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2012
DOI: 10.1016/j.bmc.2012.01.033
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Phosphodiesterase inhibitors. Part 3: Design, synthesis and structure–activity relationships of dual PDE3/4-inhibitory fused bicyclic heteroaromatic-dihydropyridazinones with anti-inflammatory and bronchodilatory activity

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Cited by 42 publications
(19 citation statements)
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“…DME25 has been reported to have an inhibitory effect on the phosphorylation of the FAK pathway, while treatment with a FAK inhibitor significantly enhanced the effect of DME25 on the FAK pathway [241]. YZX has also demonstrated the ability to not only inhibit the growth of colorectal cancer cells and lung cancer cells but also to suppress the formation of mouse peritoneal tumor nodules in vivo.…”
Section: Yangzheng Xiaojimentioning
confidence: 99%
“…DME25 has been reported to have an inhibitory effect on the phosphorylation of the FAK pathway, while treatment with a FAK inhibitor significantly enhanced the effect of DME25 on the FAK pathway [241]. YZX has also demonstrated the ability to not only inhibit the growth of colorectal cancer cells and lung cancer cells but also to suppress the formation of mouse peritoneal tumor nodules in vivo.…”
Section: Yangzheng Xiaojimentioning
confidence: 99%
“…Subsequently, the interaction between integrins and the cell cytoskeleton system is triggered (76). It has been reported that DME25 exhibited an inhibitory effect on the phosphorylation of the FAK pathway, and that the addition of a FAK inhibitor significantly enhanced the effect of DME25 on the FAK pathway (77). In addition, it was revealed that YZXJ not only inhibited the growth of colorectal and lung cancer cells, but also suppressed the formation of mouse peritoneal tumour nodules in an in vivo study.…”
Section: Tcm Regulates the Adhesion And Motility Of Cancer Cellsmentioning
confidence: 99%
“…The nitration of N ‐(3‐methoxyphenyl)acetamide ( 12 ) also afforded the undesired N ‐(5‐methoxy‐2‐nitrophenyl)acetamide ( 14 ) as a major product rather than 13 (Scheme ). We then adopted a functional group transformation approach starting with 3‐methoxy‐2‐nitrobenzoic acid ( 5 ) that was converted to a Boc‐protected aniline derivative ( 15 ) (Scheme ). The N ‐deprotection of 15 afforded 3‐methoxy‐2‐nitroaniline ( 16 ) that on a Sandmeyer type reaction gave the corresponding bromo derivative 17 .…”
Section: Methodsmentioning
confidence: 99%