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Specific Hydrogen Bonding of Barbiturates to Adenine Derivatives
Barbiturates form strong, specific hydrogen bonds with derivatives of adenine. This highly specific interaction which is more extensive than the hydrogen bonding between thymine (or uracil) derivatives and adenine derivatives may help to explain the different biological effects of barbiturates.
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Published in: | Nature (London) 1968-04, Vol.218 (5136), p.69-72 |
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container_end_page | 72 |
container_issue | 5136 |
container_start_page | 69 |
container_title | Nature (London) |
container_volume | 218 |
creator | KYOGOKU, YOSHIMASA LORD, R. C. RICH, ALEXANDER |
description | Barbiturates form strong, specific hydrogen bonds with derivatives of adenine. This highly specific interaction which is more extensive than the hydrogen bonding between thymine (or uracil) derivatives and adenine derivatives may help to explain the different biological effects of barbiturates. |
doi_str_mv | 10.1038/218069a0 |
format | article |
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subjects | Adenine Barbiturates Chemical Phenomena Chemistry Humanities and Social Sciences Infrared Rays Models, Theoretical multidisciplinary Protein Binding Science Science (multidisciplinary) Spectrum Analysis Thymine Uracil |
title | Specific Hydrogen Bonding of Barbiturates to Adenine Derivatives |
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