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Общее количество найденных документов : 57
Показаны документы с 1 по 20
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1.
| Salituro Inhibitors of p38
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2.
| Baskys Neuroprotective effects of mitogen-activated protein kinase (MAPK) cascade inhibitors
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| Baskys Neuroprotective effects of mitogen-activated protein kinase (MAPK) cascade inhibitors
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| Macroheterocylic compounds useful as kinase inhibitors
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| Benzazole derivatives and their use as JNK modulators
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| Selected derivatives of K252A
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| Selected derivatives of K252A
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| Inhibition of agonist-specific desensitization of 'бета'2 adrenergic receptors
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| Inhibition of agonist-specific desensitization of 'бета'2 adrenergic receptors
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10.
| Advances in kinase targeting: current clinical use and clinical trials // Trends Pharmacol. Sci., 2014. Vol. 35, N 11.-С.604-620
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| Vasodilatory effect of a novel Rho-kinase inhibitor, DL0805-2, on the rat mesenteric artery and its potential mechanisms // Cardiov. Drugs and Ther., 2014. Vol. 28, N 5.-С.415-424
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| Discovery of TAK-960: An orally available small molecule inhibitor of polo-like kinase 1 (PLK1) // Bioorg. and Med. Chem. Lett., 2013. Vol. 23, N 12.-С.3662-3666
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| Vijayakrishnan Treating inflammation with the Janus kinase inhibiror CP-690,550 // Trends Pharmacol. Sci., 2011. Vol. 32, N 1.-С.25-34
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14.
| Structure-based lead identification of ATP-competitive MK2 inhibitors // Bioorg. and Med. Chem. Lett., 2011. Vol. 21, N 12.-С.3818-3822
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| Comparative renal excretion of VX-702, a novel p38 MAPK inhibitor, and methotrexate in the perfused rat kidney mode // Drug Dev. and Ind. Pharm., 2010. Vol. 36, N 3.-С.315-322
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| Подавление активности JNK MARK в регуляции синтеза коллагена при раневом процессе // Бюл. Вост.-Сиб. науч. центра СО РАМН, 2010, N 5.-С.177-179
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| Подавление активности JNK MARK в регуляции синтеза коллагена при раневом процессе // Бюл. Вост.-Сиб. науч. центра СО РАМН, 2010, N 5.-С.177-179
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18.
| Механическая прочность рубцовой ткани в условиях подавления активности p38 MAP-киназы // Бюл. Вост.-Сиб. науч. центра СО РАМН, 2010, N 5.-С.180-181
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| Identification of 4,5-dihydro-1H-pyrazolo[4,3-h]quinazoline derivatives as a new class of orally and selective polo-like kinase 1 inhibitors // J. Med. Chem., 2010. Vol. 53, N 9.-С.3532-3551
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| Механическая прочность рубцовой ткани в условиях подавления активности p38 MAP-киназы // Бюл. Вост.-Сиб. науч. центра СО РАМН, 2010, N 5.-С.180-181
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