Hydroxybiphenylamide GroEL/ES Inhibitors Are Potent Antibacterials against Planktonic and Biofilm Forms of Staphylococcus aureus.

We recently reported the identification of a GroEL/ES inhibitor (1, N-(4-(benzo[ d]thiazol-2-ylthio)-3-chlorophenyl)-3,5-dibromo-2-hydroxybenzamide) that exhibited in vitro antibacterial effects against Staphylococcus aureus comparable to vancomycin, an antibiotic of last resort. To follow up, we have synthesized 43 compound 1 analogs to determine the most effective functional groups of the scaffold for inhibiting GroEL/ES and killing bacteria. Our results identified that the benzothiazole and hydroxyl groups are important for inhibiting GroEL/ES-mediated folding functions, with the hydroxyl essential for antibacterial effects.

Sulfonamido-2-arylbenzoxazole GroEL/ES Inhibitors as Potent Antibacterials against Methicillin-Resistant Staphylococcus aureus (MRSA).

Extending from a study we recently published examining the antitrypanosomal effects of a series of GroEL/ES inhibitors based on a pseudosymmetrical bis-sulfonamido-2-phenylbenzoxazole scaffold, here, we report the antibiotic effects of asymmetric analogs of this scaffold against a panel of bacteria known as the ESKAPE pathogens ( Enterococcus faecium, Staphylococcus aureus, Klebsiella pneumoniae, Acinetobacter baumannii, Pseudomonas aeruginosa, and Enterobacter species). While GroEL/ES inhibitors were largely ineffective against K. pneumoniae, A.

Mandibular embryonal rhabdomyosarcoma with cartilaginous metaplasia: report of a case and review of literature.

Rhabdomyosarcoma (RMS) is a malignant tumor of skeletal muscle origin and frequently involves the head and neck region. It represents the second most common pediatric soft tissue sarcoma and accounts for 3% of all childhood cancers. Here, we report a case of embryonal RMS presenting as a right-sided facial swelling in a 7-year-old boy.

Gas bubbles in the circulation of divers after ascending excursions from 300 to 250 msw.

The occurrence of intravascular bubbles in arteries and veins has been studied using pulsed Doppler ultrasound in six subjects who performed two ascending excursions each from 300 to 250 meters of seawater (msw) during a heliox saturation dive. Following decompression, high-intensity reflections could be observed not only in the venous system but also in the arteries, most notably in the carotid artery. Intravascular bubbles were more numerous during the first ascent than during the second.

Bubble dissolution physics and the treatment of decompression sickness.

The treatment of decompression sickness often involves both recompressing the victim and administering hyperbaric oxygen in the hope of more rapidly dissolving the bubbles which cause this malady. Although many hundreds of such treatments are conducted each year in the United States alone, the underlying physical principles governing the dissolution of such bubbles are not well understood and only empirically tested. In this paper, we present a mathematical theory of bubble dissolution that is verified by comparison with laboratory experiments.

Stabilization of gas cavitation nuclei by surface-active compounds.

Gas bubbles are the primary agent in producing the pathogenic effects of decompression sickness. Numerous experiments indicate that bubbles originate in water, and probably also in man, as pre-existing gas nuclei. This is surprising considering that gas phases larger than 1 micron should rise to the surface of a standing liquid, whereas smaller ones should dissolve rapidly due to surface tension.

Isobaric bubble growth: a consequence of altering atmospheric gas.

During certain treatments of decompression sickness following dives made with compressed air, the U.S. Navy advocates breathing helium-oxygen mixtures.