Results 151 to 160 of about 2,191 (200)

Acridinium Chemiluminogenic Labels-Synthesis, Analytical Performance, and Mechanism of Light Generation-A Comparison in View of Biomedical Diagnostics. [PDF]

Molecules
Krzymiński K, Zadykowicz B, Czechowska J, Rudnicki-Velasquez P, Serdiuk I, Sieradzan AK, Holec-Gąsior L.   +6 more
europepmc   +1 more source

Experiments and Calculation on New N,N-bis-Tetrahydroacridines. [PDF]

Molecules
Hrubaru MM, Draghici C, Ngounoue Kamga FA, Diacu E, Egemonye TC, Ekennia AC, Ungureanu EM.   +6 more
europepmc   +1 more source

Synthesis and antidiabetic evaluation of novel Tetrahydroacridine derivatives with computational insights. [PDF]

Sci Rep
Kadry AM, Abdellah WA, Mohamed MAA, Tolba MS.   +3 more
europepmc   +1 more source

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Synthesis and characterization of oxadisilole-fused acridines, dioxatrisilole-fused acridines and benzo[b]acridines

Tetrahedron, 2014
Abstract Oxadisilole-fused acridines, dioxatrisilole-fused acridines and benzo[b]acridines were synthesized through nucleophilic additions and aromatization reactions of arynes with 2-aminoaryl ketones or 2-aminoaryl aldehydes in good yields at room temperature.
Yali Chen, Weiguo Cao
exaly   +2 more sources

Acridines and streptomycine

Experientia, 1947
La streptomycine et les acridines ont une propriete commune, en ce qu'ils forment avec les nucleoproteides des levures de complexes electro-adsorptifs.
L, MASSART, G, PEETERS, A, VAN HOUCKE
openaire   +2 more sources

(Acridine)trimethylgallium–Acridine (2/1)

Acta Crystallographica Section C Crystal Structure Communications, 1996
The reaction of excess trimethylgallium with acridine in diethyl ether gave the title layer inclusion compound, [Ga(CH 3 ) 3 (C 13 H 9 N)].0.5C 13 H 9 N. The Ga-N bond length is 2.203 (3) A.
Sun, HS, Wang, XM, Sun, XZ, You, XZ, Wang, JZ   +4 more
openaire   +2 more sources

Acridines

ChemInform, 2005
AbstractFor Abstract see ChemInform Abstract in Full Text.
Prager, Rolf Herman, Williams, C M
openaire   +1 more source

The genetic toxicology of acridines

Mutation Research/Reviews in Genetic Toxicology, 1991
Acridine and its derivatives are planar polycyclic aromatic molecules which bind tightly but reversibly to DNA by intercalation, but do not usually covalently interact with it. Acridines have a broad spectrum of biological activities, and a number of derivatives are widely used as antibacterial, antiprotozoal and anticancer drugs. Simple acridines show
L R, Ferguson, W A, Denny
openaire   +2 more sources

Excited state characteristics of acridine dyes: acriflavine and acridine orange

Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy, 2003
The magnitude of the Stokes shift (frequency shifts in absorption and fluorescence spectra) is observed on changing the solvents and further has been used to calculate experimentally the dipole moments (ground state and excited state) of acriflavine and acridine orange dye molecules. Theoretically, dipole moments are calculated using PM 3 Model.
Vijay K, Sharma, P D, Sahare, Ramesh C, Rastogi, S K, Ghoshal, D, Mohan   +4 more
openaire   +2 more sources