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1.
Masakazu Atobe Kenji Naganuma Masashi Kawanishi Akifumi Morimoto Ken-ichi Kasahara Shigeki Ohashi Hiroko Suzuki Takahiko Hayashi Shiro Miyoshi 《Bioorganic & medicinal chemistry letters》2013,23(22):6064-6067
We describe a medicinal chemistry approach to generate a series of 2-(1H-pyrazol-1-yl)thiazole compounds that act as selective EP1 receptor antagonists. The obtained results suggest that compound 12 provides the best EP1 receptor antagonist activity and demonstrates good oral pharmacokinetics. 相似文献
2.
Atsushi Tokida Ichiro Atobe Kazuo Maeda 《Bioscience, biotechnology, and biochemistry》2013,77(11):3109-3113
Using vented charcoal filters, the adsorption efficiencies of acetaldehyde, isoprene and acetone, the major components in the vapor phase of cigarette smoke, were studied. Filter ventilation was found to raise the adsorption efficiency of the adsorbent. The effect of increasing the ventilation rate through the filter was greatest for the adsorption of acetaldehyde. In order to clarify the effects of decreases of the flow rate and the concentration caused by ventilation, the adsorption by unvented charcoal filters under varied conditions was also measured. Although both raised the adsorptions of the three components, the lowered concentration was contributed to mainly by an increase of adsorption by the vented charcoal filters. Regardless of whether the filter was perforated or not, the adsorptions of the three components depended on the volume of the air drawn in at the top of the lighted end of the cigarette. 相似文献
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The band 3 protein is the major integral protein present in the erythrocyte membrane. Two tissue-specific isoforms are also expressed in kidney alpha intercalated cells and in cardiomyocytes. It has been suggested that the cardiac isoform predominantly mediates the anion exchange in cardiomyocytes, but the role of the cytoplasmic domain of the band 3 (CDB3) protein in the cardiac tissue is unknown. In order to characterize novel associations of the CDB3 in the cardiac tissue, we performed the two-hybrid assay, using a bait comprising the region from leu 258 to leu 311 of the erythrocyte band 3, which must also be present in the cardiac isoform. The assay revealed two clones containing the C-terminal region of the alpha-cardiac actin. Immunoprecipitation of whole rat heart using an anti-actin antibody, immunoblotted with anti-human band 3, showed that actin binds to band 3 which was confirmed in the reverse assay. The confocal microscopy showed band 3 in the intercalated discs. Thus, besides the in vivo physical interaction in the Saccharomyces cerevisiae cell, we demonstrated using immunopreciptation that there is a physical association of band 3 with alpha-cardiac actin in cardiomyocyte, and we suggest that the binding occur "in situ," in the intercalated disc, a site of cell-cell contact and attachment of the sarcomere to the plasma membrane. 相似文献
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Kengo Funakoshi Tetsuo Kadota Yoshitoshi Atobe Masato Nakano Richard C. Goris Reiji Kishida 《Cell and tissue research》1999,298(1):45-54
To examine the presence of nitric oxide synthase (NOS) in the sensory system of the glossopharyngeal and vagus nerves of teleosts, nicotinamide adenine dinucleotide phosphate diaphorase (NADPHd) activity and immunoreactivity for NOS were examined in the puffer fish Takifugu niphobles. The nitrergic sensory neurons were located in the ganglia of both the glossopharyngeal and the vagal nerves. In the vagal ganglion, positive neurons were found in the subpopulations for the branchial rami and the coelomic visceral ramus, but not for the posterior ramus or the lateral line ramus. In the medulla, nitrergic afferent terminals were found in the glossopharyngeal lobe, the vagal lobe, and the commissural nucleus. In the gill structure, the nitrergic nerve fibers were seen in the nerve bundles running along the efferent branchial artery of all three gill arches. These fibers appeared to terminate in the proximal portion of the efferent filament arteries of three gill arches. On the other hand, autonomic neurons innervating the gill arches were unstained. These results suggest that nitrergic sensory neurons in the glossopharyngeal and vagal ganglia project their peripheral processes through the branchial rami to a specific portion of the branchial arteries, and they might play a role in baroreception of this fish. A possible role for nitric oxide (NO) in baroreception is also discussed. 相似文献
6.
Masakazu Atobe Natsumi Yamakawa Yasuhiro Wada Tokuhito Goto Masashi Kawanishi Takeshi Ito Makoto Saito Masahiro Takeda Takanori Tabata Hirokazu Arai 《Bioorganic & medicinal chemistry letters》2017,27(21):4828-4831
A series of indazole derivatives were identified as Sirt 1 activators though high-throughput screening. Optimization of each substituent on the indazole ring led to the identification of compound 13. Compound 13 appeared to give the best Sirt 1 activity of the compounds tested and also showed osteogenesis activity in a cell assay. Sirt 1 activators are therefore potential candidates for the treatment of osteoporosis. 相似文献
7.
Renata Buccheri de Oliveira Jane Harumi Atobe Simone Aparecida Souza Daniel Wagner de Castro Lima Santos 《Mycopathologia》2014,178(1-2):71-78
Invasive fungal infections (IFIs) represent one of the main causes of morbimortality in immunocompromised patients. Pneumocystosis, cryptococcosis and histoplasmosis are the most frequently occurring IFIs in patients with acquired immunodeficiency syndrome (AIDS). Fungi, such as Candida spp. and Aspergillus spp., may cause severe diseases during the course of an HIV infection. Following the introduction of highly active anti-retroviral therapy, there has been a marked reduction of opportunistic fungal infections, which today is 20–25 % of the number of infections observed in the mid-1990s. This study is an observational and retrospective study aimed at the characterising IFI incidence and describing the epidemiology, clinical diagnostic and therapeutic features and denouement in HIV/AIDS patients. In HIV/AIDS patients, the IFI incidence is 54.3/1,000 hospitalisation/year, with a lethality of 37.7 %. Cryptococcosis represents the main opportunistic IFI in the population, followed by histoplasmosis. Nosocomial pathogenic yeast infections are caused principally by Candida spp., with a higher candidemia incidence at our institution compared to other Brazilian centres. 相似文献
8.
Masakazu Atobe Kenji Naganuma Masashi Kawanishi Takahiko Hayashi Hiroko Suzuki Masahiro Nishida Hirokazu Arai 《Bioorganic & medicinal chemistry letters》2018,28(14):2408-2412
We describe a medicinal chemistry approach to the discovery of a novel EP1 antagonist exhibiting high potency and good pharmacokinetics. Our starting point is 1, an EP1 receptor antagonist that exhibits pharmacological efficacy in cystometry models following intravenous administration. Despite its good potency in vitro, the high lipophilicity of 1 is a concern in long-term in vivo studies. Further medicinal chemistry efforts identified 4 as an improved lead compound with good in vitro ADME profile applicable to long term in vivo studies. A rat fracture study was conducted with 4 for 4?weeks to validate its utility in bone fracture healing. The results suggest that this EP1 receptor antagonist stimulates callus formation and thus 4 has potential for enhancing fracture healing. 相似文献
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The end product of purine metabolism varies from species to species. The degradation of purines to urate is common to all
animal species, but the degradation of urate is much less complete in higher animals. The comparison of subcellular distribution,
intraperoxisomal localization forms, molecular structures, and some other properties of urate-degrading enzymes (urate oxidase,
allantoinase, and allantoicase) among animals is described. Liver urate oxidase (uricase) is located in the peroxisomes in
all animals with urate oxidase. On the basis of the comparison of intraperoxisomal localization forms, mol wt, and solubility
of liver urate oxidase among animals, it is suggested that amphibian urate oxidase is a transition form in the evolution of
aquatic animals to land animals. Allantoinase and allantoicase are different proteins in fish liver, but the two enzymes form
a complex in amphibian liver. The subcellular localization of allantoinase and allantoicase varies among fishes. Hepatic allantoinase
is located both in the peroxisomes and in the cytosol in saltwater fishes, and only in the cytosol in freshwater fishes. Hepatic
allantoicase is located on the outer surface of the, peroxisomal membrane in the mackerel group and in the peroxisomal matrix
in the sardine group. Amphibian hepatic allantoinase-allantoicase complex is probably located in the mitochondria. On the
basis of previous data, changes of allantoinase and allantoicase in molecular structure and intracellular localization during
animal evolution may be as follows: Fish liver allantoinase is a single peptide with a mol wt of 54,000, and is located both
in the peroxisomes and in the cytosol, or only in the cytosol. Fish liver allantoicase consists of two identical subunits
with a mol wt of 48,000, and is located in the peroxisomal matrix or on the outer surface of the peroxisomal membrane. The
evolution of fishes to amphibia resulted in the dissociation of allantoicase into subunits, and in the association of allantoinase
with the subunit of allantoicase. This amphibian enzyme was lost by further evolution. 相似文献