Zobrazeno 1 - 10
of 34
pro vyhledávání: '"N. F. Sepetov"'
Publikováno v:
Bioorganicheskaia khimiia. 17(10)
New analogues of atrial peptides of rat were synthesized by classical methods of peptide chemistry in solution. They contain a D-amino acid residue in the C-terminal part and a residue of mercaptopropionic acid in the N-terminal part of the molecule.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::737f05e00471fa0b43c5ee15e3b84147
https://pubmed.ncbi.nlm.nih.gov/1839496
https://pubmed.ncbi.nlm.nih.gov/1839496
Autor:
N F, Sepetov, M A, Krymsky, M V, Ovchinnikov, Z D, Bespalova, O L, Isakova, M, Soucek, M, Lebl
Publikováno v:
Peptide research. 4(5)
We reported earlier that peptides containing glycine as the third amino acid from the amino end undergo sequence rearrangement of the first two amino acid residues. In the course of this experimental verification of the suggested reaction mechanism,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::4e5da9c2ec5738ca73c36e94ec2aa25a
https://pubmed.ncbi.nlm.nih.gov/1802242
https://pubmed.ncbi.nlm.nih.gov/1802242
Publikováno v:
Bioorganicheskaia khimiia. 17(2)
Reductive cleavage of the riboflavin-binding glycoprotein from hen egg white with LiBH4/tert-BuOH followed by NaBH4 treatment gave rise to oligosaccharide alditols. After fractionation by HPLC two individual oligosaccharide alditols of a hybrid type
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::19de8ce11b84bf1e6f9b6674e5df7804
https://pubmed.ncbi.nlm.nih.gov/1863284
https://pubmed.ncbi.nlm.nih.gov/1863284
Publikováno v:
Peptides 1990 ISBN: 9789072199089
Peptides 1990
Peptides 1990
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a4fb500063f6b6a40ec711ecb4d2b10c
https://doi.org/10.1007/978-94-011-3034-9_283
https://doi.org/10.1007/978-94-011-3034-9_283
Publikováno v:
Peptides 1990 ISBN: 9789072199089
Peptides 1990
Peptides 1990
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::be671a560bd1808760047631014477c4
https://doi.org/10.1007/978-94-011-3034-9_34
https://doi.org/10.1007/978-94-011-3034-9_34
Publikováno v:
Bioorganicheskaia khimiia. 16(7)
Using LiBH4/ButOH treatment, oligosaccharides were cleaved off the hen egg white riboflavin-binding glycoprotein. HPLC led to the isolation of four fucose-containing oligosaccharide alditols, whose structure was elucidated by means of 1H NMR 500 MHz
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::48763fb33cfe442467c9bf7553d9e202
https://pubmed.ncbi.nlm.nih.gov/2242056
https://pubmed.ncbi.nlm.nih.gov/2242056
Publikováno v:
Bulletin of the Academy of Sciences of the USSR Division of Chemical Science. 29:1499-1503
A stereospecific migration of the axial substituent (either methyl or acyl group) from the geminal node was discovered when propyne is acylated with the cis- and trans-4-tert-butyl-1-methylcyclohexanoylcarbonyl cations.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4fe2d792cd7e5e76ec5d1d99adb0253f
https://doi.org/10.1007/bf01168282
https://doi.org/10.1007/bf01168282
Autor:
V. P. Dobrynin, A. P. Skoldinov, N. F. Sepetov, G. A. Romanova, S. S. Trofimov, R. U. Ostrovskaya, O. L. Isakova, T. A. Gudasheva
Publikováno v:
Bulletin of Experimental Biology and Medicine. 104:1561-1564
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bb88ea32bc9a3efb8d857e64657a3697
https://doi.org/10.1007/bf00845081
https://doi.org/10.1007/bf00845081
Publikováno v:
Chemistry of Heterocyclic Compounds. 18:1040-1043
The structure of substituted 3H,6H-6-sila-3-azaaceanthrylenes was confirmed as a result of an analysis of the PMR spectra and by the spectra at 360 MHz. Computer analysis of the ABCD spectrum of the phenylene protons demonstrated the characteristic n
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d877e8f8fd35444aa0f9deeb84184c94
https://doi.org/10.1007/bf00503189
https://doi.org/10.1007/bf00503189
Publikováno v:
Chemistry of Heterocyclic Compounds. 16:1003-1006
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5f790597aacafc61343bee2aaee5bdd7
https://doi.org/10.1007/bf00496597
https://doi.org/10.1007/bf00496597