Small molecule inhibitors of NF-kB and JAK/STAT signal transduction pathways as promising anti-inflammatory therapeutics.

In the current review, we discuss the role of NF-kB and JAK/STAT signaling pathways and their small molecule regulators in the therapy of inflammatory diseases. Considering potential harmful effects directly assigned to the COX-2 inhibition, novel therapeutically-relevant biological targets such as NF-kB and JAK/STAT signaling pathways have received a growing attention. Here we summarize recent progress in the identification and development of novel, clinically approved or evaluated small molecule regulators of these signaling cascades as promising anti-inflammatory therapeutics. In addition, we illustrate key structural modifications and bioisosteric transformations among these inhibitors to provide a helpful basis for further development of novel small molecule anti-inflammatory agents.

Compound library design for target families.

Chemogenomics is a modern approach to analysis of the biological effect of a wide array of small molecule compounds on a large set of homologous receptors or other macromolecular drug targets. However, the relative productivity of the method and the extremely high-cost procedure jointly force the scientist to use additional computational tools for rational compound library design and selection. The present chapter will focus specifically on application of a predictive mapping computational technology in the context of the fundamental principles of chemogenomic approach to foster rational drug design and derive information from the simultaneous biological evaluation of multiple compounds on a set of coherent biological targets.

New approaches to the treatment of inflammatory disease : focus on small-molecule inhibitors of signal transduction pathways.

This 'state-of-the-art' review specifically focuses on alternative signalling pathways deeply involved in acute and chronic inflammatory responses initiated by various pathological stimuli. The accumulated scientific knowledge has already revealed key biological targets, such as COX-2, and related pro-inflammatory mediators (cytokines and chemokines, interleukins [ILs], tumour necrosis factor [TNF]-alpha, migration inhibition factor [MIF], interferon [IFN]-gamma and matrix metalloproteinases [MMPs]) implicated in uncontrolled, destructive inflammatory reaction. A number of physiologically active agents are currently approved for market or are under active investigation in different clinical trials. However, recent findings have exposed the fatal adverse effects directly associated with drug therapy based on COX-2 inhibition. Given these possible harmful outcomes, a range of novel therapeutically relevant biological targets that include nuclear transcription factor (NF-kappaB), p38 mitogen-activated protein kinases (MAPK) and Janus protein tyrosine kinases and signal transducers and activators of transcription (JAK/STAT) signalling pathways has received growing attention. Here we discuss recent progress in the identification and development of novel, clinically approved or evaluated small-molecule regulators of these signalling cascades as promising anti-inflammatory drugs.

Novel formulation for enhancing efficiency of tebuconazole.

A novel formulation of tebuconazole in microemulsion state was prepared in this work. The microemulsion was formed due to the presence of a special system of surfactants, namely ethoxylated castor oil and fatty acid amides. Biological effect of suspension concentrate and microemulsion formulations of tebuconazole with the same concentration of active ingredient was investigated in the field experiments. The experiments demonstrated excellent efficiency of the microemulsion containing 60 g/l of tebuconazole against broad spectrum of crop diseases and infections including smut diseases, root rots and moulds in comparison to suspension concentrate at the same application rate.

Novel formulation for enhancing efficiency of metribuzin.

The biological efficiency of systemic herbicide metribuzin in water dispersible granules (WG) and solution colloid concentrate (SCC) formulations was studied in field experiments. Metribuzin formulation in SCC state was prepared by the addition of a mixture of anionic and non-ionic surfactants and alkoxylated sorbitan esters as specific adjuvants. The ability of herbicide formulation containing Metribuzin in SCC state to provide increases in control of broadleaf and grassy weeds in comparison to WG was observed. The possibility to reduce application rate of Metribuzin from high-dose to low-dose without losing efficacy of weed control was demonstrated.

Use of growth regulator of cytokinin type for enhancement and modification of herbicide activity.

The herbicidal action of Betanal Express (BPAM) on Chine jute (Abutilon theophrasti) weed was studied in the presence of a new plant growth regulator of urea type, N-phenyl-N-(1,2,4-triazol-4-yl)urea (PhenylTriazolylUrea, PTU). In the past years, Chine jute has become a major limiting factor in sugar beet production in the southern Russia due to its resistance to BPAM which is an essential herbicide widely used for sugar beet protection. When PTU was added to BPAM, the combination appeared to be more effective than the herbicide alone. The influence of phytohormone PTU was observed at very low application rate of 20-100 g/ha, thus herbicide dose in the ecosystem was reduced. The main visual signs of herbicidal action of the combination BPAM + PTU on Chine jute were inhibition of growth of overground plant and stem, leaves changes and sharp inhibition of root growth. No sugar beet injury was observed when this tank mixture was used. It was found that enhanced performance of the novel herbicide formulation is determined by increased herbicidal action of Ethofumesate, one of the active ingredients of BPAM.

Conjugates of oligonucleotides with polyaromatic fluorophores as promising DNA probes.

Conjugates of pyrene and perylene with oligodeoxynucleotides were synthesized and tested as hybridisation probes. A 13-mer containing a 3-peryleneacetic acid residue attached to the 5' end through a hexamethylenediamine linker showed no response in the fluorescent spectrum upon hybridisation to the complementary sequence. At the same time, pyrene-labelled probes are sensitive to duplex formation. A pyrene pseudonucleotide unit based on 4-(1-pyrenyl)-1,3-butanediol can be introduced into any predetermined position(s) of the oligonucleotide chain. The probes polylabelled in this fashion displayed considerable changes in the excimer-to-monomer fluorescence intensity ratio after duplex formation. The internal location of two pyrene residues in the probe provides a drastic enhancement of excimer fluorescence (approximately 470 nm) upon hybridisation. When two pyrene units were brought into close proximity to two pyrenes in the complementary strand upon duplex formation, strong excimer emission at approximately 450 nm was detected. This effect provides a basis for a sensor construction designed to detect nucleic acid hybridisation.

[Novel reagent for labeling of biomolecules--activated derivative of pyrene dichromophore with excimeric fluorescence]. / Novyi reagent dlia mecheniia biomolekul--aktivirovannoe proizvodnoe pirenovogo bikhromofora s éksimernoi fluorestsentsiei.

N-[2-(1-pyrenyl)ethyl]-1-pyrenylacetamide, bis[2-(1-pyrenyl)ethyl]amine, and N,N-bis[2-(1-pyrenyl)ethyl]succinamide were synthesized from 1-pyrenylacetic acid. These compounds contain adjacent pyrene residues and display excimer fluorescence. The latter compound, as a pentafluorophenyl ester, was used to prepare fluorescently labeled oligodeoxyribonucleotide (5)CAGGAAACAGCTATGAC. For N,N-bis[2-(1-pyrenyl)ethyl]succinamide, the excimer-to-monomer fluorescence ratio and intensity of fluorescence in water-methanol solutions changed in the presence of single-stranded and double-stranded oligonucleotides, upon attachment to an oligonucleotide, and upon hybridization of the resulting conjugate with the complementary nucleotide sequence.