Antioxidant treatments have been expected to be a novel therapeutics for various oxidative stress-mediated disorders. Our previous study revealed that 5-hydroxyoxindole and its 3-phenacyl-3-hydroxy derivatives showed excellent antioxidant activities such as 1,1-diphenyl-2-picrylhydrazyl (DPPH) radical scavenging activity and lipid-peroxidation inhibitory activity. However, the DPPH radical scav...

The systematic synthesis and photophysical, electrochemical and computational studies on an extended series of triphenylamine-[C≡C-1,4-C6H2(OR)2]n-C≡C-diphenyl-1,3,4-oxadiazole dyad molecules (the OR groups are at 2,5-positions of the para-phenylene ring and R = C6H13; n = 0-5, compounds 1, 2, 3, 4 and 5, respectively) are reported. Related molecules with identical end groups, triphenylamine-C≡...

The title compound, C(21)H(19)NO, belongs to the family of α-amino-ketones. The structure contains three benzene rings, two of which [the phenyl ring in the 1-position (B) and the methylaniline ring (A)] are nearly coplanar [dihedral angle = 5.4 (1)°], whereas the phenyl ring in the 2-position (C) is nearly normal to them [dihedral angles = 81.8 (1) and 87.0 (1)° for A/C and B/C, respectively]....

The syntheses, the biological evaluation, and the structure-activity relationships of a novel series of 1,8-dihydroxy-9(10H)-anthracenones bearing acyl-, alkyl-, or alkylidene-linked aromatic substituents in the 10-position are described. The phenylacyl and phenylalkylidene analogs were far more potent inhibitors of 5-lipoxygenase (5-LO) from bovine polymorphonuclear leukocytes (IC50 values in ...

We performed a detailed in vitro pharmacological characterization of two arylpiperazine derivatives, compound N-(4-cyanophenylmethyl)-4-(2-diphenyl)-1-piperazinehexanamide (LP-211) previously identified as a high-affinity brain penetrant ligand for 5-hydroxytryptamine (serotonin) type 7 (5-HT7) receptors, and its analog N-benzyl-4-(2-diphenyl)-1-piperazinehexanamide (MEL-9). Both ligands exhibi...

The reaction of benzil, 1-alkyl-2-arylethanediamine dihydrochloride and sodium acetate trihydrate gave the target molecule dihydropyrazine derivatives 30-34. The compounds have been characterized on the basis of their FT-IR, 1H NMR and 13C NMR spectroscopies. All the compounds are screened for their antibacterial activity against Staphylococcus aureus, Klebsiella pneumoniae, Pseudomonas aerugin...