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排序方式: 共有3496条查询结果,搜索用时 15 毫秒
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Geometriae Dedicata - We show that an Anosov map has a geodesic axis on the curve graph of the torus. The direct corollary of our result is the stable translation length of an Anosov map on the... 相似文献
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Kikuchi Shin Koga Nobuyoshi Yamazaki Atsushi 《Journal of Thermal Analysis and Calorimetry》2019,137(4):1211-1224
Journal of Thermal Analysis and Calorimetry - Thermal behaviors of two different siliceous concretes used in a sodium-cooled fast reactor were comparatively investigated in a temperature range from... 相似文献
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Dr. Jaebong Jang Dr. Ciric To Dr. Dries J. H. De Clercq Dr. Eunyoung Park Charles M. Ponthier Bo Hee Shin Mierzhati Mushajiang Dr. Radosław P. Nowak Dr. Eric S. Fischer Dr. Michael J. Eck Dr. Pasi A. Jänne Dr. Nathanael S. Gray 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2020,132(34):14589-14597
Targeting epidermal growth factor receptor (EGFR) through an allosteric mechanism provides a potential therapeutic strategy to overcome drug-resistant EGFR mutations that emerge within the ATP binding site. Here, we develop an allosteric EGFR degrader, DDC-01-163, which can selectively inhibit the proliferation of L858R/T790M (L/T) mutant Ba/F3 cells while leaving wildtype EGFR Ba/F3 cells unaffected. DDC-01-163 is also effective against osimertinib-resistant cells with L/T/C797S and L/T/L718Q EGFR mutations. When combined with an ATP-site EGFR inhibitor, osimertinib, the anti-proliferative activity of DDC-01-163 against L858R/T790M EGFR-Ba/F3 cells is enhanced. Collectively, DDC-01-163 is a promising allosteric EGFR degrader with selective activity against various clinically relevant EGFR mutants as a single agent and when combined with an ATP-site inhibitor. Our data suggests that targeted protein degradation is a promising drug development approach for mutant EGFR. 相似文献
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Hoyeon Lee Soojin Uhm Jung‐Won Shin Hyun Mi Jeon Sun Dongbang Hyo Sung Jung Yun‐Cheol Na Prof. Chulhun Kang Prof. Jong Seung Kim 《化学:亚洲杂志》2015,10(12):2695-2700
A galactose‐appended drug delivery system released camptothecin (CPT) to lysosomes of HepG2 hepatoma cells, resulting in the cell resistance to the anticancer drug. We found that the resistance to CPT is caused by alteration of the drug release from the prodrug in lysosomes, emphasizing that the final delivery locations may critically influence drug efficacy. 相似文献
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Effect of branched alkyl side chains on the performance of thin‐film transistors and photovoltaic cells fabricated with isoindigo‐based conjugated polymers 下载免费PDF全文
Gi Eun Park Jicheol Shin Dae Hee Lee Min Ju Cho Dong Hoon Choi 《Journal of polymer science. Part A, Polymer chemistry》2015,53(10):1226-1234
New isoindigo and di(thienyl)ethylene‐containing π‐extended conjugated polymers with different branched side chains were synthesized to investigate their physical properties and device performance in thin‐film transistors and photovoltaic cells. 11‐Butyltricosane (S3) and 11‐heptyltricosane (S6) groups were used as side‐chain moieties tethered to isoindigo units. The linking groups between the polymer backbone and bifurcation point in the branched side chain differ in the two polymers (i.e., PIDTE‐S3 and PIDTE‐S6 ). The polymers bearing S6 side chains showed much better charge transport behavior than those with S3 side chains. Thermally annealed PIDTE‐S6 film exhibited an outstanding hole mobility of 4.07 cm2 V?1 s?1 under ambient conditions. Furthermore, bulk heterojunction organic photovoltaic cells made from a blend film of PIDTE‐S3 and (6,6)‐phenyl C61‐butyric acid methyl ester demonstrated promising device performance with a power conversion efficiency in the range of 4.9–5.0%. © 2015 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 2015 , 53, 1226–1234 相似文献
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Dr. Wan‐Ling Liu Ni‐Shin Yang Ya‐Ting Chen Stephen Lirio Cheng‐You Wu Prof. Chia‐Her Lin Prof. Hsi‐Ya Huang 《Chemistry (Weinheim an der Bergstrasse, Germany)》2015,21(1):115-119
A green and sustainable strategy synthesizes clinical medicine warfarin anticoagulant by using lipase‐supported metal–organic framework (MOF) bioreactors (see scheme). These findings may be beneficial for future studies in the industrial production of chemical, pharmaceutical, and agrochemical precursors. 相似文献
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