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Synthesis and cytotoxic activity of new acridine-thiazolidine derivativesBARROS, Francisco W. A; GONCALVES SILVA, Teresinha; LINS GALDINO, Suely et al.Bioorganic & medicinal chemistry. 2012, Vol 20, Num 11, pp 3533-3539, issn 0968-0896, 7 p.Article

A rapid method of enumarating microorganisms from beef, using an acridine orange direct-count techniqueWALLS, I; SHERIDAN, J. J; LEVETT, P. N et al.Irish journal of food science and technology. 1989, Vol 13, Num 1, pp 23-31, issn 0332-0375, 9 p.Article

Excimer of 9-Aminoacridine Hydrochloride Hydrate in Confined Medium: An Integrated Experimental and Theoretical StudyMITRA, Piyali; CHAKRABORTY, Brotati; BHATTACHARYYA, Dhananjay et al.The journal of physical chemistry. A. 2013, Vol 117, Num 7, pp 1428-1438, issn 1089-5639, 11 p.Article

DNA binding acridine-thiazolidinone agents affecting intracellular glutathionePAULIKOVA, Helena; VANTOVA, Zuzana; HUNAKOVA, L'uba et al.Bioorganic & medicinal chemistry. 2012, Vol 20, Num 24, pp 7139-7148, issn 0968-0896, 10 p.Article

Magnetic behaviour of polyfluoroacridine-based organic molecular materialsCAMPIGLIO, P; CAMPIONE, M; SASSELLA, A et al.The European physical journal. B, Condensed matter physics (Print). 2010, Vol 73, Num 4, pp 495-501, issn 1434-6028, 7 p.Article

Synthesis of N-acridinyl-N'-alkylguanidines : Dramatic influence of amine to guanidine replacement on the physicochemical propertiesZEGHIDA, Walid; DEBRAY, Julien; MICHEL, Carine et al.Bioorganic & medicinal chemistry letters (Print). 2008, Vol 18, Num 17, pp 4779-4782, issn 0960-894X, 4 p.Article

Anaerobic microbial degradation of acridine and the application of remote fiber spectroscopy to monitor the transformation processKNEZOVICH, J. P; BISHOP, D. J; KULP, T. J et al.Environmental toxicology and chemistry. 1990, Vol 9, Num 10, pp 1235-1243, issn 0730-7268Article

Organocatalytic Asymmetric 1,4-Addition of Aldehydes to Acridiniums Catalyzed by a Diarylprolinol Silyl EtherTAO LIANG; JIAN XIAO; ZHIYI XIONG et al.Journal of organic chemistry. 2012, Vol 77, Num 7, pp 3583-3588, issn 0022-3263, 6 p.Article

One-Pot Synthesis of Novel Antiproliferative 9-AminoacridinesGELLERMAN, Gary; WAINTRAUB, Sagiv; ALBECK, Amnon et al.European journal of organic chemistry (Print). 2011, Num 22, pp 4176-4182, issn 1434-193X, 7 p.Article

An efficient ultrasound-promoted method for the one-pot synthesis of 7,10,11,12-tetrahydrobenzo[c]acridin-8(9H)-one derivativesHONGJUN ZANG; YONG ZHANG; YAPING ZANG et al.Ultrasonics sonochemistry. 2010, Vol 17, Num 3, pp 495-499, issn 1350-4177, 5 p.Article

Synthesis of Acridines by the [4 + 2] Annulation of Arynes and 2-Aminoaryl KetonesROGNESS, Donald C; LAROCK, Richard C.Journal of organic chemistry. 2010, Vol 75, Num 7, pp 2289-2295, issn 0022-3263, 7 p.Article

Unusual reactivities of acridine derivatives in catalytic hydrogenation. A combined experimental and theoretical studyMIGNON, Pierre; TIANO, Martin; BELMONT, Philippe et al.Journal of molecular catalysis. A, Chemical. 2013, Vol 371, pp 63-69, issn 1381-1169, 7 p.Article

DNA-templated click chemistry for creation of novel DNA binding moleculesIMOTO, Shuhei; HIROHAMA, Tomoya; NAGATSUGI, Fumi et al.Bioorganic & medicinal chemistry letters (Print). 2008, Vol 18, Num 20, pp 5660-5663, issn 0960-894X, 4 p.Article

Synthesis and characterization of a trigalactosylated bisacridine compound to target DNA to hepatocytesHAENSLER, J; SZOKA, F. C.Bioconjugate chemistry. 1993, Vol 4, Num 1, pp 85-93, issn 1043-1802Article

Tuning the Emission Properties of Fluorescent Ligands by Changing pH: The Unusual Case of an Acridine-Containing Polyamine MacrocyclePUCCIONI, Stefano; BAZZICALUPI, Carla; GELLINI, Cristina et al.The journal of physical chemistry. A. 2013, Vol 117, Num 18, pp 3798-3808, issn 1089-5639, 11 p.Article

Formation of Acridones by Ethylene Extrusion in the Reaction of Arynes with β-Lactams and DihydroquinolinonesYUESI FANG; ROGNESS, Donald C; LAROCK, Richard C et al.Journal of organic chemistry. 2012, Vol 77, Num 14, pp 6262-6270, issn 0022-3263, 9 p.Article

Replacement of a Thiourea-S with an Amidine-NH Donor Group in a Platinum―Acridine Antitumor Compound Reduces the Metal's Reactivity with Cysteine SulfurZHIDONG MA; LU RAO; BIERBACH, Ulrich et al.Journal of medicinal chemistry (Print). 2009, Vol 52, Num 10, pp 3424-3427, issn 0022-2623, 4 p.Article

Synthesis and photophysical behaviors of temperature/ pH-sensitive polymeric materials. I. Vinyl monomer bearing 9-aminoacridine and polymersXIAOLIN GUAN; XINYU LIU; ZHIXING SU et al.European polymer journal. 2007, Vol 43, Num 7, pp 3094-3105, issn 0014-3057, 12 p.Article

Fluorescent Acridine-Based Receptors for H2PO4MARTI-CENTELLES, Vicente; ISABEL BURGUETE, M; GALINDO, Francisco et al.Journal of organic chemistry. 2012, Vol 77, Num 1, pp 490-500, issn 0022-3263, 11 p.Article

Acridine derivatives as anti-BVDV agentsTONELLI, Michele; VETTORETTI, Gerolamo; GILIBERTI, Gabriele et al.Antiviral research. 2011, Vol 91, Num 2, pp 133-141, issn 0166-3542, 9 p.Article

Synthesis and DNA photocleavage by a pyridine-linked bis-acridine chromophore in the presence of copper(II): Ionic strength effectsGRANT, Kathryn B; TERRY, Carla A; GUDE, Lourdes et al.Bioorganic & medicinal chemistry letters (Print). 2011, Vol 21, Num 3, pp 1047-1051, issn 0960-894X, 5 p.Article

Synthesis of novel heme-interacting acridone derivatives to prevent free heme-mediated protein oxidation and degradationPAL, Chinmay; MILAN KUMAR KUNDU; BANDYOPADHYAY, Uday et al.Bioorganic & medicinal chemistry letters (Print). 2011, Vol 21, Num 12, pp 3563-3567, issn 0960-894X, 5 p.Article

Solvent-free preparation of co-crystals of phenazine and acridine with vanillinBRAGA, Dario; GREPIONI, Fabrizia; MAINI, Lucia et al.Thermochimica acta. 2010, Vol 507-08, pp 1-8, issn 0040-6031, 8 p.Article

Novel acridine-based compounds that exhibit an anti-pancreatic cancer activity are catalytic inhibitors of human topoisomerase IIOPPEGARD, Lisa M; OUGOLKOV, Andrei V; LUCHINI, Doris N et al.European journal of pharmacology. 2009, Vol 602, Num 2-3, pp 223-229, issn 0014-2999, 7 p.Article

Absorption and fluorescence spectra of the solutions of polymer Shiff bases based on diamine fluorophores : Influence of the acidity of the mediumSILING, S. A; LOZINSKAYA, E. I; BORISEVICH, YU. E et al.Polymer science. Series A. 1996, Vol 38, Num 7, pp 801-805Article

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