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studied O-alkylation of 4-[(1H-azol-1-yl)methyl]phenols with various alkylating agents, e.g., n


N - [( пиридин 4-карбониламино) карбамотиоил] фуран -2- карбоксамид - новая, связывающая рибсому бактерий перспективная антимикробная молекулаN - [( пиридин 4-карбониламино) карбамотиоил] фуран -2- карбоксамид - новая, связывающая рибсому

derivatives gives a mixture of N1 - and N3 -monosubstituted products, and the profound N



N-6-methyladenosine (m(6)A) RNA modification, a dynamic and reversible process, is essential

not yet been investigated. Methods: Data from three independent cohorts from the USA (n=1

) lncRNAs genes with COPD. DNA samples from COPD patients (N = 703) and healthy individuals (N = 655

total of 28 4-oxo-N-phenyl-1,4-dihydroquinoline-3-carboxamide derivatives were designed and synthesized

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