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Synthesis of d-(+)-camphor-based: N -acylhydrazones and their antiviral activityThe design and synthesis of a series of novel d-(+)-camphor N-acylhydrazones exhibiting inhibitory

CAMPHOR AND FENCHONE N-ACYLHYDRAZONES AS INHIBITORS OF HANTAAN VIRUS CAUSING HFRSCAMPHOR AND FENCHONE N-ACYLHYDRAZONES AS INHIBITORS OF HANTAAN VIRUS CAUSING HFRS

New class of hantaan virus inhibitors based on conjugation of the isoindole fragment to (+)-camphor or (−)-fenchone hydrazonesvThis work presents the design and synthesis of camphor, fenchone, and norcamphor N

Mono-and sesquiterpenes as a starting platform for the development of antiviral drugs

Genotoxicological safety assessment of a new antiparkinsonian substance ((1r,2r,6s)-3-methyl-6-(prop-1-en-2-yl)cyclohex-3-ene-1,2-diol)

Genotoxicological safety assessment of a new antiparkinsonian substance ((1r,2r,6s)-3-methyl-6-(prop-1-en-2-yl)cyclohex-3-ene-1,2-diol)

The action of monoterpenoids with promising antiparkinsonian activity on fertility of Drosophila melanogaster

Synthesis and Antiviral Activity of Camphene Derivatives against Different Types of Viruses influenza virus A/PR/8/34 (H1N1), Ebola virus (EBOV), and the Hantaan virus. The lead-compound 2a

Soloxolone methyl inhibits influenza virus replication and reduces virus-induced lung inflammation that SM exhibits antiviral activity against the H1N1 influenza A virus in a dose-dependent manner causing

Cyano Enone-Bearing Triterpenoid Soloxolone Methyl Inhibits Epithelial-Mesenchymal Transition of Human Lung Adenocarcinoma Cells In Vitro and Metastasis of Murine Melanoma In Vivo metalloproteinases MMP-2/-9 and c-Jun N-terminal protein kinase 1 (JNK1) can be considered as hypothetical primary

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