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acridone

Known as: 9(10H)-acridone, 9-azaanthracen-10-one 
National Institutes of Health

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Acridones

Papers overview

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2012
2012
Induction of mouthpart deformities in chironomid larvae exposed to contaminated sediments.
2007
2007
Design, Synthesis, and Evaluation of 10-N-Substituted Acridones as Novel Chemosensitizers in Plasmodium falciparum
ABSTRACT A series of novel 10-N-substituted acridones, bearing alkyl side chains with tertiary amine groups at the terminal… 
2007
2007
Design, synthesis and biological evaluation of new oligopyrrole carboxamides linked with tricyclic DNA-intercalators as potential DNA ligands or topoisomerase inhibitors.
Highly Cited
2007
Highly Cited
2007
An acridone‐producing novel multifunctional type III polyketide synthase from Huperzia serrata
A cDNA encoding a novel plant type III polyketide synthase was cloned and sequenced from the Chinese club moss Huperzia serrata… 
2002
2002
Design and synthesis of some new pyranoxanthenone aminoderivatives with cytotoxic activity.
2001
2001
Bioactive acridone alkaloids from Swinglea glutinosa.
A new prenylated acridone alkaloid, 1,3,5-trihydroxy-2,8-bis(3-methylbut-2-enyl)-10-methyl-9-acridone (1), was isolated from the… 
2000
2000
Specificities of functionally expressed chalcone and acridone synthases from Ruta graveolens.
The common rue, Ruta graveolens L., expresses two types of closely related polyketide synthases that condense three malonyl-CoAs… 
Highly Cited
1997
Highly Cited
1997
ER-27319, an acridone-related compound, inhibits release of antigen-induced allergic mediators from mast cells by selective inhibition of fcepsilon receptor I-mediated activation of Syk.
Engagement of the mast cell high-affinity receptor for immunoglobulin E (IgE), FcepsilonRI, induces tyrosine phosphorylation of… 
1988
1988
Acronycine Epoxide: A New Acridone Alkaloid from Several Sarcomelicope Species
(1) Koller, G., Russ, H. (1937) Monatsh. Chem. 70,54. (2) Santesson, J. (1969) Acta Chem. Scand, 23, 3270. (3) Dutton, M. F… 
1977
1977
Thiolytic cleavage of the anti-tumour compound 4'-(9-acridinylamino)-methanesulphon-m-anisidine (m-AMSA, NSC 156 303) in blood.
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