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Jennings LD Foreman KW Rush TS Tsao DH Mosyak L Kincaid SL Sukhdeo MN Sutherland AG Ding W Kenny CH Sabus CL Liu H Dushin EG Moghazeh SL Labthavikul P Petersen PJ Tuckman M Haney SA Ruzin AV 《Bioorganic & medicinal chemistry》2004,12(19):5115-5131
The ZipA-FtsZ protein-protein interaction is a potential target for antibacterial therapy. The design and parallel synthesis of a combinatorial library of small molecules, which target the FtsZ binding area on ZipA are described. Compounds were demonstrated to bind to the FtsZ binding domain of ZipA by HSQC NMR and to inhibit cell division in a cell elongation assay. 相似文献
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Antane S Caufield CE Hu W Keeney D Labthavikul P Morris K Naughton SM Petersen PJ Rasmussen BA Singh G Yang Y 《Bioorganic & medicinal chemistry letters》2006,16(1):176-180
Pulvinones were synthesized (>180) in arrays and evaluated as inhibitors of early stage cell wall biosynthesis enzymes MurA-MurD. Several pulvinones inhibited Mur enzymes with IC(50)'s in the 1-10 microg/mL range and demonstrated antibacterial activity against Gram-positive bacteria including methicillin-resistant Staphyloccus aureus, vancomycin-resistant Enterococcus faecalis, and penicillin-resistant Streptococcus pneumoniae. 相似文献
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Li Z Francisco GD Hu W Labthavikul P Petersen PJ Severin A Singh G Yang Y Rasmussen BA Lin YI Skotnicki JS Mansour TS 《Bioorganic & medicinal chemistry letters》2003,13(15):2591-2594
Twenty-five 2-phenyl-5,6-dihydro-2H-thieno[3,2-c]pyrazol-3-ol derivatives were synthesized for evaluation as new inhibitors of bacterial cell wall biosynthesis. Many of them demonstrated good inhibitory activity against Staphylococcus aureus MurB, MurC and MurD enzymes in vitro and antimicrobial activity against gram-positive bacteria including MRSA, VRE and PRSP. However, when they were tested in the presence of 4% bovine serum albumin, the MIC values increased to greater than 128 microg/mL against PRSP. None of the compounds demonstrated activity against gram-negative bacteria at MIC <32 microg/mL. 相似文献
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Pattaraporn Sasivimolphan Vimolmas Lipipun Garnpimol Ritthidej Khanidtha Chitphet Yoshihiro Yoshida Tohru Daikoku Boonchoo Sritularak Kittisak Likhitwitayawuid Pornpen Pramyothin Masao Hattori Kimiyasu Shiraki 《AAPS PharmSciTech》2012,13(4):1266-1275
The physicochemical properties of the optimized microemulsion and the permeating ability of oxyresveratrol in microemulsion were evaluated, and the efficacy of oxyresveratrol microemulsion in cutaneous herpes simplex virus type 1 (HSV-1) infection in mice was examined. The optimized microemulsion was composed of 10% w/w of isopropyl myristate, 35% w/w of Tween 80, 35% w/w of isopropyl alcohol, and 20% w/w of water. The mean particle diameter was 9.67 ± 0.58 nm, and the solubility of oxyresveratrol in the microemulsion was 196.34 ± 0.80 mg/ml. After accelerated and long-term stability testing, the microemulsion base and oxyresveratrol-loaded microemulsion were stable. The cumulative amount of oxyresveratrol permeating through shed snake skin from microemulsion at 6 h was 93.04 times compared to that of oxyresveratrol from Vaseline, determined at 20% w/w concentration. In cutaneous HSV-1 infection in mice, oxyresveratrol microemulsion at 20%, 25%, and 30% w/w, topically applied five times daily for 7 days after infection, was significantly effective in delaying the development of skin lesions and protecting from death (p < 0.05) compared with the untreated control. Oxyresveratrol microemulsion at 25% and 30% w/w was significantly more effective than that of 30% w/w of oxyresveratrol in Vaseline (p < 0.05) and was as effective as 5% w/w of acyclovir cream, topically applied five times daily (p > 0.05). These results demonstrated that topical oxyresveratrol microemulsion at 20–30% w/w was suitable for cutaneous HSV-1 mouse infection.KEY WORDS: cutaneous infection in mice, herpes simplex virus, microemulsion, oxyresveratrol, therapeutic efficacy 相似文献
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BACKGROUND: The ventricular myocardium simultaneously secretes two natriuretic peptides useful in the evaluation of heart failure: BNP, hormonally active, and NT-proBNP, the N-terminal end, non-hormonally active, but ultimately their concentrations differ and their clearance patterns are poorly defined. METHODS: We measured NT-proBNP and BNP in patients with and without heart failure and compared their concentrations using regression analysis. RESULTS: The relationship between NT-proBNP with BNP is nonlinear. Between 45 and 70 pmol of BNP/L (class II heart failure) the slope is much higher than in other ranges and the NT-proBNP/BNP ratio reaches its maximum in patients with class II NYHA heart failure. CONCLUSIONS: The difference in concentration for NT-proBNP and BNP can be related to the diffusion across the renal basement membrane. Their ratio is nonlinear because BNP is cleared faster than in patients with class II heart failure than other classes or normal, suggesting a change in a non-renal mode of clearance. 相似文献
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Jody K. Takemoto Julia Choi Cecilia M. Shikuma Jintanat Ananworanich Kara Bennett Pairoa Praihirunkit Piranun Hongchookiat Pornpen Mathajittiphun Daniel E. LiButti Victor DeGruttola Nittaya Phanuphak Nitiya Chomchey Patcharawee Rungrojrat Nipat Teeratakulpisarn Praphan Phanuphak Tanate Jadwattanakul Mariana Gerschenson 《Mitochondrion》2012,12(5):563
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Phenyl thiazolyl urea and carbamate derivatives as new inhibitors of bacterial cell-wall biosynthesis 总被引:2,自引:0,他引:2
Francisco GD Li Z Albright JD Eudy NH Katz AH Petersen PJ Labthavikul P Singh G Yang Y Rasmussen BA Lin YI Mansour TS 《Bioorganic & medicinal chemistry letters》2004,14(1):235-238
Over 50 phenyl thiazolyl urea and carbamate derivatives were synthesized for evaluation as new inhibitors of bacterial cell-wall biosynthesis. Many of them demonstrated good activity against MurA and MurB and gram-positive bacteria including MRSA, VRE and PRSP. 3,4-Difluorophenyl 5-cyanothiazolylurea (3p) with clog P of 2.64 demonstrated antibacterial activity against both gram-positive and gram-negative bacteria. 相似文献
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