Simple synthesis of karahanaenone

1169-117

Transformation of enals and enones into the glycoside-type derivatives by electrochemical generation of phenyl seleny cation

1126-112

Stereochemistry and 13C NMR spectra of some phenyl selenoethers obtained in phenylselenoetherification of olefinic alcohols

48-5

Animal models of cardiorenal syndrome: a review

The incidence of heart failure and renal failure is increasing and is associated with poor prognosis. Moreover, these conditions do often coexist and this coexistence results in worsened outcome. Various mechanisms have been proposed as an explanation of this interrelation, including changes in hemodynamics, endothelial dysfunction, inflammation, activation of renin-angiotensin-aldosterone system, and/or sympathetic nervous system. However, the exact mechanisms initializing and maintaining this interaction are still unknown. In many experimental studies on cardiac or renal dysfunction, the function of the other organ was either not addressed or the authors failed to show any decline in its function despite histological changes. There are few studies in which the dysfunction of both heart and kidney function has been described. In this review, we discuss animal models of combined cardiorenal dysfunction. We show that translation of the results from animal studies is limited, and there is a need for new and better models of the cardiorenal interaction to improve our understanding of this syndrome. Finally, we propose several requirements that a new animal model should meet to serve as a tool for studies on the cardiorenal syndrome

Identification and characterization of antibacterial compound(s) of cockroaches (Periplaneta americana)

Infectious diseases remain a significant threat to human health, contributing to more than 17 million deaths, annually. With the worsening trends of drug resistance, there is a need for newer and more powerful antimicrobial agents. We hypothesized that animals living in polluted environments are potential source of antimicrobials. Under polluted milieus, organisms such as cockroaches encounter different types of microbes, including superbugs. Such creatures survive the onslaught of superbugs and are able to ward off disease by producing antimicrobial substances. Here, we characterized antibacterial properties in extracts of various body organs of cockroaches (Periplaneta americana) and showed potent antibacterial activity in crude brain extract against methicillin-resistant Staphylococcus aureus and neuropathogenic E. coli K1. The size-exclusion spin columns revealed that the active compound(s) are less than 10 kDa in molecular mass. Using cytotoxicity assays, it was observed that pre-treatment of bacteria with lysates inhibited bacteria-mediated host cell cytotoxicity. Using spectra obtained with LC-MS on Agilent 1290 infinity liquid chromatograph, coupled with an Agilent 6460 triple quadruple mass spectrometer, tissues lysates were analyzed. Among hundreds of compounds, only a few homologous compounds were identified that contained isoquinoline group, chromene derivatives, thiazine groups, imidazoles, pyrrole containing analogs, sulfonamides, furanones, flavanones, and known to possess broad-spectrum antimicrobial properties, and possess anti-inflammatory, anti-tumour, and analgesic properties. Further identification, characterization and functional studies using individual compounds can act as a breakthrough in developing novel therapeutics against various pathogens including superbugs

Ring closure reaction of 4-tert-butyl-4- penten-1-ol with electrophilic reagents

101-105The reaction of 4-tert-butyl-4-penten-1-ol <span style="font-size:15.5pt; mso-bidi-font-size:9.5pt">3<span style="font-size:15.5pt;mso-bidi-font-size: 9.5pt"> with some electrophilic reagents (such as mineral acids, mercuric acetate, peracids) has been investigated. It is found that in the acid (H2SO4)catalysed reaction of 3, the products of 1,2- methyl rearrangement are produced. The oxymercuration/demercuration reaction of 3 and its reaction with meta-chloroperbenzoic acid afford in high yields exclusively Markovnikov-type products.   </span

The Molecular-structure of the Steroidal Isoxazolidine Products Derived From (z)-3-beta, 17-beta-diacetoxy-19-nor-5, 10-secoandrost-1(10)-en-5-one

X-Ray analysis of the steroidal isoxazolidine derivatives 2 and 3b, which are formed (the latter as the corresponding diacetate 3a) in the reaction of (Z)-3beta, 17beta-diacetoxy-19-nor-5,10-secoandrost-l(lo)-en-5-one (1) with N-methylhydroxylamine, has revealed that both compounds (and therefore also 3a) have the same cis-1beta,5beta-epoxyimino bridge structure. The conformations of the two molecular skeletons are compared