Mono-α-carbamoylethylthio-Substituted Pyrazolo[3,4-d]pyrimidines: the Position of Substitution
Тип публикации: Journal Article
Дата публикации: 1991-01-01
scimago Q3
wos Q4
БС3
SJR: 0.279
CiteScore: 2.6
Impact factor: 0.9
ISSN: 00049425, 14450038
General Chemistry
Краткое описание
Pyrazolo [3,4-d] pyrimidines are a general class of compounds which exhibit adenosine receptor affinity. One particular compound, α-{6-(1α-carbamoylethylthio)-1-phenylpyrazolo-[3,4-d]pyrimidin-4-ylthio} propionamide (1a), has been shown to have antagonist activity an order of magnitude greater than theophylline at the A1 adenosine receptor. The synthesis, structural elucidation by n.m.r. spectroscopy, and adenosine receptor affinity of the mono-α- carbamoylethylthio analogue is now reported.
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Scammells P., Tucker D. Mono-α-carbamoylethylthio-Substituted Pyrazolo[3,4-d]pyrimidines: the Position of Substitution // Australian Journal of Chemistry. 1991. Vol. 44. No. 5. p. 753.
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Scammells P., Tucker D. Mono-α-carbamoylethylthio-Substituted Pyrazolo[3,4-d]pyrimidines: the Position of Substitution // Australian Journal of Chemistry. 1991. Vol. 44. No. 5. p. 753.
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TY - JOUR
DO - 10.1071/CH9910753
UR - https://doi.org/10.1071/CH9910753
TI - Mono-α-carbamoylethylthio-Substituted Pyrazolo[3,4-d]pyrimidines: the Position of Substitution
T2 - Australian Journal of Chemistry
AU - Scammells, Peter
AU - Tucker, DJ
PY - 1991
DA - 1991/01/01
PB - CSIRO Publishing
SP - 753
IS - 5
VL - 44
SN - 0004-9425
SN - 1445-0038
ER -
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@article{1991_Scammells,
author = {Peter Scammells and DJ Tucker},
title = {Mono-α-carbamoylethylthio-Substituted Pyrazolo[3,4-d]pyrimidines: the Position of Substitution},
journal = {Australian Journal of Chemistry},
year = {1991},
volume = {44},
publisher = {CSIRO Publishing},
month = {jan},
url = {https://doi.org/10.1071/CH9910753},
number = {5},
pages = {753},
doi = {10.1071/CH9910753}
}
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MLA
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Scammells, Peter, and DJ Tucker. “Mono-α-carbamoylethylthio-Substituted Pyrazolo[3,4-d]pyrimidines: the Position of Substitution.” Australian Journal of Chemistry, vol. 44, no. 5, Jan. 1991, p. 753. https://doi.org/10.1071/CH9910753.