Results 11 to 20 of about 29 (23)

Synthesis of quinoline/naphthalene-containing azaphenothiazines and their potent in vitro antioxidant properties. [PDF]

open access: yesMed Chem Res, 2015
Jeleń M   +5 more
europepmc   +1 more source

The immunosuppressive activities of newly synthesized azaphenothiazines in human and mouse models. [PDF]

open access: yesCell Mol Biol Lett, 2009
Zimecki M   +5 more
europepmc   +1 more source

New phenylcyclopropane-carbohydrazide furan derivatives with potent anticancer activity and EGFR inhibitory potential. [PDF]

open access: yesRSC Adv
Patagani S   +6 more
europepmc   +1 more source

The Interaction of Structural Analogues of Phenothiazines in p53-Dependent Cellular Signaling Pathways. [PDF]

open access: yesACS Omega
Giercuszkiewicz-Haśnik K   +4 more
europepmc   +1 more source

Study of the Lipophilicity of Tetracyclic Anticancer Azaphenothiazines. [PDF]

open access: yesBiomolecules
Jeleń M   +3 more
europepmc   +1 more source

Novel 8-trifluoromethylquinobenzothiazines-Synthesis and Evaluation for Antiproliferative and Antibacterial Activity. [PDF]

open access: yesPharmaceuticals (Basel)
Klimoszek D   +5 more
europepmc   +1 more source

A Study of Antioxidant, Antihyperlipidemic, and Anti-Glycation Effects of Alkylsulfonic Acids with Quinobenzothiazinyl Substituents: In Vitro and In Silico Investigations. [PDF]

open access: yesAntioxidants (Basel)
Anamalay K   +10 more
europepmc   +1 more source
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Study of the lipophilicity of novel diquinothiazines

Journal of Planar Chromatography – Modern TLC, 2006
The lipophilicity of twenty new diquinothiazines has been determined by reversed-phase thin-layer chromatography on RP-18 silica plates with acetone-aqueous TRIS (tris(hydroxymethyl) aminomethane) buffer as mobile phase. The R M values were linearly dependent on the concentration of acetone. The R M0 values were determined by linear extrapolation to 0%
Małgorzata Nowak, Krystian Pluta
openaire   +1 more source

Synthesis of new pentacyclic diquinothiazines

Journal of Heterocyclic Chemistry, 2007
Abstractmagnified imageReactions of 2,2′‐dichloro‐3,3′‐diquinolinyl sulfide 1 with ammonia derivatives and various primary alkylamines and arylamines proceeded as a thiazine ring closure to form linear annulated pentacyclic 6H‐diquinothiazine 2H and 6‐substituted derivatives 2 with alkyl, alkylaryl, aryl and heteroaryl substituents in moderate to good ...
Małgorzata Nowak   +3 more
openaire   +1 more source

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