Results 141 to 150 of about 2,161 (179)
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Bioorganicheskaia khimiia, 1985
Psychosine prepared from bovine brain cerebroside was used for synthesis of galactosphingolipids with DL-, D-, or L-2-hydroxyhexadecanoic acids and 6-(2'-anthroyl) hexanoic acid. Psychosine was N-acetyl with p-nitrophenyl 2-acetoxyhexadecanoates in the presence of hydroxybenzotriazole to give cerebrosides. The 6-(2'-anthroyl)hexanoic acid reaction with
E V, Dokolina +4 more
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Psychosine prepared from bovine brain cerebroside was used for synthesis of galactosphingolipids with DL-, D-, or L-2-hydroxyhexadecanoic acids and 6-(2'-anthroyl) hexanoic acid. Psychosine was N-acetyl with p-nitrophenyl 2-acetoxyhexadecanoates in the presence of hydroxybenzotriazole to give cerebrosides. The 6-(2'-anthroyl)hexanoic acid reaction with
E V, Dokolina +4 more
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1970
Cerebrosides contain three moieties: a fatty amine, a fatty acid, and a hexose. The fatty amine is usually sphingosine, an 18-carbon straight-chain primary amine characterized by 2 hydroxyls (one of them allylic) and 1 amine group. A small amount of dihydrosphingosine occurs also.
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Cerebrosides contain three moieties: a fatty amine, a fatty acid, and a hexose. The fatty amine is usually sphingosine, an 18-carbon straight-chain primary amine characterized by 2 hydroxyls (one of them allylic) and 1 amine group. A small amount of dihydrosphingosine occurs also.
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A general method for the preparation of cerebrosides
Archives of Biochemistry and Biophysics, 1953Abstract A new method applicable to spleen and brain tissue for the large-scale preparation of cerebrosides is described. The procedure involves the extraction of total lipides from fresh tissue with a boiling mixture of chloroform-methanol and the isolation of the cerebrosides by virtue of their property of accumulating at the interphase zone when ...
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Chemistry of Phosphatides and Cerebrosides
Physiological Reviews, 1952W D, CELMER, H E, CARTER
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Cerebrosides and cerebroside sulfates of the brain of the harp seal
Chemistry of Natural Compounds, 1984S. G. Batrakov +4 more
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Lonijaposides, novel cerebrosides from Lonicera japonica
Tetrahedron, 2006Neeraj Kumar, Bikram Singh
exaly
Cerebrosides from the Roots of Serratula chinensis
Molecules, 2006Tie-Jun Ling, Tao Xia, Xiaoyi Wei
exaly

