent… Expand
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1993
1993
Over a period of 208 days a quinapyramine-resistant population was derived in vivo from a quinapyramine-susceptible clone of… Expand
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Highly Cited
1991
Highly Cited
1991
The sensitivity of three Trypanosoma equiperdum clones and thirteen Trypanosoma evansi clones originating from the People's… Expand
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1989
1989
A Trypanosoma brucei brucei stock resistant to diminazene aceturate, isometamidium chloride, quinapyramine sulfate, and Mel B was… Expand
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Highly Cited
1987
Highly Cited
1987
The drug sensitivity of seven Trypanosoma vivax-isolates from Kenya and Somalia was examined. With the exception of diminazene… Expand
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1971
1971
  • B. Gill
  • Transactions of the Royal Society of Tropical…
  • 1971
  • Corpus ID: 34998768
Abstract A strain of T. evansi was made drug-fast to quinapyramine, suramin, stilbamidine and tryparsamide, respectively by… Expand
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1960
1960
  • F. Hawking, A. Sen
  • British journal of pharmacology and chemotherapy
  • 1960
  • Corpus ID: 8916817
Homidium, quinapyramine, and suramin (Group II compounds) produce their trypanocidal effect in vivo only after a latent period of… Expand
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