2′,3′-seco pyrimidine nucleosides and nucleotides, including structural analogues of 3′:5′-cyclic CMP and UMP, and their behaviour in several enzyme systems
1
Institute of Biochemistry and Biophysics, Academy of Sciences, 02-532 Warszawa, Poland.
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3
Institute of Biochemistry & Biophysics, Academy of Sciences, 02-532 Warszawa, Poland
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Publication type: Journal Article
Publication date: 1986-05-01
scimago Q2
wos Q3
SJR: 0.748
CiteScore: 4.9
Impact factor: 2.2
ISSN: 0006291X, 10902104
PubMed ID:
3718515
Biochemistry
Molecular Biology
Cell Biology
Biophysics
Abstract
Cyclization of 2',3'-seco-5'- CMP and UMP with dicyclohexylcarbodiimide leads to 2',3'-seco-3':5'- cCMP and cUMP, formal structural analogues of 3':5'- cCMP and cUMP. POCl3 phosphorylation of 2',3'-secocytidine gave the same product in 50% yield, plus three additional seco nucleotides, one of which was independently obtained by enzymatic phosphorylation with the wheat shoot phosphotransferase system. The behaviour of these nucleotides has been examined in several enzyme systems. In particular, the seco 3':5'- cyclic phosphates are resistant to beef heart cyclic nucleotide phosphodiesterase, but are slowly hydrolyzed to the monophosphates by higher plant cyclic nucleotide phosphodiesterase.
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Lassota P. et al. 2′,3′-seco pyrimidine nucleosides and nucleotides, including structural analogues of 3′:5′-cyclic CMP and UMP, and their behaviour in several enzyme systems // Biochemical and Biophysical Research Communications. 1986. Vol. 137. No. 1. pp. 453-460.
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Lassota P., Kazimierczuk Z., Zan Kowalczewska M., Shugar D. 2′,3′-seco pyrimidine nucleosides and nucleotides, including structural analogues of 3′:5′-cyclic CMP and UMP, and their behaviour in several enzyme systems // Biochemical and Biophysical Research Communications. 1986. Vol. 137. No. 1. pp. 453-460.
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RIS
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TY - JOUR
DO - 10.1016/0006-291x(86)91231-3
UR - https://doi.org/10.1016/0006-291x(86)91231-3
TI - 2′,3′-seco pyrimidine nucleosides and nucleotides, including structural analogues of 3′:5′-cyclic CMP and UMP, and their behaviour in several enzyme systems
T2 - Biochemical and Biophysical Research Communications
AU - Lassota, P
AU - Kazimierczuk, Z.
AU - Zan Kowalczewska, M
AU - Shugar, D.
PY - 1986
DA - 1986/05/01
PB - Elsevier
SP - 453-460
IS - 1
VL - 137
PMID - 3718515
SN - 0006-291X
SN - 1090-2104
ER -
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BibTex (up to 50 authors)
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@article{1986_Lassota,
author = {P Lassota and Z. Kazimierczuk and M Zan Kowalczewska and D. Shugar},
title = {2′,3′-seco pyrimidine nucleosides and nucleotides, including structural analogues of 3′:5′-cyclic CMP and UMP, and their behaviour in several enzyme systems},
journal = {Biochemical and Biophysical Research Communications},
year = {1986},
volume = {137},
publisher = {Elsevier},
month = {may},
url = {https://doi.org/10.1016/0006-291x(86)91231-3},
number = {1},
pages = {453--460},
doi = {10.1016/0006-291x(86)91231-3}
}
Cite this
MLA
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Lassota, P., et al. “2′,3′-seco pyrimidine nucleosides and nucleotides, including structural analogues of 3′:5′-cyclic CMP and UMP, and their behaviour in several enzyme systems.” Biochemical and Biophysical Research Communications, vol. 137, no. 1, May. 1986, pp. 453-460. https://doi.org/10.1016/0006-291x(86)91231-3.