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91.
Huang S Lin R Yu Y Lu Y Connolly PJ Chiu G Li S Emanuel SL Middleton SA 《Bioorganic & medicinal chemistry letters》2007,17(5):1243-1245
The novel compound 3-(1H-benzimidazol-2-yl)-5-isoquinolin-4-ylpyrazolo[1,2-b]pyridine was discovered to be a potent CDK1 inhibitor. Described here is the chemistry for its synthesis, including Pd(II) catalyzed Stille coupling reaction and sulfur(0) induced benzimidazole formation. Its effects on VEGFR-2 kinase activity and tumour cell proliferation are also described. 相似文献
92.
Lin R Connolly PJ Lu Y Chiu G Li S Yu Y Huang S Li X Emanuel SL Middleton SA Gruninger RH Adams M Fuentes-Pesquera AR Greenberger LM 《Bioorganic & medicinal chemistry letters》2007,17(15):4297-4302
A series of 3,5-disubstituted pyrazolo[3,4-b]pyridine cyclin-dependent kinase (CDK) inhibitors was synthesized. These compounds showed potent and selective CDK inhibitory activities and inhibited in vitro cellular proliferation in cultured human tumor cells. Selected compounds were evaluated in an in vivo tumor xenograft model. The synthesis and biological evaluation of these pyrazolo[3,4-b]pyridines and related compounds are reported. 相似文献
93.
94.
Lin R Chiu G Yu Y Connolly PJ Li S Lu Y Adams M Fuentes-Pesquera AR Emanuel SL Greenberger LM 《Bioorganic & medicinal chemistry letters》2007,17(16):4557-4561
Two series of 3,4-disubstituted pyrazole analogues, 3-(benzimidazol-2-yl)-4-[2-(pyridin-3-yl)-vinyl]-pyrazoles (2) and 3-(imidazol-2-yl)-4-[2-(pyridin-3-yl)-vinyl]-pyrazoles (3), were synthesized as novel cyclin-dependent kinase (CDK) inhibitors. Representative compounds showed potent and selective CDK inhibitory activities and inhibited in vitro cellular proliferation in various human tumor cells. The design, synthesis, and preliminary biological evaluation of these pyrazole compounds are reported. 相似文献
95.
Alpi A Amrhein N Bertl A Blatt MR Blumwald E Cervone F Dainty J De Michelis MI Epstein E Galston AW Goldsmith MH Hawes C Hell R Hetherington A Hofte H Juergens G Leaver CJ Moroni A Murphy A Oparka K Perata P Quader H Rausch T Ritzenthaler C Rivetta A Robinson DG Sanders D Scheres B Schumacher K Sentenac H Slayman CL Soave C Somerville C Taiz L Thiel G Wagner R 《Trends in plant science》2007,12(4):135-136
96.
Amarildo Emanuel Correia Jordão Bruno Cogliati Bernard Ernesto Jensch-Junior Leandro Nogueira Pressinotti Osório Miguel Parra Francisco Javier Hernandez-Blazquez José Roberto Machado Cunha da Silva 《Polar Biology》2007,30(3):387-390
The Notothenia coriiceps liver is commonly infected with parasites, reducing the hepatic mass and inducing the regeneration. In order to better understand
the effect of nutrient influx on hepatic regeneration at 0°C, a usual mammal hepatotrophic factor (HF) solution was injected
into ten fish (HF group), while ten fish were injected with saline solution (control), twice a day, for 15 days. The liver
and carcass weight were measured, and samples were obtained for histological studies. The HF group presented a higher liver/carcass
weight (62.5%) than control group. This increase in liver mass was due mainly to hepatocytes hypertrophy, including nuclear
size increase and cytoplasmic inclusions of glycogen. Hyperplasia is also observed, although to a lesser extent. The hepatic
reaction to HF in Antarctic fish was here demonstrated for the first time, helping to understand the liver response to seasonal
nutrient. 相似文献
97.
Xiaoyan Lin Lucy Thorne Zhinan Jin Loubna A. Hammad Serena Li Jerome Deval Ian G. Goodfellow C. Cheng Kao 《Nucleic acids research》2015,43(1):446-460
The replication enzyme of RNA viruses must preferentially recognize their RNAs in an environment that contains an abundance of cellular RNAs. The factors responsible for specific RNA recognition are not well understood, in part because viral RNA synthesis takes place within enzyme complexes associated with modified cellular membrane compartments. Recombinant RNA-dependent RNA polymerases (RdRps) from the human norovirus and the murine norovirus (MNV) were found to preferentially recognize RNA segments that contain the promoter and a short template sequence for subgenomic RNA synthesis. Both the promoter and template sequence contribute to stable RdRp binding, accurate initiation of the subgenomic RNAs and efficient RNA synthesis. Using a method that combines RNA crosslinking and mass spectrometry, residues near the template channel of the MNV RdRp were found to contact the hairpin RNA motif. Mutations in the hairpin contact site in the MNV RdRp reduced MNV replication and virus production in cells. This work demonstrates that the specific recognition of the norovirus subgenomic promoter is through binding by the viral RdRp. 相似文献
98.
Vânia C. S. Pankievicz Fernanda P. do Amaral Karina F. D. N. Santos Beverly Agtuca Youwen Xu Michael J. Schueller Ana Carolina M. Arisi Maria. B.R. Steffens Emanuel M. de Souza Fábio O. Pedrosa Gary Stacey Richard A. Ferrieri 《The Plant journal : for cell and molecular biology》2015,81(6):907-919
Nitrogen‐fixing rhizobacteria can promote plant growth; however, it is controversial whether biological nitrogen fixation (BNF) from associative interaction contributes to growth promotion. The roots of Setaria viridis, a model C4 grass, were effectively colonized by bacterial inoculants resulting in a significant enhancement of growth. Nitrogen‐13 tracer studies provided direct evidence for tracer uptake by the host plant and incorporation into protein. Indeed, plants showed robust growth under nitrogen‐limiting conditions when inoculated with an ammonium‐excreting strain of Azospirillum brasilense. 11C‐labeling experiments showed that patterns in central carbon metabolism and resource allocation exhibited by nitrogen‐starved plants were largely reversed by bacterial inoculation, such that they resembled plants grown under nitrogen‐sufficient conditions. Adoption of S. viridis as a model should promote research into the mechanisms of associative nitrogen fixation with the ultimate goal of greater adoption of BNF for sustainable crop production. 相似文献
99.
Navarrete-Vazquez G Chávez-Silva F Argotte-Ramos R Rodríguez-Gutiérrez Mdel C Chan-Bacab MJ Cedillo-Rivera R Moo-Puc R Hernández-Nuñez E 《Bioorganic & medicinal chemistry letters》2011,21(10):3168-3171
We have synthesized two new benzologues of Nitazoxanide (NIT) and Tizoxanide (TIZ), using a short synthetic route. Both compounds were tested in vitro against six protozoa (Giardia intestinalis, Trichomonas vaginalis, Entamoeba histolytica, Plasmodium berghei, Leishmania mexicana and Trypanosoma cruzi). Compound 1 (benzologue of NIT) showed broad antiprotozoal effect against all parasites tested, showing IC50’s <5μM. This compound was five-times more active than NIT, and 18-times more potent than metronidazole against G. intestinalis. It was 10-times more active than pentamidine against L. mexicana, and it was sevenfold more potent than benznidazole versus T. cruzi. This compound could be considered as a new broad spectrum antiprotozoal agent. 相似文献
100.
Improta G Zupa A Fillmore H Deng J Aieta M Musto P Liotta LA Broaddus W Petricoin EF Wulfkuhle JD 《Journal of proteome research》2011,10(7):3089-3097
Brain metastases are the most common fatal complication of systemic cancer, especially of lung (40-50%) and breast (20-30%) cancers. In this era of personalized therapy, there is a critical need to uncover the signaling architecture of brain metastases; however, little is known about what signaling pathways are activated in the context of the brain microenvironment. Using a unique study set of 42 brain metastases from patients with breast or nonsmall cell lung cancer (NSCLC), the phosphorylation/activation states of 128 key signaling proteins involved in cancer signaling were measured in laser capture microdissected tumor epithelium using reverse phase protein microarray (RPMA) technology. Distinct pathway activation subgroups from both breast and lung metastases were underpinned by, among others, ERBB2, AKT, mTOR, EGFR, SMAD, and ERK-p38 signaling. Breast cancer metastases showed significantly (p < 0.05) higher activation of the c-ERBB2/IGFR-AKT pathway network compared to NSCLC metastases, whereas NSCLC metastases to the brain exhibited higher relative levels of many members of the EGFR-ERK signaling network. Protein pathway activation mapping using RPMA revealed both the heterogeneity of signaling networks in brain metastases that would require a prior stratification to targeted therapies as well as the requirement of direct analysis of the metastatic lesion. 相似文献