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The following terms were not found in PubMed: 8-benzoyl-3-, 2-dihydroxyhex-3-enyl, -9-hydroxy-8-methoxy-2-methyl-4-oxa-7-azaspiro
Unknown fields were ignored: [4.4]
Page 1
Synthesis and Aminomethylation of 2-Amino-4-(2-chlorophenyl)-6-(dicyanomethyl)-1,4-dihydropyridine-3,5-dicarbonitrile N-Methylmorpholinium Salt.
Russ J Gen Chem. 2022;92(5):779-790. doi: 10.1134/S1070363222050061. Epub 2022 Jun 14.
Russ J Gen Chem. 2022.
PMID: 35729943
Free PMC article.
Sequential reaction of 2-chlorobenzaldehyde, cyanothioacetamide, and malononitrile dimer in the presence of an excess of N-methylmorpholine resulted in the formation of N-methylmorphlinium salt of 2-amino-4-(2-chlorophenyl)-6-(dicyanomethyl)-1,4-dihydropyridine-3,5-dicarbo …
Sequential reaction of 2-chlorobenzaldehyde, cyanothioacetamide, and malononitrile dimer in the presence of an excess of N-methylmorpholine …
Metabolism of the lipid peroxidation product 4-hydroxynonenal by isolated hepatocytes and by liver cytosolic fractions.
Esterbauer H, Zollner H, Lang J.
Esterbauer H, et al.
Biochem J. 1985 Jun 1;228(2):363-73. doi: 10.1042/bj2280363.
Biochem J. 1985.
PMID: 3160340
Free PMC article.
The various findings strongly suggest that hepatocytes and rat liver cytosol respectively convert 4-hydroxynonenal enzymically is the corresponding alcohol, non-2-ene-1,4-diol, according to the equation: CH3-[CH2]4-CH(OH)-CH = CH-CHO + NADH + H+----CH3 …
The various findings strongly suggest that hepatocytes and rat liver cytosol respectively convert 4-hydroxynonenal enzymically is the corres …
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